MedsFacts Reports covering METHYLPREDNISOLONE
Directory listing ordered by most common adverse events for METHYLPREDNISOLONE
Please choose an event type to view the corresponding MedsFacts report:
PYREXIA ( 1069 FDA reports)
DYSPNOEA ( 741 FDA reports)
PNEUMONIA ( 713 FDA reports)
PAIN ( 696 FDA reports)
DIARRHOEA ( 649 FDA reports)
SEPSIS ( 639 FDA reports)
NAUSEA ( 611 FDA reports)
ANAEMIA ( 598 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 580 FDA reports)
VOMITING ( 559 FDA reports)
DRUG INEFFECTIVE ( 553 FDA reports)
ANXIETY ( 544 FDA reports)
HEADACHE ( 538 FDA reports)
HYPERTENSION ( 524 FDA reports)
THROMBOCYTOPENIA ( 524 FDA reports)
RESPIRATORY FAILURE ( 504 FDA reports)
ASTHENIA ( 460 FDA reports)
FATIGUE ( 454 FDA reports)
ABDOMINAL PAIN ( 450 FDA reports)
RENAL FAILURE ( 443 FDA reports)
HYPOTENSION ( 442 FDA reports)
MULTI-ORGAN FAILURE ( 438 FDA reports)
ARTHRALGIA ( 396 FDA reports)
BACK PAIN ( 388 FDA reports)
RENAL FAILURE ACUTE ( 388 FDA reports)
BLOOD CREATININE INCREASED ( 384 FDA reports)
INFECTION ( 376 FDA reports)
DEPRESSION ( 369 FDA reports)
RENAL IMPAIRMENT ( 348 FDA reports)
CONVULSION ( 344 FDA reports)
NEUTROPENIA ( 337 FDA reports)
INJURY ( 335 FDA reports)
PAIN IN EXTREMITY ( 332 FDA reports)
CHEST PAIN ( 331 FDA reports)
OEDEMA PERIPHERAL ( 331 FDA reports)
PANCYTOPENIA ( 326 FDA reports)
RASH ( 326 FDA reports)
MYOCARDIAL INFARCTION ( 322 FDA reports)
PLEURAL EFFUSION ( 318 FDA reports)
TRANSPLANT REJECTION ( 316 FDA reports)
URINARY TRACT INFECTION ( 314 FDA reports)
PULMONARY EMBOLISM ( 309 FDA reports)
DIZZINESS ( 307 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 307 FDA reports)
DEEP VEIN THROMBOSIS ( 303 FDA reports)
CONDITION AGGRAVATED ( 302 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 298 FDA reports)
FALL ( 292 FDA reports)
DIABETES MELLITUS ( 288 FDA reports)
MALAISE ( 275 FDA reports)
SEPTIC SHOCK ( 271 FDA reports)
COUGH ( 262 FDA reports)
HYPOAESTHESIA ( 258 FDA reports)
TACHYCARDIA ( 254 FDA reports)
LEUKOPENIA ( 250 FDA reports)
HAEMOGLOBIN DECREASED ( 243 FDA reports)
GRAFT VERSUS HOST DISEASE ( 242 FDA reports)
HAEMODIALYSIS ( 241 FDA reports)
PLATELET COUNT DECREASED ( 241 FDA reports)
WEIGHT DECREASED ( 234 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 230 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 229 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 226 FDA reports)
DEHYDRATION ( 224 FDA reports)
EMOTIONAL DISTRESS ( 219 FDA reports)
PARAESTHESIA ( 217 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 216 FDA reports)
HYPERGLYCAEMIA ( 215 FDA reports)
CARDIAC FAILURE ( 211 FDA reports)
CONFUSIONAL STATE ( 211 FDA reports)
CARDIAC ARREST ( 210 FDA reports)
ASPERGILLOSIS ( 208 FDA reports)
CEREBROVASCULAR ACCIDENT ( 207 FDA reports)
WEIGHT INCREASED ( 207 FDA reports)
FEBRILE NEUTROPENIA ( 206 FDA reports)
DEATH ( 205 FDA reports)
DRUG INTERACTION ( 203 FDA reports)
CONSTIPATION ( 201 FDA reports)
STAPHYLOCOCCAL INFECTION ( 200 FDA reports)
INSOMNIA ( 199 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 197 FDA reports)
BRONCHITIS ( 196 FDA reports)
MUSCULAR WEAKNESS ( 194 FDA reports)
ERYTHEMA ( 193 FDA reports)
HERPES ZOSTER ( 189 FDA reports)
SINUSITIS ( 188 FDA reports)
GAIT DISTURBANCE ( 186 FDA reports)
LOSS OF CONSCIOUSNESS ( 186 FDA reports)
OSTEONECROSIS OF JAW ( 183 FDA reports)
ATRIAL FIBRILLATION ( 182 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 182 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 182 FDA reports)
PRURITUS ( 182 FDA reports)
DECREASED APPETITE ( 181 FDA reports)
OEDEMA ( 177 FDA reports)
CHILLS ( 176 FDA reports)
HEPATIC FAILURE ( 175 FDA reports)
PULMONARY OEDEMA ( 175 FDA reports)
RESPIRATORY DISTRESS ( 174 FDA reports)
OSTEOARTHRITIS ( 173 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 171 FDA reports)
BLOOD PRESSURE INCREASED ( 171 FDA reports)
OSTEONECROSIS ( 170 FDA reports)
TENDON RUPTURE ( 167 FDA reports)
LUNG INFILTRATION ( 166 FDA reports)
BONE DISORDER ( 165 FDA reports)
CELLULITIS ( 165 FDA reports)
DISEASE PROGRESSION ( 165 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 165 FDA reports)
SOMNOLENCE ( 162 FDA reports)
TREMOR ( 161 FDA reports)
OSTEOMYELITIS ( 161 FDA reports)
PROTEINURIA ( 157 FDA reports)
IMPAIRED HEALING ( 155 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 154 FDA reports)
GASTRITIS ( 154 FDA reports)
INTERSTITIAL LUNG DISEASE ( 154 FDA reports)
LYMPHADENOPATHY ( 153 FDA reports)
ASCITES ( 152 FDA reports)
ABDOMINAL PAIN UPPER ( 150 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 150 FDA reports)
HYPOXIA ( 149 FDA reports)
PNEUMOTHORAX ( 149 FDA reports)
HEPATIC ENZYME INCREASED ( 148 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 148 FDA reports)
CHOLELITHIASIS ( 147 FDA reports)
DISEASE RECURRENCE ( 146 FDA reports)
HYPERHIDROSIS ( 146 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 146 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 145 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 145 FDA reports)
DYSPHAGIA ( 145 FDA reports)
HYPERLIPIDAEMIA ( 145 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 144 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 143 FDA reports)
HYPONATRAEMIA ( 143 FDA reports)
PSEUDOMONAS INFECTION ( 142 FDA reports)
HAEMORRHAGE ( 138 FDA reports)
PERITONITIS ( 135 FDA reports)
ASTHMA ( 134 FDA reports)
CHEST DISCOMFORT ( 134 FDA reports)
MYALGIA ( 133 FDA reports)
BRADYCARDIA ( 131 FDA reports)
MUCOSAL INFLAMMATION ( 131 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 130 FDA reports)
BLOOD BILIRUBIN INCREASED ( 129 FDA reports)
BONE PAIN ( 129 FDA reports)
TENDONITIS ( 129 FDA reports)
BLOOD GLUCOSE INCREASED ( 128 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 128 FDA reports)
MUSCLE SPASMS ( 127 FDA reports)
POST PROCEDURAL COMPLICATION ( 127 FDA reports)
BONE MARROW FAILURE ( 126 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 126 FDA reports)
LIVER TRANSPLANT REJECTION ( 126 FDA reports)
HYPERKALAEMIA ( 125 FDA reports)
LEUKOCYTOSIS ( 125 FDA reports)
OLIGURIA ( 123 FDA reports)
NEUROPATHY PERIPHERAL ( 122 FDA reports)
BLOOD UREA INCREASED ( 121 FDA reports)
INFUSION RELATED REACTION ( 121 FDA reports)
CARDIO-RESPIRATORY ARREST ( 118 FDA reports)
CANDIDIASIS ( 117 FDA reports)
HAEMATURIA ( 117 FDA reports)
HYPERSENSITIVITY ( 117 FDA reports)
METABOLIC ACIDOSIS ( 116 FDA reports)
BLOOD PRESSURE DECREASED ( 115 FDA reports)
SPINAL OSTEOARTHRITIS ( 115 FDA reports)
HEART RATE INCREASED ( 114 FDA reports)
PAIN IN JAW ( 114 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 112 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 112 FDA reports)
PALPITATIONS ( 112 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 111 FDA reports)
LUNG DISORDER ( 111 FDA reports)
SYNCOPE ( 111 FDA reports)
URTICARIA ( 111 FDA reports)
RESPIRATORY DISORDER ( 110 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 110 FDA reports)
OXYGEN SATURATION DECREASED ( 110 FDA reports)
LIVER DISORDER ( 109 FDA reports)
ROTATOR CUFF SYNDROME ( 109 FDA reports)
RHEUMATOID ARTHRITIS ( 108 FDA reports)
SWELLING ( 108 FDA reports)
ABDOMINAL DISTENSION ( 108 FDA reports)
METASTASES TO BONE ( 108 FDA reports)
HALLUCINATION ( 107 FDA reports)
HEPATITIS ( 107 FDA reports)
MENTAL STATUS CHANGES ( 107 FDA reports)
HYPOKALAEMIA ( 106 FDA reports)
CHOLESTASIS ( 105 FDA reports)
CORONARY ARTERY DISEASE ( 105 FDA reports)
INFLAMMATION ( 105 FDA reports)
LUNG INFECTION ( 105 FDA reports)
ANGINA PECTORIS ( 103 FDA reports)
SLEEP APNOEA SYNDROME ( 103 FDA reports)
VISION BLURRED ( 102 FDA reports)
ANHEDONIA ( 102 FDA reports)
HAEMATOMA ( 102 FDA reports)
ARTHRITIS ( 101 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 101 FDA reports)
ENCEPHALOPATHY ( 101 FDA reports)
NEPHROTIC SYNDROME ( 99 FDA reports)
WHEEZING ( 99 FDA reports)
SINUS TACHYCARDIA ( 98 FDA reports)
DYSPEPSIA ( 98 FDA reports)
MITRAL VALVE INCOMPETENCE ( 98 FDA reports)
AGRANULOCYTOSIS ( 96 FDA reports)
DYSARTHRIA ( 95 FDA reports)
SWELLING FACE ( 95 FDA reports)
TOOTH EXTRACTION ( 95 FDA reports)
CARDIAC DISORDER ( 94 FDA reports)
CEREBRAL HAEMORRHAGE ( 94 FDA reports)
DRUG HYPERSENSITIVITY ( 94 FDA reports)
ENTEROCOCCAL INFECTION ( 94 FDA reports)
GASTROENTERITIS ( 94 FDA reports)
BALANCE DISORDER ( 93 FDA reports)
LYMPHOCELE ( 93 FDA reports)
TUBERCULOSIS ( 93 FDA reports)
VASCULITIS ( 93 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 92 FDA reports)
ARRHYTHMIA ( 91 FDA reports)
ATELECTASIS ( 91 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 91 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 90 FDA reports)
BLOOD CALCIUM DECREASED ( 90 FDA reports)
COMA ( 90 FDA reports)
GASTROINTESTINAL DISORDER ( 90 FDA reports)
HAEMATOCRIT DECREASED ( 90 FDA reports)
JAUNDICE ( 90 FDA reports)
MEMORY IMPAIRMENT ( 90 FDA reports)
VISUAL IMPAIRMENT ( 90 FDA reports)
CEREBRAL INFARCTION ( 89 FDA reports)
NECK PAIN ( 89 FDA reports)
HAEMORRHOIDS ( 88 FDA reports)
THROMBOSIS ( 88 FDA reports)
SUICIDAL IDEATION ( 87 FDA reports)
URINARY INCONTINENCE ( 87 FDA reports)
EXOSTOSIS ( 87 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 87 FDA reports)
COLITIS ( 86 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 86 FDA reports)
MALNUTRITION ( 86 FDA reports)
NERVOUS SYSTEM DISORDER ( 86 FDA reports)
RHABDOMYOLYSIS ( 86 FDA reports)
SKIN LESION ( 86 FDA reports)
RENAL DISORDER ( 85 FDA reports)
BRAIN OEDEMA ( 85 FDA reports)
MYOPATHY ( 85 FDA reports)
PANCREATITIS ( 85 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 84 FDA reports)
BONE LESION ( 84 FDA reports)
EMPHYSEMA ( 84 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 83 FDA reports)
GALLBLADDER DISORDER ( 83 FDA reports)
MUSCULOSKELETAL PAIN ( 83 FDA reports)
NEPHROPATHY TOXIC ( 83 FDA reports)
NASOPHARYNGITIS ( 82 FDA reports)
CARDIOMYOPATHY ( 81 FDA reports)
FEELING ABNORMAL ( 81 FDA reports)
RENAL TUBULAR NECROSIS ( 81 FDA reports)
DIALYSIS ( 80 FDA reports)
LEUKOENCEPHALOPATHY ( 80 FDA reports)
ANURIA ( 79 FDA reports)
BRONCHOPNEUMONIA ( 79 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 79 FDA reports)
LYMPHOPENIA ( 79 FDA reports)
OVERDOSE ( 79 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 79 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 78 FDA reports)
BURSITIS ( 78 FDA reports)
DRUG TOXICITY ( 78 FDA reports)
AGITATION ( 77 FDA reports)
ANOREXIA ( 77 FDA reports)
CHOLANGITIS ( 77 FDA reports)
ESCHERICHIA INFECTION ( 77 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 77 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 76 FDA reports)
FUNGAL INFECTION ( 76 FDA reports)
HYPERCHOLESTEROLAEMIA ( 76 FDA reports)
BACTERAEMIA ( 75 FDA reports)
CATARACT ( 75 FDA reports)
HAEMOPTYSIS ( 75 FDA reports)
ACUTE RESPIRATORY FAILURE ( 74 FDA reports)
NO THERAPEUTIC RESPONSE ( 74 FDA reports)
STOMATITIS ( 74 FDA reports)
TOOTHACHE ( 74 FDA reports)
RENAL FAILURE CHRONIC ( 73 FDA reports)
SCAR ( 73 FDA reports)
PANCREATITIS ACUTE ( 73 FDA reports)
PNEUMONITIS ( 73 FDA reports)
DISORIENTATION ( 72 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 72 FDA reports)
CHOLECYSTITIS ACUTE ( 71 FDA reports)
ECONOMIC PROBLEM ( 71 FDA reports)
HYPOPHAGIA ( 71 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 71 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 71 FDA reports)
RECTAL HAEMORRHAGE ( 71 FDA reports)
SHOCK ( 71 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 71 FDA reports)
WOUND INFECTION ( 71 FDA reports)
BK VIRUS INFECTION ( 70 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 70 FDA reports)
DYSURIA ( 70 FDA reports)
NEOPLASM MALIGNANT ( 70 FDA reports)
CHOLECYSTITIS ( 69 FDA reports)
LETHARGY ( 69 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 69 FDA reports)
PRIMARY SEQUESTRUM ( 69 FDA reports)
PULMONARY HYPERTENSION ( 69 FDA reports)
UNEVALUABLE EVENT ( 69 FDA reports)
PULMONARY HAEMORRHAGE ( 68 FDA reports)
VENTRICULAR HYPERTROPHY ( 68 FDA reports)
VERTIGO ( 68 FDA reports)
BLOOD ALBUMIN DECREASED ( 68 FDA reports)
HEMIPARESIS ( 68 FDA reports)
JOINT SWELLING ( 68 FDA reports)
OFF LABEL USE ( 68 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 67 FDA reports)
CIRCULATORY COLLAPSE ( 67 FDA reports)
CONTUSION ( 67 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 67 FDA reports)
DIVERTICULUM ( 67 FDA reports)
HEPATOTOXICITY ( 67 FDA reports)
HYDRONEPHROSIS ( 67 FDA reports)
HYPOTHYROIDISM ( 67 FDA reports)
LUNG NEOPLASM ( 67 FDA reports)
MOUTH ULCERATION ( 67 FDA reports)
PERICARDIAL EFFUSION ( 67 FDA reports)
CARDIOMEGALY ( 66 FDA reports)
LUPUS NEPHRITIS ( 66 FDA reports)
STRESS ( 66 FDA reports)
TRANSAMINASES INCREASED ( 66 FDA reports)
PSYCHOTIC DISORDER ( 65 FDA reports)
PYELONEPHRITIS ( 65 FDA reports)
RADICULOPATHY ( 65 FDA reports)
HEPATIC STEATOSIS ( 65 FDA reports)
HEPATITIS C ( 65 FDA reports)
INFLUENZA LIKE ILLNESS ( 64 FDA reports)
MENISCUS LESION ( 64 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 64 FDA reports)
NIGHT SWEATS ( 64 FDA reports)
OSTEOPOROSIS ( 64 FDA reports)
POST PROCEDURAL BILE LEAK ( 64 FDA reports)
CARDIOVASCULAR DISORDER ( 63 FDA reports)
FISTULA ( 63 FDA reports)
GLOMERULONEPHRITIS ( 63 FDA reports)
HAEMODYNAMIC INSTABILITY ( 63 FDA reports)
HIATUS HERNIA ( 63 FDA reports)
RESPIRATORY TRACT INFECTION ( 63 FDA reports)
SHOCK HAEMORRHAGIC ( 63 FDA reports)
TYPE 2 DIABETES MELLITUS ( 63 FDA reports)
RASH ERYTHEMATOUS ( 62 FDA reports)
STEM CELL TRANSPLANT ( 62 FDA reports)
ABDOMINAL DISCOMFORT ( 62 FDA reports)
APHASIA ( 62 FDA reports)
GRAND MAL CONVULSION ( 62 FDA reports)
MYOCARDIAL ISCHAEMIA ( 62 FDA reports)
BACTERIAL INFECTION ( 61 FDA reports)
BLOOD POTASSIUM DECREASED ( 61 FDA reports)
DISTURBANCE IN ATTENTION ( 61 FDA reports)
HOT FLUSH ( 61 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 61 FDA reports)
MENTAL DISORDER ( 61 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 61 FDA reports)
SINUS DISORDER ( 61 FDA reports)
SURGERY ( 61 FDA reports)
TACHYPNOEA ( 61 FDA reports)
ANAPHYLACTIC REACTION ( 60 FDA reports)
DRY MOUTH ( 60 FDA reports)
HEMIPLEGIA ( 60 FDA reports)
NEPHROLITHIASIS ( 60 FDA reports)
OROPHARYNGEAL PAIN ( 60 FDA reports)
PHYSICAL DISABILITY ( 60 FDA reports)
ANGIOEDEMA ( 59 FDA reports)
EPILEPSY ( 59 FDA reports)
HYPERBILIRUBINAEMIA ( 59 FDA reports)
HYPOALBUMINAEMIA ( 59 FDA reports)
ILEUS ( 59 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 59 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 59 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 59 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 59 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 59 FDA reports)
SKIN ULCER ( 58 FDA reports)
URINE OUTPUT DECREASED ( 58 FDA reports)
WOUND DEHISCENCE ( 58 FDA reports)
AMNESIA ( 58 FDA reports)
CUSHINGOID ( 58 FDA reports)
DYSKINESIA ( 58 FDA reports)
MELAENA ( 58 FDA reports)
ABSCESS ( 57 FDA reports)
CARDIAC MURMUR ( 57 FDA reports)
COAGULOPATHY ( 57 FDA reports)
DYSPNOEA EXERTIONAL ( 57 FDA reports)
FEAR ( 57 FDA reports)
KAPOSI'S SARCOMA ( 57 FDA reports)
PURULENT DISCHARGE ( 57 FDA reports)
VENTRICULAR TACHYCARDIA ( 57 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 56 FDA reports)
THERAPY NON-RESPONDER ( 56 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 56 FDA reports)
ARTHROPATHY ( 56 FDA reports)
LOOSE TOOTH ( 56 FDA reports)
NEURALGIA ( 56 FDA reports)
PLANTAR FASCIITIS ( 56 FDA reports)
PRODUCTIVE COUGH ( 56 FDA reports)
HEPATOMEGALY ( 55 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 55 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 54 FDA reports)
CROHN'S DISEASE ( 54 FDA reports)
IMMUNOSUPPRESSION ( 54 FDA reports)
OESOPHAGITIS ( 54 FDA reports)
TOOTH ABSCESS ( 54 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 54 FDA reports)
UNRESPONSIVE TO STIMULI ( 54 FDA reports)
VIRAL INFECTION ( 54 FDA reports)
PULMONARY TUBERCULOSIS ( 53 FDA reports)
SPLENOMEGALY ( 53 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 53 FDA reports)
HAEMATOCHEZIA ( 53 FDA reports)
HAEMOLYTIC ANAEMIA ( 53 FDA reports)
ALOPECIA ( 52 FDA reports)
BACTERIAL SEPSIS ( 52 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 52 FDA reports)
OSTEOPENIA ( 52 FDA reports)
CARPAL TUNNEL SYNDROME ( 51 FDA reports)
METASTASES TO LUNG ( 51 FDA reports)
PROTHROMBIN TIME PROLONGED ( 51 FDA reports)
RENAL ARTERY STENOSIS ( 50 FDA reports)
UPPER LIMB FRACTURE ( 50 FDA reports)
URINARY RETENTION ( 50 FDA reports)
ZYGOMYCOSIS ( 50 FDA reports)
EJECTION FRACTION DECREASED ( 50 FDA reports)
HIP FRACTURE ( 50 FDA reports)
HYPERTHYROIDISM ( 50 FDA reports)
HYPOGLYCAEMIA ( 50 FDA reports)
BODY TEMPERATURE INCREASED ( 49 FDA reports)
LARGE INTESTINE PERFORATION ( 49 FDA reports)
MECHANICAL VENTILATION ( 49 FDA reports)
MOBILITY DECREASED ( 49 FDA reports)
ORAL HERPES ( 49 FDA reports)
SERUM SICKNESS ( 49 FDA reports)
SPEECH DISORDER ( 49 FDA reports)
SPINAL COMPRESSION FRACTURE ( 49 FDA reports)
TOOTH DISORDER ( 49 FDA reports)
RIB FRACTURE ( 48 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 48 FDA reports)
CHOLECYSTITIS CHRONIC ( 48 FDA reports)
DECREASED INTEREST ( 48 FDA reports)
EPISTAXIS ( 48 FDA reports)
FAECAL INCONTINENCE ( 48 FDA reports)
GRAFT DYSFUNCTION ( 48 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 48 FDA reports)
NEUROTOXICITY ( 48 FDA reports)
ABORTION SPONTANEOUS ( 47 FDA reports)
CARDIOGENIC SHOCK ( 47 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 47 FDA reports)
COLITIS ULCERATIVE ( 47 FDA reports)
MAJOR DEPRESSION ( 47 FDA reports)
PULMONARY FIBROSIS ( 47 FDA reports)
RASH MACULO-PAPULAR ( 47 FDA reports)
RESPIRATORY DEPRESSION ( 47 FDA reports)
SKIN EXFOLIATION ( 47 FDA reports)
TOOTH LOSS ( 47 FDA reports)
URETERIC OBSTRUCTION ( 46 FDA reports)
VISUAL ACUITY REDUCED ( 46 FDA reports)
ARTERIOSCLEROSIS ( 46 FDA reports)
BONE DENSITY DECREASED ( 46 FDA reports)
CYSTITIS HAEMORRHAGIC ( 46 FDA reports)
ECZEMA ( 46 FDA reports)
ESCHERICHIA SEPSIS ( 46 FDA reports)
FIBROMYALGIA ( 46 FDA reports)
FLUSHING ( 46 FDA reports)
GINGIVAL SWELLING ( 46 FDA reports)
HERPES SIMPLEX ( 46 FDA reports)
LACTIC ACIDOSIS ( 46 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 46 FDA reports)
ABNORMAL BEHAVIOUR ( 45 FDA reports)
DELIRIUM ( 45 FDA reports)
DIPLOPIA ( 45 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 45 FDA reports)
MALIGNANT MELANOMA ( 45 FDA reports)
PSEUDOMONAL SEPSIS ( 45 FDA reports)
PYELONEPHRITIS ACUTE ( 45 FDA reports)
SEDATION ( 45 FDA reports)
SERUM FERRITIN INCREASED ( 45 FDA reports)
STRONGYLOIDIASIS ( 45 FDA reports)
TENDON DISORDER ( 45 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 44 FDA reports)
EMOTIONAL DISORDER ( 44 FDA reports)
HEPATIC NECROSIS ( 44 FDA reports)
INTESTINAL OBSTRUCTION ( 44 FDA reports)
JOINT INJURY ( 44 FDA reports)
NECROSIS ( 44 FDA reports)
OBESITY ( 44 FDA reports)
PNEUMATOSIS INTESTINALIS ( 44 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 44 FDA reports)
ADRENAL INSUFFICIENCY ( 43 FDA reports)
DELUSION ( 43 FDA reports)
DEVICE RELATED INFECTION ( 43 FDA reports)
DRUG LEVEL INCREASED ( 43 FDA reports)
EAR PAIN ( 43 FDA reports)
LYMPHOMA ( 43 FDA reports)
MULTIPLE INJURIES ( 43 FDA reports)
MYELODYSPLASTIC SYNDROME ( 43 FDA reports)
PHARYNGEAL OEDEMA ( 43 FDA reports)
PHARYNGITIS ( 43 FDA reports)
PLATELET COUNT INCREASED ( 43 FDA reports)
RESPIRATORY ARREST ( 43 FDA reports)
TENOSYNOVITIS ( 43 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 42 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 42 FDA reports)
VAGINAL HAEMORRHAGE ( 42 FDA reports)
BONE DEBRIDEMENT ( 42 FDA reports)
CERVICAL DYSPLASIA ( 42 FDA reports)
DEBRIDEMENT ( 42 FDA reports)
DENTURE WEARER ( 42 FDA reports)
DYSPHONIA ( 42 FDA reports)
ENTEROBACTER INFECTION ( 42 FDA reports)
GRAFT COMPLICATION ( 42 FDA reports)
MIGRAINE ( 42 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 42 FDA reports)
PNEUMONIA KLEBSIELLA ( 42 FDA reports)
AGGRESSION ( 41 FDA reports)
BLISTER ( 41 FDA reports)
EAR INFECTION ( 41 FDA reports)
HEPATITIS B ( 41 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 41 FDA reports)
LIVER TRANSPLANT ( 41 FDA reports)
RESTLESSNESS ( 41 FDA reports)
STEVENS-JOHNSON SYNDROME ( 41 FDA reports)
TRANSPLANT FAILURE ( 41 FDA reports)
TREATMENT NONCOMPLIANCE ( 41 FDA reports)
RENAL CELL CARCINOMA ( 40 FDA reports)
RESTLESS LEGS SYNDROME ( 40 FDA reports)
SYNOVITIS ( 40 FDA reports)
TONSILLITIS ( 40 FDA reports)
TREATMENT FAILURE ( 40 FDA reports)
TUMOUR LYSIS SYNDROME ( 40 FDA reports)
ANAPHYLACTIC SHOCK ( 40 FDA reports)
APLASTIC ANAEMIA ( 40 FDA reports)
BRAIN ABSCESS ( 40 FDA reports)
CYTOLYTIC HEPATITIS ( 40 FDA reports)
FLUID OVERLOAD ( 40 FDA reports)
GINGIVITIS ( 40 FDA reports)
JAW OPERATION ( 40 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 40 FDA reports)
MULTIPLE SCLEROSIS ( 40 FDA reports)
PLEURISY ( 40 FDA reports)
BRONCHOSPASM ( 39 FDA reports)
CEREBRAL ISCHAEMIA ( 39 FDA reports)
CULTURE URINE POSITIVE ( 39 FDA reports)
CYANOSIS ( 39 FDA reports)
DRY EYE ( 39 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 39 FDA reports)
HEPATITIS CHOLESTATIC ( 39 FDA reports)
IGA NEPHROPATHY ( 39 FDA reports)
KLEBSIELLA INFECTION ( 39 FDA reports)
PNEUMONIA BACTERIAL ( 39 FDA reports)
SUBDURAL HAEMATOMA ( 39 FDA reports)
RESPIRATORY RATE INCREASED ( 38 FDA reports)
SKIN DISORDER ( 38 FDA reports)
ADENOVIRUS INFECTION ( 38 FDA reports)
BASAL CELL CARCINOMA ( 38 FDA reports)
CANDIDA SEPSIS ( 38 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 38 FDA reports)
EDENTULOUS ( 38 FDA reports)
EYE PAIN ( 38 FDA reports)
HYPERCALCAEMIA ( 38 FDA reports)
HYPERTHERMIA ( 38 FDA reports)
JOINT DISLOCATION ( 38 FDA reports)
NASAL CONGESTION ( 38 FDA reports)
NOCARDIOSIS ( 38 FDA reports)
OSTEITIS ( 38 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 38 FDA reports)
AUTOIMMUNE HEPATITIS ( 37 FDA reports)
BASEDOW'S DISEASE ( 37 FDA reports)
BLOOD CULTURE POSITIVE ( 37 FDA reports)
CAESAREAN SECTION ( 37 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 37 FDA reports)
CHRONIC SINUSITIS ( 37 FDA reports)
DERMATITIS ( 37 FDA reports)
DIVERTICULITIS ( 37 FDA reports)
DRUG RESISTANCE ( 37 FDA reports)
EXPOSED BONE IN JAW ( 37 FDA reports)
FEELING HOT ( 37 FDA reports)
HEAD INJURY ( 37 FDA reports)
LOBAR PNEUMONIA ( 37 FDA reports)
PALLOR ( 37 FDA reports)
PNEUMONIA ASPIRATION ( 37 FDA reports)
PROCEDURAL COMPLICATION ( 37 FDA reports)
TINNITUS ( 37 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 37 FDA reports)
RALES ( 36 FDA reports)
RENAL CYST ( 36 FDA reports)
SUDDEN DEATH ( 36 FDA reports)
TENDERNESS ( 36 FDA reports)
ABDOMINAL PAIN LOWER ( 36 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 36 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 36 FDA reports)
AORTIC ANEURYSM ( 36 FDA reports)
BREAST CANCER ( 36 FDA reports)
COLON CANCER ( 36 FDA reports)
COMPRESSION FRACTURE ( 36 FDA reports)
COORDINATION ABNORMAL ( 36 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 36 FDA reports)
DRUG EFFECT DECREASED ( 36 FDA reports)
GENERALISED OEDEMA ( 36 FDA reports)
HEPATIC ENCEPHALOPATHY ( 36 FDA reports)
HERPES VIRUS INFECTION ( 36 FDA reports)
INFLUENZA ( 36 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 36 FDA reports)
LIGAMENT RUPTURE ( 36 FDA reports)
MULTIPLE MYELOMA ( 36 FDA reports)
ORAL PAIN ( 36 FDA reports)
PARALYSIS ( 36 FDA reports)
POLYURIA ( 36 FDA reports)
DIVERTICULUM INTESTINAL ( 35 FDA reports)
FACE OEDEMA ( 35 FDA reports)
FACIAL PAIN ( 35 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 35 FDA reports)
HYPOAESTHESIA ORAL ( 35 FDA reports)
ILEUS PARALYTIC ( 35 FDA reports)
NEPHRECTOMY ( 35 FDA reports)
ODYNOPHAGIA ( 35 FDA reports)
ORAL CANDIDIASIS ( 35 FDA reports)
ORAL DISORDER ( 35 FDA reports)
ORTHOPNOEA ( 35 FDA reports)
PATHOLOGICAL FRACTURE ( 35 FDA reports)
RENAL TUBULAR ATROPHY ( 35 FDA reports)
RHINORRHOEA ( 35 FDA reports)
SCOLIOSIS ( 35 FDA reports)
SPINAL COLUMN STENOSIS ( 35 FDA reports)
TOOTH INFECTION ( 35 FDA reports)
TOXIC ENCEPHALOPATHY ( 35 FDA reports)
VIITH NERVE PARALYSIS ( 35 FDA reports)
RASH GENERALISED ( 34 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 34 FDA reports)
RENAL INJURY ( 34 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 34 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 34 FDA reports)
