MedsFacts Reports covering CYCLOPHOSPHAMIDE
Directory listing ordered by most common adverse events for CYCLOPHOSPHAMIDE
Please choose an event type to view the corresponding MedsFacts report:
FEBRILE NEUTROPENIA ( 4212 FDA reports)
NEUTROPENIA ( 2894 FDA reports)
PYREXIA ( 2893 FDA reports)
PNEUMONIA ( 1880 FDA reports)
DIARRHOEA ( 1702 FDA reports)
SEPSIS ( 1670 FDA reports)
NAUSEA ( 1576 FDA reports)
THROMBOCYTOPENIA ( 1515 FDA reports)
ANAEMIA ( 1499 FDA reports)
DYSPNOEA ( 1444 FDA reports)
INFECTION ( 1434 FDA reports)
VOMITING ( 1385 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1215 FDA reports)
PANCYTOPENIA ( 1178 FDA reports)
MUCOSAL INFLAMMATION ( 1076 FDA reports)
HYPOTENSION ( 1067 FDA reports)
DEATH ( 1035 FDA reports)
PLATELET COUNT DECREASED ( 1028 FDA reports)
RESPIRATORY FAILURE ( 1006 FDA reports)
FATIGUE ( 1006 FDA reports)
HAEMOGLOBIN DECREASED ( 927 FDA reports)
LEUKOPENIA ( 927 FDA reports)
PLEURAL EFFUSION ( 872 FDA reports)
RENAL FAILURE ( 872 FDA reports)
DRUG INEFFECTIVE ( 851 FDA reports)
MULTI-ORGAN FAILURE ( 834 FDA reports)
SEPTIC SHOCK ( 813 FDA reports)
ASTHENIA ( 782 FDA reports)
ABDOMINAL PAIN ( 768 FDA reports)
DEHYDRATION ( 756 FDA reports)
MYELODYSPLASTIC SYNDROME ( 753 FDA reports)
PAIN ( 719 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 712 FDA reports)
GRAFT VERSUS HOST DISEASE ( 709 FDA reports)
PULMONARY EMBOLISM ( 703 FDA reports)
HEADACHE ( 698 FDA reports)
DISEASE PROGRESSION ( 697 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 695 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 671 FDA reports)
RENAL FAILURE ACUTE ( 670 FDA reports)
NEUTROPHIL COUNT DECREASED ( 661 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 624 FDA reports)
OSTEONECROSIS ( 622 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 594 FDA reports)
INTERSTITIAL LUNG DISEASE ( 591 FDA reports)
COUGH ( 574 FDA reports)
RASH ( 570 FDA reports)
BONE MARROW FAILURE ( 568 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 554 FDA reports)
CARDIAC FAILURE ( 546 FDA reports)
MALAISE ( 541 FDA reports)
STOMATITIS ( 531 FDA reports)
WEIGHT DECREASED ( 530 FDA reports)
CONVULSION ( 522 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 518 FDA reports)
HYPERTENSION ( 502 FDA reports)
HERPES ZOSTER ( 490 FDA reports)
NEUROPATHY PERIPHERAL ( 485 FDA reports)
BACK PAIN ( 478 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 475 FDA reports)
TACHYCARDIA ( 474 FDA reports)
DEEP VEIN THROMBOSIS ( 473 FDA reports)
NEUTROPENIC SEPSIS ( 473 FDA reports)
CHILLS ( 472 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 468 FDA reports)
ARTHRALGIA ( 449 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 448 FDA reports)
CHEST PAIN ( 447 FDA reports)
CONSTIPATION ( 442 FDA reports)
ATRIAL FIBRILLATION ( 433 FDA reports)
DIZZINESS ( 431 FDA reports)
HYPOKALAEMIA ( 427 FDA reports)
HYPOXIA ( 426 FDA reports)
ASCITES ( 418 FDA reports)
PAIN IN EXTREMITY ( 415 FDA reports)
RENAL IMPAIRMENT ( 414 FDA reports)
STAPHYLOCOCCAL INFECTION ( 412 FDA reports)
HEPATIC FAILURE ( 412 FDA reports)
OEDEMA PERIPHERAL ( 410 FDA reports)
BLOOD BILIRUBIN INCREASED ( 408 FDA reports)
STEM CELL TRANSPLANT ( 406 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 398 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 397 FDA reports)
CONFUSIONAL STATE ( 395 FDA reports)
HEPATITIS B ( 395 FDA reports)
BLOOD CREATININE INCREASED ( 383 FDA reports)
DRUG TOXICITY ( 383 FDA reports)
SYNCOPE ( 383 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 379 FDA reports)
URINARY TRACT INFECTION ( 377 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 375 FDA reports)
LYMPHOPENIA ( 371 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 368 FDA reports)
CONDITION AGGRAVATED ( 367 FDA reports)
CARDIAC ARREST ( 359 FDA reports)
BONE PAIN ( 356 FDA reports)
LUNG INFILTRATION ( 350 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 348 FDA reports)
OEDEMA ( 347 FDA reports)
CYSTITIS HAEMORRHAGIC ( 338 FDA reports)
DECREASED APPETITE ( 335 FDA reports)
PULMONARY OEDEMA ( 334 FDA reports)
PNEUMONITIS ( 329 FDA reports)
LIVER DISORDER ( 328 FDA reports)
PARAESTHESIA ( 328 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 326 FDA reports)
CELLULITIS ( 319 FDA reports)
ERYTHEMA ( 319 FDA reports)
LYMPHADENOPATHY ( 317 FDA reports)
RESPIRATORY DISTRESS ( 315 FDA reports)
DRUG INTERACTION ( 311 FDA reports)
DEPRESSION ( 297 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 293 FDA reports)
TUMOUR LYSIS SYNDROME ( 290 FDA reports)
EJECTION FRACTION DECREASED ( 288 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 288 FDA reports)
NEOPLASM MALIGNANT ( 286 FDA reports)
ANXIETY ( 285 FDA reports)
HYPONATRAEMIA ( 285 FDA reports)
HAEMATOCRIT DECREASED ( 284 FDA reports)
MYALGIA ( 284 FDA reports)
AGRANULOCYTOSIS ( 282 FDA reports)
CARDIOMYOPATHY ( 282 FDA reports)
FALL ( 278 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 276 FDA reports)
MUSCULAR WEAKNESS ( 276 FDA reports)
MYOCARDIAL INFARCTION ( 272 FDA reports)
DYSPHAGIA ( 271 FDA reports)
FUNGAL INFECTION ( 270 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 264 FDA reports)
LUNG DISORDER ( 258 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 257 FDA reports)
HEPATOTOXICITY ( 255 FDA reports)
MULTIPLE MYELOMA ( 255 FDA reports)
HAEMATURIA ( 253 FDA reports)
NEUROTOXICITY ( 248 FDA reports)
ATELECTASIS ( 247 FDA reports)
CEREBRAL HAEMORRHAGE ( 247 FDA reports)
ORAL CANDIDIASIS ( 244 FDA reports)
CARDIO-RESPIRATORY ARREST ( 243 FDA reports)
LOSS OF CONSCIOUSNESS ( 240 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 238 FDA reports)
HYPERGLYCAEMIA ( 238 FDA reports)
ANOREXIA ( 237 FDA reports)
PRURITUS ( 237 FDA reports)
ALOPECIA ( 235 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 234 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 233 FDA reports)
VENOOCCLUSIVE DISEASE ( 233 FDA reports)
HYPERSENSITIVITY ( 232 FDA reports)
COLITIS ( 231 FDA reports)
HYPOAESTHESIA ( 231 FDA reports)
CANDIDIASIS ( 230 FDA reports)
LUNG INFECTION ( 228 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 227 FDA reports)
DISEASE RECURRENCE ( 226 FDA reports)
THROMBOSIS ( 226 FDA reports)
PERICARDIAL EFFUSION ( 225 FDA reports)
EPISTAXIS ( 224 FDA reports)
OSTEONECROSIS OF JAW ( 222 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 221 FDA reports)
SINUSITIS ( 218 FDA reports)
HEPATITIS ( 215 FDA reports)
ASPERGILLOSIS ( 212 FDA reports)
BACTERAEMIA ( 212 FDA reports)
WEIGHT INCREASED ( 212 FDA reports)
TREMOR ( 210 FDA reports)
LYMPHOMA ( 210 FDA reports)
HAEMORRHAGE ( 209 FDA reports)
PULMONARY FIBROSIS ( 209 FDA reports)
BACTERIAL INFECTION ( 208 FDA reports)
OSTEOMYELITIS ( 208 FDA reports)
OXYGEN SATURATION DECREASED ( 207 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 204 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 202 FDA reports)
BONE DISORDER ( 201 FDA reports)
ABDOMINAL PAIN UPPER ( 200 FDA reports)
FEBRILE BONE MARROW APLASIA ( 200 FDA reports)
SOMNOLENCE ( 200 FDA reports)
PAIN IN JAW ( 197 FDA reports)
ABDOMINAL DISTENSION ( 194 FDA reports)
CEREBROVASCULAR ACCIDENT ( 193 FDA reports)
BLOOD CULTURE POSITIVE ( 192 FDA reports)
HEART RATE INCREASED ( 192 FDA reports)
ENCEPHALOPATHY ( 188 FDA reports)
NERVOUS SYSTEM DISORDER ( 187 FDA reports)
HYPERBILIRUBINAEMIA ( 185 FDA reports)
COMA ( 184 FDA reports)
HAEMATOTOXICITY ( 184 FDA reports)
HYPOCALCAEMIA ( 184 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 184 FDA reports)
BLOOD PRESSURE DECREASED ( 182 FDA reports)
PULMONARY HAEMORRHAGE ( 181 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 180 FDA reports)
PSEUDOMONAS INFECTION ( 180 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 180 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 180 FDA reports)
LEUKOENCEPHALOPATHY ( 180 FDA reports)
APLASIA ( 176 FDA reports)
HAEMODIALYSIS ( 176 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 176 FDA reports)
LEUKOCYTOSIS ( 175 FDA reports)
BODY TEMPERATURE INCREASED ( 174 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 172 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 172 FDA reports)
PANCREATITIS ( 172 FDA reports)
PNEUMOTHORAX ( 172 FDA reports)
INSOMNIA ( 171 FDA reports)
RESPIRATORY DISORDER ( 169 FDA reports)
DIABETES MELLITUS ( 168 FDA reports)
GASTRITIS ( 168 FDA reports)
HEPATIC ENZYME INCREASED ( 167 FDA reports)
TRANSAMINASES INCREASED ( 167 FDA reports)
VASCULITIS ( 167 FDA reports)
TOOTH EXTRACTION ( 166 FDA reports)
ADENOVIRUS INFECTION ( 164 FDA reports)
GAIT DISTURBANCE ( 164 FDA reports)
OFF LABEL USE ( 163 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 163 FDA reports)
PULMONARY HYPERTENSION ( 160 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 160 FDA reports)
CARDIOMEGALY ( 159 FDA reports)
COAGULOPATHY ( 159 FDA reports)
CAECITIS ( 158 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 158 FDA reports)
JAUNDICE ( 157 FDA reports)
NO THERAPEUTIC RESPONSE ( 156 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 155 FDA reports)
OROPHARYNGEAL PAIN ( 155 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 154 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 154 FDA reports)
CARDIAC DISORDER ( 152 FDA reports)
PROTEINURIA ( 151 FDA reports)
CHEST DISCOMFORT ( 150 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 150 FDA reports)
MENTAL STATUS CHANGES ( 150 FDA reports)
HEPATOMEGALY ( 149 FDA reports)
INFUSION RELATED REACTION ( 149 FDA reports)
OSTEOPOROSIS ( 149 FDA reports)
BLOOD UREA INCREASED ( 148 FDA reports)
SHOCK ( 148 FDA reports)
LETHARGY ( 147 FDA reports)
OESOPHAGITIS ( 147 FDA reports)
ACUTE RESPIRATORY FAILURE ( 146 FDA reports)
BRADYCARDIA ( 146 FDA reports)
BLOOD SODIUM DECREASED ( 143 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 142 FDA reports)
SINUS TACHYCARDIA ( 141 FDA reports)
CHOLESTASIS ( 141 FDA reports)
INFLAMMATION ( 141 FDA reports)
METASTASES TO BONE ( 141 FDA reports)
SPLENOMEGALY ( 140 FDA reports)
VISUAL ACUITY REDUCED ( 140 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 139 FDA reports)
DYSARTHRIA ( 138 FDA reports)
BK VIRUS INFECTION ( 137 FDA reports)
MUSCULOSKELETAL PAIN ( 137 FDA reports)
ENTEROCOCCAL INFECTION ( 136 FDA reports)
BRONCHITIS ( 135 FDA reports)
ENCEPHALITIS ( 135 FDA reports)
URTICARIA ( 134 FDA reports)
ARRHYTHMIA ( 133 FDA reports)
CEREBRAL INFARCTION ( 133 FDA reports)
DEVICE RELATED INFECTION ( 131 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 131 FDA reports)
METASTASIS ( 131 FDA reports)
NEPHROPATHY TOXIC ( 131 FDA reports)
VIRAL INFECTION ( 131 FDA reports)
SWELLING ( 130 FDA reports)
MUSCLE SPASMS ( 130 FDA reports)
BACTERIAL SEPSIS ( 129 FDA reports)
CYTOGENETIC ABNORMALITY ( 129 FDA reports)
HYPERHIDROSIS ( 128 FDA reports)
BLOOD GLUCOSE INCREASED ( 127 FDA reports)
BLOOD POTASSIUM DECREASED ( 127 FDA reports)
HAEMOLYTIC ANAEMIA ( 127 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 126 FDA reports)
CLOSTRIDIAL INFECTION ( 126 FDA reports)
DYSPNOEA EXERTIONAL ( 126 FDA reports)
ILEUS PARALYTIC ( 126 FDA reports)
LUNG NEOPLASM ( 126 FDA reports)
THERAPY NON-RESPONDER ( 126 FDA reports)
BONE MARROW TRANSPLANT ( 125 FDA reports)
CIRCULATORY COLLAPSE ( 125 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 124 FDA reports)
VISION BLURRED ( 123 FDA reports)
RESPIRATORY TRACT INFECTION ( 122 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 121 FDA reports)
HYPOPHAGIA ( 121 FDA reports)
BLOOD PRESSURE INCREASED ( 120 FDA reports)
COGNITIVE DISORDER ( 120 FDA reports)
NEOPLASM PROGRESSION ( 120 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 120 FDA reports)
POLYNEUROPATHY ( 119 FDA reports)
PROTHROMBIN TIME PROLONGED ( 119 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 119 FDA reports)
APHASIA ( 119 FDA reports)
DIALYSIS ( 119 FDA reports)
HEPATIC STEATOSIS ( 119 FDA reports)
ILEUS ( 119 FDA reports)
METABOLIC ACIDOSIS ( 119 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 119 FDA reports)
DYSURIA ( 118 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 118 FDA reports)
GASTROINTESTINAL DISORDER ( 117 FDA reports)
NECK PAIN ( 117 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 117 FDA reports)
DRUG HYPERSENSITIVITY ( 116 FDA reports)
IMPAIRED HEALING ( 116 FDA reports)
ESCHERICHIA INFECTION ( 115 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 114 FDA reports)
PERITONITIS ( 114 FDA reports)
PRODUCTIVE COUGH ( 114 FDA reports)
RECTAL HAEMORRHAGE ( 114 FDA reports)
ANAPHYLACTIC REACTION ( 112 FDA reports)
BREAST CANCER ( 112 FDA reports)
CARDIOTOXICITY ( 112 FDA reports)
HAEMOPTYSIS ( 112 FDA reports)
HERPES SIMPLEX ( 112 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 111 FDA reports)
TACHYPNOEA ( 111 FDA reports)
PREMATURE BABY ( 110 FDA reports)
SWELLING FACE ( 110 FDA reports)
DISORIENTATION ( 110 FDA reports)
HYPERKALAEMIA ( 110 FDA reports)
INJURY ( 110 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 108 FDA reports)
DEFORMITY ( 108 FDA reports)
NEUTROPENIC COLITIS ( 108 FDA reports)
SUDDEN DEATH ( 108 FDA reports)
VISUAL IMPAIRMENT ( 108 FDA reports)
B-CELL LYMPHOMA ( 107 FDA reports)
BLISTER ( 107 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 107 FDA reports)
MITRAL VALVE INCOMPETENCE ( 106 FDA reports)
ABSCESS ( 105 FDA reports)
HYPOALBUMINAEMIA ( 105 FDA reports)
GASTROENTERITIS ( 104 FDA reports)
GENERALISED OEDEMA ( 104 FDA reports)
CAPILLARY LEAK SYNDROME ( 103 FDA reports)
ORAL PAIN ( 103 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 103 FDA reports)
SKIN EXFOLIATION ( 102 FDA reports)
HEMIPARESIS ( 102 FDA reports)
METASTASES TO LIVER ( 102 FDA reports)
BRAIN OEDEMA ( 101 FDA reports)
IMMUNOSUPPRESSION ( 101 FDA reports)
BRONCHOPNEUMONIA ( 100 FDA reports)
TRANSPLANT REJECTION ( 100 FDA reports)
FLUID OVERLOAD ( 99 FDA reports)
HAEMATEMESIS ( 99 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 98 FDA reports)
GRAND MAL CONVULSION ( 98 FDA reports)
GUILLAIN-BARRE SYNDROME ( 98 FDA reports)
RASH ERYTHEMATOUS ( 98 FDA reports)
PNEUMONIA FUNGAL ( 97 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 97 FDA reports)
CHOLELITHIASIS ( 97 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 97 FDA reports)
LUNG NEOPLASM MALIGNANT ( 96 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 96 FDA reports)
BRONCHIECTASIS ( 95 FDA reports)
DENTAL CARIES ( 95 FDA reports)
INTESTINAL OBSTRUCTION ( 95 FDA reports)
LUNG CONSOLIDATION ( 95 FDA reports)
MOUTH ULCERATION ( 95 FDA reports)
NEUTROPENIC INFECTION ( 95 FDA reports)
BONE LESION ( 94 FDA reports)
BONE MARROW DEPRESSION ( 94 FDA reports)
FLUID RETENTION ( 94 FDA reports)
LEUKAEMIA RECURRENT ( 94 FDA reports)
OPPORTUNISTIC INFECTION ( 94 FDA reports)
ENGRAFTMENT SYNDROME ( 93 FDA reports)
HAEMATOCHEZIA ( 93 FDA reports)
PANCREATITIS ACUTE ( 93 FDA reports)
PULMONARY TOXICITY ( 93 FDA reports)
WHEEZING ( 92 FDA reports)
HAEMORRHOIDS ( 92 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 92 FDA reports)
PALPITATIONS ( 91 FDA reports)
RENAL DISORDER ( 91 FDA reports)
SKIN ULCER ( 91 FDA reports)
URINARY INCONTINENCE ( 91 FDA reports)
URINE OUTPUT DECREASED ( 90 FDA reports)
CYTOLYTIC HEPATITIS ( 90 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 90 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 90 FDA reports)
EMBOLISM ( 90 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 90 FDA reports)
ATAXIA ( 89 FDA reports)
ENTERITIS ( 89 FDA reports)
BLINDNESS ( 88 FDA reports)
EMOTIONAL DISTRESS ( 88 FDA reports)
HEARING IMPAIRED ( 88 FDA reports)
PSEUDOMONAL SEPSIS ( 88 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 88 FDA reports)
STEVENS-JOHNSON SYNDROME ( 88 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 87 FDA reports)
AMNESIA ( 86 FDA reports)
CARDIOVASCULAR DISORDER ( 86 FDA reports)
ORAL INTAKE REDUCED ( 86 FDA reports)
SKIN LESION ( 86 FDA reports)
TRANSPLANT FAILURE ( 84 FDA reports)
BALANCE DISORDER ( 84 FDA reports)
CATHETER RELATED INFECTION ( 84 FDA reports)
DIVERTICULITIS ( 84 FDA reports)
EPILEPSY ( 84 FDA reports)
FLUSHING ( 84 FDA reports)
MEMORY IMPAIRMENT ( 84 FDA reports)
MYOCARDIAL ISCHAEMIA ( 84 FDA reports)
NEPHROTIC SYNDROME ( 84 FDA reports)
ACUTE HEPATIC FAILURE ( 83 FDA reports)
ELECTROLYTE IMBALANCE ( 83 FDA reports)
GASTROINTESTINAL TOXICITY ( 83 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 83 FDA reports)
OSTEOARTHRITIS ( 83 FDA reports)
STREPTOCOCCAL INFECTION ( 83 FDA reports)
POLLAKIURIA ( 82 FDA reports)
POST PROCEDURAL COMPLICATION ( 82 FDA reports)
PREMATURE MENOPAUSE ( 82 FDA reports)
HEPATIC ENCEPHALOPATHY ( 82 FDA reports)
MALIGNANT MELANOMA ( 82 FDA reports)
MYOCARDITIS ( 82 FDA reports)
INFLUENZA ( 81 FDA reports)
RENAL FAILURE CHRONIC ( 81 FDA reports)
RIB FRACTURE ( 81 FDA reports)
SQUAMOUS CELL CARCINOMA ( 81 FDA reports)
SUBDURAL HAEMATOMA ( 81 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 81 FDA reports)
VENTRICULAR TACHYCARDIA ( 81 FDA reports)
PHARYNGITIS ( 80 FDA reports)
ABDOMINAL DISCOMFORT ( 80 FDA reports)
HAEMOLYSIS ( 80 FDA reports)
BLOOD ALBUMIN DECREASED ( 79 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 79 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 79 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 79 FDA reports)
MELAENA ( 79 FDA reports)
OSTEOPENIA ( 79 FDA reports)
RESPIRATORY RATE INCREASED ( 79 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 79 FDA reports)
RASH MACULO-PAPULAR ( 78 FDA reports)
AGITATION ( 78 FDA reports)
APLASIA PURE RED CELL ( 78 FDA reports)
ESCHERICHIA SEPSIS ( 78 FDA reports)
METASTASES TO LUNG ( 78 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 77 FDA reports)
GRANULOCYTOPENIA ( 77 FDA reports)
INFLUENZA LIKE ILLNESS ( 77 FDA reports)
JC VIRUS INFECTION ( 77 FDA reports)
PETECHIAE ( 77 FDA reports)
PNEUMONIA BACTERIAL ( 77 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 77 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 76 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 76 FDA reports)
DYSPEPSIA ( 76 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 75 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 75 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 75 FDA reports)
HYPERCALCAEMIA ( 75 FDA reports)
INTESTINAL PERFORATION ( 75 FDA reports)
ADVERSE DRUG REACTION ( 74 FDA reports)
CATARACT ( 74 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 74 FDA reports)
HEPATIC NECROSIS ( 74 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 74 FDA reports)
KLEBSIELLA INFECTION ( 74 FDA reports)
VERTIGO ( 74 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 73 FDA reports)
HEPATITIS FULMINANT ( 73 FDA reports)
HYPOPHOSPHATAEMIA ( 72 FDA reports)
HYPOTHYROIDISM ( 71 FDA reports)
NEUROLOGICAL SYMPTOM ( 71 FDA reports)
ORTHOSTATIC HYPOTENSION ( 71 FDA reports)
SPEECH DISORDER ( 71 FDA reports)
RHINORRHOEA ( 70 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 70 FDA reports)
T-CELL LYMPHOMA ( 70 FDA reports)
CYSTITIS ( 70 FDA reports)
ENGRAFT FAILURE ( 70 FDA reports)
ERYSIPELAS ( 70 FDA reports)
HYPOGLYCAEMIA ( 70 FDA reports)
CONTUSION ( 69 FDA reports)
PULMONARY CONGESTION ( 69 FDA reports)
PNEUMONIA ASPIRATION ( 68 FDA reports)
PRIMARY SEQUESTRUM ( 68 FDA reports)
SPINAL COMPRESSION FRACTURE ( 68 FDA reports)
TENDERNESS ( 68 FDA reports)
GASTRIC ULCER ( 68 FDA reports)
HYPERURICAEMIA ( 68 FDA reports)
HYPOMAGNESAEMIA ( 68 FDA reports)
LOWER LIMB FRACTURE ( 68 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 68 FDA reports)
CHOLECYSTITIS ( 67 FDA reports)
CULTURE URINE POSITIVE ( 67 FDA reports)
DRUG EFFECT DECREASED ( 67 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 67 FDA reports)
ANGINA PECTORIS ( 66 FDA reports)
BONE MARROW DISORDER ( 66 FDA reports)
CONJUNCTIVITIS ( 66 FDA reports)
CYANOSIS ( 66 FDA reports)
EAR PAIN ( 66 FDA reports)
HEPATOSPLENOMEGALY ( 66 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 66 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 65 FDA reports)
ACUTE PULMONARY OEDEMA ( 65 FDA reports)
BASAL CELL CARCINOMA ( 65 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 65 FDA reports)
DELIRIUM ( 65 FDA reports)
DRUG RESISTANCE ( 65 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 65 FDA reports)
PALLOR ( 65 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 64 FDA reports)
ARTHRITIS ( 64 FDA reports)
BRONCHOSPASM ( 64 FDA reports)
IMMUNODEFICIENCY ( 64 FDA reports)
NECROSIS ( 64 FDA reports)
RESPIRATORY ARREST ( 64 FDA reports)
SENSORY DISTURBANCE ( 64 FDA reports)
SKIN TOXICITY ( 64 FDA reports)
WEGENER'S GRANULOMATOSIS ( 64 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 63 FDA reports)
RHABDOMYOLYSIS ( 63 FDA reports)
SKIN INFECTION ( 63 FDA reports)
ANURIA ( 63 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 63 FDA reports)
COORDINATION ABNORMAL ( 63 FDA reports)
ENTEROCOLITIS ( 63 FDA reports)
FIBROSIS ( 63 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 63 FDA reports)
LEUKAEMIA ( 63 FDA reports)
LOBAR PNEUMONIA ( 63 FDA reports)
ACIDOSIS ( 62 FDA reports)
CHEST X-RAY ABNORMAL ( 62 FDA reports)
DEAFNESS ( 62 FDA reports)
DIPLOPIA ( 62 FDA reports)
HALLUCINATION ( 62 FDA reports)
HYPERLIPIDAEMIA ( 62 FDA reports)
MENTAL DISORDER ( 62 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 61 FDA reports)
UNRESPONSIVE TO STIMULI ( 61 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 60 FDA reports)
SPINAL OSTEOARTHRITIS ( 60 FDA reports)
TOOTHACHE ( 60 FDA reports)
TOXIC SKIN ERUPTION ( 60 FDA reports)
URINARY RETENTION ( 60 FDA reports)
VENOUS THROMBOSIS ( 60 FDA reports)
VENTRICULAR FIBRILLATION ( 60 FDA reports)
VENTRICULAR HYPOKINESIA ( 60 FDA reports)
AMENORRHOEA ( 60 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 60 FDA reports)
NASAL CONGESTION ( 60 FDA reports)
APLASTIC ANAEMIA ( 59 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 59 FDA reports)
FACIAL PALSY ( 59 FDA reports)
NEUROPATHY ( 59 FDA reports)
PRESYNCOPE ( 59 FDA reports)
TUBERCULOSIS ( 59 FDA reports)
PREMATURE LABOUR ( 58 FDA reports)
STATUS EPILEPTICUS ( 58 FDA reports)
GINGIVITIS ( 58 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 57 FDA reports)
FACIAL PAIN ( 57 FDA reports)
HERPES VIRUS INFECTION ( 57 FDA reports)
HYPOVOLAEMIA ( 57 FDA reports)
MALNUTRITION ( 57 FDA reports)
OVARIAN FAILURE ( 57 FDA reports)
RALES ( 57 FDA reports)
TOOTH DISORDER ( 57 FDA reports)
SCAR ( 56 FDA reports)
ABNORMAL BEHAVIOUR ( 56 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 56 FDA reports)
DISCOMFORT ( 56 FDA reports)
ENTEROCOCCAL SEPSIS ( 56 FDA reports)
ERYTHEMA MULTIFORME ( 56 FDA reports)
EYE PAIN ( 56 FDA reports)
FISTULA ( 56 FDA reports)
GASTROINTESTINAL NECROSIS ( 56 FDA reports)
ORAL DISORDER ( 56 FDA reports)
ASTHMA ( 55 FDA reports)
BURNING SENSATION ( 55 FDA reports)
FAILURE TO THRIVE ( 55 FDA reports)
HYPERTHERMIA ( 55 FDA reports)
MASS ( 55 FDA reports)
MYOSITIS ( 55 FDA reports)
OVERDOSE ( 55 FDA reports)
PERICARDITIS ( 55 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 54 FDA reports)
VARICELLA ( 54 FDA reports)
CANDIDA SEPSIS ( 54 FDA reports)
COLON CANCER ( 54 FDA reports)
DERMATITIS EXFOLIATIVE ( 54 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 54 FDA reports)
ENCEPHALITIS HERPES ( 54 FDA reports)
HAEMATOMA ( 54 FDA reports)
JOINT SWELLING ( 54 FDA reports)
NEPHROLITHIASIS ( 54 FDA reports)
CARDIOGENIC SHOCK ( 53 FDA reports)
CEREBRAL ISCHAEMIA ( 53 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 53 FDA reports)
FEELING ABNORMAL ( 53 FDA reports)
JAW DISORDER ( 53 FDA reports)
NERVOUSNESS ( 53 FDA reports)
NIGHT SWEATS ( 53 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 53 FDA reports)
PREGNANCY ( 53 FDA reports)
SYSTEMIC CANDIDA ( 53 FDA reports)
TROPONIN INCREASED ( 53 FDA reports)
PURULENT DISCHARGE ( 52 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 52 FDA reports)
ZYGOMYCOSIS ( 52 FDA reports)
ANHEDONIA ( 52 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 52 FDA reports)
DISTURBANCE IN ATTENTION ( 52 FDA reports)
METASTASES TO LYMPH NODES ( 52 FDA reports)
MYELOPATHY ( 52 FDA reports)
HODGKIN'S DISEASE ( 51 FDA reports)
HOT FLUSH ( 51 FDA reports)
MIGRAINE ( 51 FDA reports)
MYOPATHY ( 51 FDA reports)
NEOPLASM RECURRENCE ( 51 FDA reports)
NEUTROPHIL COUNT INCREASED ( 51 FDA reports)
OTITIS MEDIA ( 51 FDA reports)
PNEUMOMEDIASTINUM ( 51 FDA reports)
RENAL TUBULAR NECROSIS ( 51 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 51 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 51 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 50 FDA reports)
PLEURITIC PAIN ( 50 FDA reports)
UROSEPSIS ( 50 FDA reports)
BLOOD CALCIUM DECREASED ( 50 FDA reports)
CLOSTRIDIUM COLITIS ( 50 FDA reports)
CORONARY ARTERY DISEASE ( 50 FDA reports)
HAEMOGLOBIN ABNORMAL ( 50 FDA reports)
HEMIPLEGIA ( 50 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 50 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 50 FDA reports)
MOBILITY DECREASED ( 50 FDA reports)
NASAL SEPTUM DISORDER ( 50 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 50 FDA reports)
ANAPHYLACTIC SHOCK ( 49 FDA reports)
CAESAREAN SECTION ( 49 FDA reports)
HEPATITIS CHOLESTATIC ( 49 FDA reports)
HYPERCHOLESTEROLAEMIA ( 49 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 49 FDA reports)
RASH GENERALISED ( 49 FDA reports)
RECURRENT CANCER ( 49 FDA reports)
TOOTH ABSCESS ( 49 FDA reports)
UNEVALUABLE EVENT ( 49 FDA reports)
PATHOGEN RESISTANCE ( 48 FDA reports)
PLEURAL FIBROSIS ( 48 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 48 FDA reports)
ACUTE CORONARY SYNDROME ( 48 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 48 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 48 FDA reports)
DEMYELINATION ( 48 FDA reports)
FAECAL INCONTINENCE ( 48 FDA reports)
GLIOMA ( 48 FDA reports)
HYDRONEPHROSIS ( 48 FDA reports)
HYPOTONIA ( 48 FDA reports)
ISCHAEMIC STROKE ( 48 FDA reports)
LIVER TRANSPLANT ( 48 FDA reports)
NEURALGIA ( 48 FDA reports)
OLIGURIA ( 48 FDA reports)
ADVERSE EVENT ( 47 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 47 FDA reports)
AREFLEXIA ( 47 FDA reports)
CARDIOPULMONARY FAILURE ( 47 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 47 FDA reports)
FACE OEDEMA ( 47 FDA reports)
GASTROINTESTINAL PERFORATION ( 47 FDA reports)
LIVER INJURY ( 47 FDA reports)
PATHOLOGICAL FRACTURE ( 47 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 47 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 46 FDA reports)
SKIN DISORDER ( 46 FDA reports)
ABASIA ( 46 FDA reports)
BLADDER CANCER ( 46 FDA reports)
COMPRESSION FRACTURE ( 46 FDA reports)
DYSGEUSIA ( 46 FDA reports)
ESCHERICHIA BACTERAEMIA ( 46 FDA reports)
EXOSTOSIS ( 46 FDA reports)
FIBRIN D DIMER INCREASED ( 46 FDA reports)
GASTRIC CANCER ( 46 FDA reports)
PAIN OF SKIN ( 46 FDA reports)
PARALYSIS ( 46 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 45 FDA reports)
ASEPTIC NECROSIS BONE ( 45 FDA reports)
BONE MARROW TOXICITY ( 45 FDA reports)
BRAIN HERNIATION ( 45 FDA reports)
BURKITT'S LYMPHOMA ( 45 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 45 FDA reports)
DRUG LEVEL INCREASED ( 45 FDA reports)
ENDOCARDITIS ( 45 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 45 FDA reports)
ODYNOPHAGIA ( 45 FDA reports)
ABDOMINAL PAIN LOWER ( 44 FDA reports)
ANAL ABSCESS ( 44 FDA reports)
CANDIDA PNEUMONIA ( 44 FDA reports)
FOETAL GROWTH RESTRICTION ( 44 FDA reports)
HEPATIC CIRRHOSIS ( 44 FDA reports)
HYDROCEPHALUS ( 44 FDA reports)
HYPERPYREXIA ( 44 FDA reports)
INTESTINAL ISCHAEMIA ( 44 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 44 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 44 FDA reports)
ORAL HERPES ( 44 FDA reports)
ORGANISING PNEUMONIA ( 44 FDA reports)
PSYCHOTIC DISORDER ( 44 FDA reports)
REFRACTORY ANAEMIA ( 44 FDA reports)
SERUM FERRITIN INCREASED ( 44 FDA reports)
SUICIDAL IDEATION ( 44 FDA reports)
SWOLLEN TONGUE ( 44 FDA reports)
TREATMENT FAILURE ( 44 FDA reports)
PHOTOPHOBIA ( 43 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 43 FDA reports)
RHEUMATOID ARTHRITIS ( 43 FDA reports)
SKIN HYPERPIGMENTATION ( 43 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 43 FDA reports)
TOXIC ENCEPHALOPATHY ( 43 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 43 FDA reports)
BRAIN ABSCESS ( 43 FDA reports)
CACHEXIA ( 43 FDA reports)
IRON DEFICIENCY ANAEMIA ( 43 FDA reports)
LABORATORY TEST ABNORMAL ( 43 FDA reports)
MOUTH HAEMORRHAGE ( 43 FDA reports)
MYELOID LEUKAEMIA ( 43 FDA reports)
ATRIAL FLUTTER ( 42 FDA reports)
CEREBELLAR SYNDROME ( 42 FDA reports)
CSF PROTEIN INCREASED ( 42 FDA reports)
DRUG ERUPTION ( 42 FDA reports)
EMPHYSEMA ( 42 FDA reports)
GASTRIC PERFORATION ( 42 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 42 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 42 FDA reports)
LOCAL SWELLING ( 42 FDA reports)
NODULE ( 42 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 42 FDA reports)
PURULENCE ( 42 FDA reports)
PROCTALGIA ( 41 FDA reports)
PURPURA ( 41 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 41 FDA reports)
SURGERY ( 41 FDA reports)
CEREBRAL ATROPHY ( 41 FDA reports)
CYTOKINE RELEASE SYNDROME ( 41 FDA reports)
HAEMODYNAMIC INSTABILITY ( 41 FDA reports)
MUCORMYCOSIS ( 41 FDA reports)
MUCOUS MEMBRANE DISORDER ( 41 FDA reports)
MYELITIS TRANSVERSE ( 41 FDA reports)
BRONCHOSTENOSIS ( 40 FDA reports)
DECUBITUS ULCER ( 40 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 40 FDA reports)
EOSINOPHILIA ( 40 FDA reports)
EXTRAVASATION ( 40 FDA reports)
EYE SWELLING ( 40 FDA reports)
GASTRIC HAEMORRHAGE ( 40 FDA reports)
HEPATITIS ACUTE ( 40 FDA reports)
LARGE INTESTINE PERFORATION ( 40 FDA reports)
LIPASE INCREASED ( 40 FDA reports)
MECHANICAL VENTILATION ( 40 FDA reports)
MEDICATION ERROR ( 40 FDA reports)
NASOPHARYNGITIS ( 40 FDA reports)
PARAPLEGIA ( 40 FDA reports)
PLASMACYTOMA ( 40 FDA reports)
RESTLESSNESS ( 40 FDA reports)
SCLERODERMA ( 40 FDA reports)
SKIN DISCOLOURATION ( 40 FDA reports)
VAGINAL HAEMORRHAGE ( 40 FDA reports)
RASH PAPULAR ( 39 FDA reports)
RENAL CYST ( 39 FDA reports)
ABORTION SPONTANEOUS ( 39 FDA reports)
BACTERIAL TEST POSITIVE ( 39 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 39 FDA reports)
BLOOD POTASSIUM INCREASED ( 39 FDA reports)
FUNGAL SEPSIS ( 39 FDA reports)
HEPATIC LESION ( 39 FDA reports)
IRRITABILITY ( 39 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 39 FDA reports)
NEOPLASM ( 39 FDA reports)
ACUTE LEUKAEMIA ( 38 FDA reports)
BLOOD DISORDER ( 38 FDA reports)
BLOOD MAGNESIUM DECREASED ( 38 FDA reports)
BREAST CANCER FEMALE ( 38 FDA reports)
CARDIAC FAILURE ACUTE ( 38 FDA reports)
CARDIAC TAMPONADE ( 38 FDA reports)
CATHETER RELATED COMPLICATION ( 38 FDA reports)
DERMATITIS ( 38 FDA reports)
DYSKINESIA ( 38 FDA reports)
GINGIVAL BLEEDING ( 38 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 38 FDA reports)
HEAD INJURY ( 38 FDA reports)
JOINT STIFFNESS ( 38 FDA reports)
LEFT VENTRICULAR FAILURE ( 38 FDA reports)
NYSTAGMUS ( 38 FDA reports)
POOR QUALITY SLEEP ( 38 FDA reports)
RASH PRURITIC ( 38 FDA reports)
SENSORY LOSS ( 38 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 38 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 38 FDA reports)
SINUS DISORDER ( 37 FDA reports)
CENTRAL LINE INFECTION ( 37 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 37 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 37 FDA reports)
HEPATITIS C ( 37 FDA reports)
LIVER ABSCESS ( 37 FDA reports)
MOTOR DYSFUNCTION ( 37 FDA reports)
NEUROBLASTOMA ( 37 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 37 FDA reports)
ARTHROPATHY ( 36 FDA reports)
BRAIN NEOPLASM ( 36 FDA reports)
DILATATION VENTRICULAR ( 36 FDA reports)
ENCEPHALITIS VIRAL ( 36 FDA reports)
EXPOSED BONE IN JAW ( 36 FDA reports)
HYPERNATRAEMIA ( 36 FDA reports)
JAW OPERATION ( 36 FDA reports)
KAPOSI'S SARCOMA ( 36 FDA reports)
PERFORMANCE STATUS DECREASED ( 36 FDA reports)
PHOTOSENSITIVITY REACTION ( 36 FDA reports)
RECTAL ULCER ( 36 FDA reports)
VENTRICULAR DYSFUNCTION ( 36 FDA reports)
PLATELET COUNT ABNORMAL ( 35 FDA reports)
RADIATION PNEUMONITIS ( 35 FDA reports)
SEQUESTRECTOMY ( 35 FDA reports)
THROMBOPHLEBITIS ( 35 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 35 FDA reports)
ANGIOEDEMA ( 35 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 35 FDA reports)
CARDIAC MURMUR ( 35 FDA reports)
COLITIS ISCHAEMIC ( 35 FDA reports)
CUSHING'S SYNDROME ( 35 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 35 FDA reports)
ENDOTRACHEAL INTUBATION ( 35 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 35 FDA reports)
FEELING HOT ( 35 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 35 FDA reports)
HYPOTHERMIA ( 35 FDA reports)
LACRIMATION INCREASED ( 35 FDA reports)
LUPUS NEPHRITIS ( 35 FDA reports)
METASTASES TO SPINE ( 35 FDA reports)
METASTATIC NEOPLASM ( 35 FDA reports)
MUSCLE RUPTURE ( 35 FDA reports)
ABSCESS JAW ( 34 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 34 FDA reports)
APHTHOUS STOMATITIS ( 34 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 34 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 34 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 34 FDA reports)
DIVERTICULAR PERFORATION ( 34 FDA reports)
EATING DISORDER ( 34 FDA reports)
ILL-DEFINED DISORDER ( 34 FDA reports)
INTRA-UTERINE DEATH ( 34 FDA reports)
LACTIC ACIDOSIS ( 34 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 34 FDA reports)
PHARYNGEAL OEDEMA ( 34 FDA reports)
PLATELET COUNT INCREASED ( 34 FDA reports)
PLATELET DISORDER ( 34 FDA reports)
PROSTATE CANCER ( 34 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 34 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 34 FDA reports)
RHINITIS ALLERGIC ( 34 FDA reports)
SPLEEN DISORDER ( 34 FDA reports)
TREATMENT NONCOMPLIANCE ( 34 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 34 FDA reports)
PERIPHERAL ISCHAEMIA ( 33 FDA reports)
PNEUMATOSIS INTESTINALIS ( 33 FDA reports)
PROCEDURAL COMPLICATION ( 33 FDA reports)
PROTEIN TOTAL DECREASED ( 33 FDA reports)
SKIN NECROSIS ( 33 FDA reports)
SLEEP APNOEA SYNDROME ( 33 FDA reports)
STREPTOCOCCAL SEPSIS ( 33 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 33 FDA reports)
TACHYARRHYTHMIA ( 33 FDA reports)
ABDOMINAL TENDERNESS ( 33 FDA reports)
ADENOVIRAL HEPATITIS ( 33 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 33 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 33 FDA reports)
ASPIRATION ( 33 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 33 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 33 FDA reports)
CHOLANGITIS ( 33 FDA reports)
CHOLECYSTITIS ACUTE ( 33 FDA reports)
CUSHINGOID ( 33 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 33 FDA reports)
HIATUS HERNIA ( 33 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 33 FDA reports)
JAUNDICE CHOLESTATIC ( 33 FDA reports)
JUGULAR VEIN THROMBOSIS ( 33 FDA reports)
LOCALISED INFECTION ( 33 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 33 FDA reports)
MASTECTOMY ( 33 FDA reports)
NECROTISING FASCIITIS ( 33 FDA reports)
PARONYCHIA ( 33 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 32 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 32 FDA reports)
BREAST CANCER RECURRENT ( 32 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 32 FDA reports)
CYSTITIS VIRAL ( 32 FDA reports)
DEMENTIA ( 32 FDA reports)
DIASTOLIC DYSFUNCTION ( 32 FDA reports)
DRUG INTOLERANCE ( 32 FDA reports)
ENTEROBACTER INFECTION ( 32 FDA reports)
FAECALOMA ( 32 FDA reports)
INFERTILITY ( 32 FDA reports)
INJECTION SITE PAIN ( 32 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 32 FDA reports)
MYELOMA RECURRENCE ( 32 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 32 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 32 FDA reports)
OPTIC ATROPHY ( 32 FDA reports)
PERIODONTAL DISEASE ( 32 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 32 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 32 FDA reports)
VIITH NERVE PARALYSIS ( 32 FDA reports)
WOUND INFECTION ( 32 FDA reports)
PERTUSSIS ( 31 FDA reports)
PHYSICAL DISABILITY ( 31 FDA reports)
PLASMACYTOSIS ( 31 FDA reports)
PRIMARY HYPOGONADISM ( 31 FDA reports)
PULMONARY MYCOSIS ( 31 FDA reports)
PULMONARY TUBERCULOSIS ( 31 FDA reports)
RETINAL HAEMORRHAGE ( 31 FDA reports)
SCOLIOSIS ( 31 FDA reports)
TENDONITIS ( 31 FDA reports)
TOXOPLASMOSIS ( 31 FDA reports)
VISUAL DISTURBANCE ( 31 FDA reports)
WOUND DEBRIDEMENT ( 31 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 31 FDA reports)
CULTURE POSITIVE ( 31 FDA reports)
DYSAESTHESIA ( 31 FDA reports)
EYELID OEDEMA ( 31 FDA reports)
GENE MUTATION ( 31 FDA reports)
HAEMORRHAGIC DIATHESIS ( 31 FDA reports)
HILAR LYMPHADENOPATHY ( 31 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 31 FDA reports)
METAPLASIA ( 31 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 31 FDA reports)
ALVEOLITIS ( 30 FDA reports)
BLOOD AMYLASE INCREASED ( 30 FDA reports)
CEREBRAL HAEMATOMA ( 30 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 30 FDA reports)
EYE IRRITATION ( 30 FDA reports)
HEPATITIS TOXIC ( 30 FDA reports)
HYPERKERATOSIS ( 30 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 30 FDA reports)
LEUKAEMIA PLASMACYTIC ( 30 FDA reports)
MANTLE CELL LYMPHOMA ( 30 FDA reports)
MENINGITIS ( 30 FDA reports)
MICROANGIOPATHY ( 30 FDA reports)
NOCARDIOSIS ( 30 FDA reports)
PHLEBITIS ( 30 FDA reports)
SPINAL FRACTURE ( 30 FDA reports)
TINNITUS ( 30 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 30 FDA reports)
TOOTH LOSS ( 30 FDA reports)
PLEURISY ( 29 FDA reports)
PULMONARY MASS ( 29 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 29 FDA reports)
SEPSIS SYNDROME ( 29 FDA reports)
SHOCK HAEMORRHAGIC ( 29 FDA reports)
SPLENIC INFARCTION ( 29 FDA reports)
VENTRICULAR HYPERTROPHY ( 29 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 29 FDA reports)
BONE SARCOMA ( 29 FDA reports)
COLITIS ULCERATIVE ( 29 FDA reports)
DECREASED INTEREST ( 29 FDA reports)
DIVERTICULUM ( 29 FDA reports)
EAR INFECTION ( 29 FDA reports)
GRANULOMA ( 29 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 29 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 29 FDA reports)
MYELITIS ( 29 FDA reports)
OVARIAN CANCER ( 29 FDA reports)
ABORTION INDUCED ( 28 FDA reports)
ANGIOPATHY ( 28 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 28 FDA reports)
BLOOD URIC ACID INCREASED ( 28 FDA reports)
BONE MARROW NECROSIS ( 28 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 28 FDA reports)
COMPLETED SUICIDE ( 28 FDA reports)
ECZEMA ( 28 FDA reports)
FOOT FRACTURE ( 28 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 28 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 28 FDA reports)
METABOLIC DISORDER ( 28 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 28 FDA reports)
SKIN EROSION ( 28 FDA reports)
THROAT TIGHTNESS ( 28 FDA reports)
VIRAEMIA ( 28 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 27 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 27 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 27 FDA reports)
SLEEP DISORDER ( 27 FDA reports)
TOOTH INFECTION ( 27 FDA reports)
VENTRICULAR ARRHYTHMIA ( 27 FDA reports)
AORTIC VALVE INCOMPETENCE ( 27 FDA reports)
BACILLUS INFECTION ( 27 FDA reports)
CARDIAC AMYLOIDOSIS ( 27 FDA reports)
COMA HEPATIC ( 27 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 27 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 27 FDA reports)
FUNGAEMIA ( 27 FDA reports)
HYPOPROTEINAEMIA ( 27 FDA reports)
INTESTINAL HAEMORRHAGE ( 27 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 27 FDA reports)
ORTHOPNOEA ( 27 FDA reports)
OSTEOMYELITIS CHRONIC ( 27 FDA reports)
OSTEOSCLEROSIS ( 27 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 27 FDA reports)
PARESIS ( 27 FDA reports)
ACTINOMYCOSIS ( 26 FDA reports)
ACUTE SINUSITIS ( 26 FDA reports)
ADENOCARCINOMA ( 26 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 26 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 26 FDA reports)
CRYING ( 26 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 26 FDA reports)
DUODENAL ULCER ( 26 FDA reports)
DYSPHONIA ( 26 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 26 FDA reports)
FEMUR FRACTURE ( 26 FDA reports)
GALLBLADDER DISORDER ( 26 FDA reports)
HEART RATE DECREASED ( 26 FDA reports)
MUSCLE TWITCHING ( 26 FDA reports)
NEPHROPATHY ( 26 FDA reports)
OLIGOHYDRAMNIOS ( 26 FDA reports)
OSTEOLYSIS ( 26 FDA reports)
OVARIAN ATROPHY ( 26 FDA reports)
PARAPARESIS ( 26 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 26 FDA reports)
POOR PERSONAL HYGIENE ( 26 FDA reports)
ROAD TRAFFIC ACCIDENT ( 26 FDA reports)
SPINAL CORD DISORDER ( 26 FDA reports)
SUBILEUS ( 26 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 26 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 26 FDA reports)
PERIPHERAL COLDNESS ( 25 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 25 FDA reports)
STENOTROPHOMONAS INFECTION ( 25 FDA reports)
VIRAL LOAD INCREASED ( 25 FDA reports)
ABDOMINAL ABSCESS ( 25 FDA reports)
ARTERIOSCLEROSIS ( 25 FDA reports)
BLOOD COUNT ABNORMAL ( 25 FDA reports)
BODY TEMPERATURE DECREASED ( 25 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 25 FDA reports)
CHROMOSOME ABNORMALITY ( 25 FDA reports)
CULTURE STOOL POSITIVE ( 25 FDA reports)
CYST ( 25 FDA reports)
DIVERTICULUM INTESTINAL ( 25 FDA reports)
EROSIVE OESOPHAGITIS ( 25 FDA reports)
FAECES DISCOLOURED ( 25 FDA reports)
FLUID INTAKE REDUCED ( 25 FDA reports)
FOLLICULITIS ( 25 FDA reports)
GANGRENE ( 25 FDA reports)
HEPATIC FIBROSIS ( 25 FDA reports)
HEPATOCELLULAR DAMAGE ( 25 FDA reports)
HYPOVOLAEMIC SHOCK ( 25 FDA reports)
JOINT EFFUSION ( 25 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 25 FDA reports)
LYMPHOEDEMA ( 25 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 25 FDA reports)
PARTIAL SEIZURES ( 25 FDA reports)
AMYLOIDOSIS ( 24 FDA reports)
APHAGIA ( 24 FDA reports)
APNOEA ( 24 FDA reports)
AUTOIMMUNE DISORDER ( 24 FDA reports)
AZOTAEMIA ( 24 FDA reports)
BEDRIDDEN ( 24 FDA reports)
BREAST CANCER METASTATIC ( 24 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 24 FDA reports)
CEREBRAL FUNGAL INFECTION ( 24 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 24 FDA reports)
DEAFNESS NEUROSENSORY ( 24 FDA reports)
DELAYED ENGRAFTMENT ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
DUODENITIS ( 24 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 24 FDA reports)
FOETAL GROWTH RETARDATION ( 24 FDA reports)
FUNGAL SKIN INFECTION ( 24 FDA reports)
GINGIVAL PAIN ( 24 FDA reports)
HYPERTHYROIDISM ( 24 FDA reports)
HYPERVENTILATION ( 24 FDA reports)
INTESTINAL ULCER ( 24 FDA reports)
LYMPHADENECTOMY ( 24 FDA reports)
MANIA ( 24 FDA reports)
MARROW HYPERPLASIA ( 24 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 24 FDA reports)
NAIL DISORDER ( 24 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 24 FDA reports)
