Please choose an event type to view the corresponding MedsFacts report:

PYREXIA ( 1579 FDA reports)
DIARRHOEA ( 1111 FDA reports)
PNEUMONIA ( 1086 FDA reports)
NAUSEA ( 1071 FDA reports)
FEBRILE NEUTROPENIA ( 1037 FDA reports)
PAIN ( 982 FDA reports)
DYSPNOEA ( 890 FDA reports)
ANAEMIA ( 826 FDA reports)
FATIGUE ( 812 FDA reports)
RENAL FAILURE ACUTE ( 811 FDA reports)
NEUTROPENIA ( 807 FDA reports)
THROMBOCYTOPENIA ( 800 FDA reports)
VOMITING ( 767 FDA reports)
HYPOTENSION ( 722 FDA reports)
ANXIETY ( 707 FDA reports)
SEPSIS ( 674 FDA reports)
HEADACHE ( 634 FDA reports)
PANCYTOPENIA ( 627 FDA reports)
ASTHENIA ( 594 FDA reports)
RASH ( 589 FDA reports)
HERPES ZOSTER ( 579 FDA reports)
RENAL FAILURE ( 579 FDA reports)
PLATELET COUNT DECREASED ( 578 FDA reports)
INFECTION ( 567 FDA reports)
BACK PAIN ( 555 FDA reports)
DEATH ( 538 FDA reports)
DEHYDRATION ( 534 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 534 FDA reports)
ARTHRALGIA ( 532 FDA reports)
ABDOMINAL PAIN ( 523 FDA reports)
HAEMOGLOBIN DECREASED ( 516 FDA reports)
DRUG INEFFECTIVE ( 515 FDA reports)
OEDEMA PERIPHERAL ( 515 FDA reports)
DIZZINESS ( 485 FDA reports)
RESPIRATORY FAILURE ( 479 FDA reports)
DEPRESSION ( 475 FDA reports)
BLOOD CREATININE INCREASED ( 468 FDA reports)
CHEST PAIN ( 461 FDA reports)
CONFUSIONAL STATE ( 461 FDA reports)
NEUROPATHY PERIPHERAL ( 459 FDA reports)
FALL ( 453 FDA reports)
PLEURAL EFFUSION ( 442 FDA reports)
HYPERTENSION ( 431 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 429 FDA reports)
INJURY ( 423 FDA reports)
MULTIPLE MYELOMA ( 423 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 421 FDA reports)
PAIN IN EXTREMITY ( 417 FDA reports)
COUGH ( 411 FDA reports)
MUCOSAL INFLAMMATION ( 394 FDA reports)
OSTEONECROSIS OF JAW ( 387 FDA reports)
CONSTIPATION ( 380 FDA reports)
INSOMNIA ( 367 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 356 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 353 FDA reports)
DEEP VEIN THROMBOSIS ( 353 FDA reports)
CONVULSION ( 352 FDA reports)
BLOOD BILIRUBIN INCREASED ( 348 FDA reports)
HYPOKALAEMIA ( 344 FDA reports)
HYPOAESTHESIA ( 342 FDA reports)
MULTI-ORGAN FAILURE ( 341 FDA reports)
MALAISE ( 337 FDA reports)
GRAFT VERSUS HOST DISEASE ( 334 FDA reports)
DECREASED APPETITE ( 331 FDA reports)
ATRIAL FIBRILLATION ( 326 FDA reports)
CHILLS ( 324 FDA reports)
DISEASE PROGRESSION ( 324 FDA reports)
WEIGHT DECREASED ( 321 FDA reports)
RENAL IMPAIRMENT ( 320 FDA reports)
STAPHYLOCOCCAL INFECTION ( 310 FDA reports)
PULMONARY EMBOLISM ( 307 FDA reports)
URINARY TRACT INFECTION ( 294 FDA reports)
BONE DISORDER ( 285 FDA reports)
MYALGIA ( 285 FDA reports)
SEPTIC SHOCK ( 282 FDA reports)
MENTAL STATUS CHANGES ( 280 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 275 FDA reports)
TACHYCARDIA ( 275 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 269 FDA reports)
CELLULITIS ( 266 FDA reports)
CONDITION AGGRAVATED ( 266 FDA reports)
PRURITUS ( 266 FDA reports)
LEUKOPENIA ( 264 FDA reports)
PARAESTHESIA ( 264 FDA reports)
OEDEMA ( 262 FDA reports)
BONE PAIN ( 261 FDA reports)
DRUG INTERACTION ( 259 FDA reports)
SINUSITIS ( 258 FDA reports)
SOMNOLENCE ( 254 FDA reports)
SPINAL OSTEOARTHRITIS ( 254 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 251 FDA reports)
MUSCLE SPASMS ( 246 FDA reports)
ERYTHEMA ( 245 FDA reports)
OSTEOARTHRITIS ( 244 FDA reports)
EMOTIONAL DISTRESS ( 240 FDA reports)
HYPOXIA ( 239 FDA reports)
ATELECTASIS ( 238 FDA reports)
SYNCOPE ( 237 FDA reports)
WEIGHT INCREASED ( 233 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 233 FDA reports)
HAEMATOCRIT DECREASED ( 233 FDA reports)
MUSCULAR WEAKNESS ( 232 FDA reports)
OSTEONECROSIS ( 231 FDA reports)
TREMOR ( 228 FDA reports)
STOMATITIS ( 225 FDA reports)
VISION BLURRED ( 223 FDA reports)
BLOOD UREA INCREASED ( 222 FDA reports)
STEM CELL TRANSPLANT ( 222 FDA reports)
ANHEDONIA ( 218 FDA reports)
BRONCHITIS ( 217 FDA reports)
DYSPHAGIA ( 217 FDA reports)
BLOOD GLUCOSE INCREASED ( 216 FDA reports)
OSTEOMYELITIS ( 216 FDA reports)
NEUTROPHIL COUNT DECREASED ( 215 FDA reports)
GAIT DISTURBANCE ( 214 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 212 FDA reports)
PULMONARY OEDEMA ( 211 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 207 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 202 FDA reports)
LUNG INFILTRATION ( 202 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 201 FDA reports)
LIVER DISORDER ( 198 FDA reports)
ABDOMINAL PAIN UPPER ( 197 FDA reports)
BLOOD PRESSURE INCREASED ( 196 FDA reports)
HAEMODIALYSIS ( 196 FDA reports)
SWELLING ( 195 FDA reports)
MYOCARDIAL INFARCTION ( 194 FDA reports)
OSTEOPENIA ( 193 FDA reports)
HYPERGLYCAEMIA ( 191 FDA reports)
LOSS OF CONSCIOUSNESS ( 190 FDA reports)
BRADYCARDIA ( 185 FDA reports)
DYSPEPSIA ( 185 FDA reports)
PAIN IN JAW ( 184 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 181 FDA reports)
ASCITES ( 179 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 176 FDA reports)
RESPIRATORY DISTRESS ( 176 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 174 FDA reports)
CARDIAC ARREST ( 172 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 171 FDA reports)
INTERSTITIAL LUNG DISEASE ( 169 FDA reports)
HALLUCINATION ( 168 FDA reports)
BONE LESION ( 167 FDA reports)
BONE MARROW FAILURE ( 166 FDA reports)
DRUG TOXICITY ( 166 FDA reports)
HYPONATRAEMIA ( 166 FDA reports)
OSTEOPOROSIS ( 166 FDA reports)
AGITATION ( 165 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 163 FDA reports)
PERICARDIAL EFFUSION ( 163 FDA reports)
DEFORMITY ( 162 FDA reports)
CARDIAC FAILURE ( 161 FDA reports)
DIABETES MELLITUS ( 160 FDA reports)
EPISTAXIS ( 160 FDA reports)
HAEMORRHOIDS ( 159 FDA reports)
HEPATIC FAILURE ( 159 FDA reports)
IMPAIRED HEALING ( 159 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 157 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 156 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 156 FDA reports)
HERPES SIMPLEX ( 156 FDA reports)
CHEST DISCOMFORT ( 155 FDA reports)
HYPERSENSITIVITY ( 153 FDA reports)
OROPHARYNGEAL PAIN ( 153 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 151 FDA reports)
CEREBROVASCULAR ACCIDENT ( 150 FDA reports)
ABDOMINAL DISTENSION ( 148 FDA reports)
NECK PAIN ( 148 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 147 FDA reports)
ENCEPHALOPATHY ( 145 FDA reports)
TOOTH EXTRACTION ( 145 FDA reports)
FUNGAL INFECTION ( 144 FDA reports)
MUSCULOSKELETAL PAIN ( 144 FDA reports)
NEUTROPENIC SEPSIS ( 144 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 143 FDA reports)
LYMPHADENOPATHY ( 142 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 142 FDA reports)
HYPOPHAGIA ( 141 FDA reports)
CARDIOMEGALY ( 140 FDA reports)
GASTRITIS ( 140 FDA reports)
HAEMATURIA ( 140 FDA reports)
DYSPNOEA EXERTIONAL ( 137 FDA reports)
MIGRAINE ( 136 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 134 FDA reports)
HYPERKALAEMIA ( 134 FDA reports)
CHOLELITHIASIS ( 133 FDA reports)
EXOSTOSIS ( 133 FDA reports)
HAEMORRHAGE ( 133 FDA reports)
MITRAL VALVE INCOMPETENCE ( 133 FDA reports)
NEUROTOXICITY ( 133 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 133 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 133 FDA reports)
DYSARTHRIA ( 132 FDA reports)
CORONARY ARTERY DISEASE ( 130 FDA reports)
HEPATOMEGALY ( 130 FDA reports)
SINUS TACHYCARDIA ( 130 FDA reports)
CEREBRAL HAEMORRHAGE ( 129 FDA reports)
HYPERHIDROSIS ( 129 FDA reports)
RIB FRACTURE ( 129 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 128 FDA reports)
CANDIDIASIS ( 128 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 128 FDA reports)
RECTAL HAEMORRHAGE ( 128 FDA reports)
RENAL FAILURE CHRONIC ( 128 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 127 FDA reports)
HEPATOTOXICITY ( 126 FDA reports)
RENAL DISORDER ( 126 FDA reports)
DYSURIA ( 124 FDA reports)
LUNG DISORDER ( 124 FDA reports)
ORAL PAIN ( 124 FDA reports)
JOINT SWELLING ( 123 FDA reports)
RASH ERYTHEMATOUS ( 123 FDA reports)
URTICARIA ( 123 FDA reports)
VISUAL ACUITY REDUCED ( 123 FDA reports)
FLUID OVERLOAD ( 120 FDA reports)
HYPOMAGNESAEMIA ( 120 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 119 FDA reports)
NEOPLASM MALIGNANT ( 119 FDA reports)
BLOOD POTASSIUM DECREASED ( 118 FDA reports)
HEPATIC ENZYME INCREASED ( 118 FDA reports)
LETHARGY ( 118 FDA reports)
METASTASES TO BONE ( 118 FDA reports)
DYSGEUSIA ( 117 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 117 FDA reports)
HYPERBILIRUBINAEMIA ( 117 FDA reports)
HYPOTHYROIDISM ( 116 FDA reports)
BACTERIAL INFECTION ( 115 FDA reports)
BLOOD SODIUM DECREASED ( 115 FDA reports)
GINGIVAL BLEEDING ( 114 FDA reports)
URINARY RETENTION ( 114 FDA reports)
BLOOD CULTURE POSITIVE ( 113 FDA reports)
FEELING ABNORMAL ( 113 FDA reports)
PNEUMONITIS ( 113 FDA reports)
ALOPECIA ( 112 FDA reports)
ASPERGILLOSIS ( 112 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 111 FDA reports)
APHASIA ( 110 FDA reports)
DISEASE RECURRENCE ( 110 FDA reports)
HEART RATE INCREASED ( 110 FDA reports)
HIATUS HERNIA ( 110 FDA reports)
SUICIDAL IDEATION ( 109 FDA reports)
ARTHRITIS ( 108 FDA reports)
BLISTER ( 108 FDA reports)
CATARACT ( 108 FDA reports)
DRUG HYPERSENSITIVITY ( 107 FDA reports)
OXYGEN SATURATION DECREASED ( 107 FDA reports)
BACTERAEMIA ( 106 FDA reports)
DIVERTICULUM ( 106 FDA reports)
THROMBOSIS ( 106 FDA reports)
VISUAL IMPAIRMENT ( 106 FDA reports)
ANOREXIA ( 105 FDA reports)
ARTHROPATHY ( 105 FDA reports)
COLITIS ( 104 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 104 FDA reports)
JAUNDICE ( 104 FDA reports)
NERVOUS SYSTEM DISORDER ( 104 FDA reports)
RASH MACULO-PAPULAR ( 104 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 104 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 103 FDA reports)
MOUTH ULCERATION ( 103 FDA reports)
NEPHROPATHY TOXIC ( 103 FDA reports)
DELIRIUM ( 102 FDA reports)
DISORIENTATION ( 102 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 102 FDA reports)
OVERDOSE ( 102 FDA reports)
TRANSAMINASES INCREASED ( 102 FDA reports)
TUMOUR LYSIS SYNDROME ( 101 FDA reports)
CYSTITIS HAEMORRHAGIC ( 101 FDA reports)
STEVENS-JOHNSON SYNDROME ( 101 FDA reports)
ABDOMINAL DISCOMFORT ( 100 FDA reports)
CONTUSION ( 100 FDA reports)
DIVERTICULITIS ( 100 FDA reports)
ORAL HERPES ( 100 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 100 FDA reports)
BLOOD PRESSURE DECREASED ( 99 FDA reports)
COMA ( 99 FDA reports)
DECREASED INTEREST ( 99 FDA reports)
EYE PAIN ( 99 FDA reports)
LUNG NEOPLASM ( 99 FDA reports)
PROTHROMBIN TIME PROLONGED ( 99 FDA reports)
ENCEPHALITIS ( 98 FDA reports)
MYELODYSPLASTIC SYNDROME ( 98 FDA reports)
SKIN EXFOLIATION ( 98 FDA reports)
ASTHMA ( 97 FDA reports)
STRESS ( 97 FDA reports)
SWELLING FACE ( 97 FDA reports)
TOOTH ABSCESS ( 96 FDA reports)
PRODUCTIVE COUGH ( 96 FDA reports)
PALPITATIONS ( 95 FDA reports)
PANCREATITIS ( 95 FDA reports)
PULMONARY CONGESTION ( 95 FDA reports)
RASH PRURITIC ( 95 FDA reports)
AMNESIA ( 94 FDA reports)
BLOOD CALCIUM DECREASED ( 94 FDA reports)
HYPERLIPIDAEMIA ( 94 FDA reports)
SLEEP DISORDER ( 94 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 93 FDA reports)
ENTEROCOCCAL INFECTION ( 93 FDA reports)
HYPERCALCAEMIA ( 93 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 93 FDA reports)
LOOSE TOOTH ( 93 FDA reports)
ORAL DISORDER ( 93 FDA reports)
OSTEOLYSIS ( 93 FDA reports)
BLOOD ALBUMIN DECREASED ( 92 FDA reports)
ORTHOSTATIC HYPOTENSION ( 92 FDA reports)
SCAR ( 92 FDA reports)
SPEECH DISORDER ( 92 FDA reports)
DIALYSIS ( 91 FDA reports)
DRY SKIN ( 91 FDA reports)
INFUSION RELATED REACTION ( 91 FDA reports)
ROTATOR CUFF SYNDROME ( 90 FDA reports)
BASAL CELL CARCINOMA ( 89 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 89 FDA reports)
ORAL CANDIDIASIS ( 89 FDA reports)
SKIN LESION ( 89 FDA reports)
TOOTHACHE ( 89 FDA reports)
DEVICE RELATED INFECTION ( 88 FDA reports)
NEPHROLITHIASIS ( 88 FDA reports)
ATAXIA ( 87 FDA reports)
CEREBRAL INFARCTION ( 87 FDA reports)
DISABILITY ( 87 FDA reports)
HAEMATOCHEZIA ( 87 FDA reports)
PLASMACYTOMA ( 87 FDA reports)
TOOTH DISORDER ( 87 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 86 FDA reports)
WOUND DEHISCENCE ( 86 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 86 FDA reports)
CHOLESTASIS ( 86 FDA reports)
ENCEPHALITIS HERPES ( 86 FDA reports)
RENAL CYST ( 86 FDA reports)
CARDIAC MURMUR ( 85 FDA reports)
LIFE EXPECTANCY SHORTENED ( 85 FDA reports)
RHABDOMYOLYSIS ( 85 FDA reports)
DISCOMFORT ( 84 FDA reports)
HERPES VIRUS INFECTION ( 84 FDA reports)
PNEUMONIA FUNGAL ( 84 FDA reports)
EAR PAIN ( 82 FDA reports)
EJECTION FRACTION DECREASED ( 82 FDA reports)
INFLAMMATION ( 82 FDA reports)
INFLUENZA LIKE ILLNESS ( 82 FDA reports)
MEMORY IMPAIRMENT ( 82 FDA reports)
METABOLIC ACIDOSIS ( 82 FDA reports)
NEOPLASM PROGRESSION ( 82 FDA reports)
PULMONARY FIBROSIS ( 82 FDA reports)
TRANSPLANT REJECTION ( 82 FDA reports)
VIRAL INFECTION ( 81 FDA reports)
WHEEZING ( 81 FDA reports)
HAEMOPTYSIS ( 80 FDA reports)
PROTEINURIA ( 80 FDA reports)
CARDIO-RESPIRATORY ARREST ( 79 FDA reports)
CLOSTRIDIAL INFECTION ( 79 FDA reports)
NO THERAPEUTIC RESPONSE ( 79 FDA reports)
BALANCE DISORDER ( 78 FDA reports)
BURNING SENSATION ( 78 FDA reports)
GASTROINTESTINAL DISORDER ( 78 FDA reports)
RENAL TUBULAR NECROSIS ( 78 FDA reports)
SPLENOMEGALY ( 78 FDA reports)
SUBDURAL HAEMATOMA ( 78 FDA reports)
ACUTE RESPIRATORY FAILURE ( 77 FDA reports)
BURSITIS ( 77 FDA reports)
ESCHERICHIA INFECTION ( 77 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 77 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 76 FDA reports)
EMPHYSEMA ( 76 FDA reports)
HALLUCINATION, VISUAL ( 76 FDA reports)
BLOOD POTASSIUM INCREASED ( 75 FDA reports)
COAGULOPATHY ( 75 FDA reports)
DENTAL CARIES ( 75 FDA reports)
GINGIVAL RECESSION ( 75 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 75 FDA reports)
PRIMARY SEQUESTRUM ( 75 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 75 FDA reports)
VENTRICULAR TACHYCARDIA ( 74 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 74 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 74 FDA reports)
ENGRAFTMENT SYNDROME ( 74 FDA reports)
GINGIVAL PAIN ( 74 FDA reports)
HYPERCHOLESTEROLAEMIA ( 74 FDA reports)
COLONIC POLYP ( 73 FDA reports)
COMPRESSION FRACTURE ( 73 FDA reports)
GRAND MAL CONVULSION ( 73 FDA reports)
LYMPHOPENIA ( 73 FDA reports)
SLEEP APNOEA SYNDROME ( 73 FDA reports)
TOOTH FRACTURE ( 73 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 72 FDA reports)
URINARY INCONTINENCE ( 72 FDA reports)
LEUKOCYTOSIS ( 72 FDA reports)
LYMPHOMA ( 72 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 72 FDA reports)
NIGHT SWEATS ( 72 FDA reports)
PNEUMOTHORAX ( 72 FDA reports)
ACTINIC KERATOSIS ( 71 FDA reports)
ARRHYTHMIA ( 71 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 71 FDA reports)
HAEMATEMESIS ( 71 FDA reports)
PHARYNGITIS ( 71 FDA reports)
RASH GENERALISED ( 71 FDA reports)
ROAD TRAFFIC ACCIDENT ( 71 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 71 FDA reports)
UNRESPONSIVE TO STIMULI ( 71 FDA reports)
TINNITUS ( 70 FDA reports)
ACIDOSIS ( 70 FDA reports)
HEPATITIS ( 70 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 70 FDA reports)
SPINAL DISORDER ( 70 FDA reports)
ELECTROLYTE IMBALANCE ( 69 FDA reports)
JAW OPERATION ( 69 FDA reports)
LUNG INFECTION ( 69 FDA reports)
SINUS BRADYCARDIA ( 69 FDA reports)
ABSCESS ( 68 FDA reports)
FACIAL PAIN ( 68 FDA reports)
HEPATIC STEATOSIS ( 68 FDA reports)
HYPOCALCAEMIA ( 68 FDA reports)
HYPOPHOSPHATAEMIA ( 68 FDA reports)
MASTICATION DISORDER ( 68 FDA reports)
RESPIRATORY DISORDER ( 68 FDA reports)
VERTIGO ( 68 FDA reports)
BODY TEMPERATURE INCREASED ( 67 FDA reports)
NERVOUSNESS ( 67 FDA reports)
SQUAMOUS CELL CARCINOMA ( 67 FDA reports)
ANGIOEDEMA ( 66 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 66 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 66 FDA reports)
IRRITABILITY ( 66 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 66 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 66 FDA reports)
PULMONARY HYPERTENSION ( 66 FDA reports)
RASH MACULAR ( 66 FDA reports)
AORTIC VALVE INCOMPETENCE ( 65 FDA reports)
BRAIN OEDEMA ( 65 FDA reports)
DRY EYE ( 65 FDA reports)
ECCHYMOSIS ( 65 FDA reports)
GINGIVAL INFECTION ( 65 FDA reports)
NEURALGIA ( 65 FDA reports)
RESTLESS LEGS SYNDROME ( 65 FDA reports)
TENDERNESS ( 65 FDA reports)
VENOOCCLUSIVE DISEASE ( 65 FDA reports)
ARTERIOSCLEROSIS ( 64 FDA reports)
HYPOALBUMINAEMIA ( 64 FDA reports)
IRRITABLE BOWEL SYNDROME ( 64 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 64 FDA reports)
MALNUTRITION ( 64 FDA reports)
OESOPHAGITIS ( 64 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 64 FDA reports)
RHEUMATOID ARTHRITIS ( 64 FDA reports)
BRONCHOPNEUMONIA ( 63 FDA reports)
DIPLOPIA ( 63 FDA reports)
DRY MOUTH ( 63 FDA reports)
OFF LABEL USE ( 63 FDA reports)
SINUS DISORDER ( 63 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 63 FDA reports)
VITREOUS FLOATERS ( 63 FDA reports)
VISUAL DISTURBANCE ( 62 FDA reports)
GINGIVAL SWELLING ( 62 FDA reports)
HAEMATOMA ( 62 FDA reports)
JOINT STIFFNESS ( 62 FDA reports)
MASS ( 62 FDA reports)
MOUTH HAEMORRHAGE ( 62 FDA reports)
PHYSICAL DISABILITY ( 62 FDA reports)
PNEUMONIA ASPIRATION ( 62 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 62 FDA reports)
CULTURE URINE POSITIVE ( 61 FDA reports)
GINGIVITIS ( 61 FDA reports)
PRESYNCOPE ( 61 FDA reports)
RESPIRATORY TRACT INFECTION ( 61 FDA reports)
HEPATIC CYST ( 60 FDA reports)
MOBILITY DECREASED ( 60 FDA reports)
OBESITY ( 60 FDA reports)
PETECHIAE ( 60 FDA reports)
PSYCHOTIC DISORDER ( 60 FDA reports)
UNEVALUABLE EVENT ( 60 FDA reports)
VENTRICULAR HYPERTROPHY ( 59 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 59 FDA reports)
ENGRAFT FAILURE ( 59 FDA reports)
RHINORRHOEA ( 59 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 58 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 58 FDA reports)
HOT FLUSH ( 58 FDA reports)
JOINT EFFUSION ( 58 FDA reports)
LEUKOENCEPHALOPATHY ( 58 FDA reports)
MENTAL IMPAIRMENT ( 58 FDA reports)
PULMONARY HAEMORRHAGE ( 58 FDA reports)
SKIN ULCER ( 58 FDA reports)
BONE MARROW TRANSPLANT ( 57 FDA reports)
CARPAL TUNNEL SYNDROME ( 57 FDA reports)
DRUG LEVEL INCREASED ( 57 FDA reports)
GALLBLADDER DISORDER ( 57 FDA reports)
SKIN DISCOLOURATION ( 57 FDA reports)
TACHYPNOEA ( 57 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 57 FDA reports)
CHOLECYSTITIS ( 56 FDA reports)
COGNITIVE DISORDER ( 56 FDA reports)
GASTROENTERITIS ( 56 FDA reports)
HYPERURICAEMIA ( 56 FDA reports)
METASTASES TO LIVER ( 56 FDA reports)
PALLOR ( 56 FDA reports)
SPONDYLOLISTHESIS ( 56 FDA reports)
ABASIA ( 55 FDA reports)
AZOTAEMIA ( 55 FDA reports)
FLUSHING ( 55 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 55 FDA reports)
PNEUMONIA BACTERIAL ( 55 FDA reports)
SKIN INDURATION ( 55 FDA reports)
VASCULITIS ( 55 FDA reports)
SURGERY ( 54 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 54 FDA reports)
AORTIC STENOSIS ( 54 FDA reports)
GENERALISED OEDEMA ( 54 FDA reports)
HEPATITIS B ( 54 FDA reports)
LUMBAR SPINAL STENOSIS ( 54 FDA reports)
POLLAKIURIA ( 54 FDA reports)
PSEUDOMONAS INFECTION ( 54 FDA reports)
SINUS CONGESTION ( 54 FDA reports)
SKIN DISORDER ( 54 FDA reports)
SKIN HYPERTROPHY ( 54 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 53 FDA reports)
HEPATOSPLENOMEGALY ( 53 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 53 FDA reports)
RASH PAPULAR ( 53 FDA reports)
SKIN TIGHTNESS ( 53 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 53 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 53 FDA reports)
ABNORMAL BEHAVIOUR ( 52 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 52 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 52 FDA reports)
DYSKINESIA ( 52 FDA reports)
EYE SWELLING ( 52 FDA reports)
GLAUCOMA ( 52 FDA reports)