AREFLEXIA ( 34 FDA reports)
COGNITIVE DISORDER ( 34 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 34 FDA reports)
CORONARY ARTERY OCCLUSION ( 34 FDA reports)
DISSEMINATED TUBERCULOSIS ( 34 FDA reports)
DYSTONIA ( 34 FDA reports)
ECCHYMOSIS ( 34 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 34 FDA reports)
FRACTURE ( 34 FDA reports)
HAEMOLYSIS ( 34 FDA reports)
ILL-DEFINED DISORDER ( 34 FDA reports)
ISCHAEMIA ( 34 FDA reports)
KIDNEY FIBROSIS ( 34 FDA reports)
MITRAL VALVE PROLAPSE ( 34 FDA reports)
PANIC ATTACK ( 34 FDA reports)
PATHOGEN RESISTANCE ( 34 FDA reports)
PETECHIAE ( 34 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 33 FDA reports)
CEREBRAL ATROPHY ( 33 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 33 FDA reports)
DEMENTIA ( 33 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 33 FDA reports)
FOOT FRACTURE ( 33 FDA reports)
GASTRIC ULCER ( 33 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 33 FDA reports)
NEUTROPHIL COUNT DECREASED ( 33 FDA reports)
PERIARTHRITIS ( 33 FDA reports)
SENSORY DISTURBANCE ( 33 FDA reports)
SKIN DISCOLOURATION ( 33 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 33 FDA reports)
TRISMUS ( 33 FDA reports)
RASH PRURITIC ( 32 FDA reports)
UROSEPSIS ( 32 FDA reports)
ABDOMINAL TENDERNESS ( 32 FDA reports)
ATRIOVENTRICULAR BLOCK ( 32 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 32 FDA reports)
EATING DISORDER ( 32 FDA reports)
ENDOCARDITIS ( 32 FDA reports)
GINGIVAL PAIN ( 32 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 32 FDA reports)
HEPATITIS ACUTE ( 32 FDA reports)
INJECTION SITE PAIN ( 32 FDA reports)
INTESTINAL PERFORATION ( 32 FDA reports)
MANIA ( 32 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 32 FDA reports)
NEPHROPATHY ( 32 FDA reports)
ACUTE CORONARY SYNDROME ( 31 FDA reports)
BRONCHIECTASIS ( 31 FDA reports)
CARDIAC FIBRILLATION ( 31 FDA reports)
CHEST X-RAY ABNORMAL ( 31 FDA reports)
CLEFT LIP AND PALATE ( 31 FDA reports)
CUSHING'S SYNDROME ( 31 FDA reports)
ESCHERICHIA BACTERAEMIA ( 31 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 31 FDA reports)
FLATULENCE ( 31 FDA reports)
GRAFT LOSS ( 31 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 31 FDA reports)
JAW DISORDER ( 31 FDA reports)
JAW FRACTURE ( 31 FDA reports)
JOINT EFFUSION ( 31 FDA reports)
MEDICATION ERROR ( 31 FDA reports)
METASTASES TO LIVER ( 31 FDA reports)
MOOD SWINGS ( 31 FDA reports)
MUSCULOSKELETAL DISORDER ( 31 FDA reports)
OSTEOSCLEROSIS ( 31 FDA reports)
PERIODONTAL DISEASE ( 31 FDA reports)
RENAL PAIN ( 31 FDA reports)
RENAL TUBULAR DISORDER ( 31 FDA reports)
SENSORY LOSS ( 31 FDA reports)
VARICELLA ( 31 FDA reports)
VARICOSE VEIN ( 31 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 31 FDA reports)
PULMONARY CONGESTION ( 30 FDA reports)
RHONCHI ( 30 FDA reports)
SEROMA ( 30 FDA reports)
SKIN NECROSIS ( 30 FDA reports)
SLEEP DISORDER ( 30 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 30 FDA reports)
ABDOMINAL ABSCESS ( 30 FDA reports)
ANAPHYLACTOID REACTION ( 30 FDA reports)
ATAXIA ( 30 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 30 FDA reports)
CATARACT OPERATION ( 30 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 30 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 30 FDA reports)
DRUG DEPENDENCE ( 30 FDA reports)
ELECTROLYTE IMBALANCE ( 30 FDA reports)
HEART RATE IRREGULAR ( 30 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 30 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 30 FDA reports)
HYPOCALCAEMIA ( 30 FDA reports)
HYPOMAGNESAEMIA ( 30 FDA reports)
IMPLANT SITE INFECTION ( 30 FDA reports)
LUNG NEOPLASM MALIGNANT ( 30 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 30 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 30 FDA reports)
POLYNEUROPATHY ( 30 FDA reports)
PRESYNCOPE ( 30 FDA reports)
ABASIA ( 29 FDA reports)
ACUTE PULMONARY OEDEMA ( 29 FDA reports)
APLASIA ( 29 FDA reports)
ENTEROCOLITIS ( 29 FDA reports)
IRRITABLE BOWEL SYNDROME ( 29 FDA reports)
MASS ( 29 FDA reports)
PERIODONTITIS ( 29 FDA reports)
ROAD TRAFFIC ACCIDENT ( 29 FDA reports)
SKIN PAPILLOMA ( 29 FDA reports)
SUICIDE ATTEMPT ( 29 FDA reports)
ULCER ( 29 FDA reports)
VENTRICULAR FIBRILLATION ( 29 FDA reports)
WALKING AID USER ( 29 FDA reports)
SUBCUTANEOUS ABSCESS ( 28 FDA reports)
SWOLLEN TONGUE ( 28 FDA reports)
TARDIVE DYSKINESIA ( 28 FDA reports)
VENOUS THROMBOSIS ( 28 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 28 FDA reports)
ANGINA UNSTABLE ( 28 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 28 FDA reports)
APLASIA PURE RED CELL ( 28 FDA reports)
ASPIRATION ( 28 FDA reports)
CLOSTRIDIAL INFECTION ( 28 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 28 FDA reports)
DEPRESSED MOOD ( 28 FDA reports)
DERMATITIS CONTACT ( 28 FDA reports)
DILATATION ATRIAL ( 28 FDA reports)
DRUG ABUSE ( 28 FDA reports)
EXCORIATION ( 28 FDA reports)
FEBRILE BONE MARROW APLASIA ( 28 FDA reports)
FEMUR FRACTURE ( 28 FDA reports)
GINGIVAL ULCERATION ( 28 FDA reports)
HYPERURICAEMIA ( 28 FDA reports)
INCORRECT DOSE ADMINISTERED ( 28 FDA reports)
ISCHAEMIC STROKE ( 28 FDA reports)
LABORATORY TEST ABNORMAL ( 28 FDA reports)
LUNG CONSOLIDATION ( 28 FDA reports)
MASTICATION DISORDER ( 28 FDA reports)
MOUTH HAEMORRHAGE ( 28 FDA reports)
MUSCLE TWITCHING ( 28 FDA reports)
NERVOUSNESS ( 28 FDA reports)
PHLEBITIS ( 28 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 27 FDA reports)
ADVERSE EVENT ( 27 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 27 FDA reports)
BLOOD POTASSIUM INCREASED ( 27 FDA reports)
BLOOD URINE PRESENT ( 27 FDA reports)
CHOLECYSTECTOMY ( 27 FDA reports)
CYST ( 27 FDA reports)
DISCOMFORT ( 27 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 27 FDA reports)
FLUID RETENTION ( 27 FDA reports)
GINGIVAL RECESSION ( 27 FDA reports)
GLAUCOMA ( 27 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 27 FDA reports)
HEPATOSPLENOMEGALY ( 27 FDA reports)
NEUTROPHIL COUNT INCREASED ( 27 FDA reports)
OVARIAN CYST ( 27 FDA reports)
PEPTIC ULCER ( 27 FDA reports)
PERIPHERAL COLDNESS ( 27 FDA reports)
PLEURITIC PAIN ( 27 FDA reports)
SPINAL FRACTURE ( 27 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 27 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 27 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 27 FDA reports)
WOUND HAEMORRHAGE ( 27 FDA reports)
PSORIASIS ( 26 FDA reports)
SOFT TISSUE INFLAMMATION ( 26 FDA reports)
SYNOVIAL CYST ( 26 FDA reports)
TOOTH FRACTURE ( 26 FDA reports)
ABSCESS LIMB ( 26 FDA reports)
BLOOD SODIUM DECREASED ( 26 FDA reports)
BURNING SENSATION ( 26 FDA reports)
CONJUNCTIVITIS ( 26 FDA reports)
CORONARY ARTERY STENOSIS ( 26 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 26 FDA reports)
DEFORMITY ( 26 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 26 FDA reports)
ENCEPHALITIS ( 26 FDA reports)
FACIAL PALSY ( 26 FDA reports)
FIBRIN D DIMER INCREASED ( 26 FDA reports)
GOITRE ( 26 FDA reports)
HEPATIC CIRRHOSIS ( 26 FDA reports)
HEPATOBILIARY DISEASE ( 26 FDA reports)
HODGKIN'S DISEASE ( 26 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 26 FDA reports)
HYPOVENTILATION ( 26 FDA reports)
INCISIONAL HERNIA ( 26 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 26 FDA reports)
LARYNGEAL OEDEMA ( 26 FDA reports)
NEUROLOGICAL SYMPTOM ( 26 FDA reports)
NEUROPATHY ( 26 FDA reports)
NEUTROPENIC SEPSIS ( 26 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 26 FDA reports)
PARAPLEGIA ( 26 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 26 FDA reports)
POSTOPERATIVE INFECTION ( 26 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 25 FDA reports)
ANGIOPATHY ( 25 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 25 FDA reports)
DERMATOMYOSITIS ( 25 FDA reports)
DILATATION VENTRICULAR ( 25 FDA reports)
ERYTHEMA INFECTIOSUM ( 25 FDA reports)
EYELID OEDEMA ( 25 FDA reports)
GASTRIC DISORDER ( 25 FDA reports)
GASTROINTESTINAL NECROSIS ( 25 FDA reports)
GENERALISED ERYTHEMA ( 25 FDA reports)
GOUT ( 25 FDA reports)
GRANULOMA ( 25 FDA reports)
HAEMATOTOXICITY ( 25 FDA reports)
HAEMOTHORAX ( 25 FDA reports)
HALLUCINATION, VISUAL ( 25 FDA reports)
HERNIA ( 25 FDA reports)
HYPERPLASIA ( 25 FDA reports)
HYPOTHERMIA ( 25 FDA reports)
INGROWING NAIL ( 25 FDA reports)
LUMBAR RADICULOPATHY ( 25 FDA reports)
MENINGITIS ASEPTIC ( 25 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 25 FDA reports)
ORGANISING PNEUMONIA ( 25 FDA reports)
PELVIC PAIN ( 25 FDA reports)
PLEURAL FIBROSIS ( 25 FDA reports)
POLLAKIURIA ( 25 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 25 FDA reports)
PREGNANCY ( 25 FDA reports)
RASH MACULAR ( 25 FDA reports)
RHINITIS ( 25 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 24 FDA reports)
REFLUX OESOPHAGITIS ( 24 FDA reports)
RHINITIS ALLERGIC ( 24 FDA reports)
SINUS BRADYCARDIA ( 24 FDA reports)
STATUS EPILEPTICUS ( 24 FDA reports)
STRABISMUS ( 24 FDA reports)
STRESS FRACTURE ( 24 FDA reports)
TERATOGENICITY ( 24 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 24 FDA reports)
WOUND SECRETION ( 24 FDA reports)
ABDOMINAL INFECTION ( 24 FDA reports)
ACINETOBACTER INFECTION ( 24 FDA reports)
AORTIC DISSECTION ( 24 FDA reports)
ATRIAL FLUTTER ( 24 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 24 FDA reports)
IRRITABILITY ( 24 FDA reports)
LACRIMATION INCREASED ( 24 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 24 FDA reports)
OPPORTUNISTIC INFECTION ( 24 FDA reports)
ABORTION INDUCED ( 23 FDA reports)
ABSCESS DRAINAGE ( 23 FDA reports)
ACNE ( 23 FDA reports)
AORTIC VALVE INCOMPETENCE ( 23 FDA reports)
BONE MARROW TRANSPLANT ( 23 FDA reports)
BRAIN HERNIATION ( 23 FDA reports)
CAPILLARITIS ( 23 FDA reports)
DRUG ERUPTION ( 23 FDA reports)
ENDOTRACHEAL INTUBATION ( 23 FDA reports)
ERECTILE DYSFUNCTION ( 23 FDA reports)
GASTRIC POLYPS ( 23 FDA reports)
GASTROINTESTINAL ULCER ( 23 FDA reports)
HAEMANGIOMA ( 23 FDA reports)
HAEMORRHAGIC DIATHESIS ( 23 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 23 FDA reports)
HYDROCEPHALUS ( 23 FDA reports)
HYPOPROTEINAEMIA ( 23 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 23 FDA reports)
MENINGITIS ( 23 FDA reports)
MUCORMYCOSIS ( 23 FDA reports)
NEOPLASM PROGRESSION ( 23 FDA reports)
PNEUMOMEDIASTINUM ( 23 FDA reports)
QUADRIPLEGIA ( 23 FDA reports)
TENOSYNOVITIS STENOSANS ( 23 FDA reports)
THYROID CANCER ( 23 FDA reports)
THYROID NEOPLASM ( 23 FDA reports)
URETERIC STENOSIS ( 23 FDA reports)
UTERINE HAEMORRHAGE ( 23 FDA reports)
PURPURA ( 22 FDA reports)
RENAL TRANSPLANT ( 22 FDA reports)
SCIATICA ( 22 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 22 FDA reports)
ANEURYSM ( 22 FDA reports)
ANGER ( 22 FDA reports)
ANGIOSARCOMA ( 22 FDA reports)
BLINDNESS ( 22 FDA reports)
BLOOD CHLORIDE DECREASED ( 22 FDA reports)
BLOOD GLUCOSE DECREASED ( 22 FDA reports)
BONE MARROW DEPRESSION ( 22 FDA reports)
BONE OPERATION ( 22 FDA reports)
CARDIAC FAILURE ACUTE ( 22 FDA reports)
CERVIX CARCINOMA ( 22 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 22 FDA reports)
DEPENDENCE ( 22 FDA reports)
DYSPLASIA ( 22 FDA reports)
GASTRITIS EROSIVE ( 22 FDA reports)
HAEMATEMESIS ( 22 FDA reports)
HEARING IMPAIRED ( 22 FDA reports)
HEART TRANSPLANT REJECTION ( 22 FDA reports)
HIP ARTHROPLASTY ( 22 FDA reports)
HORDEOLUM ( 22 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 22 FDA reports)
LIMB INJURY ( 22 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 22 FDA reports)
MYDRIASIS ( 22 FDA reports)
MYOSITIS ( 22 FDA reports)
NEURITIS ( 22 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 22 FDA reports)
PLASMACYTOMA ( 22 FDA reports)
PROPOFOL INFUSION SYNDROME ( 22 FDA reports)
APNOEA ( 21 FDA reports)
CALCIPHYLAXIS ( 21 FDA reports)
CHROMATURIA ( 21 FDA reports)
COLITIS ISCHAEMIC ( 21 FDA reports)
CYSTITIS ( 21 FDA reports)
CYTOKINE RELEASE SYNDROME ( 21 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 21 FDA reports)
DENTAL CARE ( 21 FDA reports)
DIABETIC KETOACIDOSIS ( 21 FDA reports)
ENGRAFTMENT SYNDROME ( 21 FDA reports)
GANGRENE ( 21 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 21 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 21 FDA reports)
HYPOVOLAEMIA ( 21 FDA reports)
INCOHERENT ( 21 FDA reports)
INTRA-UTERINE DEATH ( 21 FDA reports)
KLEBSIELLA SEPSIS ( 21 FDA reports)
LACERATION ( 21 FDA reports)
LUNG ADENOCARCINOMA ( 21 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 21 FDA reports)
MENORRHAGIA ( 21 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 21 FDA reports)
MONOCLONAL GAMMOPATHY ( 21 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 21 FDA reports)
PARANOIA ( 21 FDA reports)
POLYP ( 21 FDA reports)
PORTAL VEIN THROMBOSIS ( 21 FDA reports)
RADIATION ASSOCIATED PAIN ( 21 FDA reports)
RADIUS FRACTURE ( 21 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 21 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 21 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 21 FDA reports)
TOXOPLASMOSIS ( 21 FDA reports)
VISUAL DISTURBANCE ( 21 FDA reports)
WOUND ( 21 FDA reports)
RADIOTHERAPY ( 20 FDA reports)
SKIN LACERATION ( 20 FDA reports)
STREPTOCOCCAL INFECTION ( 20 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 20 FDA reports)
TONGUE INJURY ( 20 FDA reports)
TOOTH IMPACTED ( 20 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 20 FDA reports)
ABSCESS JAW ( 20 FDA reports)
ACIDOSIS ( 20 FDA reports)
B-CELL LYMPHOMA ( 20 FDA reports)
BILIARY COLIC ( 20 FDA reports)
BREAST PAIN ( 20 FDA reports)
BRONCHOSTENOSIS ( 20 FDA reports)
CERVICAL SPINAL STENOSIS ( 20 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 20 FDA reports)
COLECTOMY ( 20 FDA reports)
DYSSTASIA ( 20 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 20 FDA reports)
ENTEROCOCCAL SEPSIS ( 20 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 20 FDA reports)
ERYSIPELAS ( 20 FDA reports)
ERYTHEMA MULTIFORME ( 20 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 20 FDA reports)
EYE MOVEMENT DISORDER ( 20 FDA reports)
FACE INJURY ( 20 FDA reports)
GASTRIC HAEMORRHAGE ( 20 FDA reports)
HYPERTONIA ( 20 FDA reports)
IRON DEFICIENCY ANAEMIA ( 20 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 20 FDA reports)
LICHENOID KERATOSIS ( 20 FDA reports)
LIVER ABSCESS ( 20 FDA reports)
LYMPHADENITIS ( 20 FDA reports)
METASTASES TO SPINE ( 20 FDA reports)
METATARSALGIA ( 20 FDA reports)
MICROANGIOPATHY ( 20 FDA reports)
MOOD ALTERED ( 20 FDA reports)
MOTOR DYSFUNCTION ( 20 FDA reports)
MUSCLE DISORDER ( 20 FDA reports)
PERICARDITIS ( 20 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 20 FDA reports)
PNEUMONIA FUNGAL ( 20 FDA reports)
POST HERPETIC NEURALGIA ( 20 FDA reports)
BIPOLAR DISORDER ( 19 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 19 FDA reports)
BREATH SOUNDS ABNORMAL ( 19 FDA reports)
CARDIOPULMONARY FAILURE ( 19 FDA reports)
CUBITAL TUNNEL SYNDROME ( 19 FDA reports)
CYSTOCELE ( 19 FDA reports)
DECUBITUS ULCER ( 19 FDA reports)
DIASTOLIC DYSFUNCTION ( 19 FDA reports)
DRUG LEVEL DECREASED ( 19 FDA reports)
EAR DISCOMFORT ( 19 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 19 FDA reports)
ENDODONTIC PROCEDURE ( 19 FDA reports)
EOSINOPHILIA ( 19 FDA reports)
EPICONDYLITIS ( 19 FDA reports)
GROIN PAIN ( 19 FDA reports)
HYPERNATRAEMIA ( 19 FDA reports)
HYPERREFLEXIA ( 19 FDA reports)
HYPOREFLEXIA ( 19 FDA reports)
HYPOVOLAEMIC SHOCK ( 19 FDA reports)
IMPAIRED WORK ABILITY ( 19 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 19 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 19 FDA reports)
LACUNAR INFARCTION ( 19 FDA reports)
LYMPHOEDEMA ( 19 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 19 FDA reports)
METASTASES TO LYMPH NODES ( 19 FDA reports)
MICTURITION URGENCY ( 19 FDA reports)
MOVEMENT DISORDER ( 19 FDA reports)
NASAL SEPTUM DISORDER ( 19 FDA reports)
NEUTROPENIC INFECTION ( 19 FDA reports)
NYSTAGMUS ( 19 FDA reports)
ORAL CAVITY FISTULA ( 19 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 19 FDA reports)
PROCTALGIA ( 19 FDA reports)
PROTEIN TOTAL DECREASED ( 19 FDA reports)
PULMONARY INFARCTION ( 19 FDA reports)
PYURIA ( 19 FDA reports)
SINUS ARRHYTHMIA ( 19 FDA reports)
SPUTUM CULTURE POSITIVE ( 19 FDA reports)
SURGICAL PROCEDURE REPEATED ( 19 FDA reports)
SYSTEMIC CANDIDA ( 19 FDA reports)
WALKING DISABILITY ( 19 FDA reports)
PRURITUS GENERALISED ( 18 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 18 FDA reports)
PULSE ABSENT ( 18 FDA reports)
RASH PUSTULAR ( 18 FDA reports)
RECTOCELE ( 18 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 18 FDA reports)
THYROTOXIC CRISIS ( 18 FDA reports)
TROPONIN INCREASED ( 18 FDA reports)
UVEITIS ( 18 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 18 FDA reports)
ARTERIAL DISORDER ( 18 FDA reports)
ARTHRITIS BACTERIAL ( 18 FDA reports)
ATROPHIC VULVOVAGINITIS ( 18 FDA reports)
BILIARY DYSKINESIA ( 18 FDA reports)
BRAIN STEM SYNDROME ( 18 FDA reports)
CAROTID ARTERY STENOSIS ( 18 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 18 FDA reports)
DIABETIC NEUROPATHY ( 18 FDA reports)
DUODENAL ULCER ( 18 FDA reports)
DYSGEUSIA ( 18 FDA reports)
ESSENTIAL HYPERTENSION ( 18 FDA reports)
FUNGAL SKIN INFECTION ( 18 FDA reports)
GAZE PALSY ( 18 FDA reports)
GINGIVAL DISORDER ( 18 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 18 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 18 FDA reports)
HEART RATE DECREASED ( 18 FDA reports)
HYPERPYREXIA ( 18 FDA reports)
HYPOPHOSPHATAEMIA ( 18 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 18 FDA reports)
INJECTION SITE ERYTHEMA ( 18 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 18 FDA reports)
JUVENILE ARTHRITIS ( 18 FDA reports)
LUNG TRANSPLANT REJECTION ( 18 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 18 FDA reports)
NOCTURIA ( 18 FDA reports)
OESOPHAGITIS ULCERATIVE ( 18 FDA reports)
PARVOVIRUS INFECTION ( 18 FDA reports)
PHOTOPHOBIA ( 18 FDA reports)
POSTURE ABNORMAL ( 18 FDA reports)
PREMATURE BABY ( 18 FDA reports)
ACTINOMYCOSIS ( 17 FDA reports)
APPENDICITIS ( 17 FDA reports)
AUTOIMMUNE THYROIDITIS ( 17 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 17 FDA reports)
BRAIN NEOPLASM ( 17 FDA reports)
CALCINOSIS ( 17 FDA reports)
CARDIAC VALVE DISEASE ( 17 FDA reports)
CATHETER RELATED INFECTION ( 17 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 17 FDA reports)
COLD SWEAT ( 17 FDA reports)
DEAFNESS NEUROSENSORY ( 17 FDA reports)
DENTAL FISTULA ( 17 FDA reports)
DEVICE OCCLUSION ( 17 FDA reports)
DRUG INTOLERANCE ( 17 FDA reports)
DYSPHEMIA ( 17 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 17 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 17 FDA reports)
ENGRAFT FAILURE ( 17 FDA reports)
FLANK PAIN ( 17 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 17 FDA reports)
HEMIANOPIA ( 17 FDA reports)
HYPERTENSIVE CRISIS ( 17 FDA reports)
HYPOACUSIS ( 17 FDA reports)
HYPOTONIA ( 17 FDA reports)
JUGULAR VEIN THROMBOSIS ( 17 FDA reports)
LUMBAR SPINAL STENOSIS ( 17 FDA reports)
LUNG ABSCESS ( 17 FDA reports)
NECROTISING FASCIITIS ( 17 FDA reports)
NODULE ( 17 FDA reports)
OCULAR HYPERTENSION ( 17 FDA reports)
OEDEMA MUCOSAL ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
ORTHOSTATIC HYPOTENSION ( 17 FDA reports)
PARAESTHESIA ORAL ( 17 FDA reports)
PELVIC FRACTURE ( 17 FDA reports)
PROSTATE CANCER ( 17 FDA reports)
RADICULAR PAIN ( 17 FDA reports)
SEQUESTRECTOMY ( 17 FDA reports)
SERRATIA INFECTION ( 17 FDA reports)
SPONDYLOLISTHESIS ( 17 FDA reports)
TELANGIECTASIA ( 17 FDA reports)
THROAT IRRITATION ( 17 FDA reports)
TRACHEOBRONCHITIS ( 17 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 17 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 17 FDA reports)
URINOMA ( 17 FDA reports)
VASCULAR PSEUDOANEURYSM ( 17 FDA reports)
WOUND DRAINAGE ( 17 FDA reports)
PULMONARY MASS ( 16 FDA reports)
PULMONARY TOXICITY ( 16 FDA reports)
PUPIL FIXED ( 16 FDA reports)
RECTAL FISSURE ( 16 FDA reports)
RIGHT VENTRICULAR FAILURE ( 16 FDA reports)
SARCOIDOSIS ( 16 FDA reports)
SEBORRHOEIC KERATOSIS ( 16 FDA reports)
SPUTUM PURULENT ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
THROMBOPHLEBITIS ( 16 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 16 FDA reports)
VASCULAR CALCIFICATION ( 16 FDA reports)
WEGENER'S GRANULOMATOSIS ( 16 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 16 FDA reports)
BILE DUCT OBSTRUCTION ( 16 FDA reports)
BILE DUCT STENOSIS ( 16 FDA reports)
BIPOLAR I DISORDER ( 16 FDA reports)
BODY TEMPERATURE DECREASED ( 16 FDA reports)
BONE LOSS ( 16 FDA reports)
CARDIOTOXICITY ( 16 FDA reports)
CEREBRAL DISORDER ( 16 FDA reports)
COLONIC POLYP ( 16 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 16 FDA reports)
CREPITATIONS ( 16 FDA reports)
DERMATITIS EXFOLIATIVE ( 16 FDA reports)
DEVICE FAILURE ( 16 FDA reports)
DEVICE RELATED SEPSIS ( 16 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 16 FDA reports)
EMBOLISM ( 16 FDA reports)
FIBROSIS ( 16 FDA reports)
FOOT DEFORMITY ( 16 FDA reports)
FUNGAEMIA ( 16 FDA reports)
HAND FRACTURE ( 16 FDA reports)
HEPATIC CYST ( 16 FDA reports)
HEPATIC LESION ( 16 FDA reports)
HEPATITIS TOXIC ( 16 FDA reports)
HEPATOCELLULAR DAMAGE ( 16 FDA reports)
IMMUNODEFICIENCY ( 16 FDA reports)
INTESTINAL ISCHAEMIA ( 16 FDA reports)
LIVER GRAFT LOSS ( 16 FDA reports)
METASTASIS ( 16 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 16 FDA reports)
MUSCLE ATROPHY ( 16 FDA reports)
MUSCLE RIGIDITY ( 16 FDA reports)
MUSCLE TIGHTNESS ( 16 FDA reports)
NIGHTMARE ( 16 FDA reports)
OPEN WOUND ( 16 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 16 FDA reports)
OXYGEN SUPPLEMENTATION ( 16 FDA reports)
PARESIS ( 16 FDA reports)
PARTIAL SEIZURES ( 16 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
ACINETOBACTER TEST POSITIVE ( 15 FDA reports)
ACUTE ABDOMEN ( 15 FDA reports)
ADENOCARCINOMA ( 15 FDA reports)
ALVEOLOPLASTY ( 15 FDA reports)
ANAL ABSCESS ( 15 FDA reports)
ANGIOFIBROMA ( 15 FDA reports)
APHTHOUS STOMATITIS ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 15 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 15 FDA reports)
AZOTAEMIA ( 15 FDA reports)
BLADDER DISORDER ( 15 FDA reports)
BLOOD BICARBONATE DECREASED ( 15 FDA reports)
BLOOD URIC ACID INCREASED ( 15 FDA reports)
BONE SCAN ABNORMAL ( 15 FDA reports)
BREAST RECONSTRUCTION ( 15 FDA reports)
CAPILLARY LEAK SYNDROME ( 15 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 15 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 15 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 15 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 15 FDA reports)
CSF PROTEIN INCREASED ( 15 FDA reports)
DEAFNESS ( 15 FDA reports)
DERMATITIS BULLOUS ( 15 FDA reports)
DRUG DOSE OMISSION ( 15 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 15 FDA reports)
EOSINOPHIL COUNT INCREASED ( 15 FDA reports)
EXANTHEM ( 15 FDA reports)
FAECES DISCOLOURED ( 15 FDA reports)
FEELING COLD ( 15 FDA reports)
HEPATIC ARTERY STENOSIS ( 15 FDA reports)
HYPOKINESIA ( 15 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 15 FDA reports)
INJECTION SITE REACTION ( 15 FDA reports)
JOINT SPRAIN ( 15 FDA reports)
LYMPHOCYTIC INFILTRATION ( 15 FDA reports)
METABOLIC DISORDER ( 15 FDA reports)
NO ADVERSE EVENT ( 15 FDA reports)
PARAPSORIASIS ( 15 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 15 FDA reports)
PERONEAL NERVE PALSY ( 15 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 15 FDA reports)
PO2 DECREASED ( 15 FDA reports)
PROCTITIS ( 15 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 15 FDA reports)
PULMONARY RADIATION INJURY ( 15 FDA reports)
PULSE ABNORMAL ( 15 FDA reports)
RECTAL ABSCESS ( 15 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 15 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 15 FDA reports)
RENAL INFARCT ( 15 FDA reports)
RESPIRATORY ACIDOSIS ( 15 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 15 FDA reports)
SPINAL DISORDER ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 15 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 15 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 15 FDA reports)
TENDON INJURY ( 15 FDA reports)
THROAT TIGHTNESS ( 15 FDA reports)