PANIC ATTACK ( 24 FDA reports)
PAPILLOEDEMA ( 24 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 24 FDA reports)
PORTAL VEIN THROMBOSIS ( 24 FDA reports)
RESPIRATORY ALKALOSIS ( 24 FDA reports)
SCIATICA ( 24 FDA reports)
SINUS BRADYCARDIA ( 24 FDA reports)
SKIN NODULE ( 24 FDA reports)
VITREOUS FLOATERS ( 24 FDA reports)
QUADRIPARESIS ( 23 FDA reports)
RASH PUSTULAR ( 23 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 23 FDA reports)
SINUS CONGESTION ( 23 FDA reports)
SPUTUM CULTURE POSITIVE ( 23 FDA reports)
TRAUMATIC HAEMATOMA ( 23 FDA reports)
TYPE 2 DIABETES MELLITUS ( 23 FDA reports)
WHITE BLOOD CELL DISORDER ( 23 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 23 FDA reports)
AORTIC STENOSIS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 23 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 23 FDA reports)
CEREBRAL DISORDER ( 23 FDA reports)
COLONIC POLYP ( 23 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 23 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 23 FDA reports)
CREPITATIONS ( 23 FDA reports)
DISSEMINATED TUBERCULOSIS ( 23 FDA reports)
DYSPLASIA ( 23 FDA reports)
ERYTHEMA INFECTIOSUM ( 23 FDA reports)
FEMORAL NECK FRACTURE ( 23 FDA reports)
FLANK PAIN ( 23 FDA reports)
HEPATIC INFECTION FUNGAL ( 23 FDA reports)
HERPES ZOSTER DISSEMINATED ( 23 FDA reports)
IRON DEFICIENCY ( 23 FDA reports)
LARGE INTESTINAL ULCER ( 23 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 23 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 23 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 23 FDA reports)
MULTIPLE FRACTURES ( 23 FDA reports)
MUSCLE ATROPHY ( 23 FDA reports)
MYDRIASIS ( 23 FDA reports)
OPTIC NEURITIS ( 23 FDA reports)
ADRENAL INSUFFICIENCY ( 22 FDA reports)
ARTERIAL THROMBOSIS ( 22 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 22 FDA reports)
BLOOD GLUCOSE DECREASED ( 22 FDA reports)
BONE DEBRIDEMENT ( 22 FDA reports)
BREATH SOUNDS ABNORMAL ( 22 FDA reports)
BURSITIS ( 22 FDA reports)
CHRONIC SINUSITIS ( 22 FDA reports)
DEBRIDEMENT ( 22 FDA reports)
DISEASE COMPLICATION ( 22 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 22 FDA reports)
DYSPHASIA ( 22 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 22 FDA reports)
FACIAL PARESIS ( 22 FDA reports)
FEELING COLD ( 22 FDA reports)
GAZE PALSY ( 22 FDA reports)
GLIOSIS ( 22 FDA reports)
GOITRE ( 22 FDA reports)
HAEMOPHILUS INFECTION ( 22 FDA reports)
HEPATIC CYST ( 22 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 22 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 22 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 22 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 22 FDA reports)
LUNG ADENOCARCINOMA ( 22 FDA reports)
MOOD SWINGS ( 22 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 22 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 22 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 22 FDA reports)
OBESITY ( 22 FDA reports)
ORAL INFECTION ( 22 FDA reports)
PERITONITIS BACTERIAL ( 22 FDA reports)
PNEUMONIA HERPES VIRAL ( 22 FDA reports)
PROTEIN URINE PRESENT ( 22 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 22 FDA reports)
RHINITIS ( 22 FDA reports)
RHONCHI ( 22 FDA reports)
SOFT TISSUE INFECTION ( 22 FDA reports)
STRIDOR ( 22 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 22 FDA reports)
SUPERINFECTION ( 22 FDA reports)
THYROID CANCER ( 22 FDA reports)
TIC ( 22 FDA reports)
TONSILLITIS ( 22 FDA reports)
PARVOVIRUS INFECTION ( 21 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 21 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 21 FDA reports)
RENAL TUBULAR DISORDER ( 21 FDA reports)
RESPIRATORY DEPRESSION ( 21 FDA reports)
SKIN INDURATION ( 21 FDA reports)
SPINAL DISORDER ( 21 FDA reports)
SPLENIC ABSCESS ( 21 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 21 FDA reports)
SYSTEMIC MYCOSIS ( 21 FDA reports)
THROMBOSIS IN DEVICE ( 21 FDA reports)
TOOTH FRACTURE ( 21 FDA reports)
TRACHEITIS ( 21 FDA reports)
TRANSFUSION REACTION ( 21 FDA reports)
TROPONIN I INCREASED ( 21 FDA reports)
URETERIC OBSTRUCTION ( 21 FDA reports)
BACTERIA STOOL IDENTIFIED ( 21 FDA reports)
BONE DENSITY DECREASED ( 21 FDA reports)
BONE OPERATION ( 21 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 21 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 21 FDA reports)
CORONARY ARTERY OCCLUSION ( 21 FDA reports)
CSF TEST ABNORMAL ( 21 FDA reports)
DRY MOUTH ( 21 FDA reports)
DRY SKIN ( 21 FDA reports)
EMOTIONAL DISORDER ( 21 FDA reports)
HEPATIC ATROPHY ( 21 FDA reports)
HIP ARTHROPLASTY ( 21 FDA reports)
HYPERPARATHYROIDISM ( 21 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 21 FDA reports)
INCONTINENCE ( 21 FDA reports)
LYMPHANGITIS ( 21 FDA reports)
METASTASES TO PLEURA ( 21 FDA reports)
MOOD ALTERED ( 21 FDA reports)
MUSCLE DISORDER ( 21 FDA reports)
MYOCLONUS ( 21 FDA reports)
NERVE INJURY ( 21 FDA reports)
NEUTROPHIL COUNT ( 21 FDA reports)
NOCTURIA ( 21 FDA reports)
NON-CARDIAC CHEST PAIN ( 21 FDA reports)
ORAL DISCOMFORT ( 21 FDA reports)
PARANEOPLASTIC SYNDROME ( 21 FDA reports)
ALVEOLITIS ALLERGIC ( 20 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 20 FDA reports)
ANAL FISSURE ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 20 FDA reports)
BIOPSY LYMPH GLAND ( 20 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 20 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 20 FDA reports)
BONE LOSS ( 20 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 20 FDA reports)
CROHN'S DISEASE ( 20 FDA reports)
DILATATION ATRIAL ( 20 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 20 FDA reports)
DYSPNOEA AT REST ( 20 FDA reports)
ECCHYMOSIS ( 20 FDA reports)
EOSINOPHIL COUNT INCREASED ( 20 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 20 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 20 FDA reports)
FULL BLOOD COUNT DECREASED ( 20 FDA reports)
GROIN PAIN ( 20 FDA reports)
HIP FRACTURE ( 20 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 20 FDA reports)
HYPERTROPHY ( 20 FDA reports)
IMMUNE SYSTEM DISORDER ( 20 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 20 FDA reports)
MACULOPATHY ( 20 FDA reports)
MEDICAL DEVICE COMPLICATION ( 20 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 20 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 20 FDA reports)
MONOCYTE COUNT INCREASED ( 20 FDA reports)
MUCOSAL HAEMORRHAGE ( 20 FDA reports)
NON-SMALL CELL LUNG CANCER ( 20 FDA reports)
ONYCHOMYCOSIS ( 20 FDA reports)
ORAL SOFT TISSUE DISORDER ( 20 FDA reports)
PANCREATIC CARCINOMA ( 20 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 20 FDA reports)
PNEUMONIA VIRAL ( 20 FDA reports)
PREMATURE DELIVERY ( 20 FDA reports)
PROSTATOMEGALY ( 20 FDA reports)
PUPIL FIXED ( 20 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 20 FDA reports)
RESPIRATORY ACIDOSIS ( 20 FDA reports)
RHABDOMYOSARCOMA ( 20 FDA reports)
ROTATOR CUFF SYNDROME ( 20 FDA reports)
SEPTIC EMBOLUS ( 20 FDA reports)
SKIN PAPILLOMA ( 20 FDA reports)
STRESS ( 20 FDA reports)
TRAUMATIC LUNG INJURY ( 20 FDA reports)
UTERINE LEIOMYOMA ( 20 FDA reports)
VOCAL CORD PARALYSIS ( 20 FDA reports)
WOUND COMPLICATION ( 20 FDA reports)
PERIORBITAL OEDEMA ( 19 FDA reports)
PNEUMONIA ASPERGILLUS ( 19 FDA reports)
PNEUMONIA KLEBSIELLA ( 19 FDA reports)
PNEUMONITIS CHEMICAL ( 19 FDA reports)
PORTAL HYPERTENSION ( 19 FDA reports)
PULMONARY CALCIFICATION ( 19 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 19 FDA reports)
PULSE ABSENT ( 19 FDA reports)
PYELONEPHRITIS ( 19 FDA reports)
PYLORIC STENOSIS ( 19 FDA reports)
RADIATION INJURY ( 19 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 19 FDA reports)
SICCA SYNDROME ( 19 FDA reports)
SKIN FIBROSIS ( 19 FDA reports)
SKIN TIGHTNESS ( 19 FDA reports)
SUBCUTANEOUS NODULE ( 19 FDA reports)
THYROID NEOPLASM ( 19 FDA reports)
TONSIL CANCER ( 19 FDA reports)
WOUND DEHISCENCE ( 19 FDA reports)
ABDOMINAL INFECTION ( 19 FDA reports)
AGGRESSION ( 19 FDA reports)
APPENDICITIS ( 19 FDA reports)
BLOOD URINE PRESENT ( 19 FDA reports)
BRONCHIOLITIS ( 19 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 19 FDA reports)
CARDIAC PACEMAKER INSERTION ( 19 FDA reports)
CASTLEMAN'S DISEASE ( 19 FDA reports)
CERVICAL DYSPLASIA ( 19 FDA reports)
DENTURE WEARER ( 19 FDA reports)
DERMATITIS ALLERGIC ( 19 FDA reports)
DIABETIC KETOACIDOSIS ( 19 FDA reports)
DRUG ADMINISTRATION ERROR ( 19 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 19 FDA reports)
EYE MOVEMENT DISORDER ( 19 FDA reports)
FOOD INTOLERANCE ( 19 FDA reports)
GASTROINTESTINAL ULCER ( 19 FDA reports)
HAEMANGIOMA ( 19 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 19 FDA reports)
HAPTOGLOBIN DECREASED ( 19 FDA reports)
HEPATIC CONGESTION ( 19 FDA reports)
HICCUPS ( 19 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 19 FDA reports)
HYPERREFLEXIA ( 19 FDA reports)
HYPOACUSIS ( 19 FDA reports)
HYPOCOAGULABLE STATE ( 19 FDA reports)
HYPOREFLEXIA ( 19 FDA reports)
INCORRECT DOSE ADMINISTERED ( 19 FDA reports)
ISCHAEMIA ( 19 FDA reports)
KIDNEY FIBROSIS ( 19 FDA reports)
LIP SWELLING ( 19 FDA reports)
MASTICATION DISORDER ( 19 FDA reports)
MENOPAUSE ( 19 FDA reports)
MONOPLEGIA ( 19 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 19 FDA reports)
NOROVIRUS TEST POSITIVE ( 19 FDA reports)
ANAL HAEMORRHAGE ( 18 FDA reports)
ANAPHYLACTOID REACTION ( 18 FDA reports)
ANISOCYTOSIS ( 18 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 18 FDA reports)
AZOOSPERMIA ( 18 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 18 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 18 FDA reports)
BILE DUCT CANCER ( 18 FDA reports)
BREAST RECONSTRUCTION ( 18 FDA reports)
CHYLOTHORAX ( 18 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 18 FDA reports)
COLLAPSE OF LUNG ( 18 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 18 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 18 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 18 FDA reports)
DIZZINESS POSTURAL ( 18 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 18 FDA reports)
EYE DISCHARGE ( 18 FDA reports)
EYELID PTOSIS ( 18 FDA reports)
GLOMERULONEPHRITIS ( 18 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 18 FDA reports)
GRANULOCYTE COUNT DECREASED ( 18 FDA reports)
GRANULOCYTES ABNORMAL ( 18 FDA reports)
H1N1 INFLUENZA ( 18 FDA reports)
HALLUCINATION, VISUAL ( 18 FDA reports)
HEPATITIS D ( 18 FDA reports)
HOSPITALISATION ( 18 FDA reports)
HYPOAESTHESIA ORAL ( 18 FDA reports)
HYPOVENTILATION ( 18 FDA reports)
IATROGENIC INJURY ( 18 FDA reports)
LIFE EXPECTANCY SHORTENED ( 18 FDA reports)
MOVEMENT DISORDER ( 18 FDA reports)
MUCOSAL ULCERATION ( 18 FDA reports)
MYOCARDIAL FIBROSIS ( 18 FDA reports)
OESOPHAGEAL ULCER ( 18 FDA reports)
ONYCHOLYSIS ( 18 FDA reports)
PARALYSIS FLACCID ( 18 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 18 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 18 FDA reports)
PLANTAR FASCIITIS ( 18 FDA reports)
POST HERPETIC NEURALGIA ( 18 FDA reports)
RADIOTHERAPY ( 18 FDA reports)
RASH VESICULAR ( 18 FDA reports)
RESPIRATORY TRACT CONGESTION ( 18 FDA reports)
RETINITIS ( 18 FDA reports)
TONGUE DISORDER ( 18 FDA reports)
TRANSPLANT ( 18 FDA reports)
ULCER ( 18 FDA reports)
PEPTIC ULCER ( 17 FDA reports)
PIGMENTATION DISORDER ( 17 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 17 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 17 FDA reports)
SARCOIDOSIS ( 17 FDA reports)
SCEDOSPORIUM INFECTION ( 17 FDA reports)
SICK SINUS SYNDROME ( 17 FDA reports)
SKIN HYPERTROPHY ( 17 FDA reports)
SOLITARY KIDNEY ( 17 FDA reports)
STILLBIRTH ( 17 FDA reports)
VASCULITIS CEREBRAL ( 17 FDA reports)
VENOUS THROMBOSIS LIMB ( 17 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
WALKING AID USER ( 17 FDA reports)
WOUND ( 17 FDA reports)
ACCIDENTAL OVERDOSE ( 17 FDA reports)
APRAXIA ( 17 FDA reports)
ATRIAL TACHYCARDIA ( 17 FDA reports)
BEHCET'S SYNDROME ( 17 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 17 FDA reports)
BIOPSY BREAST ABNORMAL ( 17 FDA reports)
BLADDER DISORDER ( 17 FDA reports)
BLOOD CREATINE INCREASED ( 17 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 17 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 17 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 17 FDA reports)
BLOOD SODIUM INCREASED ( 17 FDA reports)
BONE EROSION ( 17 FDA reports)
BONE SWELLING ( 17 FDA reports)
BRAIN SCAN ABNORMAL ( 17 FDA reports)
BREAST DISCHARGE ( 17 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 17 FDA reports)
DENTAL OPERATION ( 17 FDA reports)
DIABETES INSIPIDUS ( 17 FDA reports)
DRUG CLEARANCE DECREASED ( 17 FDA reports)
GASTRIC DISORDER ( 17 FDA reports)
GASTROENTERITIS NOROVIRUS ( 17 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 17 FDA reports)
GINGIVAL INFECTION ( 17 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 17 FDA reports)
HAEMOSIDEROSIS ( 17 FDA reports)
HEPATIC NEOPLASM ( 17 FDA reports)
HYPERAMMONAEMIA ( 17 FDA reports)
HYPERTRANSAMINASAEMIA ( 17 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 17 FDA reports)
INCOHERENT ( 17 FDA reports)
INCREASED TENDENCY TO BRUISE ( 17 FDA reports)
INTRACARDIAC THROMBUS ( 17 FDA reports)
INTRACRANIAL HYPOTENSION ( 17 FDA reports)
JOINT DISLOCATION ( 17 FDA reports)
LOOSE TOOTH ( 17 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
MELANOCYTIC NAEVUS ( 17 FDA reports)
METASTASES TO MENINGES ( 17 FDA reports)
METASTASES TO SKIN ( 17 FDA reports)
MULTI-ORGAN DISORDER ( 17 FDA reports)
MYELOFIBROSIS ( 17 FDA reports)
ONCOLOGIC COMPLICATION ( 17 FDA reports)
OPTIC NEUROPATHY ( 17 FDA reports)
ORAL CAVITY FISTULA ( 17 FDA reports)
OSTEITIS ( 17 FDA reports)
PARAESTHESIA ORAL ( 17 FDA reports)
PAROSMIA ( 17 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 16 FDA reports)
AFFECT LABILITY ( 16 FDA reports)
ANGER ( 16 FDA reports)
ANTITHROMBIN III DECREASED ( 16 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 16 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 16 FDA reports)
BIOPSY BONE ABNORMAL ( 16 FDA reports)
BLOOD CREATININE DECREASED ( 16 FDA reports)
BLOOD PH DECREASED ( 16 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 16 FDA reports)
CATHETER SITE RELATED REACTION ( 16 FDA reports)
DIFFICULTY IN WALKING ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 16 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 16 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 16 FDA reports)
EWING'S SARCOMA ( 16 FDA reports)
GINGIVAL SWELLING ( 16 FDA reports)
IIIRD NERVE PARALYSIS ( 16 FDA reports)
INFECTIOUS PERITONITIS ( 16 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 16 FDA reports)
ISCHAEMIC HEPATITIS ( 16 FDA reports)
JC VIRUS TEST POSITIVE ( 16 FDA reports)
LUNG HYPERINFLATION ( 16 FDA reports)
LYMPHATIC DISORDER ( 16 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 16 FDA reports)
LYMPHOCYTOSIS ( 16 FDA reports)
MICTURITION URGENCY ( 16 FDA reports)
OEDEMA MOUTH ( 16 FDA reports)
OPEN WOUND ( 16 FDA reports)
OVARIAN CYST ( 16 FDA reports)
PERSONALITY CHANGE ( 16 FDA reports)
PITTING OEDEMA ( 16 FDA reports)
PO2 DECREASED ( 16 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 16 FDA reports)
RADICULOPATHY ( 16 FDA reports)
RECALL PHENOMENON ( 16 FDA reports)
RESTLESS LEGS SYNDROME ( 16 FDA reports)
SALIVARY GLAND CANCER ( 16 FDA reports)
SERUM SICKNESS ( 16 FDA reports)
SKIN PLAQUE ( 16 FDA reports)
SOFT TISSUE DISORDER ( 16 FDA reports)
SPLENIC RUPTURE ( 16 FDA reports)
STRONGYLOIDIASIS ( 16 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 16 FDA reports)
SYNDACTYLY ( 16 FDA reports)
SYSTOLIC DYSFUNCTION ( 16 FDA reports)
TESTICULAR DISORDER ( 16 FDA reports)
VISUAL FIELD DEFECT ( 16 FDA reports)
WATER INTOXICATION ( 16 FDA reports)
PELVIC PAIN ( 15 FDA reports)
PNEUMONIA ADENOVIRAL ( 15 FDA reports)
PROCEDURAL PAIN ( 15 FDA reports)
PROTEIN URINE ABSENT ( 15 FDA reports)
PSORIASIS ( 15 FDA reports)
PULMONARY NECROSIS ( 15 FDA reports)
QUADRIPLEGIA ( 15 FDA reports)
RAYNAUD'S PHENOMENON ( 15 FDA reports)
SEROMA ( 15 FDA reports)
SINUS HEADACHE ( 15 FDA reports)
SKIN CANCER ( 15 FDA reports)
THROAT IRRITATION ( 15 FDA reports)
UTERINE CANCER ( 15 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 15 FDA reports)
WRONG DRUG ADMINISTERED ( 15 FDA reports)
BENIGN BREAST NEOPLASM ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 15 FDA reports)
BLOOD PRESSURE ABNORMAL ( 15 FDA reports)
BRAIN DEATH ( 15 FDA reports)
BREAST PROSTHESIS REMOVAL ( 15 FDA reports)
BRONCHIAL DISORDER ( 15 FDA reports)
CARDIAC VALVE DISEASE ( 15 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 15 FDA reports)
CEREBROVASCULAR DISORDER ( 15 FDA reports)
CORONARY ARTERY STENOSIS ( 15 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 15 FDA reports)
DRY EYE ( 15 FDA reports)
EMBOLISM VENOUS ( 15 FDA reports)
EMPYEMA ( 15 FDA reports)
GASTROINTESTINAL INFECTION ( 15 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 15 FDA reports)
GINGIVAL DISORDER ( 15 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 15 FDA reports)
HEPATIC ENZYME ABNORMAL ( 15 FDA reports)
HYPERSOMNIA ( 15 FDA reports)
INFARCTION ( 15 FDA reports)
JOINT CONTRACTURE ( 15 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 15 FDA reports)
LIGHT CHAIN ANALYSIS ( 15 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 15 FDA reports)
MASS EXCISION ( 15 FDA reports)
MENINGITIS BACTERIAL ( 15 FDA reports)
MENSTRUAL DISORDER ( 15 FDA reports)
MENSTRUATION IRREGULAR ( 15 FDA reports)
METAPNEUMOVIRUS INFECTION ( 15 FDA reports)
MUTISM ( 15 FDA reports)
NEUROGENIC BLADDER ( 15 FDA reports)
OCULAR HYPERAEMIA ( 15 FDA reports)
OEDEMA MUCOSAL ( 15 FDA reports)
PANCREATIC DISORDER ( 15 FDA reports)
PARATHYROID TUMOUR BENIGN ( 15 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 14 FDA reports)
AMAUROSIS ( 14 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 14 FDA reports)
ANGIOSARCOMA ( 14 FDA reports)
AORTIC VALVE SCLEROSIS ( 14 FDA reports)
ASPERGILLUS TEST POSITIVE ( 14 FDA reports)
AXILLARY VEIN THROMBOSIS ( 14 FDA reports)
BENCE JONES PROTEINURIA ( 14 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 14 FDA reports)
BILE DUCT OBSTRUCTION ( 14 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 14 FDA reports)
BLOOD CHLORIDE INCREASED ( 14 FDA reports)
BLOOD LACTIC ACID INCREASED ( 14 FDA reports)
BREAST PAIN ( 14 FDA reports)
BRONCHIAL OBSTRUCTION ( 14 FDA reports)
CARDIAC CIRRHOSIS ( 14 FDA reports)
CARPAL TUNNEL SYNDROME ( 14 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 14 FDA reports)
CITROBACTER INFECTION ( 14 FDA reports)
CORYNEBACTERIUM INFECTION ( 14 FDA reports)
CULTURE WOUND POSITIVE ( 14 FDA reports)
DEPRESSED MOOD ( 14 FDA reports)
DESMOID TUMOUR ( 14 FDA reports)
DEVICE RELATED SEPSIS ( 14 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 14 FDA reports)
DRUG TOLERANCE DECREASED ( 14 FDA reports)
ESCHERICHIA TEST POSITIVE ( 14 FDA reports)
FANCONI SYNDROME ( 14 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 14 FDA reports)
HEPATORENAL SYNDROME ( 14 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 14 FDA reports)
HYPOGONADISM ( 14 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 14 FDA reports)
INGUINAL MASS ( 14 FDA reports)
KLEBSIELLA SEPSIS ( 14 FDA reports)
LARYNGEAL OEDEMA ( 14 FDA reports)
LEFT ATRIAL DILATATION ( 14 FDA reports)
LYMPH NODE PAIN ( 14 FDA reports)
MACULAR OEDEMA ( 14 FDA reports)
MEDULLOBLASTOMA ( 14 FDA reports)
MENINGEAL DISORDER ( 14 FDA reports)
MENINGITIS ASEPTIC ( 14 FDA reports)
MENISCUS LESION ( 14 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
NON-HODGKIN'S LYMPHOMA UNSPECIFIED HISTOLOGY AGGRESSIVE ( 14 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 14 FDA reports)
OPTIC NERVE DISORDER ( 14 FDA reports)
ORAL MUCOSA EROSION ( 14 FDA reports)
ORGAN FAILURE ( 14 FDA reports)
OVARIAN CANCER METASTATIC ( 14 FDA reports)
PCO2 DECREASED ( 14 FDA reports)
PNEUMATOSIS ( 14 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 14 FDA reports)
PRE-ECLAMPSIA ( 14 FDA reports)
PROCTITIS ( 14 FDA reports)
PULMONARY SEPSIS ( 14 FDA reports)
RENAL INFARCT ( 14 FDA reports)
RENAL TRANSPLANT ( 14 FDA reports)
RENAL TUBULAR ACIDOSIS ( 14 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 14 FDA reports)
SUBCUTANEOUS ABSCESS ( 14 FDA reports)
SUICIDE ATTEMPT ( 14 FDA reports)
TENOSYNOVITIS ( 14 FDA reports)
TETANY ( 14 FDA reports)
THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 14 FDA reports)
THYMUS ENLARGEMENT ( 14 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 14 FDA reports)
URINE ANALYSIS ABNORMAL ( 14 FDA reports)
VANISHING BILE DUCT SYNDROME ( 14 FDA reports)
VARICES OESOPHAGEAL ( 14 FDA reports)
PERINEAL ULCERATION ( 13 FDA reports)
PERIODONTITIS ( 13 FDA reports)
PERITONEAL DIALYSIS ( 13 FDA reports)
PLEURAL HAEMORRHAGE ( 13 FDA reports)
PNEUMOCOCCAL SEPSIS ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
PULMONARY THROMBOSIS ( 13 FDA reports)
REFLUX OESOPHAGITIS ( 13 FDA reports)
SKIN REACTION ( 13 FDA reports)
SMALL FOR DATES BABY ( 13 FDA reports)
SPLENIC VEIN THROMBOSIS ( 13 FDA reports)
SPUTUM PURULENT ( 13 FDA reports)
SUBDURAL HAEMORRHAGE ( 13 FDA reports)
SUDDEN CARDIAC DEATH ( 13 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 13 FDA reports)
TONSILLAR HYPERTROPHY ( 13 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 13 FDA reports)
TRISMUS ( 13 FDA reports)
TUMOUR MARKER INCREASED ( 13 FDA reports)
TUMOUR NECROSIS ( 13 FDA reports)
URETERIC STENOSIS ( 13 FDA reports)
VIRAL MYOCARDITIS ( 13 FDA reports)
VIRAL TEST POSITIVE ( 13 FDA reports)
ABDOMINAL MASS ( 13 FDA reports)
ACNE ( 13 FDA reports)
ACUTE LUNG INJURY ( 13 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 13 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 13 FDA reports)
BLINDNESS CORTICAL ( 13 FDA reports)
BLOOD ALBUMIN INCREASED ( 13 FDA reports)
BLOOD CALCIUM INCREASED ( 13 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 13 FDA reports)
BLOOD UREA DECREASED ( 13 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 13 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 13 FDA reports)
CANDIDA TEST POSITIVE ( 13 FDA reports)
CHROMATURIA ( 13 FDA reports)
DYSLALIA ( 13 FDA reports)
EFFUSION ( 13 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 13 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 13 FDA reports)
ESCHAR ( 13 FDA reports)
FEBRILE INFECTION ( 13 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 13 FDA reports)
FLATULENCE ( 13 FDA reports)
GASTROINTESTINAL OEDEMA ( 13 FDA reports)
GINGIVAL ATROPHY ( 13 FDA reports)
HEPATIC HAEMORRHAGE ( 13 FDA reports)
HEPATOCELLULAR INJURY ( 13 FDA reports)
HYPERTENSIVE CRISIS ( 13 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 13 FDA reports)
JAW FRACTURE ( 13 FDA reports)
KLEBSIELLA BACTERAEMIA ( 13 FDA reports)
LABORATORY TEST INTERFERENCE ( 13 FDA reports)
LARYNGEAL STENOSIS ( 13 FDA reports)
LEUKAEMIA CUTIS ( 13 FDA reports)
LOCALISED OEDEMA ( 13 FDA reports)
LUNG INJURY ( 13 FDA reports)
LYMPHOCYTE COUNT ( 13 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 13 FDA reports)
MALLORY-WEISS SYNDROME ( 13 FDA reports)
MENTAL IMPAIRMENT ( 13 FDA reports)
METASTASES TO ADRENALS ( 13 FDA reports)
NEUROBLASTOMA RECURRENT ( 13 FDA reports)
PARAPROTEINAEMIA ( 13 FDA reports)
ABSCESS INTESTINAL ( 12 FDA reports)
ACINETOBACTER INFECTION ( 12 FDA reports)
ACUTE ABDOMEN ( 12 FDA reports)
ACUTE PSYCHOSIS ( 12 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 12 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 12 FDA reports)
AORTIC CALCIFICATION ( 12 FDA reports)
ARTHRITIS BACTERIAL ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
AUTOIMMUNE THYROIDITIS ( 12 FDA reports)
BILIARY TRACT DISORDER ( 12 FDA reports)
BLAST CELLS PRESENT ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 12 FDA reports)
BRAIN INJURY ( 12 FDA reports)
BREAST MASS ( 12 FDA reports)
BRONCHIAL CARCINOMA ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
BURKITT'S LYMPHOMA RECURRENT ( 12 FDA reports)
CATHETER REMOVAL ( 12 FDA reports)
CAUDA EQUINA SYNDROME ( 12 FDA reports)
CELLULITIS GANGRENOUS ( 12 FDA reports)
CHROMOSOMAL DELETION ( 12 FDA reports)
COLD SWEAT ( 12 FDA reports)
COLON CANCER METASTATIC ( 12 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 12 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 12 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 12 FDA reports)
DRUG DOSE OMISSION ( 12 FDA reports)
ERYTHEMA OF EYELID ( 12 FDA reports)
EVAN'S SYNDROME ( 12 FDA reports)
EVANS SYNDROME ( 12 FDA reports)
FACIAL NERVE DISORDER ( 12 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 12 FDA reports)
FOREIGN BODY TRAUMA ( 12 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 12 FDA reports)
GASTROENTERITIS VIRAL ( 12 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 12 FDA reports)
GENERALISED ERYTHEMA ( 12 FDA reports)
GLUCOSE URINE PRESENT ( 12 FDA reports)
HAEMOTHORAX ( 12 FDA reports)
HEMIANOPIA ( 12 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 12 FDA reports)
HEPATIC VEIN OCCLUSION ( 12 FDA reports)
HEPATITIS VIRAL ( 12 FDA reports)
HIRSUTISM ( 12 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 12 FDA reports)
HYPERCAPNIA ( 12 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 12 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 12 FDA reports)
ILEAL PERFORATION ( 12 FDA reports)
INDURATION ( 12 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 12 FDA reports)
INJECTION SITE PHLEBITIS ( 12 FDA reports)
LABILE BLOOD PRESSURE ( 12 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 12 FDA reports)
LEG AMPUTATION ( 12 FDA reports)
LIPODYSTROPHY ACQUIRED ( 12 FDA reports)
LIVEDO RETICULARIS ( 12 FDA reports)
LUNG ABSCESS ( 12 FDA reports)
MASTOID DISORDER ( 12 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 12 FDA reports)
MICROGNATHIA ( 12 FDA reports)
MIDDLE EAR EFFUSION ( 12 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 12 FDA reports)
MONOCYTE COUNT DECREASED ( 12 FDA reports)
MONOCYTOSIS ( 12 FDA reports)
MUCOSAL EROSION ( 12 FDA reports)
MYOCLONIC EPILEPSY ( 12 FDA reports)
NASAL DISCOMFORT ( 12 FDA reports)
NEONATAL DISORDER ( 12 FDA reports)
OESOPHAGEAL CARCINOMA ( 12 FDA reports)
PANCREATIC PSEUDOCYST ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 12 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PERONEAL NERVE PALSY ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
PHARYNGEAL INFLAMMATION ( 12 FDA reports)
PLASMABLASTIC LYMPHOMA ( 12 FDA reports)
PNEUMONIA LEGIONELLA ( 12 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 12 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 12 FDA reports)
PROTEUS INFECTION ( 12 FDA reports)
PROTHROMBIN TIME SHORTENED ( 12 FDA reports)
PULMONARY GRANULOMA ( 12 FDA reports)
QUALITY OF LIFE DECREASED ( 12 FDA reports)
RASH MORBILLIFORM ( 12 FDA reports)
RENAL CELL CARCINOMA ( 12 FDA reports)
RIGHT VENTRICULAR FAILURE ( 12 FDA reports)
SKIN BURNING SENSATION ( 12 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 12 FDA reports)
SPINAL CORD COMPRESSION ( 12 FDA reports)
SPUTUM DISCOLOURED ( 12 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 12 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 12 FDA reports)
STENOTROPHOMONAS SEPSIS ( 12 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 12 FDA reports)
SYNCOPE VASOVAGAL ( 12 FDA reports)
SYNOVIAL CYST ( 12 FDA reports)
SYSTEMIC SCLEROSIS ( 12 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 12 FDA reports)
UPPER LIMB FRACTURE ( 12 FDA reports)
URINE ABNORMALITY ( 12 FDA reports)
VULVOVAGINAL DRYNESS ( 12 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 12 FDA reports)
X-RAY ABNORMAL ( 12 FDA reports)
PELVIC KIDNEY ( 11 FDA reports)
POLYARTHRITIS ( 11 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 11 FDA reports)
RED BLOOD CELL ABNORMALITY ( 11 FDA reports)
RELAPSING FEVER ( 11 FDA reports)
RENAL HAEMORRHAGE ( 11 FDA reports)
RENAL TUBULAR ATROPHY ( 11 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 11 FDA reports)
SCAB ( 11 FDA reports)
SCROTAL OEDEMA ( 11 FDA reports)
SECRETION DISCHARGE ( 11 FDA reports)
SINUS ARRHYTHMIA ( 11 FDA reports)
SKIN FRAGILITY ( 11 FDA reports)
SPLENECTOMY ( 11 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 11 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 11 FDA reports)
TONIC CONVULSION ( 11 FDA reports)
TRACHEOSTOMY ( 11 FDA reports)
UTERINE HAEMORRHAGE ( 11 FDA reports)
VIRAL DNA TEST POSITIVE ( 11 FDA reports)
VIRAL SKIN INFECTION ( 11 FDA reports)
VIRUS URINE TEST POSITIVE ( 11 FDA reports)
VITAMIN D DEFICIENCY ( 11 FDA reports)
VITH NERVE PARALYSIS ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
WHITE BLOOD CELL COUNT ( 11 FDA reports)
WOUND DRAINAGE ( 11 FDA reports)
ABDOMINAL RIGIDITY ( 11 FDA reports)
ABSCESS ORAL ( 11 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 11 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ACUTE PRERENAL FAILURE ( 11 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 11 FDA reports)
AMMONIA INCREASED ( 11 FDA reports)
ANAEMIA MACROCYTIC ( 11 FDA reports)
ANAL FISTULA ( 11 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 11 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 11 FDA reports)
BIOPSY LIVER ABNORMAL ( 11 FDA reports)
BLAST CELL COUNT INCREASED ( 11 FDA reports)
BLOOD CHLORIDE DECREASED ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BLOOD PH INCREASED ( 11 FDA reports)
BLOOD SODIUM ABNORMAL ( 11 FDA reports)
BREAST CANCER IN SITU ( 11 FDA reports)
BREAST NEOPLASM ( 11 FDA reports)
BRONCHOPNEUMOPATHY ( 11 FDA reports)
CALCULUS URINARY ( 11 FDA reports)
CARDIAC HYPERTROPHY ( 11 FDA reports)
CATHETER SITE ERYTHEMA ( 11 FDA reports)
CHOLECYSTITIS CHRONIC ( 11 FDA reports)
CLINODACTYLY ( 11 FDA reports)
COMMUNICATION DISORDER ( 11 FDA reports)
COMPLEX PARTIAL SEIZURES ( 11 FDA reports)
CRANIAL NERVE DISORDER ( 11 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 11 FDA reports)
DENTAL PLAQUE ( 11 FDA reports)
DEVELOPMENTAL DELAY ( 11 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 11 FDA reports)
DIPLEGIA ( 11 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 11 FDA reports)
ENDOPHTHALMITIS ( 11 FDA reports)
ENTEROBACTER SEPSIS ( 11 FDA reports)
ENTEROVESICAL FISTULA ( 11 FDA reports)
EPIGASTRIC DISCOMFORT ( 11 FDA reports)
ERYTHROLEUKAEMIA ( 11 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 11 FDA reports)
EXTRADURAL HAEMATOMA ( 11 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 11 FDA reports)
EXTRASKELETAL OSSIFICATION ( 11 FDA reports)
EYE DISORDER ( 11 FDA reports)
FACET JOINT SYNDROME ( 11 FDA reports)
FASCIITIS ( 11 FDA reports)
GASTRITIS EROSIVE ( 11 FDA reports)
GINGIVAL ERYTHEMA ( 11 FDA reports)
HALLUCINATION, AUDITORY ( 11 FDA reports)
HEART RATE IRREGULAR ( 11 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 11 FDA reports)
HYPERTONIA ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
LACUNAR INFARCTION ( 11 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 11 FDA reports)
LIFE SUPPORT ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
MENIERE'S DISEASE ( 11 FDA reports)
MENINGISM ( 11 FDA reports)
MENOPAUSAL SYMPTOMS ( 11 FDA reports)
METASTASES TO PERITONEUM ( 11 FDA reports)
MICROCYTOSIS ( 11 FDA reports)
MIOSIS ( 11 FDA reports)
MONOPARESIS ( 11 FDA reports)
MULTIPLE SCLEROSIS ( 11 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 11 FDA reports)
NEPHRITIS ( 11 FDA reports)
NEUTROPHILIA ( 11 FDA reports)
ORAL SURGERY ( 11 FDA reports)
OTORRHOEA ( 11 FDA reports)
AGEUSIA ( 10 FDA reports)
ALVEOLAR OSTEITIS ( 10 FDA reports)
AORTIC ANEURYSM ( 10 FDA reports)
ATRIAL THROMBOSIS ( 10 FDA reports)
ATROPHY ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 10 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 10 FDA reports)
BREAST TENDERNESS ( 10 FDA reports)
CARBON DIOXIDE DECREASED ( 10 FDA reports)
CATHETER SITE PAIN ( 10 FDA reports)
CELL DEATH ( 10 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 10 FDA reports)
CEREBELLAR ATAXIA ( 10 FDA reports)
CHIMERISM ( 10 FDA reports)
CHOLECYSTECTOMY ( 10 FDA reports)
DEAFNESS BILATERAL ( 10 FDA reports)
DEPRESSIVE SYMPTOM ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DEVICE DISLOCATION ( 10 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 10 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 10 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
EXERCISE TOLERANCE DECREASED ( 10 FDA reports)
FEMORAL ARTERY OCCLUSION ( 10 FDA reports)
FIBROUS HISTIOCYTOMA ( 10 FDA reports)
FOLLICULAR MUCINOSIS ( 10 FDA reports)
FOOT DEFORMITY ( 10 FDA reports)
FRACTURE NONUNION ( 10 FDA reports)
FUNGAL TEST POSITIVE ( 10 FDA reports)
FUSARIUM INFECTION ( 10 FDA reports)
GLOSSITIS ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 10 FDA reports)
GROWTH RETARDATION ( 10 FDA reports)
HAEMANGIOMA OF SPLEEN ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HEPATIC INFARCTION ( 10 FDA reports)
HEPATIC PAIN ( 10 FDA reports)
HEPATOBILIARY DISEASE ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
HYPERPHOSPHATAEMIA ( 10 FDA reports)
HYPOKINESIA ( 10 FDA reports)
ILEAL STENOSIS ( 10 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 10 FDA reports)
IRITIS ( 10 FDA reports)
LACTOBACILLUS INFECTION ( 10 FDA reports)
LISTERIOSIS ( 10 FDA reports)
LYMPHOCYTIC INFILTRATION ( 10 FDA reports)
MACULAR HOLE ( 10 FDA reports)
MALIGNANT MELANOMA IN SITU ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
NEPHROSCLEROSIS ( 10 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 10 FDA reports)
OESOPHAGEAL PAIN ( 10 FDA reports)
PAPULE ( 10 FDA reports)
PERIORBITAL HAEMATOMA ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PNEUMOPERITONEUM ( 10 FDA reports)
POSTURING ( 10 FDA reports)
PULMONARY VASCULITIS ( 10 FDA reports)
RADIATION SKIN INJURY ( 10 FDA reports)
RETICULOCYTE COUNT DECREASED ( 10 FDA reports)
RETINAL DETACHMENT ( 10 FDA reports)
RETROPERITONEAL FIBROSIS ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
SEDATION ( 10 FDA reports)
SENSATION OF FOREIGN BODY ( 10 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 10 FDA reports)
SUBDURAL EFFUSION ( 10 FDA reports)
SWEAT GLAND TUMOUR ( 10 FDA reports)
TONGUE NEOPLASM ( 10 FDA reports)
ULNA FRACTURE ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 10 FDA reports)
VENA CAVA THROMBOSIS ( 10 FDA reports)
WEST NILE VIRAL INFECTION ( 10 FDA reports)
PELVIC ABSCESS ( 9 FDA reports)
PERITONEAL HAEMORRHAGE ( 9 FDA reports)
POLYMYOSITIS ( 9 FDA reports)
POLYURIA ( 9 FDA reports)
POOR VENOUS ACCESS ( 9 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 9 FDA reports)
PROSTATITIS ( 9 FDA reports)
PRURITUS GENERALISED ( 9 FDA reports)
PYOGENIC GRANULOMA ( 9 FDA reports)
RASH MACULAR ( 9 FDA reports)
RENAL VEIN THROMBOSIS ( 9 FDA reports)
RESPIRATION ABNORMAL ( 9 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 9 FDA reports)
RESPIRATORY RATE DECREASED ( 9 FDA reports)
RETICULOCYTE COUNT INCREASED ( 9 FDA reports)
SENSITIVITY OF TEETH ( 9 FDA reports)
SIGMOIDITIS ( 9 FDA reports)
SINUSITIS FUNGAL ( 9 FDA reports)
TEETH BRITTLE ( 9 FDA reports)
TRICHOSPORON INFECTION ( 9 FDA reports)
TRISOMY 21 ( 9 FDA reports)
TUMOUR HAEMORRHAGE ( 9 FDA reports)
URETERIC DILATATION ( 9 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 9 FDA reports)
UVEITIS ( 9 FDA reports)
VAGINAL INFECTION ( 9 FDA reports)
VASCULAR ACCESS COMPLICATION ( 9 FDA reports)
VIRAL PHARYNGITIS ( 9 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 9 FDA reports)
XEROSIS ( 9 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ANGIONEUROTIC OEDEMA ( 9 FDA reports)
ANTIBODY TEST POSITIVE ( 9 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 9 FDA reports)
ARACHNOIDITIS ( 9 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 9 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
BACTERIA URINE IDENTIFIED ( 9 FDA reports)
BIOPSY ( 9 FDA reports)
BLOOD BICARBONATE DECREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 9 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 9 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 9 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 9 FDA reports)
BRAIN STEM INFARCTION ( 9 FDA reports)
BRONCHIAL SECRETION RETENTION ( 9 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 9 FDA reports)
BURKITT'S LEUKAEMIA ( 9 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 9 FDA reports)
CARDIAC ENZYMES INCREASED ( 9 FDA reports)
CATHETER SITE DISCHARGE ( 9 FDA reports)
CATHETER SITE INFECTION ( 9 FDA reports)
CLONIC CONVULSION ( 9 FDA reports)
CONGENITAL FOOT MALFORMATION ( 9 FDA reports)
CRYSTAL URINE PRESENT ( 9 FDA reports)
CYTOKINE STORM ( 9 FDA reports)
DYSPHEMIA ( 9 FDA reports)
DYSPRAXIA ( 9 FDA reports)
ENCEPHALITIC INFECTION ( 9 FDA reports)
ERECTILE DYSFUNCTION ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
FACTOR VIII DEFICIENCY ( 9 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 9 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 9 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 9 FDA reports)
GINGIVAL ULCERATION ( 9 FDA reports)
GLIOBLASTOMA MULTIFORME ( 9 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 9 FDA reports)
GROWTH HORMONE DEFICIENCY ( 9 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 9 FDA reports)
HIP SURGERY ( 9 FDA reports)
HYPERVISCOSITY SYNDROME ( 9 FDA reports)
HYPOAESTHESIA FACIAL ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 9 FDA reports)
INADEQUATE ANALGESIA ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INTENTIONAL DRUG MISUSE ( 9 FDA reports)
INTESTINAL INFARCTION ( 9 FDA reports)
INTESTINAL MASS ( 9 FDA reports)
LISTLESS ( 9 FDA reports)
LOSS OF PROPRIOCEPTION ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 9 FDA reports)
LYMPHOMA TRANSFORMATION ( 9 FDA reports)
MAJOR DEPRESSION ( 9 FDA reports)
MASTITIS ( 9 FDA reports)
MASTOIDITIS ( 9 FDA reports)
MILLER FISHER SYNDROME ( 9 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 9 FDA reports)
MUSCULOSKELETAL DISORDER ( 9 FDA reports)
NECROTISING COLITIS ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
NEURITIS ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 9 FDA reports)
OBSTRUCTION GASTRIC ( 9 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 9 FDA reports)
ACANTHAMOEBA INFECTION ( 8 FDA reports)
AFFECTIVE DISORDER ( 8 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 8 FDA reports)
ALVEOLAR PROTEINOSIS ( 8 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 8 FDA reports)
ANORECTAL DISORDER ( 8 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 8 FDA reports)
AXILLARY MASS ( 8 FDA reports)
BACK INJURY ( 8 FDA reports)
BENIGN GASTRIC NEOPLASM ( 8 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
BILE DUCT STONE ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 8 FDA reports)
BIPOLAR DISORDER ( 8 FDA reports)
BLOOD CREATININE ABNORMAL ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BODY HEIGHT BELOW NORMAL ( 8 FDA reports)
BREAST CYST ( 8 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 8 FDA reports)
BREATH ODOUR ( 8 FDA reports)
BURKITT'S LYMPHOMA STAGE III ( 8 FDA reports)
CAMPYLOBACTER INFECTION ( 8 FDA reports)
CATHETER SEPSIS ( 8 FDA reports)
CELL MARKER INCREASED ( 8 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 8 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 8 FDA reports)
CHEST WALL PAIN ( 8 FDA reports)
CHOKING ( 8 FDA reports)
CITROBACTER SEPSIS ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
CNS VENTRICULITIS ( 8 FDA reports)
COLLAGEN DISORDER ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 8 FDA reports)
CONDUCTIVE DEAFNESS ( 8 FDA reports)
CONGENITAL ANOMALY ( 8 FDA reports)
CONGENITAL HAND MALFORMATION ( 8 FDA reports)
CORONA VIRUS INFECTION ( 8 FDA reports)
CRYPTOCOCCOSIS ( 8 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 8 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DISINHIBITION ( 8 FDA reports)
DUODENAL ULCER PERFORATION ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 8 FDA reports)
DYSSTASIA ( 8 FDA reports)
DYSTONIA ( 8 FDA reports)
EAR DISCOMFORT ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
ECZEMA EYELIDS ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
ENCEPHALITIS ENTEROVIRAL ( 8 FDA reports)
ENTROPION ( 8 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 8 FDA reports)
ERYTHEMA NODOSUM ( 8 FDA reports)
EXCORIATION ( 8 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FANCONI SYNDROME ACQUIRED ( 8 FDA reports)
FEAR ( 8 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 8 FDA reports)
FRACTURE ( 8 FDA reports)
GASTRITIS HAEMORRHAGIC ( 8 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 8 FDA reports)
GENITAL HERPES ( 8 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 8 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 8 FDA reports)
GLOMERULOSCLEROSIS ( 8 FDA reports)
GOUTY ARTHRITIS ( 8 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 8 FDA reports)
HEPATITIS B DNA INCREASED ( 8 FDA reports)
HIV INFECTION ( 8 FDA reports)
HUMERUS FRACTURE ( 8 FDA reports)
HYPERPLASIA ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 8 FDA reports)
INTESTINAL FISTULA ( 8 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 8 FDA reports)
JAUNDICE NEONATAL ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
JUGULAR VEIN DISTENSION ( 8 FDA reports)
KERATITIS ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
LICHEN PLANUS ( 8 FDA reports)
LIPOMA ( 8 FDA reports)
LIVER SCAN ABNORMAL ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
MACROCYTOSIS ( 8 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 8 FDA reports)
MALIGNANT GLIOMA ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
MEGAKARYOCYTES INCREASED ( 8 FDA reports)
MENINGITIS VIRAL ( 8 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 8 FDA reports)
MUSCLE HAEMORRHAGE ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MYCOBACTERIAL INFECTION ( 8 FDA reports)
MYOPIA ( 8 FDA reports)
NAIL DYSTROPHY ( 8 FDA reports)
NAIL-PATELLA SYNDROME ( 8 FDA reports)
NASAL DISORDER ( 8 FDA reports)
NECK MASS ( 8 FDA reports)
OCULAR TOXICITY ( 8 FDA reports)
OESOPHAGEAL PERFORATION ( 8 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
OESOPHAGEAL STENOSIS ( 8 FDA reports)
ONYCHOMADESIS ( 8 FDA reports)
ORAL FUNGAL INFECTION ( 8 FDA reports)
ORAL MUCOSAL DISORDER ( 8 FDA reports)
ORAL NEOPLASM BENIGN ( 8 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 8 FDA reports)
OXYGEN SUPPLEMENTATION ( 8 FDA reports)
PARANOIA ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PAST-POINTING ( 8 FDA reports)
PCO2 INCREASED ( 8 FDA reports)
PERINEURIAL CYST ( 8 FDA reports)
PLEURAL DISORDER ( 8 FDA reports)
PNEUMOCOCCAL INFECTION ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 8 FDA reports)
PULMONARY INFARCTION ( 8 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 8 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 8 FDA reports)