ILEUS PARALYTIC ( 52 FDA reports)
MYOPATHY ( 52 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 52 FDA reports)
SYNOVIAL CYST ( 51 FDA reports)
VENOUS INSUFFICIENCY ( 51 FDA reports)
DISTURBANCE IN ATTENTION ( 51 FDA reports)
ENDODONTIC PROCEDURE ( 51 FDA reports)
FAILURE TO THRIVE ( 51 FDA reports)
HYPOACUSIS ( 51 FDA reports)
HYPOGLYCAEMIA ( 51 FDA reports)
NOCTURIA ( 51 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 51 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 51 FDA reports)
SOFT TISSUE INFLAMMATION ( 51 FDA reports)
SPINAL COMPRESSION FRACTURE ( 51 FDA reports)
DRUG INTOLERANCE ( 50 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 50 FDA reports)
FLUID RETENTION ( 50 FDA reports)
GINGIVAL DISORDER ( 50 FDA reports)
HEAD INJURY ( 50 FDA reports)
INCORRECT DOSE ADMINISTERED ( 50 FDA reports)
OCULAR HYPERAEMIA ( 50 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 50 FDA reports)
AGRANULOCYTOSIS ( 49 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 49 FDA reports)
COORDINATION ABNORMAL ( 49 FDA reports)
FISTULA ( 49 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 49 FDA reports)
MENINGITIS ( 49 FDA reports)
SHOCK ( 49 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 48 FDA reports)
BLINDNESS ( 48 FDA reports)
BLOOD MAGNESIUM DECREASED ( 48 FDA reports)
CEREBRAL ATROPHY ( 48 FDA reports)
FOOT DEFORMITY ( 48 FDA reports)
INFLUENZA ( 48 FDA reports)
LOBAR PNEUMONIA ( 48 FDA reports)
LOCALISED INFECTION ( 48 FDA reports)
TREATMENT NONCOMPLIANCE ( 48 FDA reports)
THERAPY NON-RESPONDER ( 47 FDA reports)
URINE OUTPUT DECREASED ( 47 FDA reports)
DEAFNESS ( 47 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 47 FDA reports)
HIP FRACTURE ( 47 FDA reports)
HYPOVOLAEMIA ( 47 FDA reports)
LUNG CONSOLIDATION ( 47 FDA reports)
MYOCARDIAL ISCHAEMIA ( 47 FDA reports)
PROTEIN TOTAL DECREASED ( 47 FDA reports)
RALES ( 47 FDA reports)
BK VIRUS INFECTION ( 46 FDA reports)
CAPILLARY LEAK SYNDROME ( 46 FDA reports)
DEBRIDEMENT ( 46 FDA reports)
FACIAL PALSY ( 46 FDA reports)
METASTASES TO SPINE ( 46 FDA reports)
MYELOMA RECURRENCE ( 46 FDA reports)
OSTEITIS ( 46 FDA reports)
POST PROCEDURAL COMPLICATION ( 46 FDA reports)
RESTLESSNESS ( 46 FDA reports)
STREPTOCOCCAL INFECTION ( 46 FDA reports)
TRANSPLANT FAILURE ( 46 FDA reports)
TOOTH LOSS ( 45 FDA reports)
APLASIA PURE RED CELL ( 45 FDA reports)
ATRIAL TACHYCARDIA ( 45 FDA reports)
CHRONIC SINUSITIS ( 45 FDA reports)
HYPERNATRAEMIA ( 45 FDA reports)
MENTAL DISORDER ( 45 FDA reports)
ODYNOPHAGIA ( 45 FDA reports)
RADICULOPATHY ( 45 FDA reports)
BACTERIAL SEPSIS ( 44 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 44 FDA reports)
CARDIAC DISORDER ( 44 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 44 FDA reports)
DYSPHONIA ( 44 FDA reports)
FACE OEDEMA ( 44 FDA reports)
HAEMOLYTIC ANAEMIA ( 44 FDA reports)
RASH VESICULAR ( 44 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 44 FDA reports)
ACTINOMYCOSIS ( 43 FDA reports)
ADRENAL INSUFFICIENCY ( 43 FDA reports)
CROHN'S DISEASE ( 43 FDA reports)
DRUG ERUPTION ( 43 FDA reports)
ESCHERICHIA BACTERAEMIA ( 43 FDA reports)
MELAENA ( 43 FDA reports)
NIGHTMARE ( 43 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 43 FDA reports)
SCIATICA ( 43 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 42 FDA reports)
CIRCULATORY COLLAPSE ( 42 FDA reports)
DRUG RESISTANCE ( 42 FDA reports)
FOOT FRACTURE ( 42 FDA reports)
ILEUS ( 42 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 42 FDA reports)
NASOPHARYNGITIS ( 42 FDA reports)
PSEUDOMONAL SEPSIS ( 42 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 42 FDA reports)
THROMBOPHLEBITIS ( 41 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 41 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 41 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 41 FDA reports)
FIBROSIS ( 41 FDA reports)
MUSCLE STRAIN ( 41 FDA reports)
MUSCLE TWITCHING ( 41 FDA reports)
NODULE ( 41 FDA reports)
PLEURITIC PAIN ( 41 FDA reports)
SCOLIOSIS ( 41 FDA reports)
BACTERIAL DISEASE CARRIER ( 40 FDA reports)
CARDIOMYOPATHY ( 40 FDA reports)
CATHETER RELATED INFECTION ( 40 FDA reports)
CONJUNCTIVITIS ( 40 FDA reports)
DIABETIC KETOACIDOSIS ( 40 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 40 FDA reports)
HAEMOLYSIS ( 40 FDA reports)
JAW DISORDER ( 40 FDA reports)
MYOCLONUS ( 40 FDA reports)
PERFORMANCE STATUS DECREASED ( 40 FDA reports)
PURULENT DISCHARGE ( 40 FDA reports)
SINOATRIAL BLOCK ( 40 FDA reports)
SPINAL COLUMN STENOSIS ( 40 FDA reports)
TOOTH INFECTION ( 40 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 40 FDA reports)
ABORTION SPONTANEOUS ( 39 FDA reports)
ATRIAL FLUTTER ( 39 FDA reports)
BRONCHIECTASIS ( 39 FDA reports)
CEREBRAL ISCHAEMIA ( 39 FDA reports)
CHOLECYSTITIS CHRONIC ( 39 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 39 FDA reports)
EOSINOPHIL COUNT INCREASED ( 39 FDA reports)
FAECAL INCONTINENCE ( 39 FDA reports)
FAECES DISCOLOURED ( 39 FDA reports)
HEPATIC LESION ( 39 FDA reports)
HEPATITIS CHOLESTATIC ( 39 FDA reports)
HYPERKERATOSIS ( 39 FDA reports)
NASAL CONGESTION ( 39 FDA reports)
OTITIS MEDIA ( 39 FDA reports)
PROCTALGIA ( 39 FDA reports)
ABDOMINAL PAIN LOWER ( 38 FDA reports)
ACUTE SINUSITIS ( 38 FDA reports)
AGGRESSION ( 38 FDA reports)
APHTHOUS STOMATITIS ( 38 FDA reports)
DECUBITUS ULCER ( 38 FDA reports)
DENTAL PROSTHESIS USER ( 38 FDA reports)
ECZEMA ( 38 FDA reports)
ENDOCARDITIS ( 38 FDA reports)
FEAR ( 38 FDA reports)
GOUT ( 38 FDA reports)
HEARING IMPAIRED ( 38 FDA reports)
HEPATIC NECROSIS ( 38 FDA reports)
INTESTINAL OBSTRUCTION ( 38 FDA reports)
RESPIRATORY ARREST ( 38 FDA reports)
SERUM FERRITIN INCREASED ( 38 FDA reports)
SKIN INFECTION ( 38 FDA reports)
SKIN TOXICITY ( 38 FDA reports)
TYPE 2 DIABETES MELLITUS ( 38 FDA reports)
VAGINAL HAEMORRHAGE ( 38 FDA reports)
X-RAY ABNORMAL ( 37 FDA reports)
ADENOVIRUS INFECTION ( 37 FDA reports)
ADVERSE DRUG REACTION ( 37 FDA reports)
BARRETT'S OESOPHAGUS ( 37 FDA reports)
CATARACT OPERATION ( 37 FDA reports)
CHEST X-RAY ABNORMAL ( 37 FDA reports)
DERMAL CYST ( 37 FDA reports)
ERYTHEMA MULTIFORME ( 37 FDA reports)
IMMUNOSUPPRESSION ( 37 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 37 FDA reports)
KLEBSIELLA INFECTION ( 37 FDA reports)
MENISCUS LESION ( 37 FDA reports)
PHLEBITIS ( 37 FDA reports)
PROSTATE CANCER ( 37 FDA reports)
RASH PUSTULAR ( 37 FDA reports)
SCAB ( 37 FDA reports)
SEBORRHOEIC DERMATITIS ( 37 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 37 FDA reports)
ANURIA ( 36 FDA reports)
BONE DEBRIDEMENT ( 36 FDA reports)
CARDIOPULMONARY FAILURE ( 36 FDA reports)
CERVICAL SPINAL STENOSIS ( 36 FDA reports)
CYST ( 36 FDA reports)
ECONOMIC PROBLEM ( 36 FDA reports)
FEELING HOT ( 36 FDA reports)
FLANK PAIN ( 36 FDA reports)
HEPATITIS C ( 36 FDA reports)
HYPERCOAGULATION ( 36 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 36 FDA reports)
LARYNGITIS ( 36 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 36 FDA reports)
NYSTAGMUS ( 36 FDA reports)
PARAESTHESIA ORAL ( 36 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 36 FDA reports)
TENDONITIS ( 36 FDA reports)
ANAPHYLACTIC REACTION ( 35 FDA reports)
BLOOD CHLORIDE DECREASED ( 35 FDA reports)
BREAST CANCER METASTATIC ( 35 FDA reports)
CACHEXIA ( 35 FDA reports)
CHOLANGITIS ( 35 FDA reports)
FIBROMYALGIA ( 35 FDA reports)
GINGIVAL ABSCESS ( 35 FDA reports)
LACTIC ACIDOSIS ( 35 FDA reports)
NEUROPATHY ( 35 FDA reports)
OLIGURIA ( 35 FDA reports)
PANCREATITIS ACUTE ( 35 FDA reports)
PLEURAL FIBROSIS ( 35 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 35 FDA reports)
PRESBYOPIA ( 35 FDA reports)
REFLUX OESOPHAGITIS ( 35 FDA reports)
RETINITIS ( 35 FDA reports)
SEROTONIN SYNDROME ( 35 FDA reports)
SKIN FIBROSIS ( 35 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 34 FDA reports)
BREAST PAIN ( 34 FDA reports)
EAR INFECTION ( 34 FDA reports)
HEMIPARESIS ( 34 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 34 FDA reports)
INTESTINAL PERFORATION ( 34 FDA reports)
KERATITIS HERPETIC ( 34 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 34 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 34 FDA reports)
PAIN OF SKIN ( 34 FDA reports)
PERITONITIS ( 34 FDA reports)
PREGNANCY ( 34 FDA reports)
SENSORY DISTURBANCE ( 34 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 34 FDA reports)
VAGINAL INFECTION ( 34 FDA reports)
VIITH NERVE PARALYSIS ( 33 FDA reports)
ENTEROCOLITIS ( 33 FDA reports)
MELANOCYTIC NAEVUS ( 33 FDA reports)
NEUROLOGICAL SYMPTOM ( 33 FDA reports)
ORAL SURGERY ( 33 FDA reports)
PELVIC FRACTURE ( 33 FDA reports)
PLASMACYTOSIS ( 33 FDA reports)
SKIN PAPILLOMA ( 33 FDA reports)
SPINAL DEFORMITY ( 33 FDA reports)
STREPTOCOCCAL SEPSIS ( 33 FDA reports)
ABSCESS DRAINAGE ( 32 FDA reports)
BLOOD CALCIUM INCREASED ( 32 FDA reports)
BLOOD URINE PRESENT ( 32 FDA reports)
CYSTITIS ( 32 FDA reports)
DELUSION ( 32 FDA reports)
DRUG DOSE OMISSION ( 32 FDA reports)
DRUG EFFECT DECREASED ( 32 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 32 FDA reports)
GINGIVAL ULCERATION ( 32 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 32 FDA reports)
NEPHROPATHY ( 32 FDA reports)
NEPHROTIC SYNDROME ( 32 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 32 FDA reports)
POLYNEUROPATHY ( 32 FDA reports)
RENAL PAIN ( 32 FDA reports)
RETCHING ( 32 FDA reports)
SUICIDE ATTEMPT ( 32 FDA reports)
SWOLLEN TONGUE ( 32 FDA reports)
TONGUE DISORDER ( 31 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 31 FDA reports)
ASPERGILLUS TEST POSITIVE ( 31 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 31 FDA reports)
BLOOD CREATINE INCREASED ( 31 FDA reports)
BREAST CANCER ( 31 FDA reports)
DIVERTICULUM INTESTINAL ( 31 FDA reports)
EMOTIONAL DISORDER ( 31 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 31 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 31 FDA reports)
HYPERAESTHESIA ( 31 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 31 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 31 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 31 FDA reports)
PANIC ATTACK ( 31 FDA reports)
PERICARDITIS ( 31 FDA reports)
RESPIRATORY RATE INCREASED ( 31 FDA reports)
AREFLEXIA ( 30 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 30 FDA reports)
BONE SCAN ABNORMAL ( 30 FDA reports)
BREAST MASS ( 30 FDA reports)
CSF PROTEIN INCREASED ( 30 FDA reports)
DERMATITIS EXFOLIATIVE ( 30 FDA reports)
EPILEPSY ( 30 FDA reports)
EXPOSED BONE IN JAW ( 30 FDA reports)
EYELID OEDEMA ( 30 FDA reports)
FLATULENCE ( 30 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 30 FDA reports)
HEART DISEASE CONGENITAL ( 30 FDA reports)
HYPERTONIC BLADDER ( 30 FDA reports)
INCREASED TENDENCY TO BRUISE ( 30 FDA reports)
INGUINAL HERNIA ( 30 FDA reports)
INTESTINAL ISCHAEMIA ( 30 FDA reports)
OSTEOSCLEROSIS ( 30 FDA reports)
PHOTOPHOBIA ( 30 FDA reports)
SCOTOMA ( 30 FDA reports)
THIRST ( 30 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 29 FDA reports)
TOOTH IMPACTED ( 29 FDA reports)
TORSADE DE POINTES ( 29 FDA reports)
VARICELLA ( 29 FDA reports)
ABDOMINAL TENDERNESS ( 29 FDA reports)
ACUTE CORONARY SYNDROME ( 29 FDA reports)
BLOOD BICARBONATE DECREASED ( 29 FDA reports)
DRUG DEPENDENCE ( 29 FDA reports)
ENCEPHALITIS VIRAL ( 29 FDA reports)
FEMUR FRACTURE ( 29 FDA reports)
FRACTURED SACRUM ( 29 FDA reports)
HAEMATOTOXICITY ( 29 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 29 FDA reports)
HUMERUS FRACTURE ( 29 FDA reports)
LARGE INTESTINE PERFORATION ( 29 FDA reports)
LEFT ATRIAL DILATATION ( 29 FDA reports)
LIPASE INCREASED ( 29 FDA reports)
LOCAL SWELLING ( 29 FDA reports)
MEDICATION ERROR ( 29 FDA reports)
PHARYNGEAL OEDEMA ( 29 FDA reports)
PHOTOPSIA ( 29 FDA reports)
PROSTATITIS ( 29 FDA reports)
RAYNAUD'S PHENOMENON ( 29 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 29 FDA reports)
SERUM SICKNESS ( 29 FDA reports)
STATUS EPILEPTICUS ( 29 FDA reports)
ASTIGMATISM ( 28 FDA reports)
CHOLECYSTITIS ACUTE ( 28 FDA reports)
CHROMATURIA ( 28 FDA reports)
DENTURE WEARER ( 28 FDA reports)
EATING DISORDER ( 28 FDA reports)
ESCHERICHIA SEPSIS ( 28 FDA reports)
EXTRASYSTOLES ( 28 FDA reports)
GINGIVAL OEDEMA ( 28 FDA reports)
ILL-DEFINED DISORDER ( 28 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 28 FDA reports)
LABORATORY TEST ABNORMAL ( 28 FDA reports)
LIBIDO DECREASED ( 28 FDA reports)
LIVER TRANSPLANT REJECTION ( 28 FDA reports)
MANTLE CELL LYMPHOMA ( 28 FDA reports)
MICTURITION URGENCY ( 28 FDA reports)
MOOD ALTERED ( 28 FDA reports)
MOVEMENT DISORDER ( 28 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 28 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 28 FDA reports)
PLEURISY ( 28 FDA reports)
PULMONARY MYCOSIS ( 28 FDA reports)
RHINITIS ALLERGIC ( 28 FDA reports)
SKIN HYPERPIGMENTATION ( 28 FDA reports)
SPUTUM CULTURE POSITIVE ( 28 FDA reports)
STRESS URINARY INCONTINENCE ( 28 FDA reports)
TOXIC SKIN ERUPTION ( 28 FDA reports)
TRACHEOBRONCHITIS ( 28 FDA reports)
TRIGGER FINGER ( 27 FDA reports)
UMBILICAL HERNIA ( 27 FDA reports)
VENTRICULAR FIBRILLATION ( 27 FDA reports)
WOUND ( 27 FDA reports)
ANGIOPATHY ( 27 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 27 FDA reports)
BODY TEMPERATURE DECREASED ( 27 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 27 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 27 FDA reports)
EXCORIATION ( 27 FDA reports)
GASTRITIS EROSIVE ( 27 FDA reports)
INCOHERENT ( 27 FDA reports)
LEUKAEMIA PLASMACYTIC ( 27 FDA reports)
LUNG NEOPLASM MALIGNANT ( 27 FDA reports)
MULTIPLE SCLEROSIS ( 27 FDA reports)
NEPHRITIS INTERSTITIAL ( 27 FDA reports)
OCULAR ICTERUS ( 27 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 26 FDA reports)
ANGINA PECTORIS ( 26 FDA reports)
ATRIAL SEPTAL DEFECT ( 26 FDA reports)
BLADDER CANCER ( 26 FDA reports)
BLOOD GLUCOSE DECREASED ( 26 FDA reports)
BONE MARROW DISORDER ( 26 FDA reports)
CAECITIS ( 26 FDA reports)
DEVICE FAILURE ( 26 FDA reports)
DILATATION VENTRICULAR ( 26 FDA reports)
DRUG ADMINISTRATION ERROR ( 26 FDA reports)
DYSSTASIA ( 26 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 26 FDA reports)
GASTRIC ULCER ( 26 FDA reports)
GINGIVAL EROSION ( 26 FDA reports)
GRANULOMA ( 26 FDA reports)
HICCUPS ( 26 FDA reports)
HYDRONEPHROSIS ( 26 FDA reports)
HYPOMANIA ( 26 FDA reports)
INTRAOCULAR LENS IMPLANT ( 26 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 26 FDA reports)
MECHANICAL VENTILATION ( 26 FDA reports)
METASTASES TO LUNG ( 26 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 26 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 26 FDA reports)
NECROTISING RETINITIS ( 26 FDA reports)
PULMONARY GRANULOMA ( 26 FDA reports)
PURULENCE ( 26 FDA reports)
PYELONEPHRITIS ( 26 FDA reports)
RETINAL DETACHMENT ( 26 FDA reports)
UTERINE CANCER ( 26 FDA reports)
VENTRICULAR HYPOKINESIA ( 26 FDA reports)
TENDON DISORDER ( 25 FDA reports)
ABNORMAL DREAMS ( 25 FDA reports)
ADVERSE EVENT ( 25 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 25 FDA reports)
ANTITHROMBIN III DECREASED ( 25 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 25 FDA reports)
BRONCHOSPASM ( 25 FDA reports)
CARDIOGENIC SHOCK ( 25 FDA reports)
CUSHINGOID ( 25 FDA reports)
DENTAL OPERATION ( 25 FDA reports)
DERMATITIS BULLOUS ( 25 FDA reports)
ENTEROCOCCAL SEPSIS ( 25 FDA reports)
FUNGAEMIA ( 25 FDA reports)
GASTROINTESTINAL TOXICITY ( 25 FDA reports)
HODGKIN'S DISEASE ( 25 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 25 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 25 FDA reports)
LIVER ABSCESS ( 25 FDA reports)
MACULAR HOLE ( 25 FDA reports)
MERALGIA PARAESTHETICA ( 25 FDA reports)
MUSCLE ATROPHY ( 25 FDA reports)
NECROSIS ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 25 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 25 FDA reports)
ORAL INFECTION ( 25 FDA reports)
PATHOGEN RESISTANCE ( 25 FDA reports)
PELVIC PAIN ( 25 FDA reports)
PHOTOSENSITIVITY REACTION ( 25 FDA reports)
POST HERPETIC NEURALGIA ( 25 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 25 FDA reports)
PSORIASIS ( 25 FDA reports)
ACUTE HEPATIC FAILURE ( 24 FDA reports)
AMAUROSIS FUGAX ( 24 FDA reports)
ANGIOLIPOMA ( 24 FDA reports)
APLASTIC ANAEMIA ( 24 FDA reports)
ASPIRATION ( 24 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 24 FDA reports)
BLOOD CHLORIDE INCREASED ( 24 FDA reports)
BLOOD URIC ACID INCREASED ( 24 FDA reports)
BONE OPERATION ( 24 FDA reports)
CARDIOVASCULAR DISORDER ( 24 FDA reports)
CEREBRAL ARTERY STENOSIS ( 24 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 24 FDA reports)
DEVELOPMENTAL DELAY ( 24 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 24 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 24 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 24 FDA reports)
GROIN PAIN ( 24 FDA reports)
HAEMODYNAMIC INSTABILITY ( 24 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 24 FDA reports)
OSTEOMYELITIS CHRONIC ( 24 FDA reports)
PARTIAL SEIZURES ( 24 FDA reports)
PITUITARY ENLARGEMENT ( 24 FDA reports)
POLYARTERITIS NODOSA ( 24 FDA reports)
PYURIA ( 24 FDA reports)
RENAL INJURY ( 24 FDA reports)
RHINITIS ( 24 FDA reports)
SPINAL FRACTURE ( 24 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 24 FDA reports)
THROMBOPHLEBITIS MIGRANS ( 24 FDA reports)
THYROID DISORDER ( 24 FDA reports)
VENTRICULAR ARRHYTHMIA ( 24 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 24 FDA reports)
VASCULAR ANOMALY ( 23 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 23 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 23 FDA reports)
ATRIOVENTRICULAR BLOCK ( 23 FDA reports)
AUTOIMMUNE HEPATITIS ( 23 FDA reports)
BONE ATROPHY ( 23 FDA reports)
BREAST TENDERNESS ( 23 FDA reports)
CARDIAC FAILURE ACUTE ( 23 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 23 FDA reports)
DEMENTIA ( 23 FDA reports)
DERMATITIS ( 23 FDA reports)
DIFFICULTY IN WALKING ( 23 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 23 FDA reports)
EYE DISORDER ( 23 FDA reports)
GOITRE ( 23 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 23 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 23 FDA reports)
HEPATIC ENCEPHALOPATHY ( 23 FDA reports)
INJECTION SITE PAIN ( 23 FDA reports)
INJECTION SITE REACTION ( 23 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 23 FDA reports)
JOINT INJURY ( 23 FDA reports)
LIP SWELLING ( 23 FDA reports)
MUCOUS MEMBRANE DISORDER ( 23 FDA reports)
MYOSITIS ( 23 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 23 FDA reports)
POLYURIA ( 23 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 23 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 23 FDA reports)
SOFT TISSUE INFECTION ( 23 FDA reports)
ADJUSTMENT DISORDER ( 22 FDA reports)
AFFECTIVE DISORDER ( 22 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 22 FDA reports)
BONE DENSITY DECREASED ( 22 FDA reports)
BONE GRAFT ( 22 FDA reports)
CENTRAL LINE INFECTION ( 22 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 22 FDA reports)
CYTOLYTIC HEPATITIS ( 22 FDA reports)
GENITAL HERPES ( 22 FDA reports)
GRAFT DYSFUNCTION ( 22 FDA reports)
HEART RATE IRREGULAR ( 22 FDA reports)
HYPOTONIA ( 22 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 22 FDA reports)
MALIGNANT MELANOMA ( 22 FDA reports)
METASTASES TO LYMPH NODES ( 22 FDA reports)
METASTATIC NEOPLASM ( 22 FDA reports)
MOUTH INJURY ( 22 FDA reports)
ORAL DISCOMFORT ( 22 FDA reports)
ORGANISING PNEUMONIA ( 22 FDA reports)
OSTEORADIONECROSIS ( 22 FDA reports)
PARAPROTEINAEMIA ( 22 FDA reports)
PROTEIN URINE PRESENT ( 22 FDA reports)
PURPURA ( 22 FDA reports)
SEPSIS SYNDROME ( 22 FDA reports)
SEPTIC EMBOLUS ( 22 FDA reports)
TRANSFUSION REACTION ( 22 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 22 FDA reports)
UROSEPSIS ( 22 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 22 FDA reports)
VITAMIN B12 DEFICIENCY ( 22 FDA reports)
SYSTEMIC CANDIDA ( 21 FDA reports)