TOBACCO ABUSE ( 15 FDA reports)
TRACHEOSTOMY ( 15 FDA reports)
UTERINE LEIOMYOMA ( 15 FDA reports)
PROTEIN URINE PRESENT ( 14 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 14 FDA reports)
RASH PAPULAR ( 14 FDA reports)
SPINAL LAMINECTOMY ( 14 FDA reports)
SPLENIC INFARCTION ( 14 FDA reports)
SUBCUTANEOUS NODULE ( 14 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 14 FDA reports)
T-CELL LYMPHOMA ( 14 FDA reports)
ACUTE HEPATIC FAILURE ( 14 FDA reports)
ANIMAL BITE ( 14 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 14 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 14 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 14 FDA reports)
BILE DUCT STONE ( 14 FDA reports)
BILIARY ISCHAEMIA ( 14 FDA reports)
BLEEDING TIME PROLONGED ( 14 FDA reports)
BLOOD AMYLASE INCREASED ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
CEREBELLAR INFARCTION ( 14 FDA reports)
CLOSTRIDIUM COLITIS ( 14 FDA reports)
CORONARY ARTERY BYPASS ( 14 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 14 FDA reports)
DROP ATTACKS ( 14 FDA reports)
DRUG ABUSER ( 14 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 14 FDA reports)
DYSLIPIDAEMIA ( 14 FDA reports)
DYSMENORRHOEA ( 14 FDA reports)
EMBOLISM VENOUS ( 14 FDA reports)
EYE IRRITATION ( 14 FDA reports)
FUNGAL SEPSIS ( 14 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 14 FDA reports)
GRIMACING ( 14 FDA reports)
GROWTH RETARDATION ( 14 FDA reports)
HEARING AID USER ( 14 FDA reports)
HEPATORENAL SYNDROME ( 14 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 14 FDA reports)
HYPERAMMONAEMIA ( 14 FDA reports)
HYPERCAPNIA ( 14 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 14 FDA reports)
IATROGENIC INJURY ( 14 FDA reports)
IMMUNE SYSTEM DISORDER ( 14 FDA reports)
INGUINAL HERNIA ( 14 FDA reports)
INJECTION SITE HAEMORRHAGE ( 14 FDA reports)
INTERVERTEBRAL DISCITIS ( 14 FDA reports)
INTESTINAL ULCER ( 14 FDA reports)
JC VIRUS INFECTION ( 14 FDA reports)
JOINT ARTHROPLASTY ( 14 FDA reports)
KIDNEY MALFORMATION ( 14 FDA reports)
LIP SWELLING ( 14 FDA reports)
LIVER INJURY ( 14 FDA reports)
LOCALISED INFECTION ( 14 FDA reports)
MACULOPATHY ( 14 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 14 FDA reports)
MYOCARDITIS ( 14 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 14 FDA reports)
PARALYSIS FLACCID ( 14 FDA reports)
PERITONEAL DIALYSIS ( 14 FDA reports)
POLYARTHRITIS ( 14 FDA reports)
POLYMYOSITIS ( 14 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 13 FDA reports)
ANKLE FRACTURE ( 13 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 13 FDA reports)
ARTERIOVENOUS FISTULA ( 13 FDA reports)
ATRIAL TACHYCARDIA ( 13 FDA reports)
BEDRIDDEN ( 13 FDA reports)
BLADDER CANCER ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 13 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 13 FDA reports)
BONE MARROW TOXICITY ( 13 FDA reports)
BRAIN STEM INFARCTION ( 13 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 13 FDA reports)
CALCULUS URINARY ( 13 FDA reports)
COLECTOMY TOTAL ( 13 FDA reports)
COLONIC OBSTRUCTION ( 13 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 13 FDA reports)
CRYPTOCOCCOSIS ( 13 FDA reports)
DENTAL CARIES ( 13 FDA reports)
DIABETES INSIPIDUS ( 13 FDA reports)
DIFFICULTY IN WALKING ( 13 FDA reports)
ERUCTATION ( 13 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 13 FDA reports)
EYELID PTOSIS ( 13 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 13 FDA reports)
FUNGAL ENDOCARDITIS ( 13 FDA reports)
GENERAL SYMPTOM ( 13 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 13 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 13 FDA reports)
H1N1 INFLUENZA ( 13 FDA reports)
HALLUCINATION, AUDITORY ( 13 FDA reports)
HALLUCINATIONS, MIXED ( 13 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 13 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
KIDNEY ENLARGEMENT ( 13 FDA reports)
LABYRINTHITIS ( 13 FDA reports)
LARGE INTESTINAL ULCER ( 13 FDA reports)
LEUKOPLAKIA ORAL ( 13 FDA reports)
MALABSORPTION ( 13 FDA reports)
MENTAL IMPAIRMENT ( 13 FDA reports)
METASTASES TO SKIN ( 13 FDA reports)
MITRAL VALVE DISEASE ( 13 FDA reports)
MULTI-ORGAN DISORDER ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 13 FDA reports)
NON-CARDIAC CHEST PAIN ( 13 FDA reports)
ORAL SURGERY ( 13 FDA reports)
OSTEOLYSIS ( 13 FDA reports)
OSTEOPOROTIC FRACTURE ( 13 FDA reports)
PANCREATIC DISORDER ( 13 FDA reports)
PARAPARESIS ( 13 FDA reports)
PERITONEAL CANDIDIASIS ( 13 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 13 FDA reports)
PREMATURE LABOUR ( 13 FDA reports)
PYELOCALIECTASIS ( 13 FDA reports)
RENAL GRAFT LOSS ( 13 FDA reports)
RENAL MASS ( 13 FDA reports)
RENAL TUBULAR ACIDOSIS ( 13 FDA reports)
RENAL VEIN THROMBOSIS ( 13 FDA reports)
SICK SINUS SYNDROME ( 13 FDA reports)
SKIN REACTION ( 13 FDA reports)
STOMACH DISCOMFORT ( 13 FDA reports)
TOOTH REPAIR ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
TRICUSPID VALVE DISEASE ( 13 FDA reports)
VENOOCCLUSIVE DISEASE ( 13 FDA reports)
VENOUS INSUFFICIENCY ( 13 FDA reports)
VISUAL FIELD DEFECT ( 13 FDA reports)
WHEELCHAIR USER ( 13 FDA reports)
PULMONARY GRANULOMA ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
REPERFUSION INJURY ( 12 FDA reports)
SEROSITIS ( 12 FDA reports)
SKIN BURNING SENSATION ( 12 FDA reports)
SKIN NODULE ( 12 FDA reports)
SPINAL CORD DISORDER ( 12 FDA reports)
SPLENIC LESION ( 12 FDA reports)
STRESS SYMPTOMS ( 12 FDA reports)
THIRST ( 12 FDA reports)
THYROID CYST ( 12 FDA reports)
TONGUE DISORDER ( 12 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 12 FDA reports)
TYPE 1 DIABETES MELLITUS ( 12 FDA reports)
VERBAL ABUSE ( 12 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 12 FDA reports)
VERTIGO POSITIONAL ( 12 FDA reports)
ACUTE LUNG INJURY ( 12 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
ALVEOLITIS ALLERGIC ( 12 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 12 FDA reports)
AORTIC STENOSIS ( 12 FDA reports)
APRAXIA ( 12 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 12 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 12 FDA reports)
ASCITES INFECTION ( 12 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 12 FDA reports)
BLINDNESS UNILATERAL ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
BLOOD DISORDER ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
BRUXISM ( 12 FDA reports)
CARDIAC VALVE VEGETATION ( 12 FDA reports)
CAROTID ARTERY DISEASE ( 12 FDA reports)
CEREBROVASCULAR DISORDER ( 12 FDA reports)
CERVICAL SPINE FLATTENING ( 12 FDA reports)
COLOSTOMY ( 12 FDA reports)
CRYING ( 12 FDA reports)
CUTANEOUS TUBERCULOSIS ( 12 FDA reports)
DECREASED ACTIVITY ( 12 FDA reports)
DEMYELINATION ( 12 FDA reports)
DIVERTICULAR PERFORATION ( 12 FDA reports)
DRUG ADMINISTRATION ERROR ( 12 FDA reports)
DYSTHYMIC DISORDER ( 12 FDA reports)
ESCHAR ( 12 FDA reports)
EXOPHTHALMOS ( 12 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 12 FDA reports)
GALACTORRHOEA ( 12 FDA reports)
GASTRITIS HAEMORRHAGIC ( 12 FDA reports)
GASTROINTESTINAL PAIN ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
GUILLAIN-BARRE SYNDROME ( 12 FDA reports)
HAPTOGLOBIN DECREASED ( 12 FDA reports)
HEPATIC ENZYME ABNORMAL ( 12 FDA reports)
HEPATIC NEOPLASM ( 12 FDA reports)
HEPATITIS FULMINANT ( 12 FDA reports)
HYPERPARATHYROIDISM ( 12 FDA reports)
ILEITIS ( 12 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
ISCHAEMIC HEPATITIS ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
MENINGIOMA ( 12 FDA reports)
METASTASES TO PLEURA ( 12 FDA reports)
MICTURITION FREQUENCY DECREASED ( 12 FDA reports)
MUSCLE SPASTICITY ( 12 FDA reports)
MYELOMA RECURRENCE ( 12 FDA reports)
NEPHRITIC SYNDROME ( 12 FDA reports)
PALATAL DISORDER ( 12 FDA reports)
PAPILLOEDEMA ( 12 FDA reports)
PEPTIC ULCER PERFORATION ( 12 FDA reports)
PERINEPHRIC ABSCESS ( 12 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 12 FDA reports)
PERIPHERAL ISCHAEMIA ( 12 FDA reports)
PERITONEAL DISORDER ( 12 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 12 FDA reports)
PNEUMOPERITONEUM ( 12 FDA reports)
PRESCRIBED OVERDOSE ( 12 FDA reports)
PROCEDURAL PAIN ( 12 FDA reports)
ABDOMINAL HAEMATOMA ( 11 FDA reports)
ABDOMINAL NEOPLASM ( 11 FDA reports)
ACANTHAMOEBA INFECTION ( 11 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ALVEOLITIS ( 11 FDA reports)
AMENORRHOEA ( 11 FDA reports)
AORTIC VALVE DISEASE ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 11 FDA reports)
BLINDNESS CORTICAL ( 11 FDA reports)
BLOOD CHLORIDE INCREASED ( 11 FDA reports)
CARDIAC HYPERTROPHY ( 11 FDA reports)
CATHETER REMOVAL ( 11 FDA reports)
CEREBELLAR SYNDROME ( 11 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 11 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 11 FDA reports)
CLONIC CONVULSION ( 11 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 11 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 11 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 11 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 11 FDA reports)
ECTOPIC PREGNANCY ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 11 FDA reports)
ENTERITIS INFECTIOUS ( 11 FDA reports)
EPIDURAL LIPOMATOSIS ( 11 FDA reports)
EVANS SYNDROME ( 11 FDA reports)
EXTUBATION ( 11 FDA reports)
FACIAL PARESIS ( 11 FDA reports)
FEMORAL NECK FRACTURE ( 11 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 11 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 11 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 11 FDA reports)
GLOSSITIS ( 11 FDA reports)
GRANULOCYTOPENIA ( 11 FDA reports)
GRIP STRENGTH DECREASED ( 11 FDA reports)
HEPATIC FIBROSIS ( 11 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 11 FDA reports)
HISTOPLASMOSIS ( 11 FDA reports)
HYPERKERATOSIS ( 11 FDA reports)
HYPERPHAGIA ( 11 FDA reports)
HYPERTENSIVE HEART DISEASE ( 11 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 11 FDA reports)
INDUCED LABOUR ( 11 FDA reports)
INJECTION SITE SWELLING ( 11 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 11 FDA reports)
INTESTINAL INFARCTION ( 11 FDA reports)
INTRAOCULAR LENS IMPLANT ( 11 FDA reports)
LICHEN PLANUS ( 11 FDA reports)
LIPASE INCREASED ( 11 FDA reports)
LYMPHOCYTOSIS ( 11 FDA reports)
MASKED FACIES ( 11 FDA reports)
MEDICAL DEVICE COMPLICATION ( 11 FDA reports)
MORTON'S NEUROMA ( 11 FDA reports)
MUSCLE FATIGUE ( 11 FDA reports)
MUSCLE HAEMORRHAGE ( 11 FDA reports)
MUSCLE RUPTURE ( 11 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 11 FDA reports)
MYOPATHY TOXIC ( 11 FDA reports)
MYOPIA ( 11 FDA reports)
NEOPLASM ( 11 FDA reports)
ORCHITIS ( 11 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 11 FDA reports)
OTITIS MEDIA ( 11 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 11 FDA reports)
PLASMAPHERESIS ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 11 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 11 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 11 FDA reports)
PROTRUSION TONGUE ( 11 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 11 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 11 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 11 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 11 FDA reports)
RENAL HAEMORRHAGE ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
RETINAL DETACHMENT ( 11 FDA reports)
RETINOPATHY ( 11 FDA reports)
SNORING ( 11 FDA reports)
STUPOR ( 11 FDA reports)
SYSTEMIC MYCOSIS ( 11 FDA reports)
TACHYARRHYTHMIA ( 11 FDA reports)
THINKING ABNORMAL ( 11 FDA reports)
TROPONIN I INCREASED ( 11 FDA reports)
URINE ANALYSIS ABNORMAL ( 11 FDA reports)
VARICES OESOPHAGEAL ( 11 FDA reports)
VENTRICULAR DYSFUNCTION ( 11 FDA reports)
VENTRICULAR HYPOKINESIA ( 11 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 11 FDA reports)
VULVAL CANCER STAGE 0 ( 11 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 10 FDA reports)
PRURIGO ( 10 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 10 FDA reports)
RADICULITIS ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RETCHING ( 10 FDA reports)
SKIN TEST POSITIVE ( 10 FDA reports)
SKIN TOXICITY ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
SUBACUTE HEPATIC FAILURE ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
TONGUE ULCERATION ( 10 FDA reports)
TORSADE DE POINTES ( 10 FDA reports)
URINARY ANASTOMOTIC LEAK ( 10 FDA reports)
VASCULAR OCCLUSION ( 10 FDA reports)
VASCULITIS CEREBRAL ( 10 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 10 FDA reports)
VESICOURETERIC REFLUX ( 10 FDA reports)
VOCAL CORD PARALYSIS ( 10 FDA reports)
VULVAR DYSPLASIA ( 10 FDA reports)
ABSCESS FUNGAL ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 10 FDA reports)
ACUTE SINUSITIS ( 10 FDA reports)
AMAUROSIS FUGAX ( 10 FDA reports)
ANASTOMOTIC LEAK ( 10 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 10 FDA reports)
ATHEROSCLEROSIS ( 10 FDA reports)
ATRIAL SEPTAL DEFECT ( 10 FDA reports)
BACK DISORDER ( 10 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
BOWEL SOUNDS ABNORMAL ( 10 FDA reports)
BREAST CANCER FEMALE ( 10 FDA reports)
BREAST MASS ( 10 FDA reports)
BULLOUS LUNG DISEASE ( 10 FDA reports)
CATATONIA ( 10 FDA reports)
CELL MARKER INCREASED ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 10 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 10 FDA reports)
DYSAESTHESIA ( 10 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
ENCEPHALITIS HERPES ( 10 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 10 FDA reports)
EPIDERMOLYSIS ( 10 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 10 FDA reports)
ESCHERICHIA TEST POSITIVE ( 10 FDA reports)
EUPHORIC MOOD ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
FAILURE TO THRIVE ( 10 FDA reports)
FORAMEN MAGNUM STENOSIS ( 10 FDA reports)
FUNGAL PERITONITIS ( 10 FDA reports)
FUNGUS CULTURE POSITIVE ( 10 FDA reports)
GASTRIC CANCER ( 10 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
GLUCOSE URINE PRESENT ( 10 FDA reports)
GRAFT THROMBOSIS ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HUNGER ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
INCREASED TENDENCY TO BRUISE ( 10 FDA reports)
INFECTIOUS PERITONITIS ( 10 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 10 FDA reports)
INTESTINAL HAEMORRHAGE ( 10 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 10 FDA reports)
JOINT INSTABILITY ( 10 FDA reports)
JOINT STIFFNESS ( 10 FDA reports)
KELOID SCAR ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
LARYNGOCELE ( 10 FDA reports)
LIPOMA ( 10 FDA reports)
LIVEDO RETICULARIS ( 10 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 10 FDA reports)
MEDIASTINAL DISORDER ( 10 FDA reports)
MEDICAL DEVICE REMOVAL ( 10 FDA reports)
MUSCLE STRAIN ( 10 FDA reports)
MYELITIS TRANSVERSE ( 10 FDA reports)
MYOCLONUS ( 10 FDA reports)
NASAL CAVITY CANCER ( 10 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 10 FDA reports)
OESOPHAGEAL DISORDER ( 10 FDA reports)
ORAL INTAKE REDUCED ( 10 FDA reports)
OROPHARYNGEAL BLISTERING ( 10 FDA reports)
PANCREATITIS CHRONIC ( 10 FDA reports)
PELIOSIS HEPATIS ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
PILONIDAL CYST ( 10 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 10 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 10 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 10 FDA reports)
ACARODERMATITIS ( 9 FDA reports)
ACUTE PRERENAL FAILURE ( 9 FDA reports)
ALCOHOL ABUSE ( 9 FDA reports)
ALLERGY TO ANIMAL ( 9 FDA reports)
ANGIONEUROTIC OEDEMA ( 9 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 9 FDA reports)
ARTERIOSPASM CORONARY ( 9 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 9 FDA reports)
AXONAL NEUROPATHY ( 9 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BLADDER DILATATION ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BLOOD PROLACTIN INCREASED ( 9 FDA reports)
BLOOD VISCOSITY INCREASED ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
BREAST CANCER METASTATIC ( 9 FDA reports)
BREAST CANCER RECURRENT ( 9 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 9 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX SEPSIS ( 9 FDA reports)
CALCULUS URETERIC ( 9 FDA reports)
CARDIAC TAMPONADE ( 9 FDA reports)
CEREBRAL ASPERGILLOSIS ( 9 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 9 FDA reports)
CERVICAL MYELOPATHY ( 9 FDA reports)
CERVICOBRACHIAL SYNDROME ( 9 FDA reports)
CLONUS ( 9 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 9 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 9 FDA reports)
COOMBS TEST POSITIVE ( 9 FDA reports)
CORONARY ANGIOPLASTY ( 9 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 9 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 9 FDA reports)
CORONARY ARTERY THROMBOSIS ( 9 FDA reports)
CROUP INFECTIOUS ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DUODENAL POLYP ( 9 FDA reports)
DUODENITIS ( 9 FDA reports)
DYSPAREUNIA ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
EMPYEMA ( 9 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 9 FDA reports)
EPIGASTRIC DISCOMFORT ( 9 FDA reports)
EXERCISE TOLERANCE DECREASED ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
EYE INFECTION ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
FAECALOMA ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 9 FDA reports)
GASTRIC PERFORATION ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
GINGIVAL EROSION ( 9 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 9 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 9 FDA reports)
HEAD DISCOMFORT ( 9 FDA reports)
HIV INFECTION ( 9 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 9 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 9 FDA reports)
INGROWN HAIR ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 9 FDA reports)
KLEBSIELLA BACTERAEMIA ( 9 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 9 FDA reports)
LEUKAEMIA RECURRENT ( 9 FDA reports)
LIGAMENT LAXITY ( 9 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 9 FDA reports)
MUCOSAL HAEMORRHAGE ( 9 FDA reports)
MYCOBACTERIAL INFECTION ( 9 FDA reports)
MYOPATHY STEROID ( 9 FDA reports)
NEUROMYELITIS OPTICA ( 9 FDA reports)
OCULAR HYPERAEMIA ( 9 FDA reports)
ONYCHOMYCOSIS ( 9 FDA reports)
ORAL FUNGAL INFECTION ( 9 FDA reports)
ORAL PRURITUS ( 9 FDA reports)
OTITIS MEDIA ACUTE ( 9 FDA reports)
PAINFUL RESPIRATION ( 9 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 9 FDA reports)
PANNICULITIS ( 9 FDA reports)
PATHOLOGICAL GAMBLING ( 9 FDA reports)
PNEUMONIA ASPERGILLUS ( 9 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 9 FDA reports)
PNEUMONIA ESCHERICHIA ( 9 FDA reports)
PNEUMONIA LEGIONELLA ( 9 FDA reports)
PORTAL HYPERTENSION ( 9 FDA reports)
RADICAL HYSTERECTOMY ( 9 FDA reports)
REFLUX LARYNGITIS ( 9 FDA reports)
RENAL CORTICAL NECROSIS ( 9 FDA reports)
RENAL ISCHAEMIA ( 9 FDA reports)
RETROPERITONEAL INFECTION ( 9 FDA reports)
SACROILIITIS ( 9 FDA reports)
SALMONELLA SEPSIS ( 9 FDA reports)
SALPINGO-OOPHORECTOMY ( 9 FDA reports)
SCOTOMA ( 9 FDA reports)
SENSATION OF PRESSURE ( 9 FDA reports)
SKIN HAEMORRHAGE ( 9 FDA reports)
SKIN INFECTION ( 9 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 9 FDA reports)
SOFT TISSUE INFECTION ( 9 FDA reports)
SOMATOFORM DISORDER ( 9 FDA reports)
SPINAL FUSION SURGERY ( 9 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 9 FDA reports)
SPUTUM ABNORMAL ( 9 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 9 FDA reports)
TEMPORAL ARTERITIS ( 9 FDA reports)
TENDON PAIN ( 9 FDA reports)
THROMBOCYTOSIS ( 9 FDA reports)
THYROIDITIS ( 9 FDA reports)
TRANSFUSION REACTION ( 9 FDA reports)
URINARY TRACT DISORDER ( 9 FDA reports)
VASCULAR SKIN DISORDER ( 9 FDA reports)
VIRAEMIA ( 9 FDA reports)
WITHDRAWAL SYNDROME ( 9 FDA reports)
X-RAY ABNORMAL ( 9 FDA reports)
PUPILS UNEQUAL ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
REFLEXES ABNORMAL ( 8 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SINUS CONGESTION ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SMALL INTESTINAL PERFORATION ( 8 FDA reports)
SMALL INTESTINAL RESECTION ( 8 FDA reports)
SOMNAMBULISM ( 8 FDA reports)
STATUS ASTHMATICUS ( 8 FDA reports)
STRESS URINARY INCONTINENCE ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
THORACIC CAVITY DRAINAGE ( 8 FDA reports)
THYROTOXIC PERIODIC PARALYSIS ( 8 FDA reports)
THYROXINE FREE DECREASED ( 8 FDA reports)
TONGUE DISCOLOURATION ( 8 FDA reports)
URINARY CASTS ( 8 FDA reports)
URINARY FISTULA ( 8 FDA reports)
VASCULAR GRAFT OCCLUSION ( 8 FDA reports)
VENA CAVA THROMBOSIS ( 8 FDA reports)
VITAL CAPACITY DECREASED ( 8 FDA reports)
VITREOUS HAEMORRHAGE ( 8 FDA reports)
WOUND ABSCESS ( 8 FDA reports)
ABDOMINAL WALL ABSCESS ( 8 FDA reports)
ABORTION ( 8 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 8 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
ACUTE PSYCHOSIS ( 8 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
ALTERNARIA INFECTION ( 8 FDA reports)
AMYLOIDOSIS ( 8 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 8 FDA reports)
ANEURYSM RUPTURED ( 8 FDA reports)
AORTIC BYPASS ( 8 FDA reports)
AORTIC CALCIFICATION ( 8 FDA reports)
ARTERITIS ( 8 FDA reports)
ARTHRITIS INFECTIVE ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 8 FDA reports)
ATROPHY ( 8 FDA reports)
BIOPSY ( 8 FDA reports)
BLEPHARITIS ( 8 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BLOOD PH INCREASED ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BURSITIS INFECTIVE ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 8 FDA reports)
CATARACT NUCLEAR ( 8 FDA reports)
CATHETER PLACEMENT ( 8 FDA reports)
CEREBRAL THROMBOSIS ( 8 FDA reports)
CEREBROVASCULAR SPASM ( 8 FDA reports)
CHOREA ( 8 FDA reports)
CHORIORETINOPATHY ( 8 FDA reports)
CLUMSINESS ( 8 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 8 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 8 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 8 FDA reports)
ENCEPHALITIS VIRAL ( 8 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 8 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 8 FDA reports)
EROSIVE DUODENITIS ( 8 FDA reports)
ERYTHEMA NODOSUM ( 8 FDA reports)
EXCITABILITY ( 8 FDA reports)
EXTRADURAL ABSCESS ( 8 FDA reports)
EXTRAVASATION ( 8 FDA reports)
FLUID INTAKE REDUCED ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
FOOD ALLERGY ( 8 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 8 FDA reports)
GINGIVAL INFECTION ( 8 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 8 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 8 FDA reports)
GOUTY ARTHRITIS ( 8 FDA reports)
HEPATIC HAEMATOMA ( 8 FDA reports)
HYDROCELE ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
ILEAL PERFORATION ( 8 FDA reports)
ILEOSTOMY ( 8 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 8 FDA reports)
INFECTED SKIN ULCER ( 8 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 8 FDA reports)
INJECTION SITE IRRITATION ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 8 FDA reports)
INTESTINAL RESECTION ( 8 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
LEFT VENTRICULAR FAILURE ( 8 FDA reports)
LEUKAEMIA ( 8 FDA reports)
LIGAMENT INJURY ( 8 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 8 FDA reports)
LINEAR IGA DISEASE ( 8 FDA reports)
LIPOHYPERTROPHY ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
MENOPAUSAL SYMPTOMS ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
METASTASES TO ADRENALS ( 8 FDA reports)
METASTATIC NEOPLASM ( 8 FDA reports)
METRORRHAGIA ( 8 FDA reports)
MUCOUS MEMBRANE DISORDER ( 8 FDA reports)
MUSCLE NECROSIS ( 8 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
NASAL SEPTUM DEVIATION ( 8 FDA reports)
NECROSIS ISCHAEMIC ( 8 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 8 FDA reports)
OSTEOCHONDROSIS ( 8 FDA reports)
OVARIAN MASS ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PANCREATIC NEOPLASM ( 8 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 8 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 8 FDA reports)
PERITONITIS BACTERIAL ( 8 FDA reports)
PERSECUTORY DELUSION ( 8 FDA reports)
PRESBYOPIA ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
ABDOMINAL HERNIA ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ACQUIRED HAEMOPHILIA ( 7 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 7 FDA reports)