RENAL ATROPHY ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
RESPIRATORY MONILIASIS ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
RETINAL DEGENERATION ( 8 FDA reports)
RHEUMATOID NODULE ( 8 FDA reports)
SALMONELLOSIS ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SCAN ABNORMAL ( 8 FDA reports)
SECONDARY SEQUESTRUM ( 8 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 8 FDA reports)
SKIN MASS ( 8 FDA reports)
SMALL INTESTINAL PERFORATION ( 8 FDA reports)
SOFT TISSUE NECROSIS ( 8 FDA reports)
SOPOR ( 8 FDA reports)
SPONDYLITIS ( 8 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 8 FDA reports)
TENDON DISORDER ( 8 FDA reports)
THIRST ( 8 FDA reports)
THYROID MASS ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
TONGUE ULCERATION ( 8 FDA reports)
TOOTH HYPOPLASIA ( 8 FDA reports)
TOXIC NODULAR GOITRE ( 8 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
TROPONIN T INCREASED ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 8 FDA reports)
URETHRAL HAEMORRHAGE ( 8 FDA reports)
URINARY TRACT OBSTRUCTION ( 8 FDA reports)
VASODILATATION ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
WALKING DISABILITY ( 8 FDA reports)
WEIGHT BEARING DIFFICULTY ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
PELVIC FLUID COLLECTION ( 7 FDA reports)
PEMPHIGUS ( 7 FDA reports)
PERICARDIAL HAEMORRHAGE ( 7 FDA reports)
PERICARDITIS CONSTRICTIVE ( 7 FDA reports)
PERIORBITAL CELLULITIS ( 7 FDA reports)
PERIOSTITIS ( 7 FDA reports)
PHLEBITIS SUPERFICIAL ( 7 FDA reports)
PHLEBOTHROMBOSIS ( 7 FDA reports)
PNEUMONIA NECROTISING ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PRODUCT QUALITY ISSUE ( 7 FDA reports)
PROTEIN TOTAL INCREASED ( 7 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 7 FDA reports)
PRURIGO ( 7 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 7 FDA reports)
PULSE ABNORMAL ( 7 FDA reports)
PUPILS UNEQUAL ( 7 FDA reports)
RECTAL CANCER ( 7 FDA reports)
RECTAL FISSURE ( 7 FDA reports)
RENAL CANCER ( 7 FDA reports)
RENAL NECROSIS ( 7 FDA reports)
RENAL VASCULITIS ( 7 FDA reports)
RETINAL VASCULITIS ( 7 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 7 FDA reports)
RIGHT ATRIAL DILATATION ( 7 FDA reports)
ROTAVIRUS INFECTION ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SHOULDER PAIN ( 7 FDA reports)
SJOGREN'S SYNDROME ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SKIN INJURY ( 7 FDA reports)
SMALL INTESTINE ULCER ( 7 FDA reports)
SNORING ( 7 FDA reports)
SPINAL DEFORMITY ( 7 FDA reports)
SPIROMETRY ABNORMAL ( 7 FDA reports)
STARING ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SUPRAPUBIC PAIN ( 7 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 7 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
TELANGIECTASIA ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
THALAMIC INFARCTION ( 7 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TOXIC NEUROPATHY ( 7 FDA reports)
TRACHEOBRONCHITIS ( 7 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
URINARY TRACT DISORDER ( 7 FDA reports)
URINARY TRACT INFECTION VIRAL ( 7 FDA reports)
VESTIBULAR DISORDER ( 7 FDA reports)
VIRAL RASH ( 7 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 7 FDA reports)
ABDOMINAL NEOPLASM ( 7 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 7 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 7 FDA reports)
ACUTE STRESS DISORDER ( 7 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 7 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 7 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 7 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 7 FDA reports)
ARTERIAL DISORDER ( 7 FDA reports)
ARTHRITIS INFECTIVE ( 7 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 7 FDA reports)
BLADDER PAIN ( 7 FDA reports)
BLINDNESS UNILATERAL ( 7 FDA reports)
BLOOD BICARBONATE INCREASED ( 7 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 7 FDA reports)
BLOOD CORTISOL DECREASED ( 7 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 7 FDA reports)
BONE DENSITY INCREASED ( 7 FDA reports)
BONE INFARCTION ( 7 FDA reports)
BONE SCAN ABNORMAL ( 7 FDA reports)
BORRELIA INFECTION ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BRONCHOPLEURAL FISTULA ( 7 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 7 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 7 FDA reports)
CATHETER SITE HAEMORRHAGE ( 7 FDA reports)
CEREBELLAR ATROPHY ( 7 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 7 FDA reports)
CEREBRAL ASPERGILLOSIS ( 7 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CHOLECYSTITIS INFECTIVE ( 7 FDA reports)
COMPARTMENT SYNDROME ( 7 FDA reports)
COR PULMONALE ( 7 FDA reports)
CORONARY ARTERY BYPASS ( 7 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DENTAL CLEANING ( 7 FDA reports)
DENTAL TREATMENT ( 7 FDA reports)
DERMATOMYOSITIS ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE ( 7 FDA reports)
ENDOMETRIAL CANCER ( 7 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 7 FDA reports)
ENDOTOXIC SHOCK ( 7 FDA reports)
EPIDURAL LIPOMATOSIS ( 7 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 7 FDA reports)
EWING'S SARCOMA RECURRENT ( 7 FDA reports)
EXFOLIATIVE RASH ( 7 FDA reports)
EXTRASYSTOLES ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 7 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 7 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
FURUNCLE ( 7 FDA reports)
GASTRIC MUCOSAL LESION ( 7 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GENERAL NUTRITION DISORDER ( 7 FDA reports)
GLIOBLASTOMA ( 7 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 7 FDA reports)
GOUT ( 7 FDA reports)
GRAFT COMPLICATION ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 7 FDA reports)
HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HEPATORENAL FAILURE ( 7 FDA reports)
HORMONE LEVEL ABNORMAL ( 7 FDA reports)
HYPERTONIC BLADDER ( 7 FDA reports)
HYPOPERFUSION ( 7 FDA reports)
ILEITIS ( 7 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCISION SITE INFECTION ( 7 FDA reports)
INFECTED LYMPHOCELE ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
INTESTINAL DILATATION ( 7 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 7 FDA reports)
INVESTIGATION ( 7 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 7 FDA reports)
LACERATION ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 7 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
LYMPHOMATOID PAPULOSIS ( 7 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 7 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 7 FDA reports)
MEDIASTINAL MASS ( 7 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 7 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 7 FDA reports)
METASTASES TO BONE MARROW ( 7 FDA reports)
MICTURITION DISORDER ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MONONEUROPATHY MULTIPLEX ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
MUSCLE NECROSIS ( 7 FDA reports)
MUSCLE SPASTICITY ( 7 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 7 FDA reports)
MYOPATHY STEROID ( 7 FDA reports)
NEPHROBLASTOMA ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 7 FDA reports)
OPHTHALMOPLEGIA ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
OSTEORADIONECROSIS ( 7 FDA reports)
PANCREATIC ATROPHY ( 7 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 7 FDA reports)
PARANASAL SINUS DISCOMFORT ( 7 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 7 FDA reports)
PAROTITIS ( 7 FDA reports)
ABDOMINAL SYMPTOM ( 6 FDA reports)
ABSCESS FUNGAL ( 6 FDA reports)
ABULIA ( 6 FDA reports)
ACID FAST BACILLI INFECTION ( 6 FDA reports)
ACQUIRED HAEMOPHILIA ( 6 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 6 FDA reports)
ANAEMIA NEONATAL ( 6 FDA reports)
ANAL DISCOMFORT ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
AORTIC THROMBOSIS ( 6 FDA reports)
AORTIC VALVE STENOSIS ( 6 FDA reports)
APATHY ( 6 FDA reports)
APPETITE DISORDER ( 6 FDA reports)
BACTEROIDES INFECTION ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BILIARY DRAINAGE ( 6 FDA reports)
BIOPSY SKIN ABNORMAL ( 6 FDA reports)
BLADDER TELANGIECTASIA ( 6 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
BLAST CELL CRISIS ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 6 FDA reports)
BLOOD IRON INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 6 FDA reports)
BONE NEOPLASM ( 6 FDA reports)
BOVINE TUBERCULOSIS ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BRAIN DAMAGE ( 6 FDA reports)
BREAST CELLULITIS ( 6 FDA reports)
BREAST OPERATION ( 6 FDA reports)
CALCULUS URETERIC ( 6 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 6 FDA reports)
CARDIAC OUTPUT DECREASED ( 6 FDA reports)
CARDIAC VALVE VEGETATION ( 6 FDA reports)
CARDITIS ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
CATARACT OPERATION ( 6 FDA reports)
CATHETER THROMBOSIS ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM ENTEROVIRAL INFECTION ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 6 FDA reports)
CEREBRAL CALCIFICATION ( 6 FDA reports)
CEREBRAL THROMBOSIS ( 6 FDA reports)
CERVIX CARCINOMA ( 6 FDA reports)
CHROMOSOMAL MUTATION ( 6 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COLECTOMY ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 6 FDA reports)
CONUS MEDULLARIS SYNDROME ( 6 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DENTAL PROSTHESIS USER ( 6 FDA reports)
DEPRESSION SUICIDAL ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DERMOID CYST ( 6 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 6 FDA reports)
DIABETIC COMA ( 6 FDA reports)
ECTHYMA ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 6 FDA reports)
ENTEROBACTER BACTERAEMIA ( 6 FDA reports)
ENTEROCOLITIS VIRAL ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA ( 6 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FAT EMBOLISM ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FLUID IMBALANCE ( 6 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 6 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 6 FDA reports)
FUNGUS STOOL IDENTIFIED ( 6 FDA reports)
GAS GANGRENE ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTRIC VOLVULUS ( 6 FDA reports)
GASTROENTERITIS SALMONELLA ( 6 FDA reports)
GASTROINTESTINAL CARCINOMA ( 6 FDA reports)
GASTROINTESTINAL FISTULA ( 6 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 6 FDA reports)
GASTROSPLENIC FISTULA ( 6 FDA reports)
HAEMARTHROSIS ( 6 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 6 FDA reports)
HAEMORRHAGIC ANAEMIA ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HEMIANOPIA HOMONYMOUS ( 6 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 6 FDA reports)
HEPATITIS B VIRUS ( 6 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERAEMIA ( 6 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 6 FDA reports)
HYPOCHROMASIA ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
HYPOURICAEMIA ( 6 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 6 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 6 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 6 FDA reports)
INTUBATION ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
KLIPPEL-FEIL SYNDROME ( 6 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 6 FDA reports)
LARYNGEAL CANCER ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LENTIGO ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
LYMPH NODE PALPABLE ( 6 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 6 FDA reports)
MENORRHAGIA ( 6 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 6 FDA reports)
METASTASES TO THE MEDIASTINUM ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MICROCEPHALY ( 6 FDA reports)
MICROSCOPIC POLYANGIITIS ( 6 FDA reports)
MUCOUS STOOLS ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
MYELOBLASTOMA ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 6 FDA reports)
NEPHRITIC SYNDROME ( 6 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 6 FDA reports)
NEUROCYSTICERCOSIS ( 6 FDA reports)
NO ADVERSE EFFECT ( 6 FDA reports)
NORMAL NEWBORN ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
NUCHAL RIGIDITY ( 6 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 6 FDA reports)
OVARIAN DISORDER ( 6 FDA reports)
PACHYMENINGITIS ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 6 FDA reports)
PERITONEAL EFFUSION ( 6 FDA reports)
PETIT MAL EPILEPSY ( 6 FDA reports)
PHARYNGEAL ULCERATION ( 6 FDA reports)
PLEURAL INFECTION ( 6 FDA reports)
PNEUMATURIA ( 6 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 6 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 6 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
POROKERATOSIS ( 6 FDA reports)
POSTRENAL FAILURE ( 6 FDA reports)
PRINZMETAL ANGINA ( 6 FDA reports)
PROCTOCOLITIS ( 6 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 6 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 6 FDA reports)
PURPURA FULMINANS ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RADIAL NERVE PALSY ( 6 FDA reports)
RADIUS FRACTURE ( 6 FDA reports)
REGRESSIVE BEHAVIOUR ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 6 FDA reports)
RHINITIS HYPERTROPHIC ( 6 FDA reports)
RICKETS ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SARCOMA ( 6 FDA reports)
SARCOMA METASTATIC ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SENSE OF OPPRESSION ( 6 FDA reports)
SHIFT TO THE LEFT ( 6 FDA reports)
SKELETAL INJURY ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 6 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 6 FDA reports)
STOMATOCOCCAL INFECTION ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 6 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 6 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
TESTIS CANCER ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
THYROIDITIS ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 6 FDA reports)
UTERINE ENLARGEMENT ( 6 FDA reports)
VAGINAL OBSTRUCTION ( 6 FDA reports)
VASCULITIC RASH ( 6 FDA reports)
VIRAL DIARRHOEA ( 6 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 6 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 6 FDA reports)
PELIOSIS HEPATIS ( 5 FDA reports)
PERIPHERAL NERVE PALSY ( 5 FDA reports)
PERITONEAL CARCINOMA ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POSTMENOPAUSE ( 5 FDA reports)
POSTOPERATIVE ADHESION ( 5 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 5 FDA reports)
POSTURE ABNORMAL ( 5 FDA reports)
PRECOCIOUS PUBERTY ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PRODUCT COLOUR ISSUE ( 5 FDA reports)
PROSTRATION ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
PULMONARY HILUM MASS ( 5 FDA reports)
PULSE PRESSURE DECREASED ( 5 FDA reports)
PYELONEPHRITIS FUNGAL ( 5 FDA reports)
PYOTHORAX ( 5 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 5 FDA reports)
RADIATION MUCOSITIS ( 5 FDA reports)
RENAL AMYLOIDOSIS ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL HYPERTENSION ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RETINAL DYSTROPHY ( 5 FDA reports)
RETINAL OEDEMA ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
RICHTER'S SYNDROME ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SENSORIMOTOR DISORDER ( 5 FDA reports)
SEPSIS NEONATAL ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN CHAPPED ( 5 FDA reports)
SKIN DEPIGMENTATION ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SMEAR CERVIX ABNORMAL ( 5 FDA reports)
SPINAL ANAESTHESIA ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SPINAL CORD OEDEMA ( 5 FDA reports)
SPLENIC LESION ( 5 FDA reports)
STRESS CARDIOMYOPATHY ( 5 FDA reports)
SUBACUTE HEPATIC FAILURE ( 5 FDA reports)
SUBDURAL HYGROMA ( 5 FDA reports)
SUDDEN HEARING LOSS ( 5 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
THERAPEUTIC EMBOLISATION ( 5 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
THROMBOTIC STROKE ( 5 FDA reports)
TRACHEAL STENOSIS ( 5 FDA reports)
TRANSFUSION MICROCHIMERISM ( 5 FDA reports)
TRANSIENT PSYCHOSIS ( 5 FDA reports)
TRIGEMINAL NERVE DISORDER ( 5 FDA reports)
TUMOUR FLARE ( 5 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 5 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
UTERINE MASS ( 5 FDA reports)
VAGINAL CELLULITIS ( 5 FDA reports)
VASCULAR GRAFT COMPLICATION ( 5 FDA reports)
VASCULAR PSEUDOANEURYSM ( 5 FDA reports)
VEILLONELLA INFECTION ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
VISCERAL LEISHMANIASIS ( 5 FDA reports)
VITILIGO ( 5 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 5 FDA reports)
ABDOMINAL WALL DISORDER ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 5 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
AMBLYOPIA STRABISMIC ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
APOPTOSIS ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
ASPERGILLOMA ( 5 FDA reports)
ATONIC SEIZURES ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
AXONAL NEUROPATHY ( 5 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 5 FDA reports)
BASAL GANGLION DEGENERATION ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 5 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
BLOOD OSMOLARITY INCREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BLOOD URINE ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BRAIN STEM HAEMORRHAGE ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST ABSCESS ( 5 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 5 FDA reports)
BRONCHOSCOPY ABNORMAL ( 5 FDA reports)
BURSA DISORDER ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
CAROTID ARTERY THROMBOSIS ( 5 FDA reports)
CATHETER SITE CELLULITIS ( 5 FDA reports)
CATHETER SITE SWELLING ( 5 FDA reports)
CELLULITIS ORBITAL ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CEREBELLAR TUMOUR ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CERVICAL SPINAL STENOSIS ( 5 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 5 FDA reports)
CHALAZION ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHORIORETINAL ATROPHY ( 5 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 5 FDA reports)
COLON NEOPLASM ( 5 FDA reports)
COLOUR BLINDNESS ( 5 FDA reports)
COMA SCALE ABNORMAL ( 5 FDA reports)
COMPLEMENT FACTOR DECREASED ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CORNEAL NEOVASCULARISATION ( 5 FDA reports)
CORNEAL OPACITY ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CRYOGLOBULINAEMIA ( 5 FDA reports)
CSF BACTERIA IDENTIFIED ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
CYST REMOVAL ( 5 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 5 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 5 FDA reports)
DENERVATION ATROPHY ( 5 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DIARRHOEA INFECTIOUS ( 5 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DUODENAL PERFORATION ( 5 FDA reports)
DYSMORPHISM ( 5 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 5 FDA reports)
EJECTION FRACTION ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 5 FDA reports)
ENCEPHALITIS POST VARICELLA ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENDOCARDIAL FIBROSIS ( 5 FDA reports)
ENTEROVIRUS INFECTION ( 5 FDA reports)
EPIDERMAL NECROSIS ( 5 FDA reports)
EPIDERMOLYSIS ( 5 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE INFECTION BACTERIAL ( 5 FDA reports)
FAT TISSUE INCREASED ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
FOETAL DEATH ( 5 FDA reports)
GASTROINTESTINAL EROSION ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GRANULOCYTOSIS ( 5 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 5 FDA reports)
GRUNTING ( 5 FDA reports)
HAEMOGLOBIN ( 5 FDA reports)
HEART TRANSPLANT ( 5 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 5 FDA reports)
HEPATIC INFECTION ( 5 FDA reports)
HEPATITIS C VIRUS TEST ( 5 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 5 FDA reports)
HERPES OESOPHAGITIS ( 5 FDA reports)
HERPES SIMPLEX HEPATITIS ( 5 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HODGKIN'S DISEASE STAGE II ( 5 FDA reports)
HYDROURETER ( 5 FDA reports)
HYPERPROTEINAEMIA ( 5 FDA reports)
HYPOCAPNIA ( 5 FDA reports)
HYPOSMIA ( 5 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
ILEAL ULCER ( 5 FDA reports)
ILIAC VEIN THROMBOSIS ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 5 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INJECTION SITE EXTRAVASATION ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
INTESTINAL STENOSIS ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
IRIDOCYCLITIS ( 5 FDA reports)
KERATITIS INTERSTITIAL ( 5 FDA reports)
KIDNEY MALFORMATION ( 5 FDA reports)
KLEBSIELLA TEST POSITIVE ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
LAPAROTOMY ( 5 FDA reports)
LASER THERAPY ( 5 FDA reports)
LEUKODYSTROPHY ( 5 FDA reports)
LEUKOSTASIS ( 5 FDA reports)
LICHENOID KERATOSIS ( 5 FDA reports)
LIGAMENT LAXITY ( 5 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LIPASE ABNORMAL ( 5 FDA reports)
LIPOSARCOMA ( 5 FDA reports)
LIVER TENDERNESS ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LUPUS PNEUMONITIS ( 5 FDA reports)
LYMPHOCELE ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MALIGNANT ASCITES ( 5 FDA reports)
MARASMUS ( 5 FDA reports)
MECHANICAL ILEUS ( 5 FDA reports)
MEDIASTINUM NEOPLASM ( 5 FDA reports)
MENINGITIS ENTEROVIRAL ( 5 FDA reports)
MENINGITIS LISTERIA ( 5 FDA reports)
MENINGITIS TUBERCULOUS ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 5 FDA reports)
METASTASES TO HEART ( 5 FDA reports)
METASTASES TO KIDNEY ( 5 FDA reports)
MICROALBUMINURIA ( 5 FDA reports)
MICROSPORIDIA INFECTION ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MUCOSAL INFECTION ( 5 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
NAIL DISCOLOURATION ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NECROSIS ISCHAEMIC ( 5 FDA reports)
NECROTISING RETINITIS ( 5 FDA reports)
NEONATAL HYPOTENSION ( 5 FDA reports)
NEPHRECTOMY ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
ONYCHOCLASIS ( 5 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 5 FDA reports)
ORCHITIS ( 5 FDA reports)
OSTEOTOMY ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABSCESS NECK ( 4 FDA reports)
ABSCESS RUPTURE ( 4 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 4 FDA reports)
ADENOCARCINOMA PANCREAS ( 4 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
ADRENAL MASS ( 4 FDA reports)
ALBUMINURIA ( 4 FDA reports)
ANAL ULCER ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
ARTERIAL RUPTURE ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTHRITIS REACTIVE ( 4 FDA reports)
ARTHROTOXICITY ( 4 FDA reports)
ASCITES INFECTION ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
ATRIAL HYPERTROPHY ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
AURICULAR SWELLING ( 4 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 4 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 4 FDA reports)
B-LYMPHOCYTE ABNORMALITIES ( 4 FDA reports)
BACILLARY ANGIOMATOSIS ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
BICYTOPENIA ( 4 FDA reports)
BILIARY TRACT INFECTION ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 4 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 4 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 4 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE MARROW ISCHAEMIA ( 4 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN COMPRESSION ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BREAST DISCOMFORT ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST INFECTION ( 4 FDA reports)
BRONCHITIS BACTERIAL ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
BRONCHOPULMONARY DISEASE ( 4 FDA reports)
BURNING SENSATION MUCOSAL ( 4 FDA reports)
BUTTERFLY RASH ( 4 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CAPILLARY DISORDER ( 4 FDA reports)
CARBON DIOXIDE INCREASED ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 4 FDA reports)
CD4/CD8 RATIO DECREASED ( 4 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CEREBROSCLEROSIS ( 4 FDA reports)
CHLOROMA ( 4 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 4 FDA reports)
CHORIORETINITIS ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
CLONUS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 4 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 4 FDA reports)
COLONIC FISTULA ( 4 FDA reports)
COMPLICATION OF PREGNANCY ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 4 FDA reports)
CONGENITAL NOSE MALFORMATION ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CSF CULTURE POSITIVE ( 4 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 4 FDA reports)
CUTANEOUS TUBERCULOSIS ( 4 FDA reports)
CYTOLOGY ABNORMAL ( 4 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 4 FDA reports)
CYTOMEGALOVIRUS TEST ( 4 FDA reports)
DECREASED VIBRATORY SENSE ( 4 FDA reports)
DELUSION OF GRANDEUR ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 4 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIAPHRAGMATIC DISORDER ( 4 FDA reports)
DIASTOLIC HYPOTENSION ( 4 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 4 FDA reports)
DIZZINESS EXERTIONAL ( 4 FDA reports)
DRUG CLEARANCE INCREASED ( 4 FDA reports)
DRUG LEVEL FLUCTUATING ( 4 FDA reports)
DUODENAL STENOSIS ( 4 FDA reports)
DYSENTERY ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDOCRINE DISORDER ( 4 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
FLIGHT OF IDEAS ( 4 FDA reports)
FLOPPY INFANT ( 4 FDA reports)
FOETAL MALNUTRITION ( 4 FDA reports)
FUNGAL ENDOCARDITIS ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTRODUODENAL ULCER ( 4 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT DYSFUNCTION ( 4 FDA reports)
GRAFT LOSS ( 4 FDA reports)
GRANULOCYTES MATURATION ARREST ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMORRHAGIC ASCITES ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEART TRANSPLANT REJECTION ( 4 FDA reports)
HEPATIC ISCHAEMIA ( 4 FDA reports)
HEPATITIS B VIRUS TEST ( 4 FDA reports)
HEPATITIS E ( 4 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 4 FDA reports)
HETEROTAXIA ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HY'S LAW CASE ( 4 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 4 FDA reports)
HYPERCHLORHYDRIA ( 4 FDA reports)
HYPERMETABOLISM ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
IMPLANT SITE REACTION ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INFECTION PARASITIC ( 4 FDA reports)
INFUSION SITE BRUISING ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE VASCULITIS ( 4 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
JEJUNITIS ( 4 FDA reports)
JOINT SURGERY ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KOUNIS SYNDROME ( 4 FDA reports)
LARYNGEAL DISORDER ( 4 FDA reports)
LEUKAEMIC INFILTRATION ( 4 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 4 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 4 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LIPOMATOSIS ( 4 FDA reports)
LIVE BIRTH ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 4 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MALARIA ( 4 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 4 FDA reports)
METASTASES TO OVARY ( 4 FDA reports)
METASTASES TO RETROPERITONEUM ( 4 FDA reports)
METASTASES TO SALIVARY GLAND ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
MYELOCYTOSIS ( 4 FDA reports)
MYOPERICARDITIS ( 4 FDA reports)
NASAL CAVITY CANCER ( 4 FDA reports)
NEPHRITIS AUTOIMMUNE ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NERVE ROOT LESION ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUROPATHIC PAIN ( 4 FDA reports)
NEUTROPENIA NEONATAL ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NIKOLSKY'S SIGN ( 4 FDA reports)
NOCARDIA SEPSIS ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OCULAR SURFACE DISEASE ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
OSTEOCHONDRITIS ( 4 FDA reports)
OSTEOCHONDROSIS ( 4 FDA reports)
OSTEOMA CUTIS ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERITONEAL INFECTION ( 4 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 4 FDA reports)
PHAEHYPHOMYCOSIS ( 4 FDA reports)
PHALANGEAL AGENESIS ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PNEUMONIA ESCHERICHIA ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYSEROSITIS ( 4 FDA reports)
POOR SUCKING REFLEX ( 4 FDA reports)
POSITIVE ROMBERGISM ( 4 FDA reports)
POST PROCEDURAL VOMITING ( 4 FDA reports)
POSTICTAL STATE ( 4 FDA reports)
POSTPARTUM DEPRESSION ( 4 FDA reports)
POTENTIATING DRUG INTERACTION ( 4 FDA reports)
PRESSURE OF SPEECH ( 4 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 4 FDA reports)
PROTEIN C DECREASED ( 4 FDA reports)
PROTEIN S DECREASED ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PSEUDOBULBAR PALSY ( 4 FDA reports)
PSOAS ABSCESS ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PYURIA ( 4 FDA reports)
RADIATION NECROSIS ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RADICULITIS BRACHIAL ( 4 FDA reports)
RECTAL PERFORATION ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 4 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 4 FDA reports)
RENAL ANEURYSM ( 4 FDA reports)
RENAL HYPERTROPHY ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RHABDOMYOSARCOMA RECURRENT ( 4 FDA reports)
SALIVARY GLAND NEOPLASM ( 4 FDA reports)
SCLEREMA ( 4 FDA reports)
SCROTAL INFECTION ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SINUSITIS BACTERIAL ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 4 FDA reports)
SPUTUM ABNORMAL ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 4 FDA reports)
STEATORRHOEA ( 4 FDA reports)
STRESS ULCER ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THREATENED LABOUR ( 4 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TOOTH REPAIR ( 4 FDA reports)
TRANSFUSION ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
TURNER'S SYNDROME ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
VACCINATION FAILURE ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VAGINAL INFLAMMATION ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VASCULITIS GASTROINTESTINAL ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VEIN DISORDER ( 4 FDA reports)
VENOUS STENOSIS ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VITAMIN B12 INCREASED ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 4 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 3 FDA reports)
PERIDIVERTICULAR ABSCESS ( 3 FDA reports)
PERITONSILLAR ABSCESS ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PERSISTENT GENERALISED LYMPHADENOPATHY ( 3 FDA reports)
PHALANGEAL HYPOPLASIA ( 3 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 3 FDA reports)
PHLEBOSCLEROSIS ( 3 FDA reports)
PHRENIC NERVE PARALYSIS ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
PLASTIC SURGERY ( 3 FDA reports)
PLATELET AGGREGATION ( 3 FDA reports)
PLATELET COUNT ( 3 FDA reports)
PLEURAL INFECTION BACTERIAL ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PLEUROPERICARDITIS ( 3 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 3 FDA reports)
POEMS SYNDROME ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
PORPHYRIA NON-ACUTE ( 3 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POST PROCEDURAL NAUSEA ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTMATURE BABY ( 3 FDA reports)
POSTPARTUM HAEMORRHAGE ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRIMITIVE NEUROECTODERMAL TUMOUR ( 3 FDA reports)
PROSTATE CANCER STAGE IV ( 3 FDA reports)
PROSTHESIS IMPLANTATION ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY VASCULAR DISORDER ( 3 FDA reports)
PUNCTURE SITE INFECTION ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RED BLOOD CELLS URINE ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
RENAL AGENESIS ( 3 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL SALT-WASTING SYNDROME ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RETCHING ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RHABDOMYOMA ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RHEUMATOID VASCULITIS ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SALIVARY GLAND ADENOMA ( 3 FDA reports)
SALMONELLA SEPSIS ( 3 FDA reports)
SALMONELLA TEST POSITIVE ( 3 FDA reports)
SCLERODACTYLIA ( 3 FDA reports)
SCLERODERMA RENAL CRISIS ( 3 FDA reports)
SECONDARY SEXUAL CHARACTERISTICS ABSENCE ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SMALL INTESTINAL STENOSIS ( 3 FDA reports)
SODIUM RETENTION ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPLENIC HAEMATOMA ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SUPERINFECTION BACTERIAL ( 3 FDA reports)
SWEAT GLAND DISORDER ( 3 FDA reports)
SYRINGOMYELIA ( 3 FDA reports)
T-CELL LYMPHOMA REFRACTORY ( 3 FDA reports)
TANGENTIALITY ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TERMINAL DRIBBLING ( 3 FDA reports)
THROMBECTOMY ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOOTH DEPOSIT ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOOTH EROSION ( 3 FDA reports)
TOXIC OPTIC NEUROPATHY ( 3 FDA reports)
TOXIC SHOCK SYNDROME ( 3 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TRANSAMINASES ABNORMAL ( 3 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 3 FDA reports)
TRICHIASIS ( 3 FDA reports)
TUMOUR ULCERATION ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
URAEMIC ENCEPHALOPATHY ( 3 FDA reports)
UREAPLASMA INFECTION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
UROGENITAL HAEMORRHAGE ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOUS HAEMORRHAGE ( 3 FDA reports)
VENTRICULAR DYSKINESIA ( 3 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 3 FDA reports)
VIIITH NERVE LESION ( 3 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 3 FDA reports)
VOCAL CORD PARESIS ( 3 FDA reports)
VULVAR EROSION ( 3 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND NECROSIS ( 3 FDA reports)
XANTHOGRANULOMA ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 3 FDA reports)
ABSCESS DRAINAGE ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACALCULIA ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ADENOVIRUS TEST POSITIVE ( 3 FDA reports)
ADMINISTRATION SITE PAIN ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA RECURRENT ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANAPLASTIC THYROID CANCER ( 3 FDA reports)
ANDROGENETIC ALOPECIA ( 3 FDA reports)
ANGIOSCLEROSIS ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ANOTIA ( 3 FDA reports)
ANTI-THYROID ANTIBODY ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 3 FDA reports)
AURA ( 3 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
BACILLUS TEST POSITIVE ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BACTERIAL DISEASE CARRIER ( 3 FDA reports)
BACTERIAL PERICARDITIS ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BARTHOLIN'S ABSCESS ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BENIGN COLONIC NEOPLASM ( 3 FDA reports)
BILE DUCT STENT INSERTION ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BILIARY TRACT DILATION PROCEDURE ( 3 FDA reports)
BIOPSY LUNG ABNORMAL ( 3 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 3 FDA reports)
BLADDER HYPERTROPHY ( 3 FDA reports)
BLAST CELL PROLIFERATION ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD HIV RNA INCREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD STEM CELL HARVEST ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN MIDLINE SHIFT ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
BRONCHIAL HAEMORRHAGE ( 3 FDA reports)
BRUCELLOSIS ( 3 FDA reports)
BULLOUS LUNG DISEASE ( 3 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 3 FDA reports)
CALCIUM IONISED DECREASED ( 3 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC INFECTION ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAROTID BRUIT ( 3 FDA reports)
CAST REMOVAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBRAL HYGROMA ( 3 FDA reports)
CERUMEN REMOVAL ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHEST WALL MASS ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 3 FDA reports)
CHRONIC TONSILLITIS ( 3 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 3 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 3 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLON GANGRENE ( 3 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONJUNCTIVAL OEDEMA ( 3 FDA reports)
CONNECTIVE TISSUE DISORDER ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
COXSACKIE VIRAL INFECTION ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CSF CELL COUNT ABNORMAL ( 3 FDA reports)
CSF GLUCOSE ABNORMAL ( 3 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 3 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CSF VIRUS IDENTIFIED ( 3 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 3 FDA reports)
CYTOMEGALOVIRUS MYELOMENINGORADICULITIS ( 3 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DISTRACTIBILITY ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG HALF-LIFE INCREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
EAR INFECTION BACTERIAL ( 3 FDA reports)
ECCENTRIC FIXATION ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 3 FDA reports)
ENDOCERVICAL CURETTAGE ( 3 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EPIPHYSIOLYSIS ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYELID VASCULAR DISORDER ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III RECURRENT ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
FROSTBITE ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
GASTRIC ATONY ( 3 FDA reports)
GASTRIC CANCER STAGE IV ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
GLIAL SCAR ( 3 FDA reports)
GLYCOGEN STORAGE DISORDER ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HANTAVIRUS PULMONARY INFECTION ( 3 FDA reports)
HBV DNA INCREASED ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEPATIC AMOEBIASIS ( 3 FDA reports)
HEPATIC CANDIDIASIS ( 3 FDA reports)
HEPATIC SIDEROSIS ( 3 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 3 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS INFECTIOUS ( 3 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 3 FDA reports)
HIV TEST POSITIVE ( 3 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 3 FDA reports)
HUMORAL IMMUNE DEFECT ( 3 FDA reports)
HUNGRY BONE SYNDROME ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERTROPHIC SCAR ( 3 FDA reports)
HYPOMETABOLISM ( 3 FDA reports)
IGA NEPHROPATHY ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 3 FDA reports)
IMMUNODEFICIENCY CONGENITAL ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INFECTION REACTIVATION ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INFESTATION ( 3 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
JAUNDICE HEPATOCELLULAR ( 3 FDA reports)
JOINT DESTRUCTION ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KRABBE'S DISEASE ( 3 FDA reports)
LABOUR INDUCTION ( 3 FDA reports)
LARYNGOSCOPY ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LEGIONELLA INFECTION ( 3 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 3 FDA reports)
LEGIONELLA TEST POSITIVE ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LEUKAEMIC INFILTRATION GINGIVA ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LHERMITTE'S SIGN ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
LYMPHOHISTIOCYTOSIS ( 3 FDA reports)
MALIGNANT TRANSFORMATION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 3 FDA reports)
MEDICAL DEVICE REMOVAL ( 3 FDA reports)
MENINGITIS HERPES ( 3 FDA reports)
MENINGITIS TOXOPLASMAL ( 3 FDA reports)
MENINGOENCEPHALITIS ADENOVIRAL ( 3 FDA reports)
MENINGORRHAGIA ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 3 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METAL POISONING ( 3 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 3 FDA reports)
METASTASES TO EYE ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
METHYLOBACTERIUM INFECTION ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MOYAMOYA DISEASE ( 3 FDA reports)
MUCOSAL EXFOLIATION ( 3 FDA reports)
MULTIMORBIDITY ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYCOTIC ANEURYSM ( 3 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 3 FDA reports)
NEONATAL CHOLESTASIS ( 3 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 3 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 3 FDA reports)
NODAL ARRHYTHMIA ( 3 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESOPHAGEAL INFECTION ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPTIC NERVE INFARCTION ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 3 FDA reports)
ORCHIDECTOMY ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
OSTEOMYELITIS BACTERIAL ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PARANEOPLASTIC DERMATOMYOSITIS ( 3 FDA reports)
PARENTERAL NUTRITION ( 3 FDA reports)
PAROTIDECTOMY ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 2 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 2 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADENOVIRAL UPPER RESPIRATORY INFECTION ( 2 FDA reports)
ADIPOSIS DOLOROSA ( 2 FDA reports)
AESTHESIONEUROBLASTOMA ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
AIDS DEMENTIA COMPLEX ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALEXIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALLOIMMUNISATION ( 2 FDA reports)
ALOPECIA AREATA ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMINO ACID LEVEL INCREASED ( 2 FDA reports)
AMINOACIDURIA ( 2 FDA reports)
AMOEBIASIS ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 2 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-GAD ANTIBODY ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
APPENDICEAL MUCOCOELE ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPLICATION SITE CELLULITIS ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ASTRINGENT THERAPY ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BABESIOSIS ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY ISCHAEMIA ( 2 FDA reports)
BILIARY SPHINCTEROTOMY ( 2 FDA reports)
BLADDER FIBROSIS ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLADDER PERFORATION ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD AMYLASE ABNORMAL ( 2 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN ( 2 FDA reports)
BLOOD CHROMIUM DECREASED ( 2 FDA reports)
BLOOD CHROMIUM INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN NEGATIVE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 2 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 2 FDA reports)
BLOOD THROMBIN INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BODY FAT DISORDER ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BULBAR PALSY ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CANCER IN REMISSION ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBROVASCULAR SPASM ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHOLESTEATOMA ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHORIOCARCINOMA ( 2 FDA reports)