TROPONIN INCREASED ( 21 FDA reports)
ARTHRITIS BACTERIAL ( 21 FDA reports)
BLEPHARITIS ( 21 FDA reports)
BONE MARROW DEPRESSION ( 21 FDA reports)
CARDIAC TAMPONADE ( 21 FDA reports)
CLOSTRIDIUM COLITIS ( 21 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 21 FDA reports)
DERMATOSIS ( 21 FDA reports)
DILATATION ATRIAL ( 21 FDA reports)
EAR CONGESTION ( 21 FDA reports)
EAR DISCOMFORT ( 21 FDA reports)
ERECTILE DYSFUNCTION ( 21 FDA reports)
EXOPHTHALMOS ( 21 FDA reports)
FEMORAL NECK FRACTURE ( 21 FDA reports)
FIBRIN D DIMER INCREASED ( 21 FDA reports)
FLUID INTAKE REDUCED ( 21 FDA reports)
HAEMATOCRIT ABNORMAL ( 21 FDA reports)
HALLUCINATIONS, MIXED ( 21 FDA reports)
HYPOAESTHESIA ORAL ( 21 FDA reports)
IMMUNOGLOBULINS DECREASED ( 21 FDA reports)
INJECTION SITE ERYTHEMA ( 21 FDA reports)
LACERATION ( 21 FDA reports)
LEUKAEMIA ( 21 FDA reports)
LIP ULCERATION ( 21 FDA reports)
MARROW HYPERPLASIA ( 21 FDA reports)
MASTOIDITIS ( 21 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 21 FDA reports)
PERIPHERAL COLDNESS ( 21 FDA reports)
PLATELET DISORDER ( 21 FDA reports)
RASH MORBILLIFORM ( 21 FDA reports)
SKIN PLAQUE ( 21 FDA reports)
SUDDEN DEATH ( 21 FDA reports)
ABORTION MISSED ( 20 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 20 FDA reports)
ACUTE PULMONARY OEDEMA ( 20 FDA reports)
ANKLE FRACTURE ( 20 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 20 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 20 FDA reports)
BREATH SOUNDS ABNORMAL ( 20 FDA reports)
DEPRESSED MOOD ( 20 FDA reports)
ENTERITIS ( 20 FDA reports)
HEMIPLEGIA ( 20 FDA reports)
HEPATIC FIBROSIS ( 20 FDA reports)
HOSPITALISATION ( 20 FDA reports)
IMMUNE SYSTEM DISORDER ( 20 FDA reports)
INGROWING NAIL ( 20 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 20 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 20 FDA reports)
JOINT CONTRACTURE ( 20 FDA reports)
LEUKAEMIA RECURRENT ( 20 FDA reports)
MAJOR DEPRESSION ( 20 FDA reports)
MENIERE'S DISEASE ( 20 FDA reports)
METASTASES TO THORAX ( 20 FDA reports)
METRORRHAGIA ( 20 FDA reports)
OESOPHAGEAL STENOSIS ( 20 FDA reports)
OPPORTUNISTIC INFECTION ( 20 FDA reports)
ORAL INTAKE REDUCED ( 20 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 20 FDA reports)
PERIVASCULAR DERMATITIS ( 20 FDA reports)
PHLEBOLITH ( 20 FDA reports)
PULMONARY TOXICITY ( 20 FDA reports)
QUALITY OF LIFE DECREASED ( 20 FDA reports)
SUBCUTANEOUS ABSCESS ( 20 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 20 FDA reports)
VENOUS THROMBOSIS LIMB ( 20 FDA reports)
VIRAL PHARYNGITIS ( 19 FDA reports)
WALKING AID USER ( 19 FDA reports)
WOUND INFECTION ( 19 FDA reports)
AMYLOIDOSIS ( 19 FDA reports)
ANGINA UNSTABLE ( 19 FDA reports)
BLEPHAROSPASM ( 19 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 19 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 19 FDA reports)
BUNDLE BRANCH BLOCK ( 19 FDA reports)
CAROTID ARTERY STENOSIS ( 19 FDA reports)
CEREBRAL ASPERGILLOSIS ( 19 FDA reports)
CLEFT PALATE ( 19 FDA reports)
EMBOLISM ( 19 FDA reports)
ENTEROVESICAL FISTULA ( 19 FDA reports)
EPISCLERITIS ( 19 FDA reports)
GANGRENE ( 19 FDA reports)
GLOMERULONEPHRITIS ( 19 FDA reports)
GLOSSODYNIA ( 19 FDA reports)
H1N1 INFLUENZA ( 19 FDA reports)
HAEMATOCRIT INCREASED ( 19 FDA reports)
HALLUCINATION, AUDITORY ( 19 FDA reports)
HYPERTENSIVE CRISIS ( 19 FDA reports)
HYPOKINESIA ( 19 FDA reports)
LYMPHOEDEMA ( 19 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 19 FDA reports)
MUSCULOSKELETAL DISORDER ( 19 FDA reports)
PCO2 DECREASED ( 19 FDA reports)
PERIODONTITIS ( 19 FDA reports)
PERIORBITAL OEDEMA ( 19 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 19 FDA reports)
PRODUCT QUALITY ISSUE ( 19 FDA reports)
RETINAL INFARCTION ( 19 FDA reports)
SENSORY LOSS ( 19 FDA reports)
SOFT TISSUE DISORDER ( 19 FDA reports)
SPINAL CORD COMPRESSION ( 19 FDA reports)
ACCIDENTAL OVERDOSE ( 18 FDA reports)
ALVEOLITIS ALLERGIC ( 18 FDA reports)
ANGER ( 18 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 18 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 18 FDA reports)
BLADDER DISORDER ( 18 FDA reports)
BLINDNESS UNILATERAL ( 18 FDA reports)
BONE CYST ( 18 FDA reports)
BONE LOSS ( 18 FDA reports)
BREAST CYST ( 18 FDA reports)
CEREBROVASCULAR DISORDER ( 18 FDA reports)
CORYNEBACTERIUM INFECTION ( 18 FDA reports)
DIZZINESS POSTURAL ( 18 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 18 FDA reports)
EYE INFLAMMATION ( 18 FDA reports)
EYE LASER SURGERY ( 18 FDA reports)
FACIAL BONES FRACTURE ( 18 FDA reports)
FEELING COLD ( 18 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 18 FDA reports)
JAUNDICE CHOLESTATIC ( 18 FDA reports)
LUMBAR RADICULOPATHY ( 18 FDA reports)
MELANOSIS COLI ( 18 FDA reports)
MONONEUROPATHY MULTIPLEX ( 18 FDA reports)
MOOD SWINGS ( 18 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 18 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 18 FDA reports)
NODAL ARRHYTHMIA ( 18 FDA reports)
ORTHOPNOEA ( 18 FDA reports)
PARAPARESIS ( 18 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 18 FDA reports)
PRURITUS GENERALISED ( 18 FDA reports)
PULMONARY INFARCTION ( 18 FDA reports)
RESPIRATORY DEPRESSION ( 18 FDA reports)
SEBORRHOEIC KERATOSIS ( 18 FDA reports)
SKIN CHAPPED ( 18 FDA reports)
SPUTUM PURULENT ( 18 FDA reports)
TENDON RUPTURE ( 18 FDA reports)
THINKING ABNORMAL ( 18 FDA reports)
TONGUE INJURY ( 18 FDA reports)
TOXIC ENCEPHALOPATHY ( 18 FDA reports)
URINARY HESITATION ( 18 FDA reports)
VULVOVAGINAL DRYNESS ( 18 FDA reports)
WOUND COMPLICATION ( 18 FDA reports)
WOUND SECRETION ( 18 FDA reports)
THROMBOSED VARICOSE VEIN ( 17 FDA reports)
TOOTH EROSION ( 17 FDA reports)
TREATMENT FAILURE ( 17 FDA reports)
TROPONIN I INCREASED ( 17 FDA reports)
AORTIC CALCIFICATION ( 17 FDA reports)
APLASIA ( 17 FDA reports)
BACILLUS INFECTION ( 17 FDA reports)
BLOOD DISORDER ( 17 FDA reports)
BRAIN HERNIATION ( 17 FDA reports)
BREAST ENLARGEMENT ( 17 FDA reports)
BRONCHITIS VIRAL ( 17 FDA reports)
CANDIDA TEST POSITIVE ( 17 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 17 FDA reports)
CATHETER SITE INFECTION ( 17 FDA reports)
COLONOSCOPY ( 17 FDA reports)
CYANOSIS ( 17 FDA reports)
CYTOKINE RELEASE SYNDROME ( 17 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 17 FDA reports)
DEMYELINATION ( 17 FDA reports)
DROOLING ( 17 FDA reports)
ENTEROBACTER INFECTION ( 17 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 17 FDA reports)
FELTY'S SYNDROME ( 17 FDA reports)
GASTROINTESTINAL INFECTION ( 17 FDA reports)
HEPATITIS ACUTE ( 17 FDA reports)
HYDROCEPHALUS ( 17 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 17 FDA reports)
INTENTIONAL OVERDOSE ( 17 FDA reports)
JAW FRACTURE ( 17 FDA reports)
KYPHOSIS ( 17 FDA reports)
LARYNGITIS VIRAL ( 17 FDA reports)
MANIA ( 17 FDA reports)
MENINGITIS ASEPTIC ( 17 FDA reports)
MITRAL VALVE CALCIFICATION ( 17 FDA reports)
MONOCYTOSIS ( 17 FDA reports)
MOTOR DYSFUNCTION ( 17 FDA reports)
MULTIPLE INJURIES ( 17 FDA reports)
MUSCLE RUPTURE ( 17 FDA reports)
MYELITIS TRANSVERSE ( 17 FDA reports)
OESOPHAGEAL PAIN ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
PARANOIA ( 17 FDA reports)
PERIODONTAL DISEASE ( 17 FDA reports)
POOR VENOUS ACCESS ( 17 FDA reports)
PROTEIN URINE ( 17 FDA reports)
RADIOTHERAPY ( 17 FDA reports)
RADIUS FRACTURE ( 17 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 17 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 17 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 17 FDA reports)
SARCOIDOSIS ( 17 FDA reports)
SEROMA ( 17 FDA reports)
SHOCK HAEMORRHAGIC ( 17 FDA reports)
SKIN NODULE ( 17 FDA reports)
SKIN ODOUR ABNORMAL ( 17 FDA reports)
SUBCUTANEOUS NODULE ( 17 FDA reports)
ABSCESS JAW ( 16 FDA reports)
ACINETOBACTER INFECTION ( 16 FDA reports)
ACROCHORDON ( 16 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 16 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 16 FDA reports)
AORTIC ANEURYSM ( 16 FDA reports)
AORTIC VALVE DISEASE ( 16 FDA reports)
ATROPHIC VULVOVAGINITIS ( 16 FDA reports)
BILE DUCT OBSTRUCTION ( 16 FDA reports)
BLOOD AMYLASE INCREASED ( 16 FDA reports)
BRADYCARDIA NEONATAL ( 16 FDA reports)
CATHETER RELATED COMPLICATION ( 16 FDA reports)
CHOREOATHETOSIS ( 16 FDA reports)
DERMATITIS ALLERGIC ( 16 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 16 FDA reports)
DYSTONIA ( 16 FDA reports)
EOSINOPHILIA ( 16 FDA reports)
EYE PRURITUS ( 16 FDA reports)
FULL BLOOD COUNT DECREASED ( 16 FDA reports)
FURUNCLE ( 16 FDA reports)
HYPERAMMONAEMIA ( 16 FDA reports)
HYPOTHERMIA ( 16 FDA reports)
IMMUNODEFICIENCY ( 16 FDA reports)
IRON DEFICIENCY ANAEMIA ( 16 FDA reports)
KAPOSI'S SARCOMA ( 16 FDA reports)
KERATITIS ( 16 FDA reports)
KLEBSIELLA BACTERAEMIA ( 16 FDA reports)
LACRIMATION INCREASED ( 16 FDA reports)
METASTASIS ( 16 FDA reports)
NEUTROPHIL COUNT INCREASED ( 16 FDA reports)
OCCULT BLOOD POSITIVE ( 16 FDA reports)
OESOPHAGEAL SPASM ( 16 FDA reports)
PEPTIC ULCER ( 16 FDA reports)
PLATELET COUNT INCREASED ( 16 FDA reports)
POOR PERSONAL HYGIENE ( 16 FDA reports)
PREMATURE BABY ( 16 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 16 FDA reports)
SINUS ARRHYTHMIA ( 16 FDA reports)
SYSTEMIC MYCOSIS ( 16 FDA reports)
TACHYARRHYTHMIA ( 16 FDA reports)
THROAT TIGHTNESS ( 16 FDA reports)
UPPER LIMB FRACTURE ( 16 FDA reports)
VARICOSE VEIN ( 16 FDA reports)
TONSILLITIS ( 15 FDA reports)
TOXOPLASMOSIS ( 15 FDA reports)
TRANSFUSION ( 15 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 15 FDA reports)
AGEUSIA ( 15 FDA reports)
ANOGENITAL WARTS ( 15 FDA reports)
ANXIETY DISORDER ( 15 FDA reports)
AORTIC VALVE SCLEROSIS ( 15 FDA reports)
APATHY ( 15 FDA reports)
APNOEA ( 15 FDA reports)
ASPIRATION PLEURAL CAVITY ( 15 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 15 FDA reports)
BLINDNESS TRANSIENT ( 15 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 15 FDA reports)
BRADYARRHYTHMIA ( 15 FDA reports)
BRAIN DEATH ( 15 FDA reports)
BRUXISM ( 15 FDA reports)
CALCULUS URETERIC ( 15 FDA reports)
CHOLECYSTECTOMY ( 15 FDA reports)
CHOROIDAL DETACHMENT ( 15 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 15 FDA reports)
CONGENITAL JAW MALFORMATION ( 15 FDA reports)
COSTOCHONDRITIS ( 15 FDA reports)
CRYING ( 15 FDA reports)
CYSTOCELE ( 15 FDA reports)
DERMATITIS CONTACT ( 15 FDA reports)
DIASTOLIC DYSFUNCTION ( 15 FDA reports)
ECTOPIC PREGNANCY ( 15 FDA reports)
ENDOTRACHEAL INTUBATION ( 15 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 15 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 15 FDA reports)
EYE IRRITATION ( 15 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 15 FDA reports)
FALLOT'S TETRALOGY ( 15 FDA reports)
FUNGAL SKIN INFECTION ( 15 FDA reports)
HEART RATE DECREASED ( 15 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 15 FDA reports)
HERPES ZOSTER DISSEMINATED ( 15 FDA reports)
HYPERMETABOLISM ( 15 FDA reports)
HYPERREFLEXIA ( 15 FDA reports)
HYPERSOMNIA ( 15 FDA reports)
INCONTINENCE ( 15 FDA reports)
INFANTILE APNOEIC ATTACK ( 15 FDA reports)
INFECTED SEBACEOUS CYST ( 15 FDA reports)
JAUNDICE NEONATAL ( 15 FDA reports)
KNEE OPERATION ( 15 FDA reports)
LERICHE SYNDROME ( 15 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 15 FDA reports)
MASS EXCISION ( 15 FDA reports)
MENOPAUSE ( 15 FDA reports)
MICROTIA ( 15 FDA reports)
MYDRIASIS ( 15 FDA reports)
MYOPIA ( 15 FDA reports)
NASAL ULCER ( 15 FDA reports)
NEPHRITIS ( 15 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 15 FDA reports)
NON-CARDIAC CHEST PAIN ( 15 FDA reports)
ONYCHOMYCOSIS ( 15 FDA reports)
OSTEOMA ( 15 FDA reports)
PERONEAL NERVE PALSY ( 15 FDA reports)
PITTING OEDEMA ( 15 FDA reports)
PNEUMOCOCCAL SEPSIS ( 15 FDA reports)
PORTAL HYPERTENSION ( 15 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 15 FDA reports)
PULSE ABSENT ( 15 FDA reports)
SCLERODERMA ( 15 FDA reports)
SNORING ( 15 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 15 FDA reports)
STUPOR ( 15 FDA reports)
ABSCESS LIMB ( 14 FDA reports)
ACTINIC ELASTOSIS ( 14 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 14 FDA reports)
BACTERIA STOOL IDENTIFIED ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BLOOD COUNT ABNORMAL ( 14 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 14 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
BRAIN ABSCESS ( 14 FDA reports)
BREAST CANCER FEMALE ( 14 FDA reports)
CANDIDA SEPSIS ( 14 FDA reports)
CATHETER REMOVAL ( 14 FDA reports)
COLON ADENOMA ( 14 FDA reports)
COMMUNICATION DISORDER ( 14 FDA reports)
DEPRESSIVE SYMPTOM ( 14 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 14 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 14 FDA reports)
ESSENTIAL HYPERTENSION ( 14 FDA reports)
EYE DISCHARGE ( 14 FDA reports)
FOLLICULITIS ( 14 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 14 FDA reports)
GASTRIC DISORDER ( 14 FDA reports)
GLYCOSURIA ( 14 FDA reports)
GRAFT COMPLICATION ( 14 FDA reports)
GYNAECOMASTIA ( 14 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 14 FDA reports)
IMPAIRED DRIVING ABILITY ( 14 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 14 FDA reports)
INTENTIONAL DRUG MISUSE ( 14 FDA reports)
LARGE INTESTINAL ULCER ( 14 FDA reports)
LIMB DISCOMFORT ( 14 FDA reports)
LOCALISED OEDEMA ( 14 FDA reports)
MASTECTOMY ( 14 FDA reports)
MEDICAL DEVICE COMPLICATION ( 14 FDA reports)
MENINGITIS VIRAL ( 14 FDA reports)
METABOLIC DISORDER ( 14 FDA reports)
MUSCLE TIGHTNESS ( 14 FDA reports)
ORAL FIBROMA ( 14 FDA reports)
PATHOLOGICAL FRACTURE ( 14 FDA reports)
PNEUMATOSIS INTESTINALIS ( 14 FDA reports)
PNEUMOMEDIASTINUM ( 14 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 14 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 14 FDA reports)
PSYCHIATRIC SYMPTOM ( 14 FDA reports)
PULMONARY TUBERCULOSIS ( 14 FDA reports)
RADIATION INJURY ( 14 FDA reports)
RADICULAR PAIN ( 14 FDA reports)
RECTOCELE ( 14 FDA reports)
SKIN CANCER ( 14 FDA reports)
THROAT IRRITATION ( 14 FDA reports)
TRANSPLANT ( 14 FDA reports)
TUMOUR FLARE ( 14 FDA reports)
UMBILICAL HERNIA REPAIR ( 14 FDA reports)
VASCULAR CALCIFICATION ( 14 FDA reports)
VENA CAVA THROMBOSIS ( 14 FDA reports)
WOUND DRAINAGE ( 14 FDA reports)
XEROSIS ( 14 FDA reports)
TUBERCULOSIS ( 13 FDA reports)
UTERINE LEIOMYOMA ( 13 FDA reports)
VENTRICULAR DYSFUNCTION ( 13 FDA reports)
ABDOMINAL ABSCESS ( 13 FDA reports)
ABSCESS ORAL ( 13 FDA reports)
ADHESION ( 13 FDA reports)
AFFECT LABILITY ( 13 FDA reports)
AMMONIA INCREASED ( 13 FDA reports)
BACK INJURY ( 13 FDA reports)
BLADDER SPASM ( 13 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 13 FDA reports)
BLOOD PRESSURE ABNORMAL ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 13 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 13 FDA reports)
CARDIAC PACEMAKER INSERTION ( 13 FDA reports)
COLD SWEAT ( 13 FDA reports)
COLON CANCER ( 13 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 13 FDA reports)
CORNEAL DEPOSITS ( 13 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 13 FDA reports)
DEAFNESS NEUROSENSORY ( 13 FDA reports)
DRUG ABUSE ( 13 FDA reports)
DYSAESTHESIA ( 13 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 13 FDA reports)
EPIGASTRIC DISCOMFORT ( 13 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 13 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 13 FDA reports)
GRANULOCYTOPENIA ( 13 FDA reports)
HEPATIC CIRRHOSIS ( 13 FDA reports)
HEPATITIS FULMINANT ( 13 FDA reports)
HYPERVENTILATION ( 13 FDA reports)
HYPOVOLAEMIC SHOCK ( 13 FDA reports)
ILIAC ARTERY THROMBOSIS ( 13 FDA reports)
JOINT DISLOCATION ( 13 FDA reports)
KIDNEY SMALL ( 13 FDA reports)
KLEBSIELLA SEPSIS ( 13 FDA reports)
LIGAMENT RUPTURE ( 13 FDA reports)
MAXILLOFACIAL OPERATION ( 13 FDA reports)
MENINGITIS BACTERIAL ( 13 FDA reports)
METABOLIC ENCEPHALOPATHY ( 13 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 13 FDA reports)
NASAL SEPTUM DEVIATION ( 13 FDA reports)
NEPHRITIC SYNDROME ( 13 FDA reports)
NO ADVERSE EVENT ( 13 FDA reports)
PELIOSIS HEPATIS ( 13 FDA reports)
PERIORBITAL CELLULITIS ( 13 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 13 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 13 FDA reports)
POOR PERIPHERAL CIRCULATION ( 13 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 13 FDA reports)
PROTEIN TOTAL INCREASED ( 13 FDA reports)
RECURRENT CANCER ( 13 FDA reports)
RENAL ANEURYSM ( 13 FDA reports)
RENAL TUBULAR ACIDOSIS ( 13 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 13 FDA reports)
SEDATION ( 13 FDA reports)
SENSATION OF FOREIGN BODY ( 13 FDA reports)
SENSITIVITY OF TEETH ( 13 FDA reports)
SEXUAL DYSFUNCTION ( 13 FDA reports)
SINUS HEADACHE ( 13 FDA reports)
SKULL MALFORMATION ( 13 FDA reports)
SPINAL FUSION SURGERY ( 13 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 12 FDA reports)
ACUTE LEUKAEMIA ( 12 FDA reports)
ADJUSTMENT DISORDER WITH MIXED ANXIETY AND DEPRESSED MOOD ( 12 FDA reports)
ANAPHYLACTOID REACTION ( 12 FDA reports)
APRAXIA ( 12 FDA reports)
ASTERIXIS ( 12 FDA reports)
BIOPSY GINGIVAL ( 12 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 12 FDA reports)
BONE LESION EXCISION ( 12 FDA reports)
BUNION ( 12 FDA reports)
CARDIAC ANEURYSM ( 12 FDA reports)
CERVICOBRACHIAL SYNDROME ( 12 FDA reports)
COLLAPSE OF LUNG ( 12 FDA reports)
COMPLETED SUICIDE ( 12 FDA reports)
CORONARY ARTERY OCCLUSION ( 12 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 12 FDA reports)
CREPITATIONS ( 12 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 12 FDA reports)
CULTURE WOUND POSITIVE ( 12 FDA reports)
DENTAL FISTULA ( 12 FDA reports)
DEVICE DISLOCATION ( 12 FDA reports)
DRUG LEVEL DECREASED ( 12 FDA reports)
DRUG PRESCRIBING ERROR ( 12 FDA reports)
DUODENOGASTRIC REFLUX ( 12 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 12 FDA reports)
EMPYEMA ( 12 FDA reports)
EPIDIDYMITIS ( 12 FDA reports)
EYE ALLERGY ( 12 FDA reports)
FACET JOINT SYNDROME ( 12 FDA reports)
FAT NECROSIS ( 12 FDA reports)
FEELING JITTERY ( 12 FDA reports)
FIBULA FRACTURE ( 12 FDA reports)
GASTROINTESTINAL NECROSIS ( 12 FDA reports)
GUILLAIN-BARRE SYNDROME ( 12 FDA reports)
HAEMOCHROMATOSIS ( 12 FDA reports)
HAEMORRHAGIC DIATHESIS ( 12 FDA reports)
HAIR GROWTH ABNORMAL ( 12 FDA reports)
HEPATIC MASS ( 12 FDA reports)
HEPATITIS TOXIC ( 12 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 12 FDA reports)
HYPERMETROPIA ( 12 FDA reports)
HYPERPLASIA ( 12 FDA reports)
INJECTION SITE SWELLING ( 12 FDA reports)
ISCHAEMIA ( 12 FDA reports)
JC VIRUS INFECTION ( 12 FDA reports)
LICHENOID KERATOSIS ( 12 FDA reports)
LIGAMENT SPRAIN ( 12 FDA reports)
LIMB OPERATION ( 12 FDA reports)
LOWER EXTREMITY MASS ( 12 FDA reports)
MACULAR DEGENERATION ( 12 FDA reports)
MACULOPATHY ( 12 FDA reports)
METASTASES TO PELVIS ( 12 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 12 FDA reports)
MULTIPLE FRACTURES ( 12 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 12 FDA reports)
NEUROFIBROMA ( 12 FDA reports)
NEUTROPENIC INFECTION ( 12 FDA reports)
ORAL CAVITY FISTULA ( 12 FDA reports)
PARALYSIS ( 12 FDA reports)
PARESIS ( 12 FDA reports)
PEAU D'ORANGE ( 12 FDA reports)
PERITONITIS BACTERIAL ( 12 FDA reports)
PERSONALITY CHANGE ( 12 FDA reports)
PNEUMONIA KLEBSIELLA ( 12 FDA reports)
POLYP ( 12 FDA reports)
PORTAL VEIN THROMBOSIS ( 12 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
RETINAL HAEMORRHAGE ( 12 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 12 FDA reports)
SOPOR ( 12 FDA reports)
SPLENIC ABSCESS ( 12 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 12 FDA reports)
STOMACH DISCOMFORT ( 12 FDA reports)
TARDIVE DYSKINESIA ( 12 FDA reports)
TOOTH DEPOSIT ( 12 FDA reports)
UVEITIS ( 12 FDA reports)
VAGINAL DISCHARGE ( 12 FDA reports)
VASCULAR INSUFFICIENCY ( 12 FDA reports)
VISUAL FIELD DEFECT ( 12 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 11 FDA reports)
SYNOVIAL RUPTURE ( 11 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 11 FDA reports)