AFFECT LABILITY ( 7 FDA reports)
ALVEOLAR OSTEITIS ( 7 FDA reports)
AMAUROSIS ( 7 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 7 FDA reports)
ANOXIC ENCEPHALOPATHY ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
ANTITHROMBIN III DECREASED ( 7 FDA reports)
ARACHNOID CYST ( 7 FDA reports)
ARTERIAL THROMBOSIS ( 7 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 7 FDA reports)
ASTROCYTOMA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BILE DUCT NECROSIS ( 7 FDA reports)
BIOPSY GINGIVAL ( 7 FDA reports)
BIPOLAR II DISORDER ( 7 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD PRESSURE ABNORMAL ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
BONE MARROW NECROSIS ( 7 FDA reports)
BONE MARROW OEDEMA ( 7 FDA reports)
CACHEXIA ( 7 FDA reports)
CANDIDA TEST POSITIVE ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CAROTID BRUIT ( 7 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 7 FDA reports)
CEREBRAL ARTERY STENOSIS ( 7 FDA reports)
CHIMERISM ( 7 FDA reports)
CHOKING ( 7 FDA reports)
CHONDROMALACIA ( 7 FDA reports)
COAGULATION FACTOR DECREASED ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DRY THROAT ( 7 FDA reports)
DYSPHORIA ( 7 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 7 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 7 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 7 FDA reports)
EPIDERMAL NECROSIS ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
EYE INFLAMMATION ( 7 FDA reports)
FACIAL BONES FRACTURE ( 7 FDA reports)
FEMALE STERILISATION ( 7 FDA reports)
FEMORAL ARTERY OCCLUSION ( 7 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 7 FDA reports)
GASTRODUODENITIS ( 7 FDA reports)
GASTROENTERITIS SALMONELLA ( 7 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 7 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 7 FDA reports)
GESTATIONAL HYPERTENSION ( 7 FDA reports)
GINGIVAL HYPERPLASIA ( 7 FDA reports)
GLARE ( 7 FDA reports)
GLOMERULONEPHROPATHY ( 7 FDA reports)
HAEMANGIOMA OF SKIN ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HAEMOGLOBIN ABNORMAL ( 7 FDA reports)
HEPATIC INFARCTION ( 7 FDA reports)
HEPATITIS A ( 7 FDA reports)
HEPATITIS VIRAL ( 7 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 7 FDA reports)
HUMERUS FRACTURE ( 7 FDA reports)
HYDROPNEUMOTHORAX ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
HYPERTRICHOSIS ( 7 FDA reports)
HYPOPERFUSION ( 7 FDA reports)
ILLUSION ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCREASED APPETITE ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INJECTION SITE EXTRAVASATION ( 7 FDA reports)
INJECTION SITE ULCER ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
INTRACARDIAC THROMBUS ( 7 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
JUGULAR VEIN DISTENSION ( 7 FDA reports)
KIDNEY RUPTURE ( 7 FDA reports)
KLEBSIELLA TEST POSITIVE ( 7 FDA reports)
LAPAROTOMY ( 7 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 7 FDA reports)
LIFE EXPECTANCY SHORTENED ( 7 FDA reports)
LISTERIOSIS ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LOW TURNOVER OSTEOPATHY ( 7 FDA reports)
LYMPH NODE PAIN ( 7 FDA reports)
LYMPHANGITIS ( 7 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
MALIGNANT MELANOMA IN SITU ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MEGACOLON ( 7 FDA reports)
METHAEMOGLOBINAEMIA ( 7 FDA reports)
MONOPARESIS ( 7 FDA reports)
MOTION SICKNESS ( 7 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
MYELOPATHY ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
NERVE INJURY ( 7 FDA reports)
NEUROMYOPATHY ( 7 FDA reports)
ORAL NEOPLASM ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
OVARIAN NEOPLASM ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PANCREATIC NECROSIS ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PCO2 INCREASED ( 7 FDA reports)
PERICARDIAL CYST ( 7 FDA reports)
PERITONEAL HAEMORRHAGE ( 7 FDA reports)
PIGMENTATION DISORDER ( 7 FDA reports)
PLASMACYTOSIS ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POSTURING ( 7 FDA reports)
PROTEUS INFECTION ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
PYODERMA ( 7 FDA reports)
PYOTHORAX ( 7 FDA reports)
RAYNAUD'S PHENOMENON ( 7 FDA reports)
RED MAN SYNDROME ( 7 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 7 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RENAL HYPERTROPHY ( 7 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 7 FDA reports)
RESPIRATORY MONILIASIS ( 7 FDA reports)
RESPIRATORY RATE DECREASED ( 7 FDA reports)
RETINAL INFARCTION ( 7 FDA reports)
SCEDOSPORIUM INFECTION ( 7 FDA reports)
SCRATCH ( 7 FDA reports)
SICCA SYNDROME ( 7 FDA reports)
SIMPLE PARTIAL SEIZURES ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SKIN MASS ( 7 FDA reports)
SMALL FOR DATES BABY ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SPUTUM INCREASED ( 7 FDA reports)
STENOTROPHOMONAS INFECTION ( 7 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 7 FDA reports)
TEARFULNESS ( 7 FDA reports)
THYROID ADENOMA ( 7 FDA reports)
TRANSFUSION ( 7 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 7 FDA reports)
UMBILICAL CORD ABNORMALITY ( 7 FDA reports)
UNDERDOSE ( 7 FDA reports)
UPPER MOTOR NEURONE LESION ( 7 FDA reports)
URETERAL NECROSIS ( 7 FDA reports)
URETERITIS ( 7 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 7 FDA reports)
VAGINAL DISCHARGE ( 7 FDA reports)
VASCULAR GRAFT COMPLICATION ( 7 FDA reports)
VASOSPASM ( 7 FDA reports)
VENOUS STENOSIS ( 7 FDA reports)
VIRAL DNA TEST POSITIVE ( 7 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
PURULENCE ( 6 FDA reports)
QUADRIPARESIS ( 6 FDA reports)
RADIATION PNEUMONITIS ( 6 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
RETINAL VASCULITIS ( 6 FDA reports)
RHEUMATOID FACTOR INCREASED ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SCAB ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SENSATION OF FOREIGN BODY ( 6 FDA reports)
SENSORIMOTOR DISORDER ( 6 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SKIN STRIAE ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SPINAL DECOMPRESSION ( 6 FDA reports)
SPLENIC ARTERY ANEURYSM ( 6 FDA reports)
SPONDYLOLYSIS ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STENOTROPHOMONAS SEPSIS ( 6 FDA reports)
STREPTOCOCCAL SEPSIS ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 6 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
TENDON CALCIFICATION ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TENSION HEADACHE ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
TINEA CRURIS ( 6 FDA reports)
TONIC CLONIC MOVEMENTS ( 6 FDA reports)
TONSIL CANCER ( 6 FDA reports)
TONSILLAR HYPERTROPHY ( 6 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
TRICHOSPORON INFECTION ( 6 FDA reports)
TRIGEMINAL NEURALGIA ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
VAGINAL CANDIDIASIS ( 6 FDA reports)
VARICOSE VEINS VULVAL ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VERTEBRAL COLUMN MASS ( 6 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 6 FDA reports)
WOUND NECROSIS ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ABSCESS INTESTINAL ( 6 FDA reports)
ACCIDENT AT WORK ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ALCOHOL USE ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 6 FDA reports)
AMPUTATION ( 6 FDA reports)
ANAL FISTULA ( 6 FDA reports)
ANASTOMOTIC STENOSIS ( 6 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
APHAKIA ( 6 FDA reports)
ARACHNOIDITIS ( 6 FDA reports)
ARRESTED LABOUR ( 6 FDA reports)
ARTERIAL HAEMORRHAGE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BACTEROIDES INFECTION ( 6 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 6 FDA reports)
BONE METABOLISM DISORDER ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BRAIN SCAN ABNORMAL ( 6 FDA reports)
BREAST ABSCESS ( 6 FDA reports)
BREAST CANCER IN SITU ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 6 FDA reports)
BRONCHOSCOPY ( 6 FDA reports)
BUNION ( 6 FDA reports)
CAMPYLOBACTER INFECTION ( 6 FDA reports)
CANDIDURIA ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CASTLEMAN'S DISEASE ( 6 FDA reports)
CATHETERISATION CARDIAC ( 6 FDA reports)
CD4 LYMPHOCYTES ( 6 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 6 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 6 FDA reports)
CEREBRAL FUNGAL INFECTION ( 6 FDA reports)
CITROBACTER INFECTION ( 6 FDA reports)
COCCIDIOIDOMYCOSIS ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 6 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 6 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DISORDER OF ORBIT ( 6 FDA reports)
DISSOCIATION ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG LEVEL FLUCTUATING ( 6 FDA reports)
DRUG SCREEN POSITIVE ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 6 FDA reports)
ENDOMETRIOSIS ( 6 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 6 FDA reports)
EYE INFECTION FUNGAL ( 6 FDA reports)
FAMILY STRESS ( 6 FDA reports)
FEEDING DISORDER ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FINGER DEFORMITY ( 6 FDA reports)
FISTULA REPAIR ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FOETAL GROWTH RESTRICTION ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
FOOT AMPUTATION ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GINGIVAL ERYTHEMA ( 6 FDA reports)
GLOMERULOSCLEROSIS ( 6 FDA reports)
GRAFT INFECTION ( 6 FDA reports)
GRAFT ISCHAEMIA ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 6 FDA reports)
GRAVITATIONAL OEDEMA ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HAEMOGLOBINURIA ( 6 FDA reports)
HEPATIC CONGESTION ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HYPERAMYLASAEMIA ( 6 FDA reports)
HYPOCHROMIC ANAEMIA ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 6 FDA reports)
INCISIONAL HERNIA REPAIR ( 6 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 6 FDA reports)
INTESTINAL ANASTOMOSIS ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
IRON BINDING CAPACITY UNSATURATED INCREASED ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
JEJUNAL PERFORATION ( 6 FDA reports)
JOINT TUBERCULOSIS ( 6 FDA reports)
KERATITIS ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
LEUKAEMIA PLASMACYTIC ( 6 FDA reports)
LEUKODYSTROPHY ( 6 FDA reports)
LIFE SUPPORT ( 6 FDA reports)
LIGAMENT SPRAIN ( 6 FDA reports)
LIPOMATOSIS ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LUNG TRANSPLANT ( 6 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 6 FDA reports)
LYMPHOHISTIOCYTOSIS ( 6 FDA reports)
MADAROSIS ( 6 FDA reports)
MALIGNANT TUMOUR EXCISION ( 6 FDA reports)
MASTOCYTOSIS ( 6 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 6 FDA reports)
MENINGITIS TUBERCULOUS ( 6 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
MIGRAINE WITH AURA ( 6 FDA reports)
MOYAMOYA DISEASE ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 6 FDA reports)
MYOGLOBINURIA ( 6 FDA reports)
NEPHROSTOMY ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
OROANTRAL FISTULA ( 6 FDA reports)
OVERWORK ( 6 FDA reports)
PANCREATIC ABSCESS ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PARKINSON'S DISEASE ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PLATELET COUNT ABNORMAL ( 6 FDA reports)
PLEOCYTOSIS ( 6 FDA reports)
POISONING ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PREMATURE DELIVERY ( 6 FDA reports)
PRODUCT CONTAMINATION ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
ABNORMAL DREAMS ( 5 FDA reports)
ACCELERATED HYPERTENSION ( 5 FDA reports)
ACCIDENT AT HOME ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
ACID FAST BACILLI INFECTION ( 5 FDA reports)
ACINETOBACTER BACTERAEMIA ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 5 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 5 FDA reports)
ADIPOSIS DOLOROSA ( 5 FDA reports)
ADRENAL NEOPLASM ( 5 FDA reports)
ANAEMIA MEGALOBLASTIC ( 5 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 5 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANAL FISSURE EXCISION ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANOPLASTY ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
BACTERIAL PYELONEPHRITIS ( 5 FDA reports)
BACTERIAL TOXAEMIA ( 5 FDA reports)
BASAL GANGLION DEGENERATION ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 5 FDA reports)
BIOPSY LIVER ABNORMAL ( 5 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 5 FDA reports)
BLADDER IRRITATION ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLAST CELL CRISIS ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BONE LESION EXCISION ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BREAST CELLULITIS ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 5 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CATHETER SITE RELATED REACTION ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL CALCIFICATION ( 5 FDA reports)
CEREBRAL MICROANGIOPATHY ( 5 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 5 FDA reports)
CHEST WALL OPERATION ( 5 FDA reports)
CHOLANGITIS SUPPURATIVE ( 5 FDA reports)
CHRONIC FATIGUE SYNDROME ( 5 FDA reports)
COLON CANCER METASTATIC ( 5 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 5 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 5 FDA reports)
CONJUNCTIVAL OEDEMA ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 5 FDA reports)
CSF TEST ABNORMAL ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
CYSTITIS VIRAL ( 5 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 5 FDA reports)
DEAFNESS UNILATERAL ( 5 FDA reports)
DIABETIC COMA ( 5 FDA reports)
DIABETIC MICROANGIOPATHY ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRUG-INDUCED LIVER INJURY ( 5 FDA reports)
DURAL FISTULA ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
ENTEROBACTER SEPSIS ( 5 FDA reports)
ENTEROVESICAL FISTULA ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
EPIGLOTTITIS ( 5 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
EYES SUNKEN ( 5 FDA reports)
FACIAL SPASM ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FAT EMBOLISM ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
FOOD INTOLERANCE ( 5 FDA reports)
FOREIGN BODY ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GASTROINTESTINAL OEDEMA ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 5 FDA reports)
GOUTY TOPHUS ( 5 FDA reports)
GROWTH HORMONE DEFICIENCY ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEMIANOPIA HOMONYMOUS ( 5 FDA reports)
HEPATIC ARTERY ANEURYSM ( 5 FDA reports)
HEPATIC HAEMORRHAGE ( 5 FDA reports)
HEPATOCELLULAR INJURY ( 5 FDA reports)
HYPOGONADISM ( 5 FDA reports)
HYPOPITUITARISM ( 5 FDA reports)
IIIRD NERVE PARALYSIS ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCISION SITE PAIN ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFECTIVE TENOSYNOVITIS ( 5 FDA reports)
INJECTION SITE BURNING ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
INJECTION SITE STINGING ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INTERNAL HERNIA ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTRACRANIAL HAEMATOMA ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
KERATOMILEUSIS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LATENT TUBERCULOSIS ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
LUNG HYPERINFLATION ( 5 FDA reports)
LYMPHATIC DUCT RUPTURE ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 5 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 5 FDA reports)
MAXILLOFACIAL OPERATION ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MELANOMATOUS MENINGITIS ( 5 FDA reports)
MENINGITIS BACTERIAL ( 5 FDA reports)
METASTASES TO KIDNEY ( 5 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 5 FDA reports)
MUCOUS STOOLS ( 5 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 5 FDA reports)
MYCOTIC ANEURYSM ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYOCLONIC EPILEPSY ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
NAIL OPERATION ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
OLIGODENDROGLIOMA ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
OSTEOGENESIS IMPERFECTA ( 5 FDA reports)
OSTEOMA ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PANCREATITIS NECROTISING ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARTNER STRESS ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PERIRENAL HAEMATOMA ( 5 FDA reports)
PHARYNGEAL INFLAMMATION ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
PLACENTAL DISORDER ( 5 FDA reports)
PLASTIC SURGERY ( 5 FDA reports)
PNEUMONIA LIPOID ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
POTENTIATING DRUG INTERACTION ( 5 FDA reports)
POVERTY OF THOUGHT CONTENT ( 5 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 5 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PROCTOCOLECTOMY ( 5 FDA reports)
PROLAPSE REPAIR ( 5 FDA reports)
PULMONARY EOSINOPHILIA ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
PULMONARY SEPSIS ( 5 FDA reports)
PULMONARY VASCULITIS ( 5 FDA reports)
PYONEPHROSIS ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RENAL ABSCESS ( 5 FDA reports)
RENAL NECROSIS ( 5 FDA reports)
RENAL VEIN OCCLUSION ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 5 FDA reports)
RETINITIS ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
RHEUMATOID NODULE ( 5 FDA reports)
RHINOPLASTY ( 5 FDA reports)
SALMONELLOSIS ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
STARING ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
TOE AMPUTATION ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TONIC CONVULSION ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
UTERINE CANCER ( 5 FDA reports)
UTERINE DISORDER ( 5 FDA reports)
UTERINE PROLAPSE REPAIR ( 5 FDA reports)
VAGINAL INFECTION ( 5 FDA reports)
VEIN DISORDER ( 5 FDA reports)
VOCAL CORD DISORDER ( 5 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 5 FDA reports)
WAXY FLEXIBILITY ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
WOUND COMPLICATION ( 5 FDA reports)
WOUND DECOMPOSITION ( 5 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 4 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 4 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 4 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 4 FDA reports)
PSOAS ABSCESS ( 4 FDA reports)
PSYCHOLOGICAL TRAUMA ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
RECTAL LESION ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
RED BLOOD CELL ABNORMALITY ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 4 FDA reports)
REFRACTORY ANAEMIA ( 4 FDA reports)
RENAL ANEURYSM ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETICULOCYTE COUNT INCREASED ( 4 FDA reports)
RETROPERITONEAL ABSCESS ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 4 FDA reports)
SECONDARY HYPERTENSION ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SMALL CELL CARCINOMA ( 4 FDA reports)
SOLITARY KIDNEY ( 4 FDA reports)
SPINAL SHOCK ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SUPPORTIVE CARE ( 4 FDA reports)
SYSTEMIC SCLEROSIS ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 4 FDA reports)
THYROID GLAND ABSCESS ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONSILLAR DISORDER ( 4 FDA reports)
TONSILLECTOMY ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
TORULOPSIS INFECTION ( 4 FDA reports)
TRACHEAL ULCER ( 4 FDA reports)
TRANSFUSION MICROCHIMERISM ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 4 FDA reports)
TRIGEMINAL NERVE DISORDER ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TUBERCULOUS PLEURISY ( 4 FDA reports)
TUMOUR INVASION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
ULCERATIVE KERATITIS ( 4 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 4 FDA reports)
URACHAL ABSCESS ( 4 FDA reports)
UREAPLASMA INFECTION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URINARY SEDIMENT PRESENT ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE TRANSITIONAL CELLS PRESENT ( 4 FDA reports)
UTERINE POLYP ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VASCULAR HEADACHE ( 4 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VIRAL HEPATITIS CARRIER ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VIRAL TEST POSITIVE ( 4 FDA reports)
VISCERAL LEISHMANIASIS ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
VON WILLEBRAND'S FACTOR ACTIVITY INCREASED ( 4 FDA reports)
VON WILLEBRAND'S FACTOR ANTIGEN INCREASED ( 4 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 4 FDA reports)
WEIGHT BEARING DIFFICULTY ( 4 FDA reports)
WOUND EVISCERATION ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL SEPSIS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABSCESS BACTERIAL ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
ADHESION ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 4 FDA reports)
AEROMONA INFECTION ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ALOPECIA EFFLUVIUM ( 4 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 4 FDA reports)
ANAL FISSURE ( 4 FDA reports)
ANKLE DEFORMITY ( 4 FDA reports)
ANO-RECTAL STENOSIS ( 4 FDA reports)
ANORECTAL STENOSIS ( 4 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 4 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
APATHY ( 4 FDA reports)
APHONIA ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 4 FDA reports)
ASPERGILLOMA ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 4 FDA reports)
BILE ACID MALABSORPTION ( 4 FDA reports)
BILIARY DRAINAGE ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLOOD ARSENIC INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BRONCHIAL CARCINOMA ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BRONCHIAL SECRETION RETENTION ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CALCULUS BLADDER ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CARTILAGE ATROPHY ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CATHETER SEPSIS ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CENTRAL OBESITY ( 4 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 4 FDA reports)
CEREBROSPINAL FISTULA ( 4 FDA reports)
CERVIX DISORDER ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CHOREOATHETOSIS ( 4 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 4 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONCENTRIC SCLEROSIS ( 4 FDA reports)
CONJUNCTIVAL PALLOR ( 4 FDA reports)
CONTRAST MEDIA REACTION ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CRACKLES LUNG ( 4 FDA reports)
CRYOFIBRINOGENAEMIA ( 4 FDA reports)
CRYOGLOBULINAEMIA ( 4 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 4 FDA reports)
CSF GRANULOCYTE COUNT ABNORMAL ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CULTURE THROAT POSITIVE ( 4 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 4 FDA reports)
CYTOMEGALOVIRUS DUODENITIS ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 4 FDA reports)
DISTRIBUTIVE SHOCK ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG THERAPY ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ENTEROCOLITIS FUNGAL ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
EOSINOPHILIC LEUKAEMIA ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPENDYMOMA ( 4 FDA reports)
EPIDERMOLYSIS BULLOSA ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 4 FDA reports)
EYE INFECTION TOXOPLASMAL ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
EYELID PAIN ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FAT NECROSIS ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FIBROUS HISTIOCYTOMA ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FOETAL HEART RATE ABNORMAL ( 4 FDA reports)
FRACTURE DISPLACEMENT ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 4 FDA reports)
FUNGAL TEST POSITIVE ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTRITIS BACTERIAL ( 4 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 4 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 4 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL TOXICITY ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HELICOBACTER SEPSIS ( 4 FDA reports)
HELLP SYNDROME ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 4 FDA reports)
HEPATIC VEIN OCCLUSION ( 4 FDA reports)
HEPATIC VEIN STENOSIS ( 4 FDA reports)
HEPATITIS C RNA INCREASED ( 4 FDA reports)