CHORIORETINAL DISORDER ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLD AGGLUTININS POSITIVE ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONGENITAL AORTIC ANOMALY ( 2 FDA reports)
CONGENITAL CEREBRAL CYST ( 2 FDA reports)
CONGENITAL NAIL DISORDER ( 2 FDA reports)
CONGENITAL RENAL DISORDER ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL OPACITY CONGENITAL ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORYNEBACTERIUM SEPSIS ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
CROSSMATCH INCOMPATIBLE ( 2 FDA reports)
CSF GLUCOSE INCREASED ( 2 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
CSF MONOCYTE COUNT POSITIVE ( 2 FDA reports)
CSF PROTEIN ABNORMAL ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS URINARY TRACT INFECTION ( 2 FDA reports)
CYTOTOXIC OEDEMA ( 2 FDA reports)
DACTYLITIS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELAYED SLEEP PHASE ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS DIAPER ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DIFFUSE AXONAL INJURY ( 2 FDA reports)
DIFFUSE VASCULITIS ( 2 FDA reports)
DISTRIBUTIVE SHOCK ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DUCHENNE MUSCULAR DYSTROPHY ( 2 FDA reports)
DWARFISM ( 2 FDA reports)
DYSPONESIS ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
DYSTROPHIC CALCIFICATION ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ENCEPHALITIS PROTOZOAL ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
ENTEROVIRUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIC CELLULITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 2 FDA reports)
EPSTEIN-BARR VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
EROSIVE BALANITIS ( 2 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 2 FDA reports)
EWING'S SARCOMA METASTATIC ( 2 FDA reports)
EXCHANGE BLOOD TRANSFUSION ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) RECURRENT ( 2 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE INFECTION TOXOPLASMAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FACTOR VII DEFICIENCY ( 2 FDA reports)
FAECALURIA ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FALLOT'S TETRALOGY ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FIBRILLARY GLOMERULONEPHRITIS ( 2 FDA reports)
FINGER HYPOPLASIA ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FIXED ERUPTION ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETAL HEART RATE DISORDER ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC ILEUS ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROENTERITIS RADIATION ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL ENDOSCOPIC THERAPY ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL INFECTION FUNGAL ( 2 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 2 FDA reports)
GERM CELL CANCER ( 2 FDA reports)
GERSTMANN'S SYNDROME ( 2 FDA reports)
GINGIVAL CANCER ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVAL OPERATION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GLUCOCORTICOID DEFICIENCY ( 2 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 2 FDA reports)
GOODPASTURE'S SYNDROME ( 2 FDA reports)
GRAM STAIN POSITIVE ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMANGIOMA CONGENITAL ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOBLASTOMA ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HERNIAL EVENTRATION ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HERPETIC STOMATITIS ( 2 FDA reports)
HIGH ARCHED PALATE ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIGH GRADE B-CELL LYMPHOMA BURKITT-LIKE LYMPHOMA ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 2 FDA reports)
HUMAN RHINOVIRUS TEST POSITIVE ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGONADISM FEMALE ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
HYPOTELORISM OF ORBIT ( 2 FDA reports)
ICHTHYOSIS ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
IMMUNOTACTOID GLOMERULONEPHRITIS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED INSULIN SECRETION ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
IMPLANT SITE EXTRAVASATION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTION MASKED ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFECTIVE THROMBOSIS ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY PSEUDOTUMOUR ( 2 FDA reports)
INFUSION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN RESISTANT DIABETES ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ANASTOMOSIS ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IVTH NERVE PARESIS ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
JEJUNAL STENOSIS ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL NEOPLASM ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LEIOMYOSARCOMA RECURRENT ( 2 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 2 FDA reports)
LEUKOPENIA NEONATAL ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIGHT CHAIN DISEASE ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOCAL ANAESTHESIA ( 2 FDA reports)
LOW SET EARS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUDWIG ANGINA ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG CYST ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
LYMPHOMA AIDS RELATED ( 2 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 2 FDA reports)
LYMPHOSTASIS ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT LYMPHOMA UNCLASSIFIABLE HIGH GRADE ( 2 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MANTLE CELL LYMPHOMA REFRACTORY ( 2 FDA reports)
MAXILLOFACIAL OPERATION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 2 FDA reports)
MEDIASTINAL ABSCESS ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 2 FDA reports)
MENINGIOMA MALIGNANT ( 2 FDA reports)
MENINGOCOCCAL BACTERAEMIA ( 2 FDA reports)
MENINGOENCEPHALITIS AMOEBIC ( 2 FDA reports)
METASTASES TO LARGE INTESTINE ( 2 FDA reports)
METASTASES TO NECK ( 2 FDA reports)
METASTASES TO OESOPHAGUS ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
METASTASES TO THORAX ( 2 FDA reports)
METASTASES TO TRACHEA ( 2 FDA reports)
METASTASES TO UTERUS ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUCOSAL NECROSIS ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 2 FDA reports)
MYCOSIS FUNGOIDES RECURRENT ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL PIGMENTATION ( 2 FDA reports)
NASAL CAVITY PACKING ( 2 FDA reports)
NASAL FLARING ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 2 FDA reports)
NEONATAL APNOEIC ATTACK ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEURILEMMOMA ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NEUROMYELITIS OPTICA ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NOCARDIA TEST POSITIVE ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
OLFACTORY NERVE DISORDER ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
ORO-PHARYNGEAL ASPERGILLOSIS ( 2 FDA reports)
OROANTRAL FISTULA ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
ORTHOSTATIC TREMOR ( 2 FDA reports)
OSSICLE DISORDER ( 2 FDA reports)
OSTEOSARCOMA METASTATIC ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PAGET-SCHROETTER SYNDROME ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PALATITIS ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PANNICULITIS LOBULAR ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARACENTESIS ABDOMEN ( 2 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 2 FDA reports)
PARESIS CRANIAL NERVE ( 2 FDA reports)
PAROTID GLAND INFLAMMATION ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERICARDIAL FIBROSIS ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 2 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED RECURRENT ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED STAGE IV ( 2 FDA reports)
PERIPORTAL OEDEMA ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONEAL TUBERCULOSIS ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNX DISCOMFORT ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHOTOPHERESIS ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLASMA CELLS INCREASED ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLASMINOGEN DECREASED ( 2 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
PORTAL VEIN FLOW DECREASED ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
PRECURSOR B-LYMPHOBLASTIC LYMPHOMA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROCTOSTOMY ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSITTACOSIS ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY ALVEOLAR MICROLITHIASIS ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYOMYOSITIS ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL HAEMATOMA ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL LIPOMATOSIS ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY DEPTH DECREASED ( 2 FDA reports)
RESPIRATORY PARALYSIS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RESPIRATORY TRACT OEDEMA ( 2 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETROPERITONEAL MASS ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 2 FDA reports)
SARCOMA UTERUS ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SECONDARY HYPOTHYROIDISM ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SIGNET-RING CELL CARCINOMA ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN SENSITISATION ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOFT TISSUE INFLAMMATION ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL CORD HAEMORRHAGE ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPLENIC NECROSIS ( 2 FDA reports)
SPOROTRICHOSIS ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STAPHYLOMA ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STOMATITIS RADIATION ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE NEONATAL ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE II ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
T-CELL LYMPHOMA STAGE III ( 2 FDA reports)
TABLET PHYSICAL ISSUE ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 2 FDA reports)
TERATOGENICITY ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
TESTICULAR NEOPLASM ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THERAPY RESPONDER ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
TONGUE CARCINOMA STAGE I ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONSILLAR ULCER ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TORUS FRACTURE ( 2 FDA reports)
TRACHEAL DEVIATION ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRICHOSTASIS SPINULOSA ( 2 FDA reports)
TRICHOTILLOMANIA ( 2 FDA reports)
TRISOMY 8 ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY BLADDER ATROPHY ( 2 FDA reports)
URINARY BLADDER SARCOMA ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URINE OSMOLARITY DECREASED ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
URINE PHOSPHORUS INCREASED ( 2 FDA reports)
URINE POTASSIUM INCREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VAGINAL ABSCESS ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VENA CAVA FILTER INSERTION ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENTOUSE EXTRACTION ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VIRAL HEPATITIS CARRIER ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VIRAL TITRE DECREASED ( 2 FDA reports)
VIRAL VASCULITIS ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAMIN A INCREASED ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN D INCREASED ( 2 FDA reports)
VITH NERVE DISORDER ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
VULVOVAGINAL ADHESION ( 2 FDA reports)
WEIGHT DECREASE NEONATAL ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WOUND INFECTION FUNGAL ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PENICILLIOSIS ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDITIS FUNGAL ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL EFFLUENT LEUKOCYTE COUNT INCREASED ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHAGOCYTOSIS ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLASMIN INHIBITOR DECREASED ( 1 FDA reports)
PLATELET AGGREGATION INHIBITION ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLATELET TOXICITY ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
PNEUMONIA TOXOPLASMAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYMERASE CHAIN REACTION ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PRECIPITATE LABOUR ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRIMARY AMYLOIDOSIS ( 1 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROCALCITONIN ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT CLOSURE ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOXANTHOMA ELASTICUM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PUBERTY ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERY ANEURYSM ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTATE BASOPHILIA ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE DISCHARGE ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYOMETRA ( 1 FDA reports)
RADIAL NERVE LESION ( 1 FDA reports)
RADIATION PERICARDITIS ( 1 FDA reports)
RADIATION RETINOPATHY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION PRESENT ( 1 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL NUCLEATED MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH EXCESS BLASTS IN TRANSFORMATION ( 1 FDA reports)
REFRACTORY CANCER ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY RATE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RETICULIN INCREASED ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINITIS VIRAL ( 1 FDA reports)
RETINOBLASTOMA UNILATERAL ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIGHT AORTIC ARCH ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND CANCER RECURRENT ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SECONDARY HYPERTHYROIDISM ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SEMEN ABNORMAL ( 1 FDA reports)
SEPSIS PASTEURELLA ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SEZARY CELLS INCREASED ( 1 FDA reports)
SHORTENED CERVIX ( 1 FDA reports)
SHRINKING LUNG SYNDROME ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN FLAP NECROSIS ( 1 FDA reports)
SKIN GRAFT REJECTION ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOLITARY KIDNEY SECONDARY ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
SPHEROCYTIC ANAEMIA ( 1 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINAL VASCULAR DISORDER ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC INFECTION FUNGAL ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBACUTE SCLEROSING PANENCEPHALITIS ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPERINFECTION FUNGAL ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPPORTIVE CARE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
SYSTEMIC SCLEROSIS PULMONARY ( 1 FDA reports)
T-CELL CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
T-LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR FAILURE PRIMARY ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYMUS HYPERTROPHY ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRACE ELEMENT DEFICIENCY ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSFUSION WITH INCOMPATIBLE BLOOD ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRICUSPID VALVE CALCIFICATION ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
ULTRASOUND BLADDER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNRELATED DONOR BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL CYST ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL POLYP ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
UV LIGHT THERAPY ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL EXFOLIATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL STRICTURE ( 1 FDA reports)
VARICELLA POST VACCINE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VIBRATORY SENSE INCREASED ( 1 FDA reports)
VIRAL UVEITIS ( 1 FDA reports)
VIRILISM ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VIRUS BODY FLUID IDENTIFIED ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VITAL CAPACITY ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA RECURRENT ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHIPPLE'S DISEASE ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
XANTHOMATOSIS ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABORTED PREGNANCY ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION SPONTANEOUS INCOMPLETE ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACHROMOTRICHIA ACQUIRED ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 1 FDA reports)
ACQUIRED PROTEIN S DEFICIENCY ( 1 FDA reports)
ACRODERMATITIS ( 1 FDA reports)
ACRODYNIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ADRENOLEUKODYSTROPHY ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALEUKAEMIC LEUKAEMIA ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALVEOLAR SOFT PART SARCOMA METASTATIC ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANDROGENS ABNORMAL ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANISEIKONIA ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOMALY OF ORBIT, CONGENITAL ( 1 FDA reports)
ANOPHTHALMOS ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTHRAX ( 1 FDA reports)
ANTI-GAD ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 1 FDA reports)
ANTISYNTHETASE SYNDROME ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHERESIS ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERITIS INFECTIVE ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS FUNGAL ( 1 FDA reports)
ARTHRITIS SALMONELLA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLUS TEST ( 1 FDA reports)
ASPIRATION JOINT ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATAXIA TELANGIECTASIA ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AUDITORY MEATUS EXTERNAL EROSION ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE NEUROPATHY ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AUTOSOMAL CHROMOSOME ANOMALY ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
B-CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 1 FDA reports)
BACTERIAL PROSTATITIS ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTEROIDES TEST POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BARTONELLA TEST POSITIVE ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BENIGN FAMILIAL HAEMATURIA ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF LACRIMAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN SPLEEN TUMOUR ( 1 FDA reports)
BETA 2 MICROGLOBULIN ABNORMAL ( 1 FDA reports)
BILE DUCT CANCER STAGE IV ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED NORMAL ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NECK OPERATION ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD COPPER DECREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD GALACTOSE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GONADOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD GONADOTROPHIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TEST NORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE LESION EXCISION ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORRELIA BURGDORFERI SEROLOGY NEGATIVE ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BROWN-SEQUARD SYNDROME ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED ABNORMAL ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CAMPTODACTYLY CONGENITAL ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CANDIDA OSTEOMYELITIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE CAECUM ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARCINOMA IN SITU OF EYE ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CARPUS CURVUS ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELL-MEDIATED CYTOTOXICITY ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM FUNCTION TEST ABNORMAL ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL SARCOIDOSIS ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 1 FDA reports)
CERVIX INFLAMMATION ( 1 FDA reports)
CHEMICAL CYSTITIS ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CHEMOTHERAPY NEUROTOXICITY ATTENUATION ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHRONIC EOSINOPHILIC LEUKAEMIA ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLD AGGLUTININS ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON FISTULA REPAIR ( 1 FDA reports)
COLONIC PERFORATION POSTOPERATIVE ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL CLEFT HAND ( 1 FDA reports)
CONGENITAL EYELID MALFORMATION ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL OSTEODYSTROPHY ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRALATERAL BREAST CANCER ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 1 FDA reports)
CRYPTOCOCCUS ANTIGEN POSITIVE ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF LACTATE ABNORMAL ( 1 FDA reports)
CSF PROTEIN ( 1 FDA reports)
CSF PROTEIN DECREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS AMYLOIDOSIS ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYST ASPIRATION ABNORMAL ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOMEGALOVIRUS PROCTOCOLITIS ( 1 FDA reports)
DACRYOCANALICULITIS ( 1 FDA reports)
DACRYOCYSTITIS ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMATOFIBROSARCOMA ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DESMOPLASTIC SMALL ROUND CELL TUMOUR ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DONOR LEUKOCYTE INFUSION ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRAIN OF CEREBRAL SUBDURAL SPACE ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSTROPHIA MYOTONICA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMBOLISM INFECTIVE ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENCEPHALITIS INFLUENZAL ( 1 FDA reports)
ENCEPHALOMYELITIS ( 1 FDA reports)
ENDOMETRIAL DYSPLASIA ( 1 FDA reports)
ENDOMETRIAL SARCOMA ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENLARGED CLITORIS ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENZYME INDUCTION ( 1 FDA reports)
EOSINOPHILIC LEUKAEMIA ( 1 FDA reports)
EPIPHYSEAL DISORDER ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHROBLAST COUNT NORMAL ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPOSURE VIA FATHER ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYEGLASSES THERAPY ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FAMILIAL MEDITERRANEAN FEVER ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FIBRIN DECREASED ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL HAEMOGLOBIN INCREASED ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III REFRACTORY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FREE HAEMOGLOBIN PRESENT ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRONTAL LOBE EPILEPSY ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGAL RHINITIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRIC CANCER STAGE IV WITH METASTASES ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC TUBE RECONSTRUCTION ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GEOTRICHUM INFECTION ( 1 FDA reports)
GESTATIONAL TROPHOBLASTIC TUMOUR ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GITELMAN'S SYNDROME ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GROWTH ACCELERATED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCOLPOS ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ARTERY FLOW DECREASED ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATITIS D VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS E ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIPPOCAMPAL SCLEROSIS ( 1 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 1 FDA reports)
HISTIOCYTOSIS ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY RECURRENT ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE IV ( 1 FDA reports)
HODGKIN'S DISEASE REFRACTORY ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HTLV-1 ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN ANTI-MOUSE ANTIBODY INCREASED ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERCHOLIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERKERATOSIS FOLLICULARIS ET PARAFOLLICULARIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOGLOSSAL NERVE PARESIS ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IDIOPATHIC LENTICULAR MUCOCUTANEOUS PIGMENTATION ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOGLOBULIN THERAPY ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE OEDEMA ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERLEUKIN LEVEL DECREASED ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL TRANSPLANT ( 1 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRIS HYPOPIGMENTATION ( 1 FDA reports)
IRIS NEOVASCULARISATION ( 1 FDA reports)
IRIS OPERATION ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARYNGEAL HAEMATOMA ( 1 FDA reports)
LARYNGOSCOPY ABNORMAL ( 1 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 1 FDA reports)
LASEGUE'S TEST POSITIVE ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGIONELLA TEST ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKAEMIA MONOCYTIC ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LICHEN MYXOEDEMATOSUS ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIGHT CHAIN ANALYSIS DECREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LISTERIA ENCEPHALITIS ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LONG QT SYNDROME CONGENITAL ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODE FIBROSIS ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
MACRODACTYLY ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 1 FDA reports)
MALIGNANT MELANOMA STAGE II ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MASTOID EFFUSION ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MAXIMAL VOLUNTARY VENTILATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEGAKARYOCYTES ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGEAL LEUKAEMIA ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS STREPTOCOCCAL ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PHARYNX ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
MICRODACTYLY ( 1 FDA reports)
MICROGLOSSIA ( 1 FDA reports)
MICROSTOMIA ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MISMATCHED DONOR BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUMPS ANTIBODY TEST POSITIVE ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE FLAP OPERATION ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUTAGENIC EFFECT ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIUM KANSASII PNEUMONIA ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES REFRACTORY ( 1 FDA reports)
MYCOSIS FUNGOIDES STAGE IV ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYELOID METAPLASIA ( 1 FDA reports)
MYOCARDITIS BACTERIAL ( 1 FDA reports)
MYOCARDITIS MYCOTIC ( 1 FDA reports)
MYOCARDITIS TOXOPLASMAL ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NASAL CAVITY MASS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NATURAL KILLER-CELL LEUKAEMIA ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NECROTISING SCLERITIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURILEMMOMA MALIGNANT ( 1 FDA reports)
NEURITIS CRANIAL ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OCULAR VASCULITIS ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGECTOMY ( 1 FDA reports)
OESTRADIOL ABNORMAL ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC PATHWAY INJURY ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORBITAL APEX SYNDROME ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OROTICACIDURIA ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOSARCOMA LOCALISED ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN NECROSIS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC INFARCTION ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC LEAK ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPILLOMA EXCISION ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAINFLUENZAE VIRAL LARYNGOTRACHEOBRONCHITIS ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ANAL SPHINCTER ( 1 FDA reports)
NEUTROPENIA ( 2894 FDA reports)
PYREXIA ( 2893 FDA reports)
PNEUMONIA ( 1880 FDA reports)
DIARRHOEA ( 1702 FDA reports)
SEPSIS ( 1670 FDA reports)
NAUSEA ( 1576 FDA reports)
THROMBOCYTOPENIA ( 1515 FDA reports)
ANAEMIA ( 1499 FDA reports)
DYSPNOEA ( 1444 FDA reports)
INFECTION ( 1434 FDA reports)
VOMITING ( 1385 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1215 FDA reports)
PANCYTOPENIA ( 1178 FDA reports)
MUCOSAL INFLAMMATION ( 1076 FDA reports)
HYPOTENSION ( 1067 FDA reports)
DEATH ( 1035 FDA reports)
PLATELET COUNT DECREASED ( 1028 FDA reports)
RESPIRATORY FAILURE ( 1006 FDA reports)
FATIGUE ( 1006 FDA reports)
HAEMOGLOBIN DECREASED ( 927 FDA reports)
LEUKOPENIA ( 927 FDA reports)
PLEURAL EFFUSION ( 872 FDA reports)
RENAL FAILURE ( 872 FDA reports)
DRUG INEFFECTIVE ( 851 FDA reports)
MULTI-ORGAN FAILURE ( 834 FDA reports)
SEPTIC SHOCK ( 813 FDA reports)
ASTHENIA ( 782 FDA reports)
ABDOMINAL PAIN ( 768 FDA reports)
DEHYDRATION ( 756 FDA reports)
MYELODYSPLASTIC SYNDROME ( 753 FDA reports)
PAIN ( 719 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 712 FDA reports)
GRAFT VERSUS HOST DISEASE ( 709 FDA reports)
PULMONARY EMBOLISM ( 703 FDA reports)
HEADACHE ( 698 FDA reports)
DISEASE PROGRESSION ( 697 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 695 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 671 FDA reports)
RENAL FAILURE ACUTE ( 670 FDA reports)
NEUTROPHIL COUNT DECREASED ( 661 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 624 FDA reports)
OSTEONECROSIS ( 622 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 594 FDA reports)
INTERSTITIAL LUNG DISEASE ( 591 FDA reports)
COUGH ( 574 FDA reports)
RASH ( 570 FDA reports)
BONE MARROW FAILURE ( 568 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 554 FDA reports)
CARDIAC FAILURE ( 546 FDA reports)
MALAISE ( 541 FDA reports)
STOMATITIS ( 531 FDA reports)
WEIGHT DECREASED ( 530 FDA reports)
CONVULSION ( 522 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 518 FDA reports)
HYPERTENSION ( 502 FDA reports)
HERPES ZOSTER ( 490 FDA reports)
NEUROPATHY PERIPHERAL ( 485 FDA reports)
BACK PAIN ( 478 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 475 FDA reports)
TACHYCARDIA ( 474 FDA reports)
DEEP VEIN THROMBOSIS ( 473 FDA reports)
NEUTROPENIC SEPSIS ( 473 FDA reports)
CHILLS ( 472 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 468 FDA reports)
ARTHRALGIA ( 449 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 448 FDA reports)
CHEST PAIN ( 447 FDA reports)
CONSTIPATION ( 442 FDA reports)
ATRIAL FIBRILLATION ( 433 FDA reports)
DIZZINESS ( 431 FDA reports)
HYPOKALAEMIA ( 427 FDA reports)
HYPOXIA ( 426 FDA reports)
ASCITES ( 418 FDA reports)
PAIN IN EXTREMITY ( 415 FDA reports)
RENAL IMPAIRMENT ( 414 FDA reports)
STAPHYLOCOCCAL INFECTION ( 412 FDA reports)
HEPATIC FAILURE ( 412 FDA reports)
OEDEMA PERIPHERAL ( 410 FDA reports)
BLOOD BILIRUBIN INCREASED ( 408 FDA reports)
STEM CELL TRANSPLANT ( 406 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 398 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 397 FDA reports)
CONFUSIONAL STATE ( 395 FDA reports)
HEPATITIS B ( 395 FDA reports)
BLOOD CREATININE INCREASED ( 383 FDA reports)
DRUG TOXICITY ( 383 FDA reports)
SYNCOPE ( 383 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 379 FDA reports)
URINARY TRACT INFECTION ( 377 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 375 FDA reports)
LYMPHOPENIA ( 371 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 368 FDA reports)
CONDITION AGGRAVATED ( 367 FDA reports)
CARDIAC ARREST ( 359 FDA reports)
BONE PAIN ( 356 FDA reports)
LUNG INFILTRATION ( 350 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 348 FDA reports)
OEDEMA ( 347 FDA reports)
CYSTITIS HAEMORRHAGIC ( 338 FDA reports)
DECREASED APPETITE ( 335 FDA reports)
PULMONARY OEDEMA ( 334 FDA reports)
PNEUMONITIS ( 329 FDA reports)
LIVER DISORDER ( 328 FDA reports)
PARAESTHESIA ( 328 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 326 FDA reports)
CELLULITIS ( 319 FDA reports)
ERYTHEMA ( 319 FDA reports)
LYMPHADENOPATHY ( 317 FDA reports)
RESPIRATORY DISTRESS ( 315 FDA reports)
DRUG INTERACTION ( 311 FDA reports)
DEPRESSION ( 297 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 293 FDA reports)
TUMOUR LYSIS SYNDROME ( 290 FDA reports)
EJECTION FRACTION DECREASED ( 288 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 288 FDA reports)
NEOPLASM MALIGNANT ( 286 FDA reports)
ANXIETY ( 285 FDA reports)
HYPONATRAEMIA ( 285 FDA reports)
HAEMATOCRIT DECREASED ( 284 FDA reports)
MYALGIA ( 284 FDA reports)
AGRANULOCYTOSIS ( 282 FDA reports)
CARDIOMYOPATHY ( 282 FDA reports)
FALL ( 278 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 276 FDA reports)
MUSCULAR WEAKNESS ( 276 FDA reports)
MYOCARDIAL INFARCTION ( 272 FDA reports)
DYSPHAGIA ( 271 FDA reports)
FUNGAL INFECTION ( 270 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 264 FDA reports)
LUNG DISORDER ( 258 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 257 FDA reports)
HEPATOTOXICITY ( 255 FDA reports)
MULTIPLE MYELOMA ( 255 FDA reports)
HAEMATURIA ( 253 FDA reports)
NEUROTOXICITY ( 248 FDA reports)
ATELECTASIS ( 247 FDA reports)
CEREBRAL HAEMORRHAGE ( 247 FDA reports)
ORAL CANDIDIASIS ( 244 FDA reports)
CARDIO-RESPIRATORY ARREST ( 243 FDA reports)
LOSS OF CONSCIOUSNESS ( 240 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 238 FDA reports)
HYPERGLYCAEMIA ( 238 FDA reports)
ANOREXIA ( 237 FDA reports)
PRURITUS ( 237 FDA reports)
ALOPECIA ( 235 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 234 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 233 FDA reports)
VENOOCCLUSIVE DISEASE ( 233 FDA reports)
HYPERSENSITIVITY ( 232 FDA reports)
COLITIS ( 231 FDA reports)
HYPOAESTHESIA ( 231 FDA reports)
CANDIDIASIS ( 230 FDA reports)
LUNG INFECTION ( 228 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 227 FDA reports)
DISEASE RECURRENCE ( 226 FDA reports)
THROMBOSIS ( 226 FDA reports)
PERICARDIAL EFFUSION ( 225 FDA reports)
EPISTAXIS ( 224 FDA reports)
OSTEONECROSIS OF JAW ( 222 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 221 FDA reports)
SINUSITIS ( 218 FDA reports)
HEPATITIS ( 215 FDA reports)
ASPERGILLOSIS ( 212 FDA reports)
BACTERAEMIA ( 212 FDA reports)
WEIGHT INCREASED ( 212 FDA reports)
TREMOR ( 210 FDA reports)
LYMPHOMA ( 210 FDA reports)
HAEMORRHAGE ( 209 FDA reports)
PULMONARY FIBROSIS ( 209 FDA reports)
BACTERIAL INFECTION ( 208 FDA reports)
OSTEOMYELITIS ( 208 FDA reports)
OXYGEN SATURATION DECREASED ( 207 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 204 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 202 FDA reports)
BONE DISORDER ( 201 FDA reports)
ABDOMINAL PAIN UPPER ( 200 FDA reports)
FEBRILE BONE MARROW APLASIA ( 200 FDA reports)
SOMNOLENCE ( 200 FDA reports)
PAIN IN JAW ( 197 FDA reports)
ABDOMINAL DISTENSION ( 194 FDA reports)
CEREBROVASCULAR ACCIDENT ( 193 FDA reports)
BLOOD CULTURE POSITIVE ( 192 FDA reports)
HEART RATE INCREASED ( 192 FDA reports)
ENCEPHALOPATHY ( 188 FDA reports)
NERVOUS SYSTEM DISORDER ( 187 FDA reports)
HYPERBILIRUBINAEMIA ( 185 FDA reports)
COMA ( 184 FDA reports)
HAEMATOTOXICITY ( 184 FDA reports)
HYPOCALCAEMIA ( 184 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 184 FDA reports)
BLOOD PRESSURE DECREASED ( 182 FDA reports)
PULMONARY HAEMORRHAGE ( 181 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 180 FDA reports)
PSEUDOMONAS INFECTION ( 180 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 180 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 180 FDA reports)
LEUKOENCEPHALOPATHY ( 180 FDA reports)
APLASIA ( 176 FDA reports)
HAEMODIALYSIS ( 176 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 176 FDA reports)
LEUKOCYTOSIS ( 175 FDA reports)
BODY TEMPERATURE INCREASED ( 174 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 172 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 172 FDA reports)
PANCREATITIS ( 172 FDA reports)
PNEUMOTHORAX ( 172 FDA reports)
INSOMNIA ( 171 FDA reports)
RESPIRATORY DISORDER ( 169 FDA reports)
DIABETES MELLITUS ( 168 FDA reports)
GASTRITIS ( 168 FDA reports)
HEPATIC ENZYME INCREASED ( 167 FDA reports)
TRANSAMINASES INCREASED ( 167 FDA reports)
VASCULITIS ( 167 FDA reports)
TOOTH EXTRACTION ( 166 FDA reports)
ADENOVIRUS INFECTION ( 164 FDA reports)
GAIT DISTURBANCE ( 164 FDA reports)
OFF LABEL USE ( 163 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 163 FDA reports)
PULMONARY HYPERTENSION ( 160 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 160 FDA reports)
CARDIOMEGALY ( 159 FDA reports)
COAGULOPATHY ( 159 FDA reports)
CAECITIS ( 158 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 158 FDA reports)
JAUNDICE ( 157 FDA reports)
NO THERAPEUTIC RESPONSE ( 156 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 155 FDA reports)
OROPHARYNGEAL PAIN ( 155 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 154 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 154 FDA reports)
CARDIAC DISORDER ( 152 FDA reports)
PROTEINURIA ( 151 FDA reports)
CHEST DISCOMFORT ( 150 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 150 FDA reports)
MENTAL STATUS CHANGES ( 150 FDA reports)
HEPATOMEGALY ( 149 FDA reports)
INFUSION RELATED REACTION ( 149 FDA reports)
OSTEOPOROSIS ( 149 FDA reports)
BLOOD UREA INCREASED ( 148 FDA reports)
SHOCK ( 148 FDA reports)
LETHARGY ( 147 FDA reports)
OESOPHAGITIS ( 147 FDA reports)
ACUTE RESPIRATORY FAILURE ( 146 FDA reports)
BRADYCARDIA ( 146 FDA reports)
BLOOD SODIUM DECREASED ( 143 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 142 FDA reports)
SINUS TACHYCARDIA ( 141 FDA reports)
CHOLESTASIS ( 141 FDA reports)
INFLAMMATION ( 141 FDA reports)
METASTASES TO BONE ( 141 FDA reports)
SPLENOMEGALY ( 140 FDA reports)
VISUAL ACUITY REDUCED ( 140 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 139 FDA reports)
DYSARTHRIA ( 138 FDA reports)
BK VIRUS INFECTION ( 137 FDA reports)
MUSCULOSKELETAL PAIN ( 137 FDA reports)
ENTEROCOCCAL INFECTION ( 136 FDA reports)
BRONCHITIS ( 135 FDA reports)
ENCEPHALITIS ( 135 FDA reports)
URTICARIA ( 134 FDA reports)
ARRHYTHMIA ( 133 FDA reports)
CEREBRAL INFARCTION ( 133 FDA reports)
DEVICE RELATED INFECTION ( 131 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 131 FDA reports)
METASTASIS ( 131 FDA reports)
NEPHROPATHY TOXIC ( 131 FDA reports)
VIRAL INFECTION ( 131 FDA reports)
SWELLING ( 130 FDA reports)
MUSCLE SPASMS ( 130 FDA reports)
BACTERIAL SEPSIS ( 129 FDA reports)
CYTOGENETIC ABNORMALITY ( 129 FDA reports)
HYPERHIDROSIS ( 128 FDA reports)
BLOOD GLUCOSE INCREASED ( 127 FDA reports)
BLOOD POTASSIUM DECREASED ( 127 FDA reports)
HAEMOLYTIC ANAEMIA ( 127 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 126 FDA reports)
CLOSTRIDIAL INFECTION ( 126 FDA reports)
DYSPNOEA EXERTIONAL ( 126 FDA reports)
ILEUS PARALYTIC ( 126 FDA reports)
LUNG NEOPLASM ( 126 FDA reports)
THERAPY NON-RESPONDER ( 126 FDA reports)
BONE MARROW TRANSPLANT ( 125 FDA reports)
CIRCULATORY COLLAPSE ( 125 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 124 FDA reports)
VISION BLURRED ( 123 FDA reports)
RESPIRATORY TRACT INFECTION ( 122 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 121 FDA reports)
HYPOPHAGIA ( 121 FDA reports)
BLOOD PRESSURE INCREASED ( 120 FDA reports)
COGNITIVE DISORDER ( 120 FDA reports)
NEOPLASM PROGRESSION ( 120 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 120 FDA reports)
POLYNEUROPATHY ( 119 FDA reports)
PROTHROMBIN TIME PROLONGED ( 119 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 119 FDA reports)
APHASIA ( 119 FDA reports)
DIALYSIS ( 119 FDA reports)
HEPATIC STEATOSIS ( 119 FDA reports)
ILEUS ( 119 FDA reports)
METABOLIC ACIDOSIS ( 119 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 119 FDA reports)
DYSURIA ( 118 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 118 FDA reports)
GASTROINTESTINAL DISORDER ( 117 FDA reports)
NECK PAIN ( 117 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 117 FDA reports)
DRUG HYPERSENSITIVITY ( 116 FDA reports)
IMPAIRED HEALING ( 116 FDA reports)
ESCHERICHIA INFECTION ( 115 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 114 FDA reports)
PERITONITIS ( 114 FDA reports)
PRODUCTIVE COUGH ( 114 FDA reports)
RECTAL HAEMORRHAGE ( 114 FDA reports)
ANAPHYLACTIC REACTION ( 112 FDA reports)
BREAST CANCER ( 112 FDA reports)
CARDIOTOXICITY ( 112 FDA reports)
HAEMOPTYSIS ( 112 FDA reports)
HERPES SIMPLEX ( 112 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 111 FDA reports)
TACHYPNOEA ( 111 FDA reports)
PREMATURE BABY ( 110 FDA reports)
SWELLING FACE ( 110 FDA reports)
DISORIENTATION ( 110 FDA reports)
HYPERKALAEMIA ( 110 FDA reports)
INJURY ( 110 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 108 FDA reports)
DEFORMITY ( 108 FDA reports)
NEUTROPENIC COLITIS ( 108 FDA reports)
SUDDEN DEATH ( 108 FDA reports)
VISUAL IMPAIRMENT ( 108 FDA reports)
B-CELL LYMPHOMA ( 107 FDA reports)
BLISTER ( 107 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 107 FDA reports)
MITRAL VALVE INCOMPETENCE ( 106 FDA reports)
ABSCESS ( 105 FDA reports)
HYPOALBUMINAEMIA ( 105 FDA reports)
GASTROENTERITIS ( 104 FDA reports)
GENERALISED OEDEMA ( 104 FDA reports)
CAPILLARY LEAK SYNDROME ( 103 FDA reports)
ORAL PAIN ( 103 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 103 FDA reports)
SKIN EXFOLIATION ( 102 FDA reports)
HEMIPARESIS ( 102 FDA reports)
METASTASES TO LIVER ( 102 FDA reports)
BRAIN OEDEMA ( 101 FDA reports)
IMMUNOSUPPRESSION ( 101 FDA reports)
BRONCHOPNEUMONIA ( 100 FDA reports)
TRANSPLANT REJECTION ( 100 FDA reports)
FLUID OVERLOAD ( 99 FDA reports)
HAEMATEMESIS ( 99 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 98 FDA reports)
GRAND MAL CONVULSION ( 98 FDA reports)
GUILLAIN-BARRE SYNDROME ( 98 FDA reports)
RASH ERYTHEMATOUS ( 98 FDA reports)
PNEUMONIA FUNGAL ( 97 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 97 FDA reports)
CHOLELITHIASIS ( 97 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 97 FDA reports)
LUNG NEOPLASM MALIGNANT ( 96 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 96 FDA reports)
BRONCHIECTASIS ( 95 FDA reports)
DENTAL CARIES ( 95 FDA reports)
INTESTINAL OBSTRUCTION ( 95 FDA reports)
LUNG CONSOLIDATION ( 95 FDA reports)
MOUTH ULCERATION ( 95 FDA reports)
NEUTROPENIC INFECTION ( 95 FDA reports)
BONE LESION ( 94 FDA reports)
BONE MARROW DEPRESSION ( 94 FDA reports)
FLUID RETENTION ( 94 FDA reports)
LEUKAEMIA RECURRENT ( 94 FDA reports)
OPPORTUNISTIC INFECTION ( 94 FDA reports)
ENGRAFTMENT SYNDROME ( 93 FDA reports)
HAEMATOCHEZIA ( 93 FDA reports)
PANCREATITIS ACUTE ( 93 FDA reports)
PULMONARY TOXICITY ( 93 FDA reports)
WHEEZING ( 92 FDA reports)
HAEMORRHOIDS ( 92 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 92 FDA reports)
PALPITATIONS ( 91 FDA reports)
RENAL DISORDER ( 91 FDA reports)
SKIN ULCER ( 91 FDA reports)
URINARY INCONTINENCE ( 91 FDA reports)
URINE OUTPUT DECREASED ( 90 FDA reports)