TOOTH REPAIR ( 11 FDA reports)
ULCERATIVE KERATITIS ( 11 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 11 FDA reports)
VAGINAL PROLAPSE ( 11 FDA reports)
VAGINITIS BACTERIAL ( 11 FDA reports)
VENOUS THROMBOSIS ( 11 FDA reports)
VENTRICULAR DYSKINESIA ( 11 FDA reports)
VULVAL ULCERATION ( 11 FDA reports)
ABDOMINAL MASS ( 11 FDA reports)
ACUTE PRERENAL FAILURE ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 11 FDA reports)
ANASTOMOTIC STENOSIS ( 11 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 11 FDA reports)
BACTERIAL TEST POSITIVE ( 11 FDA reports)
BARTHOLIN'S CYST ( 11 FDA reports)
BETA GLOBULIN INCREASED ( 11 FDA reports)
BLADDER PROLAPSE ( 11 FDA reports)
BLAST CELL COUNT INCREASED ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 11 FDA reports)
BLOOD IRON INCREASED ( 11 FDA reports)
BLOOD PH DECREASED ( 11 FDA reports)
BONE FISSURE ( 11 FDA reports)
BONE GIANT CELL TUMOUR ( 11 FDA reports)
BONE SWELLING ( 11 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 11 FDA reports)
CANCER PAIN ( 11 FDA reports)
CARDIAC VALVE DISEASE ( 11 FDA reports)
CATHETER PLACEMENT ( 11 FDA reports)
CELLULITIS ORBITAL ( 11 FDA reports)
CEREBELLAR SYNDROME ( 11 FDA reports)
CHEILITIS ( 11 FDA reports)
CHOREA ( 11 FDA reports)
COLPOCELE ( 11 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 11 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 11 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 11 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 11 FDA reports)
CONJUNCTIVITIS VIRAL ( 11 FDA reports)
CULTURE POSITIVE ( 11 FDA reports)
DELAYED ENGRAFTMENT ( 11 FDA reports)
DUODENAL ULCER ( 11 FDA reports)
DYSHIDROSIS ( 11 FDA reports)
DYSPHEMIA ( 11 FDA reports)
DYSPLASIA ( 11 FDA reports)
DYSPLASTIC NAEVUS ( 11 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 11 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 11 FDA reports)
ENDOSCOPY ( 11 FDA reports)
ERYTHEMA OF EYELID ( 11 FDA reports)
EXTRASKELETAL OSSIFICATION ( 11 FDA reports)
EXTRAVASATION ( 11 FDA reports)
EYELID PTOSIS ( 11 FDA reports)
FEBRILE INFECTION ( 11 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 11 FDA reports)
GASTRODUODENITIS ( 11 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 11 FDA reports)
GLOMERULOSCLEROSIS ( 11 FDA reports)
HAND FRACTURE ( 11 FDA reports)
HEPATIC ENZYME ABNORMAL ( 11 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 11 FDA reports)
HYPERPYREXIA ( 11 FDA reports)
IMPAIRED WORK ABILITY ( 11 FDA reports)
INCREASED APPETITE ( 11 FDA reports)
INFECTED SKIN ULCER ( 11 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 11 FDA reports)
INTENTION TREMOR ( 11 FDA reports)
INTERCOSTAL NEURALGIA ( 11 FDA reports)
INTRA-UTERINE DEATH ( 11 FDA reports)
KIDNEY ENLARGEMENT ( 11 FDA reports)
LACTOSE INTOLERANCE ( 11 FDA reports)
LIP PAIN ( 11 FDA reports)
LIPOMA ( 11 FDA reports)
LYMPHADENECTOMY ( 11 FDA reports)
MACROCYTOSIS ( 11 FDA reports)
MENINGIOMA ( 11 FDA reports)
MENISCUS REMOVAL ( 11 FDA reports)
NECK INJURY ( 11 FDA reports)
NOCARDIOSIS ( 11 FDA reports)
OCCIPITAL NEURALGIA ( 11 FDA reports)
OPTIC NERVE CUPPING ( 11 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 11 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 11 FDA reports)
PROSTATISM ( 11 FDA reports)
PSYCHOMOTOR RETARDATION ( 11 FDA reports)
PUPILS UNEQUAL ( 11 FDA reports)
RADIOTHERAPY TO BRAIN ( 11 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 11 FDA reports)
RENAL OSTEODYSTROPHY ( 11 FDA reports)
RENAL TUBULAR DISORDER ( 11 FDA reports)
RETICULOCYTOSIS ( 11 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 11 FDA reports)
SCLERAL OPERATION ( 11 FDA reports)
SKIN OEDEMA ( 11 FDA reports)
SUDDEN CARDIAC DEATH ( 11 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 11 FDA reports)
ABSCESS NECK ( 10 FDA reports)
ACUTE ABDOMEN ( 10 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 10 FDA reports)
ARTHROSCOPIC SURGERY ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 10 FDA reports)
BACTERIA URINE IDENTIFIED ( 10 FDA reports)
BILE DUCT STONE ( 10 FDA reports)
BILIARY TRACT DISORDER ( 10 FDA reports)
BLOOD MAGNESIUM INCREASED ( 10 FDA reports)
BLOOD UREA DECREASED ( 10 FDA reports)
BONE MARROW TOXICITY ( 10 FDA reports)
BRADYPHRENIA ( 10 FDA reports)
CATARACT NUCLEAR ( 10 FDA reports)
CLEFT LIP AND PALATE ( 10 FDA reports)
COMPLEX PARTIAL SEIZURES ( 10 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 10 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 10 FDA reports)
CSF TEST ABNORMAL ( 10 FDA reports)
CYSTOSCOPY ( 10 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 10 FDA reports)
DEPENDENCE ( 10 FDA reports)
DIVERTICULAR PERFORATION ( 10 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 10 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 10 FDA reports)
DYSPHASIA ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 10 FDA reports)
EXPIRED DRUG ADMINISTERED ( 10 FDA reports)
EYE MOVEMENT DISORDER ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
FUNGAL SEPSIS ( 10 FDA reports)
GASTRITIS HAEMORRHAGIC ( 10 FDA reports)
GENE MUTATION ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 10 FDA reports)
GLUCOSE URINE PRESENT ( 10 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 10 FDA reports)
GRANULOCYTE COUNT DECREASED ( 10 FDA reports)
HYDROPNEUMOTHORAX ( 10 FDA reports)
HYPERTELORISM OF ORBIT ( 10 FDA reports)
HYPERTHERMIA ( 10 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 10 FDA reports)
INJECTION SITE PRURITUS ( 10 FDA reports)
INTESTINAL DILATATION ( 10 FDA reports)
IRITIS ( 10 FDA reports)
JARISCH-HERXHEIMER REACTION ( 10 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 10 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 10 FDA reports)
LIP DRY ( 10 FDA reports)
LIPOMA EXCISION ( 10 FDA reports)
LUNG HYPERINFLATION ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 10 FDA reports)
LYMPHOCYTIC INFILTRATION ( 10 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 10 FDA reports)
MEDICATION RESIDUE ( 10 FDA reports)
MICROANGIOPATHY ( 10 FDA reports)
MOANING ( 10 FDA reports)
MYELITIS ( 10 FDA reports)
NECK MASS ( 10 FDA reports)
NEONATAL DISORDER ( 10 FDA reports)
NERVE ROOT COMPRESSION ( 10 FDA reports)
NERVE ROOT LESION ( 10 FDA reports)
ORGAN FAILURE ( 10 FDA reports)
OROPHARYNGEAL BLISTERING ( 10 FDA reports)
PAPILLOEDEMA ( 10 FDA reports)
PAROSMIA ( 10 FDA reports)
PELVIC ABSCESS ( 10 FDA reports)
PERIARTHRITIS ( 10 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 10 FDA reports)
PLATELET COUNT ABNORMAL ( 10 FDA reports)
PNEUMONIA VIRAL ( 10 FDA reports)
PROCEDURAL COMPLICATION ( 10 FDA reports)
PROCEDURAL PAIN ( 10 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 10 FDA reports)
RENAL ARTERY STENOSIS ( 10 FDA reports)
ROSACEA ( 10 FDA reports)
SEASONAL ALLERGY ( 10 FDA reports)
SEQUESTRECTOMY ( 10 FDA reports)
SHOULDER PAIN ( 10 FDA reports)
SINUS POLYP ( 10 FDA reports)
SKIN CANDIDA ( 10 FDA reports)
SKIN FISSURES ( 10 FDA reports)
SKIN REACTION ( 10 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 10 FDA reports)
SPLEEN DISORDER ( 10 FDA reports)
SPONDYLITIS ( 10 FDA reports)
STENT PLACEMENT ( 10 FDA reports)
SYNCOPE VASOVAGAL ( 10 FDA reports)
THROMBOCYTOPENIC PURPURA ( 10 FDA reports)
TRACHEOSTOMY ( 10 FDA reports)
TIBIA FRACTURE ( 9 FDA reports)
ULCER ( 9 FDA reports)
VITAMIN D DEFICIENCY ( 9 FDA reports)
ABDOMINAL HERNIA ( 9 FDA reports)
ACANTHAMOEBA INFECTION ( 9 FDA reports)
ACCIDENTAL EXPOSURE ( 9 FDA reports)
ADRENAL SUPPRESSION ( 9 FDA reports)
ALCOHOL USE ( 9 FDA reports)
ANAEMIA MACROCYTIC ( 9 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 9 FDA reports)
AORTIC DISORDER ( 9 FDA reports)
APICECTOMY ( 9 FDA reports)
APPENDICITIS ( 9 FDA reports)
ATROPHY ( 9 FDA reports)
BILIARY DYSKINESIA ( 9 FDA reports)
BIPOLAR DISORDER ( 9 FDA reports)
BLADDER OPERATION ( 9 FDA reports)
BLOOD SODIUM INCREASED ( 9 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 9 FDA reports)
BONE EROSION ( 9 FDA reports)
BRADYKINESIA ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
BREAST CALCIFICATIONS ( 9 FDA reports)
BREAST SWELLING ( 9 FDA reports)
CALCINOSIS ( 9 FDA reports)
CARBON DIOXIDE DECREASED ( 9 FDA reports)
CARDIOTOXICITY ( 9 FDA reports)
CEREBRAL CYST ( 9 FDA reports)
CEREBRAL DISORDER ( 9 FDA reports)
CERUMEN IMPACTION ( 9 FDA reports)
CHEST WALL PAIN ( 9 FDA reports)
CLAVICLE FRACTURE ( 9 FDA reports)
CLONUS ( 9 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 9 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 9 FDA reports)
CORNEAL DYSTROPHY ( 9 FDA reports)
CYSTITIS VIRAL ( 9 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 9 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 9 FDA reports)
DYSLALIA ( 9 FDA reports)
EDENTULOUS ( 9 FDA reports)
ENCEPHALOMALACIA ( 9 FDA reports)
EPICONDYLITIS ( 9 FDA reports)
EVAN'S SYNDROME ( 9 FDA reports)
EXFOLIATIVE RASH ( 9 FDA reports)
EYE INFECTION ( 9 FDA reports)
FIBROUS HISTIOCYTOMA ( 9 FDA reports)
FORMICATION ( 9 FDA reports)
FUNGAL OESOPHAGITIS ( 9 FDA reports)
GENERAL SYMPTOM ( 9 FDA reports)
GLIOSIS ( 9 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 9 FDA reports)
GRIP STRENGTH DECREASED ( 9 FDA reports)
HAEMOSIDEROSIS ( 9 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 9 FDA reports)
HEPATIC CONGESTION ( 9 FDA reports)
HEPATORENAL SYNDROME ( 9 FDA reports)
HETEROTAXIA ( 9 FDA reports)
HOMICIDAL IDEATION ( 9 FDA reports)
HUMAN CHORIONIC GONADOTROPIN INCREASED ( 9 FDA reports)
HYPERVISCOSITY SYNDROME ( 9 FDA reports)
IMPULSIVE BEHAVIOUR ( 9 FDA reports)
INFECTIVE TENOSYNOVITIS ( 9 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 9 FDA reports)
INTRACARDIAC THROMBUS ( 9 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 9 FDA reports)
IRON DEFICIENCY ( 9 FDA reports)
ISCHAEMIC HEPATITIS ( 9 FDA reports)
LIP DISCOLOURATION ( 9 FDA reports)
LIVER INJURY ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MENINGITIS TOXOPLASMAL ( 9 FDA reports)
METATARSUS PRIMUS VARUS ( 9 FDA reports)
MONOPARESIS ( 9 FDA reports)
NASAL CYST ( 9 FDA reports)
NASAL DISCOMFORT ( 9 FDA reports)
NECROTISING COLITIS ( 9 FDA reports)
NEURODERMATITIS ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 9 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 9 FDA reports)
OVERWEIGHT ( 9 FDA reports)
POLYDIPSIA ( 9 FDA reports)
POLYP COLORECTAL ( 9 FDA reports)
POOR QUALITY SLEEP ( 9 FDA reports)
POST LAMINECTOMY SYNDROME ( 9 FDA reports)
PULMONARY MASS ( 9 FDA reports)
PULMONARY VASCULAR DISORDER ( 9 FDA reports)
QRS AXIS ABNORMAL ( 9 FDA reports)
RADICULITIS CERVICAL ( 9 FDA reports)
RECTAL POLYP ( 9 FDA reports)
RENAL MASS ( 9 FDA reports)
REPERFUSION ARRHYTHMIA ( 9 FDA reports)
RESPIRATORY ACIDOSIS ( 9 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 9 FDA reports)
SCROTAL IRRITATION ( 9 FDA reports)
SECONDARY SEQUESTRUM ( 9 FDA reports)
SERRATIA INFECTION ( 9 FDA reports)
SPINAL COLUMN INJURY ( 9 FDA reports)
SPLENIC RUPTURE ( 9 FDA reports)
SPUTUM DISCOLOURED ( 9 FDA reports)
SUPERINFECTION ( 9 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 8 FDA reports)
ABDOMINAL NEOPLASM ( 8 FDA reports)
ABDOMINAL RIGIDITY ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 8 FDA reports)
ACNE ( 8 FDA reports)
ADENOCARCINOMA ( 8 FDA reports)
ADRENAL CARCINOMA ( 8 FDA reports)
ADRENAL MASS ( 8 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 8 FDA reports)
ANAL CANCER ( 8 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 8 FDA reports)
APPENDIX DISORDER ( 8 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BACK DISORDER ( 8 FDA reports)
BEDRIDDEN ( 8 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 8 FDA reports)
BLOOD OSMOLARITY DECREASED ( 8 FDA reports)
BLOOD TEST ABNORMAL ( 8 FDA reports)
BOWEN'S DISEASE ( 8 FDA reports)
BRONCHIAL HAEMORRHAGE ( 8 FDA reports)
BRONCHOPLEURAL FISTULA ( 8 FDA reports)
BULLOUS LUNG DISEASE ( 8 FDA reports)
CARDIAC ENZYMES INCREASED ( 8 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
CATHETER SITE ERYTHEMA ( 8 FDA reports)
CATHETER SITE PAIN ( 8 FDA reports)
CEREBELLAR HAEMATOMA ( 8 FDA reports)
CEREBRAL FUNGAL INFECTION ( 8 FDA reports)
CEREBRAL HAEMATOMA ( 8 FDA reports)
CERVICAL DYSPLASIA ( 8 FDA reports)
CHONDROMALACIA ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 8 FDA reports)
CLUMSINESS ( 8 FDA reports)
COLOSTOMY ( 8 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 8 FDA reports)
CORONARY ARTERY RESTENOSIS ( 8 FDA reports)
CYSTITIS INTERSTITIAL ( 8 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 8 FDA reports)
DENTAL NECROSIS ( 8 FDA reports)
DERMATITIS ATOPIC ( 8 FDA reports)
DIABETIC NEUROPATHY ( 8 FDA reports)
DRUG SCREEN POSITIVE ( 8 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
EFFUSION ( 8 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 8 FDA reports)
EMBOLIC STROKE ( 8 FDA reports)
ESCHAR ( 8 FDA reports)
EYE HAEMORRHAGE ( 8 FDA reports)
EYELID MARGIN CRUSTING ( 8 FDA reports)
FACIAL PARESIS ( 8 FDA reports)
FAECALOMA ( 8 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 8 FDA reports)
FEELING OF DESPAIR ( 8 FDA reports)
FOLLICULAR MUCINOSIS ( 8 FDA reports)
FOREIGN BODY TRAUMA ( 8 FDA reports)
FRACTURE ( 8 FDA reports)
FUSARIUM INFECTION ( 8 FDA reports)
GALLBLADDER ENLARGEMENT ( 8 FDA reports)
GASTRIC POLYPS ( 8 FDA reports)
GASTROENTERITIS BACTERIAL ( 8 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 8 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 8 FDA reports)
GASTROINTESTINAL PERFORATION ( 8 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 8 FDA reports)
GAZE PALSY ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HAEMORRHAGIC STROKE ( 8 FDA reports)
HAPTOGLOBIN DECREASED ( 8 FDA reports)
HEPATOCELLULAR DAMAGE ( 8 FDA reports)
HYPERCAPNIA ( 8 FDA reports)
HYPERPHOSPHATAEMIA ( 8 FDA reports)
HYPERTHYROIDISM ( 8 FDA reports)
HYPERTONIA ( 8 FDA reports)
HYPOGONADISM ( 8 FDA reports)
HYPOVENTILATION ( 8 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 8 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 8 FDA reports)
INJURY CORNEAL ( 8 FDA reports)
INTESTINAL MALROTATION ( 8 FDA reports)
JOINT LOCK ( 8 FDA reports)
LABORATORY TEST INTERFERENCE ( 8 FDA reports)
LASER THERAPY ( 8 FDA reports)
LIMB INJURY ( 8 FDA reports)
LIVER TRANSPLANT ( 8 FDA reports)
MALABSORPTION ( 8 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 8 FDA reports)
METAPNEUMOVIRUS INFECTION ( 8 FDA reports)
MICROPHTHALMOS ( 8 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 8 FDA reports)
MYCOBACTERIAL INFECTION ( 8 FDA reports)
MYOCARDITIS ( 8 FDA reports)
NAIL DYSTROPHY ( 8 FDA reports)
NEPHROGENIC ANAEMIA ( 8 FDA reports)
NEUROBLASTOMA ( 8 FDA reports)
NEUROPATHIC ULCER ( 8 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 8 FDA reports)
OESOPHAGEAL DILATATION ( 8 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 8 FDA reports)
OVARIAN CYST ( 8 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PARAPLEGIA ( 8 FDA reports)
PERIPHERAL BLOOD STEM CELL APHERESIS ( 8 FDA reports)
PERIPHERAL ISCHAEMIA ( 8 FDA reports)
PLANTAR FASCIITIS ( 8 FDA reports)
PLASMAPHERESIS ( 8 FDA reports)
PLATELET TRANSFUSION ( 8 FDA reports)
PNEUMONIA HERPES VIRAL ( 8 FDA reports)
POISONING ( 8 FDA reports)
PROSTATOMEGALY ( 8 FDA reports)
PULMONARY AIR LEAKAGE ( 8 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 8 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 8 FDA reports)
RADICULITIS ( 8 FDA reports)
RENAL HAEMATOMA ( 8 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
RESUSCITATION ( 8 FDA reports)
RETINOPATHY ( 8 FDA reports)
RHONCHI ( 8 FDA reports)
RIGHT VENTRICULAR FAILURE ( 8 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 8 FDA reports)
SIALOADENITIS ( 8 FDA reports)
SKIN SWELLING ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 8 FDA reports)
THROMBOCYTOSIS ( 8 FDA reports)
THROMBOTIC STROKE ( 8 FDA reports)
TONGUE COATED ( 8 FDA reports)
TRICHOSPORON INFECTION ( 8 FDA reports)
TUMOUR EMBOLISM ( 8 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 8 FDA reports)
UTERINE PROLAPSE ( 8 FDA reports)
VARICES OESOPHAGEAL ( 8 FDA reports)
VASCULAR CAUTERISATION ( 8 FDA reports)
VIRAEMIA ( 8 FDA reports)
VITAMIN D DECREASED ( 8 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 8 FDA reports)
WRIST FRACTURE ( 8 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
SUTURE INSERTION ( 7 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
TELANGIECTASIA ( 7 FDA reports)
TENOSYNOVITIS ( 7 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 7 FDA reports)
THYROID NEOPLASM ( 7 FDA reports)
TINEA CRURIS ( 7 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 7 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 7 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 7 FDA reports)
TRISMUS ( 7 FDA reports)
URGE INCONTINENCE ( 7 FDA reports)
VENOUS STENOSIS ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
ZYGOMYCOSIS ( 7 FDA reports)
AEROMONA INFECTION ( 7 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 7 FDA reports)
ALLODYNIA ( 7 FDA reports)
AMAUROSIS ( 7 FDA reports)
ANOSMIA ( 7 FDA reports)
APPETITE DISORDER ( 7 FDA reports)
ARACHNOIDITIS ( 7 FDA reports)
ARTHROPOD BITE ( 7 FDA reports)
ARTHROSCOPY ( 7 FDA reports)
AUTOIMMUNE DISORDER ( 7 FDA reports)
BACTERIAL DIARRHOEA ( 7 FDA reports)
BILIARY COLIC ( 7 FDA reports)
BIOPSY ( 7 FDA reports)
BIOPSY LIVER ABNORMAL ( 7 FDA reports)
BLOOD ALBUMIN INCREASED ( 7 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 7 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 7 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 7 FDA reports)
BLOOD CREATININE DECREASED ( 7 FDA reports)
BLOOD GASES ABNORMAL ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 7 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 7 FDA reports)
BONE FORMATION INCREASED ( 7 FDA reports)
BONE INFARCTION ( 7 FDA reports)
BURKITT'S LYMPHOMA ( 7 FDA reports)
CALCIPHYLAXIS ( 7 FDA reports)
CHAPPED LIPS ( 7 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 7 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 7 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
COLON OPERATION ( 7 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 7 FDA reports)
CRYSTAL URINE PRESENT ( 7 FDA reports)
CSF GLUCOSE DECREASED ( 7 FDA reports)
CSF VIRUS IDENTIFIED ( 7 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
CYSTITIS NONINFECTIVE ( 7 FDA reports)
CYSTOPEXY ( 7 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 7 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 7 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 7 FDA reports)
DEVICE OCCLUSION ( 7 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
DRUG LEVEL FLUCTUATING ( 7 FDA reports)
EJECTION FRACTION ABNORMAL ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 7 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 7 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 7 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 7 FDA reports)
ENTEROCELE ( 7 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 7 FDA reports)
EXERCISE TOLERANCE DECREASED ( 7 FDA reports)
EXTRADURAL HAEMATOMA ( 7 FDA reports)
EYELID DISORDER ( 7 FDA reports)
FACIAL SPASM ( 7 FDA reports)
FISTULA DISCHARGE ( 7 FDA reports)
FOOD INTOLERANCE ( 7 FDA reports)
GASTROENTERITIS VIRAL ( 7 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 7 FDA reports)
GINGIVAL ERYTHEMA ( 7 FDA reports)
GINGIVAL HYPERTROPHY ( 7 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 7 FDA reports)
HAEMOGLOBINURIA ( 7 FDA reports)
HALLUCINATION, OLFACTORY ( 7 FDA reports)
HEART TRANSPLANT REJECTION ( 7 FDA reports)
HERNIA ( 7 FDA reports)
HERPES OESOPHAGITIS ( 7 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 7 FDA reports)
HILAR LYMPHADENOPATHY ( 7 FDA reports)
HIP ARTHROPLASTY ( 7 FDA reports)
HIP SURGERY ( 7 FDA reports)
HIV INFECTION ( 7 FDA reports)
HYPERSEXUALITY ( 7 FDA reports)