HEPATITIS C RNA POSITIVE ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HODGKIN'S DISEASE STAGE II ( 4 FDA reports)
HOMICIDE ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 4 FDA reports)
HYPEROXALURIA ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOPNOEA ( 4 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
INTRAUTERINE INFECTION ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 4 FDA reports)
LEUKOENCEPHALOMYELITIS ( 4 FDA reports)
LEUKOPLAKIA ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LUNG LOBECTOMY ( 4 FDA reports)
LUNG NEOPLASM SURGERY ( 4 FDA reports)
LUNG OPERATION ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
LYMPHORRHOEA ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MASTOIDITIS ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
METAL POISONING ( 4 FDA reports)
METASTASES TO BONE MARROW ( 4 FDA reports)
METASTASES TO HEART ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
METASTASES TO SPLEEN ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
NEONATAL HYPONATRAEMIA ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NEUROCRYPTOCOCCOSIS ( 4 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 4 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
OPHTHALMOPLEGIA ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
OVARIAN CANCER METASTATIC ( 4 FDA reports)
OVARIAN GERM CELL CANCER STAGE III ( 4 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PALMAR ERYTHEMA ( 4 FDA reports)
PALPABLE PURPURA ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PARENTERAL NUTRITION ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PAST-POINTING ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PENIS DISORDER ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 4 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 4 FDA reports)
PERITONEAL ADHESIONS ( 4 FDA reports)
PERITONITIS SCLEROSING ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHAEHYPHOMYCOSIS ( 4 FDA reports)
PHONOPHOBIA ( 4 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 4 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PLEURAL HAEMORRHAGE ( 4 FDA reports)
PNEUMONECTOMY ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 4 FDA reports)
POST PROCEDURAL FISTULA ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 4 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 3 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALOPECIA TOTALIS ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANGIODYSPLASIA ( 3 FDA reports)
ANGIOSARCOMA METASTATIC ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANKLE OPERATION ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC EMBOLUS ( 3 FDA reports)
AORTIC RUPTURE ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTERITIS INFECTIVE ( 3 FDA reports)
ARTHRITIS FUNGAL ( 3 FDA reports)
ASPERGILLUS TEST ( 3 FDA reports)
ASPERGILLUS TEST POSITIVE ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
AUTOIMMUNE PANCREATITIS ( 3 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
AUTOMATIC BLADDER ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILIARY CYST ( 3 FDA reports)
BILIARY SPHINCTEROTOMY ( 3 FDA reports)
BILIARY TRACT INFECTION ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIOPSY KIDNEY ( 3 FDA reports)
BIOPSY LUNG ABNORMAL ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE TRIMMING ( 3 FDA reports)
BOWEN'S DISEASE ( 3 FDA reports)
BRACHIAL PLEXOPATHY ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST TENDERNESS ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHIAL ULCERATION ( 3 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARBON DIOXIDE ABNORMAL ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARDIAC ASTHMA ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDITIS ( 3 FDA reports)
CATARACT SUBCAPSULAR ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE NECROSIS ( 3 FDA reports)
CATHETER SITE OEDEMA ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL VASOCONSTRICTION ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHROMOSOMAL DELETION ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 3 FDA reports)
COMPLEMENT FACTOR DECREASED ( 3 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONDYLOMA ACUMINATUM ( 3 FDA reports)
CONJUNCTIVAL IRRITATION ( 3 FDA reports)
COR PULMONALE ACUTE ( 3 FDA reports)
CORNEAL PERFORATION ( 3 FDA reports)
CRYSTAL URINE PRESENT ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CYSTITIS BACTERIAL ( 3 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 3 FDA reports)
CYTOTOXIC OEDEMA ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DRUG TOLERANCE INCREASED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 3 FDA reports)
ENTEROBACTER BACTERAEMIA ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACTOR VIII DEFICIENCY ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GALLBLADDER PERFORATION ( 3 FDA reports)
GASTRIC CANCER STAGE IV ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 3 FDA reports)
GROIN ABSCESS ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA NEPHRITIS ( 3 FDA reports)
HEPATIC ARTERY EMBOLISM ( 3 FDA reports)
HEPATIC ARTERY OCCLUSION ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATITIS INFECTIOUS ( 3 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 3 FDA reports)
HERPES SEPSIS ( 3 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPERPROTEINAEMIA ( 3 FDA reports)
HYPERSEXUALITY ( 3 FDA reports)
HYPERSPLENISM ACQUIRED ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 3 FDA reports)
HYPOPYON ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
ILIAC ARTERY THROMBOSIS ( 3 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPLANT SITE URTICARIA ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INFECTIVE SPONDYLITIS ( 3 FDA reports)
INFESTATION ( 3 FDA reports)
INFUSION SITE THROMBOSIS ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
KERATOSIS FOLLICULAR ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
KOUNIS SYNDROME ( 3 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 3 FDA reports)
LARYNGEAL OBSTRUCTION ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LEUKAEMOID REACTION ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MASTOID DISORDER ( 3 FDA reports)
MEDIASTINITIS ( 3 FDA reports)
MENINGITIS HERPES ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METASTASES TO THORAX ( 3 FDA reports)
MICROSPORIDIA INFECTION ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MYELOCYTE COUNT INCREASED ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYOCARDIAC ABSCESS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 3 FDA reports)
NEPHROURETERECTOMY ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROPATHIC PAIN ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OCULOGYRIC CRISIS ( 3 FDA reports)
OEDEMATOUS PANCREATITIS ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
OOPHORITIS ( 3 FDA reports)
OPSOCLONUS MYOCLONUS ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
OVARIAN EPITHELIAL CANCER ( 3 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PAPILLARY THYROID CANCER ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PARANASAL SINUS DISCOMFORT ( 3 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARAOESOPHAGEAL ABSCESS ( 3 FDA reports)
PARESIS CRANIAL NERVE ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PELVIC KIDNEY ( 3 FDA reports)
PERICARDIAL DISEASE ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PERITONEAL EFFUSION ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHAEOCHROMOCYTOMA ( 3 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 3 FDA reports)
PLATELET DESTRUCTION INCREASED ( 3 FDA reports)
PLEURISY VIRAL ( 3 FDA reports)
PNEUMONIA HERPES VIRAL ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POOR SUCKING REFLEX ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
POSTRENAL FAILURE ( 3 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PSEUDALLESCHERIA INFECTION ( 3 FDA reports)
PULMONARY BULLA ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RASH FOLLICULAR ( 3 FDA reports)
REGRESSIVE BEHAVIOUR ( 3 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETINAL LASER COAGULATION ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RHINITIS HYPERTROPHIC ( 3 FDA reports)
SARCOMA METASTATIC ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCLERODACTYLIA ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SENSATION OF PRESSURE IN EAR ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SKIN GRAFT REJECTION ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBDURAL EMPYEMA ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
TARSAL TUNNEL SYNDROME ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TIC ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 3 FDA reports)
TRACHEOMALACIA ( 3 FDA reports)
TRAUMATIC FRACTURE ( 3 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 3 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
TUMOUR ULCERATION ( 3 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULAR STENT INSERTION ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VITREOUS DISORDER ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
YAWNING ( 3 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PUBIC PAIN ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY FISTULA ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
REACTION TO DRUG EXCIPIENT ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CANCER RECURRENT ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
RESECTION OF RECTUM ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETROPERITONEAL EFFUSION ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
RHABDOID TUMOUR OF THE KIDNEY ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIGHT AORTIC ARCH ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SALPINGOSTOMY ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SECONDARY HYPOGONADISM ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SECONDARY SEXUAL CHARACTERISTICS ABSENCE ( 2 FDA reports)
SECONDARY SYPHILIS ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSITISATION ( 2 FDA reports)
SERRATIA TEST POSITIVE ( 2 FDA reports)
SHRINKING LUNG SYNDROME ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKIN DYSTROPHY ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOMATOFORM DISORDER CARDIOVASCULAR ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL VASCULAR DISORDER ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLEEN PALPABLE ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STENT REMOVAL ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
STROKE VOLUME DECREASED ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SYMPTOM MASKED ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOSTOSIS ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TENSION ( 2 FDA reports)
TESTICULAR CYST ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYMUS DISORDER ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE CANCER METASTATIC ( 2 FDA reports)
TRACHEAL FISTULA ( 2 FDA reports)
TRANSIENT PSYCHOSIS ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 2 FDA reports)
TRICHOPHYTIC GRANULOMA ( 2 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URACHAL ABNORMALITY ( 2 FDA reports)
URAEMIC ENCEPHALOPATHY ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERIC PERFORATION ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE AMYLASE INCREASED ( 2 FDA reports)
URINE CYTOMEGALOVIRUS ( 2 FDA reports)
VAGINAL INFLAMMATION ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIS GASTROINTESTINAL ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VEILLONELLA INFECTION ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
VIRUS URINE TEST POSITIVE ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITREOUS ABSCESS ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VULVA CYST ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WEIGHT DECREASE NEONATAL ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ACANTHOLYSIS ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACHOLIA ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACUTE CHEST SYNDROME ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 2 FDA reports)
ADENOVIRAL HEPATITIS ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADRENOCORTICAL STEROID THERAPY ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-THYROID ANTIBODY ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTERITIS CORONARY ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHRITIS SALMONELLA ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BACILLUS TEST POSITIVE ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BALANOPOSTHITIS ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BED REST ( 2 FDA reports)
BILIARY ANASTOMOSIS ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BILOMA ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 2 FDA reports)
BLADDER CATHETER REMOVAL ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BODY HEIGHT BELOW NORMAL ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BONE TUBERCULOSIS ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIAL ANASTOMOSIS COMPLICATION ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURSA REMOVAL ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC INDEX DECREASED ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CARPUS CURVUS ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLS IN URINE ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBRAL SARCOIDOSIS ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CERVIX DYSTOCIA ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLANGITIS CHRONIC ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CHORIORETINAL DISORDER ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COLD EXPOSURE INJURY ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONUS MEDULLARIS SYNDROME ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL GRAFT REJECTION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CSF CULTURE POSITIVE ( 2 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
CUTANEOUS SARCOIDOSIS ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 2 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 2 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DURAL TEAR ( 2 FDA reports)
DWARFISM ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
ENCEPHALITIS ALLERGIC ( 2 FDA reports)
ENCEPHALITIS AUTOIMMUNE ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTEROBACTER PNEUMONIA ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
ETHANOL GELATION TEST POSITIVE ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EXTRAVASATION BLOOD ( 2 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FACTOR IX DEFICIENCY ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FACTOR XI DEFICIENCY ( 2 FDA reports)
FACTOR XII DEFICIENCY ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FASCIAL OPERATION ( 2 FDA reports)
FIBRILLARY GLOMERULONEPHRITIS ( 2 FDA reports)
FIBRIN ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FUNGAL DNA TEST POSITIVE ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
GALLBLADDER ABSCESS ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRITIS FUNGAL ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOSSECTOMY ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
HAEMANGIOMA REMOVAL ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOGLOBINAEMIA ( 2 FDA reports)
HAEMOPERFUSION ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HEAD LAG ABNORMAL ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HLA MARKER STUDY POSITIVE ( 2 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 2 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERURICOSURIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
IATROGENIC INFECTION ( 2 FDA reports)
IIIRD NERVE DISORDER ( 2 FDA reports)
ILEOCOLOSTOMY ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INFECTIOUS DISEASE CARRIER ( 2 FDA reports)
INFECTIVE ANEURYSM ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTRANASAL FUNGAL INFECTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KABUKI MAKE-UP SYNDROME ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL GRANULOMA ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEGIONELLA TEST ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LISTERIA ENCEPHALITIS ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
LYMPHOMA TRANSFORMATION ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MACULE ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGEAL NEOPLASM ( 2 FDA reports)
MENINGITIS CANDIDA ( 2 FDA reports)
MENINGITIS ENTEROCOCCAL ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENINGORADICULITIS ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 2 FDA reports)
MESENTERIC HAEMORRHAGE ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO NECK ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTATIC CARCINOID TUMOUR ( 2 FDA reports)
MICROSCOPIC POLYANGIITIS ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MISCARRIAGE OF PARTNER ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 2 FDA reports)
NECROTISING RETINITIS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROFIBROMA ( 2 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NOCARDIA SEPSIS ( 2 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
OCULOMOTOR STUDY ABNORMAL ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGAN TRANSPLANT ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PANCREATECTOMY ( 2 FDA reports)
PANCREATIC ENZYMES ABNORMAL ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAPROTEINAEMIA ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
PELVIC CONGESTION ( 2 FDA reports)
PELVIC POUCH PROCEDURE ( 2 FDA reports)
PERICARDITIS INFECTIVE ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PHAGOCYTOSIS ( 2 FDA reports)
PLACENTAL HYPERTROPHY ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
POROKERATOSIS ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
PORTAL VEIN STENOSIS ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALEXIA ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPERS' DISEASE ( 1 FDA reports)
ALPHA-1 ACID GLYCOPROTEIN INCREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANCER METASTATIC ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APGAR SCORE ABNORMAL ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ARTERIAL ANEURYSM REPAIR ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
BACILLARY ANGIOMATOSIS ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BARTONELLOSIS ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BIOPSY CHORIONIC VILLOUS ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIOPSY VOCAL CORD ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CALCULUS REMOVAL ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREECH DELIVERY ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOGRAM ABNORMAL ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CAPILLARY FRAGILITY INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC INDEX INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMOSIDERIN DEPOSITION ( 1 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA STAGE III ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMOBLASTOMYCOSIS ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION DISORDER NEONATAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLD AGGLUTININS ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLORECTOSTOMY ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL CYSTIC LUNG ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CRANIAL NERVE OPERATION ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
CRYSTAL NEPHROPATHY ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST ASPIRATION ABNORMAL ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYTAPHERESIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
CYTOMEGALOVIRUS MUCOCUTANEOUS ULCER ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIFFUSE MESANGIAL SCLEROSIS ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DILUTIONAL COAGULOPATHY ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIRECT INFECTION TRANSMISSION ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCRINE NEOPLASM MALIGNANT ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY LARGE BOWEL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPINEPHRINE ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EWING'S SARCOMA METASTATIC ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPOSURE VIA SEMEN ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRANODAL NK/T-CELL LYMPHOMA, NASAL TYPE ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR IX INHIBITION ( 1 FDA reports)
FACTOR XIII DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FALLOPIAN TUBE DISORDER ( 1 FDA reports)
FAMILIAL HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
FEAR OF PREGNANCY ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL RHINITIS ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOODPASTURE'S SYNDROME ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HASHIMOTO'S ENCEPHALOPATHY ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CYST INFECTION ( 1 FDA reports)
HEPATIC ENZYME ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOPULMONARY SYNDROME ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HODGKIN'S DISEASE REFRACTORY ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE I INFECTION ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPALLAESTHESIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE EXTRAVASATION ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKODERMA ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN MYXOEDEMATOSUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER AND PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
LIVER AND SMALL INTESTINE TRANSPLANT ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT TRANSFORMATION ( 1 FDA reports)
MARBURG'S VARIANT MULTIPLE SCLEROSIS ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEGAKARYOCYTES ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOCUTANEOUS ULCERATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIUM KANSASII PNEUMONIA ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDITIS MYCOTIC ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NATURAL KILLER CELL COUNT INCREASED ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTIC PRESERVATION INJURY OF GRAFT ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROBLASTOMA ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROBLASTOMA RECURRENT ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NONINFECTIVE BRONCHITIS ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGITIS BACTERIAL ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ORAL ALLERGY SYNDROME ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORBITAL APEX SYNDROME ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSMOLAR GAP ABNORMAL ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OSTEOSARCOMA LOCALISED ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN HAEMORRHAGE ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 1 FDA reports)
PARANEOPLASTIC CEREBELLAR DEGENERATION ( 1 FDA reports)
PARANEOPLASTIC DERMATOMYOSITIS ( 1 FDA reports)
PARASITIC TEST POSITIVE ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERICARDITIS FUNGAL ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTODYNAMIC THERAPY ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA TOXOPLASMAL ( 1 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 1 FDA reports)
PNEUMORETROPERITONEUM ( 1 FDA reports)
POIKILODERMA ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-ENGRAFTMENT IMMUNE REACTION ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PRIMARY HYPOTHYROIDISM ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOPARALYSIS ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 1 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VEIN OCCLUSION ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL AGENESIS ( 1 FDA reports)
RENAL AND PANCREAS TRANSPLANT ( 1 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL HAEMANGIOMA ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL SALT-WASTING SYNDROME ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENAL TUBERCULOSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALMONELLA TEST POSITIVE ( 1 FDA reports)