CYTOLYTIC HEPATITIS ( 90 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 90 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 90 FDA reports)
EMBOLISM ( 90 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 90 FDA reports)
ATAXIA ( 89 FDA reports)
ENTERITIS ( 89 FDA reports)
BLINDNESS ( 88 FDA reports)
EMOTIONAL DISTRESS ( 88 FDA reports)
HEARING IMPAIRED ( 88 FDA reports)
PSEUDOMONAL SEPSIS ( 88 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 88 FDA reports)
STEVENS-JOHNSON SYNDROME ( 88 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 87 FDA reports)
AMNESIA ( 86 FDA reports)
CARDIOVASCULAR DISORDER ( 86 FDA reports)
ORAL INTAKE REDUCED ( 86 FDA reports)
SKIN LESION ( 86 FDA reports)
TRANSPLANT FAILURE ( 84 FDA reports)
BALANCE DISORDER ( 84 FDA reports)
CATHETER RELATED INFECTION ( 84 FDA reports)
DIVERTICULITIS ( 84 FDA reports)
EPILEPSY ( 84 FDA reports)
FLUSHING ( 84 FDA reports)
MEMORY IMPAIRMENT ( 84 FDA reports)
MYOCARDIAL ISCHAEMIA ( 84 FDA reports)
NEPHROTIC SYNDROME ( 84 FDA reports)
ACUTE HEPATIC FAILURE ( 83 FDA reports)
ELECTROLYTE IMBALANCE ( 83 FDA reports)
GASTROINTESTINAL TOXICITY ( 83 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 83 FDA reports)
OSTEOARTHRITIS ( 83 FDA reports)
STREPTOCOCCAL INFECTION ( 83 FDA reports)
POLLAKIURIA ( 82 FDA reports)
POST PROCEDURAL COMPLICATION ( 82 FDA reports)
PREMATURE MENOPAUSE ( 82 FDA reports)
HEPATIC ENCEPHALOPATHY ( 82 FDA reports)
MALIGNANT MELANOMA ( 82 FDA reports)
MYOCARDITIS ( 82 FDA reports)
INFLUENZA ( 81 FDA reports)
RENAL FAILURE CHRONIC ( 81 FDA reports)
RIB FRACTURE ( 81 FDA reports)
SQUAMOUS CELL CARCINOMA ( 81 FDA reports)
SUBDURAL HAEMATOMA ( 81 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 81 FDA reports)
VENTRICULAR TACHYCARDIA ( 81 FDA reports)
PHARYNGITIS ( 80 FDA reports)
ABDOMINAL DISCOMFORT ( 80 FDA reports)
HAEMOLYSIS ( 80 FDA reports)
BLOOD ALBUMIN DECREASED ( 79 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 79 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 79 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 79 FDA reports)
MELAENA ( 79 FDA reports)
OSTEOPENIA ( 79 FDA reports)
RESPIRATORY RATE INCREASED ( 79 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 79 FDA reports)
RASH MACULO-PAPULAR ( 78 FDA reports)
AGITATION ( 78 FDA reports)
APLASIA PURE RED CELL ( 78 FDA reports)
ESCHERICHIA SEPSIS ( 78 FDA reports)
METASTASES TO LUNG ( 78 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 77 FDA reports)
GRANULOCYTOPENIA ( 77 FDA reports)
INFLUENZA LIKE ILLNESS ( 77 FDA reports)
JC VIRUS INFECTION ( 77 FDA reports)
PETECHIAE ( 77 FDA reports)
PNEUMONIA BACTERIAL ( 77 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 77 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 76 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 76 FDA reports)
DYSPEPSIA ( 76 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 75 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 75 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 75 FDA reports)
HYPERCALCAEMIA ( 75 FDA reports)
INTESTINAL PERFORATION ( 75 FDA reports)
ADVERSE DRUG REACTION ( 74 FDA reports)
CATARACT ( 74 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 74 FDA reports)
HEPATIC NECROSIS ( 74 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 74 FDA reports)
KLEBSIELLA INFECTION ( 74 FDA reports)
VERTIGO ( 74 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 73 FDA reports)
HEPATITIS FULMINANT ( 73 FDA reports)
HYPOPHOSPHATAEMIA ( 72 FDA reports)
HYPOTHYROIDISM ( 71 FDA reports)
NEUROLOGICAL SYMPTOM ( 71 FDA reports)
ORTHOSTATIC HYPOTENSION ( 71 FDA reports)
SPEECH DISORDER ( 71 FDA reports)
RHINORRHOEA ( 70 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 70 FDA reports)
T-CELL LYMPHOMA ( 70 FDA reports)
CYSTITIS ( 70 FDA reports)
ENGRAFT FAILURE ( 70 FDA reports)
ERYSIPELAS ( 70 FDA reports)
HYPOGLYCAEMIA ( 70 FDA reports)
CONTUSION ( 69 FDA reports)
PULMONARY CONGESTION ( 69 FDA reports)
PNEUMONIA ASPIRATION ( 68 FDA reports)
PRIMARY SEQUESTRUM ( 68 FDA reports)
SPINAL COMPRESSION FRACTURE ( 68 FDA reports)
TENDERNESS ( 68 FDA reports)
GASTRIC ULCER ( 68 FDA reports)
HYPERURICAEMIA ( 68 FDA reports)
HYPOMAGNESAEMIA ( 68 FDA reports)
LOWER LIMB FRACTURE ( 68 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 68 FDA reports)
CHOLECYSTITIS ( 67 FDA reports)
CULTURE URINE POSITIVE ( 67 FDA reports)
DRUG EFFECT DECREASED ( 67 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 67 FDA reports)
ANGINA PECTORIS ( 66 FDA reports)
BONE MARROW DISORDER ( 66 FDA reports)
CONJUNCTIVITIS ( 66 FDA reports)
CYANOSIS ( 66 FDA reports)
EAR PAIN ( 66 FDA reports)
HEPATOSPLENOMEGALY ( 66 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 66 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 65 FDA reports)
ACUTE PULMONARY OEDEMA ( 65 FDA reports)
BASAL CELL CARCINOMA ( 65 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 65 FDA reports)
DELIRIUM ( 65 FDA reports)
DRUG RESISTANCE ( 65 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 65 FDA reports)
PALLOR ( 65 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 64 FDA reports)
ARTHRITIS ( 64 FDA reports)
BRONCHOSPASM ( 64 FDA reports)
IMMUNODEFICIENCY ( 64 FDA reports)
NECROSIS ( 64 FDA reports)
RESPIRATORY ARREST ( 64 FDA reports)
SENSORY DISTURBANCE ( 64 FDA reports)
SKIN TOXICITY ( 64 FDA reports)
WEGENER'S GRANULOMATOSIS ( 64 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 63 FDA reports)
RHABDOMYOLYSIS ( 63 FDA reports)
SKIN INFECTION ( 63 FDA reports)
ANURIA ( 63 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 63 FDA reports)
COORDINATION ABNORMAL ( 63 FDA reports)
ENTEROCOLITIS ( 63 FDA reports)
FIBROSIS ( 63 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 63 FDA reports)
LEUKAEMIA ( 63 FDA reports)
LOBAR PNEUMONIA ( 63 FDA reports)
ACIDOSIS ( 62 FDA reports)
CHEST X-RAY ABNORMAL ( 62 FDA reports)
DEAFNESS ( 62 FDA reports)
DIPLOPIA ( 62 FDA reports)
HALLUCINATION ( 62 FDA reports)
HYPERLIPIDAEMIA ( 62 FDA reports)
MENTAL DISORDER ( 62 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 61 FDA reports)
UNRESPONSIVE TO STIMULI ( 61 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 60 FDA reports)
SPINAL OSTEOARTHRITIS ( 60 FDA reports)
TOOTHACHE ( 60 FDA reports)
TOXIC SKIN ERUPTION ( 60 FDA reports)
URINARY RETENTION ( 60 FDA reports)
VENOUS THROMBOSIS ( 60 FDA reports)
VENTRICULAR FIBRILLATION ( 60 FDA reports)
VENTRICULAR HYPOKINESIA ( 60 FDA reports)
AMENORRHOEA ( 60 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 60 FDA reports)
NASAL CONGESTION ( 60 FDA reports)
APLASTIC ANAEMIA ( 59 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 59 FDA reports)
FACIAL PALSY ( 59 FDA reports)
NEUROPATHY ( 59 FDA reports)
PRESYNCOPE ( 59 FDA reports)
TUBERCULOSIS ( 59 FDA reports)
PREMATURE LABOUR ( 58 FDA reports)
STATUS EPILEPTICUS ( 58 FDA reports)
GINGIVITIS ( 58 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 57 FDA reports)
FACIAL PAIN ( 57 FDA reports)
HERPES VIRUS INFECTION ( 57 FDA reports)
HYPOVOLAEMIA ( 57 FDA reports)
MALNUTRITION ( 57 FDA reports)
OVARIAN FAILURE ( 57 FDA reports)
RALES ( 57 FDA reports)
TOOTH DISORDER ( 57 FDA reports)
SCAR ( 56 FDA reports)
ABNORMAL BEHAVIOUR ( 56 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 56 FDA reports)
DISCOMFORT ( 56 FDA reports)
ENTEROCOCCAL SEPSIS ( 56 FDA reports)
ERYTHEMA MULTIFORME ( 56 FDA reports)
EYE PAIN ( 56 FDA reports)
FISTULA ( 56 FDA reports)
GASTROINTESTINAL NECROSIS ( 56 FDA reports)
ORAL DISORDER ( 56 FDA reports)
ASTHMA ( 55 FDA reports)
BURNING SENSATION ( 55 FDA reports)
FAILURE TO THRIVE ( 55 FDA reports)
HYPERTHERMIA ( 55 FDA reports)
MASS ( 55 FDA reports)
MYOSITIS ( 55 FDA reports)
OVERDOSE ( 55 FDA reports)
PERICARDITIS ( 55 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 54 FDA reports)
VARICELLA ( 54 FDA reports)
CANDIDA SEPSIS ( 54 FDA reports)
COLON CANCER ( 54 FDA reports)
DERMATITIS EXFOLIATIVE ( 54 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 54 FDA reports)
ENCEPHALITIS HERPES ( 54 FDA reports)
HAEMATOMA ( 54 FDA reports)
JOINT SWELLING ( 54 FDA reports)
NEPHROLITHIASIS ( 54 FDA reports)
CARDIOGENIC SHOCK ( 53 FDA reports)
CEREBRAL ISCHAEMIA ( 53 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 53 FDA reports)
FEELING ABNORMAL ( 53 FDA reports)
JAW DISORDER ( 53 FDA reports)
NERVOUSNESS ( 53 FDA reports)
NIGHT SWEATS ( 53 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 53 FDA reports)
PREGNANCY ( 53 FDA reports)
SYSTEMIC CANDIDA ( 53 FDA reports)
TROPONIN INCREASED ( 53 FDA reports)
PURULENT DISCHARGE ( 52 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 52 FDA reports)
ZYGOMYCOSIS ( 52 FDA reports)
ANHEDONIA ( 52 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 52 FDA reports)
DISTURBANCE IN ATTENTION ( 52 FDA reports)
METASTASES TO LYMPH NODES ( 52 FDA reports)
MYELOPATHY ( 52 FDA reports)
HODGKIN'S DISEASE ( 51 FDA reports)
HOT FLUSH ( 51 FDA reports)
MIGRAINE ( 51 FDA reports)
MYOPATHY ( 51 FDA reports)
NEOPLASM RECURRENCE ( 51 FDA reports)
NEUTROPHIL COUNT INCREASED ( 51 FDA reports)
OTITIS MEDIA ( 51 FDA reports)
PNEUMOMEDIASTINUM ( 51 FDA reports)
RENAL TUBULAR NECROSIS ( 51 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 51 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 51 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 50 FDA reports)
PLEURITIC PAIN ( 50 FDA reports)
UROSEPSIS ( 50 FDA reports)
BLOOD CALCIUM DECREASED ( 50 FDA reports)
CLOSTRIDIUM COLITIS ( 50 FDA reports)
CORONARY ARTERY DISEASE ( 50 FDA reports)
HAEMOGLOBIN ABNORMAL ( 50 FDA reports)
HEMIPLEGIA ( 50 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 50 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 50 FDA reports)
MOBILITY DECREASED ( 50 FDA reports)
NASAL SEPTUM DISORDER ( 50 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 50 FDA reports)
ANAPHYLACTIC SHOCK ( 49 FDA reports)
CAESAREAN SECTION ( 49 FDA reports)
HEPATITIS CHOLESTATIC ( 49 FDA reports)
HYPERCHOLESTEROLAEMIA ( 49 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 49 FDA reports)
RASH GENERALISED ( 49 FDA reports)
RECURRENT CANCER ( 49 FDA reports)
TOOTH ABSCESS ( 49 FDA reports)
UNEVALUABLE EVENT ( 49 FDA reports)
PATHOGEN RESISTANCE ( 48 FDA reports)
PLEURAL FIBROSIS ( 48 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 48 FDA reports)
ACUTE CORONARY SYNDROME ( 48 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 48 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 48 FDA reports)
DEMYELINATION ( 48 FDA reports)
FAECAL INCONTINENCE ( 48 FDA reports)
GLIOMA ( 48 FDA reports)
HYDRONEPHROSIS ( 48 FDA reports)
HYPOTONIA ( 48 FDA reports)
ISCHAEMIC STROKE ( 48 FDA reports)
LIVER TRANSPLANT ( 48 FDA reports)
NEURALGIA ( 48 FDA reports)
OLIGURIA ( 48 FDA reports)
ADVERSE EVENT ( 47 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 47 FDA reports)
AREFLEXIA ( 47 FDA reports)
CARDIOPULMONARY FAILURE ( 47 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 47 FDA reports)
FACE OEDEMA ( 47 FDA reports)
GASTROINTESTINAL PERFORATION ( 47 FDA reports)
LIVER INJURY ( 47 FDA reports)
PATHOLOGICAL FRACTURE ( 47 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 47 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 46 FDA reports)
SKIN DISORDER ( 46 FDA reports)
ABASIA ( 46 FDA reports)
BLADDER CANCER ( 46 FDA reports)
COMPRESSION FRACTURE ( 46 FDA reports)
DYSGEUSIA ( 46 FDA reports)
ESCHERICHIA BACTERAEMIA ( 46 FDA reports)
EXOSTOSIS ( 46 FDA reports)
FIBRIN D DIMER INCREASED ( 46 FDA reports)
GASTRIC CANCER ( 46 FDA reports)
PAIN OF SKIN ( 46 FDA reports)
PARALYSIS ( 46 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 45 FDA reports)
ASEPTIC NECROSIS BONE ( 45 FDA reports)
BONE MARROW TOXICITY ( 45 FDA reports)
BRAIN HERNIATION ( 45 FDA reports)
BURKITT'S LYMPHOMA ( 45 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 45 FDA reports)
DRUG LEVEL INCREASED ( 45 FDA reports)
ENDOCARDITIS ( 45 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 45 FDA reports)
ODYNOPHAGIA ( 45 FDA reports)
ABDOMINAL PAIN LOWER ( 44 FDA reports)
ANAL ABSCESS ( 44 FDA reports)
CANDIDA PNEUMONIA ( 44 FDA reports)
FOETAL GROWTH RESTRICTION ( 44 FDA reports)
HEPATIC CIRRHOSIS ( 44 FDA reports)
HYDROCEPHALUS ( 44 FDA reports)
HYPERPYREXIA ( 44 FDA reports)
INTESTINAL ISCHAEMIA ( 44 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 44 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 44 FDA reports)
ORAL HERPES ( 44 FDA reports)
ORGANISING PNEUMONIA ( 44 FDA reports)
PSYCHOTIC DISORDER ( 44 FDA reports)
REFRACTORY ANAEMIA ( 44 FDA reports)
SERUM FERRITIN INCREASED ( 44 FDA reports)
SUICIDAL IDEATION ( 44 FDA reports)
SWOLLEN TONGUE ( 44 FDA reports)
TREATMENT FAILURE ( 44 FDA reports)
PHOTOPHOBIA ( 43 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 43 FDA reports)
RHEUMATOID ARTHRITIS ( 43 FDA reports)
SKIN HYPERPIGMENTATION ( 43 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 43 FDA reports)
TOXIC ENCEPHALOPATHY ( 43 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 43 FDA reports)
BRAIN ABSCESS ( 43 FDA reports)
CACHEXIA ( 43 FDA reports)
IRON DEFICIENCY ANAEMIA ( 43 FDA reports)
LABORATORY TEST ABNORMAL ( 43 FDA reports)
MOUTH HAEMORRHAGE ( 43 FDA reports)
MYELOID LEUKAEMIA ( 43 FDA reports)
ATRIAL FLUTTER ( 42 FDA reports)
CEREBELLAR SYNDROME ( 42 FDA reports)
CSF PROTEIN INCREASED ( 42 FDA reports)
DRUG ERUPTION ( 42 FDA reports)
EMPHYSEMA ( 42 FDA reports)
GASTRIC PERFORATION ( 42 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 42 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 42 FDA reports)
LOCAL SWELLING ( 42 FDA reports)
NODULE ( 42 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 42 FDA reports)
PURULENCE ( 42 FDA reports)
PROCTALGIA ( 41 FDA reports)
PURPURA ( 41 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 41 FDA reports)
SURGERY ( 41 FDA reports)
CEREBRAL ATROPHY ( 41 FDA reports)
CYTOKINE RELEASE SYNDROME ( 41 FDA reports)
HAEMODYNAMIC INSTABILITY ( 41 FDA reports)
MUCORMYCOSIS ( 41 FDA reports)
MUCOUS MEMBRANE DISORDER ( 41 FDA reports)
MYELITIS TRANSVERSE ( 41 FDA reports)
BRONCHOSTENOSIS ( 40 FDA reports)
DECUBITUS ULCER ( 40 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 40 FDA reports)
EOSINOPHILIA ( 40 FDA reports)
EXTRAVASATION ( 40 FDA reports)
EYE SWELLING ( 40 FDA reports)
GASTRIC HAEMORRHAGE ( 40 FDA reports)
HEPATITIS ACUTE ( 40 FDA reports)
LARGE INTESTINE PERFORATION ( 40 FDA reports)
LIPASE INCREASED ( 40 FDA reports)
MECHANICAL VENTILATION ( 40 FDA reports)
MEDICATION ERROR ( 40 FDA reports)
NASOPHARYNGITIS ( 40 FDA reports)
PARAPLEGIA ( 40 FDA reports)
PLASMACYTOMA ( 40 FDA reports)
RESTLESSNESS ( 40 FDA reports)
SCLERODERMA ( 40 FDA reports)
SKIN DISCOLOURATION ( 40 FDA reports)
VAGINAL HAEMORRHAGE ( 40 FDA reports)
RASH PAPULAR ( 39 FDA reports)
RENAL CYST ( 39 FDA reports)
ABORTION SPONTANEOUS ( 39 FDA reports)
BACTERIAL TEST POSITIVE ( 39 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 39 FDA reports)
BLOOD POTASSIUM INCREASED ( 39 FDA reports)
FUNGAL SEPSIS ( 39 FDA reports)
HEPATIC LESION ( 39 FDA reports)
IRRITABILITY ( 39 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 39 FDA reports)
NEOPLASM ( 39 FDA reports)
ACUTE LEUKAEMIA ( 38 FDA reports)
BLOOD DISORDER ( 38 FDA reports)
BLOOD MAGNESIUM DECREASED ( 38 FDA reports)
BREAST CANCER FEMALE ( 38 FDA reports)
CARDIAC FAILURE ACUTE ( 38 FDA reports)
CARDIAC TAMPONADE ( 38 FDA reports)
CATHETER RELATED COMPLICATION ( 38 FDA reports)
DERMATITIS ( 38 FDA reports)
DYSKINESIA ( 38 FDA reports)
GINGIVAL BLEEDING ( 38 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 38 FDA reports)
HEAD INJURY ( 38 FDA reports)
JOINT STIFFNESS ( 38 FDA reports)
LEFT VENTRICULAR FAILURE ( 38 FDA reports)
NYSTAGMUS ( 38 FDA reports)
POOR QUALITY SLEEP ( 38 FDA reports)
RASH PRURITIC ( 38 FDA reports)
SENSORY LOSS ( 38 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 38 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 38 FDA reports)
SINUS DISORDER ( 37 FDA reports)
CENTRAL LINE INFECTION ( 37 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 37 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 37 FDA reports)
HEPATITIS C ( 37 FDA reports)
LIVER ABSCESS ( 37 FDA reports)
MOTOR DYSFUNCTION ( 37 FDA reports)
NEUROBLASTOMA ( 37 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 37 FDA reports)
ARTHROPATHY ( 36 FDA reports)
BRAIN NEOPLASM ( 36 FDA reports)
DILATATION VENTRICULAR ( 36 FDA reports)
ENCEPHALITIS VIRAL ( 36 FDA reports)
EXPOSED BONE IN JAW ( 36 FDA reports)
HYPERNATRAEMIA ( 36 FDA reports)
JAW OPERATION ( 36 FDA reports)
KAPOSI'S SARCOMA ( 36 FDA reports)
PERFORMANCE STATUS DECREASED ( 36 FDA reports)
PHOTOSENSITIVITY REACTION ( 36 FDA reports)
RECTAL ULCER ( 36 FDA reports)
VENTRICULAR DYSFUNCTION ( 36 FDA reports)
PLATELET COUNT ABNORMAL ( 35 FDA reports)
RADIATION PNEUMONITIS ( 35 FDA reports)
SEQUESTRECTOMY ( 35 FDA reports)
THROMBOPHLEBITIS ( 35 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 35 FDA reports)
ANGIOEDEMA ( 35 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 35 FDA reports)
CARDIAC MURMUR ( 35 FDA reports)
COLITIS ISCHAEMIC ( 35 FDA reports)
CUSHING'S SYNDROME ( 35 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 35 FDA reports)
ENDOTRACHEAL INTUBATION ( 35 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 35 FDA reports)
FEELING HOT ( 35 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 35 FDA reports)
HYPOTHERMIA ( 35 FDA reports)
LACRIMATION INCREASED ( 35 FDA reports)
LUPUS NEPHRITIS ( 35 FDA reports)
METASTASES TO SPINE ( 35 FDA reports)
METASTATIC NEOPLASM ( 35 FDA reports)
MUSCLE RUPTURE ( 35 FDA reports)
ABSCESS JAW ( 34 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 34 FDA reports)
APHTHOUS STOMATITIS ( 34 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 34 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 34 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 34 FDA reports)
DIVERTICULAR PERFORATION ( 34 FDA reports)
EATING DISORDER ( 34 FDA reports)
ILL-DEFINED DISORDER ( 34 FDA reports)
INTRA-UTERINE DEATH ( 34 FDA reports)
LACTIC ACIDOSIS ( 34 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 34 FDA reports)
PHARYNGEAL OEDEMA ( 34 FDA reports)
PLATELET COUNT INCREASED ( 34 FDA reports)
PLATELET DISORDER ( 34 FDA reports)
PROSTATE CANCER ( 34 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 34 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 34 FDA reports)
RHINITIS ALLERGIC ( 34 FDA reports)
SPLEEN DISORDER ( 34 FDA reports)
TREATMENT NONCOMPLIANCE ( 34 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 34 FDA reports)
PERIPHERAL ISCHAEMIA ( 33 FDA reports)
PNEUMATOSIS INTESTINALIS ( 33 FDA reports)
PROCEDURAL COMPLICATION ( 33 FDA reports)
PROTEIN TOTAL DECREASED ( 33 FDA reports)
SKIN NECROSIS ( 33 FDA reports)
SLEEP APNOEA SYNDROME ( 33 FDA reports)
STREPTOCOCCAL SEPSIS ( 33 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 33 FDA reports)
TACHYARRHYTHMIA ( 33 FDA reports)
ABDOMINAL TENDERNESS ( 33 FDA reports)
ADENOVIRAL HEPATITIS ( 33 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 33 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 33 FDA reports)
ASPIRATION ( 33 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 33 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 33 FDA reports)
CHOLANGITIS ( 33 FDA reports)
CHOLECYSTITIS ACUTE ( 33 FDA reports)
CUSHINGOID ( 33 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 33 FDA reports)
HIATUS HERNIA ( 33 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 33 FDA reports)
JAUNDICE CHOLESTATIC ( 33 FDA reports)
JUGULAR VEIN THROMBOSIS ( 33 FDA reports)
LOCALISED INFECTION ( 33 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 33 FDA reports)
MASTECTOMY ( 33 FDA reports)
NECROTISING FASCIITIS ( 33 FDA reports)
PARONYCHIA ( 33 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 32 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 32 FDA reports)
BREAST CANCER RECURRENT ( 32 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 32 FDA reports)
CYSTITIS VIRAL ( 32 FDA reports)
DEMENTIA ( 32 FDA reports)
DIASTOLIC DYSFUNCTION ( 32 FDA reports)
DRUG INTOLERANCE ( 32 FDA reports)
ENTEROBACTER INFECTION ( 32 FDA reports)
FAECALOMA ( 32 FDA reports)
INFERTILITY ( 32 FDA reports)
INJECTION SITE PAIN ( 32 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 32 FDA reports)
MYELOMA RECURRENCE ( 32 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 32 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 32 FDA reports)
OPTIC ATROPHY ( 32 FDA reports)
PERIODONTAL DISEASE ( 32 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 32 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 32 FDA reports)
VIITH NERVE PARALYSIS ( 32 FDA reports)
WOUND INFECTION ( 32 FDA reports)
PERTUSSIS ( 31 FDA reports)
PHYSICAL DISABILITY ( 31 FDA reports)
PLASMACYTOSIS ( 31 FDA reports)
PRIMARY HYPOGONADISM ( 31 FDA reports)
PULMONARY MYCOSIS ( 31 FDA reports)
PULMONARY TUBERCULOSIS ( 31 FDA reports)
RETINAL HAEMORRHAGE ( 31 FDA reports)
SCOLIOSIS ( 31 FDA reports)
TENDONITIS ( 31 FDA reports)
TOXOPLASMOSIS ( 31 FDA reports)
VISUAL DISTURBANCE ( 31 FDA reports)
WOUND DEBRIDEMENT ( 31 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 31 FDA reports)
CULTURE POSITIVE ( 31 FDA reports)
DYSAESTHESIA ( 31 FDA reports)
EYELID OEDEMA ( 31 FDA reports)
GENE MUTATION ( 31 FDA reports)
HAEMORRHAGIC DIATHESIS ( 31 FDA reports)
HILAR LYMPHADENOPATHY ( 31 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 31 FDA reports)
METAPLASIA ( 31 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 31 FDA reports)
ALVEOLITIS ( 30 FDA reports)
BLOOD AMYLASE INCREASED ( 30 FDA reports)
CEREBRAL HAEMATOMA ( 30 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 30 FDA reports)
EYE IRRITATION ( 30 FDA reports)
HEPATITIS TOXIC ( 30 FDA reports)
HYPERKERATOSIS ( 30 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 30 FDA reports)
LEUKAEMIA PLASMACYTIC ( 30 FDA reports)
MANTLE CELL LYMPHOMA ( 30 FDA reports)
MENINGITIS ( 30 FDA reports)
MICROANGIOPATHY ( 30 FDA reports)
NOCARDIOSIS ( 30 FDA reports)
PHLEBITIS ( 30 FDA reports)
SPINAL FRACTURE ( 30 FDA reports)
TINNITUS ( 30 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 30 FDA reports)
TOOTH LOSS ( 30 FDA reports)
PLEURISY ( 29 FDA reports)
PULMONARY MASS ( 29 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 29 FDA reports)
SEPSIS SYNDROME ( 29 FDA reports)
SHOCK HAEMORRHAGIC ( 29 FDA reports)
SPLENIC INFARCTION ( 29 FDA reports)
VENTRICULAR HYPERTROPHY ( 29 FDA reports)
BLOOD LUTEINISING HORMONE INCREASED ( 29 FDA reports)
BONE SARCOMA ( 29 FDA reports)
COLITIS ULCERATIVE ( 29 FDA reports)
DECREASED INTEREST ( 29 FDA reports)
DIVERTICULUM ( 29 FDA reports)
EAR INFECTION ( 29 FDA reports)
GRANULOMA ( 29 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 29 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 29 FDA reports)
MYELITIS ( 29 FDA reports)
OVARIAN CANCER ( 29 FDA reports)
ABORTION INDUCED ( 28 FDA reports)
ANGIOPATHY ( 28 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 28 FDA reports)
BLOOD URIC ACID INCREASED ( 28 FDA reports)
BONE MARROW NECROSIS ( 28 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 28 FDA reports)
COMPLETED SUICIDE ( 28 FDA reports)
ECZEMA ( 28 FDA reports)
FOOT FRACTURE ( 28 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 28 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 28 FDA reports)
METABOLIC DISORDER ( 28 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 28 FDA reports)
SKIN EROSION ( 28 FDA reports)
THROAT TIGHTNESS ( 28 FDA reports)
VIRAEMIA ( 28 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 27 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 27 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 27 FDA reports)
SLEEP DISORDER ( 27 FDA reports)
TOOTH INFECTION ( 27 FDA reports)
VENTRICULAR ARRHYTHMIA ( 27 FDA reports)
AORTIC VALVE INCOMPETENCE ( 27 FDA reports)
BACILLUS INFECTION ( 27 FDA reports)
CARDIAC AMYLOIDOSIS ( 27 FDA reports)
COMA HEPATIC ( 27 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 27 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 27 FDA reports)
FUNGAEMIA ( 27 FDA reports)
HYPOPROTEINAEMIA ( 27 FDA reports)
INTESTINAL HAEMORRHAGE ( 27 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 27 FDA reports)
ORTHOPNOEA ( 27 FDA reports)
OSTEOMYELITIS CHRONIC ( 27 FDA reports)
OSTEOSCLEROSIS ( 27 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 27 FDA reports)
PARESIS ( 27 FDA reports)
ACTINOMYCOSIS ( 26 FDA reports)
ACUTE SINUSITIS ( 26 FDA reports)
ADENOCARCINOMA ( 26 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 26 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 26 FDA reports)
CRYING ( 26 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 26 FDA reports)
DUODENAL ULCER ( 26 FDA reports)
DYSPHONIA ( 26 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 26 FDA reports)
FEMUR FRACTURE ( 26 FDA reports)
GALLBLADDER DISORDER ( 26 FDA reports)
HEART RATE DECREASED ( 26 FDA reports)
MUSCLE TWITCHING ( 26 FDA reports)
NEPHROPATHY ( 26 FDA reports)
OLIGOHYDRAMNIOS ( 26 FDA reports)
OSTEOLYSIS ( 26 FDA reports)
OVARIAN ATROPHY ( 26 FDA reports)
PARAPARESIS ( 26 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 26 FDA reports)
POOR PERSONAL HYGIENE ( 26 FDA reports)
ROAD TRAFFIC ACCIDENT ( 26 FDA reports)
SPINAL CORD DISORDER ( 26 FDA reports)
SUBILEUS ( 26 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 26 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 26 FDA reports)
PERIPHERAL COLDNESS ( 25 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 25 FDA reports)
STENOTROPHOMONAS INFECTION ( 25 FDA reports)
VIRAL LOAD INCREASED ( 25 FDA reports)
ABDOMINAL ABSCESS ( 25 FDA reports)
ARTERIOSCLEROSIS ( 25 FDA reports)
BLOOD COUNT ABNORMAL ( 25 FDA reports)
BODY TEMPERATURE DECREASED ( 25 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 25 FDA reports)
CHROMOSOME ABNORMALITY ( 25 FDA reports)
CULTURE STOOL POSITIVE ( 25 FDA reports)
CYST ( 25 FDA reports)
DIVERTICULUM INTESTINAL ( 25 FDA reports)
EROSIVE OESOPHAGITIS ( 25 FDA reports)
FAECES DISCOLOURED ( 25 FDA reports)
FLUID INTAKE REDUCED ( 25 FDA reports)
FOLLICULITIS ( 25 FDA reports)
GANGRENE ( 25 FDA reports)
HEPATIC FIBROSIS ( 25 FDA reports)
HEPATOCELLULAR DAMAGE ( 25 FDA reports)
HYPOVOLAEMIC SHOCK ( 25 FDA reports)
JOINT EFFUSION ( 25 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 25 FDA reports)
LYMPHOEDEMA ( 25 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 25 FDA reports)
PARTIAL SEIZURES ( 25 FDA reports)
AMYLOIDOSIS ( 24 FDA reports)
APHAGIA ( 24 FDA reports)
APNOEA ( 24 FDA reports)
AUTOIMMUNE DISORDER ( 24 FDA reports)
AZOTAEMIA ( 24 FDA reports)
BEDRIDDEN ( 24 FDA reports)
BREAST CANCER METASTATIC ( 24 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 24 FDA reports)
CEREBRAL FUNGAL INFECTION ( 24 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 24 FDA reports)
DEAFNESS NEUROSENSORY ( 24 FDA reports)
DELAYED ENGRAFTMENT ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
DUODENITIS ( 24 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 24 FDA reports)
FOETAL GROWTH RETARDATION ( 24 FDA reports)
FUNGAL SKIN INFECTION ( 24 FDA reports)
GINGIVAL PAIN ( 24 FDA reports)
HYPERTHYROIDISM ( 24 FDA reports)
HYPERVENTILATION ( 24 FDA reports)
INTESTINAL ULCER ( 24 FDA reports)
LYMPHADENECTOMY ( 24 FDA reports)
MANIA ( 24 FDA reports)
MARROW HYPERPLASIA ( 24 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 24 FDA reports)
NAIL DISORDER ( 24 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 24 FDA reports)
PANIC ATTACK ( 24 FDA reports)
PAPILLOEDEMA ( 24 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 24 FDA reports)
PORTAL VEIN THROMBOSIS ( 24 FDA reports)
RESPIRATORY ALKALOSIS ( 24 FDA reports)
SCIATICA ( 24 FDA reports)
SINUS BRADYCARDIA ( 24 FDA reports)
SKIN NODULE ( 24 FDA reports)
VITREOUS FLOATERS ( 24 FDA reports)
QUADRIPARESIS ( 23 FDA reports)
RASH PUSTULAR ( 23 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 23 FDA reports)
SINUS CONGESTION ( 23 FDA reports)
SPUTUM CULTURE POSITIVE ( 23 FDA reports)
TRAUMATIC HAEMATOMA ( 23 FDA reports)
TYPE 2 DIABETES MELLITUS ( 23 FDA reports)
WHITE BLOOD CELL DISORDER ( 23 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 23 FDA reports)
AORTIC STENOSIS ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 23 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 23 FDA reports)
CEREBRAL DISORDER ( 23 FDA reports)
COLONIC POLYP ( 23 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 23 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 23 FDA reports)
CREPITATIONS ( 23 FDA reports)
DISSEMINATED TUBERCULOSIS ( 23 FDA reports)
DYSPLASIA ( 23 FDA reports)
ERYTHEMA INFECTIOSUM ( 23 FDA reports)
FEMORAL NECK FRACTURE ( 23 FDA reports)
FLANK PAIN ( 23 FDA reports)
HEPATIC INFECTION FUNGAL ( 23 FDA reports)
HERPES ZOSTER DISSEMINATED ( 23 FDA reports)
IRON DEFICIENCY ( 23 FDA reports)
LARGE INTESTINAL ULCER ( 23 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 23 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 23 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 23 FDA reports)
MULTIPLE FRACTURES ( 23 FDA reports)
MUSCLE ATROPHY ( 23 FDA reports)
MYDRIASIS ( 23 FDA reports)
OPTIC NEURITIS ( 23 FDA reports)
ADRENAL INSUFFICIENCY ( 22 FDA reports)
ARTERIAL THROMBOSIS ( 22 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 22 FDA reports)
BLOOD GLUCOSE DECREASED ( 22 FDA reports)
BONE DEBRIDEMENT ( 22 FDA reports)
BREATH SOUNDS ABNORMAL ( 22 FDA reports)
BURSITIS ( 22 FDA reports)
CHRONIC SINUSITIS ( 22 FDA reports)
DEBRIDEMENT ( 22 FDA reports)
DISEASE COMPLICATION ( 22 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 22 FDA reports)
DYSPHASIA ( 22 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 22 FDA reports)
FACIAL PARESIS ( 22 FDA reports)
FEELING COLD ( 22 FDA reports)
GAZE PALSY ( 22 FDA reports)
GLIOSIS ( 22 FDA reports)
GOITRE ( 22 FDA reports)
HAEMOPHILUS INFECTION ( 22 FDA reports)
HEPATIC CYST ( 22 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 22 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 22 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 22 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 22 FDA reports)
LUNG ADENOCARCINOMA ( 22 FDA reports)
MOOD SWINGS ( 22 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 22 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 22 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 22 FDA reports)
OBESITY ( 22 FDA reports)
ORAL INFECTION ( 22 FDA reports)
PERITONITIS BACTERIAL ( 22 FDA reports)
PNEUMONIA HERPES VIRAL ( 22 FDA reports)
PROTEIN URINE PRESENT ( 22 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 22 FDA reports)
RHINITIS ( 22 FDA reports)
RHONCHI ( 22 FDA reports)
SOFT TISSUE INFECTION ( 22 FDA reports)
STRIDOR ( 22 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 22 FDA reports)
SUPERINFECTION ( 22 FDA reports)
THYROID CANCER ( 22 FDA reports)
TIC ( 22 FDA reports)
TONSILLITIS ( 22 FDA reports)
PARVOVIRUS INFECTION ( 21 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 21 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 21 FDA reports)
RENAL TUBULAR DISORDER ( 21 FDA reports)
RESPIRATORY DEPRESSION ( 21 FDA reports)
SKIN INDURATION ( 21 FDA reports)
SPINAL DISORDER ( 21 FDA reports)
SPLENIC ABSCESS ( 21 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 21 FDA reports)
SYSTEMIC MYCOSIS ( 21 FDA reports)
THROMBOSIS IN DEVICE ( 21 FDA reports)
TOOTH FRACTURE ( 21 FDA reports)
TRACHEITIS ( 21 FDA reports)
TRANSFUSION REACTION ( 21 FDA reports)
TROPONIN I INCREASED ( 21 FDA reports)
URETERIC OBSTRUCTION ( 21 FDA reports)
BACTERIA STOOL IDENTIFIED ( 21 FDA reports)
BONE DENSITY DECREASED ( 21 FDA reports)
BONE OPERATION ( 21 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 21 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 21 FDA reports)
CORONARY ARTERY OCCLUSION ( 21 FDA reports)
CSF TEST ABNORMAL ( 21 FDA reports)
DRY MOUTH ( 21 FDA reports)
DRY SKIN ( 21 FDA reports)
EMOTIONAL DISORDER ( 21 FDA reports)
HEPATIC ATROPHY ( 21 FDA reports)
HIP ARTHROPLASTY ( 21 FDA reports)
HYPERPARATHYROIDISM ( 21 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 21 FDA reports)
INCONTINENCE ( 21 FDA reports)
LYMPHANGITIS ( 21 FDA reports)
METASTASES TO PLEURA ( 21 FDA reports)
MOOD ALTERED ( 21 FDA reports)
MUSCLE DISORDER ( 21 FDA reports)
MYOCLONUS ( 21 FDA reports)
NERVE INJURY ( 21 FDA reports)
NEUTROPHIL COUNT ( 21 FDA reports)
NOCTURIA ( 21 FDA reports)
NON-CARDIAC CHEST PAIN ( 21 FDA reports)
ORAL DISCOMFORT ( 21 FDA reports)
PARANEOPLASTIC SYNDROME ( 21 FDA reports)
ALVEOLITIS ALLERGIC ( 20 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 20 FDA reports)
ANAL FISSURE ( 20 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 20 FDA reports)
BIOPSY LYMPH GLAND ( 20 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 20 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 20 FDA reports)
BONE LOSS ( 20 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 20 FDA reports)
CROHN'S DISEASE ( 20 FDA reports)
DILATATION ATRIAL ( 20 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 20 FDA reports)
DYSPNOEA AT REST ( 20 FDA reports)
ECCHYMOSIS ( 20 FDA reports)
EOSINOPHIL COUNT INCREASED ( 20 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 20 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 20 FDA reports)
FULL BLOOD COUNT DECREASED ( 20 FDA reports)
GROIN PAIN ( 20 FDA reports)
HIP FRACTURE ( 20 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 20 FDA reports)
HYPERTROPHY ( 20 FDA reports)
IMMUNE SYSTEM DISORDER ( 20 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 20 FDA reports)
MACULOPATHY ( 20 FDA reports)
MEDICAL DEVICE COMPLICATION ( 20 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 20 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 20 FDA reports)
MONOCYTE COUNT INCREASED ( 20 FDA reports)
MUCOSAL HAEMORRHAGE ( 20 FDA reports)
NON-SMALL CELL LUNG CANCER ( 20 FDA reports)
ONYCHOMYCOSIS ( 20 FDA reports)
ORAL SOFT TISSUE DISORDER ( 20 FDA reports)
PANCREATIC CARCINOMA ( 20 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 20 FDA reports)
PNEUMONIA VIRAL ( 20 FDA reports)
PREMATURE DELIVERY ( 20 FDA reports)
PROSTATOMEGALY ( 20 FDA reports)
PUPIL FIXED ( 20 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 20 FDA reports)
RESPIRATORY ACIDOSIS ( 20 FDA reports)
RHABDOMYOSARCOMA ( 20 FDA reports)
ROTATOR CUFF SYNDROME ( 20 FDA reports)
SEPTIC EMBOLUS ( 20 FDA reports)
SKIN PAPILLOMA ( 20 FDA reports)
STRESS ( 20 FDA reports)
TRAUMATIC LUNG INJURY ( 20 FDA reports)
UTERINE LEIOMYOMA ( 20 FDA reports)
VOCAL CORD PARALYSIS ( 20 FDA reports)
WOUND COMPLICATION ( 20 FDA reports)
PERIORBITAL OEDEMA ( 19 FDA reports)
PNEUMONIA ASPERGILLUS ( 19 FDA reports)
PNEUMONIA KLEBSIELLA ( 19 FDA reports)
PNEUMONITIS CHEMICAL ( 19 FDA reports)
PORTAL HYPERTENSION ( 19 FDA reports)
PULMONARY CALCIFICATION ( 19 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 19 FDA reports)
PULSE ABSENT ( 19 FDA reports)
PYELONEPHRITIS ( 19 FDA reports)
PYLORIC STENOSIS ( 19 FDA reports)
RADIATION INJURY ( 19 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 19 FDA reports)
SICCA SYNDROME ( 19 FDA reports)
SKIN FIBROSIS ( 19 FDA reports)
SKIN TIGHTNESS ( 19 FDA reports)
SUBCUTANEOUS NODULE ( 19 FDA reports)
THYROID NEOPLASM ( 19 FDA reports)
TONSIL CANCER ( 19 FDA reports)
WOUND DEHISCENCE ( 19 FDA reports)
ABDOMINAL INFECTION ( 19 FDA reports)
AGGRESSION ( 19 FDA reports)
APPENDICITIS ( 19 FDA reports)
BLOOD URINE PRESENT ( 19 FDA reports)
BRONCHIOLITIS ( 19 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 19 FDA reports)
CARDIAC PACEMAKER INSERTION ( 19 FDA reports)
CASTLEMAN'S DISEASE ( 19 FDA reports)
CERVICAL DYSPLASIA ( 19 FDA reports)
DENTURE WEARER ( 19 FDA reports)
DERMATITIS ALLERGIC ( 19 FDA reports)
DIABETIC KETOACIDOSIS ( 19 FDA reports)
DRUG ADMINISTRATION ERROR ( 19 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 19 FDA reports)
EYE MOVEMENT DISORDER ( 19 FDA reports)
FOOD INTOLERANCE ( 19 FDA reports)
GASTROINTESTINAL ULCER ( 19 FDA reports)
HAEMANGIOMA ( 19 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 19 FDA reports)
HAPTOGLOBIN DECREASED ( 19 FDA reports)
HEPATIC CONGESTION ( 19 FDA reports)
HICCUPS ( 19 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 19 FDA reports)
HYPERREFLEXIA ( 19 FDA reports)
HYPOACUSIS ( 19 FDA reports)
HYPOCOAGULABLE STATE ( 19 FDA reports)
HYPOREFLEXIA ( 19 FDA reports)
INCORRECT DOSE ADMINISTERED ( 19 FDA reports)
ISCHAEMIA ( 19 FDA reports)
KIDNEY FIBROSIS ( 19 FDA reports)
LIP SWELLING ( 19 FDA reports)
MASTICATION DISORDER ( 19 FDA reports)
MENOPAUSE ( 19 FDA reports)
MONOPLEGIA ( 19 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 19 FDA reports)
NOROVIRUS TEST POSITIVE ( 19 FDA reports)
ANAL HAEMORRHAGE ( 18 FDA reports)
ANAPHYLACTOID REACTION ( 18 FDA reports)
ANISOCYTOSIS ( 18 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 18 FDA reports)
AZOOSPERMIA ( 18 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 18 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 18 FDA reports)
BILE DUCT CANCER ( 18 FDA reports)
BREAST RECONSTRUCTION ( 18 FDA reports)
CHYLOTHORAX ( 18 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 18 FDA reports)
COLLAPSE OF LUNG ( 18 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 18 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 18 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 18 FDA reports)
DIZZINESS POSTURAL ( 18 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 18 FDA reports)
EYE DISCHARGE ( 18 FDA reports)
EYELID PTOSIS ( 18 FDA reports)
GLOMERULONEPHRITIS ( 18 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 18 FDA reports)
GRANULOCYTE COUNT DECREASED ( 18 FDA reports)
GRANULOCYTES ABNORMAL ( 18 FDA reports)
H1N1 INFLUENZA ( 18 FDA reports)
HALLUCINATION, VISUAL ( 18 FDA reports)
HEPATITIS D ( 18 FDA reports)
HOSPITALISATION ( 18 FDA reports)
HYPOAESTHESIA ORAL ( 18 FDA reports)
HYPOVENTILATION ( 18 FDA reports)
IATROGENIC INJURY ( 18 FDA reports)
LIFE EXPECTANCY SHORTENED ( 18 FDA reports)
MOVEMENT DISORDER ( 18 FDA reports)
MUCOSAL ULCERATION ( 18 FDA reports)
MYOCARDIAL FIBROSIS ( 18 FDA reports)
OESOPHAGEAL ULCER ( 18 FDA reports)
ONYCHOLYSIS ( 18 FDA reports)
PARALYSIS FLACCID ( 18 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 18 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 18 FDA reports)
PLANTAR FASCIITIS ( 18 FDA reports)
POST HERPETIC NEURALGIA ( 18 FDA reports)
RADIOTHERAPY ( 18 FDA reports)
RASH VESICULAR ( 18 FDA reports)
RESPIRATORY TRACT CONGESTION ( 18 FDA reports)
RETINITIS ( 18 FDA reports)
TONGUE DISORDER ( 18 FDA reports)
TRANSPLANT ( 18 FDA reports)
ULCER ( 18 FDA reports)
PEPTIC ULCER ( 17 FDA reports)
PIGMENTATION DISORDER ( 17 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 17 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 17 FDA reports)
SARCOIDOSIS ( 17 FDA reports)
SCEDOSPORIUM INFECTION ( 17 FDA reports)
SICK SINUS SYNDROME ( 17 FDA reports)
SKIN HYPERTROPHY ( 17 FDA reports)
SOLITARY KIDNEY ( 17 FDA reports)
STILLBIRTH ( 17 FDA reports)
VASCULITIS CEREBRAL ( 17 FDA reports)
VENOUS THROMBOSIS LIMB ( 17 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 17 FDA reports)
WALKING AID USER ( 17 FDA reports)
WOUND ( 17 FDA reports)
ACCIDENTAL OVERDOSE ( 17 FDA reports)
APRAXIA ( 17 FDA reports)
ATRIAL TACHYCARDIA ( 17 FDA reports)
BEHCET'S SYNDROME ( 17 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 17 FDA reports)
BIOPSY BREAST ABNORMAL ( 17 FDA reports)
BLADDER DISORDER ( 17 FDA reports)
BLOOD CREATINE INCREASED ( 17 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN ABNORMAL ( 17 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 17 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 17 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 17 FDA reports)
BLOOD SODIUM INCREASED ( 17 FDA reports)
BONE EROSION ( 17 FDA reports)
BONE SWELLING ( 17 FDA reports)
BRAIN SCAN ABNORMAL ( 17 FDA reports)
BREAST DISCHARGE ( 17 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 17 FDA reports)
DENTAL OPERATION ( 17 FDA reports)
DIABETES INSIPIDUS ( 17 FDA reports)
DRUG CLEARANCE DECREASED ( 17 FDA reports)
GASTRIC DISORDER ( 17 FDA reports)
GASTROENTERITIS NOROVIRUS ( 17 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 17 FDA reports)
GINGIVAL INFECTION ( 17 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 17 FDA reports)
HAEMOSIDEROSIS ( 17 FDA reports)
HEPATIC NEOPLASM ( 17 FDA reports)
HYPERAMMONAEMIA ( 17 FDA reports)
HYPERTRANSAMINASAEMIA ( 17 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 17 FDA reports)
INCOHERENT ( 17 FDA reports)
INCREASED TENDENCY TO BRUISE ( 17 FDA reports)
INTRACARDIAC THROMBUS ( 17 FDA reports)
INTRACRANIAL HYPOTENSION ( 17 FDA reports)
JOINT DISLOCATION ( 17 FDA reports)
LOOSE TOOTH ( 17 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 17 FDA reports)
MELANOCYTIC NAEVUS ( 17 FDA reports)
METASTASES TO MENINGES ( 17 FDA reports)
METASTASES TO SKIN ( 17 FDA reports)
MULTI-ORGAN DISORDER ( 17 FDA reports)
MYELOFIBROSIS ( 17 FDA reports)
ONCOLOGIC COMPLICATION ( 17 FDA reports)
OPTIC NEUROPATHY ( 17 FDA reports)
ORAL CAVITY FISTULA ( 17 FDA reports)
OSTEITIS ( 17 FDA reports)
PARAESTHESIA ORAL ( 17 FDA reports)
PAROSMIA ( 17 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 16 FDA reports)
AFFECT LABILITY ( 16 FDA reports)
ANGER ( 16 FDA reports)
ANTITHROMBIN III DECREASED ( 16 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 16 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 16 FDA reports)
BIOPSY BONE ABNORMAL ( 16 FDA reports)
BLOOD CREATININE DECREASED ( 16 FDA reports)
BLOOD PH DECREASED ( 16 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 16 FDA reports)
CATHETER SITE RELATED REACTION ( 16 FDA reports)
DIFFICULTY IN WALKING ( 16 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 16 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 16 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 16 FDA reports)
EWING'S SARCOMA ( 16 FDA reports)
GINGIVAL SWELLING ( 16 FDA reports)
IIIRD NERVE PARALYSIS ( 16 FDA reports)
INFECTIOUS PERITONITIS ( 16 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 16 FDA reports)
ISCHAEMIC HEPATITIS ( 16 FDA reports)
JC VIRUS TEST POSITIVE ( 16 FDA reports)
LUNG HYPERINFLATION ( 16 FDA reports)
LYMPHATIC DISORDER ( 16 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 16 FDA reports)
LYMPHOCYTOSIS ( 16 FDA reports)
MICTURITION URGENCY ( 16 FDA reports)
OEDEMA MOUTH ( 16 FDA reports)
OPEN WOUND ( 16 FDA reports)
OVARIAN CYST ( 16 FDA reports)
PERSONALITY CHANGE ( 16 FDA reports)