HYPOREFLEXIA ( 7 FDA reports)
HYSTERECTOMY ( 7 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 7 FDA reports)
IMPULSE-CONTROL DISORDER ( 7 FDA reports)
INCREASED VENTRICULAR AFTERLOAD ( 7 FDA reports)
INFECTIOUS PERITONITIS ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INJECTION SITE HAEMATOMA ( 7 FDA reports)
INJECTION SITE HAEMORRHAGE ( 7 FDA reports)
INJECTION SITE INDURATION ( 7 FDA reports)
INJECTION SITE RASH ( 7 FDA reports)
INTENTIONAL SELF-INJURY ( 7 FDA reports)
INTERVERTEBRAL DISCITIS ( 7 FDA reports)
INTESTINAL ULCER ( 7 FDA reports)
ISCHAEMIC STROKE ( 7 FDA reports)
JOINT CREPITATION ( 7 FDA reports)
JOINT INSTABILITY ( 7 FDA reports)
JOINT SURGERY ( 7 FDA reports)
KIDNEY INFECTION ( 7 FDA reports)
KYPHOSCOLIOSIS ( 7 FDA reports)
LACTOBACILLUS INFECTION ( 7 FDA reports)
LACUNAR INFARCTION ( 7 FDA reports)
LENTIGO ( 7 FDA reports)
LIPOHYPERTROPHY ( 7 FDA reports)
LISTERIOSIS ( 7 FDA reports)
LYMPH NODE PALPABLE ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
MACULAR OEDEMA ( 7 FDA reports)
MALIGNANT MESENTERIC NEOPLASM ( 7 FDA reports)
MANDIBULAR PROSTHESIS USER ( 7 FDA reports)
MEAN CELL VOLUME INCREASED ( 7 FDA reports)
MENORRHAGIA ( 7 FDA reports)
MENSTRUATION IRREGULAR ( 7 FDA reports)
METASTATIC PAIN ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MOUTH CYST ( 7 FDA reports)
MUCOSAL ULCERATION ( 7 FDA reports)
MULTIPLE DRUG OVERDOSE ( 7 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
NEOPLASM ( 7 FDA reports)
NEURITIS ( 7 FDA reports)
NEUROPATHIC ARTHROPATHY ( 7 FDA reports)
ONYCHALGIA ( 7 FDA reports)
OPEN REDUCTION OF FRACTURE ( 7 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 7 FDA reports)
OROPHARYNGEAL SPASM ( 7 FDA reports)
OSTEOMALACIA ( 7 FDA reports)
OTITIS EXTERNA ( 7 FDA reports)
OTITIS MEDIA ACUTE ( 7 FDA reports)
OVARIAN DISORDER ( 7 FDA reports)
PANCREATIC ATROPHY ( 7 FDA reports)
PARKINSONISM ( 7 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 7 FDA reports)
PELVIC FLUID COLLECTION ( 7 FDA reports)
PERICARDIAL HAEMORRHAGE ( 7 FDA reports)
PERIORBITAL HAEMORRHAGE ( 7 FDA reports)
PIGMENTATION DISORDER ( 7 FDA reports)
PLEURECTOMY ( 7 FDA reports)
PNEUMONIA ASPERGILLUS ( 7 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 7 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 7 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 7 FDA reports)
PNEUMONITIS CHEMICAL ( 7 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 7 FDA reports)
POSTERIOR CAPSULE OPACIFICATION ( 7 FDA reports)
PUPIL FIXED ( 7 FDA reports)
RED BLOOD CELLS CSF POSITIVE ( 7 FDA reports)
RETINAL VEIN OCCLUSION ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SKIN NECROSIS ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
SPINAL LAMINECTOMY ( 7 FDA reports)
STARING ( 7 FDA reports)
STASIS DERMATITIS ( 7 FDA reports)
STENOTROPHOMONAS INFECTION ( 7 FDA reports)
STRIDOR ( 7 FDA reports)
ABDOMINAL OPERATION ( 6 FDA reports)
ABSCESS INTESTINAL ( 6 FDA reports)
ACCIDENT ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 6 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 6 FDA reports)
ADRENAL DISORDER ( 6 FDA reports)
ALOPECIA AREATA ( 6 FDA reports)
ALVEOLITIS ( 6 FDA reports)
ALVEOLOPLASTY ( 6 FDA reports)
ANAL ABSCESS ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
ANAL FISTULA ( 6 FDA reports)
ANORECTAL DISCOMFORT ( 6 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
APHONIA ( 6 FDA reports)
ASBESTOSIS ( 6 FDA reports)
ASEPTIC NECROSIS BONE ( 6 FDA reports)
ASPHYXIA ( 6 FDA reports)
AUTONOMIC NEUROPATHY ( 6 FDA reports)
BILE DUCT NECROSIS ( 6 FDA reports)
BILE DUCT STENOSIS ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BILIARY SEPSIS ( 6 FDA reports)
BIOPSY BONE MARROW ( 6 FDA reports)
BLADDER NECK OPERATION ( 6 FDA reports)
BLADDER PERFORATION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BONE FISTULA ( 6 FDA reports)
BONE FRAGMENTATION ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 6 FDA reports)
CANDIDA PNEUMONIA ( 6 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CATARACT CONGENITAL ( 6 FDA reports)
CATHETER SEPSIS ( 6 FDA reports)
CATHETER SITE HAEMORRHAGE ( 6 FDA reports)
CATHETERISATION VENOUS ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 6 FDA reports)
CEREBELLAR INFARCTION ( 6 FDA reports)
CNS VENTRICULITIS ( 6 FDA reports)
COLOBOMA ( 6 FDA reports)
COLON POLYPECTOMY ( 6 FDA reports)
COLONIC OBSTRUCTION ( 6 FDA reports)
COLONIC STENOSIS ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 6 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 6 FDA reports)
CORNEAL OPERATION ( 6 FDA reports)
CORNEAL TRANSPLANT ( 6 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
CRYOGLOBULINAEMIA ( 6 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 6 FDA reports)
CRYSTALLURIA ( 6 FDA reports)
CULTURE STOOL POSITIVE ( 6 FDA reports)
CUSHING'S SYNDROME ( 6 FDA reports)
CYCLOTHYMIC DISORDER ( 6 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DERMATOPHYTOSIS ( 6 FDA reports)
DEVICE RELATED SEPSIS ( 6 FDA reports)
DIABETIC COMA ( 6 FDA reports)
DISEASE COMPLICATION ( 6 FDA reports)
DRUG DISPENSING ERROR ( 6 FDA reports)
DRUG-INDUCED LIVER INJURY ( 6 FDA reports)
DUODENAL ULCER PERFORATION ( 6 FDA reports)
DUODENITIS ( 6 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 6 FDA reports)
ENCEPHALITIS POST VARICELLA ( 6 FDA reports)
ENTERITIS INFECTIOUS ( 6 FDA reports)
EROSIVE OESOPHAGITIS ( 6 FDA reports)
ERUCTATION ( 6 FDA reports)
ERYSIPELAS ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
FASCIITIS ( 6 FDA reports)
FEEDING TUBE COMPLICATION ( 6 FDA reports)
FLAT AFFECT ( 6 FDA reports)
FLUID IMBALANCE ( 6 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 6 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 6 FDA reports)
FRACTURE DISPLACEMENT ( 6 FDA reports)
GAMMOPATHY ( 6 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 6 FDA reports)
GENERALISED ANXIETY DISORDER ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
GINGIVECTOMY ( 6 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 6 FDA reports)
GLOSSITIS ( 6 FDA reports)
HAEMOGLOBIN ABNORMAL ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEMIANOPIA HOMONYMOUS ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HEPATITIS VIRAL ( 6 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 6 FDA reports)
HORDEOLUM ( 6 FDA reports)
HYPERAMYLASAEMIA ( 6 FDA reports)
HYPERTENSIVE HEART DISEASE ( 6 FDA reports)
HYPOPERFUSION ( 6 FDA reports)
HYPOPNOEA ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 6 FDA reports)
INADEQUATE ANALGESIA ( 6 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 6 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 6 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 6 FDA reports)
INTESTINAL HAEMORRHAGE ( 6 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 6 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 6 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 6 FDA reports)
IRON OVERLOAD ( 6 FDA reports)
JOINT DESTRUCTION ( 6 FDA reports)
JOINT SPRAIN ( 6 FDA reports)
JUGULAR VEIN THROMBOSIS ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LIFE SUPPORT ( 6 FDA reports)
LOSS OF LIBIDO ( 6 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
LUNG ABSCESS ( 6 FDA reports)
LUNG INJURY ( 6 FDA reports)
LYMPH NODE PAIN ( 6 FDA reports)
LYMPHOCELE ( 6 FDA reports)
MALIGNANT MELANOMA IN SITU ( 6 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 6 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 6 FDA reports)
MEDIASTINAL DISORDER ( 6 FDA reports)
METABOLIC ALKALOSIS ( 6 FDA reports)
METASTASES TO SKIN ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MONOCLONAL GAMMOPATHY ( 6 FDA reports)
MORAXELLA INFECTION ( 6 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 6 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 6 FDA reports)
NASAL VESTIBULITIS ( 6 FDA reports)
NEOPLASM RECURRENCE ( 6 FDA reports)
NERVE COMPRESSION ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
NEUROSIS ( 6 FDA reports)
NEUTROPENIC COLITIS ( 6 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 6 FDA reports)
NIKOLSKY'S SIGN ( 6 FDA reports)
NODAL RHYTHM ( 6 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 6 FDA reports)
OEDEMA MOUTH ( 6 FDA reports)
OESOPHAGEAL RUPTURE ( 6 FDA reports)
OESOPHAGEAL ULCER ( 6 FDA reports)
ORAL SOFT TISSUE DISORDER ( 6 FDA reports)
OXYGEN SUPPLEMENTATION ( 6 FDA reports)
PANCREATIC DISORDER ( 6 FDA reports)
PANCREATIC DUCT DILATATION ( 6 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 6 FDA reports)
PATHOLOGICAL GAMBLING ( 6 FDA reports)
PELVIC DISCOMFORT ( 6 FDA reports)
PELVIC PROLAPSE ( 6 FDA reports)
PERIORBITAL HAEMATOMA ( 6 FDA reports)
PERSEVERATION ( 6 FDA reports)
PNEUMATOSIS ( 6 FDA reports)
PNEUMONIA LEGIONELLA ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 6 FDA reports)
POSTNASAL DRIP ( 6 FDA reports)
PROTEUS INFECTION ( 6 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 6 FDA reports)
PTERYGIUM ( 6 FDA reports)
PULMONARY SEPSIS ( 6 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 6 FDA reports)
PYELONEPHRITIS ACUTE ( 6 FDA reports)
RADICULITIS LUMBOSACRAL ( 6 FDA reports)
RECTAL CANCER ( 6 FDA reports)
RED BLOOD CELL ABNORMALITY ( 6 FDA reports)
RENAL COLIC ( 6 FDA reports)
RENAL VEIN THROMBOSIS ( 6 FDA reports)
RESPIRATION ABNORMAL ( 6 FDA reports)
RESPIRATORY RATE DECREASED ( 6 FDA reports)
RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
RETINAL OEDEMA ( 6 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
SCAN ABNORMAL ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SENSATION OF HEAVINESS ( 6 FDA reports)
SHOULDER OPERATION ( 6 FDA reports)
SKIN EROSION ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SPLENECTOMY ( 6 FDA reports)
SPLENIC GRANULOMA ( 6 FDA reports)
SPLENIC LESION ( 6 FDA reports)
SPONDYLITIC MYELOPATHY ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
TALIPES ( 6 FDA reports)
TEARFULNESS ( 6 FDA reports)
TEETH BRITTLE ( 6 FDA reports)
TEMPORAL ARTERITIS ( 6 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 6 FDA reports)
TONGUE OEDEMA ( 6 FDA reports)
TONGUE ULCERATION ( 6 FDA reports)
TRACHEAL DEVIATION ( 6 FDA reports)
TUMOUR INVASION ( 6 FDA reports)
URETERIC OBSTRUCTION ( 6 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 6 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 6 FDA reports)
URINE ABNORMALITY ( 6 FDA reports)
URINE ANALYSIS ABNORMAL ( 6 FDA reports)
UTEROVAGINAL PROLAPSE ( 6 FDA reports)
VANISHING BILE DUCT SYNDROME ( 6 FDA reports)
VASOCONSTRICTION ( 6 FDA reports)
VENTRICULAR HYPOPLASIA ( 6 FDA reports)
VERTEBROPLASTY ( 6 FDA reports)
VIRAL DNA TEST POSITIVE ( 6 FDA reports)
VOCAL CORD PARESIS ( 6 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 6 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 6 FDA reports)
WEST NILE VIRAL INFECTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 6 FDA reports)
TESTICULAR PAIN ( 5 FDA reports)
TINEA VERSICOLOUR ( 5 FDA reports)
TONGUE ERUPTION ( 5 FDA reports)
TYPE 1 DIABETES MELLITUS ( 5 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 5 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINARY SEDIMENT ABNORMAL ( 5 FDA reports)
UTERINE ENLARGEMENT ( 5 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 5 FDA reports)
VASODILATATION ( 5 FDA reports)
VERTEBRAL ARTERY THROMBOSIS ( 5 FDA reports)
VERTIGO POSITIONAL ( 5 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
VITREOUS DETACHMENT ( 5 FDA reports)
WISDOM TEETH REMOVAL ( 5 FDA reports)
WOUND NECROSIS ( 5 FDA reports)
WOUND TREATMENT ( 5 FDA reports)
ABDOMINAL INFECTION ( 5 FDA reports)
ABDOMINAL SEPSIS ( 5 FDA reports)
ABNORMAL SENSATION IN EYE ( 5 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 5 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 5 FDA reports)
ACUTE POLYNEUROPATHY ( 5 FDA reports)
ADNEXA UTERI MASS ( 5 FDA reports)
ADRENAL ADENOMA ( 5 FDA reports)
ADVERSE REACTION ( 5 FDA reports)
ALCOHOL ABUSE ( 5 FDA reports)
AMENORRHOEA ( 5 FDA reports)
ANORECTAL DISORDER ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APPLICATION SITE IRRITATION ( 5 FDA reports)
APPLICATION SITE PAIN ( 5 FDA reports)
ARTHRITIS INFECTIVE ( 5 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 5 FDA reports)
AURA ( 5 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 5 FDA reports)
BASILAR MIGRAINE ( 5 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 5 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
BLOOD BLISTER ( 5 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 5 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 5 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 5 FDA reports)
BONE TRIMMING ( 5 FDA reports)
BRAIN CONTUSION ( 5 FDA reports)
BRAIN MIDLINE SHIFT ( 5 FDA reports)
BRAIN STEM SYNDROME ( 5 FDA reports)
BREAST LUMP REMOVAL ( 5 FDA reports)
BREATH ODOUR ( 5 FDA reports)
BRONCHITIS CHRONIC ( 5 FDA reports)
BULIMIA NERVOSA ( 5 FDA reports)
BUTTERFLY RASH ( 5 FDA reports)
CARDIAC AMYLOIDOSIS ( 5 FDA reports)
CARDIAC FAILURE CHRONIC ( 5 FDA reports)
CARDIAC FLUTTER ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CATHETER SITE SWELLING ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 5 FDA reports)
CEREBELLAR HAEMORRHAGE ( 5 FDA reports)
CEREBRAL THROMBOSIS ( 5 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 5 FDA reports)
CHOLANGITIS ACUTE ( 5 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 5 FDA reports)
CLONIC CONVULSION ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 5 FDA reports)
CORNEAL GRAFT REJECTION ( 5 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 5 FDA reports)
COTARD'S SYNDROME ( 5 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 5 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 5 FDA reports)
CUTIS LAXA ( 5 FDA reports)
CYTOTOXIC OEDEMA ( 5 FDA reports)
DELUSION OF GRANDEUR ( 5 FDA reports)
DENTAL IMPLANTATION ( 5 FDA reports)
DEVICE MALFUNCTION ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DISINHIBITION ( 5 FDA reports)
DOUBLE OUTLET RIGHT VENTRICLE ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DYSTHYMIC DISORDER ( 5 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 5 FDA reports)
ELECTROLYTE DEPLETION ( 5 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 5 FDA reports)
ENTEROBACTER BACTERAEMIA ( 5 FDA reports)
ENTEROBACTER PNEUMONIA ( 5 FDA reports)
ERYTHEMA INFECTIOSUM ( 5 FDA reports)
ESCHERICHIA TEST POSITIVE ( 5 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 5 FDA reports)
EYE INFECTION FUNGAL ( 5 FDA reports)
FAECES PALE ( 5 FDA reports)
FANCONI SYNDROME ACQUIRED ( 5 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 5 FDA reports)
FUNGAL TEST POSITIVE ( 5 FDA reports)
FUNGUS CULTURE POSITIVE ( 5 FDA reports)
GASTROENTERITIS RADIATION ( 5 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 5 FDA reports)
GASTROINTESTINAL TRACT IRRITATION ( 5 FDA reports)
HAEMANGIOMA ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMARTHROSIS ( 5 FDA reports)
HAEMATOPOIETIC STEM CELL MOBILISATION ( 5 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 5 FDA reports)
HAEMORRHOID OPERATION ( 5 FDA reports)
HAEMOTHORAX ( 5 FDA reports)
HEART INJURY ( 5 FDA reports)
HEAT STROKE ( 5 FDA reports)
HEPATIC ARTERY OCCLUSION ( 5 FDA reports)
HEPATIC SIDEROSIS ( 5 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 5 FDA reports)
HERPES OPHTHALMIC ( 5 FDA reports)
HERPES ZOSTER OTICUS ( 5 FDA reports)
HYDROURETER ( 5 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 5 FDA reports)
HYPERMAGNESAEMIA ( 5 FDA reports)
HYPERPARATHYROIDISM ( 5 FDA reports)
HYPERPHAGIA ( 5 FDA reports)
HYPERTROPHY OF TONGUE PAPILLAE ( 5 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 5 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 5 FDA reports)
INCISION SITE HAEMORRHAGE ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
INFECTIOUS DISEASE CARRIER ( 5 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 5 FDA reports)
INFUSION SITE HAEMATOMA ( 5 FDA reports)
INFUSION SITE SWELLING ( 5 FDA reports)
INGUINAL HERNIA REPAIR ( 5 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
JC VIRUS TEST POSITIVE ( 5 FDA reports)
JOINT ABSCESS ( 5 FDA reports)
LARYNGEAL HAEMORRHAGE ( 5 FDA reports)
LIMB DEFORMITY ( 5 FDA reports)
LIPODYSTROPHY ACQUIRED ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 5 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 5 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 5 FDA reports)
MEGAKARYOCYTES INCREASED ( 5 FDA reports)
MEIBOMIANITIS ( 5 FDA reports)
MENINGISM ( 5 FDA reports)
MENINGITIS HERPES ( 5 FDA reports)
MENINGORRHAGIA ( 5 FDA reports)
METAPLASIA ( 5 FDA reports)
METHAEMOGLOBINAEMIA ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MITRAL VALVE STENOSIS ( 5 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 5 FDA reports)
MUSCLE FATIGUE ( 5 FDA reports)
MUSCLE SPASTICITY ( 5 FDA reports)
MYELOFIBROSIS ( 5 FDA reports)
MYOPATHY STEROID ( 5 FDA reports)
NAIL DISORDER ( 5 FDA reports)
NASAL OBSTRUCTION ( 5 FDA reports)
NEGATIVISM ( 5 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 5 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 5 FDA reports)
NERVE INJURY ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 5 FDA reports)
OEDEMA MUCOSAL ( 5 FDA reports)
OESOPHAGEAL DISORDER ( 5 FDA reports)
OPEN ANGLE GLAUCOMA ( 5 FDA reports)
OPTIC ATROPHY ( 5 FDA reports)
OPTIC NEUROPATHY ( 5 FDA reports)
ORCHITIS ( 5 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 5 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
OVARIAN MASS ( 5 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 5 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 5 FDA reports)
PATELLA FRACTURE ( 5 FDA reports)
PEMPHIGOID ( 5 FDA reports)
PERIDIVERTICULAR ABSCESS ( 5 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 5 FDA reports)
PINGUECULA ( 5 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POLYPECTOMY ( 5 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 5 FDA reports)
POST PROCEDURAL BILE LEAK ( 5 FDA reports)
POST THROMBOTIC SYNDROME ( 5 FDA reports)
POSTICTAL STATE ( 5 FDA reports)
POSTOPERATIVE ILEUS ( 5 FDA reports)
POSTURING ( 5 FDA reports)
PRE-ECLAMPSIA ( 5 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 5 FDA reports)
PROPOFOL INFUSION SYNDROME ( 5 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 5 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 5 FDA reports)
PULPITIS DENTAL ( 5 FDA reports)
QUADRIPARESIS ( 5 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
RELAPSING FEVER ( 5 FDA reports)
RENAL STONE REMOVAL ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
RESORPTION BONE INCREASED ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 5 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
RHINOVIRUS INFECTION ( 5 FDA reports)
RIB DEFORMITY ( 5 FDA reports)
RIGHT ATRIAL DILATATION ( 5 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
ROTAVIRUS INFECTION ( 5 FDA reports)
SCLERITIS ( 5 FDA reports)
SHOULDER DEFORMITY ( 5 FDA reports)
SICCA SYNDROME ( 5 FDA reports)
SIMPLE PARTIAL SEIZURES ( 5 FDA reports)
SPINA BIFIDA OCCULTA ( 5 FDA reports)
STENT OCCLUSION ( 5 FDA reports)
STRABISMUS ( 5 FDA reports)
STRESS SYMPTOMS ( 5 FDA reports)
SUNBURN ( 5 FDA reports)
ABDOMINAL ADHESIONS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 4 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALCOHOL POISONING ( 4 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 4 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 4 FDA reports)
ANGIOMYOLIPOMA ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANOXIC ENCEPHALOPATHY ( 4 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
APPENDICECTOMY ( 4 FDA reports)
APPLICATION SITE SWELLING ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ASTEATOSIS ( 4 FDA reports)
B-CELL LYMPHOMA STAGE III ( 4 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BIOPSY SKIN ABNORMAL ( 4 FDA reports)