SALPINGO-OOPHORITIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCHNITZLER'S SYNDROME ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DEGENERATIVE DISORDER ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMOOTH MUSCLE CELL NEOPLASM ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPASTIC PARAPLEGIA ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINAL MENINGIOMA BENIGN ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURFACTANT PROTEIN INCREASED ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC ASPIRATION ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYMIC CANCER METASTATIC ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRANSFUSION WITH INCOMPATIBLE BLOOD ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT ABSCESS ( 1 FDA reports)
TRANSURETHRAL BLADDER RESECTION ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRIGEMINAL NERVE ABLATION ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TROPICAL SPASTIC PARESIS ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUBERCULOSIS OF INTRATHORACIC LYMPH NODES ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS AND UVEITIS SYNDROME ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TUMOUR RELATED COMPLICATION ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASONIC ANGIOGRAM ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC FISTULA ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL FISTULA ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY BLADDER SARCOMA ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 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 SODIUM INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENTOUSE EXTRACTION ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VESTIBULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL SINUSITIS ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN C DECREASED ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)
DYSPNOEA ( 741 FDA reports)
PNEUMONIA ( 713 FDA reports)
PAIN ( 696 FDA reports)
DIARRHOEA ( 649 FDA reports)
SEPSIS ( 639 FDA reports)
NAUSEA ( 611 FDA reports)
ANAEMIA ( 598 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 580 FDA reports)
VOMITING ( 559 FDA reports)
DRUG INEFFECTIVE ( 553 FDA reports)
ANXIETY ( 544 FDA reports)
HEADACHE ( 538 FDA reports)
HYPERTENSION ( 524 FDA reports)
THROMBOCYTOPENIA ( 524 FDA reports)
RESPIRATORY FAILURE ( 504 FDA reports)
ASTHENIA ( 460 FDA reports)
FATIGUE ( 454 FDA reports)
ABDOMINAL PAIN ( 450 FDA reports)
RENAL FAILURE ( 443 FDA reports)
HYPOTENSION ( 442 FDA reports)
MULTI-ORGAN FAILURE ( 438 FDA reports)
ARTHRALGIA ( 396 FDA reports)
BACK PAIN ( 388 FDA reports)
RENAL FAILURE ACUTE ( 388 FDA reports)
BLOOD CREATININE INCREASED ( 384 FDA reports)
INFECTION ( 376 FDA reports)
DEPRESSION ( 369 FDA reports)
RENAL IMPAIRMENT ( 348 FDA reports)
CONVULSION ( 344 FDA reports)
NEUTROPENIA ( 337 FDA reports)
INJURY ( 335 FDA reports)
PAIN IN EXTREMITY ( 332 FDA reports)
CHEST PAIN ( 331 FDA reports)
OEDEMA PERIPHERAL ( 331 FDA reports)
PANCYTOPENIA ( 326 FDA reports)
RASH ( 326 FDA reports)
MYOCARDIAL INFARCTION ( 322 FDA reports)
PLEURAL EFFUSION ( 318 FDA reports)
TRANSPLANT REJECTION ( 316 FDA reports)
URINARY TRACT INFECTION ( 314 FDA reports)
PULMONARY EMBOLISM ( 309 FDA reports)
DIZZINESS ( 307 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 307 FDA reports)
DEEP VEIN THROMBOSIS ( 303 FDA reports)
CONDITION AGGRAVATED ( 302 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 298 FDA reports)
FALL ( 292 FDA reports)
DIABETES MELLITUS ( 288 FDA reports)
MALAISE ( 275 FDA reports)
SEPTIC SHOCK ( 271 FDA reports)
COUGH ( 262 FDA reports)
HYPOAESTHESIA ( 258 FDA reports)
TACHYCARDIA ( 254 FDA reports)
LEUKOPENIA ( 250 FDA reports)
HAEMOGLOBIN DECREASED ( 243 FDA reports)
GRAFT VERSUS HOST DISEASE ( 242 FDA reports)
HAEMODIALYSIS ( 241 FDA reports)
PLATELET COUNT DECREASED ( 241 FDA reports)
WEIGHT DECREASED ( 234 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 230 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 229 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 226 FDA reports)
DEHYDRATION ( 224 FDA reports)
EMOTIONAL DISTRESS ( 219 FDA reports)
PARAESTHESIA ( 217 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 216 FDA reports)
HYPERGLYCAEMIA ( 215 FDA reports)
CARDIAC FAILURE ( 211 FDA reports)
CONFUSIONAL STATE ( 211 FDA reports)
CARDIAC ARREST ( 210 FDA reports)
ASPERGILLOSIS ( 208 FDA reports)
CEREBROVASCULAR ACCIDENT ( 207 FDA reports)
WEIGHT INCREASED ( 207 FDA reports)
FEBRILE NEUTROPENIA ( 206 FDA reports)
DEATH ( 205 FDA reports)
DRUG INTERACTION ( 203 FDA reports)
CONSTIPATION ( 201 FDA reports)
STAPHYLOCOCCAL INFECTION ( 200 FDA reports)
INSOMNIA ( 199 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 197 FDA reports)
BRONCHITIS ( 196 FDA reports)
MUSCULAR WEAKNESS ( 194 FDA reports)
ERYTHEMA ( 193 FDA reports)
HERPES ZOSTER ( 189 FDA reports)
SINUSITIS ( 188 FDA reports)
GAIT DISTURBANCE ( 186 FDA reports)
LOSS OF CONSCIOUSNESS ( 186 FDA reports)
OSTEONECROSIS OF JAW ( 183 FDA reports)
ATRIAL FIBRILLATION ( 182 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 182 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 182 FDA reports)
PRURITUS ( 182 FDA reports)
DECREASED APPETITE ( 181 FDA reports)
OEDEMA ( 177 FDA reports)
CHILLS ( 176 FDA reports)
HEPATIC FAILURE ( 175 FDA reports)
PULMONARY OEDEMA ( 175 FDA reports)
RESPIRATORY DISTRESS ( 174 FDA reports)
OSTEOARTHRITIS ( 173 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 171 FDA reports)
BLOOD PRESSURE INCREASED ( 171 FDA reports)
OSTEONECROSIS ( 170 FDA reports)
TENDON RUPTURE ( 167 FDA reports)
LUNG INFILTRATION ( 166 FDA reports)
BONE DISORDER ( 165 FDA reports)
CELLULITIS ( 165 FDA reports)
DISEASE PROGRESSION ( 165 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 165 FDA reports)
SOMNOLENCE ( 162 FDA reports)
TREMOR ( 161 FDA reports)
OSTEOMYELITIS ( 161 FDA reports)
PROTEINURIA ( 157 FDA reports)
IMPAIRED HEALING ( 155 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 154 FDA reports)
GASTRITIS ( 154 FDA reports)
INTERSTITIAL LUNG DISEASE ( 154 FDA reports)
LYMPHADENOPATHY ( 153 FDA reports)
ASCITES ( 152 FDA reports)
ABDOMINAL PAIN UPPER ( 150 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 150 FDA reports)
HYPOXIA ( 149 FDA reports)
PNEUMOTHORAX ( 149 FDA reports)
HEPATIC ENZYME INCREASED ( 148 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 148 FDA reports)
CHOLELITHIASIS ( 147 FDA reports)
DISEASE RECURRENCE ( 146 FDA reports)
HYPERHIDROSIS ( 146 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 146 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 145 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 145 FDA reports)
DYSPHAGIA ( 145 FDA reports)
HYPERLIPIDAEMIA ( 145 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 144 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 143 FDA reports)
HYPONATRAEMIA ( 143 FDA reports)
PSEUDOMONAS INFECTION ( 142 FDA reports)
HAEMORRHAGE ( 138 FDA reports)
PERITONITIS ( 135 FDA reports)
ASTHMA ( 134 FDA reports)
CHEST DISCOMFORT ( 134 FDA reports)
MYALGIA ( 133 FDA reports)
BRADYCARDIA ( 131 FDA reports)
MUCOSAL INFLAMMATION ( 131 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 130 FDA reports)
BLOOD BILIRUBIN INCREASED ( 129 FDA reports)
BONE PAIN ( 129 FDA reports)
TENDONITIS ( 129 FDA reports)
BLOOD GLUCOSE INCREASED ( 128 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 128 FDA reports)
MUSCLE SPASMS ( 127 FDA reports)
POST PROCEDURAL COMPLICATION ( 127 FDA reports)
BONE MARROW FAILURE ( 126 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 126 FDA reports)
LIVER TRANSPLANT REJECTION ( 126 FDA reports)
HYPERKALAEMIA ( 125 FDA reports)
LEUKOCYTOSIS ( 125 FDA reports)
OLIGURIA ( 123 FDA reports)
NEUROPATHY PERIPHERAL ( 122 FDA reports)
BLOOD UREA INCREASED ( 121 FDA reports)
INFUSION RELATED REACTION ( 121 FDA reports)
CARDIO-RESPIRATORY ARREST ( 118 FDA reports)
CANDIDIASIS ( 117 FDA reports)
HAEMATURIA ( 117 FDA reports)
HYPERSENSITIVITY ( 117 FDA reports)
METABOLIC ACIDOSIS ( 116 FDA reports)
BLOOD PRESSURE DECREASED ( 115 FDA reports)
SPINAL OSTEOARTHRITIS ( 115 FDA reports)
HEART RATE INCREASED ( 114 FDA reports)
PAIN IN JAW ( 114 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 112 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 112 FDA reports)
PALPITATIONS ( 112 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 111 FDA reports)
LUNG DISORDER ( 111 FDA reports)
SYNCOPE ( 111 FDA reports)
URTICARIA ( 111 FDA reports)
RESPIRATORY DISORDER ( 110 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 110 FDA reports)
OXYGEN SATURATION DECREASED ( 110 FDA reports)
LIVER DISORDER ( 109 FDA reports)
ROTATOR CUFF SYNDROME ( 109 FDA reports)
RHEUMATOID ARTHRITIS ( 108 FDA reports)
SWELLING ( 108 FDA reports)
ABDOMINAL DISTENSION ( 108 FDA reports)
METASTASES TO BONE ( 108 FDA reports)
HALLUCINATION ( 107 FDA reports)
HEPATITIS ( 107 FDA reports)
MENTAL STATUS CHANGES ( 107 FDA reports)
HYPOKALAEMIA ( 106 FDA reports)
CHOLESTASIS ( 105 FDA reports)
CORONARY ARTERY DISEASE ( 105 FDA reports)
INFLAMMATION ( 105 FDA reports)
LUNG INFECTION ( 105 FDA reports)
ANGINA PECTORIS ( 103 FDA reports)
SLEEP APNOEA SYNDROME ( 103 FDA reports)
VISION BLURRED ( 102 FDA reports)
ANHEDONIA ( 102 FDA reports)
HAEMATOMA ( 102 FDA reports)
ARTHRITIS ( 101 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 101 FDA reports)
ENCEPHALOPATHY ( 101 FDA reports)
NEPHROTIC SYNDROME ( 99 FDA reports)
WHEEZING ( 99 FDA reports)
SINUS TACHYCARDIA ( 98 FDA reports)
DYSPEPSIA ( 98 FDA reports)
MITRAL VALVE INCOMPETENCE ( 98 FDA reports)
AGRANULOCYTOSIS ( 96 FDA reports)
DYSARTHRIA ( 95 FDA reports)
SWELLING FACE ( 95 FDA reports)
TOOTH EXTRACTION ( 95 FDA reports)
CARDIAC DISORDER ( 94 FDA reports)
CEREBRAL HAEMORRHAGE ( 94 FDA reports)
DRUG HYPERSENSITIVITY ( 94 FDA reports)
ENTEROCOCCAL INFECTION ( 94 FDA reports)
GASTROENTERITIS ( 94 FDA reports)
BALANCE DISORDER ( 93 FDA reports)
LYMPHOCELE ( 93 FDA reports)
TUBERCULOSIS ( 93 FDA reports)
VASCULITIS ( 93 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 92 FDA reports)
ARRHYTHMIA ( 91 FDA reports)
ATELECTASIS ( 91 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 91 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 90 FDA reports)
BLOOD CALCIUM DECREASED ( 90 FDA reports)
COMA ( 90 FDA reports)
GASTROINTESTINAL DISORDER ( 90 FDA reports)
HAEMATOCRIT DECREASED ( 90 FDA reports)
JAUNDICE ( 90 FDA reports)
MEMORY IMPAIRMENT ( 90 FDA reports)
VISUAL IMPAIRMENT ( 90 FDA reports)
CEREBRAL INFARCTION ( 89 FDA reports)
NECK PAIN ( 89 FDA reports)
HAEMORRHOIDS ( 88 FDA reports)
THROMBOSIS ( 88 FDA reports)
SUICIDAL IDEATION ( 87 FDA reports)
URINARY INCONTINENCE ( 87 FDA reports)
EXOSTOSIS ( 87 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 87 FDA reports)
COLITIS ( 86 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 86 FDA reports)
MALNUTRITION ( 86 FDA reports)
NERVOUS SYSTEM DISORDER ( 86 FDA reports)
RHABDOMYOLYSIS ( 86 FDA reports)
SKIN LESION ( 86 FDA reports)
RENAL DISORDER ( 85 FDA reports)
BRAIN OEDEMA ( 85 FDA reports)
MYOPATHY ( 85 FDA reports)
PANCREATITIS ( 85 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 84 FDA reports)
BONE LESION ( 84 FDA reports)
EMPHYSEMA ( 84 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 83 FDA reports)
GALLBLADDER DISORDER ( 83 FDA reports)
MUSCULOSKELETAL PAIN ( 83 FDA reports)
NEPHROPATHY TOXIC ( 83 FDA reports)
NASOPHARYNGITIS ( 82 FDA reports)
CARDIOMYOPATHY ( 81 FDA reports)
FEELING ABNORMAL ( 81 FDA reports)
RENAL TUBULAR NECROSIS ( 81 FDA reports)
DIALYSIS ( 80 FDA reports)
LEUKOENCEPHALOPATHY ( 80 FDA reports)
ANURIA ( 79 FDA reports)
BRONCHOPNEUMONIA ( 79 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 79 FDA reports)
LYMPHOPENIA ( 79 FDA reports)
OVERDOSE ( 79 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 79 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 78 FDA reports)
BURSITIS ( 78 FDA reports)
DRUG TOXICITY ( 78 FDA reports)
AGITATION ( 77 FDA reports)
ANOREXIA ( 77 FDA reports)
CHOLANGITIS ( 77 FDA reports)
ESCHERICHIA INFECTION ( 77 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 77 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 76 FDA reports)
FUNGAL INFECTION ( 76 FDA reports)
HYPERCHOLESTEROLAEMIA ( 76 FDA reports)
BACTERAEMIA ( 75 FDA reports)
CATARACT ( 75 FDA reports)
HAEMOPTYSIS ( 75 FDA reports)
ACUTE RESPIRATORY FAILURE ( 74 FDA reports)
NO THERAPEUTIC RESPONSE ( 74 FDA reports)
STOMATITIS ( 74 FDA reports)
TOOTHACHE ( 74 FDA reports)
RENAL FAILURE CHRONIC ( 73 FDA reports)
SCAR ( 73 FDA reports)
PANCREATITIS ACUTE ( 73 FDA reports)
PNEUMONITIS ( 73 FDA reports)
DISORIENTATION ( 72 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 72 FDA reports)
CHOLECYSTITIS ACUTE ( 71 FDA reports)
ECONOMIC PROBLEM ( 71 FDA reports)
HYPOPHAGIA ( 71 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 71 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 71 FDA reports)
RECTAL HAEMORRHAGE ( 71 FDA reports)
SHOCK ( 71 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 71 FDA reports)
WOUND INFECTION ( 71 FDA reports)
BK VIRUS INFECTION ( 70 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 70 FDA reports)
DYSURIA ( 70 FDA reports)
NEOPLASM MALIGNANT ( 70 FDA reports)
CHOLECYSTITIS ( 69 FDA reports)
LETHARGY ( 69 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 69 FDA reports)
PRIMARY SEQUESTRUM ( 69 FDA reports)
PULMONARY HYPERTENSION ( 69 FDA reports)
UNEVALUABLE EVENT ( 69 FDA reports)
PULMONARY HAEMORRHAGE ( 68 FDA reports)
VENTRICULAR HYPERTROPHY ( 68 FDA reports)
VERTIGO ( 68 FDA reports)
BLOOD ALBUMIN DECREASED ( 68 FDA reports)
HEMIPARESIS ( 68 FDA reports)
JOINT SWELLING ( 68 FDA reports)
OFF LABEL USE ( 68 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 67 FDA reports)
CIRCULATORY COLLAPSE ( 67 FDA reports)
CONTUSION ( 67 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 67 FDA reports)
DIVERTICULUM ( 67 FDA reports)
HEPATOTOXICITY ( 67 FDA reports)
HYDRONEPHROSIS ( 67 FDA reports)
HYPOTHYROIDISM ( 67 FDA reports)
LUNG NEOPLASM ( 67 FDA reports)
MOUTH ULCERATION ( 67 FDA reports)
PERICARDIAL EFFUSION ( 67 FDA reports)
CARDIOMEGALY ( 66 FDA reports)
LUPUS NEPHRITIS ( 66 FDA reports)
STRESS ( 66 FDA reports)
TRANSAMINASES INCREASED ( 66 FDA reports)
PSYCHOTIC DISORDER ( 65 FDA reports)
PYELONEPHRITIS ( 65 FDA reports)
RADICULOPATHY ( 65 FDA reports)
HEPATIC STEATOSIS ( 65 FDA reports)
HEPATITIS C ( 65 FDA reports)
INFLUENZA LIKE ILLNESS ( 64 FDA reports)
MENISCUS LESION ( 64 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 64 FDA reports)
NIGHT SWEATS ( 64 FDA reports)
OSTEOPOROSIS ( 64 FDA reports)
POST PROCEDURAL BILE LEAK ( 64 FDA reports)
CARDIOVASCULAR DISORDER ( 63 FDA reports)
FISTULA ( 63 FDA reports)
GLOMERULONEPHRITIS ( 63 FDA reports)
HAEMODYNAMIC INSTABILITY ( 63 FDA reports)
HIATUS HERNIA ( 63 FDA reports)
RESPIRATORY TRACT INFECTION ( 63 FDA reports)
SHOCK HAEMORRHAGIC ( 63 FDA reports)
TYPE 2 DIABETES MELLITUS ( 63 FDA reports)
RASH ERYTHEMATOUS ( 62 FDA reports)
STEM CELL TRANSPLANT ( 62 FDA reports)
ABDOMINAL DISCOMFORT ( 62 FDA reports)
APHASIA ( 62 FDA reports)
GRAND MAL CONVULSION ( 62 FDA reports)
MYOCARDIAL ISCHAEMIA ( 62 FDA reports)
BACTERIAL INFECTION ( 61 FDA reports)
BLOOD POTASSIUM DECREASED ( 61 FDA reports)
DISTURBANCE IN ATTENTION ( 61 FDA reports)
HOT FLUSH ( 61 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 61 FDA reports)
MENTAL DISORDER ( 61 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 61 FDA reports)
SINUS DISORDER ( 61 FDA reports)
SURGERY ( 61 FDA reports)
TACHYPNOEA ( 61 FDA reports)
ANAPHYLACTIC REACTION ( 60 FDA reports)
DRY MOUTH ( 60 FDA reports)
HEMIPLEGIA ( 60 FDA reports)
NEPHROLITHIASIS ( 60 FDA reports)
OROPHARYNGEAL PAIN ( 60 FDA reports)
PHYSICAL DISABILITY ( 60 FDA reports)
ANGIOEDEMA ( 59 FDA reports)
EPILEPSY ( 59 FDA reports)
HYPERBILIRUBINAEMIA ( 59 FDA reports)
HYPOALBUMINAEMIA ( 59 FDA reports)
ILEUS ( 59 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 59 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 59 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 59 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 59 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 59 FDA reports)
SKIN ULCER ( 58 FDA reports)
URINE OUTPUT DECREASED ( 58 FDA reports)
WOUND DEHISCENCE ( 58 FDA reports)
AMNESIA ( 58 FDA reports)
CUSHINGOID ( 58 FDA reports)
DYSKINESIA ( 58 FDA reports)
MELAENA ( 58 FDA reports)
ABSCESS ( 57 FDA reports)
CARDIAC MURMUR ( 57 FDA reports)
COAGULOPATHY ( 57 FDA reports)
DYSPNOEA EXERTIONAL ( 57 FDA reports)
FEAR ( 57 FDA reports)
KAPOSI'S SARCOMA ( 57 FDA reports)
PURULENT DISCHARGE ( 57 FDA reports)
VENTRICULAR TACHYCARDIA ( 57 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 56 FDA reports)
THERAPY NON-RESPONDER ( 56 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 56 FDA reports)
ARTHROPATHY ( 56 FDA reports)
LOOSE TOOTH ( 56 FDA reports)
NEURALGIA ( 56 FDA reports)
PLANTAR FASCIITIS ( 56 FDA reports)
PRODUCTIVE COUGH ( 56 FDA reports)
HEPATOMEGALY ( 55 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 55 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 54 FDA reports)
CROHN'S DISEASE ( 54 FDA reports)
IMMUNOSUPPRESSION ( 54 FDA reports)
OESOPHAGITIS ( 54 FDA reports)
TOOTH ABSCESS ( 54 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 54 FDA reports)
UNRESPONSIVE TO STIMULI ( 54 FDA reports)
VIRAL INFECTION ( 54 FDA reports)
PULMONARY TUBERCULOSIS ( 53 FDA reports)
SPLENOMEGALY ( 53 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 53 FDA reports)
HAEMATOCHEZIA ( 53 FDA reports)
HAEMOLYTIC ANAEMIA ( 53 FDA reports)
ALOPECIA ( 52 FDA reports)
BACTERIAL SEPSIS ( 52 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 52 FDA reports)
OSTEOPENIA ( 52 FDA reports)
CARPAL TUNNEL SYNDROME ( 51 FDA reports)
METASTASES TO LUNG ( 51 FDA reports)
PROTHROMBIN TIME PROLONGED ( 51 FDA reports)
RENAL ARTERY STENOSIS ( 50 FDA reports)
UPPER LIMB FRACTURE ( 50 FDA reports)
URINARY RETENTION ( 50 FDA reports)
ZYGOMYCOSIS ( 50 FDA reports)
EJECTION FRACTION DECREASED ( 50 FDA reports)
HIP FRACTURE ( 50 FDA reports)
HYPERTHYROIDISM ( 50 FDA reports)
HYPOGLYCAEMIA ( 50 FDA reports)
BODY TEMPERATURE INCREASED ( 49 FDA reports)
LARGE INTESTINE PERFORATION ( 49 FDA reports)
MECHANICAL VENTILATION ( 49 FDA reports)
MOBILITY DECREASED ( 49 FDA reports)
ORAL HERPES ( 49 FDA reports)
SERUM SICKNESS ( 49 FDA reports)
SPEECH DISORDER ( 49 FDA reports)
SPINAL COMPRESSION FRACTURE ( 49 FDA reports)
TOOTH DISORDER ( 49 FDA reports)
RIB FRACTURE ( 48 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 48 FDA reports)
CHOLECYSTITIS CHRONIC ( 48 FDA reports)
DECREASED INTEREST ( 48 FDA reports)
EPISTAXIS ( 48 FDA reports)
FAECAL INCONTINENCE ( 48 FDA reports)
GRAFT DYSFUNCTION ( 48 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 48 FDA reports)
NEUROTOXICITY ( 48 FDA reports)
ABORTION SPONTANEOUS ( 47 FDA reports)
CARDIOGENIC SHOCK ( 47 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 47 FDA reports)
COLITIS ULCERATIVE ( 47 FDA reports)
MAJOR DEPRESSION ( 47 FDA reports)
PULMONARY FIBROSIS ( 47 FDA reports)
RASH MACULO-PAPULAR ( 47 FDA reports)
RESPIRATORY DEPRESSION ( 47 FDA reports)
SKIN EXFOLIATION ( 47 FDA reports)
TOOTH LOSS ( 47 FDA reports)
URETERIC OBSTRUCTION ( 46 FDA reports)
VISUAL ACUITY REDUCED ( 46 FDA reports)
ARTERIOSCLEROSIS ( 46 FDA reports)
BONE DENSITY DECREASED ( 46 FDA reports)
CYSTITIS HAEMORRHAGIC ( 46 FDA reports)
ECZEMA ( 46 FDA reports)
ESCHERICHIA SEPSIS ( 46 FDA reports)
FIBROMYALGIA ( 46 FDA reports)
FLUSHING ( 46 FDA reports)
GINGIVAL SWELLING ( 46 FDA reports)
HERPES SIMPLEX ( 46 FDA reports)
LACTIC ACIDOSIS ( 46 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 46 FDA reports)
ABNORMAL BEHAVIOUR ( 45 FDA reports)
DELIRIUM ( 45 FDA reports)
DIPLOPIA ( 45 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 45 FDA reports)
MALIGNANT MELANOMA ( 45 FDA reports)
PSEUDOMONAL SEPSIS ( 45 FDA reports)
PYELONEPHRITIS ACUTE ( 45 FDA reports)
SEDATION ( 45 FDA reports)
SERUM FERRITIN INCREASED ( 45 FDA reports)
STRONGYLOIDIASIS ( 45 FDA reports)
TENDON DISORDER ( 45 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 44 FDA reports)
EMOTIONAL DISORDER ( 44 FDA reports)
HEPATIC NECROSIS ( 44 FDA reports)
INTESTINAL OBSTRUCTION ( 44 FDA reports)
JOINT INJURY ( 44 FDA reports)
NECROSIS ( 44 FDA reports)
OBESITY ( 44 FDA reports)
PNEUMATOSIS INTESTINALIS ( 44 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 44 FDA reports)
ADRENAL INSUFFICIENCY ( 43 FDA reports)
DELUSION ( 43 FDA reports)
DEVICE RELATED INFECTION ( 43 FDA reports)
DRUG LEVEL INCREASED ( 43 FDA reports)
EAR PAIN ( 43 FDA reports)
LYMPHOMA ( 43 FDA reports)
MULTIPLE INJURIES ( 43 FDA reports)
MYELODYSPLASTIC SYNDROME ( 43 FDA reports)
PHARYNGEAL OEDEMA ( 43 FDA reports)
PHARYNGITIS ( 43 FDA reports)
PLATELET COUNT INCREASED ( 43 FDA reports)
RESPIRATORY ARREST ( 43 FDA reports)
TENOSYNOVITIS ( 43 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 42 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 42 FDA reports)
VAGINAL HAEMORRHAGE ( 42 FDA reports)
BONE DEBRIDEMENT ( 42 FDA reports)
CERVICAL DYSPLASIA ( 42 FDA reports)
DEBRIDEMENT ( 42 FDA reports)
DENTURE WEARER ( 42 FDA reports)
DYSPHONIA ( 42 FDA reports)
ENTEROBACTER INFECTION ( 42 FDA reports)
GRAFT COMPLICATION ( 42 FDA reports)
MIGRAINE ( 42 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 42 FDA reports)
PNEUMONIA KLEBSIELLA ( 42 FDA reports)
AGGRESSION ( 41 FDA reports)
BLISTER ( 41 FDA reports)
EAR INFECTION ( 41 FDA reports)
HEPATITIS B ( 41 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 41 FDA reports)
LIVER TRANSPLANT ( 41 FDA reports)
RESTLESSNESS ( 41 FDA reports)
STEVENS-JOHNSON SYNDROME ( 41 FDA reports)
TRANSPLANT FAILURE ( 41 FDA reports)
TREATMENT NONCOMPLIANCE ( 41 FDA reports)
RENAL CELL CARCINOMA ( 40 FDA reports)
RESTLESS LEGS SYNDROME ( 40 FDA reports)
SYNOVITIS ( 40 FDA reports)
TONSILLITIS ( 40 FDA reports)
TREATMENT FAILURE ( 40 FDA reports)
TUMOUR LYSIS SYNDROME ( 40 FDA reports)
ANAPHYLACTIC SHOCK ( 40 FDA reports)
APLASTIC ANAEMIA ( 40 FDA reports)
BRAIN ABSCESS ( 40 FDA reports)
CYTOLYTIC HEPATITIS ( 40 FDA reports)
FLUID OVERLOAD ( 40 FDA reports)
GINGIVITIS ( 40 FDA reports)
JAW OPERATION ( 40 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 40 FDA reports)
MULTIPLE SCLEROSIS ( 40 FDA reports)
PLEURISY ( 40 FDA reports)
BRONCHOSPASM ( 39 FDA reports)
CEREBRAL ISCHAEMIA ( 39 FDA reports)
CULTURE URINE POSITIVE ( 39 FDA reports)
CYANOSIS ( 39 FDA reports)
DRY EYE ( 39 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 39 FDA reports)
HEPATITIS CHOLESTATIC ( 39 FDA reports)
IGA NEPHROPATHY ( 39 FDA reports)
KLEBSIELLA INFECTION ( 39 FDA reports)
PNEUMONIA BACTERIAL ( 39 FDA reports)
SUBDURAL HAEMATOMA ( 39 FDA reports)
RESPIRATORY RATE INCREASED ( 38 FDA reports)
SKIN DISORDER ( 38 FDA reports)
ADENOVIRUS INFECTION ( 38 FDA reports)
BASAL CELL CARCINOMA ( 38 FDA reports)
CANDIDA SEPSIS ( 38 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 38 FDA reports)
EDENTULOUS ( 38 FDA reports)
EYE PAIN ( 38 FDA reports)
HYPERCALCAEMIA ( 38 FDA reports)
HYPERTHERMIA ( 38 FDA reports)
JOINT DISLOCATION ( 38 FDA reports)
NASAL CONGESTION ( 38 FDA reports)
NOCARDIOSIS ( 38 FDA reports)
OSTEITIS ( 38 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 38 FDA reports)
AUTOIMMUNE HEPATITIS ( 37 FDA reports)
BASEDOW'S DISEASE ( 37 FDA reports)
BLOOD CULTURE POSITIVE ( 37 FDA reports)
CAESAREAN SECTION ( 37 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 37 FDA reports)
CHRONIC SINUSITIS ( 37 FDA reports)
DERMATITIS ( 37 FDA reports)
DIVERTICULITIS ( 37 FDA reports)
DRUG RESISTANCE ( 37 FDA reports)
EXPOSED BONE IN JAW ( 37 FDA reports)
FEELING HOT ( 37 FDA reports)
HEAD INJURY ( 37 FDA reports)
LOBAR PNEUMONIA ( 37 FDA reports)
PALLOR ( 37 FDA reports)
PNEUMONIA ASPIRATION ( 37 FDA reports)
PROCEDURAL COMPLICATION ( 37 FDA reports)