PITTING OEDEMA ( 16 FDA reports)
PO2 DECREASED ( 16 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 16 FDA reports)
RADICULOPATHY ( 16 FDA reports)
RECALL PHENOMENON ( 16 FDA reports)
RESTLESS LEGS SYNDROME ( 16 FDA reports)
SALIVARY GLAND CANCER ( 16 FDA reports)
SERUM SICKNESS ( 16 FDA reports)
SKIN PLAQUE ( 16 FDA reports)
SOFT TISSUE DISORDER ( 16 FDA reports)
SPLENIC RUPTURE ( 16 FDA reports)
STRONGYLOIDIASIS ( 16 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 16 FDA reports)
SYNDACTYLY ( 16 FDA reports)
SYSTOLIC DYSFUNCTION ( 16 FDA reports)
TESTICULAR DISORDER ( 16 FDA reports)
VISUAL FIELD DEFECT ( 16 FDA reports)
WATER INTOXICATION ( 16 FDA reports)
PELVIC PAIN ( 15 FDA reports)
PNEUMONIA ADENOVIRAL ( 15 FDA reports)
PROCEDURAL PAIN ( 15 FDA reports)
PROTEIN URINE ABSENT ( 15 FDA reports)
PSORIASIS ( 15 FDA reports)
PULMONARY NECROSIS ( 15 FDA reports)
QUADRIPLEGIA ( 15 FDA reports)
RAYNAUD'S PHENOMENON ( 15 FDA reports)
SEROMA ( 15 FDA reports)
SINUS HEADACHE ( 15 FDA reports)
SKIN CANCER ( 15 FDA reports)
THROAT IRRITATION ( 15 FDA reports)
UTERINE CANCER ( 15 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 15 FDA reports)
WRONG DRUG ADMINISTERED ( 15 FDA reports)
BENIGN BREAST NEOPLASM ( 15 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 15 FDA reports)
BLOOD PRESSURE ABNORMAL ( 15 FDA reports)
BRAIN DEATH ( 15 FDA reports)
BREAST PROSTHESIS REMOVAL ( 15 FDA reports)
BRONCHIAL DISORDER ( 15 FDA reports)
CARDIAC VALVE DISEASE ( 15 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 15 FDA reports)
CEREBROVASCULAR DISORDER ( 15 FDA reports)
CORONARY ARTERY STENOSIS ( 15 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 15 FDA reports)
DRY EYE ( 15 FDA reports)
EMBOLISM VENOUS ( 15 FDA reports)
EMPYEMA ( 15 FDA reports)
GASTROINTESTINAL INFECTION ( 15 FDA reports)
GIANT CELL TUMOUR OF TENDON SHEATH ( 15 FDA reports)
GINGIVAL DISORDER ( 15 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 15 FDA reports)
HEPATIC ENZYME ABNORMAL ( 15 FDA reports)
HYPERSOMNIA ( 15 FDA reports)
INFARCTION ( 15 FDA reports)
JOINT CONTRACTURE ( 15 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 15 FDA reports)
LIGHT CHAIN ANALYSIS ( 15 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 15 FDA reports)
MASS EXCISION ( 15 FDA reports)
MENINGITIS BACTERIAL ( 15 FDA reports)
MENSTRUAL DISORDER ( 15 FDA reports)
MENSTRUATION IRREGULAR ( 15 FDA reports)
METAPNEUMOVIRUS INFECTION ( 15 FDA reports)
MUTISM ( 15 FDA reports)
NEUROGENIC BLADDER ( 15 FDA reports)
OCULAR HYPERAEMIA ( 15 FDA reports)
OEDEMA MUCOSAL ( 15 FDA reports)
PANCREATIC DISORDER ( 15 FDA reports)
PARATHYROID TUMOUR BENIGN ( 15 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 14 FDA reports)
AMAUROSIS ( 14 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 14 FDA reports)
ANGIOSARCOMA ( 14 FDA reports)
AORTIC VALVE SCLEROSIS ( 14 FDA reports)
ASPERGILLUS TEST POSITIVE ( 14 FDA reports)
AXILLARY VEIN THROMBOSIS ( 14 FDA reports)
BENCE JONES PROTEINURIA ( 14 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 14 FDA reports)
BILE DUCT OBSTRUCTION ( 14 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 14 FDA reports)
BLOOD CHLORIDE INCREASED ( 14 FDA reports)
BLOOD LACTIC ACID INCREASED ( 14 FDA reports)
BREAST PAIN ( 14 FDA reports)
BRONCHIAL OBSTRUCTION ( 14 FDA reports)
CARDIAC CIRRHOSIS ( 14 FDA reports)
CARPAL TUNNEL SYNDROME ( 14 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 14 FDA reports)
CITROBACTER INFECTION ( 14 FDA reports)
CORYNEBACTERIUM INFECTION ( 14 FDA reports)
CULTURE WOUND POSITIVE ( 14 FDA reports)
DEPRESSED MOOD ( 14 FDA reports)
DESMOID TUMOUR ( 14 FDA reports)
DEVICE RELATED SEPSIS ( 14 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 14 FDA reports)
DRUG TOLERANCE DECREASED ( 14 FDA reports)
ESCHERICHIA TEST POSITIVE ( 14 FDA reports)
FANCONI SYNDROME ( 14 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 14 FDA reports)
HEPATORENAL SYNDROME ( 14 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 14 FDA reports)
HYPOGONADISM ( 14 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 14 FDA reports)
INGUINAL MASS ( 14 FDA reports)
KLEBSIELLA SEPSIS ( 14 FDA reports)
LARYNGEAL OEDEMA ( 14 FDA reports)
LEFT ATRIAL DILATATION ( 14 FDA reports)
LYMPH NODE PAIN ( 14 FDA reports)
MACULAR OEDEMA ( 14 FDA reports)
MEDULLOBLASTOMA ( 14 FDA reports)
MENINGEAL DISORDER ( 14 FDA reports)
MENINGITIS ASEPTIC ( 14 FDA reports)
MENISCUS LESION ( 14 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 14 FDA reports)
NEPHRITIS INTERSTITIAL ( 14 FDA reports)
NON-HODGKIN'S LYMPHOMA UNSPECIFIED HISTOLOGY AGGRESSIVE ( 14 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 14 FDA reports)
OPTIC NERVE DISORDER ( 14 FDA reports)
ORAL MUCOSA EROSION ( 14 FDA reports)
ORGAN FAILURE ( 14 FDA reports)
OVARIAN CANCER METASTATIC ( 14 FDA reports)
PCO2 DECREASED ( 14 FDA reports)
PNEUMATOSIS ( 14 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 14 FDA reports)
PRE-ECLAMPSIA ( 14 FDA reports)
PROCTITIS ( 14 FDA reports)
PULMONARY SEPSIS ( 14 FDA reports)
RENAL INFARCT ( 14 FDA reports)
RENAL TRANSPLANT ( 14 FDA reports)
RENAL TUBULAR ACIDOSIS ( 14 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 14 FDA reports)
SUBCUTANEOUS ABSCESS ( 14 FDA reports)
SUICIDE ATTEMPT ( 14 FDA reports)
TENOSYNOVITIS ( 14 FDA reports)
TETANY ( 14 FDA reports)
THROMBOCYTOPENIC PURPURA ( 14 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 14 FDA reports)
THYMUS ENLARGEMENT ( 14 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 14 FDA reports)
URINE ANALYSIS ABNORMAL ( 14 FDA reports)
VANISHING BILE DUCT SYNDROME ( 14 FDA reports)
VARICES OESOPHAGEAL ( 14 FDA reports)
PERINEAL ULCERATION ( 13 FDA reports)
PERIODONTITIS ( 13 FDA reports)
PERITONEAL DIALYSIS ( 13 FDA reports)
PLEURAL HAEMORRHAGE ( 13 FDA reports)
PNEUMOCOCCAL SEPSIS ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
PULMONARY THROMBOSIS ( 13 FDA reports)
REFLUX OESOPHAGITIS ( 13 FDA reports)
SKIN REACTION ( 13 FDA reports)
SMALL FOR DATES BABY ( 13 FDA reports)
SPLENIC VEIN THROMBOSIS ( 13 FDA reports)
SPUTUM PURULENT ( 13 FDA reports)
SUBDURAL HAEMORRHAGE ( 13 FDA reports)
SUDDEN CARDIAC DEATH ( 13 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 13 FDA reports)
TONSILLAR HYPERTROPHY ( 13 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 13 FDA reports)
TRISMUS ( 13 FDA reports)
TUMOUR MARKER INCREASED ( 13 FDA reports)
TUMOUR NECROSIS ( 13 FDA reports)
URETERIC STENOSIS ( 13 FDA reports)
VIRAL MYOCARDITIS ( 13 FDA reports)
VIRAL TEST POSITIVE ( 13 FDA reports)
ABDOMINAL MASS ( 13 FDA reports)
ACNE ( 13 FDA reports)
ACUTE LUNG INJURY ( 13 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 13 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 13 FDA reports)
BLINDNESS CORTICAL ( 13 FDA reports)
BLOOD ALBUMIN INCREASED ( 13 FDA reports)
BLOOD CALCIUM INCREASED ( 13 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 13 FDA reports)
BLOOD UREA DECREASED ( 13 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 13 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 13 FDA reports)
CANDIDA TEST POSITIVE ( 13 FDA reports)
CHROMATURIA ( 13 FDA reports)
DYSLALIA ( 13 FDA reports)
EFFUSION ( 13 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 13 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 13 FDA reports)
ESCHAR ( 13 FDA reports)
FEBRILE INFECTION ( 13 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 13 FDA reports)
FLATULENCE ( 13 FDA reports)
GASTROINTESTINAL OEDEMA ( 13 FDA reports)
GINGIVAL ATROPHY ( 13 FDA reports)
HEPATIC HAEMORRHAGE ( 13 FDA reports)
HEPATOCELLULAR INJURY ( 13 FDA reports)
HYPERTENSIVE CRISIS ( 13 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 13 FDA reports)
JAW FRACTURE ( 13 FDA reports)
KLEBSIELLA BACTERAEMIA ( 13 FDA reports)
LABORATORY TEST INTERFERENCE ( 13 FDA reports)
LARYNGEAL STENOSIS ( 13 FDA reports)
LEUKAEMIA CUTIS ( 13 FDA reports)
LOCALISED OEDEMA ( 13 FDA reports)
LUNG INJURY ( 13 FDA reports)
LYMPHOCYTE COUNT ( 13 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 13 FDA reports)
MALLORY-WEISS SYNDROME ( 13 FDA reports)
MENTAL IMPAIRMENT ( 13 FDA reports)
METASTASES TO ADRENALS ( 13 FDA reports)
NEUROBLASTOMA RECURRENT ( 13 FDA reports)
PARAPROTEINAEMIA ( 13 FDA reports)
ABSCESS INTESTINAL ( 12 FDA reports)
ACINETOBACTER INFECTION ( 12 FDA reports)
ACUTE ABDOMEN ( 12 FDA reports)
ACUTE PSYCHOSIS ( 12 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 12 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 12 FDA reports)
AORTIC CALCIFICATION ( 12 FDA reports)
ARTHRITIS BACTERIAL ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK ( 12 FDA reports)
AUTOIMMUNE THYROIDITIS ( 12 FDA reports)
BILIARY TRACT DISORDER ( 12 FDA reports)
BLAST CELLS PRESENT ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 12 FDA reports)
BRAIN INJURY ( 12 FDA reports)
BREAST MASS ( 12 FDA reports)
BRONCHIAL CARCINOMA ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
BURKITT'S LYMPHOMA RECURRENT ( 12 FDA reports)
CATHETER REMOVAL ( 12 FDA reports)
CAUDA EQUINA SYNDROME ( 12 FDA reports)
CELLULITIS GANGRENOUS ( 12 FDA reports)
CHROMOSOMAL DELETION ( 12 FDA reports)
COLD SWEAT ( 12 FDA reports)
COLON CANCER METASTATIC ( 12 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 12 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 12 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 12 FDA reports)
DRUG DOSE OMISSION ( 12 FDA reports)
ERYTHEMA OF EYELID ( 12 FDA reports)
EVAN'S SYNDROME ( 12 FDA reports)
EVANS SYNDROME ( 12 FDA reports)
FACIAL NERVE DISORDER ( 12 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 12 FDA reports)
FOREIGN BODY TRAUMA ( 12 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 12 FDA reports)
GASTROENTERITIS VIRAL ( 12 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 12 FDA reports)
GENERALISED ERYTHEMA ( 12 FDA reports)
GLUCOSE URINE PRESENT ( 12 FDA reports)
HAEMOTHORAX ( 12 FDA reports)
HEMIANOPIA ( 12 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 12 FDA reports)
HEPATIC VEIN OCCLUSION ( 12 FDA reports)
HEPATITIS VIRAL ( 12 FDA reports)
HIRSUTISM ( 12 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 12 FDA reports)
HYPERCAPNIA ( 12 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 12 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 12 FDA reports)
ILEAL PERFORATION ( 12 FDA reports)
INDURATION ( 12 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 12 FDA reports)
INJECTION SITE PHLEBITIS ( 12 FDA reports)
LABILE BLOOD PRESSURE ( 12 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 12 FDA reports)
LEG AMPUTATION ( 12 FDA reports)
LIPODYSTROPHY ACQUIRED ( 12 FDA reports)
LIVEDO RETICULARIS ( 12 FDA reports)
LUNG ABSCESS ( 12 FDA reports)
MASTOID DISORDER ( 12 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 12 FDA reports)
MICROGNATHIA ( 12 FDA reports)
MIDDLE EAR EFFUSION ( 12 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 12 FDA reports)
MONOCYTE COUNT DECREASED ( 12 FDA reports)
MONOCYTOSIS ( 12 FDA reports)
MUCOSAL EROSION ( 12 FDA reports)
MYOCLONIC EPILEPSY ( 12 FDA reports)
NASAL DISCOMFORT ( 12 FDA reports)
NEONATAL DISORDER ( 12 FDA reports)
OESOPHAGEAL CARCINOMA ( 12 FDA reports)
PANCREATIC PSEUDOCYST ( 12 FDA reports)
PARKINSONISM ( 12 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 12 FDA reports)
PERIRECTAL ABSCESS ( 12 FDA reports)
PERONEAL NERVE PALSY ( 12 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 12 FDA reports)
PHARYNGEAL INFLAMMATION ( 12 FDA reports)
PLASMABLASTIC LYMPHOMA ( 12 FDA reports)
PNEUMONIA LEGIONELLA ( 12 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 12 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 12 FDA reports)
PROTEUS INFECTION ( 12 FDA reports)
PROTHROMBIN TIME SHORTENED ( 12 FDA reports)
PULMONARY GRANULOMA ( 12 FDA reports)
QUALITY OF LIFE DECREASED ( 12 FDA reports)
RASH MORBILLIFORM ( 12 FDA reports)
RENAL CELL CARCINOMA ( 12 FDA reports)
RIGHT VENTRICULAR FAILURE ( 12 FDA reports)
SKIN BURNING SENSATION ( 12 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 12 FDA reports)
SPINAL CORD COMPRESSION ( 12 FDA reports)
SPUTUM DISCOLOURED ( 12 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 12 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 12 FDA reports)
STENOTROPHOMONAS SEPSIS ( 12 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 12 FDA reports)
SYNCOPE VASOVAGAL ( 12 FDA reports)
SYNOVIAL CYST ( 12 FDA reports)
SYSTEMIC SCLEROSIS ( 12 FDA reports)
TUBERCULOSIS OF CENTRAL NERVOUS SYSTEM ( 12 FDA reports)
UPPER LIMB FRACTURE ( 12 FDA reports)
URINE ABNORMALITY ( 12 FDA reports)
VULVOVAGINAL DRYNESS ( 12 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 12 FDA reports)
X-RAY ABNORMAL ( 12 FDA reports)
PELVIC KIDNEY ( 11 FDA reports)
POLYARTHRITIS ( 11 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 11 FDA reports)
POST PROCEDURAL HAEMATOMA ( 11 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 11 FDA reports)
RED BLOOD CELL ABNORMALITY ( 11 FDA reports)
RELAPSING FEVER ( 11 FDA reports)
RENAL HAEMORRHAGE ( 11 FDA reports)
RENAL TUBULAR ATROPHY ( 11 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 11 FDA reports)
SCAB ( 11 FDA reports)
SCROTAL OEDEMA ( 11 FDA reports)
SECRETION DISCHARGE ( 11 FDA reports)
SINUS ARRHYTHMIA ( 11 FDA reports)
SKIN FRAGILITY ( 11 FDA reports)
SPLENECTOMY ( 11 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 11 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 11 FDA reports)
TONIC CONVULSION ( 11 FDA reports)
TRACHEOSTOMY ( 11 FDA reports)
UTERINE HAEMORRHAGE ( 11 FDA reports)
VIRAL DNA TEST POSITIVE ( 11 FDA reports)
VIRAL SKIN INFECTION ( 11 FDA reports)
VIRUS URINE TEST POSITIVE ( 11 FDA reports)
VITAMIN D DEFICIENCY ( 11 FDA reports)
VITH NERVE PARALYSIS ( 11 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 11 FDA reports)
WHITE BLOOD CELL COUNT ( 11 FDA reports)
WOUND DRAINAGE ( 11 FDA reports)
ABDOMINAL RIGIDITY ( 11 FDA reports)
ABSCESS ORAL ( 11 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 11 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ACUTE PRERENAL FAILURE ( 11 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 11 FDA reports)
AMMONIA INCREASED ( 11 FDA reports)
ANAEMIA MACROCYTIC ( 11 FDA reports)
ANAL FISTULA ( 11 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 11 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 11 FDA reports)
BIOPSY LIVER ABNORMAL ( 11 FDA reports)
BLAST CELL COUNT INCREASED ( 11 FDA reports)
BLOOD CHLORIDE DECREASED ( 11 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 11 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 11 FDA reports)
BLOOD PH INCREASED ( 11 FDA reports)
BLOOD SODIUM ABNORMAL ( 11 FDA reports)
BREAST CANCER IN SITU ( 11 FDA reports)
BREAST NEOPLASM ( 11 FDA reports)
BRONCHOPNEUMOPATHY ( 11 FDA reports)
CALCULUS URINARY ( 11 FDA reports)
CARDIAC HYPERTROPHY ( 11 FDA reports)
CATHETER SITE ERYTHEMA ( 11 FDA reports)
CHOLECYSTITIS CHRONIC ( 11 FDA reports)
CLINODACTYLY ( 11 FDA reports)
COMMUNICATION DISORDER ( 11 FDA reports)
COMPLEX PARTIAL SEIZURES ( 11 FDA reports)
CRANIAL NERVE DISORDER ( 11 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 11 FDA reports)
DENTAL PLAQUE ( 11 FDA reports)
DEVELOPMENTAL DELAY ( 11 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 11 FDA reports)
DIPLEGIA ( 11 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 11 FDA reports)
ENDOPHTHALMITIS ( 11 FDA reports)
ENTEROBACTER SEPSIS ( 11 FDA reports)
ENTEROVESICAL FISTULA ( 11 FDA reports)
EPIGASTRIC DISCOMFORT ( 11 FDA reports)
ERYTHROLEUKAEMIA ( 11 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 11 FDA reports)
EXTRADURAL HAEMATOMA ( 11 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 11 FDA reports)
EXTRASKELETAL OSSIFICATION ( 11 FDA reports)
EYE DISORDER ( 11 FDA reports)
FACET JOINT SYNDROME ( 11 FDA reports)
FASCIITIS ( 11 FDA reports)
GASTRITIS EROSIVE ( 11 FDA reports)
GINGIVAL ERYTHEMA ( 11 FDA reports)
HALLUCINATION, AUDITORY ( 11 FDA reports)
HEART RATE IRREGULAR ( 11 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 11 FDA reports)
HYPERTONIA ( 11 FDA reports)
INJECTION SITE ERYTHEMA ( 11 FDA reports)
JOINT SPRAIN ( 11 FDA reports)
LACUNAR INFARCTION ( 11 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 11 FDA reports)
LIFE SUPPORT ( 11 FDA reports)
LIP ULCERATION ( 11 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 11 FDA reports)
MENIERE'S DISEASE ( 11 FDA reports)
MENINGISM ( 11 FDA reports)
MENOPAUSAL SYMPTOMS ( 11 FDA reports)
METASTASES TO PERITONEUM ( 11 FDA reports)
MICROCYTOSIS ( 11 FDA reports)
MIOSIS ( 11 FDA reports)
MONOPARESIS ( 11 FDA reports)
MULTIPLE SCLEROSIS ( 11 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 11 FDA reports)
NEPHRITIS ( 11 FDA reports)
NEUTROPHILIA ( 11 FDA reports)
ORAL SURGERY ( 11 FDA reports)
OTORRHOEA ( 11 FDA reports)
AGEUSIA ( 10 FDA reports)
ALVEOLAR OSTEITIS ( 10 FDA reports)
AORTIC ANEURYSM ( 10 FDA reports)
ATRIAL THROMBOSIS ( 10 FDA reports)
ATROPHY ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 10 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 10 FDA reports)
BREAST TENDERNESS ( 10 FDA reports)
CARBON DIOXIDE DECREASED ( 10 FDA reports)
CATHETER SITE PAIN ( 10 FDA reports)
CELL DEATH ( 10 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 10 FDA reports)
CEREBELLAR ATAXIA ( 10 FDA reports)
CHIMERISM ( 10 FDA reports)
CHOLECYSTECTOMY ( 10 FDA reports)
DEAFNESS BILATERAL ( 10 FDA reports)
DEPRESSIVE SYMPTOM ( 10 FDA reports)
DERMATITIS BULLOUS ( 10 FDA reports)
DEVICE DISLOCATION ( 10 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 10 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 10 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 10 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 10 FDA reports)
EXERCISE TOLERANCE DECREASED ( 10 FDA reports)
FEMORAL ARTERY OCCLUSION ( 10 FDA reports)
FIBROUS HISTIOCYTOMA ( 10 FDA reports)
FOLLICULAR MUCINOSIS ( 10 FDA reports)
FOOT DEFORMITY ( 10 FDA reports)
FRACTURE NONUNION ( 10 FDA reports)
FUNGAL TEST POSITIVE ( 10 FDA reports)
FUSARIUM INFECTION ( 10 FDA reports)
GLOSSITIS ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 10 FDA reports)
GROWTH RETARDATION ( 10 FDA reports)
HAEMANGIOMA OF SPLEEN ( 10 FDA reports)
HAEMORRHAGIC STROKE ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HEPATIC INFARCTION ( 10 FDA reports)
HEPATIC PAIN ( 10 FDA reports)
HEPATOBILIARY DISEASE ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
HYPERPHOSPHATAEMIA ( 10 FDA reports)
HYPOKINESIA ( 10 FDA reports)
ILEAL STENOSIS ( 10 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 10 FDA reports)
IRITIS ( 10 FDA reports)
LACTOBACILLUS INFECTION ( 10 FDA reports)
LISTERIOSIS ( 10 FDA reports)
LYMPHOCYTIC INFILTRATION ( 10 FDA reports)
MACULAR HOLE ( 10 FDA reports)
MALIGNANT MELANOMA IN SITU ( 10 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 10 FDA reports)
NEPHROSCLEROSIS ( 10 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 10 FDA reports)
OESOPHAGEAL PAIN ( 10 FDA reports)
PAPULE ( 10 FDA reports)
PERIORBITAL HAEMATOMA ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PNEUMOPERITONEUM ( 10 FDA reports)
POSTURING ( 10 FDA reports)
PULMONARY VASCULITIS ( 10 FDA reports)
RADIATION SKIN INJURY ( 10 FDA reports)
RETICULOCYTE COUNT DECREASED ( 10 FDA reports)
RETINAL DETACHMENT ( 10 FDA reports)
RETROPERITONEAL FIBROSIS ( 10 FDA reports)
RETROPERITONEAL HAEMATOMA ( 10 FDA reports)
SEDATION ( 10 FDA reports)
SENSATION OF FOREIGN BODY ( 10 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 10 FDA reports)
SUBDURAL EFFUSION ( 10 FDA reports)
SWEAT GLAND TUMOUR ( 10 FDA reports)
TONGUE NEOPLASM ( 10 FDA reports)
ULNA FRACTURE ( 10 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 10 FDA reports)
VENA CAVA THROMBOSIS ( 10 FDA reports)
WEST NILE VIRAL INFECTION ( 10 FDA reports)
PELVIC ABSCESS ( 9 FDA reports)
PERITONEAL HAEMORRHAGE ( 9 FDA reports)
POLYMYOSITIS ( 9 FDA reports)
POLYURIA ( 9 FDA reports)
POOR VENOUS ACCESS ( 9 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 9 FDA reports)
PROSTATITIS ( 9 FDA reports)
PRURITUS GENERALISED ( 9 FDA reports)
PYOGENIC GRANULOMA ( 9 FDA reports)
RASH MACULAR ( 9 FDA reports)
RENAL VEIN THROMBOSIS ( 9 FDA reports)
RESPIRATION ABNORMAL ( 9 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 9 FDA reports)
RESPIRATORY RATE DECREASED ( 9 FDA reports)
RETICULOCYTE COUNT INCREASED ( 9 FDA reports)
SENSITIVITY OF TEETH ( 9 FDA reports)
SIGMOIDITIS ( 9 FDA reports)
SINUSITIS FUNGAL ( 9 FDA reports)
TEETH BRITTLE ( 9 FDA reports)
TRICHOSPORON INFECTION ( 9 FDA reports)
TRISOMY 21 ( 9 FDA reports)
TUMOUR HAEMORRHAGE ( 9 FDA reports)
URETERIC DILATATION ( 9 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 9 FDA reports)
UVEITIS ( 9 FDA reports)
VAGINAL INFECTION ( 9 FDA reports)
VASCULAR ACCESS COMPLICATION ( 9 FDA reports)
VIRAL PHARYNGITIS ( 9 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 9 FDA reports)
XEROSIS ( 9 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 9 FDA reports)
ANGINA UNSTABLE ( 9 FDA reports)
ANGIONEUROTIC OEDEMA ( 9 FDA reports)
ANTIBODY TEST POSITIVE ( 9 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 9 FDA reports)
ARACHNOIDITIS ( 9 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 9 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 9 FDA reports)
AUTONOMIC NEUROPATHY ( 9 FDA reports)
BACTERIA URINE IDENTIFIED ( 9 FDA reports)
BIOPSY ( 9 FDA reports)
BLOOD BICARBONATE DECREASED ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 9 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 9 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 9 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 9 FDA reports)
BRAIN STEM INFARCTION ( 9 FDA reports)
BRONCHIAL SECRETION RETENTION ( 9 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 9 FDA reports)
BURKITT'S LEUKAEMIA ( 9 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 9 FDA reports)
CARDIAC ENZYMES INCREASED ( 9 FDA reports)
CATHETER SITE DISCHARGE ( 9 FDA reports)
CATHETER SITE INFECTION ( 9 FDA reports)
CLONIC CONVULSION ( 9 FDA reports)
CONGENITAL FOOT MALFORMATION ( 9 FDA reports)
CRYSTAL URINE PRESENT ( 9 FDA reports)
CYTOKINE STORM ( 9 FDA reports)
DYSPHEMIA ( 9 FDA reports)
DYSPRAXIA ( 9 FDA reports)
ENCEPHALITIC INFECTION ( 9 FDA reports)
ERECTILE DYSFUNCTION ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
FACTOR VIII DEFICIENCY ( 9 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 9 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 9 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 9 FDA reports)
GINGIVAL ULCERATION ( 9 FDA reports)
GLIOBLASTOMA MULTIFORME ( 9 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 9 FDA reports)
GROWTH HORMONE DEFICIENCY ( 9 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 9 FDA reports)
HIP SURGERY ( 9 FDA reports)
HYPERVISCOSITY SYNDROME ( 9 FDA reports)
HYPOAESTHESIA FACIAL ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 9 FDA reports)
INADEQUATE ANALGESIA ( 9 FDA reports)
INGUINAL HERNIA ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INTENTIONAL DRUG MISUSE ( 9 FDA reports)
INTESTINAL INFARCTION ( 9 FDA reports)
INTESTINAL MASS ( 9 FDA reports)
LISTLESS ( 9 FDA reports)
LOSS OF PROPRIOCEPTION ( 9 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 9 FDA reports)
LYMPHOMA TRANSFORMATION ( 9 FDA reports)
MAJOR DEPRESSION ( 9 FDA reports)
MASTITIS ( 9 FDA reports)
MASTOIDITIS ( 9 FDA reports)
MILLER FISHER SYNDROME ( 9 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 9 FDA reports)
MUSCULOSKELETAL DISORDER ( 9 FDA reports)
NECROTISING COLITIS ( 9 FDA reports)
NEOPLASM SKIN ( 9 FDA reports)
NEURITIS ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 9 FDA reports)
OBSTRUCTION GASTRIC ( 9 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 9 FDA reports)
ACANTHAMOEBA INFECTION ( 8 FDA reports)
AFFECTIVE DISORDER ( 8 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 8 FDA reports)
ALVEOLAR PROTEINOSIS ( 8 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 8 FDA reports)
ANORECTAL DISORDER ( 8 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 8 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 8 FDA reports)
AXILLARY MASS ( 8 FDA reports)
BACK INJURY ( 8 FDA reports)
BENIGN GASTRIC NEOPLASM ( 8 FDA reports)
BILE DUCT STENOSIS ( 8 FDA reports)
BILE DUCT STONE ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BIOPSY MUCOSA ABNORMAL ( 8 FDA reports)
BIPOLAR DISORDER ( 8 FDA reports)
BLOOD CREATININE ABNORMAL ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BODY HEIGHT BELOW NORMAL ( 8 FDA reports)
BREAST CYST ( 8 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 8 FDA reports)
BREATH ODOUR ( 8 FDA reports)
BURKITT'S LYMPHOMA STAGE III ( 8 FDA reports)
CAMPYLOBACTER INFECTION ( 8 FDA reports)
CATHETER SEPSIS ( 8 FDA reports)
CELL MARKER INCREASED ( 8 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 8 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 8 FDA reports)
CHEST WALL PAIN ( 8 FDA reports)
CHOKING ( 8 FDA reports)
CITROBACTER SEPSIS ( 8 FDA reports)
CLUSTER HEADACHE ( 8 FDA reports)
CNS VENTRICULITIS ( 8 FDA reports)
COLLAGEN DISORDER ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 8 FDA reports)
CONDUCTIVE DEAFNESS ( 8 FDA reports)
CONGENITAL ANOMALY ( 8 FDA reports)
CONGENITAL HAND MALFORMATION ( 8 FDA reports)
CORONA VIRUS INFECTION ( 8 FDA reports)
CRYPTOCOCCOSIS ( 8 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 8 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DISINHIBITION ( 8 FDA reports)
DUODENAL ULCER PERFORATION ( 8 FDA reports)
DYSLIPIDAEMIA ( 8 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 8 FDA reports)
DYSSTASIA ( 8 FDA reports)
DYSTONIA ( 8 FDA reports)
EAR DISCOMFORT ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
ECZEMA EYELIDS ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 8 FDA reports)
EMBOLISM ARTERIAL ( 8 FDA reports)
ENCEPHALITIS ENTEROVIRAL ( 8 FDA reports)
ENTROPION ( 8 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 8 FDA reports)
ERYTHEMA NODOSUM ( 8 FDA reports)
EXCORIATION ( 8 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 8 FDA reports)
FACIAL BONES FRACTURE ( 8 FDA reports)
FANCONI SYNDROME ACQUIRED ( 8 FDA reports)
FEAR ( 8 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 8 FDA reports)
FRACTURE ( 8 FDA reports)
GASTRITIS HAEMORRHAGIC ( 8 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 8 FDA reports)
GENITAL HERPES ( 8 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 8 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 8 FDA reports)
GLOMERULOSCLEROSIS ( 8 FDA reports)
GOUTY ARTHRITIS ( 8 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 8 FDA reports)
HEPATITIS B DNA INCREASED ( 8 FDA reports)
HIV INFECTION ( 8 FDA reports)
HUMERUS FRACTURE ( 8 FDA reports)
HYPERPLASIA ( 8 FDA reports)
IMMUNOGLOBULINS DECREASED ( 8 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 8 FDA reports)
INTESTINAL FISTULA ( 8 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 8 FDA reports)
JAUNDICE NEONATAL ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
JUGULAR VEIN DISTENSION ( 8 FDA reports)
KERATITIS ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
LICHEN PLANUS ( 8 FDA reports)
LIPOMA ( 8 FDA reports)
LIVER SCAN ABNORMAL ( 8 FDA reports)
LUNG CANCER METASTATIC ( 8 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 8 FDA reports)
MACROCYTOSIS ( 8 FDA reports)
MALIGNANT BREAST LUMP REMOVAL ( 8 FDA reports)
MALIGNANT GLIOMA ( 8 FDA reports)
MAMMARY DUCT ECTASIA ( 8 FDA reports)
MEGAKARYOCYTES INCREASED ( 8 FDA reports)
MENINGITIS VIRAL ( 8 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 8 FDA reports)
MUSCLE HAEMORRHAGE ( 8 FDA reports)
MUSCLE STRAIN ( 8 FDA reports)
MYCOBACTERIAL INFECTION ( 8 FDA reports)
MYOPIA ( 8 FDA reports)
NAIL DYSTROPHY ( 8 FDA reports)
NAIL-PATELLA SYNDROME ( 8 FDA reports)
NASAL DISORDER ( 8 FDA reports)
NECK MASS ( 8 FDA reports)
OCULAR TOXICITY ( 8 FDA reports)
OESOPHAGEAL PERFORATION ( 8 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 8 FDA reports)
OESOPHAGEAL STENOSIS ( 8 FDA reports)
ONYCHOMADESIS ( 8 FDA reports)
ORAL FUNGAL INFECTION ( 8 FDA reports)
ORAL MUCOSAL DISORDER ( 8 FDA reports)
ORAL NEOPLASM BENIGN ( 8 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 8 FDA reports)
OXYGEN SUPPLEMENTATION ( 8 FDA reports)
PARANOIA ( 8 FDA reports)
PARKINSON'S DISEASE ( 8 FDA reports)
PAROTID GLAND ENLARGEMENT ( 8 FDA reports)
PAST-POINTING ( 8 FDA reports)
PCO2 INCREASED ( 8 FDA reports)
PERINEURIAL CYST ( 8 FDA reports)
PLEURAL DISORDER ( 8 FDA reports)
PNEUMOCOCCAL INFECTION ( 8 FDA reports)
POLYP COLORECTAL ( 8 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 8 FDA reports)
PULMONARY INFARCTION ( 8 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 8 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 8 FDA reports)
RENAL ATROPHY ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
RESPIRATORY MONILIASIS ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
RETINAL DEGENERATION ( 8 FDA reports)
RHEUMATOID NODULE ( 8 FDA reports)
SALMONELLOSIS ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SCAN ABNORMAL ( 8 FDA reports)
SECONDARY SEQUESTRUM ( 8 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 8 FDA reports)
SKIN MASS ( 8 FDA reports)
SMALL INTESTINAL PERFORATION ( 8 FDA reports)
SOFT TISSUE NECROSIS ( 8 FDA reports)
SOPOR ( 8 FDA reports)
SPONDYLITIS ( 8 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 8 FDA reports)
TENDON DISORDER ( 8 FDA reports)
THIRST ( 8 FDA reports)
THYROID MASS ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
TONGUE ULCERATION ( 8 FDA reports)
TOOTH HYPOPLASIA ( 8 FDA reports)
TOXIC NODULAR GOITRE ( 8 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 8 FDA reports)
TROPONIN T INCREASED ( 8 FDA reports)
TYPE 1 DIABETES MELLITUS ( 8 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 8 FDA reports)
URETHRAL HAEMORRHAGE ( 8 FDA reports)
URINARY TRACT OBSTRUCTION ( 8 FDA reports)
VASODILATATION ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
WALKING DISABILITY ( 8 FDA reports)
WEIGHT BEARING DIFFICULTY ( 8 FDA reports)
WOUND SECRETION ( 8 FDA reports)
PELVIC FLUID COLLECTION ( 7 FDA reports)
PEMPHIGUS ( 7 FDA reports)
PERICARDIAL HAEMORRHAGE ( 7 FDA reports)
PERICARDITIS CONSTRICTIVE ( 7 FDA reports)
PERIORBITAL CELLULITIS ( 7 FDA reports)
PERIOSTITIS ( 7 FDA reports)
PHLEBITIS SUPERFICIAL ( 7 FDA reports)
PHLEBOTHROMBOSIS ( 7 FDA reports)
PNEUMONIA NECROTISING ( 7 FDA reports)
POLYCYTHAEMIA ( 7 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 7 FDA reports)
PRODUCT QUALITY ISSUE ( 7 FDA reports)
PROTEIN TOTAL INCREASED ( 7 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 7 FDA reports)
PRURIGO ( 7 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 7 FDA reports)
PULSE ABNORMAL ( 7 FDA reports)
PUPILS UNEQUAL ( 7 FDA reports)
RECTAL CANCER ( 7 FDA reports)
RECTAL FISSURE ( 7 FDA reports)
RENAL CANCER ( 7 FDA reports)
RENAL NECROSIS ( 7 FDA reports)
RENAL VASCULITIS ( 7 FDA reports)
RETINAL VASCULITIS ( 7 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 7 FDA reports)
RIGHT ATRIAL DILATATION ( 7 FDA reports)
ROTAVIRUS INFECTION ( 7 FDA reports)
SEROSITIS ( 7 FDA reports)
SHOULDER PAIN ( 7 FDA reports)
SJOGREN'S SYNDROME ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SKIN INJURY ( 7 FDA reports)
SMALL INTESTINE ULCER ( 7 FDA reports)
SNORING ( 7 FDA reports)
SPINAL DEFORMITY ( 7 FDA reports)
SPIROMETRY ABNORMAL ( 7 FDA reports)
STARING ( 7 FDA reports)
STRABISMUS ( 7 FDA reports)
SUPRAPUBIC PAIN ( 7 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 7 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 7 FDA reports)
TELANGIECTASIA ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
THALAMIC INFARCTION ( 7 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 7 FDA reports)
TIBIA FRACTURE ( 7 FDA reports)
TORSADE DE POINTES ( 7 FDA reports)
TOXIC NEUROPATHY ( 7 FDA reports)
TRACHEOBRONCHITIS ( 7 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
URINARY TRACT DISORDER ( 7 FDA reports)
URINARY TRACT INFECTION VIRAL ( 7 FDA reports)
VESTIBULAR DISORDER ( 7 FDA reports)
VIRAL RASH ( 7 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 7 FDA reports)
ABDOMINAL NEOPLASM ( 7 FDA reports)
ABNORMAL FAECES ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 7 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 7 FDA reports)
ACUTE STRESS DISORDER ( 7 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 7 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 7 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 7 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 7 FDA reports)
ARTERIAL DISORDER ( 7 FDA reports)
ARTHRITIS INFECTIVE ( 7 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 7 FDA reports)
BLADDER PAIN ( 7 FDA reports)
BLINDNESS UNILATERAL ( 7 FDA reports)
BLOOD BICARBONATE INCREASED ( 7 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 7 FDA reports)
BLOOD CORTISOL DECREASED ( 7 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 7 FDA reports)
BONE DENSITY INCREASED ( 7 FDA reports)
BONE INFARCTION ( 7 FDA reports)
BONE SCAN ABNORMAL ( 7 FDA reports)
BORRELIA INFECTION ( 7 FDA reports)
BOWEL SOUNDS ABNORMAL ( 7 FDA reports)
BRONCHOPLEURAL FISTULA ( 7 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 7 FDA reports)
CARBOHYDRATE ANTIGEN 15-3 INCREASED ( 7 FDA reports)
CATHETER SITE HAEMORRHAGE ( 7 FDA reports)
CEREBELLAR ATROPHY ( 7 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 7 FDA reports)
CEREBRAL ASPERGILLOSIS ( 7 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 7 FDA reports)
CHEMOTHERAPY ( 7 FDA reports)
CHLOASMA ( 7 FDA reports)
CHOLECYSTITIS INFECTIVE ( 7 FDA reports)
COMPARTMENT SYNDROME ( 7 FDA reports)
COR PULMONALE ( 7 FDA reports)
CORONARY ARTERY BYPASS ( 7 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 7 FDA reports)
DEAFNESS UNILATERAL ( 7 FDA reports)
DENTAL CLEANING ( 7 FDA reports)
DENTAL TREATMENT ( 7 FDA reports)
DERMATOMYOSITIS ( 7 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 7 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
DUPUYTREN'S CONTRACTURE ( 7 FDA reports)
ENDOMETRIAL CANCER ( 7 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 7 FDA reports)
ENDOTOXIC SHOCK ( 7 FDA reports)
EPIDURAL LIPOMATOSIS ( 7 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 7 FDA reports)
EWING'S SARCOMA RECURRENT ( 7 FDA reports)
EXFOLIATIVE RASH ( 7 FDA reports)
EXTRASYSTOLES ( 7 FDA reports)
EYE HAEMORRHAGE ( 7 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 7 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 7 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 7 FDA reports)
FURUNCLE ( 7 FDA reports)
GASTRIC MUCOSAL LESION ( 7 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GENERAL NUTRITION DISORDER ( 7 FDA reports)
GLIOBLASTOMA ( 7 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 7 FDA reports)
GOUT ( 7 FDA reports)
GRAFT COMPLICATION ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 7 FDA reports)
HAEMOGLOBIN INCREASED ( 7 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 7 FDA reports)
HEPATORENAL FAILURE ( 7 FDA reports)
HORMONE LEVEL ABNORMAL ( 7 FDA reports)
HYPERTONIC BLADDER ( 7 FDA reports)
HYPOPERFUSION ( 7 FDA reports)
ILEITIS ( 7 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCISION SITE INFECTION ( 7 FDA reports)
INFECTED LYMPHOCELE ( 7 FDA reports)
INGROWING NAIL ( 7 FDA reports)
INTESTINAL DILATATION ( 7 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 7 FDA reports)
INVESTIGATION ( 7 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 7 FDA reports)
LACERATION ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 7 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
LYMPHOMATOID PAPULOSIS ( 7 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 7 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 7 FDA reports)
MEDIASTINAL MASS ( 7 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 7 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 7 FDA reports)
METASTASES TO BONE MARROW ( 7 FDA reports)
MICTURITION DISORDER ( 7 FDA reports)
MITRAL VALVE DISEASE ( 7 FDA reports)
MONONEUROPATHY MULTIPLEX ( 7 FDA reports)
MUSCLE CONTRACTURE ( 7 FDA reports)
MUSCLE NECROSIS ( 7 FDA reports)
MUSCLE SPASTICITY ( 7 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 7 FDA reports)
MYOPATHY STEROID ( 7 FDA reports)
NEPHROBLASTOMA ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 7 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 7 FDA reports)
OPHTHALMOPLEGIA ( 7 FDA reports)
OS TRIGONUM SYNDROME ( 7 FDA reports)
OSTEORADIONECROSIS ( 7 FDA reports)
PANCREATIC ATROPHY ( 7 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 7 FDA reports)
PANCREATITIS NECROTISING ( 7 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 7 FDA reports)
PARANASAL SINUS DISCOMFORT ( 7 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 7 FDA reports)
PAROTITIS ( 7 FDA reports)
ABDOMINAL SYMPTOM ( 6 FDA reports)
ABSCESS FUNGAL ( 6 FDA reports)
ABULIA ( 6 FDA reports)
ACID FAST BACILLI INFECTION ( 6 FDA reports)
ACQUIRED HAEMOPHILIA ( 6 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 6 FDA reports)
ANAEMIA NEONATAL ( 6 FDA reports)
ANAL DISCOMFORT ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
AORTIC THROMBOSIS ( 6 FDA reports)
AORTIC VALVE STENOSIS ( 6 FDA reports)
APATHY ( 6 FDA reports)
APPETITE DISORDER ( 6 FDA reports)
BACTEROIDES INFECTION ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BILIARY DRAINAGE ( 6 FDA reports)
BIOPSY SKIN ABNORMAL ( 6 FDA reports)
BLADDER TELANGIECTASIA ( 6 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 6 FDA reports)
BLAST CELL CRISIS ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 6 FDA reports)
BLOOD IRON INCREASED ( 6 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 6 FDA reports)
BLOOD MAGNESIUM INCREASED ( 6 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 6 FDA reports)
BONE NEOPLASM ( 6 FDA reports)
BOVINE TUBERCULOSIS ( 6 FDA reports)
BRADYPHRENIA ( 6 FDA reports)
BRAIN DAMAGE ( 6 FDA reports)
BREAST CELLULITIS ( 6 FDA reports)
BREAST OPERATION ( 6 FDA reports)
CALCULUS URETERIC ( 6 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 6 FDA reports)
CARDIAC OUTPUT DECREASED ( 6 FDA reports)
CARDIAC VALVE VEGETATION ( 6 FDA reports)
CARDITIS ( 6 FDA reports)
CAROTID ARTERY STENOSIS ( 6 FDA reports)
CATARACT OPERATION ( 6 FDA reports)
CATHETER THROMBOSIS ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM ENTEROVIRAL INFECTION ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 6 FDA reports)
CEREBRAL CALCIFICATION ( 6 FDA reports)
CEREBRAL THROMBOSIS ( 6 FDA reports)
CERVIX CARCINOMA ( 6 FDA reports)
CHROMOSOMAL MUTATION ( 6 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
COAGULATION TIME PROLONGED ( 6 FDA reports)
COLECTOMY ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 6 FDA reports)
CONUS MEDULLARIS SYNDROME ( 6 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 6 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 6 FDA reports)
CROUP INFECTIOUS ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DENTAL PROSTHESIS USER ( 6 FDA reports)
DEPRESSION SUICIDAL ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DERMOID CYST ( 6 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 6 FDA reports)
DIABETIC COMA ( 6 FDA reports)
ECTHYMA ( 6 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 6 FDA reports)
ENTEROBACTER BACTERAEMIA ( 6 FDA reports)
ENTEROCOLITIS VIRAL ( 6 FDA reports)
EOSINOPHILIC PNEUMONIA ( 6 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 6 FDA reports)
EPHELIDES ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
FACE INJURY ( 6 FDA reports)
FAT EMBOLISM ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FLUID IMBALANCE ( 6 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 6 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 6 FDA reports)
FUNGUS STOOL IDENTIFIED ( 6 FDA reports)
GAS GANGRENE ( 6 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 6 FDA reports)
GASTRIC VOLVULUS ( 6 FDA reports)
GASTROENTERITIS SALMONELLA ( 6 FDA reports)
GASTROINTESTINAL CARCINOMA ( 6 FDA reports)
GASTROINTESTINAL FISTULA ( 6 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 6 FDA reports)
GASTROSPLENIC FISTULA ( 6 FDA reports)
HAEMARTHROSIS ( 6 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 6 FDA reports)
HAEMORRHAGIC ANAEMIA ( 6 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 6 FDA reports)
HEMIANOPIA HOMONYMOUS ( 6 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 6 FDA reports)
HEPATITIS B VIRUS ( 6 FDA reports)
HEPATITIS CHRONIC ACTIVE ( 6 FDA reports)
HYDROPNEUMOTHORAX ( 6 FDA reports)
HYPERAEMIA ( 6 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 6 FDA reports)
HYPOCHROMASIA ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
HYPOURICAEMIA ( 6 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 6 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 6 FDA reports)
INFUSION SITE EXTRAVASATION ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 6 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 6 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 6 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 6 FDA reports)
INTUBATION ( 6 FDA reports)
IRRITABLE BOWEL SYNDROME ( 6 FDA reports)
KLIPPEL-FEIL SYNDROME ( 6 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 6 FDA reports)
LARYNGEAL CANCER ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LENTIGO ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUMBAR SPINAL STENOSIS ( 6 FDA reports)
LYMPH NODE PALPABLE ( 6 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 6 FDA reports)
MAMMOPLASTY ( 6 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 6 FDA reports)
MENORRHAGIA ( 6 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 6 FDA reports)
METASTASES TO THE MEDIASTINUM ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MICROCEPHALY ( 6 FDA reports)
MICROSCOPIC POLYANGIITIS ( 6 FDA reports)
MUCOUS STOOLS ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MUSCLE RIGIDITY ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
MYELOBLASTOMA ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 6 FDA reports)
NEPHRITIC SYNDROME ( 6 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 6 FDA reports)
NEUROCYSTICERCOSIS ( 6 FDA reports)
NO ADVERSE EFFECT ( 6 FDA reports)
NORMAL NEWBORN ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
NUCHAL RIGIDITY ( 6 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 6 FDA reports)
OVARIAN DISORDER ( 6 FDA reports)
PACHYMENINGITIS ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 6 FDA reports)