BLADDER PAIN ( 4 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 4 FDA reports)
BLINDNESS CORTICAL ( 4 FDA reports)
BLOOD BICARBONATE INCREASED ( 4 FDA reports)
BLOOD LACTIC ACID INCREASED ( 4 FDA reports)
BLOOD OSMOLARITY INCREASED ( 4 FDA reports)
BLOOD PH INCREASED ( 4 FDA reports)
BLOOD URIC ACID DECREASED ( 4 FDA reports)
BLOODY DISCHARGE ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BONE ABSCESS ( 4 FDA reports)
BONE DEFORMITY ( 4 FDA reports)
BONE DENSITY INCREASED ( 4 FDA reports)
BOWEL SOUNDS ABNORMAL ( 4 FDA reports)
BRAIN NEOPLASM ( 4 FDA reports)
BRAIN STEM HAEMORRHAGE ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BREAST CANCER IN SITU ( 4 FDA reports)
BREAST CANCER STAGE I ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BREAST RECONSTRUCTION ( 4 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
CAESAREAN SECTION ( 4 FDA reports)
CALCIUM IONISED DECREASED ( 4 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 4 FDA reports)
CAPNOCYTOPHAGIA INFECTION ( 4 FDA reports)
CARCINOMA IN SITU ( 4 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
CAROTID ARTERY INSUFFICIENCY ( 4 FDA reports)
CATATONIA ( 4 FDA reports)
CERVIX CARCINOMA STAGE 0 ( 4 FDA reports)
CHEST WALL MASS ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHONDROCALCINOSIS ( 4 FDA reports)
CHORIOAMNIONITIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 4 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 4 FDA reports)
COAGULATION TEST ABNORMAL ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COLONOSCOPY ABNORMAL ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
CONGENITAL DIAPHRAGMATIC HERNIA ( 4 FDA reports)
CONGENITAL MITRAL VALVE STENOSIS ( 4 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CORNEAL DISORDER ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORNEAL SCAR ( 4 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CULTURE THROAT POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 4 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 4 FDA reports)
CYTOREDUCTIVE SURGERY ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DEFAECATION URGENCY ( 4 FDA reports)
DENTAL CARE ( 4 FDA reports)
DEVICE INEFFECTIVE ( 4 FDA reports)
DIABETIC RETINOPATHY ( 4 FDA reports)
DIPLEGIA ( 4 FDA reports)
DRUG DETOXIFICATION ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
DYSLIPIDAEMIA ( 4 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 4 FDA reports)
EAR DISORDER ( 4 FDA reports)
ECTHYMA ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
EMBOLISM VENOUS ( 4 FDA reports)
ENCEPHALOMYELITIS ( 4 FDA reports)
ENDOTOXIC SHOCK ( 4 FDA reports)
ENERGY INCREASED ( 4 FDA reports)
ENTHESOPATHY ( 4 FDA reports)
EYE NAEVUS ( 4 FDA reports)
EYE OPERATION ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FEBRILE CONVULSION ( 4 FDA reports)
FEELING DRUNK ( 4 FDA reports)
FINGER DEFORMITY ( 4 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GALLBLADDER POLYP ( 4 FDA reports)
GALLOP RHYTHM PRESENT ( 4 FDA reports)
GASTRIC HAEMORRHAGE ( 4 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 4 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 4 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 4 FDA reports)
GASTROSTOMY TUBE INSERTION ( 4 FDA reports)
GINGIVAL OPERATION ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMATOSPERMIA ( 4 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HEART SOUNDS ABNORMAL ( 4 FDA reports)
HELICOBACTER SEPSIS ( 4 FDA reports)
HEPATIC NEOPLASM ( 4 FDA reports)
HEPATIC PAIN ( 4 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 4 FDA reports)
HERPES DERMATITIS ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
HIRSUTISM ( 4 FDA reports)
HISTOPLASMOSIS ( 4 FDA reports)
HORMONE LEVEL ABNORMAL ( 4 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 4 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPEROSMOLAR STATE ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
INCISION SITE COMPLICATION ( 4 FDA reports)
INCISION SITE HAEMATOMA ( 4 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 4 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
INJECTION SITE URTICARIA ( 4 FDA reports)
INTERMITTENT CLAUDICATION ( 4 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 4 FDA reports)
INTESTINAL RESECTION ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
JOINT ARTHROPLASTY ( 4 FDA reports)
JUGULAR VEIN DISTENSION ( 4 FDA reports)
KERATOACANTHOMA ( 4 FDA reports)
KERATOSIS FOLLICULAR ( 4 FDA reports)
KLEBSIELLA TEST POSITIVE ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LABILE BLOOD PRESSURE ( 4 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 4 FDA reports)
LIP DISORDER ( 4 FDA reports)
LIP HAEMORRHAGE ( 4 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
MADAROSIS ( 4 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 4 FDA reports)
MEDIASTINITIS ( 4 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 4 FDA reports)
METASTASES TO PLEURA ( 4 FDA reports)
MICROCOCCUS INFECTION ( 4 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCLE INJURY ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 4 FDA reports)
MYOCARDIAL FIBROSIS ( 4 FDA reports)
MYOPERICARDITIS ( 4 FDA reports)
NASAL SEPTUM PERFORATION ( 4 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 4 FDA reports)
NEONATAL PNEUMONIA ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NERVE ROOT INJURY LUMBAR ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
OEDEMA GENITAL ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 4 FDA reports)
OPEN WOUND ( 4 FDA reports)
OPHTHALMOPLEGIA ( 4 FDA reports)
ORAL DISCHARGE ( 4 FDA reports)
OSTECTOMY ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PANCREATIC PSEUDOCYST ( 4 FDA reports)
PAST-POINTING ( 4 FDA reports)
PERICARDIAL DISEASE ( 4 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 4 FDA reports)
PERIODONTAL OPERATION ( 4 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHARYNGEAL INFLAMMATION ( 4 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 4 FDA reports)
PNEUMONIA HAEMOPHILUS ( 4 FDA reports)
POLYDACTYLY ( 4 FDA reports)
POST POLIO SYNDROME ( 4 FDA reports)
POST PROCEDURAL URINE LEAK ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PULMONARY VALVE STENOSIS CONGENITAL ( 4 FDA reports)
PUSTULAR PSORIASIS ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RED BLOOD CELLS URINE ( 4 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 4 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 4 FDA reports)
RENAL AMYLOIDOSIS ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RENAL NEOPLASM ( 4 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 4 FDA reports)
RETICULOCYTE COUNT INCREASED ( 4 FDA reports)
RETINOIC ACID SYNDROME ( 4 FDA reports)
RETROVIRAL INFECTION ( 4 FDA reports)
SENSATION OF PRESSURE ( 4 FDA reports)
SINGLE UMBILICAL ARTERY ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SKIN DEPIGMENTATION ( 4 FDA reports)
SKIN DESQUAMATION ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
SMALL INTESTINE CARCINOMA ( 4 FDA reports)
SPINAL CLAUDICATION ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPINAL CORD OPERATION ( 4 FDA reports)
SPINAL HAEMANGIOMA ( 4 FDA reports)
SPINAL OPERATION ( 4 FDA reports)
STENT REMOVAL ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
STRONGYLOIDIASIS ( 4 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 4 FDA reports)
T-CELL LYMPHOMA STAGE III ( 4 FDA reports)
TENDON GRAFT ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE DRY ( 4 FDA reports)
TRACHEAL INJURY ( 4 FDA reports)
TRIGEMINAL NEURALGIA ( 4 FDA reports)
TUMOUR PAIN ( 4 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 4 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 4 FDA reports)
URETHRAL OBSTRUCTION ( 4 FDA reports)
URINARY TRACT INFECTION VIRAL ( 4 FDA reports)
URINE AMPHETAMINE POSITIVE ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
UTERINE MASS ( 4 FDA reports)
VAGINAL CANDIDIASIS ( 4 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 4 FDA reports)
VASCULAR OPERATION ( 4 FDA reports)
VASCULAR STENOSIS ( 4 FDA reports)
VASCULITIS NECROTISING ( 4 FDA reports)
VEILLONELLA INFECTION ( 4 FDA reports)
VENOUS HAEMORRHAGE ( 4 FDA reports)
VENOUS STENT INSERTION ( 4 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 4 FDA reports)
VESICAL FISTULA ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VIROLOGIC FAILURE ( 4 FDA reports)
VIRUS CULTURE POSITIVE ( 4 FDA reports)
VITRITIS ( 4 FDA reports)
VOCAL CORD THICKENING ( 4 FDA reports)
VULVOVAGINAL DISCOMFORT ( 4 FDA reports)
VULVOVAGINAL PAIN ( 4 FDA reports)
WEIGHT BEARING DIFFICULTY ( 4 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 4 FDA reports)
WOUND DEBRIDEMENT ( 4 FDA reports)
WOUND EVISCERATION ( 4 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
TENOSYNOVITIS STENOSANS ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THALASSAEMIA ALPHA ( 3 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THYROID CANCER ( 3 FDA reports)
THYROID MASS ( 3 FDA reports)
TONGUE BITING ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TRACHEAL ULCER ( 3 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 3 FDA reports)
TRAUMATIC LUNG INJURY ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
ULCER HAEMORRHAGE ( 3 FDA reports)
URETERIC STENOSIS ( 3 FDA reports)
URINE OUTPUT INCREASED ( 3 FDA reports)
UTERINE DISORDER ( 3 FDA reports)
UTERINE STENOSIS ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VIRAL LABYRINTHITIS ( 3 FDA reports)
VIRAL VASCULITIS ( 3 FDA reports)
VITAL CAPACITY DECREASED ( 3 FDA reports)
VOCAL CORD POLYP ( 3 FDA reports)
VULVAL CANCER STAGE 0 ( 3 FDA reports)
VULVAR DYSPLASIA ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WEGENER'S GRANULOMATOSIS ( 3 FDA reports)
WHEELCHAIR USER ( 3 FDA reports)
WHITE BLOOD CELL ANALYSIS ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WOUND HAEMORRHAGE ( 3 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 3 FDA reports)
WRONG DRUG ADMINISTERED ( 3 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 3 FDA reports)
XANTHOCHROMIA ( 3 FDA reports)
YELLOW SKIN ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABSCESS FUNGAL ( 3 FDA reports)
ABULIA ( 3 FDA reports)
ACANTHOLYSIS ( 3 FDA reports)
ACINETOBACTER BACTERAEMIA ( 3 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 3 FDA reports)
ACQUIRED HAEMOPHILIA ( 3 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 3 FDA reports)
ACUTE PSYCHOSIS ( 3 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 3 FDA reports)
ADENOVIRAL HEPATITIS ( 3 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
ANKYLOGLOSSIA CONGENITAL ( 3 FDA reports)
ANOGENITAL DYSPLASIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC ANEURYSM RUPTURE ( 3 FDA reports)
AORTIC BRUIT ( 3 FDA reports)
AORTIC DILATATION ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE ERYTHEMA ( 3 FDA reports)
APPLICATION SITE RASH ( 3 FDA reports)
ARTERIAL RUPTURE ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 3 FDA reports)
ARTERY DISSECTION ( 3 FDA reports)
ASPERGILLOMA ( 3 FDA reports)
ASPERGILLOSIS ORAL ( 3 FDA reports)
ATHEROSCLEROSIS ( 3 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BACTERIAL TOXAEMIA ( 3 FDA reports)
BACTEROIDES TEST POSITIVE ( 3 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
BENIGN LUNG NEOPLASM ( 3 FDA reports)
BLADDER DIVERTICULUM ( 3 FDA reports)
BLADDER OBSTRUCTION ( 3 FDA reports)
BLAST CELL COUNT DECREASED ( 3 FDA reports)
BLAST CELLS PRESENT ( 3 FDA reports)
BLIGHTED OVUM ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD HIV RNA INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BODY MASS INDEX INCREASED ( 3 FDA reports)
BRADYPNOEA ( 3 FDA reports)
BRAIN COMPRESSION ( 3 FDA reports)
BRAIN MALFORMATION ( 3 FDA reports)
BRAIN SCAN ABNORMAL ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BRONCHIAL ULCERATION ( 3 FDA reports)
BRONCHOPULMONARY DISEASE ( 3 FDA reports)
BRONCHOSCOPY ABNORMAL ( 3 FDA reports)
BURKITT'S LYMPHOMA STAGE III ( 3 FDA reports)
CALCULUS URINARY ( 3 FDA reports)
CANDIDURIA ( 3 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CAROTID BRUIT ( 3 FDA reports)
CATARACT SUBCAPSULAR ( 3 FDA reports)
CATHETER SITE CELLULITIS ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
CELLULITIS GANGRENOUS ( 3 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 3 FDA reports)
CELLULITIS STREPTOCOCCAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBELLAR ATAXIA ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL CALCIFICATION ( 3 FDA reports)
CEREBROVASCULAR SPASM ( 3 FDA reports)
CHORIORETINOPATHY ( 3 FDA reports)
CHROMOSOME ABNORMALITY ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COLD AGGLUTININS POSITIVE ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COMPARTMENT SYNDROME ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 3 FDA reports)
CONGENITAL HAND MALFORMATION ( 3 FDA reports)
CONJUNCTIVAL OEDEMA ( 3 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 3 FDA reports)
COOMBS TEST POSITIVE ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORNEAL OPACITY CONGENITAL ( 3 FDA reports)
CORONAVIRUS TEST POSITIVE ( 3 FDA reports)
CORYNEBACTERIUM SEPSIS ( 3 FDA reports)
CRANIAL NERVE PARALYSIS ( 3 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 3 FDA reports)
CRYPTORCHISM ( 3 FDA reports)
CSF CULTURE POSITIVE ( 3 FDA reports)
CSF NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CYTOKINE STORM ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEAFNESS TRANSITORY ( 3 FDA reports)
DERMATITIS ACNEIFORM ( 3 FDA reports)
DEVICE BREAKAGE ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC EYE DISEASE ( 3 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 3 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 3 FDA reports)
DRUG EFFECT INCREASED ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
ECHOLALIA ( 3 FDA reports)
ECZEMA ASTEATOTIC ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 3 FDA reports)
ENCEPHALITIS TOXIC ( 3 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 3 FDA reports)
ENDOMETRIOSIS ( 3 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 3 FDA reports)
ENTEROCUTANEOUS FISTULA ( 3 FDA reports)
EROSIVE DUODENITIS ( 3 FDA reports)
ERYTHEMA NODOSUM ( 3 FDA reports)
EXCITABILITY ( 3 FDA reports)
EYE INFECTION TOXOPLASMAL ( 3 FDA reports)
EYE INFECTION VIRAL ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACE INJURY ( 3 FDA reports)
FACIAL NEURALGIA ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
FEAR OF DISEASE ( 3 FDA reports)
FEBRILE BONE MARROW APLASIA ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FIBRINOUS BRONCHITIS ( 3 FDA reports)
FOETAL HEART RATE ABNORMAL ( 3 FDA reports)
FOLATE DEFICIENCY ( 3 FDA reports)
FOOT AMPUTATION ( 3 FDA reports)
FUNISITIS ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 3 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 3 FDA reports)
GENITAL DISORDER FEMALE ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GOUTY ARTHRITIS ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
GRANDIOSITY ( 3 FDA reports)
GRANULOCYTE COUNT INCREASED ( 3 FDA reports)
GRANULOCYTOSIS ( 3 FDA reports)
HAEMANGIOMA OF SPLEEN ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGIC INFARCTION ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATIC TRAUMA ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HEPATORENAL FAILURE ( 3 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 3 FDA reports)
HERNIA REPAIR ( 3 FDA reports)
HERPES SEPSIS ( 3 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 3 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 3 FDA reports)
HOSTILITY ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYPERADRENALISM ( 3 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 3 FDA reports)
HYPERCHROMASIA ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPERTROPHY ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
HYPOTHERMIA NEONATAL ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
INCISION SITE PAIN ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INFLUENZA B VIRUS TEST POSITIVE ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
INFUSION SITE EXTRAVASATION ( 3 FDA reports)
INFUSION SITE INFECTION ( 3 FDA reports)
INJECTION SITE EXTRAVASATION ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INJECTION SITE VESICLES ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
KARNOFSKY SCALE WORSENED ( 3 FDA reports)
KERATOMILEUSIS ( 3 FDA reports)
LABOUR COMPLICATION ( 3 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 3 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIGAMENT PAIN ( 3 FDA reports)
LINEAR IGA DISEASE ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPOATROPHY ( 3 FDA reports)
LIVER TENDERNESS ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LUNG TRANSPLANT REJECTION ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPH NODE CALCIFICATION ( 3 FDA reports)
LYMPHATIC DISORDER ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 3 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 3 FDA reports)
MALIGNANT HYPERTENSION ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MANTLE CELL LYMPHOMA RECURRENT ( 3 FDA reports)
MASKED FACIES ( 3 FDA reports)
MEAN CELL VOLUME DECREASED ( 3 FDA reports)
MEGACOLON ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
METAMORPHOPSIA ( 3 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 3 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 3 FDA reports)
MICROCYTIC ANAEMIA ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 3 FDA reports)
MUCORMYCOSIS ( 3 FDA reports)
MUCOSAL DRYNESS ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUCOSAL HAEMORRHAGE ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MUSCLE ENZYME INCREASED ( 3 FDA reports)
MUSCLE HAEMORRHAGE ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 3 FDA reports)
NAIL INFECTION ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEONATAL ASPIRATION ( 3 FDA reports)
NEPHRECTOMY ( 3 FDA reports)
NEUROBLASTOMA RECURRENT ( 3 FDA reports)
NEURODEGENERATIVE DISORDER ( 3 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 3 FDA reports)
NEUROPATHIC PAIN ( 3 FDA reports)
NEUROSYPHILIS ( 3 FDA reports)
NEUTROPHIL COUNT ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
NUCHAL RIGIDITY ( 3 FDA reports)
OBSESSIVE THOUGHTS ( 3 FDA reports)
OBSTRUCTIVE UROPATHY ( 3 FDA reports)
OCULAR VASCULITIS ( 3 FDA reports)
OESOPHAGEAL MUCOSAL HYPERPLASIA ( 3 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
ORAL DYSAESTHESIA ( 3 FDA reports)
ORAL MUCOSA ATROPHY ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
ORAL MUCOSAL DISORDER ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
OROPHARYNGEAL SWELLING ( 3 FDA reports)
ORTHODONTIC APPLIANCE USER ( 3 FDA reports)
OSTEOMYELITIS ACUTE ( 3 FDA reports)
OSTEOSYNTHESIS ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
OXYGEN SATURATION ABNORMAL ( 3 FDA reports)
PAINFUL RESPIRATION ( 3 FDA reports)
PALMAR ERYTHEMA ( 3 FDA reports)
PANCREATIC DUCT OBSTRUCTION ( 3 FDA reports)
PANCREATIC ENZYMES INCREASED ( 3 FDA reports)
PANCREATIC MASS ( 3 FDA reports)
PANIC REACTION ( 3 FDA reports)
PAPILLOMA VIRAL INFECTION ( 3 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 3 FDA reports)
PARKINSON'S DISEASE ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PCO2 INCREASED ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERITONEAL DIALYSIS ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 3 FDA reports)
PLEOCYTOSIS ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PLEURAL INFECTION ( 3 FDA reports)
PLEURAL RUB ( 3 FDA reports)
PNEUMATURIA ( 3 FDA reports)
PNEUMOCOCCAL INFECTION ( 3 FDA reports)
PNEUMONIA NECROTISING ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
POIKILODERMA ( 3 FDA reports)
POROCARCINOMA ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST PROCEDURAL INFECTION ( 3 FDA reports)