TINNITUS ( 37 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 37 FDA reports)
RALES ( 36 FDA reports)
RENAL CYST ( 36 FDA reports)
SUDDEN DEATH ( 36 FDA reports)
TENDERNESS ( 36 FDA reports)
ABDOMINAL PAIN LOWER ( 36 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 36 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 36 FDA reports)
AORTIC ANEURYSM ( 36 FDA reports)
BREAST CANCER ( 36 FDA reports)
COLON CANCER ( 36 FDA reports)
COMPRESSION FRACTURE ( 36 FDA reports)
COORDINATION ABNORMAL ( 36 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 36 FDA reports)
DRUG EFFECT DECREASED ( 36 FDA reports)
GENERALISED OEDEMA ( 36 FDA reports)
HEPATIC ENCEPHALOPATHY ( 36 FDA reports)
HERPES VIRUS INFECTION ( 36 FDA reports)
INFLUENZA ( 36 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 36 FDA reports)
LIGAMENT RUPTURE ( 36 FDA reports)
MULTIPLE MYELOMA ( 36 FDA reports)
ORAL PAIN ( 36 FDA reports)
PARALYSIS ( 36 FDA reports)
POLYURIA ( 36 FDA reports)
DIVERTICULUM INTESTINAL ( 35 FDA reports)
FACE OEDEMA ( 35 FDA reports)
FACIAL PAIN ( 35 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 35 FDA reports)
HYPOAESTHESIA ORAL ( 35 FDA reports)
ILEUS PARALYTIC ( 35 FDA reports)
NEPHRECTOMY ( 35 FDA reports)
ODYNOPHAGIA ( 35 FDA reports)
ORAL CANDIDIASIS ( 35 FDA reports)
ORAL DISORDER ( 35 FDA reports)
ORTHOPNOEA ( 35 FDA reports)
PATHOLOGICAL FRACTURE ( 35 FDA reports)
RENAL TUBULAR ATROPHY ( 35 FDA reports)
RHINORRHOEA ( 35 FDA reports)
SCOLIOSIS ( 35 FDA reports)
SPINAL COLUMN STENOSIS ( 35 FDA reports)
TOOTH INFECTION ( 35 FDA reports)
TOXIC ENCEPHALOPATHY ( 35 FDA reports)
VIITH NERVE PARALYSIS ( 35 FDA reports)
RASH GENERALISED ( 34 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 34 FDA reports)
RENAL INJURY ( 34 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 34 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 34 FDA reports)
AREFLEXIA ( 34 FDA reports)
COGNITIVE DISORDER ( 34 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 34 FDA reports)
CORONARY ARTERY OCCLUSION ( 34 FDA reports)
DISSEMINATED TUBERCULOSIS ( 34 FDA reports)
DYSTONIA ( 34 FDA reports)
ECCHYMOSIS ( 34 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 34 FDA reports)
FRACTURE ( 34 FDA reports)
HAEMOLYSIS ( 34 FDA reports)
ILL-DEFINED DISORDER ( 34 FDA reports)
ISCHAEMIA ( 34 FDA reports)
KIDNEY FIBROSIS ( 34 FDA reports)
MITRAL VALVE PROLAPSE ( 34 FDA reports)
PANIC ATTACK ( 34 FDA reports)
PATHOGEN RESISTANCE ( 34 FDA reports)
PETECHIAE ( 34 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 33 FDA reports)
CEREBRAL ATROPHY ( 33 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 33 FDA reports)
DEMENTIA ( 33 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 33 FDA reports)
FOOT FRACTURE ( 33 FDA reports)
GASTRIC ULCER ( 33 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 33 FDA reports)
NEUTROPHIL COUNT DECREASED ( 33 FDA reports)
PERIARTHRITIS ( 33 FDA reports)
SENSORY DISTURBANCE ( 33 FDA reports)
SKIN DISCOLOURATION ( 33 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 33 FDA reports)
TRISMUS ( 33 FDA reports)
RASH PRURITIC ( 32 FDA reports)
UROSEPSIS ( 32 FDA reports)
ABDOMINAL TENDERNESS ( 32 FDA reports)
ATRIOVENTRICULAR BLOCK ( 32 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 32 FDA reports)
EATING DISORDER ( 32 FDA reports)
ENDOCARDITIS ( 32 FDA reports)
GINGIVAL PAIN ( 32 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 32 FDA reports)
HEPATITIS ACUTE ( 32 FDA reports)
INJECTION SITE PAIN ( 32 FDA reports)
INTESTINAL PERFORATION ( 32 FDA reports)
MANIA ( 32 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 32 FDA reports)
NEPHROPATHY ( 32 FDA reports)
ACUTE CORONARY SYNDROME ( 31 FDA reports)
BRONCHIECTASIS ( 31 FDA reports)
CARDIAC FIBRILLATION ( 31 FDA reports)
CHEST X-RAY ABNORMAL ( 31 FDA reports)
CLEFT LIP AND PALATE ( 31 FDA reports)
CUSHING'S SYNDROME ( 31 FDA reports)
ESCHERICHIA BACTERAEMIA ( 31 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 31 FDA reports)
FLATULENCE ( 31 FDA reports)
GRAFT LOSS ( 31 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 31 FDA reports)
JAW DISORDER ( 31 FDA reports)
JAW FRACTURE ( 31 FDA reports)
JOINT EFFUSION ( 31 FDA reports)
MEDICATION ERROR ( 31 FDA reports)
METASTASES TO LIVER ( 31 FDA reports)
MOOD SWINGS ( 31 FDA reports)
MUSCULOSKELETAL DISORDER ( 31 FDA reports)
OSTEOSCLEROSIS ( 31 FDA reports)
PERIODONTAL DISEASE ( 31 FDA reports)
RENAL PAIN ( 31 FDA reports)
RENAL TUBULAR DISORDER ( 31 FDA reports)
SENSORY LOSS ( 31 FDA reports)
VARICELLA ( 31 FDA reports)
VARICOSE VEIN ( 31 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 31 FDA reports)
PULMONARY CONGESTION ( 30 FDA reports)
RHONCHI ( 30 FDA reports)
SEROMA ( 30 FDA reports)
SKIN NECROSIS ( 30 FDA reports)
SLEEP DISORDER ( 30 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 30 FDA reports)
ABDOMINAL ABSCESS ( 30 FDA reports)
ANAPHYLACTOID REACTION ( 30 FDA reports)
ATAXIA ( 30 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 30 FDA reports)
CATARACT OPERATION ( 30 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 30 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 30 FDA reports)
DRUG DEPENDENCE ( 30 FDA reports)
ELECTROLYTE IMBALANCE ( 30 FDA reports)
HEART RATE IRREGULAR ( 30 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 30 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 30 FDA reports)
HYPOCALCAEMIA ( 30 FDA reports)
HYPOMAGNESAEMIA ( 30 FDA reports)
IMPLANT SITE INFECTION ( 30 FDA reports)
LUNG NEOPLASM MALIGNANT ( 30 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 30 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 30 FDA reports)
POLYNEUROPATHY ( 30 FDA reports)
PRESYNCOPE ( 30 FDA reports)
ABASIA ( 29 FDA reports)
ACUTE PULMONARY OEDEMA ( 29 FDA reports)
APLASIA ( 29 FDA reports)
ENTEROCOLITIS ( 29 FDA reports)
IRRITABLE BOWEL SYNDROME ( 29 FDA reports)
MASS ( 29 FDA reports)
PERIODONTITIS ( 29 FDA reports)
ROAD TRAFFIC ACCIDENT ( 29 FDA reports)
SKIN PAPILLOMA ( 29 FDA reports)
SUICIDE ATTEMPT ( 29 FDA reports)
ULCER ( 29 FDA reports)
VENTRICULAR FIBRILLATION ( 29 FDA reports)
WALKING AID USER ( 29 FDA reports)
SUBCUTANEOUS ABSCESS ( 28 FDA reports)
SWOLLEN TONGUE ( 28 FDA reports)
TARDIVE DYSKINESIA ( 28 FDA reports)
VENOUS THROMBOSIS ( 28 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 28 FDA reports)
ANGINA UNSTABLE ( 28 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 28 FDA reports)
APLASIA PURE RED CELL ( 28 FDA reports)
ASPIRATION ( 28 FDA reports)
CLOSTRIDIAL INFECTION ( 28 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 28 FDA reports)
DEPRESSED MOOD ( 28 FDA reports)
DERMATITIS CONTACT ( 28 FDA reports)
DILATATION ATRIAL ( 28 FDA reports)
DRUG ABUSE ( 28 FDA reports)
EXCORIATION ( 28 FDA reports)
FEBRILE BONE MARROW APLASIA ( 28 FDA reports)
FEMUR FRACTURE ( 28 FDA reports)
GINGIVAL ULCERATION ( 28 FDA reports)
HYPERURICAEMIA ( 28 FDA reports)
INCORRECT DOSE ADMINISTERED ( 28 FDA reports)
ISCHAEMIC STROKE ( 28 FDA reports)
LABORATORY TEST ABNORMAL ( 28 FDA reports)
LUNG CONSOLIDATION ( 28 FDA reports)
MASTICATION DISORDER ( 28 FDA reports)
MOUTH HAEMORRHAGE ( 28 FDA reports)
MUSCLE TWITCHING ( 28 FDA reports)
NERVOUSNESS ( 28 FDA reports)
PHLEBITIS ( 28 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 27 FDA reports)
ADVERSE EVENT ( 27 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 27 FDA reports)
BLOOD POTASSIUM INCREASED ( 27 FDA reports)
BLOOD URINE PRESENT ( 27 FDA reports)
CHOLECYSTECTOMY ( 27 FDA reports)
CYST ( 27 FDA reports)
DISCOMFORT ( 27 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 27 FDA reports)
FLUID RETENTION ( 27 FDA reports)
GINGIVAL RECESSION ( 27 FDA reports)
GLAUCOMA ( 27 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 27 FDA reports)
HEPATOSPLENOMEGALY ( 27 FDA reports)
NEUTROPHIL COUNT INCREASED ( 27 FDA reports)
OVARIAN CYST ( 27 FDA reports)
PEPTIC ULCER ( 27 FDA reports)
PERIPHERAL COLDNESS ( 27 FDA reports)
PLEURITIC PAIN ( 27 FDA reports)
SPINAL FRACTURE ( 27 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 27 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 27 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 27 FDA reports)
WOUND HAEMORRHAGE ( 27 FDA reports)
PSORIASIS ( 26 FDA reports)
SOFT TISSUE INFLAMMATION ( 26 FDA reports)
SYNOVIAL CYST ( 26 FDA reports)
TOOTH FRACTURE ( 26 FDA reports)
ABSCESS LIMB ( 26 FDA reports)
BLOOD SODIUM DECREASED ( 26 FDA reports)
BURNING SENSATION ( 26 FDA reports)
CONJUNCTIVITIS ( 26 FDA reports)
CORONARY ARTERY STENOSIS ( 26 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 26 FDA reports)
DEFORMITY ( 26 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 26 FDA reports)
ENCEPHALITIS ( 26 FDA reports)
FACIAL PALSY ( 26 FDA reports)
FIBRIN D DIMER INCREASED ( 26 FDA reports)
GOITRE ( 26 FDA reports)
HEPATIC CIRRHOSIS ( 26 FDA reports)
HEPATOBILIARY DISEASE ( 26 FDA reports)
HODGKIN'S DISEASE ( 26 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 26 FDA reports)
HYPOVENTILATION ( 26 FDA reports)
INCISIONAL HERNIA ( 26 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 26 FDA reports)
LARYNGEAL OEDEMA ( 26 FDA reports)
NEUROLOGICAL SYMPTOM ( 26 FDA reports)
NEUROPATHY ( 26 FDA reports)
NEUTROPENIC SEPSIS ( 26 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 26 FDA reports)
PARAPLEGIA ( 26 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 26 FDA reports)
POSTOPERATIVE INFECTION ( 26 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 25 FDA reports)
ANGIOPATHY ( 25 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 25 FDA reports)
DERMATOMYOSITIS ( 25 FDA reports)
DILATATION VENTRICULAR ( 25 FDA reports)
ERYTHEMA INFECTIOSUM ( 25 FDA reports)
EYELID OEDEMA ( 25 FDA reports)
GASTRIC DISORDER ( 25 FDA reports)
GASTROINTESTINAL NECROSIS ( 25 FDA reports)
GENERALISED ERYTHEMA ( 25 FDA reports)
GOUT ( 25 FDA reports)
GRANULOMA ( 25 FDA reports)
HAEMATOTOXICITY ( 25 FDA reports)
HAEMOTHORAX ( 25 FDA reports)
HALLUCINATION, VISUAL ( 25 FDA reports)
HERNIA ( 25 FDA reports)
HYPERPLASIA ( 25 FDA reports)
HYPOTHERMIA ( 25 FDA reports)
INGROWING NAIL ( 25 FDA reports)
LUMBAR RADICULOPATHY ( 25 FDA reports)
MENINGITIS ASEPTIC ( 25 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 25 FDA reports)
ORGANISING PNEUMONIA ( 25 FDA reports)
PELVIC PAIN ( 25 FDA reports)
PLEURAL FIBROSIS ( 25 FDA reports)
POLLAKIURIA ( 25 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 25 FDA reports)
PREGNANCY ( 25 FDA reports)
RASH MACULAR ( 25 FDA reports)
RHINITIS ( 25 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 24 FDA reports)
REFLUX OESOPHAGITIS ( 24 FDA reports)
RHINITIS ALLERGIC ( 24 FDA reports)
SINUS BRADYCARDIA ( 24 FDA reports)
STATUS EPILEPTICUS ( 24 FDA reports)
STRABISMUS ( 24 FDA reports)
STRESS FRACTURE ( 24 FDA reports)
TERATOGENICITY ( 24 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 24 FDA reports)
WOUND SECRETION ( 24 FDA reports)
ABDOMINAL INFECTION ( 24 FDA reports)
ACINETOBACTER INFECTION ( 24 FDA reports)
AORTIC DISSECTION ( 24 FDA reports)
ATRIAL FLUTTER ( 24 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 24 FDA reports)
DISABILITY ( 24 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 24 FDA reports)
IRRITABILITY ( 24 FDA reports)
LACRIMATION INCREASED ( 24 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 24 FDA reports)
OPPORTUNISTIC INFECTION ( 24 FDA reports)
ABORTION INDUCED ( 23 FDA reports)
ABSCESS DRAINAGE ( 23 FDA reports)
ACNE ( 23 FDA reports)
AORTIC VALVE INCOMPETENCE ( 23 FDA reports)
BONE MARROW TRANSPLANT ( 23 FDA reports)
BRAIN HERNIATION ( 23 FDA reports)
CAPILLARITIS ( 23 FDA reports)
DRUG ERUPTION ( 23 FDA reports)
ENDOTRACHEAL INTUBATION ( 23 FDA reports)
ERECTILE DYSFUNCTION ( 23 FDA reports)
GASTRIC POLYPS ( 23 FDA reports)
GASTROINTESTINAL ULCER ( 23 FDA reports)
HAEMANGIOMA ( 23 FDA reports)
HAEMORRHAGIC DIATHESIS ( 23 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 23 FDA reports)
HYDROCEPHALUS ( 23 FDA reports)
HYPOPROTEINAEMIA ( 23 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 23 FDA reports)
MENINGITIS ( 23 FDA reports)
MUCORMYCOSIS ( 23 FDA reports)
NEOPLASM PROGRESSION ( 23 FDA reports)
PNEUMOMEDIASTINUM ( 23 FDA reports)
QUADRIPLEGIA ( 23 FDA reports)
TENOSYNOVITIS STENOSANS ( 23 FDA reports)
THYROID CANCER ( 23 FDA reports)
THYROID NEOPLASM ( 23 FDA reports)
URETERIC STENOSIS ( 23 FDA reports)
UTERINE HAEMORRHAGE ( 23 FDA reports)
PURPURA ( 22 FDA reports)
RENAL TRANSPLANT ( 22 FDA reports)
SCIATICA ( 22 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 22 FDA reports)
ANEURYSM ( 22 FDA reports)
ANGER ( 22 FDA reports)
ANGIOSARCOMA ( 22 FDA reports)
BLINDNESS ( 22 FDA reports)
BLOOD CHLORIDE DECREASED ( 22 FDA reports)
BLOOD GLUCOSE DECREASED ( 22 FDA reports)
BONE MARROW DEPRESSION ( 22 FDA reports)
BONE OPERATION ( 22 FDA reports)
CARDIAC FAILURE ACUTE ( 22 FDA reports)
CERVIX CARCINOMA ( 22 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 22 FDA reports)
DEPENDENCE ( 22 FDA reports)
DYSPLASIA ( 22 FDA reports)
GASTRITIS EROSIVE ( 22 FDA reports)
HAEMATEMESIS ( 22 FDA reports)
HEARING IMPAIRED ( 22 FDA reports)
HEART TRANSPLANT REJECTION ( 22 FDA reports)
HIP ARTHROPLASTY ( 22 FDA reports)
HORDEOLUM ( 22 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 22 FDA reports)
LIMB INJURY ( 22 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 22 FDA reports)
MYDRIASIS ( 22 FDA reports)
MYOSITIS ( 22 FDA reports)
NEURITIS ( 22 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 22 FDA reports)
PLASMACYTOMA ( 22 FDA reports)
PROPOFOL INFUSION SYNDROME ( 22 FDA reports)
APNOEA ( 21 FDA reports)
CALCIPHYLAXIS ( 21 FDA reports)
CHROMATURIA ( 21 FDA reports)
COLITIS ISCHAEMIC ( 21 FDA reports)
CYSTITIS ( 21 FDA reports)
CYTOKINE RELEASE SYNDROME ( 21 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 21 FDA reports)
DENTAL CARE ( 21 FDA reports)
DIABETIC KETOACIDOSIS ( 21 FDA reports)
ENGRAFTMENT SYNDROME ( 21 FDA reports)
GANGRENE ( 21 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 21 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 21 FDA reports)
HYPOVOLAEMIA ( 21 FDA reports)
INCOHERENT ( 21 FDA reports)
INTRA-UTERINE DEATH ( 21 FDA reports)
KLEBSIELLA SEPSIS ( 21 FDA reports)
LACERATION ( 21 FDA reports)
LUNG ADENOCARCINOMA ( 21 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 21 FDA reports)
MENORRHAGIA ( 21 FDA reports)
MESENTERIC VASCULAR INSUFFICIENCY ( 21 FDA reports)
MONOCLONAL GAMMOPATHY ( 21 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 21 FDA reports)
PARANOIA ( 21 FDA reports)
POLYP ( 21 FDA reports)
PORTAL VEIN THROMBOSIS ( 21 FDA reports)
RADIATION ASSOCIATED PAIN ( 21 FDA reports)
RADIUS FRACTURE ( 21 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 21 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 21 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 21 FDA reports)
TOXOPLASMOSIS ( 21 FDA reports)
VISUAL DISTURBANCE ( 21 FDA reports)
WOUND ( 21 FDA reports)
RADIOTHERAPY ( 20 FDA reports)
SKIN LACERATION ( 20 FDA reports)
STREPTOCOCCAL INFECTION ( 20 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 20 FDA reports)
TONGUE INJURY ( 20 FDA reports)
TOOTH IMPACTED ( 20 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 20 FDA reports)
ABSCESS JAW ( 20 FDA reports)
ACIDOSIS ( 20 FDA reports)
B-CELL LYMPHOMA ( 20 FDA reports)
BILIARY COLIC ( 20 FDA reports)
BREAST PAIN ( 20 FDA reports)
BRONCHOSTENOSIS ( 20 FDA reports)
CERVICAL SPINAL STENOSIS ( 20 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 20 FDA reports)
COLECTOMY ( 20 FDA reports)
DYSSTASIA ( 20 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 20 FDA reports)
ENTEROCOCCAL SEPSIS ( 20 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 20 FDA reports)
ERYSIPELAS ( 20 FDA reports)
ERYTHEMA MULTIFORME ( 20 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 20 FDA reports)
EYE MOVEMENT DISORDER ( 20 FDA reports)
FACE INJURY ( 20 FDA reports)
GASTRIC HAEMORRHAGE ( 20 FDA reports)
HYPERTONIA ( 20 FDA reports)
IRON DEFICIENCY ANAEMIA ( 20 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 20 FDA reports)
LICHENOID KERATOSIS ( 20 FDA reports)
LIVER ABSCESS ( 20 FDA reports)
LYMPHADENITIS ( 20 FDA reports)
METASTASES TO SPINE ( 20 FDA reports)
METATARSALGIA ( 20 FDA reports)
MICROANGIOPATHY ( 20 FDA reports)
MOOD ALTERED ( 20 FDA reports)
MOTOR DYSFUNCTION ( 20 FDA reports)
MUSCLE DISORDER ( 20 FDA reports)
PERICARDITIS ( 20 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 20 FDA reports)
PNEUMONIA FUNGAL ( 20 FDA reports)
POST HERPETIC NEURALGIA ( 20 FDA reports)
BIPOLAR DISORDER ( 19 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 19 FDA reports)
BREATH SOUNDS ABNORMAL ( 19 FDA reports)
CARDIOPULMONARY FAILURE ( 19 FDA reports)
CUBITAL TUNNEL SYNDROME ( 19 FDA reports)
CYSTOCELE ( 19 FDA reports)
DECUBITUS ULCER ( 19 FDA reports)
DIASTOLIC DYSFUNCTION ( 19 FDA reports)
DRUG LEVEL DECREASED ( 19 FDA reports)
EAR DISCOMFORT ( 19 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 19 FDA reports)
ENDODONTIC PROCEDURE ( 19 FDA reports)
EOSINOPHILIA ( 19 FDA reports)
EPICONDYLITIS ( 19 FDA reports)
GROIN PAIN ( 19 FDA reports)
HYPERNATRAEMIA ( 19 FDA reports)
HYPERREFLEXIA ( 19 FDA reports)
HYPOREFLEXIA ( 19 FDA reports)
HYPOVOLAEMIC SHOCK ( 19 FDA reports)
IMPAIRED WORK ABILITY ( 19 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 19 FDA reports)
INTENTIONAL DRUG MISUSE ( 19 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 19 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 19 FDA reports)
LACUNAR INFARCTION ( 19 FDA reports)
LYMPHOEDEMA ( 19 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 19 FDA reports)
METASTASES TO LYMPH NODES ( 19 FDA reports)
MICTURITION URGENCY ( 19 FDA reports)
MOVEMENT DISORDER ( 19 FDA reports)
NASAL SEPTUM DISORDER ( 19 FDA reports)
NEUTROPENIC INFECTION ( 19 FDA reports)
NYSTAGMUS ( 19 FDA reports)
ORAL CAVITY FISTULA ( 19 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 19 FDA reports)
PROCTALGIA ( 19 FDA reports)
PROTEIN TOTAL DECREASED ( 19 FDA reports)
PULMONARY INFARCTION ( 19 FDA reports)
PYURIA ( 19 FDA reports)
SINUS ARRHYTHMIA ( 19 FDA reports)
SPUTUM CULTURE POSITIVE ( 19 FDA reports)
SURGICAL PROCEDURE REPEATED ( 19 FDA reports)
SYSTEMIC CANDIDA ( 19 FDA reports)
WALKING DISABILITY ( 19 FDA reports)
PRURITUS GENERALISED ( 18 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 18 FDA reports)
PULSE ABSENT ( 18 FDA reports)
RASH PUSTULAR ( 18 FDA reports)
RECTOCELE ( 18 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 18 FDA reports)
THYROTOXIC CRISIS ( 18 FDA reports)
TROPONIN INCREASED ( 18 FDA reports)
UVEITIS ( 18 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 18 FDA reports)
ARTERIAL DISORDER ( 18 FDA reports)
ARTHRITIS BACTERIAL ( 18 FDA reports)
ATROPHIC VULVOVAGINITIS ( 18 FDA reports)
BILIARY DYSKINESIA ( 18 FDA reports)
BRAIN STEM SYNDROME ( 18 FDA reports)
CAROTID ARTERY STENOSIS ( 18 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 18 FDA reports)
DIABETIC NEUROPATHY ( 18 FDA reports)
DUODENAL ULCER ( 18 FDA reports)
DYSGEUSIA ( 18 FDA reports)
ESSENTIAL HYPERTENSION ( 18 FDA reports)
FUNGAL SKIN INFECTION ( 18 FDA reports)
GAZE PALSY ( 18 FDA reports)
GINGIVAL DISORDER ( 18 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 18 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 18 FDA reports)
HEART RATE DECREASED ( 18 FDA reports)
HYPERPYREXIA ( 18 FDA reports)
HYPOPHOSPHATAEMIA ( 18 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 18 FDA reports)
INJECTION SITE ERYTHEMA ( 18 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 18 FDA reports)
JUVENILE ARTHRITIS ( 18 FDA reports)
LUNG TRANSPLANT REJECTION ( 18 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 18 FDA reports)
NOCTURIA ( 18 FDA reports)
OESOPHAGITIS ULCERATIVE ( 18 FDA reports)
PARVOVIRUS INFECTION ( 18 FDA reports)
PHOTOPHOBIA ( 18 FDA reports)
POSTURE ABNORMAL ( 18 FDA reports)
PREMATURE BABY ( 18 FDA reports)
ACTINOMYCOSIS ( 17 FDA reports)
APPENDICITIS ( 17 FDA reports)
AUTOIMMUNE THYROIDITIS ( 17 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 17 FDA reports)
BRAIN NEOPLASM ( 17 FDA reports)
CALCINOSIS ( 17 FDA reports)
CARDIAC VALVE DISEASE ( 17 FDA reports)
CATHETER RELATED INFECTION ( 17 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 17 FDA reports)
COLD SWEAT ( 17 FDA reports)
DEAFNESS NEUROSENSORY ( 17 FDA reports)
DENTAL FISTULA ( 17 FDA reports)
DEVICE OCCLUSION ( 17 FDA reports)
DRUG INTOLERANCE ( 17 FDA reports)
DYSPHEMIA ( 17 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 17 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 17 FDA reports)
ENGRAFT FAILURE ( 17 FDA reports)
FLANK PAIN ( 17 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 17 FDA reports)
HEMIANOPIA ( 17 FDA reports)
HYPERTENSIVE CRISIS ( 17 FDA reports)
HYPOACUSIS ( 17 FDA reports)
HYPOTONIA ( 17 FDA reports)
JUGULAR VEIN THROMBOSIS ( 17 FDA reports)
LUMBAR SPINAL STENOSIS ( 17 FDA reports)
LUNG ABSCESS ( 17 FDA reports)
NECROTISING FASCIITIS ( 17 FDA reports)
NODULE ( 17 FDA reports)
OCULAR HYPERTENSION ( 17 FDA reports)
OEDEMA MUCOSAL ( 17 FDA reports)
OPTIC NEURITIS ( 17 FDA reports)
ORTHOSTATIC HYPOTENSION ( 17 FDA reports)
PARAESTHESIA ORAL ( 17 FDA reports)
PELVIC FRACTURE ( 17 FDA reports)
PROSTATE CANCER ( 17 FDA reports)
RADICULAR PAIN ( 17 FDA reports)
SEQUESTRECTOMY ( 17 FDA reports)
SERRATIA INFECTION ( 17 FDA reports)
SPONDYLOLISTHESIS ( 17 FDA reports)
TELANGIECTASIA ( 17 FDA reports)
THROAT IRRITATION ( 17 FDA reports)
TRACHEOBRONCHITIS ( 17 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 17 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 17 FDA reports)
URINOMA ( 17 FDA reports)
VASCULAR PSEUDOANEURYSM ( 17 FDA reports)
WOUND DRAINAGE ( 17 FDA reports)
PULMONARY MASS ( 16 FDA reports)
PULMONARY TOXICITY ( 16 FDA reports)
PUPIL FIXED ( 16 FDA reports)
RECTAL FISSURE ( 16 FDA reports)
RIGHT VENTRICULAR FAILURE ( 16 FDA reports)
SARCOIDOSIS ( 16 FDA reports)
SEBORRHOEIC KERATOSIS ( 16 FDA reports)
SPUTUM PURULENT ( 16 FDA reports)
SQUAMOUS CELL CARCINOMA ( 16 FDA reports)
THROMBOPHLEBITIS ( 16 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 16 FDA reports)
VASCULAR CALCIFICATION ( 16 FDA reports)
WEGENER'S GRANULOMATOSIS ( 16 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 16 FDA reports)
BILE DUCT OBSTRUCTION ( 16 FDA reports)
BILE DUCT STENOSIS ( 16 FDA reports)
BIPOLAR I DISORDER ( 16 FDA reports)
BODY TEMPERATURE DECREASED ( 16 FDA reports)
BONE LOSS ( 16 FDA reports)
CARDIOTOXICITY ( 16 FDA reports)
CEREBRAL DISORDER ( 16 FDA reports)
COLONIC POLYP ( 16 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 16 FDA reports)
CREPITATIONS ( 16 FDA reports)
DERMATITIS EXFOLIATIVE ( 16 FDA reports)
DEVICE FAILURE ( 16 FDA reports)
DEVICE RELATED SEPSIS ( 16 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 16 FDA reports)
EMBOLISM ( 16 FDA reports)
FIBROSIS ( 16 FDA reports)
FOOT DEFORMITY ( 16 FDA reports)
FUNGAEMIA ( 16 FDA reports)
HAND FRACTURE ( 16 FDA reports)
HEPATIC CYST ( 16 FDA reports)
HEPATIC LESION ( 16 FDA reports)
HEPATITIS TOXIC ( 16 FDA reports)
HEPATOCELLULAR DAMAGE ( 16 FDA reports)
IMMUNODEFICIENCY ( 16 FDA reports)
INTESTINAL ISCHAEMIA ( 16 FDA reports)
LIVER GRAFT LOSS ( 16 FDA reports)
METASTASIS ( 16 FDA reports)
MOOD DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 16 FDA reports)
MUSCLE ATROPHY ( 16 FDA reports)
MUSCLE RIGIDITY ( 16 FDA reports)
MUSCLE TIGHTNESS ( 16 FDA reports)
NIGHTMARE ( 16 FDA reports)
OPEN WOUND ( 16 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 16 FDA reports)
OXYGEN SUPPLEMENTATION ( 16 FDA reports)
PARESIS ( 16 FDA reports)
PARTIAL SEIZURES ( 16 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 16 FDA reports)
PROSTHESIS USER ( 16 FDA reports)
ACINETOBACTER TEST POSITIVE ( 15 FDA reports)
ACUTE ABDOMEN ( 15 FDA reports)
ADENOCARCINOMA ( 15 FDA reports)
ALVEOLOPLASTY ( 15 FDA reports)
ANAL ABSCESS ( 15 FDA reports)
ANGIOFIBROMA ( 15 FDA reports)
APHTHOUS STOMATITIS ( 15 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 15 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 15 FDA reports)
AZOTAEMIA ( 15 FDA reports)