PERITONEAL EFFUSION ( 6 FDA reports)
PETIT MAL EPILEPSY ( 6 FDA reports)
PHARYNGEAL ULCERATION ( 6 FDA reports)
PLEURAL INFECTION ( 6 FDA reports)
PNEUMATURIA ( 6 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 6 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 6 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 6 FDA reports)
POLYDIPSIA ( 6 FDA reports)
POROKERATOSIS ( 6 FDA reports)
POSTRENAL FAILURE ( 6 FDA reports)
PRINZMETAL ANGINA ( 6 FDA reports)
PROCTOCOLITIS ( 6 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 6 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 6 FDA reports)
PURPURA FULMINANS ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RADIAL NERVE PALSY ( 6 FDA reports)
RADIUS FRACTURE ( 6 FDA reports)
REGRESSIVE BEHAVIOUR ( 6 FDA reports)
RENAL PAIN ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 6 FDA reports)
RETINOPATHY ( 6 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 6 FDA reports)
RHINITIS HYPERTROPHIC ( 6 FDA reports)
RICKETS ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SARCOMA ( 6 FDA reports)
SARCOMA METASTATIC ( 6 FDA reports)
SCOTOMA ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SENSE OF OPPRESSION ( 6 FDA reports)
SHIFT TO THE LEFT ( 6 FDA reports)
SKELETAL INJURY ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SKIN LACERATION ( 6 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 6 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 6 FDA reports)
STOMATOCOCCAL INFECTION ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 6 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 6 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
TERATOMA ( 6 FDA reports)
TESTIS CANCER ( 6 FDA reports)
THROMBOCYTOSIS ( 6 FDA reports)
THYROIDITIS ( 6 FDA reports)
TOE AMPUTATION ( 6 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 6 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 6 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 6 FDA reports)
UTERINE ENLARGEMENT ( 6 FDA reports)
VAGINAL OBSTRUCTION ( 6 FDA reports)
VASCULITIC RASH ( 6 FDA reports)
VIRAL DIARRHOEA ( 6 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 6 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 6 FDA reports)
PELIOSIS HEPATIS ( 5 FDA reports)
PERIPHERAL NERVE PALSY ( 5 FDA reports)
PERITONEAL CARCINOMA ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POSTMENOPAUSE ( 5 FDA reports)
POSTOPERATIVE ADHESION ( 5 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 5 FDA reports)
POSTURE ABNORMAL ( 5 FDA reports)
PRECOCIOUS PUBERTY ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PRODUCT COLOUR ISSUE ( 5 FDA reports)
PROSTRATION ( 5 FDA reports)
PSYCHOMOTOR RETARDATION ( 5 FDA reports)
PULMONARY HILUM MASS ( 5 FDA reports)
PULSE PRESSURE DECREASED ( 5 FDA reports)
PYELONEPHRITIS FUNGAL ( 5 FDA reports)
PYOTHORAX ( 5 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 5 FDA reports)
RADIATION MUCOSITIS ( 5 FDA reports)
RENAL AMYLOIDOSIS ( 5 FDA reports)
RENAL ARTERY STENOSIS ( 5 FDA reports)
RENAL HYPERTENSION ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RETINAL DYSTROPHY ( 5 FDA reports)
RETINAL OEDEMA ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
RICHTER'S SYNDROME ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SENSORIMOTOR DISORDER ( 5 FDA reports)
SEPSIS NEONATAL ( 5 FDA reports)
SERRATIA INFECTION ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
SKIN CHAPPED ( 5 FDA reports)
SKIN DEPIGMENTATION ( 5 FDA reports)
SKIN NEOPLASM EXCISION ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SKIN STRIAE ( 5 FDA reports)
SMEAR CERVIX ABNORMAL ( 5 FDA reports)
SPINAL ANAESTHESIA ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SPINAL CORD OEDEMA ( 5 FDA reports)
SPLENIC LESION ( 5 FDA reports)
STRESS CARDIOMYOPATHY ( 5 FDA reports)
SUBACUTE HEPATIC FAILURE ( 5 FDA reports)
SUBDURAL HYGROMA ( 5 FDA reports)
SUDDEN HEARING LOSS ( 5 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 5 FDA reports)
TEMPERATURE INTOLERANCE ( 5 FDA reports)
THERAPEUTIC EMBOLISATION ( 5 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
THROMBOTIC STROKE ( 5 FDA reports)
TRACHEAL STENOSIS ( 5 FDA reports)
TRANSFUSION MICROCHIMERISM ( 5 FDA reports)
TRANSIENT PSYCHOSIS ( 5 FDA reports)
TRIGEMINAL NERVE DISORDER ( 5 FDA reports)
TUMOUR FLARE ( 5 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 5 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 5 FDA reports)
URINE FLOW DECREASED ( 5 FDA reports)
UTERINE MASS ( 5 FDA reports)
VAGINAL CELLULITIS ( 5 FDA reports)
VASCULAR GRAFT COMPLICATION ( 5 FDA reports)
VASCULAR PSEUDOANEURYSM ( 5 FDA reports)
VEILLONELLA INFECTION ( 5 FDA reports)
VENOUS OCCLUSION ( 5 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
VISCERAL LEISHMANIASIS ( 5 FDA reports)
VITILIGO ( 5 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 5 FDA reports)
ABDOMINAL WALL ABSCESS ( 5 FDA reports)
ABDOMINAL WALL DISORDER ( 5 FDA reports)
ADHESION ( 5 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 5 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 5 FDA reports)
AKATHISIA ( 5 FDA reports)
AMBLYOPIA STRABISMIC ( 5 FDA reports)
AMYOTROPHY ( 5 FDA reports)
ANAPLASTIC ASTROCYTOMA ( 5 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
AORTIC VALVE CALCIFICATION ( 5 FDA reports)
APOPTOSIS ( 5 FDA reports)
ARTERIAL HAEMORRHAGE ( 5 FDA reports)
ASPERGILLOMA ( 5 FDA reports)
ATONIC SEIZURES ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 5 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 5 FDA reports)
AXONAL NEUROPATHY ( 5 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 5 FDA reports)
BASAL GANGLION DEGENERATION ( 5 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 5 FDA reports)
BLEPHARITIS ( 5 FDA reports)
BLOOD GROWTH HORMONE DECREASED ( 5 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
BLOOD OSMOLARITY INCREASED ( 5 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 5 FDA reports)
BLOOD URINE ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BRAIN STEM HAEMORRHAGE ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST ABSCESS ( 5 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 5 FDA reports)
BRONCHOSCOPY ABNORMAL ( 5 FDA reports)
BURSA DISORDER ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CANDIDURIA ( 5 FDA reports)
CAROTID ARTERY OCCLUSION ( 5 FDA reports)
CAROTID ARTERY THROMBOSIS ( 5 FDA reports)
CATHETER SITE CELLULITIS ( 5 FDA reports)
CATHETER SITE SWELLING ( 5 FDA reports)
CELLULITIS ORBITAL ( 5 FDA reports)
CEREBELLAR INFARCTION ( 5 FDA reports)
CEREBELLAR TUMOUR ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CERVICAL SPINAL STENOSIS ( 5 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 5 FDA reports)
CHALAZION ( 5 FDA reports)
CHOLANGITIS SCLEROSING ( 5 FDA reports)
CHORIORETINAL ATROPHY ( 5 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 5 FDA reports)
COLON NEOPLASM ( 5 FDA reports)
COLOUR BLINDNESS ( 5 FDA reports)
COMA SCALE ABNORMAL ( 5 FDA reports)
COMPLEMENT FACTOR DECREASED ( 5 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 5 FDA reports)
CORNEAL NEOVASCULARISATION ( 5 FDA reports)
CORNEAL OPACITY ( 5 FDA reports)
CORONARY ARTERY THROMBOSIS ( 5 FDA reports)
CRYOGLOBULINAEMIA ( 5 FDA reports)
CSF BACTERIA IDENTIFIED ( 5 FDA reports)
CUTANEOUS VASCULITIS ( 5 FDA reports)
CYST REMOVAL ( 5 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 5 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 5 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 5 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 5 FDA reports)
DENERVATION ATROPHY ( 5 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DEVICE OCCLUSION ( 5 FDA reports)
DIARRHOEA INFECTIOUS ( 5 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DUODENAL PERFORATION ( 5 FDA reports)
DYSMORPHISM ( 5 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 5 FDA reports)
EJECTION FRACTION ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 5 FDA reports)
ENCEPHALITIS POST VARICELLA ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENDOCARDIAL FIBROSIS ( 5 FDA reports)
ENTEROVIRUS INFECTION ( 5 FDA reports)
EPIDERMAL NECROSIS ( 5 FDA reports)
EPIDERMOLYSIS ( 5 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYE INFECTION BACTERIAL ( 5 FDA reports)
FAT TISSUE INCREASED ( 5 FDA reports)
FEEDING DISORDER ( 5 FDA reports)
FIBROMYALGIA ( 5 FDA reports)
FOETAL DEATH ( 5 FDA reports)
GASTROINTESTINAL EROSION ( 5 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 5 FDA reports)
GENERAL SYMPTOM ( 5 FDA reports)
GESTATIONAL DIABETES ( 5 FDA reports)
GINGIVAL HYPERPLASIA ( 5 FDA reports)
GRANULOCYTOSIS ( 5 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 5 FDA reports)
GRUNTING ( 5 FDA reports)
HAEMOGLOBIN ( 5 FDA reports)
HEART TRANSPLANT ( 5 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 5 FDA reports)
HEPATIC INFECTION ( 5 FDA reports)
HEPATITIS C VIRUS TEST ( 5 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 5 FDA reports)
HERPES OESOPHAGITIS ( 5 FDA reports)
HERPES SIMPLEX HEPATITIS ( 5 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 5 FDA reports)
HISTOPLASMOSIS ( 5 FDA reports)
HODGKIN'S DISEASE STAGE II ( 5 FDA reports)
HYDROURETER ( 5 FDA reports)
HYPERPROTEINAEMIA ( 5 FDA reports)
HYPOCAPNIA ( 5 FDA reports)
HYPOSMIA ( 5 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
ILEAL ULCER ( 5 FDA reports)
ILIAC VEIN THROMBOSIS ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INFECTED SKIN ULCER ( 5 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 5 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INJECTION SITE EXTRAVASATION ( 5 FDA reports)
INJECTION SITE RASH ( 5 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 5 FDA reports)
INTESTINAL STENOSIS ( 5 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 5 FDA reports)
IRIDOCYCLITIS ( 5 FDA reports)
KERATITIS INTERSTITIAL ( 5 FDA reports)
KIDNEY MALFORMATION ( 5 FDA reports)
KLEBSIELLA TEST POSITIVE ( 5 FDA reports)
KYPHOSIS ( 5 FDA reports)
LAPAROTOMY ( 5 FDA reports)
LASER THERAPY ( 5 FDA reports)
LEUKODYSTROPHY ( 5 FDA reports)
LEUKOSTASIS ( 5 FDA reports)
LICHENOID KERATOSIS ( 5 FDA reports)
LIGAMENT LAXITY ( 5 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 5 FDA reports)
LIMB INJURY ( 5 FDA reports)
LIPASE ABNORMAL ( 5 FDA reports)
LIPOSARCOMA ( 5 FDA reports)
LIVER TENDERNESS ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
LUPUS PNEUMONITIS ( 5 FDA reports)
LYMPHOCELE ( 5 FDA reports)
MALABSORPTION ( 5 FDA reports)
MALIGNANT ASCITES ( 5 FDA reports)
MARASMUS ( 5 FDA reports)
MECHANICAL ILEUS ( 5 FDA reports)
MEDIASTINUM NEOPLASM ( 5 FDA reports)
MENINGITIS ENTEROVIRAL ( 5 FDA reports)
MENINGITIS LISTERIA ( 5 FDA reports)
MENINGITIS TUBERCULOUS ( 5 FDA reports)
METABOLIC ENCEPHALOPATHY ( 5 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 5 FDA reports)
METASTASES TO HEART ( 5 FDA reports)
METASTASES TO KIDNEY ( 5 FDA reports)
MICROALBUMINURIA ( 5 FDA reports)
MICROSPORIDIA INFECTION ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MUCOSAL INFECTION ( 5 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 5 FDA reports)
MYCOSIS FUNGOIDES ( 5 FDA reports)
NAIL DISCOLOURATION ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NECROSIS ISCHAEMIC ( 5 FDA reports)
NECROTISING RETINITIS ( 5 FDA reports)
NEONATAL HYPOTENSION ( 5 FDA reports)
NEPHRECTOMY ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
NODULE ON EXTREMITY ( 5 FDA reports)
OCCULT BLOOD POSITIVE ( 5 FDA reports)
ONYCHOCLASIS ( 5 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 5 FDA reports)
ORCHITIS ( 5 FDA reports)
OSTEOTOMY ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
PANCREATIC ENZYMES INCREASED ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABSCESS NECK ( 4 FDA reports)
ABSCESS RUPTURE ( 4 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE POLYNEUROPATHY ( 4 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 4 FDA reports)
ADENOCARCINOMA PANCREAS ( 4 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
ADRENAL MASS ( 4 FDA reports)
ALBUMINURIA ( 4 FDA reports)
ANAL ULCER ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC DISSECTION ( 4 FDA reports)
ARTERIAL RUPTURE ( 4 FDA reports)
ARTERIOSPASM CORONARY ( 4 FDA reports)
ARTHRITIS REACTIVE ( 4 FDA reports)
ARTHROTOXICITY ( 4 FDA reports)
ASCITES INFECTION ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
ATRIAL HYPERTROPHY ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
AURICULAR SWELLING ( 4 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 4 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 4 FDA reports)
B-LYMPHOCYTE ABNORMALITIES ( 4 FDA reports)
BACILLARY ANGIOMATOSIS ( 4 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 4 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
BICYTOPENIA ( 4 FDA reports)
BILIARY TRACT INFECTION ( 4 FDA reports)
BLADDER CATHETERISATION ( 4 FDA reports)
BLADDER SPASM ( 4 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 4 FDA reports)
BLOOD BLISTER ( 4 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 4 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 4 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 4 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BONE FISTULA ( 4 FDA reports)
BONE MARROW ISCHAEMIA ( 4 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 4 FDA reports)
BOWEN'S DISEASE ( 4 FDA reports)
BRACHIAL PLEXOPATHY ( 4 FDA reports)
BRADYPNOEA ( 4 FDA reports)
BRAIN COMPRESSION ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BREAST DISCOMFORT ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BREAST HYPERPLASIA ( 4 FDA reports)
BREAST INFECTION ( 4 FDA reports)
BRONCHITIS BACTERIAL ( 4 FDA reports)
BRONCHITIS VIRAL ( 4 FDA reports)
BRONCHOPULMONARY DISEASE ( 4 FDA reports)
BURNING SENSATION MUCOSAL ( 4 FDA reports)
BUTTERFLY RASH ( 4 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CAPILLARY DISORDER ( 4 FDA reports)
CARBON DIOXIDE INCREASED ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 4 FDA reports)
CD4/CD8 RATIO DECREASED ( 4 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 4 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 4 FDA reports)
CEREBROSCLEROSIS ( 4 FDA reports)
CHLOROMA ( 4 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 4 FDA reports)
CHORIORETINITIS ( 4 FDA reports)
CHRONIC FATIGUE SYNDROME ( 4 FDA reports)
CLONUS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 4 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 4 FDA reports)
COLONIC FISTULA ( 4 FDA reports)
COMPLICATION OF PREGNANCY ( 4 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 4 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 4 FDA reports)
CONGENITAL NOSE MALFORMATION ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CSF CULTURE POSITIVE ( 4 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 4 FDA reports)
CUTANEOUS TUBERCULOSIS ( 4 FDA reports)
CYTOLOGY ABNORMAL ( 4 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 4 FDA reports)
CYTOMEGALOVIRUS TEST ( 4 FDA reports)
DECREASED VIBRATORY SENSE ( 4 FDA reports)
DELUSION OF GRANDEUR ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 4 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIAPHRAGMATIC DISORDER ( 4 FDA reports)
DIASTOLIC HYPOTENSION ( 4 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 4 FDA reports)
DIZZINESS EXERTIONAL ( 4 FDA reports)
DRUG CLEARANCE INCREASED ( 4 FDA reports)
DRUG LEVEL FLUCTUATING ( 4 FDA reports)
DUODENAL STENOSIS ( 4 FDA reports)
DYSENTERY ( 4 FDA reports)
DYSPNOEA EXACERBATED ( 4 FDA reports)
ELEVATED MOOD ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ENDOCRINE DISORDER ( 4 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
EYE OEDEMA ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
FLIGHT OF IDEAS ( 4 FDA reports)
FLOPPY INFANT ( 4 FDA reports)
FOETAL MALNUTRITION ( 4 FDA reports)
FUNGAL ENDOCARDITIS ( 4 FDA reports)
FUNGAL OESOPHAGITIS ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTRODUODENAL ULCER ( 4 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
GINGIVAL RECESSION ( 4 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
GRAFT DYSFUNCTION ( 4 FDA reports)
GRAFT LOSS ( 4 FDA reports)
GRANULOCYTES MATURATION ARREST ( 4 FDA reports)
GRIMACING ( 4 FDA reports)
HAEMANGIOMA OF LIVER ( 4 FDA reports)
HAEMATOCRIT INCREASED ( 4 FDA reports)
HAEMORRHAGIC ASCITES ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HEART TRANSPLANT REJECTION ( 4 FDA reports)
HEPATIC ISCHAEMIA ( 4 FDA reports)
HEPATITIS B VIRUS TEST ( 4 FDA reports)
HEPATITIS E ( 4 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 4 FDA reports)
HETEROTAXIA ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HY'S LAW CASE ( 4 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 4 FDA reports)
HYPERCHLORHYDRIA ( 4 FDA reports)
HYPERMETABOLISM ( 4 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPOCHROMIC ANAEMIA ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
IMPLANT SITE REACTION ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 4 FDA reports)
INFECTION PARASITIC ( 4 FDA reports)
INFUSION SITE BRUISING ( 4 FDA reports)
INJECTION SITE HAEMATOMA ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
INJECTION SITE VASCULITIS ( 4 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
INTRAOCULAR LENS IMPLANT ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 4 FDA reports)
JEJUNITIS ( 4 FDA reports)
JOINT SURGERY ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KOUNIS SYNDROME ( 4 FDA reports)
LARYNGEAL DISORDER ( 4 FDA reports)
LEUKAEMIC INFILTRATION ( 4 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 4 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 4 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 4 FDA reports)
LEUKOPLAKIA ORAL ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
LIPIDS INCREASED ( 4 FDA reports)
LIPOATROPHY ( 4 FDA reports)
LIPOMATOSIS ( 4 FDA reports)
LIVE BIRTH ( 4 FDA reports)
LOCALISED OSTEOARTHRITIS ( 4 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 4 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MALARIA ( 4 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
MEAN CELL VOLUME INCREASED ( 4 FDA reports)
MEGACOLON ( 4 FDA reports)
MENINGIOMA ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
METASTASES TO GASTROINTESTINAL TRACT ( 4 FDA reports)
METASTASES TO OVARY ( 4 FDA reports)
METASTASES TO RETROPERITONEUM ( 4 FDA reports)
METASTASES TO SALIVARY GLAND ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
MOUTH CYST ( 4 FDA reports)
MULTIPLE GATED ACQUISITION SCAN ABNORMAL ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
MUSCLE ABSCESS ( 4 FDA reports)
MUSCLE CRAMP ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
MYELOCYTOSIS ( 4 FDA reports)
MYOPERICARDITIS ( 4 FDA reports)
NASAL CAVITY CANCER ( 4 FDA reports)
NEPHRITIS AUTOIMMUNE ( 4 FDA reports)
NEPHROGENIC ANAEMIA ( 4 FDA reports)
NERVE ROOT LESION ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
NEUROPATHIC PAIN ( 4 FDA reports)
NEUTROPENIA NEONATAL ( 4 FDA reports)
NIGHTMARE ( 4 FDA reports)
NIKOLSKY'S SIGN ( 4 FDA reports)
NOCARDIA SEPSIS ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 4 FDA reports)
OBSTRUCTION ( 4 FDA reports)
OCULAR ICTERUS ( 4 FDA reports)
OCULAR SURFACE DISEASE ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 4 FDA reports)
OSTEOCHONDRITIS ( 4 FDA reports)
OSTEOCHONDROSIS ( 4 FDA reports)
OSTEOMA CUTIS ( 4 FDA reports)
OSTEOMYELITIS ACUTE ( 4 FDA reports)
OSTEOPOROTIC FRACTURE ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PELVIC FRACTURE ( 4 FDA reports)
PELVIC MASS ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERITONEAL INFECTION ( 4 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 4 FDA reports)
PHAEHYPHOMYCOSIS ( 4 FDA reports)
PHALANGEAL AGENESIS ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
PNEUMONIA ESCHERICHIA ( 4 FDA reports)
PNEUMONIA MYCOPLASMAL ( 4 FDA reports)
POISONING ( 4 FDA reports)
POLYSEROSITIS ( 4 FDA reports)
POOR SUCKING REFLEX ( 4 FDA reports)
POSITIVE ROMBERGISM ( 4 FDA reports)
POST PROCEDURAL VOMITING ( 4 FDA reports)
POSTICTAL STATE ( 4 FDA reports)
POSTPARTUM DEPRESSION ( 4 FDA reports)
POTENTIATING DRUG INTERACTION ( 4 FDA reports)
PRESSURE OF SPEECH ( 4 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 4 FDA reports)
PROTEIN C DECREASED ( 4 FDA reports)
PROTEIN S DECREASED ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 4 FDA reports)
PSEUDOBULBAR PALSY ( 4 FDA reports)
PSOAS ABSCESS ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PYURIA ( 4 FDA reports)
RADIATION NECROSIS ( 4 FDA reports)
RADICULAR PAIN ( 4 FDA reports)
RADICULITIS BRACHIAL ( 4 FDA reports)
RECTAL PERFORATION ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 4 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 4 FDA reports)
RENAL ANEURYSM ( 4 FDA reports)
RENAL HYPERTROPHY ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 4 FDA reports)
RETINAL EXUDATES ( 4 FDA reports)
RHABDOMYOSARCOMA RECURRENT ( 4 FDA reports)
SALIVARY GLAND NEOPLASM ( 4 FDA reports)
SCLEREMA ( 4 FDA reports)
SCROTAL INFECTION ( 4 FDA reports)
SEXUAL DYSFUNCTION ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SINUSITIS BACTERIAL ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SPLEEN CONGESTION ( 4 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 4 FDA reports)
SPUTUM ABNORMAL ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA OF THE CERVIX ( 4 FDA reports)
STEATORRHOEA ( 4 FDA reports)
STRESS ULCER ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 4 FDA reports)
SYNOVITIS ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THREATENED LABOUR ( 4 FDA reports)
THROMBOTIC CEREBRAL INFARCTION ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TOOTH REPAIR ( 4 FDA reports)
TRANSFUSION ( 4 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 4 FDA reports)
TRICUSPID VALVE DISEASE ( 4 FDA reports)
TURNER'S SYNDROME ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
UTERINE DISORDER ( 4 FDA reports)
VACCINATION FAILURE ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VAGINAL DISORDER ( 4 FDA reports)
VAGINAL INFLAMMATION ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VASCULAR RUPTURE ( 4 FDA reports)
VASCULITIS GASTROINTESTINAL ( 4 FDA reports)
VASOSPASM ( 4 FDA reports)
VEIN DISORDER ( 4 FDA reports)
VENOUS STENOSIS ( 4 FDA reports)
VENTRICULAR FAILURE ( 4 FDA reports)
VITAMIN B12 INCREASED ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WHEELCHAIR USER ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 4 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 3 FDA reports)
PERIDIVERTICULAR ABSCESS ( 3 FDA reports)
PERITONSILLAR ABSCESS ( 3 FDA reports)
PERIVASCULAR DERMATITIS ( 3 FDA reports)
PERSISTENT GENERALISED LYMPHADENOPATHY ( 3 FDA reports)
PHALANGEAL HYPOPLASIA ( 3 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 3 FDA reports)
PHLEBOSCLEROSIS ( 3 FDA reports)
PHRENIC NERVE PARALYSIS ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
PLASTIC SURGERY ( 3 FDA reports)
PLATELET AGGREGATION ( 3 FDA reports)
PLATELET COUNT ( 3 FDA reports)
PLEURAL INFECTION BACTERIAL ( 3 FDA reports)
PLEURODESIS ( 3 FDA reports)
PLEUROPERICARDITIS ( 3 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 3 FDA reports)
POEMS SYNDROME ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
PORPHYRIA NON-ACUTE ( 3 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POST PROCEDURAL NAUSEA ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTMATURE BABY ( 3 FDA reports)
POSTPARTUM HAEMORRHAGE ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PRIMITIVE NEUROECTODERMAL TUMOUR ( 3 FDA reports)
PROSTATE CANCER STAGE IV ( 3 FDA reports)
PROSTHESIS IMPLANTATION ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY VASCULAR DISORDER ( 3 FDA reports)
PUNCTURE SITE INFECTION ( 3 FDA reports)
QRS AXIS ABNORMAL ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RECTAL ABSCESS ( 3 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
RED BLOOD CELLS URINE ( 3 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 3 FDA reports)
RENAL AGENESIS ( 3 FDA reports)
RENAL CELL CARCINOMA RECURRENT ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RENAL SALT-WASTING SYNDROME ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
RETCHING ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
RHABDOMYOMA ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RHEUMATOID VASCULITIS ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SALIVARY GLAND ADENOMA ( 3 FDA reports)
SALMONELLA SEPSIS ( 3 FDA reports)
SALMONELLA TEST POSITIVE ( 3 FDA reports)
SCLERODACTYLIA ( 3 FDA reports)
SCLERODERMA RENAL CRISIS ( 3 FDA reports)
SECONDARY SEXUAL CHARACTERISTICS ABSENCE ( 3 FDA reports)
SENSATION OF PRESSURE ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SERRATIA SEPSIS ( 3 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 3 FDA reports)
SKIN TURGOR DECREASED ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 3 FDA reports)
SMALL INTESTINAL STENOSIS ( 3 FDA reports)
SODIUM RETENTION ( 3 FDA reports)
SOMATOFORM DISORDER ( 3 FDA reports)
SPINAL HAEMATOMA ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPLENIC HAEMATOMA ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SUPERINFECTION BACTERIAL ( 3 FDA reports)
SWEAT GLAND DISORDER ( 3 FDA reports)
SYRINGOMYELIA ( 3 FDA reports)
T-CELL LYMPHOMA REFRACTORY ( 3 FDA reports)
TANGENTIALITY ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TERMINAL DRIBBLING ( 3 FDA reports)
THROMBECTOMY ( 3 FDA reports)
THYROXINE FREE INCREASED ( 3 FDA reports)
TONGUE OEDEMA ( 3 FDA reports)
TONGUE PARALYSIS ( 3 FDA reports)
TONSILLAR DISORDER ( 3 FDA reports)
TOOTH DEPOSIT ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TOOTH EROSION ( 3 FDA reports)
TOXIC OPTIC NEUROPATHY ( 3 FDA reports)
TOXIC SHOCK SYNDROME ( 3 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TRANSAMINASES ABNORMAL ( 3 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 3 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 3 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 3 FDA reports)
TRICHIASIS ( 3 FDA reports)
TUMOUR ULCERATION ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
URAEMIC ENCEPHALOPATHY ( 3 FDA reports)
UREAPLASMA INFECTION ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINARY SEDIMENT PRESENT ( 3 FDA reports)
URINARY TRACT PAIN ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 3 FDA reports)
UROGENITAL HAEMORRHAGE ( 3 FDA reports)
URTICARIA GENERALISED ( 3 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 3 FDA reports)
VAGINAL CANCER ( 3 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 3 FDA reports)
VEIN PAIN ( 3 FDA reports)
VENOUS HAEMORRHAGE ( 3 FDA reports)
VENTRICULAR DYSKINESIA ( 3 FDA reports)
VENTRICULO-PERITONEAL SHUNT ( 3 FDA reports)
VIIITH NERVE LESION ( 3 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 3 FDA reports)
VOCAL CORD PARESIS ( 3 FDA reports)
VULVAR EROSION ( 3 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WOUND ABSCESS ( 3 FDA reports)
WOUND NECROSIS ( 3 FDA reports)
XANTHOGRANULOMA ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 3 FDA reports)
ABSCESS DRAINAGE ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACALCULIA ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 3 FDA reports)
ADENOVIRUS TEST POSITIVE ( 3 FDA reports)
ADMINISTRATION SITE PAIN ( 3 FDA reports)
ADRENAL DISORDER ( 3 FDA reports)
ADRENAL NEOPLASM ( 3 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA RECURRENT ( 3 FDA reports)
ALANINE AMINOTRANSFERASE ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 3 FDA reports)
ANAL SPHINCTER ATONY ( 3 FDA reports)
ANAPLASTIC THYROID CANCER ( 3 FDA reports)
ANDROGENETIC ALOPECIA ( 3 FDA reports)
ANGIOSCLEROSIS ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ANOTIA ( 3 FDA reports)
ANTI-THYROID ANTIBODY ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
AORTIC ATHEROSCLEROSIS ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
ARTERIAL STENOSIS ( 3 FDA reports)
ARTERITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 3 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 3 FDA reports)
ATROPHIC VULVOVAGINITIS ( 3 FDA reports)
AURA ( 3 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
BACILLUS TEST POSITIVE ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BACTERIAL DISEASE CARRIER ( 3 FDA reports)
BACTERIAL PERICARDITIS ( 3 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
BARTHOLIN'S ABSCESS ( 3 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 3 FDA reports)
BASEDOW'S DISEASE ( 3 FDA reports)
BENIGN COLONIC NEOPLASM ( 3 FDA reports)
BILE DUCT STENT INSERTION ( 3 FDA reports)
BILIARY COLIC ( 3 FDA reports)
BILIARY TRACT DILATION PROCEDURE ( 3 FDA reports)
BIOPSY LUNG ABNORMAL ( 3 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 3 FDA reports)
BLADDER HYPERTROPHY ( 3 FDA reports)
BLAST CELL PROLIFERATION ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BLOOD HIV RNA INCREASED ( 3 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD STEM CELL HARVEST ( 3 FDA reports)
BLOOD TRIGLYCERIDES ( 3 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 3 FDA reports)
BRADYKINESIA ( 3 FDA reports)
BRAIN MIDLINE SHIFT ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
BRONCHIAL HAEMORRHAGE ( 3 FDA reports)
BRUCELLOSIS ( 3 FDA reports)
BULLOUS LUNG DISEASE ( 3 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 3 FDA reports)
CALCIUM IONISED DECREASED ( 3 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CARDIAC FAILURE CHRONIC ( 3 FDA reports)
CARDIAC INFECTION ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CAROTID ARTERY ATHEROMA ( 3 FDA reports)
CAROTID BRUIT ( 3 FDA reports)
CAST REMOVAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBRAL HYGROMA ( 3 FDA reports)
CERUMEN REMOVAL ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
CHEST WALL MASS ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 3 FDA reports)
CHRONIC TONSILLITIS ( 3 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 3 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 3 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 3 FDA reports)
COAGULATION TEST ABNORMAL ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLON GANGRENE ( 3 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 3 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONJUNCTIVAL OEDEMA ( 3 FDA reports)
CONNECTIVE TISSUE DISORDER ( 3 FDA reports)
CONTRAST MEDIA REACTION ( 3 FDA reports)
COXSACKIE VIRAL INFECTION ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CSF CELL COUNT ABNORMAL ( 3 FDA reports)
CSF GLUCOSE ABNORMAL ( 3 FDA reports)
CSF MYELIN BASIC PROTEIN INCREASED ( 3 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CSF VIRUS IDENTIFIED ( 3 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 3 FDA reports)
CYTOMEGALOVIRUS MYELOMENINGORADICULITIS ( 3 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 3 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 3 FDA reports)
DISTRACTIBILITY ( 3 FDA reports)
DRUG EFFECT DELAYED ( 3 FDA reports)
DRUG HALF-LIFE INCREASED ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DUODENAL POLYP ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
EAR INFECTION BACTERIAL ( 3 FDA reports)
ECCENTRIC FIXATION ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 3 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 3 FDA reports)
ENDOCERVICAL CURETTAGE ( 3 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 3 FDA reports)
EPIPHYSIOLYSIS ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 3 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
EYELID VASCULAR DISORDER ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III RECURRENT ( 3 FDA reports)
FRACTURED SACRUM ( 3 FDA reports)
FROSTBITE ( 3 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 3 FDA reports)
GASTRIC ATONY ( 3 FDA reports)
GASTRIC CANCER STAGE IV ( 3 FDA reports)
GASTRIC DILATATION ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 3 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GINGIVAL ABSCESS ( 3 FDA reports)
GLIAL SCAR ( 3 FDA reports)
GLYCOGEN STORAGE DISORDER ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
GRAVITATIONAL OEDEMA ( 3 FDA reports)
HAEMATOCRIT ABNORMAL ( 3 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAEMORRHAGIC DISORDER ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HANTAVIRUS PULMONARY INFECTION ( 3 FDA reports)
HBV DNA INCREASED ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEPATIC AMOEBIASIS ( 3 FDA reports)
HEPATIC CANDIDIASIS ( 3 FDA reports)
HEPATIC SIDEROSIS ( 3 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 3 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 3 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 3 FDA reports)
HEPATITIS INFECTIOUS ( 3 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 3 FDA reports)
HIV TEST POSITIVE ( 3 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 3 FDA reports)
HUMORAL IMMUNE DEFECT ( 3 FDA reports)
HUNGRY BONE SYNDROME ( 3 FDA reports)
HYPERACUSIS ( 3 FDA reports)
HYPERAMYLASAEMIA ( 3 FDA reports)
HYPERCHLORAEMIA ( 3 FDA reports)
HYPERTROPHIC SCAR ( 3 FDA reports)
HYPOMETABOLISM ( 3 FDA reports)
IGA NEPHROPATHY ( 3 FDA reports)
IMMOBILE ( 3 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 3 FDA reports)
IMMUNODEFICIENCY CONGENITAL ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INCORRECT STORAGE OF DRUG ( 3 FDA reports)
INFECTION REACTIVATION ( 3 FDA reports)
INFERTILITY MALE ( 3 FDA reports)
INFESTATION ( 3 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 3 FDA reports)
INFUSION SITE PAIN ( 3 FDA reports)
INFUSION SITE REACTION ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE INFECTION ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
JAUNDICE HEPATOCELLULAR ( 3 FDA reports)
JOINT DESTRUCTION ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
KIDNEY SMALL ( 3 FDA reports)
KRABBE'S DISEASE ( 3 FDA reports)
LABOUR INDUCTION ( 3 FDA reports)
LARYNGOSCOPY ( 3 FDA reports)
LEARNING DISORDER ( 3 FDA reports)
LEGIONELLA INFECTION ( 3 FDA reports)
LEGIONELLA SEROLOGY POSITIVE ( 3 FDA reports)
LEGIONELLA TEST POSITIVE ( 3 FDA reports)
LEIOMYOMA ( 3 FDA reports)
LEUKAEMIC INFILTRATION GINGIVA ( 3 FDA reports)
LEUKOCYTURIA ( 3 FDA reports)
LHERMITTE'S SIGN ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIP HAEMORRHAGE ( 3 FDA reports)
LIPOHYPERTROPHY ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LONG QT SYNDROME ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
LYMPHOHISTIOCYTOSIS ( 3 FDA reports)
MALIGNANT TRANSFORMATION ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 3 FDA reports)
MEDIASTINAL DISORDER ( 3 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 3 FDA reports)
MEDICAL DEVICE REMOVAL ( 3 FDA reports)
MENINGITIS HERPES ( 3 FDA reports)
MENINGITIS TOXOPLASMAL ( 3 FDA reports)
MENINGOENCEPHALITIS ADENOVIRAL ( 3 FDA reports)
MENINGORRHAGIA ( 3 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 3 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 3 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METAL POISONING ( 3 FDA reports)
METAMYELOCYTE COUNT INCREASED ( 3 FDA reports)
METASTASES TO EYE ( 3 FDA reports)
METASTATIC GASTRIC CANCER ( 3 FDA reports)
METHAEMOGLOBINAEMIA ( 3 FDA reports)
METHYLOBACTERIUM INFECTION ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MORPHOEA ( 3 FDA reports)
MOUTH INJURY ( 3 FDA reports)
MOYAMOYA DISEASE ( 3 FDA reports)
MUCOSAL EXFOLIATION ( 3 FDA reports)
MULTIMORBIDITY ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MYCOPLASMA INFECTION ( 3 FDA reports)
MYCOTIC ANEURYSM ( 3 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 3 FDA reports)
NEONATAL CHOLESTASIS ( 3 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NEUROENDOCRINE CARCINOMA ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 3 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 3 FDA reports)
NODAL ARRHYTHMIA ( 3 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OESOPHAGEAL INFECTION ( 3 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 3 FDA reports)
OESOPHAGOBRONCHIAL FISTULA ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPTIC NERVE INFARCTION ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
ORAL SUBMUCOSAL FIBROSIS ( 3 FDA reports)
ORCHIDECTOMY ( 3 FDA reports)
OROPHARYNGEAL BLISTERING ( 3 FDA reports)
OSTEOMALACIA ( 3 FDA reports)
OSTEOMYELITIS BACTERIAL ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PARANEOPLASTIC DERMATOMYOSITIS ( 3 FDA reports)
PARENTERAL NUTRITION ( 3 FDA reports)
PAROTIDECTOMY ( 3 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ABSCESS SOFT TISSUE ( 2 FDA reports)
ACANTHOSIS ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 2 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 2 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 2 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 2 FDA reports)
ADENOTONSILLECTOMY ( 2 FDA reports)
ADENOVIRAL UPPER RESPIRATORY INFECTION ( 2 FDA reports)
ADIPOSIS DOLOROSA ( 2 FDA reports)
AESTHESIONEUROBLASTOMA ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
AIDS DEMENTIA COMPLEX ( 2 FDA reports)
AKINESIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALEXIA ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLERGIC RESPIRATORY SYMPTOM ( 2 FDA reports)
ALLOIMMUNISATION ( 2 FDA reports)
ALOPECIA AREATA ( 2 FDA reports)
ALVEOLITIS FIBROSING ( 2 FDA reports)
AMINO ACID LEVEL INCREASED ( 2 FDA reports)
AMINOACIDURIA ( 2 FDA reports)
AMOEBIASIS ( 2 FDA reports)
AMPUTATION ( 2 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 2 FDA reports)
ANAL ATRESIA ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGIODYSPLASIA ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 2 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-GAD ANTIBODY ( 2 FDA reports)
ANTIBODY TEST ABNORMAL ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
APPENDICEAL MUCOCOELE ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPLICATION SITE CELLULITIS ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARTERIAL INJURY ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
ASTRINGENT THERAPY ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BABESIOSIS ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BACTERIAL PYELONEPHRITIS ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIARY ISCHAEMIA ( 2 FDA reports)
BILIARY SPHINCTEROTOMY ( 2 FDA reports)
BLADDER FIBROSIS ( 2 FDA reports)
BLADDER IRRITATION ( 2 FDA reports)
BLADDER PERFORATION ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD AMYLASE ABNORMAL ( 2 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN ( 2 FDA reports)
BLOOD CHROMIUM DECREASED ( 2 FDA reports)
BLOOD CHROMIUM INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN NEGATIVE ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 2 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 2 FDA reports)
BLOOD THROMBIN INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BODY FAT DISORDER ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE FRAGMENTATION ( 2 FDA reports)
BONE INFECTION ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN CANCER METASTATIC ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN MALFORMATION ( 2 FDA reports)
BREAST FIBROSIS ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREATH SOUNDS ABSENT ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRUXISM ( 2 FDA reports)
BULBAR PALSY ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURNING MOUTH SYNDROME ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 2 FDA reports)
CANCER IN REMISSION ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CATATONIA ( 2 FDA reports)
CATHETER PLACEMENT ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLULITIS STREPTOCOCCAL ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL CYST ( 2 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 2 FDA reports)
CEREBROVASCULAR SPASM ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEMICAL EYE INJURY ( 2 FDA reports)
CHEYNE-STOKES RESPIRATION ( 2 FDA reports)
CHLAMYDIAL INFECTION ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLESTATIC LIVER INJURY ( 2 FDA reports)
CHOLESTEATOMA ( 2 FDA reports)
CHONDROCALCINOSIS ( 2 FDA reports)
CHORIOCARCINOMA ( 2 FDA reports)
CHORIORETINAL DISORDER ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
CLUBBING ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLD AGGLUTININS POSITIVE ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 2 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONGENITAL AORTIC ANOMALY ( 2 FDA reports)
CONGENITAL CEREBRAL CYST ( 2 FDA reports)
CONGENITAL NAIL DISORDER ( 2 FDA reports)
CONGENITAL RENAL DISORDER ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL OPACITY CONGENITAL ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORYNEBACTERIUM SEPSIS ( 2 FDA reports)
CRACKLES LUNG ( 2 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 2 FDA reports)
CROSSMATCH INCOMPATIBLE ( 2 FDA reports)
CSF GLUCOSE INCREASED ( 2 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
CSF MONOCYTE COUNT POSITIVE ( 2 FDA reports)
CSF PROTEIN ABNORMAL ( 2 FDA reports)
CULTURE THROAT POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS URINARY TRACT INFECTION ( 2 FDA reports)
CYTOTOXIC OEDEMA ( 2 FDA reports)
DACTYLITIS ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELAYED SLEEP PHASE ( 2 FDA reports)
DENTAL FISTULA ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS DIAPER ( 2 FDA reports)
DEVICE INEFFECTIVE ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DIFFUSE AXONAL INJURY ( 2 FDA reports)
DIFFUSE VASCULITIS ( 2 FDA reports)
DISTRIBUTIVE SHOCK ( 2 FDA reports)
DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG-INDUCED LIVER INJURY ( 2 FDA reports)
DUCHENNE MUSCULAR DYSTROPHY ( 2 FDA reports)
DWARFISM ( 2 FDA reports)
DYSPONESIS ( 2 FDA reports)
DYSTHYMIC DISORDER ( 2 FDA reports)
DYSTROPHIC CALCIFICATION ( 2 FDA reports)
EAR CONGESTION ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ENCEPHALITIS PROTOZOAL ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
ENTEROVIRUS TEST POSITIVE ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EOSINOPHILIC CELLULITIS ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOMA ( 2 FDA reports)
EPSTEIN-BARR VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
EROSIVE BALANITIS ( 2 FDA reports)
ERYTHROBLAST COUNT DECREASED ( 2 FDA reports)
EWING'S SARCOMA METASTATIC ( 2 FDA reports)
EXCHANGE BLOOD TRANSFUSION ( 2 FDA reports)
EXPLORATIVE LAPAROTOMY ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) RECURRENT ( 2 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
EYE INFECTION FUNGAL ( 2 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
EYE INFECTION TOXOPLASMAL ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