POST PROCEDURAL PAIN ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 3 FDA reports)
PRESSURE OF SPEECH ( 3 FDA reports)
PROCEDURAL HYPOTENSION ( 3 FDA reports)
PROGESTERONE DECREASED ( 3 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 3 FDA reports)
PULMONARY CAVITATION ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
PULSE ABNORMAL ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL SALT-WASTING SYNDROME ( 3 FDA reports)
RENAL VESSEL DISORDER ( 3 FDA reports)
REPETITIVE STRAIN INJURY ( 3 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 3 FDA reports)
RESPIRATORY MONILIASIS ( 3 FDA reports)
RESPIRATORY MUSCLE WEAKNESS ( 3 FDA reports)
RETINAL ARTERY THROMBOSIS ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 3 FDA reports)
RETINAL VASCULITIS ( 3 FDA reports)
RETROGRADE AMNESIA ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE DECREASED ( 3 FDA reports)
SALPINGO-OOPHORECTOMY ( 3 FDA reports)
SCHISTOSOMIASIS ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SEBACEOUS CYST EXCISION ( 3 FDA reports)
SECRETION DISCHARGE ( 3 FDA reports)
SEROSITIS ( 3 FDA reports)
SICK SINUS SYNDROME ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SINUS TARSI SYNDROME ( 3 FDA reports)
SINUSITIS BACTERIAL ( 3 FDA reports)
SKIN LESION EXCISION ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SKULL FRACTURED BASE ( 3 FDA reports)
SMEAR CERVIX ABNORMAL ( 3 FDA reports)
SPLENIC INJURY ( 3 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
SPUTUM INCREASED ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STEAL SYNDROME ( 3 FDA reports)
STRABISMUS CONGENITAL ( 3 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
5'NUCLEOTIDASE INCREASED ( 2 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 2 FDA reports)
ABNORMAL WITHDRAWAL BLEEDING ( 2 FDA reports)
ABSCESS BACTERIAL ( 2 FDA reports)
ACCESSORY SPLEEN ( 2 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 2 FDA reports)
ACUTE STRESS DISORDER ( 2 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 2 FDA reports)
AGITATION NEONATAL ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALLERGIC PHARYNGITIS ( 2 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 2 FDA reports)
AMYLASE INCREASED ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ANAL ULCER ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
ANIMAL BITE ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
ANORECTAL INFECTION BACTERIAL ( 2 FDA reports)
ANOTIA ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBS ANTIBODY ( 2 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
AORTA HYPOPLASIA ( 2 FDA reports)
APGAR SCORE LOW ( 2 FDA reports)
APPENDICEAL MUCOCOELE ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE INFLAMMATION ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
ARGININOSUCCINATE SYNTHETASE DEFICIENCY ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTHRITIS FUNGAL ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ARTICULAR CALCIFICATION ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 2 FDA reports)
ATHETOSIS ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
AUTISM ( 2 FDA reports)
AUTOIMMUNE NEUROPATHY ( 2 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AXILLARY MASS ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BANDAEMIA ( 2 FDA reports)
BICYTOPENIA ( 2 FDA reports)
BILIARY CANCER METASTATIC ( 2 FDA reports)
BILIARY CYST ( 2 FDA reports)
BILIARY ISCHAEMIA ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BIOPSY BREAST ABNORMAL ( 2 FDA reports)
BIOPSY ENDOMETRIUM ABNORMAL ( 2 FDA reports)
BLAST CELL PROLIFERATION ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 2 FDA reports)
BLOOD HOMOCYSTEINE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 2 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 2 FDA reports)
BLOOD STEM CELL HARVEST FAILURE ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BONE MARROW ISCHAEMIA ( 2 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 2 FDA reports)
BONE MARROW NECROSIS ( 2 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BREAST DISCOMFORT ( 2 FDA reports)
BRONCHIAL FISTULA ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 2 FDA reports)
BRONCHOSCOPY NORMAL ( 2 FDA reports)
C-REACTIVE PROTEIN ( 2 FDA reports)
CAMPYLOBACTER INFECTION ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC HYPERTROPHY ( 2 FDA reports)
CARDIAC INFECTION ( 2 FDA reports)
CARDIOVASCULAR DECONDITIONING ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CAROTID ARTERY THROMBOSIS ( 2 FDA reports)
CAROTIDYNIA ( 2 FDA reports)
CATABOLIC STATE ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CATHETER CULTURE POSITIVE ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
CATHETER THROMBOSIS ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 2 FDA reports)
CELL MARKER INCREASED ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 2 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 2 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
CERVIX DISORDER ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHIMERISM ( 2 FDA reports)
CHLOROMA ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHONDROMA ( 2 FDA reports)
CHORDAE TENDINAE RUPTURE ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CITROBACTER SEPSIS ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
COCCIDIOIDOMYCOSIS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COLON CANCER STAGE 0 ( 2 FDA reports)
COLORECTAL CANCER METASTATIC ( 2 FDA reports)
COMMUNITY ACQUIRED INFECTION ( 2 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 2 FDA reports)
CONGENITAL ANAEMIA ( 2 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 2 FDA reports)
CONGENITAL NAIL DISORDER ( 2 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 2 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 2 FDA reports)
CORNEAL ENDOTHELIITIS ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
CORONA VIRUS INFECTION ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
CRANIAL SUTURES WIDENING ( 2 FDA reports)
CRANIOSYNOSTOSIS ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CRYOFIBRINOGENAEMIA ( 2 FDA reports)
CRYSTAL URINE ( 2 FDA reports)
CSF GLUCOSE ABNORMAL ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 2 FDA reports)
CULTURE TISSUE SPECIMEN POSITIVE ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DELIRIUM TREMENS ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DELUSIONAL PERCEPTION ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DESCEMET'S MEMBRANE DISORDER ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIABETIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIARRHOEA INFECTIOUS ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
DIGITAL ULCER ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG LEVEL CHANGED ( 2 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DRY GANGRENE ( 2 FDA reports)
DUODENITIS HAEMORRHAGIC ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMBOLISM INFECTIVE ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENCEPHALITIS ALLERGIC ( 2 FDA reports)
ENCEPHALITIS FUNGAL ( 2 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 2 FDA reports)
ENDOLYMPHATIC HYDROPS ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENDOTOXAEMIA ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
EPHELIDES ( 2 FDA reports)
EPIDERMAL NAEVUS ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
ERYTHROMELALGIA ( 2 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 2 FDA reports)
EUSTACHIAN TUBE DISORDER ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FAECAL VOLUME INCREASED ( 2 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR OF DEATH ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
FOETAL MALFORMATION ( 2 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III RECURRENT ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FRACTURED COCCYX ( 2 FDA reports)
FRONTAL SINUS OPERATIONS ( 2 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 2 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
FUNGAL PERITONITIS ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC CANCER RECURRENT ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 2 FDA reports)
GLARE ( 2 FDA reports)
GLOSSECTOMY ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
GRAM STAIN POSITIVE ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GRIEF REACTION ( 2 FDA reports)
GRIMACING ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 2 FDA reports)
HAEMOPHILUS SEPSIS ( 2 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 2 FDA reports)
HAEMORRHAGE URINARY TRACT ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAIR COLOUR CHANGES ( 2 FDA reports)
HAIR DISORDER ( 2 FDA reports)
HALO VISION ( 2 FDA reports)
HAND DEFORMITY ( 2 FDA reports)
HAPTOGLOBIN ABNORMAL ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HELICOBACTER TEST POSITIVE ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEMISENSORY NEGLECT ( 2 FDA reports)
HEPATIC ARTERY STENOSIS ( 2 FDA reports)
HEPATIC CALCIFICATION ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATITIS B CORE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIBODY POSITIVE ( 2 FDA reports)
HEPATITIS C RNA POSITIVE ( 2 FDA reports)
HERNIAL EVENTRATION ( 2 FDA reports)
HERPES PHARYNGITIS ( 2 FDA reports)
HERPES SIMPLEX DNA TEST POSITIVE ( 2 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 2 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 2 FDA reports)
HODGKIN'S DISEASE REFRACTORY ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 2 FDA reports)
HYPERKINESIA ( 2 FDA reports)
HYPOGEUSIA ( 2 FDA reports)
HYPOPYON ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
IIIRD NERVE PARALYSIS ( 2 FDA reports)
ILIAC ARTERY STENOSIS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INCISIONAL HERNIA ( 2 FDA reports)
INCLUSION BODY MYOSITIS ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 2 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE PAIN ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INGUINAL MASS ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTERTRIGO CANDIDA ( 2 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 2 FDA reports)
INTRACRANIAL HAEMATOMA ( 2 FDA reports)
INTRACRANIAL HYPOTENSION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
INTRAUTERINE INFECTION ( 2 FDA reports)
IRIS DISORDER ( 2 FDA reports)
ISCHAEMIC NEUROPATHY ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
KERATITIS INTERSTITIAL ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 2 FDA reports)
LAPAROSCOPIC STERILISATION ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LATEX ALLERGY ( 2 FDA reports)
LAZINESS ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEIOMYOSARCOMA ( 2 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 2 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 2 FDA reports)
LEUKOSTASIS ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LIGHT CHAIN DISEASE ( 2 FDA reports)
LIMB MALFORMATION ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP EXFOLIATION ( 2 FDA reports)
LIP INFECTION ( 2 FDA reports)
LIPIDS ABNORMAL ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LIPOMA OF BREAST ( 2 FDA reports)
LIPOMATOSIS ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LIVE BIRTH ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOW BIRTH WEIGHT BABY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 2 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHADENITIS FUNGAL ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 2 FDA reports)
LYMPHOHISTIOCYTOSIS ( 2 FDA reports)
LYMPHOMA TRANSFORMATION ( 2 FDA reports)
MALIGNANT PALATE NEOPLASM ( 2 FDA reports)
MANTLE CELL LYMPHOMA REFRACTORY ( 2 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 2 FDA reports)
MEASLES ( 2 FDA reports)
MECONIUM ABNORMAL ( 2 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENINGITIS FUNGAL ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 2 FDA reports)
MENOPAUSAL SYMPTOMS ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO BONE MARROW ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO PANCREAS ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTASES TO SPLEEN ( 2 FDA reports)
MICROGNATHIA ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MORBID THOUGHTS ( 2 FDA reports)
MUCOSAL DISCOLOURATION ( 2 FDA reports)
MUCOSAL INFECTION ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
NASAL CAVITY MASS ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NASAL MUCOSAL DISORDER ( 2 FDA reports)
NECROSIS ISCHAEMIC ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NECROTISING OESOPHAGITIS ( 2 FDA reports)
NEISSERIA INFECTION ( 2 FDA reports)
NEONATAL MUCOCUTANEOUS HERPES SIMPLEX ( 2 FDA reports)
NEUROENDOCRINE TUMOUR ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
NIPPLE DISORDER ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NO ADVERSE EFFECT ( 2 FDA reports)
NODAL OSTEOARTHRITIS ( 2 FDA reports)
NODULE ON EXTREMITY ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 2 FDA reports)
OESOPHAGEAL ATRESIA ( 2 FDA reports)
OESTROGEN DEFICIENCY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL PRURITUS ( 2 FDA reports)
ORTHOSIS USER ( 2 FDA reports)
ORTHOSTATIC INTOLERANCE ( 2 FDA reports)
OSTEOCHONDROSIS ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
PACHYMENINGITIS ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PAPILLOMA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PENICILLIOSIS ( 2 FDA reports)
PENILE DISCHARGE ( 2 FDA reports)
PENILE OEDEMA ( 2 FDA reports)
PERICARDITIS FUNGAL ( 2 FDA reports)
PERIOSTITIS ( 2 FDA reports)
PERIPHERAL NERVE INJURY ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PERITONEAL ADHESIONS ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHLEBITIS INFECTIVE ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PHOTODYNAMIC THERAPY ( 2 FDA reports)
PHYSIOTHERAPY ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLACENTAL DISORDER ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLASMABLASTIC LYMPHOMA ( 2 FDA reports)
PLATELET DESTRUCTION INCREASED ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL INFECTION BACTERIAL ( 2 FDA reports)
PNEUMONIA CHLAMYDIAL ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 2 FDA reports)
POLYCHROMASIA ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PREMATURE EJACULATION ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 2 FDA reports)
PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PROCTITIS ( 2 FDA reports)
PROCTITIS HERPES ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROSTATECTOMY ( 2 FDA reports)
PSITTACOSIS ( 2 FDA reports)
PTERYGIUM COLLI ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
PULMONARY HYPOPLASIA ( 2 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 2 FDA reports)
PUTAMEN HAEMORRHAGE ( 2 FDA reports)
PYODERMA ( 2 FDA reports)
RADIATION MUCOSITIS ( 2 FDA reports)
RADIATION NEUROPATHY ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RECTAL ABSCESS ( 2 FDA reports)
RECTAL CANCER STAGE 0 ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SPHEROCYTES PRESENT ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 2 FDA reports)
RED MAN SYNDROME ( 2 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL HYPERTENSION ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RESPIRATORY PARALYSIS ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RETICULOCYTOPENIA ( 2 FDA reports)
RETINAL DEPOSITS ( 2 FDA reports)
RETINAL INFILTRATES ( 2 FDA reports)
RETINAL INJURY ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETROGNATHIA ( 2 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
RHINITIS ATROPHIC ( 2 FDA reports)
RHYTHM IDIOVENTRICULAR ( 2 FDA reports)
ROTAVIRUS TEST POSITIVE ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCEDOSPORIUM INFECTION ( 2 FDA reports)
SCHIZOPHRENIA ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
SCROTAL CYST ( 2 FDA reports)
SCROTAL DISORDER ( 2 FDA reports)
SCROTAL SWELLING ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEMEN ANALYSIS ABNORMAL ( 2 FDA reports)
SHOCK HYPOGLYCAEMIC ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SINUS PERFORATION ( 2 FDA reports)
SKELETAL INJURY ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
SMALL INTESTINE ULCER ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOFT TISSUE NECROSIS ( 2 FDA reports)
SOLITARY KIDNEY ( 2 FDA reports)
SOMATOFORM DISORDER ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPASTIC DIPLEGIA ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINA BIFIDA ( 2 FDA reports)
SPINAL CORPECTOMY ( 2 FDA reports)
SPINE MALFORMATION ( 2 FDA reports)
SPLEEN PALPABLE ( 2 FDA reports)
SPLENIC INFECTION ( 2 FDA reports)
STAPHYLOMA ( 2 FDA reports)
STENOTROPHOMONAS SEPSIS ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
STEROID THERAPY ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBDURAL EFFUSION ( 2 FDA reports)
SUBDURAL EMPYEMA ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
TENSION ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
TETANY ( 2 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THOUGHT INSERTION ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TINEA INFECTION ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TONSILLAR DISORDER ( 2 FDA reports)
TONSILLAR HYPERTROPHY ( 2 FDA reports)
TONSILLECTOMY ( 2 FDA reports)
TOTAL HYSTERECTOMY ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEITIS ( 2 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 2 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 2 FDA reports)
TRAUMATIC BRAIN INJURY ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TRICHOMONIASIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
ULNAR NERVE PALSY ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
UTERINE POLYP ( 2 FDA reports)
UTERINE RUPTURE ( 2 FDA reports)
UVULITIS ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VAGINAL CELLULITIS ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VAGINAL OEDEMA ( 2 FDA reports)
VARICELLA POST VACCINE ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR ENCEPHALOPATHY ( 2 FDA reports)
VASCULAR GRAFT COMPLICATION ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VENOUS LAKE ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
VENOUS PRESSURE JUGULAR DECREASED ( 2 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 2 FDA reports)
VERTEBRAL WEDGING ( 2 FDA reports)
VESICOURETERIC REFLUX ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRAL TEST POSITIVE ( 2 FDA reports)
VISCERAL OEDEMA ( 2 FDA reports)
VITAMIN D INCREASED ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
VITREOUS OPACITIES ( 2 FDA reports)
VOMITING NEONATAL ( 2 FDA reports)
VULVA CYST ( 2 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
WOUND DECOMPOSITION ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
SYDENHAM'S CHOREA ( 1 FDA reports)
SYNOVIAL FLUID WHITE BLOOD CELLS POSITIVE ( 1 FDA reports)
SYRINGE ISSUE ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
TACHYCARDIA FOETAL ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TARSAL TUNNEL SYNDROME ( 1 FDA reports)
TEMPERATURE REGULATION DISORDER ( 1 FDA reports)
TEMPORAL LOBE EPILEPSY ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TERATOGENICITY ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THALASSAEMIA BETA ( 1 FDA reports)
THALASSAEMIA TRAIT ( 1 FDA reports)
THERAPEUTIC EMBOLISATION ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY RESPONDER ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THYROID CANCER METASTATIC ( 1 FDA reports)
THYROID PAIN ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE ATROPHY ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TONSILLAR NEOPLASM ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOTAL BILE ACIDS INCREASED ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRACHEAL NEOPLASM ( 1 FDA reports)