FACTOR VII DEFICIENCY ( 2 FDA reports)
FAECALURIA ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FALLOT'S TETRALOGY ( 2 FDA reports)
FAT NECROSIS ( 2 FDA reports)
FIBRILLARY GLOMERULONEPHRITIS ( 2 FDA reports)
FINGER HYPOPLASIA ( 2 FDA reports)
FISTULA DISCHARGE ( 2 FDA reports)
FIXED ERUPTION ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETAL HEART RATE DISORDER ( 2 FDA reports)
FOETAL HYPOKINESIA ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 2 FDA reports)
FORMICATION ( 2 FDA reports)
FRUSTRATION ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
GALLBLADDER CANCER ( 2 FDA reports)
GAMMOPATHY ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC ILEUS ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROENTERITIS RADIATION ( 2 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 2 FDA reports)
GASTROINTESTINAL ENDOSCOPIC THERAPY ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GENITAL HAEMORRHAGE ( 2 FDA reports)
GENITAL INFECTION FUNGAL ( 2 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 2 FDA reports)
GERM CELL CANCER ( 2 FDA reports)
GERSTMANN'S SYNDROME ( 2 FDA reports)
GINGIVAL CANCER ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVAL OPERATION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOBULINS INCREASED ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GLUCOCORTICOID DEFICIENCY ( 2 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 2 FDA reports)
GOODPASTURE'S SYNDROME ( 2 FDA reports)
GRAM STAIN POSITIVE ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GROIN ABSCESS ( 2 FDA reports)
HAEMANGIOMA CONGENITAL ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HELICOBACTER GASTRITIS ( 2 FDA reports)
HEPATIC HAEMATOMA ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC MASS ( 2 FDA reports)
HEPATIC RUPTURE ( 2 FDA reports)
HEPATIC TRAUMA ( 2 FDA reports)
HEPATITIS A ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HEPATOBLASTOMA ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HERNIAL EVENTRATION ( 2 FDA reports)
HERPES OPHTHALMIC ( 2 FDA reports)
HERPETIC STOMATITIS ( 2 FDA reports)
HIGH ARCHED PALATE ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HIGH GRADE B-CELL LYMPHOMA BURKITT-LIKE LYMPHOMA ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 2 FDA reports)
HUMAN RHINOVIRUS TEST POSITIVE ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPERALBUMINAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERTRICHOSIS ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOGONADISM FEMALE ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOSPADIAS ( 2 FDA reports)
HYPOTELORISM OF ORBIT ( 2 FDA reports)
ICHTHYOSIS ( 2 FDA reports)
ILEAL FISTULA ( 2 FDA reports)
IMMUNOTACTOID GLOMERULONEPHRITIS ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
IMPAIRED INSULIN SECRETION ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
IMPLANT SITE EXTRAVASATION ( 2 FDA reports)
INFECTED CYST ( 2 FDA reports)
INFECTION MASKED ( 2 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 2 FDA reports)
INFECTIVE THROMBOSIS ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY PSEUDOTUMOUR ( 2 FDA reports)
INFUSION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE BRUISING ( 2 FDA reports)
INJECTION SITE INFLAMMATION ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE OEDEMA ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN RESISTANT DIABETES ( 2 FDA reports)
INSULIN-LIKE GROWTH FACTOR DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISCITIS ( 2 FDA reports)
INTESTINAL ANASTOMOSIS ( 2 FDA reports)
INTESTINAL HYPOMOTILITY ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IVTH NERVE PARESIS ( 2 FDA reports)
JEJUNAL PERFORATION ( 2 FDA reports)
JEJUNAL STENOSIS ( 2 FDA reports)
JOINT HYPEREXTENSION ( 2 FDA reports)
KAPOSI'S VARICELLIFORM ERUPTION ( 2 FDA reports)
KAWASAKI'S DISEASE ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
LANGERHANS' CELL HISTIOCYTOSIS ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL NEOPLASM ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LEIOMYOSARCOMA RECURRENT ( 2 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 2 FDA reports)
LEUKOPENIA NEONATAL ( 2 FDA reports)
LEUKOPLAKIA ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LIGHT CHAIN DISEASE ( 2 FDA reports)
LIPIDOSIS ( 2 FDA reports)
LIVIDITY ( 2 FDA reports)
LOCAL ANAESTHESIA ( 2 FDA reports)
LOW SET EARS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUDWIG ANGINA ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG CYST ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LYME DISEASE ( 2 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 2 FDA reports)
LYMPHOMA AIDS RELATED ( 2 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 2 FDA reports)
LYMPHOSTASIS ( 2 FDA reports)
MACULE ( 2 FDA reports)
MALIGNANT LYMPHOMA UNCLASSIFIABLE HIGH GRADE ( 2 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MALIGNANT TUMOUR EXCISION ( 2 FDA reports)
MANTLE CELL LYMPHOMA REFRACTORY ( 2 FDA reports)
MAXILLOFACIAL OPERATION ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 2 FDA reports)
MEDIASTINAL ABSCESS ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 2 FDA reports)
MENINGIOMA MALIGNANT ( 2 FDA reports)
MENINGOCOCCAL BACTERAEMIA ( 2 FDA reports)
MENINGOENCEPHALITIS AMOEBIC ( 2 FDA reports)
METASTASES TO LARGE INTESTINE ( 2 FDA reports)
METASTASES TO NECK ( 2 FDA reports)
METASTASES TO OESOPHAGUS ( 2 FDA reports)
METASTASES TO PELVIS ( 2 FDA reports)
METASTASES TO SOFT TISSUE ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
METASTASES TO THORAX ( 2 FDA reports)
METASTASES TO TRACHEA ( 2 FDA reports)
METASTASES TO UTERUS ( 2 FDA reports)
MICROCOCCUS INFECTION ( 2 FDA reports)
MIGRAINE WITH AURA ( 2 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MITRAL VALVE CALCIFICATION ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUCOSAL NECROSIS ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MYCETOMA MYCOTIC ( 2 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 2 FDA reports)
MYCOSIS FUNGOIDES RECURRENT ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NAIL INFECTION ( 2 FDA reports)
NAIL PIGMENTATION ( 2 FDA reports)
NASAL CAVITY PACKING ( 2 FDA reports)
NASAL FLARING ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NASAL SEPTUM DEVIATION ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NECROTISING FASCIITIS STAPHYLOCOCCAL ( 2 FDA reports)
NEONATAL APNOEIC ATTACK ( 2 FDA reports)
NEONATAL TACHYPNOEA ( 2 FDA reports)
NEURILEMMOMA ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NEUROMYELITIS OPTICA ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUTRALISING ANTIBODIES POSITIVE ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NOCARDIA TEST POSITIVE ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
OBSTRUCTIVE UROPATHY ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OCCUPATIONAL EXPOSURE TO TOXIC AGENT ( 2 FDA reports)
OCULAR NEOPLASM ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OESOPHAGITIS ULCERATIVE ( 2 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 2 FDA reports)
OESTRADIOL INCREASED ( 2 FDA reports)
OLFACTORY NERVE DISORDER ( 2 FDA reports)
ORAL DISCHARGE ( 2 FDA reports)
ORAL DYSAESTHESIA ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
ORAL TORUS ( 2 FDA reports)
ORO-PHARYNGEAL ASPERGILLOSIS ( 2 FDA reports)
OROANTRAL FISTULA ( 2 FDA reports)
OROPHARYNGEAL PLAQUE ( 2 FDA reports)
OROPHARYNGEAL SWELLING ( 2 FDA reports)
ORTHOSTATIC TREMOR ( 2 FDA reports)
OSSICLE DISORDER ( 2 FDA reports)
OSTEOSARCOMA METASTATIC ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PAGET-SCHROETTER SYNDROME ( 2 FDA reports)
PALATAL OEDEMA ( 2 FDA reports)
PALATITIS ( 2 FDA reports)
PANCREAS INFECTION ( 2 FDA reports)
PANCREATIC CYST ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATIC NECROSIS ( 2 FDA reports)
PANCREATIC NEOPLASM ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PANNICULITIS LOBULAR ( 2 FDA reports)
PAPILLITIS ( 2 FDA reports)
PARACENTESIS ABDOMEN ( 2 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 2 FDA reports)
PARESIS CRANIAL NERVE ( 2 FDA reports)
PAROTID GLAND INFLAMMATION ( 2 FDA reports)
PEAU D'ORANGE ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PENILE PAIN ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERICARDIAL FIBROSIS ( 2 FDA reports)
PERINEAL ABSCESS ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 2 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED RECURRENT ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED STAGE IV ( 2 FDA reports)
PERIPORTAL OEDEMA ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PERITONEAL TUBERCULOSIS ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNX DISCOMFORT ( 2 FDA reports)
PHLEBITIS DEEP ( 2 FDA reports)
PHOTOPHERESIS ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLASMA CELLS INCREASED ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLASMINOGEN DECREASED ( 2 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEOCYTOSIS ( 2 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PORPHYRIA ( 2 FDA reports)
PORTAL VEIN FLOW DECREASED ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
PRECURSOR B-LYMPHOBLASTIC LYMPHOMA ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROCTOSTOMY ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PROMYELOCYTE COUNT INCREASED ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PROTRUSION TONGUE ( 2 FDA reports)
PSITTACOSIS ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
PUBIS FRACTURE ( 2 FDA reports)
PULMONARY ALVEOLAR MICROLITHIASIS ( 2 FDA reports)
PULMONARY ARTERY DILATATION ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
PYOMYOSITIS ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
REFRACTION DISORDER ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL HAEMATOMA ( 2 FDA reports)
RENAL ISCHAEMIA ( 2 FDA reports)
RENAL LIPOMATOSIS ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY DEPTH DECREASED ( 2 FDA reports)
RESPIRATORY PARALYSIS ( 2 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RESPIRATORY TRACT OEDEMA ( 2 FDA reports)
RETICULOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
RETROPERITONEAL MASS ( 2 FDA reports)
RETROPERITONEAL NEOPLASM ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 2 FDA reports)
SARCOMA UTERUS ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SECONDARY HYPERTENSION ( 2 FDA reports)
SECONDARY HYPOTHYROIDISM ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 2 FDA reports)
SHOULDER OPERATION ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SHUNT MALFUNCTION ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SIGNET-RING CELL CARCINOMA ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN SENSITISATION ( 2 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
SOFT TISSUE INFLAMMATION ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 2 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL CORD HAEMORRHAGE ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL SHOCK ( 2 FDA reports)
SPLENIC NECROSIS ( 2 FDA reports)
SPOROTRICHOSIS ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STAPHYLOMA ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STOMATITIS RADIATION ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE NEONATAL ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE II ( 2 FDA reports)
SUTURE INSERTION ( 2 FDA reports)
T-CELL LYMPHOMA STAGE III ( 2 FDA reports)
TABLET PHYSICAL ISSUE ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
TEMPORAL LOBE EPILEPSY ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SURGERY ( 2 FDA reports)
TERATOGENICITY ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TESTICULAR FAILURE ( 2 FDA reports)
TESTICULAR NEOPLASM ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 2 FDA reports)
THERAPY RESPONDER ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
TONGUE CARCINOMA STAGE I ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONSILLAR ULCER ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TORUS FRACTURE ( 2 FDA reports)
TRACHEAL DEVIATION ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
TRICHOSTASIS SPINULOSA ( 2 FDA reports)
TRICHOTILLOMANIA ( 2 FDA reports)
TRISOMY 8 ( 2 FDA reports)
TUBERCULIN TEST POSITIVE ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 2 FDA reports)
UPPER MOTOR NEURONE LESION ( 2 FDA reports)
URETERITIS ( 2 FDA reports)
URETHRAL PAIN ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY BLADDER ATROPHY ( 2 FDA reports)
URINARY BLADDER SARCOMA ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URINE OSMOLARITY DECREASED ( 2 FDA reports)
URINE OUTPUT INCREASED ( 2 FDA reports)
URINE PHOSPHORUS INCREASED ( 2 FDA reports)
URINE POTASSIUM INCREASED ( 2 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
VAGINAL ABSCESS ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR INSUFFICIENCY ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VENA CAVA FILTER INSERTION ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENOUS PRESSURE INCREASED ( 2 FDA reports)
VENTOUSE EXTRACTION ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VERTEBRAL COLUMN MASS ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VIRAL HEPATITIS CARRIER ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VIRAL TITRE DECREASED ( 2 FDA reports)
VIRAL VASCULITIS ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
VISUAL PATHWAY DISORDER ( 2 FDA reports)
VITAMIN A INCREASED ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN D INCREASED ( 2 FDA reports)
VITH NERVE DISORDER ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
VULVITIS ( 2 FDA reports)
VULVOVAGINAL ADHESION ( 2 FDA reports)
WEIGHT DECREASE NEONATAL ( 2 FDA reports)
WOUND INFECTION BACTERIAL ( 2 FDA reports)
WOUND INFECTION FUNGAL ( 2 FDA reports)
WOUND TREATMENT ( 2 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PCO2 ABNORMAL ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PENICILLIOSIS ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDITIS FUNGAL ( 1 FDA reports)
PERIHEPATIC ABSCESS ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL EFFLUENT LEUKOCYTE COUNT INCREASED ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PERONEAL MUSCULAR ATROPHY ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHAGOCYTOSIS ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHLEBITIS INFECTIVE ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PILONIDAL CYST ( 1 FDA reports)
PLASMIN INHIBITOR DECREASED ( 1 FDA reports)
PLATELET AGGREGATION INHIBITION ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLATELET TOXICITY ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL CALCIFICATION ( 1 FDA reports)
PLEURAL RUB ( 1 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA LIPOID ( 1 FDA reports)
PNEUMONIA TOXOPLASMAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTERITIS NODOSA ( 1 FDA reports)
POLYMERASE CHAIN REACTION ( 1 FDA reports)
POLYNEUROPATHY TOXIC ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ABSCESS ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PRECIPITATE LABOUR ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST FALSE POSITIVE ( 1 FDA reports)
PREPYLORIC STENOSIS ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRIMARY AMYLOIDOSIS ( 1 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROCALCITONIN ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTITIS ULCERATIVE ( 1 FDA reports)
PRODUCT CLOSURE ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PROGRESSIVE RELAPSING MULTIPLE SCLEROSIS ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROLONGED PREGNANCY ( 1 FDA reports)
PROLYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROTEIN C DEFICIENCY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOXANTHOMA ELASTICUM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PUBERTY ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERY ANEURYSM ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY SARCOIDOSIS ( 1 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
PUNCTATE BASOPHILIA ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE DISCHARGE ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYOMETRA ( 1 FDA reports)
RADIAL NERVE LESION ( 1 FDA reports)
RADIATION PERICARDITIS ( 1 FDA reports)
RADIATION RETINOPATHY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
RECTAL STENOSIS ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION PRESENT ( 1 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL NUCLEATED MORPHOLOGY PRESENT ( 1 FDA reports)
RED BLOOD CELL POIKILOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFLUX GASTRITIS ( 1 FDA reports)
REFRACTORY ANAEMIA WITH EXCESS BLASTS IN TRANSFORMATION ( 1 FDA reports)
REFRACTORY CANCER ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENOVASCULAR HYPERTENSION ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESECTION OF RECTUM ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY RATE ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 1 FDA reports)
RETICULIN INCREASED ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINITIS VIRAL ( 1 FDA reports)
RETINOBLASTOMA UNILATERAL ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
REVERSIBLE AIRWAYS OBSTRUCTION ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIGHT AORTIC ARCH ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
RUPTURED ECTOPIC PREGNANCY ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SALIVARY GLAND CANCER RECURRENT ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALIVARY GLAND PAIN ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHAMBERG'S DISEASE ( 1 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLEROEDEMA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL ERYTHEMA ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEBACEOUS CARCINOMA ( 1 FDA reports)
SECONDARY HYPERTHYROIDISM ( 1 FDA reports)
SEIZURE LIKE PHENOMENA ( 1 FDA reports)
SEMEN ABNORMAL ( 1 FDA reports)
SEPSIS PASTEURELLA ( 1 FDA reports)
SEPTAL PANNICULITIS ( 1 FDA reports)
SEZARY CELLS INCREASED ( 1 FDA reports)
SHORTENED CERVIX ( 1 FDA reports)
SHRINKING LUNG SYNDROME ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SIALOADENITIS ( 1 FDA reports)
SICKLE CELL ANAEMIA ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SINUS PAIN ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN FLAP NECROSIS ( 1 FDA reports)
SKIN GRAFT REJECTION ( 1 FDA reports)
SKIN HYPOPLASIA ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMALL INTESTINAL RESECTION ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SOLITARY KIDNEY SECONDARY ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
SPHEROCYTIC ANAEMIA ( 1 FDA reports)
SPHINGOMONAS PAUCIMOBILIS INFECTION ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPINAL CORD HERNIATION ( 1 FDA reports)
SPINAL CORD INFECTION ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL HAEMANGIOMA ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINAL VASCULAR DISORDER ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
SPINE MALFORMATION ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLENIC ARTERY ANEURYSM ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC GRANULOMA ( 1 FDA reports)
SPLENIC INFECTION FUNGAL ( 1 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STIFF-MAN SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMACH MASS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBACUTE ENDOCARDITIS ( 1 FDA reports)
SUBACUTE SCLEROSING PANENCEPHALITIS ( 1 FDA reports)
SUBDURAL EMPYEMA ( 1 FDA reports)
SUBDURAL HAEMATOMA EVACUATION ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPERINFECTION FUNGAL ( 1 FDA reports)
SUPERINFECTION LUNG ( 1 FDA reports)
SUPPORTIVE CARE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
SYSTEMIC SCLEROSIS PULMONARY ( 1 FDA reports)
T-CELL CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
T-LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
TABLET ISSUE ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TENSION ( 1 FDA reports)
TESTICULAR FAILURE PRIMARY ( 1 FDA reports)
TESTICULAR MASS ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY REGIMEN CHANGED ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
THYMUS DISORDER ( 1 FDA reports)
THYMUS HYPERTROPHY ( 1 FDA reports)
THYROXINE FREE DECREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TOOTH DECALCIFICATION ( 1 FDA reports)
TOOTH MALFORMATION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TORULOPSIS INFECTION ( 1 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRACE ELEMENT DEFICIENCY ( 1 FDA reports)
TRACHEAL INFLAMMATION ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSFUSION WITH INCOMPATIBLE BLOOD ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TRICUSPID VALVE CALCIFICATION ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TRUNCUS ARTERIOSUS PERSISTENT ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR COMPRESSION ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
TUMOUR PAIN ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
ULTRASOUND BLADDER ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
UMBILICAL HERNIA REPAIR ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNRELATED DONOR BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERAL NEOPLASM ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL CYST ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL POLYP ( 1 FDA reports)
URINARY CASTS ( 1 FDA reports)
URINARY TRACT INFECTION NEONATAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE NEOPLASM ( 1 FDA reports)
UTERINE PERFORATION ( 1 FDA reports)
UV LIGHT THERAPY ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL EXFOLIATION ( 1 FDA reports)
VAGINAL MYCOSIS ( 1 FDA reports)
VAGINAL STRICTURE ( 1 FDA reports)
VARICELLA POST VACCINE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VEIN DISCOLOURATION ( 1 FDA reports)
VENA CAVA EMBOLISM ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VIBRATORY SENSE INCREASED ( 1 FDA reports)
VIRAL UVEITIS ( 1 FDA reports)
VIRILISM ( 1 FDA reports)
VIROLOGIC FAILURE ( 1 FDA reports)
VIRUS BODY FLUID IDENTIFIED ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VITAL CAPACITY ABNORMAL ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOLUME BLOOD INCREASED ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOLVULUS OF SMALL BOWEL ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVAL ABSCESS ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVAR DYSPLASIA ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA RECURRENT ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHIPPLE'S DISEASE ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL ( 1 FDA reports)
WHITE BLOOD CELLS STOOL POSITIVE ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)
XANTHOMATOSIS ( 1 FDA reports)
YAWNING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABORTED PREGNANCY ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION SPONTANEOUS INCOMPLETE ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACHROMOTRICHIA ACQUIRED ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACOUSTIC NEUROMA ( 1 FDA reports)
ACQUIRED NIGHT BLINDNESS ( 1 FDA reports)
ACQUIRED PROTEIN S DEFICIENCY ( 1 FDA reports)
ACRODERMATITIS ( 1 FDA reports)
ACRODYNIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE ENDOCARDITIS ( 1 FDA reports)
ACUTE HAEMORRHAGIC CONJUNCTIVITIS ( 1 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 1 FDA reports)
ADENOIDAL HYPERTROPHY ( 1 FDA reports)
ADENOMA BENIGN ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
ADRENAL HAEMORRHAGE ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ADRENOLEUKODYSTROPHY ( 1 FDA reports)
AGITATED DEPRESSION ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO ABNORMAL ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALDOLASE INCREASED ( 1 FDA reports)
ALEUKAEMIC LEUKAEMIA ( 1 FDA reports)
ALLERGIC RESPIRATORY DISEASE ( 1 FDA reports)
ALLERGY TO METALS ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALVEOLAR SOFT PART SARCOMA METASTATIC ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMNIOTIC FLUID VOLUME INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANDROGENS ABNORMAL ( 1 FDA reports)
ANGIOFIBROMA ( 1 FDA reports)
ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANISEIKONIA ( 1 FDA reports)
ANKLE OPERATION ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANOMALY OF ORBIT, CONGENITAL ( 1 FDA reports)
ANOPHTHALMOS ( 1 FDA reports)
ANORECTAL CELLULITIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTHRAX ( 1 FDA reports)
ANTI-GAD ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 1 FDA reports)
ANTISYNTHETASE SYNDROME ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC INJURY ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APHERESIS ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL THERAPEUTIC PROCEDURE ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERITIS INFECTIVE ( 1 FDA reports)
ARTERITIS OBLITERANS ( 1 FDA reports)
ARTHRITIS FUNGAL ( 1 FDA reports)
ARTHRITIS SALMONELLA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPERGILLUS TEST ( 1 FDA reports)
ASPIRATION JOINT ABNORMAL ( 1 FDA reports)
ASPIRATION TRACHEAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ASTROCYTOMA ( 1 FDA reports)
ATAXIA TELANGIECTASIA ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AUDITORY MEATUS EXTERNAL EROSION ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE NEUROPATHY ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AUTOMATIC BLADDER ( 1 FDA reports)
AUTOMATISM ( 1 FDA reports)
AUTOSOMAL CHROMOSOME ANOMALY ( 1 FDA reports)
AVULSION FRACTURE ( 1 FDA reports)
B-CELL LYMPHOMA REFRACTORY ( 1 FDA reports)
B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
BACTERIA BODY FLUID IDENTIFIED ( 1 FDA reports)
BACTERIAL PROSTATITIS ( 1 FDA reports)
BACTERIAL TEST ( 1 FDA reports)
BACTEROIDES TEST POSITIVE ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BAND NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
BAROTRAUMA ( 1 FDA reports)
BARTONELLA TEST POSITIVE ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BENIGN FAMILIAL HAEMATURIA ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF LACRIMAL GLAND ( 1 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 1 FDA reports)
BENIGN OVARIAN TUMOUR ( 1 FDA reports)
BENIGN SPLEEN TUMOUR ( 1 FDA reports)
BETA 2 MICROGLOBULIN ABNORMAL ( 1 FDA reports)
BILE DUCT CANCER STAGE IV ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BIOPSY BREAST ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED NORMAL ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NECK OPERATION ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD AMINO ACID LEVEL INCREASED ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE ABNORMAL ( 1 FDA reports)
BLOOD BETA-D-GLUCAN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD COPPER DECREASED ( 1 FDA reports)
BLOOD COPPER INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD GALACTOSE INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GONADOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD GONADOTROPHIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 1 FDA reports)
BLOOD PROLACTIN DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TEST NORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE LESION EXCISION ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BORRELIA BURGDORFERI SEROLOGY NEGATIVE ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRACHIAL PLEXUS INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
BRAIN NEOPLASM BENIGN ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER MALE ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INDURATION ( 1 FDA reports)
BREAST NECROSIS ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BROWN-SEQUARD SYNDROME ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIFICATION METASTATIC ( 1 FDA reports)
CALCIPHYLAXIS ( 1 FDA reports)
CALCIUM IONISED ABNORMAL ( 1 FDA reports)
CALCIUM IONISED INCREASED ( 1 FDA reports)
CAMPTODACTYLY CONGENITAL ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CANDIDA OSTEOMYELITIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARCINOID TUMOUR OF THE CAECUM ( 1 FDA reports)
CARCINOMA IN SITU ( 1 FDA reports)
CARCINOMA IN SITU OF EYE ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIAC VALVE ABSCESS ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 1 FDA reports)
CARDIOVASCULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CARPUS CURVUS ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATARACT OPERATION COMPLICATION ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE PRURITUS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 1 FDA reports)
CELL-MEDIATED CYTOTOXICITY ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM ABSCESS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM FUNCTION TEST ABNORMAL ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL SARCOIDOSIS ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVIX CANCER METASTATIC ( 1 FDA reports)
CERVIX CERCLAGE PROCEDURE ( 1 FDA reports)
CERVIX INFLAMMATION ( 1 FDA reports)
CHEMICAL CYSTITIS ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CHEMOTHERAPY NEUROTOXICITY ATTENUATION ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 1 FDA reports)
CHORIORETINOPATHY ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHRONIC EOSINOPHILIC LEUKAEMIA ( 1 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLEFT PALATE ( 1 FDA reports)
COAGULATION FACTOR IX LEVEL DECREASED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLD AGGLUTININS ( 1 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLLAGEN-VASCULAR DISEASE ( 1 FDA reports)
COLON FISTULA REPAIR ( 1 FDA reports)
COLONIC PERFORATION POSTOPERATIVE ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CONDYLOMA ACUMINATUM ( 1 FDA reports)
CONGENITAL CLEFT HAND ( 1 FDA reports)
CONGENITAL EYELID MALFORMATION ( 1 FDA reports)
CONGENITAL ORAL MALFORMATION ( 1 FDA reports)
CONGENITAL OSTEODYSTROPHY ( 1 FDA reports)
CONGENITAL PNEUMONIA ( 1 FDA reports)
CONGENITAL VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRALATERAL BREAST CANCER ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL LESION ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
CRYOTHERAPY ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CRYPTOCOCCAL FUNGAEMIA ( 1 FDA reports)
CRYPTOCOCCUS ANTIGEN POSITIVE ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF LACTATE ABNORMAL ( 1 FDA reports)
CSF PROTEIN ( 1 FDA reports)
CSF PROTEIN DECREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS AMYLOIDOSIS ( 1 FDA reports)
CYANOSIS CENTRAL ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYST ASPIRATION ABNORMAL ( 1 FDA reports)
CYSTITIS RADIATION ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
CYTOMEGALOVIRUS PROCTOCOLITIS ( 1 FDA reports)
DACRYOCANALICULITIS ( 1 FDA reports)
DACRYOCYSTITIS ( 1 FDA reports)
DEATH OF SPOUSE ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DENTAL PULP DISORDER ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMATOFIBROSARCOMA ( 1 FDA reports)
DERMATOSIS ( 1 FDA reports)
DESMOPLASTIC SMALL ROUND CELL TUMOUR ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIABETIC VASCULAR DISORDER ( 1 FDA reports)
DIAPHRAGM MUSCLE WEAKNESS ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DONOR LEUKOCYTE INFUSION ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRAIN OF CEREBRAL SUBDURAL SPACE ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DUODENAL FISTULA ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSTROPHIA MYOTONICA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
EMBOLISM INFECTIVE ( 1 FDA reports)
EMPHYSEMATOUS BULLA ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENCEPHALITIS INFLUENZAL ( 1 FDA reports)
ENCEPHALOMYELITIS ( 1 FDA reports)
ENDOMETRIAL DYSPLASIA ( 1 FDA reports)
ENDOMETRIAL SARCOMA ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOSCOPY SMALL INTESTINE ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENLARGED CLITORIS ( 1 FDA reports)
ENLARGED UVULA ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENZYME INDUCTION ( 1 FDA reports)
EOSINOPHILIC LEUKAEMIA ( 1 FDA reports)
EPIPHYSEAL DISORDER ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHROBLAST COUNT NORMAL ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
ERYTHROSIS ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXPOSURE VIA FATHER ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EXTRAOCULAR MUSCLE DISORDER ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYE PENETRATION ( 1 FDA reports)
EYEGLASSES THERAPY ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FALLOPIAN TUBE CYST ( 1 FDA reports)
FAMILIAL MEDITERRANEAN FEVER ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FIBRIN DECREASED ( 1 FDA reports)
FIBRIN INCREASED ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
FINE MOTOR DELAY ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FOETAL CARDIAC DISORDER ( 1 FDA reports)
FOETAL HAEMOGLOBIN INCREASED ( 1 FDA reports)
FOETAL HEART RATE ABNORMAL ( 1 FDA reports)
FOETAL MALFORMATION ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III REFRACTORY ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III STAGE IV ( 1 FDA reports)
FONTANELLE BULGING ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FOREIGN BODY REACTION ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FREE HAEMOGLOBIN PRESENT ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRONTAL LOBE EPILEPSY ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL DNA TEST POSITIVE ( 1 FDA reports)
FUNGAL RHINITIS ( 1 FDA reports)
FUNGUS BODY FLUID IDENTIFIED ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER NECROSIS ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PERFORATION ( 1 FDA reports)
GANGLION ( 1 FDA reports)
GANGLIONEUROMA ( 1 FDA reports)
GASTRIC CANCER STAGE IV WITH METASTASES ( 1 FDA reports)
GASTRIC STENOSIS ( 1 FDA reports)
GASTRIC TUBE RECONSTRUCTION ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS PROTEUS ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ANASTOMOTIC LEAK ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL STOMA NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GEOTRICHUM INFECTION ( 1 FDA reports)
GESTATIONAL TROPHOBLASTIC TUMOUR ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GITELMAN'S SYNDROME ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GRAFT HAEMORRHAGE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA ANNULARE ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GROWTH ACCELERATED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCOLPOS ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HAPTOGLOBIN ABNORMAL ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEART VALVE INSUFFICIENCY ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPAPLASTIN DECREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC ARTERY FLOW DECREASED ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC ECHINOCOCCIASIS ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN ( 1 FDA reports)
HEPATITIS C RNA INCREASED ( 1 FDA reports)
HEPATITIS D VIRUS TEST POSITIVE ( 1 FDA reports)
HEPATITIS E ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIA REPAIR ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HIDRADENITIS ( 1 FDA reports)
HIPPOCAMPAL SCLEROSIS ( 1 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 1 FDA reports)
HISTIOCYTOSIS ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY RECURRENT ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE IV ( 1 FDA reports)
HODGKIN'S DISEASE REFRACTORY ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HTLV-1 ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN ANTI-MOUSE ANTIBODY INCREASED ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY ( 1 FDA reports)
HYALURONIC ACID INCREASED ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYPERCHOLIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERKERATOSIS FOLLICULARIS ET PARAFOLLICULARIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOGLOSSAL NERVE PARESIS ( 1 FDA reports)
HYPOGONADISM MALE ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
HYPOVITAMINOSIS ( 1 FDA reports)
IDIOPATHIC LENTICULAR MUCOCUTANEOUS PIGMENTATION ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMUNOGLOBULIN THERAPY ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMPAIRED FASTING GLUCOSE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IMPLANT SITE OEDEMA ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTIVE MYOSITIS ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE HAEMATOMA ( 1 FDA reports)
INFUSION SITE INDURATION ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE ULCER ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERLEUKIN LEVEL DECREASED ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL TRANSPLANT ( 1 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIS ADHESIONS ( 1 FDA reports)
IRIS HYPOPIGMENTATION ( 1 FDA reports)
IRIS NEOVASCULARISATION ( 1 FDA reports)
IRIS OPERATION ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 1 FDA reports)
LARYNGEAL HAEMATOMA ( 1 FDA reports)
LARYNGOSCOPY ABNORMAL ( 1 FDA reports)
LARYNGOTRACHEAL OEDEMA ( 1 FDA reports)
LASEGUE'S TEST POSITIVE ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEGIONELLA TEST ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LEUKAEMIA MONOCYTIC ( 1 FDA reports)
LEUKAEMOID REACTION ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LICHEN MYXOEDEMATOSUS ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIGHT CHAIN ANALYSIS DECREASED ( 1 FDA reports)
LIMB ASYMMETRY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIMB REDUCTION DEFECT ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIPASE ( 1 FDA reports)
LISTERIA ENCEPHALITIS ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LONG QT SYNDROME CONGENITAL ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 1 FDA reports)
LUMBAR PUNCTURE HEADACHE ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA METASTATIC ( 1 FDA reports)
LUPUS ENCEPHALITIS ( 1 FDA reports)
LUPUS ENTERITIS ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPH NODE FIBROSIS ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHANGIECTASIA ( 1 FDA reports)
MACRODACTYLY ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MACROSOMIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT HISTIOCYTOSIS ( 1 FDA reports)
MALIGNANT MELANOMA OF SITES OTHER THAN SKIN ( 1 FDA reports)
MALIGNANT MELANOMA STAGE II ( 1 FDA reports)
MALIGNANT NEOPLASM OF PLEURA ( 1 FDA reports)
MALIGNANT NEOPLASM OF RENAL PELVIS ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MALIGNANT NEOPLASM OF THORAX ( 1 FDA reports)
MALIGNANT NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
MALIGNANT SOFT TISSUE NEOPLASM ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANDIBULECTOMY ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTOCYTOSIS ( 1 FDA reports)
MASTOID EFFUSION ( 1 FDA reports)
MATERNAL DEATH AFFECTING FOETUS ( 1 FDA reports)
MAXIMAL VOLUNTARY VENTILATION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MEGAKARYOCYTES ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENDELSON'S SYNDROME ( 1 FDA reports)
MENINGEAL LEUKAEMIA ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS STREPTOCOCCAL ( 1 FDA reports)
MENINGOCOCCAL SEPSIS ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
MESENTERIC ARTERIOSCLEROSIS ( 1 FDA reports)
MESENTERIC LYMPHADENOPATHY ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO GALLBLADDER ( 1 FDA reports)
METASTASES TO PANCREAS ( 1 FDA reports)
METASTASES TO PHARYNX ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
MICRODACTYLY ( 1 FDA reports)
MICROGLOSSIA ( 1 FDA reports)
MICROSTOMIA ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MISMATCHED DONOR BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
MITOCHONDRIAL DNA MUTATION ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUMPS ANTIBODY TEST POSITIVE ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE FLAP OPERATION ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUTAGENIC EFFECT ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCOBACTERIUM KANSASII PNEUMONIA ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES REFRACTORY ( 1 FDA reports)
MYCOSIS FUNGOIDES STAGE IV ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYELOID METAPLASIA ( 1 FDA reports)
MYOCARDITIS BACTERIAL ( 1 FDA reports)
MYOCARDITIS MYCOTIC ( 1 FDA reports)
MYOCARDITIS TOXOPLASMAL ( 1 FDA reports)
MYODESOPSIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOKYMIA ( 1 FDA reports)
MYOTONIA ( 1 FDA reports)
NAIL BED BLEEDING ( 1 FDA reports)
NAIL BED INFLAMMATION ( 1 FDA reports)
NAIL OPERATION ( 1 FDA reports)
NASAL CAVITY MASS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL SINUS DRAINAGE ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NATURAL KILLER-CELL LEUKAEMIA ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NECROBIOSIS ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NECROTISING SCLERITIS ( 1 FDA reports)
NEGATIVISM ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NEURILEMMOMA MALIGNANT ( 1 FDA reports)
NEURITIS CRANIAL ( 1 FDA reports)
NEUROFIBROMA ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NO ADVERSE REACTION ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE I ( 1 FDA reports)
NORMAL DELIVERY ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ( 1 FDA reports)
OCULAR MYASTHENIA ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OCULAR VASCULITIS ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL ATRESIA ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESOPHAGEAL RUPTURE ( 1 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGECTOMY ( 1 FDA reports)
OESTRADIOL ABNORMAL ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OPEN REDUCTION OF FRACTURE ( 1 FDA reports)
OPSOCLONUS MYOCLONUS ( 1 FDA reports)
OPTIC DISC HAEMORRHAGE ( 1 FDA reports)
OPTIC PATHWAY INJURY ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL MUCOSAL PETECHIAE ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
ORBITAL APEX SYNDROME ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OROTICACIDURIA ( 1 FDA reports)
ORTHOSIS USER ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTECTOMY ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOSARCOMA LOCALISED ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTORHINOLARYNGOLOGICAL SURGERY ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
OVARIAN NECROSIS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC INFARCTION ( 1 FDA reports)
PANCREATIC INSUFFICIENCY ( 1 FDA reports)
PANCREATIC LEAK ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PAPILLOMA EXCISION ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARAINFLUENZAE VIRAL LARYNGOTRACHEOBRONCHITIS ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARESIS ANAL SPHINCTER ( 1 FDA reports)