TRACHEAL OBSTRUCTION ( 1 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRANSAMINASES DECREASED ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHOSTASIS SPINULOSA ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UMBILICAL ARTERY HYPOPLASIA ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
UPPER AIRWAY NECROSIS ( 1 FDA reports)
UPPER MOTOR NEURONE LESION ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETERIC DILATATION ( 1 FDA reports)
URETERITIS ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE BILIRUBIN INCREASED ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE ELECTROLYTES ABNORMAL ( 1 FDA reports)
URINE KETONE BODY ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE PROTEIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROGENITAL DISORDER ( 1 FDA reports)
UROGRAPHY ABNORMAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
VACCINATION FAILURE ( 1 FDA reports)
VAGINAL EXFOLIATION ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VAGINAL REMOVAL OF INTRAUTERINE FOREIGN BODY ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR GRAFT ( 1 FDA reports)
VASCULAR GRAFT OCCLUSION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VASOMOTOR RHINITIS ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VENOGRAM ABNORMAL ( 1 FDA reports)
VENOUS ANGIOMA OF BRAIN ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBRAL ARTERY HYPOPLASIA ( 1 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VIITH NERVE INJURY ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VIRAL OESOPHAGITIS ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VIRAL TRACHEITIS ( 1 FDA reports)
VIRUS BODY FLUID IDENTIFIED ( 1 FDA reports)
VIRUS STOOL TEST POSITIVE ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
VITREOUS DEGENERATION ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD INFLAMMATION ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)
VULVAL LEUKOPLAKIA ( 1 FDA reports)
VULVAR EROSION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 1 FDA reports)
VULVOVAGINAL ULCERATION ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WANDERING PACEMAKER ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WOUND HAEMATOMA ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
YAWNING ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL CLOTTING FACTOR ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACANTHAMOEBA KERATITIS ( 1 FDA reports)
ACCIDENTAL NEEDLE STICK ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACRODYNIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AIDS RELATED COMPLICATION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALLOIMMUNISATION ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
AMYLASE ABNORMAL ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTIC TRANSFUSION REACTION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANASTOMOTIC ULCER ( 1 FDA reports)
ANDROGEN DEFICIENCY ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANHIDROSIS ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
ANTHRAX ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGM ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT TOXICITY ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIVIRAL DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANXIETY DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APHERESIS ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE BRUISING ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE DESQUAMATION ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE NODULE ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPERGILLUS TEST ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION BONE MARROW ( 1 FDA reports)
ASTHMA EXERCISE INDUCED ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATOPY ( 1 FDA reports)
ATRIAL BIGEMINY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
ATYPICAL FIBROXANTHOMA ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME ( 1 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL TRACHEITIS ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BALANITIS CANDIDA ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILIARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY BONE MARROW NORMAL ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BIOPSY LYMPH GLAND ABNORMAL ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLADDER DISCOMFORT ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 1 FDA reports)
BLADDER REPAIR ( 1 FDA reports)
BLADDER STENOSIS ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ACID PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ETHANOL INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE NORMAL ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD LUTEINISING HORMONE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OESTROGEN DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD PRESSURE ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID DECREASED ( 1 FDA reports)
BLOOD SELENIUM INCREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 1 FDA reports)
BLOOD URINE ABSENT ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BODY TEMPERATURE ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BRACHIOCEPHALIC VEIN STENOSIS ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST FEEDING ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
BRONCHIAL ANASTOMOSIS ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL POLYP ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOSTENOSIS ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BULLOUS IMPETIGO ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAMPYLOBACTER GASTROENTERITIS ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARBUNCLE ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC CIRRHOSIS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIAC SEPTAL DEFECT ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LEUKAEMIA ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 1 FDA reports)
CEPHALHAEMATOMA ( 1 FDA reports)
CEREBELLAR ISCHAEMIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVICITIS ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHEST TUBE INSERTION ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLANGIOLITIS ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIORETINAL DISORDER ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON FISTULA REPAIR ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMMINUTED FRACTURE ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
COMPUTERISED TOMOGRAM HEAD ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL AORTIC STENOSIS ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL GENITOURINARY ABNORMALITY ( 1 FDA reports)
CONGENITAL IRIS ANOMALY ( 1 FDA reports)
CONGENITAL MEGAURETER ( 1 FDA reports)
CONGENITAL SPINAL CORD ANOMALY ( 1 FDA reports)
CONGENITAL TORTICOLLIS ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL DEGENERATION ( 1 FDA reports)
CORNEAL REFLEX DECREASED ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CRANIOPLASTY ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CREUTZFELDT-JAKOB DISEASE ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CULTURE TISSUE SPECIMEN ( 1 FDA reports)
CULTURE URINE ( 1 FDA reports)
CUTANEOUS AMYLOIDOSIS ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYANOSIS NEONATAL ( 1 FDA reports)
CYSTITIS BACTERIAL ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYTARABINE SYNDROME ( 1 FDA reports)
CYTOMEGALOVIRUS DUODENITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS MYELOMENINGORADICULITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DENTAL DISCOMFORT ( 1 FDA reports)
DENTAL PLAQUE ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DERMATITIS HERPETIFORMIS ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DERMOGRAPHISM ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION IN NEWBORN ( 1 FDA reports)
DISTRIBUTIVE SHOCK ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENAL POLYP ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPONESIS ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ECZEMA INFECTED ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENCEPHALITIS AUTOIMMUNE ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
ENCEPHALITIS POST MEASLES ( 1 FDA reports)
ENCEPHALITIS PROTOZOAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL COUNT ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 1 FDA reports)
EOSINOPHILS URINE PRESENT ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
ERYTHEMA ANNULARE ( 1 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EXPOSURE TO NOISE ( 1 FDA reports)
EXTERNAL EAR DISORDER ( 1 FDA reports)
EXTERNAL EAR INFLAMMATION ( 1 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
EXTREMITY CONTRACTURE ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
FACIAL DYSMORPHISM ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FALSE NEGATIVE LABORATORY RESULT ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEVER NEONATAL ( 1 FDA reports)
FIBRINOLYSIS INCREASED ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FILARIASIS ( 1 FDA reports)
FINGER HYPOPLASIA ( 1 FDA reports)
FLAIL CHEST ( 1 FDA reports)
FLUORESCENT IN SITU HYBRIDISATION ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FOETAL MOVEMENTS DECREASED ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA DIFFUSE SMALL CELL LYMPHOMA ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE DELAYED UNION ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAL RHINITIS ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS STOOL IDENTIFIED ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC FISTULA ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRIC ULCER SURGERY ( 1 FDA reports)
GASTRITIS FUNGAL ( 1 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL DYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT MUCOSAL DISCOLOURATION ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENITAL CANDIDIASIS ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITAL INFECTION FEMALE ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GENOTYPE DRUG RESISTANCE TEST POSITIVE ( 1 FDA reports)
GEOTRICHUM INFECTION ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLIOBLASTOMA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
GREENSTICK FRACTURE ( 1 FDA reports)
GROWING PAINS ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMOBILIA ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMOGLOBINAEMIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAIRY CELL LEUKAEMIA ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HAMARTOMA ( 1 FDA reports)
HEAD AND NECK CANCER ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEARING AID USER ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC ENZYME ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC INFECTION BACTERIAL ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATITIS INFECTIOUS ( 1 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES SIMPLEX VIRUS CONJUNCTIVITIS NEONATAL ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HETEROPHORIA ( 1 FDA reports)
HIP DEFORMITY ( 1 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 1 FDA reports)
HISTIOCYTOSIS ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HUMAN EHRLICHIOSIS ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY ( 1 FDA reports)
HUMAN RHINOVIRUS TEST POSITIVE ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPONATRAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOPHONESIS ( 1 FDA reports)
HYPOPHOSPHATAEMIC RICKETS ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILEOCOLOSTOMY ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
IMPACTED FRACTURE ( 1 FDA reports)
IMPAIRED INSULIN SECRETION ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE CELLULITIS ( 1 FDA reports)
INCISIONAL DRAINAGE ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INDIRECT INFECTION TRANSMISSION ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTED BITES ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
INFLAMMATION LOCALISED ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE PHLEBITIS ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INGUINAL HERNIA STRANGULATED ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE DISCOLOURATION ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NERVE DAMAGE ( 1 FDA reports)
INJECTION SITE PAPULE ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTERNAL FIXATION OF SPINE ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERRUPTION OF AORTIC ARCH ( 1 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL GANGRENE ( 1 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
IRIS HYPOPIGMENTATION ( 1 FDA reports)
IUCD COMPLICATION ( 1 FDA reports)
JAW LESION EXCISION ( 1 FDA reports)
JEJUNECTOMY ( 1 FDA reports)
JOINT DISLOCATION PATHOLOGICAL ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KAWASAKI'S DISEASE ( 1 FDA reports)
KERATITIS VIRAL ( 1 FDA reports)
KERATOPLASTY ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LARYNGITIS FUNGAL ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LEGIONELLA TEST ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LEUKOCYTE ANTIGEN B-27 POSITIVE ( 1 FDA reports)
LEUKOENCEPHALOMYELITIS ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOW SET EARS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
LUMBAR PUNCTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE III ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE 0 ( 1 FDA reports)
LYMPHATIC OBSTRUCTION ( 1 FDA reports)
LYMPHOBLAST COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 1 FDA reports)
MACULAR REFLEX ABNORMAL ( 1 FDA reports)
MACULAR SCAR ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT MYOPIA ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MASTOID EFFUSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDIASTINAL SHIFT ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEDICAL OBSERVATION ( 1 FDA reports)
MEDULLOBLASTOMA ( 1 FDA reports)
MEGAKARYOCYTES DECREASED ( 1 FDA reports)
MEIGE'S SYNDROME ( 1 FDA reports)
MENINGEAL NEOPLASM ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENINGOENCEPHALITIS AMOEBIC ( 1 FDA reports)
MENISCAL DEGENERATION ( 1 FDA reports)
METAMYELOCYTE COUNT ( 1 FDA reports)
METASTASES TO LARGE INTESTINE ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTATIC LYMPHOMA ( 1 FDA reports)
METASTATIC PULMONARY EMBOLISM ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIGRAINE WITH AURA ( 1 FDA reports)
MILKER'S NODULES ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY ( 1 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 1 FDA reports)
MODIFIED RADICAL MASTECTOMY ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MULTIFOCAL MICRONODULAR PNEUMOCYTE HYPERPLASIA ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOSIS FUNGOIDES STAGE IV ( 1 FDA reports)
MYELOCYTE COUNT ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOCARDITIS MYCOTIC ( 1 FDA reports)
MYOCARDITIS TOXOPLASMAL ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL FLARING ( 1 FDA reports)
NATURAL KILLER CELL COUNT DECREASED ( 1 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEONATAL INFECTION ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NERVOUS SYSTEM SURGERY ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEURON-SPECIFIC ENOLASE INCREASED ( 1 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODAL MARGINAL ZONE B-CELL LYMPHOMA ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NOROVIRUS TEST POSITIVE ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEATED RED CELLS ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OCULAR DYSMETRIA ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPHTHALMOLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
OPTIC NERVE OPERATION ( 1 FDA reports)
ORAL CAVITY NEOPLASM SURGERY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORAL TORUS ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
OROPHARYNGEAL CANCER STAGE III ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OSTEOMYELITIS FUNGAL ( 1 FDA reports)
OTITIS MEDIA FUNGAL ( 1 FDA reports)
OTOSCOPY ABNORMAL ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PACEMAKER GENERATED RHYTHM ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN MANAGEMENT ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PANCREATIC ABSCESS ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATICODUODENECTOMY ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANENCEPHALITIS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARESIS ANAL SPHINCTER ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PELVIC ORGAN INJURY ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERICARDITIS INFECTIVE ( 1 FDA reports)
PERINEAL ULCERATION ( 1 FDA reports)
PERINEPHRIC ABSCESS ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERINEPHRIC EFFUSION ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PEYRONIE'S DISEASE ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHARYNGITIS BACTERIAL ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PILONIDAL CYST CONGENITAL ( 1 FDA reports)
PITUITARY HAEMORRHAGE ( 1 FDA reports)
PLACENTAL NECROSIS ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMA CELLS PRESENT ( 1 FDA reports)
PLASTIC SURGERY ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLATELET TOXICITY ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYHYDRAMNIOS ( 1 FDA reports)
POLYMEDICATION ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POLYOMAVIRUS INTERSTITIAL NEPHRITIS ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
PORTAL VEIN FLOW DECREASED ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
PORTAL VEIN STENOSIS ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POST PROCEDURAL CONSTIPATION ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT PHYSICAL ISSUE ( 1 FDA reports)
PRODUCT USED FOR UNKNOWN INDICATION ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER STAGE I ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PROTRUSION TONGUE ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY AMYLOIDOSIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY ARTERIOVENOUS FISTULA ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASMUSSEN ENCEPHALITIS ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RELAPSING POLYCHONDRITIS ( 1 FDA reports)
RELATIONSHIP BREAKDOWN ( 1 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RESPIRATORY PAPILLOMA ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL SCAR ( 1 FDA reports)
RETINAL TELANGIECTASIA ( 1 FDA reports)
RETINAL TOXICITY ( 1 FDA reports)
RETINAL VASCULAR OCCLUSION ( 1 FDA reports)
RETINOPATHY CONGENITAL ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RETROPERITONEAL CANCER ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHEUMATIC FEVER ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALIVARY GLAND DISORDER ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCAN ABDOMEN ABNORMAL ( 1 FDA reports)
SCHISTOSOMA TEST POSITIVE ( 1 FDA reports)
SCIATIC NERVE INJURY ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 1 FDA reports)
SEMINOMA ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SIGNET-RING CELL CARCINOMA ( 1 FDA reports)
SINOBRONCHITIS ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN GRAFT REJECTION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKULL X-RAY ABNORMAL ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMEAR TEST ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPERM COUNT ZERO ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPINOCEREBELLAR ATAXIA ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
STAPHYLOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STATUS MIGRAINOSUS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STOMATOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SUDDEN INFANT DEATH SYNDROME ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)

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