BLADDER DISORDER ( 15 FDA reports)
BLOOD BICARBONATE DECREASED ( 15 FDA reports)
BLOOD URIC ACID INCREASED ( 15 FDA reports)
BONE SCAN ABNORMAL ( 15 FDA reports)
BREAST RECONSTRUCTION ( 15 FDA reports)
CAPILLARY LEAK SYNDROME ( 15 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 15 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 15 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 15 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 15 FDA reports)
CSF PROTEIN INCREASED ( 15 FDA reports)
DEAFNESS ( 15 FDA reports)
DERMATITIS BULLOUS ( 15 FDA reports)
DRUG DOSE OMISSION ( 15 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 15 FDA reports)
EOSINOPHIL COUNT INCREASED ( 15 FDA reports)
EXANTHEM ( 15 FDA reports)
FAECES DISCOLOURED ( 15 FDA reports)
FEELING COLD ( 15 FDA reports)
HEPATIC ARTERY STENOSIS ( 15 FDA reports)
HYPOKINESIA ( 15 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 15 FDA reports)
INJECTION SITE REACTION ( 15 FDA reports)
JOINT SPRAIN ( 15 FDA reports)
LYMPHOCYTIC INFILTRATION ( 15 FDA reports)
METABOLIC DISORDER ( 15 FDA reports)
NO ADVERSE EVENT ( 15 FDA reports)
PARAPSORIASIS ( 15 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 15 FDA reports)
PERONEAL NERVE PALSY ( 15 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 15 FDA reports)
PO2 DECREASED ( 15 FDA reports)
PROCTITIS ( 15 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 15 FDA reports)
PULMONARY RADIATION INJURY ( 15 FDA reports)
PULSE ABNORMAL ( 15 FDA reports)
RECTAL ABSCESS ( 15 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 15 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 15 FDA reports)
RENAL INFARCT ( 15 FDA reports)
RESPIRATORY ACIDOSIS ( 15 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 15 FDA reports)
SPINAL DISORDER ( 15 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 15 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 15 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 15 FDA reports)
TENDON INJURY ( 15 FDA reports)
THROAT TIGHTNESS ( 15 FDA reports)
TOBACCO ABUSE ( 15 FDA reports)
TRACHEOSTOMY ( 15 FDA reports)
UTERINE LEIOMYOMA ( 15 FDA reports)
PROTEIN URINE PRESENT ( 14 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 14 FDA reports)
RASH PAPULAR ( 14 FDA reports)
SPINAL LAMINECTOMY ( 14 FDA reports)
SPLENIC INFARCTION ( 14 FDA reports)
SUBCUTANEOUS NODULE ( 14 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 14 FDA reports)
T-CELL LYMPHOMA ( 14 FDA reports)
ACUTE HEPATIC FAILURE ( 14 FDA reports)
ANIMAL BITE ( 14 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 14 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 14 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 14 FDA reports)
BILE DUCT STONE ( 14 FDA reports)
BILIARY ISCHAEMIA ( 14 FDA reports)
BLEEDING TIME PROLONGED ( 14 FDA reports)
BLOOD AMYLASE INCREASED ( 14 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 14 FDA reports)
BONE NEOPLASM MALIGNANT ( 14 FDA reports)
CEREBELLAR INFARCTION ( 14 FDA reports)
CLOSTRIDIUM COLITIS ( 14 FDA reports)
CORONARY ARTERY BYPASS ( 14 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 14 FDA reports)
DROP ATTACKS ( 14 FDA reports)
DRUG ABUSER ( 14 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 14 FDA reports)
DYSLIPIDAEMIA ( 14 FDA reports)
DYSMENORRHOEA ( 14 FDA reports)
EMBOLISM VENOUS ( 14 FDA reports)
EYE IRRITATION ( 14 FDA reports)
FUNGAL SEPSIS ( 14 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 14 FDA reports)
GRIMACING ( 14 FDA reports)
GROWTH RETARDATION ( 14 FDA reports)
HEARING AID USER ( 14 FDA reports)
HEPATORENAL SYNDROME ( 14 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 14 FDA reports)
HYPERAMMONAEMIA ( 14 FDA reports)
HYPERCAPNIA ( 14 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 14 FDA reports)
IATROGENIC INJURY ( 14 FDA reports)
IMMUNE SYSTEM DISORDER ( 14 FDA reports)
INGUINAL HERNIA ( 14 FDA reports)
INJECTION SITE HAEMORRHAGE ( 14 FDA reports)
INTERVERTEBRAL DISCITIS ( 14 FDA reports)
INTESTINAL ULCER ( 14 FDA reports)
JC VIRUS INFECTION ( 14 FDA reports)
JOINT ARTHROPLASTY ( 14 FDA reports)
KIDNEY MALFORMATION ( 14 FDA reports)
LIP SWELLING ( 14 FDA reports)
LIVER INJURY ( 14 FDA reports)
LOCALISED INFECTION ( 14 FDA reports)
MACULOPATHY ( 14 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 14 FDA reports)
MYOCARDITIS ( 14 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 14 FDA reports)
PARALYSIS FLACCID ( 14 FDA reports)
PERITONEAL DIALYSIS ( 14 FDA reports)
POLYARTHRITIS ( 14 FDA reports)
POLYMYOSITIS ( 14 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 13 FDA reports)
ANKLE FRACTURE ( 13 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 13 FDA reports)
ARTERIOVENOUS FISTULA ( 13 FDA reports)
ATRIAL TACHYCARDIA ( 13 FDA reports)
BEDRIDDEN ( 13 FDA reports)
BLADDER CANCER ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 13 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 13 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 13 FDA reports)
BONE MARROW TOXICITY ( 13 FDA reports)
BRAIN STEM INFARCTION ( 13 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 13 FDA reports)
CALCULUS URINARY ( 13 FDA reports)
COLECTOMY TOTAL ( 13 FDA reports)
COLONIC OBSTRUCTION ( 13 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 13 FDA reports)
CRYPTOCOCCOSIS ( 13 FDA reports)
DENTAL CARIES ( 13 FDA reports)
DIABETES INSIPIDUS ( 13 FDA reports)
DIFFICULTY IN WALKING ( 13 FDA reports)
ERUCTATION ( 13 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 13 FDA reports)
EYELID PTOSIS ( 13 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 13 FDA reports)
FUNGAL ENDOCARDITIS ( 13 FDA reports)
GENERAL SYMPTOM ( 13 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 13 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 13 FDA reports)
H1N1 INFLUENZA ( 13 FDA reports)
HALLUCINATION, AUDITORY ( 13 FDA reports)
HALLUCINATIONS, MIXED ( 13 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 13 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 13 FDA reports)
IMPETIGO ( 13 FDA reports)
KIDNEY ENLARGEMENT ( 13 FDA reports)
LABYRINTHITIS ( 13 FDA reports)
LARGE INTESTINAL ULCER ( 13 FDA reports)
LEUKOPLAKIA ORAL ( 13 FDA reports)
MALABSORPTION ( 13 FDA reports)
MENTAL IMPAIRMENT ( 13 FDA reports)
METASTASES TO SKIN ( 13 FDA reports)
MITRAL VALVE DISEASE ( 13 FDA reports)
MULTI-ORGAN DISORDER ( 13 FDA reports)
NEPHRITIS INTERSTITIAL ( 13 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 13 FDA reports)
NON-CARDIAC CHEST PAIN ( 13 FDA reports)
ORAL SURGERY ( 13 FDA reports)
OSTEOLYSIS ( 13 FDA reports)
OSTEOPOROTIC FRACTURE ( 13 FDA reports)
PANCREATIC DISORDER ( 13 FDA reports)
PARAPARESIS ( 13 FDA reports)
PERITONEAL CANDIDIASIS ( 13 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 13 FDA reports)
PREMATURE LABOUR ( 13 FDA reports)
PYELOCALIECTASIS ( 13 FDA reports)
RENAL GRAFT LOSS ( 13 FDA reports)
RENAL MASS ( 13 FDA reports)
RENAL TUBULAR ACIDOSIS ( 13 FDA reports)
RENAL VEIN THROMBOSIS ( 13 FDA reports)
SICK SINUS SYNDROME ( 13 FDA reports)
SKIN REACTION ( 13 FDA reports)
STOMACH DISCOMFORT ( 13 FDA reports)
TOOTH REPAIR ( 13 FDA reports)
TOXIC SKIN ERUPTION ( 13 FDA reports)
TRICUSPID VALVE DISEASE ( 13 FDA reports)
VENOOCCLUSIVE DISEASE ( 13 FDA reports)
VENOUS INSUFFICIENCY ( 13 FDA reports)
VISUAL FIELD DEFECT ( 13 FDA reports)
WHEELCHAIR USER ( 13 FDA reports)
PULMONARY GRANULOMA ( 12 FDA reports)
RENAL ATROPHY ( 12 FDA reports)
REPERFUSION INJURY ( 12 FDA reports)
SEROSITIS ( 12 FDA reports)
SKIN BURNING SENSATION ( 12 FDA reports)
SKIN NODULE ( 12 FDA reports)
SPINAL CORD DISORDER ( 12 FDA reports)
SPLENIC LESION ( 12 FDA reports)
STRESS SYMPTOMS ( 12 FDA reports)
THIRST ( 12 FDA reports)
THYROID CYST ( 12 FDA reports)
TONGUE DISORDER ( 12 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 12 FDA reports)
TYPE 1 DIABETES MELLITUS ( 12 FDA reports)
VERBAL ABUSE ( 12 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 12 FDA reports)
VERTIGO POSITIONAL ( 12 FDA reports)
ACUTE LUNG INJURY ( 12 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 12 FDA reports)
ADVERSE DRUG REACTION ( 12 FDA reports)
ALVEOLITIS ALLERGIC ( 12 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 12 FDA reports)
AORTIC STENOSIS ( 12 FDA reports)
APRAXIA ( 12 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 12 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 12 FDA reports)
ASCITES INFECTION ( 12 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 12 FDA reports)
BLINDNESS UNILATERAL ( 12 FDA reports)
BLOOD CREATINE INCREASED ( 12 FDA reports)
BLOOD DISORDER ( 12 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
BRUXISM ( 12 FDA reports)
CARDIAC VALVE VEGETATION ( 12 FDA reports)
CAROTID ARTERY DISEASE ( 12 FDA reports)
CEREBROVASCULAR DISORDER ( 12 FDA reports)
CERVICAL SPINE FLATTENING ( 12 FDA reports)
COLOSTOMY ( 12 FDA reports)
CRYING ( 12 FDA reports)
CUTANEOUS TUBERCULOSIS ( 12 FDA reports)
DECREASED ACTIVITY ( 12 FDA reports)
DEMYELINATION ( 12 FDA reports)
DIVERTICULAR PERFORATION ( 12 FDA reports)
DRUG ADMINISTRATION ERROR ( 12 FDA reports)
DYSTHYMIC DISORDER ( 12 FDA reports)
ESCHAR ( 12 FDA reports)
EXOPHTHALMOS ( 12 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 12 FDA reports)
GALACTORRHOEA ( 12 FDA reports)
GASTRITIS HAEMORRHAGIC ( 12 FDA reports)
GASTROINTESTINAL PAIN ( 12 FDA reports)
GINGIVAL BLEEDING ( 12 FDA reports)
GUILLAIN-BARRE SYNDROME ( 12 FDA reports)
HAPTOGLOBIN DECREASED ( 12 FDA reports)
HEPATIC ENZYME ABNORMAL ( 12 FDA reports)
HEPATIC NEOPLASM ( 12 FDA reports)
HEPATITIS FULMINANT ( 12 FDA reports)
HYPERPARATHYROIDISM ( 12 FDA reports)
ILEITIS ( 12 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
ISCHAEMIC HEPATITIS ( 12 FDA reports)
LOCAL SWELLING ( 12 FDA reports)
MENINGIOMA ( 12 FDA reports)
METASTASES TO PLEURA ( 12 FDA reports)
MICTURITION FREQUENCY DECREASED ( 12 FDA reports)
MUSCLE SPASTICITY ( 12 FDA reports)
MYELOMA RECURRENCE ( 12 FDA reports)
NEPHRITIC SYNDROME ( 12 FDA reports)
PALATAL DISORDER ( 12 FDA reports)
PAPILLOEDEMA ( 12 FDA reports)
PEPTIC ULCER PERFORATION ( 12 FDA reports)
PERINEPHRIC ABSCESS ( 12 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 12 FDA reports)
PERIPHERAL ISCHAEMIA ( 12 FDA reports)
PERITONEAL DISORDER ( 12 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 12 FDA reports)
PNEUMOPERITONEUM ( 12 FDA reports)
PRESCRIBED OVERDOSE ( 12 FDA reports)
PROCEDURAL PAIN ( 12 FDA reports)
ABDOMINAL HAEMATOMA ( 11 FDA reports)
ABDOMINAL NEOPLASM ( 11 FDA reports)
ACANTHAMOEBA INFECTION ( 11 FDA reports)
ACTINIC KERATOSIS ( 11 FDA reports)
ALVEOLITIS ( 11 FDA reports)
AMENORRHOEA ( 11 FDA reports)
AORTIC VALVE DISEASE ( 11 FDA reports)
ARTERIAL STENOSIS ( 11 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 11 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 11 FDA reports)
BILIARY TRACT DISORDER ( 11 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 11 FDA reports)
BLINDNESS CORTICAL ( 11 FDA reports)
BLOOD CHLORIDE INCREASED ( 11 FDA reports)
CARDIAC HYPERTROPHY ( 11 FDA reports)
CATHETER REMOVAL ( 11 FDA reports)
CEREBELLAR SYNDROME ( 11 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 11 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 11 FDA reports)
CLONIC CONVULSION ( 11 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 11 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 11 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 11 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 11 FDA reports)
ECTOPIC PREGNANCY ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 11 FDA reports)
ENTERITIS INFECTIOUS ( 11 FDA reports)
EPIDURAL LIPOMATOSIS ( 11 FDA reports)
EVANS SYNDROME ( 11 FDA reports)
EXTUBATION ( 11 FDA reports)
FACIAL PARESIS ( 11 FDA reports)
FEMORAL NECK FRACTURE ( 11 FDA reports)
GALLBLADDER NON-FUNCTIONING ( 11 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 11 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 11 FDA reports)
GLOSSITIS ( 11 FDA reports)
GRANULOCYTOPENIA ( 11 FDA reports)
GRIP STRENGTH DECREASED ( 11 FDA reports)
HEPATIC FIBROSIS ( 11 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 11 FDA reports)
HISTOPLASMOSIS ( 11 FDA reports)
HYPERKERATOSIS ( 11 FDA reports)
HYPERPHAGIA ( 11 FDA reports)
HYPERTENSIVE HEART DISEASE ( 11 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 11 FDA reports)
INDUCED LABOUR ( 11 FDA reports)
INJECTION SITE SWELLING ( 11 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 11 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 11 FDA reports)
INTESTINAL INFARCTION ( 11 FDA reports)
INTRAOCULAR LENS IMPLANT ( 11 FDA reports)
LICHEN PLANUS ( 11 FDA reports)
LIPASE INCREASED ( 11 FDA reports)
LYMPHOCYTOSIS ( 11 FDA reports)
MASKED FACIES ( 11 FDA reports)
MEDICAL DEVICE COMPLICATION ( 11 FDA reports)
MORTON'S NEUROMA ( 11 FDA reports)
MUSCLE FATIGUE ( 11 FDA reports)
MUSCLE HAEMORRHAGE ( 11 FDA reports)
MUSCLE RUPTURE ( 11 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 11 FDA reports)
MYOPATHY TOXIC ( 11 FDA reports)
MYOPIA ( 11 FDA reports)
NEOPLASM ( 11 FDA reports)
ORCHITIS ( 11 FDA reports)
OROPHARYNGEAL CANCER STAGE UNSPECIFIED ( 11 FDA reports)
OTITIS MEDIA ( 11 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 11 FDA reports)
PLASMAPHERESIS ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 11 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 11 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 11 FDA reports)
PROTRUSION TONGUE ( 11 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 11 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 11 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 11 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 11 FDA reports)
RENAL HAEMORRHAGE ( 11 FDA reports)
RESPIRATION ABNORMAL ( 11 FDA reports)
RETINAL DETACHMENT ( 11 FDA reports)
RETINOPATHY ( 11 FDA reports)
SNORING ( 11 FDA reports)
STUPOR ( 11 FDA reports)
SYSTEMIC MYCOSIS ( 11 FDA reports)
TACHYARRHYTHMIA ( 11 FDA reports)
THINKING ABNORMAL ( 11 FDA reports)
TROPONIN I INCREASED ( 11 FDA reports)
URINE ANALYSIS ABNORMAL ( 11 FDA reports)
VARICES OESOPHAGEAL ( 11 FDA reports)
VENTRICULAR DYSFUNCTION ( 11 FDA reports)
VENTRICULAR HYPOKINESIA ( 11 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 11 FDA reports)
VULVAL CANCER STAGE 0 ( 11 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 10 FDA reports)
PRURIGO ( 10 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 10 FDA reports)
RADICULITIS ( 10 FDA reports)
RENAL LIPOMATOSIS ( 10 FDA reports)
RETCHING ( 10 FDA reports)
SKIN TEST POSITIVE ( 10 FDA reports)
SKIN TOXICITY ( 10 FDA reports)
SPUTUM DISCOLOURED ( 10 FDA reports)
SUBACUTE HEPATIC FAILURE ( 10 FDA reports)
THYROID DISORDER ( 10 FDA reports)
TONGUE ULCERATION ( 10 FDA reports)
TORSADE DE POINTES ( 10 FDA reports)
URINARY ANASTOMOTIC LEAK ( 10 FDA reports)
VASCULAR OCCLUSION ( 10 FDA reports)
VASCULITIS CEREBRAL ( 10 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 10 FDA reports)
VESICOURETERIC REFLUX ( 10 FDA reports)
VOCAL CORD PARALYSIS ( 10 FDA reports)
VULVAR DYSPLASIA ( 10 FDA reports)
ABSCESS FUNGAL ( 10 FDA reports)
ACCIDENTAL OVERDOSE ( 10 FDA reports)
ACUTE SINUSITIS ( 10 FDA reports)
AMAUROSIS FUGAX ( 10 FDA reports)
ANASTOMOTIC LEAK ( 10 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 10 FDA reports)
ATHEROSCLEROSIS ( 10 FDA reports)
ATRIAL SEPTAL DEFECT ( 10 FDA reports)
BACK DISORDER ( 10 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 10 FDA reports)
BOWEL SOUNDS ABNORMAL ( 10 FDA reports)
BREAST CANCER FEMALE ( 10 FDA reports)
BREAST MASS ( 10 FDA reports)
BULLOUS LUNG DISEASE ( 10 FDA reports)
CATATONIA ( 10 FDA reports)
CELL MARKER INCREASED ( 10 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 10 FDA reports)
COMPLETED SUICIDE ( 10 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 10 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 10 FDA reports)
DYSAESTHESIA ( 10 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 10 FDA reports)
DYSPLASTIC NAEVUS ( 10 FDA reports)
ENCEPHALITIS HERPES ( 10 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 10 FDA reports)
EPIDERMOLYSIS ( 10 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 10 FDA reports)
ESCHERICHIA TEST POSITIVE ( 10 FDA reports)
EUPHORIC MOOD ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
FAILURE TO THRIVE ( 10 FDA reports)
FORAMEN MAGNUM STENOSIS ( 10 FDA reports)
FUNGAL PERITONITIS ( 10 FDA reports)
FUNGUS CULTURE POSITIVE ( 10 FDA reports)
GASTRIC CANCER ( 10 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 10 FDA reports)
GLOSSODYNIA ( 10 FDA reports)
GLUCOSE URINE PRESENT ( 10 FDA reports)
GRAFT THROMBOSIS ( 10 FDA reports)
HELICOBACTER INFECTION ( 10 FDA reports)
HUNGER ( 10 FDA reports)
HYPERAESTHESIA ( 10 FDA reports)
HYPERCOAGULATION ( 10 FDA reports)
INCREASED TENDENCY TO BRUISE ( 10 FDA reports)
INFECTIOUS PERITONITIS ( 10 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 10 FDA reports)
INTESTINAL HAEMORRHAGE ( 10 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 10 FDA reports)
JOINT INSTABILITY ( 10 FDA reports)
JOINT STIFFNESS ( 10 FDA reports)
KELOID SCAR ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
LARYNGOCELE ( 10 FDA reports)
LIPOMA ( 10 FDA reports)
LIVEDO RETICULARIS ( 10 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
LOWER LIMB FRACTURE ( 10 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 10 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 10 FDA reports)
MEDIASTINAL DISORDER ( 10 FDA reports)
MEDICAL DEVICE REMOVAL ( 10 FDA reports)
MUSCLE STRAIN ( 10 FDA reports)
MYELITIS TRANSVERSE ( 10 FDA reports)
MYOCLONUS ( 10 FDA reports)
NASAL CAVITY CANCER ( 10 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 10 FDA reports)
OESOPHAGEAL DISORDER ( 10 FDA reports)
ORAL INTAKE REDUCED ( 10 FDA reports)
OROPHARYNGEAL BLISTERING ( 10 FDA reports)
PANCREATITIS CHRONIC ( 10 FDA reports)
PELIOSIS HEPATIS ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
PILONIDAL CYST ( 10 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 10 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 10 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 10 FDA reports)
ACARODERMATITIS ( 9 FDA reports)
ACUTE PRERENAL FAILURE ( 9 FDA reports)
ALCOHOL ABUSE ( 9 FDA reports)
ALLERGY TO ANIMAL ( 9 FDA reports)
ANGIONEUROTIC OEDEMA ( 9 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 9 FDA reports)
ARTERIOSPASM CORONARY ( 9 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 9 FDA reports)
AXONAL NEUROPATHY ( 9 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 9 FDA reports)
BACK INJURY ( 9 FDA reports)
BLADDER DILATATION ( 9 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 9 FDA reports)
BLOOD PROLACTIN INCREASED ( 9 FDA reports)
BLOOD VISCOSITY INCREASED ( 9 FDA reports)
BRAIN INJURY ( 9 FDA reports)
BREAST CANCER METASTATIC ( 9 FDA reports)
BREAST CANCER RECURRENT ( 9 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 9 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX SEPSIS ( 9 FDA reports)
CALCULUS URETERIC ( 9 FDA reports)
CARDIAC TAMPONADE ( 9 FDA reports)
CEREBRAL ASPERGILLOSIS ( 9 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 9 FDA reports)
CERVICAL MYELOPATHY ( 9 FDA reports)
CERVICOBRACHIAL SYNDROME ( 9 FDA reports)
CLONUS ( 9 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 9 FDA reports)
COMPLICATIONS OF TRANSPLANTED PANCREAS ( 9 FDA reports)
COOMBS TEST POSITIVE ( 9 FDA reports)
CORONARY ANGIOPLASTY ( 9 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 9 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 9 FDA reports)
CORONARY ARTERY THROMBOSIS ( 9 FDA reports)
CROUP INFECTIOUS ( 9 FDA reports)
DIAPHRAGMATIC HERNIA ( 9 FDA reports)
DUODENAL POLYP ( 9 FDA reports)
DUODENITIS ( 9 FDA reports)
DYSPAREUNIA ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 9 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 9 FDA reports)
EMPYEMA ( 9 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 9 FDA reports)
EPIGASTRIC DISCOMFORT ( 9 FDA reports)
EXERCISE TOLERANCE DECREASED ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
EYE INFECTION ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
FAECALOMA ( 9 FDA reports)
FEAR OF DEATH ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 9 FDA reports)
GASTRIC PERFORATION ( 9 FDA reports)
GASTROENTERITIS VIRAL ( 9 FDA reports)
GINGIVAL EROSION ( 9 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 9 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 9 FDA reports)
HEAD DISCOMFORT ( 9 FDA reports)
HIV INFECTION ( 9 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 9 FDA reports)
HYPERPHOSPHATAEMIA ( 9 FDA reports)
INCISIONAL DRAINAGE ( 9 FDA reports)
INCONTINENCE ( 9 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 9 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 9 FDA reports)
INGROWN HAIR ( 9 FDA reports)
INJECTION SITE INDURATION ( 9 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 9 FDA reports)
KLEBSIELLA BACTERAEMIA ( 9 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 9 FDA reports)
LEUKAEMIA RECURRENT ( 9 FDA reports)
LIGAMENT LAXITY ( 9 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 9 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 9 FDA reports)
MUCOSAL HAEMORRHAGE ( 9 FDA reports)
MYCOBACTERIAL INFECTION ( 9 FDA reports)
MYOPATHY STEROID ( 9 FDA reports)
NEUROMYELITIS OPTICA ( 9 FDA reports)
OCULAR HYPERAEMIA ( 9 FDA reports)
ONYCHOMYCOSIS ( 9 FDA reports)
ORAL FUNGAL INFECTION ( 9 FDA reports)
ORAL PRURITUS ( 9 FDA reports)
OTITIS MEDIA ACUTE ( 9 FDA reports)
PAINFUL RESPIRATION ( 9 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 9 FDA reports)
PANNICULITIS ( 9 FDA reports)
PATHOLOGICAL GAMBLING ( 9 FDA reports)
PNEUMONIA ASPERGILLUS ( 9 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 9 FDA reports)
PNEUMONIA ESCHERICHIA ( 9 FDA reports)
PNEUMONIA LEGIONELLA ( 9 FDA reports)
PORTAL HYPERTENSION ( 9 FDA reports)
RADICAL HYSTERECTOMY ( 9 FDA reports)
REFLUX LARYNGITIS ( 9 FDA reports)
RENAL CORTICAL NECROSIS ( 9 FDA reports)
RENAL ISCHAEMIA ( 9 FDA reports)
RETROPERITONEAL INFECTION ( 9 FDA reports)
SACROILIITIS ( 9 FDA reports)
SALMONELLA SEPSIS ( 9 FDA reports)
SALPINGO-OOPHORECTOMY ( 9 FDA reports)
SCOTOMA ( 9 FDA reports)
SENSATION OF PRESSURE ( 9 FDA reports)
SKIN HAEMORRHAGE ( 9 FDA reports)
SKIN INFECTION ( 9 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 9 FDA reports)
SOFT TISSUE INFECTION ( 9 FDA reports)
SOMATOFORM DISORDER ( 9 FDA reports)
SPINAL FUSION SURGERY ( 9 FDA reports)
SPINAL NERVE STIMULATOR IMPLANTATION ( 9 FDA reports)
SPUTUM ABNORMAL ( 9 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 9 FDA reports)
TEMPORAL ARTERITIS ( 9 FDA reports)
TENDON PAIN ( 9 FDA reports)
THROMBOCYTOSIS ( 9 FDA reports)
THYROIDITIS ( 9 FDA reports)
TRANSFUSION REACTION ( 9 FDA reports)
URINARY TRACT DISORDER ( 9 FDA reports)
VASCULAR SKIN DISORDER ( 9 FDA reports)
VIRAEMIA ( 9 FDA reports)
WITHDRAWAL SYNDROME ( 9 FDA reports)
X-RAY ABNORMAL ( 9 FDA reports)
PUPILS UNEQUAL ( 8 FDA reports)
RASH VESICULAR ( 8 FDA reports)
REFLEXES ABNORMAL ( 8 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 8 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 8 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 8 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SENSATION OF HEAVINESS ( 8 FDA reports)
SINUS CONGESTION ( 8 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 8 FDA reports)
SMALL INTESTINAL PERFORATION ( 8 FDA reports)
SMALL INTESTINAL RESECTION ( 8 FDA reports)
SOMNAMBULISM ( 8 FDA reports)
STATUS ASTHMATICUS ( 8 FDA reports)
STRESS URINARY INCONTINENCE ( 8 FDA reports)
SUDDEN CARDIAC DEATH ( 8 FDA reports)
THORACIC CAVITY DRAINAGE ( 8 FDA reports)
THYROTOXIC PERIODIC PARALYSIS ( 8 FDA reports)
THYROXINE FREE DECREASED ( 8 FDA reports)
TONGUE DISCOLOURATION ( 8 FDA reports)
URINARY CASTS ( 8 FDA reports)
URINARY FISTULA ( 8 FDA reports)
VASCULAR GRAFT OCCLUSION ( 8 FDA reports)
VENA CAVA THROMBOSIS ( 8 FDA reports)
VITAL CAPACITY DECREASED ( 8 FDA reports)
VITREOUS HAEMORRHAGE ( 8 FDA reports)
WOUND ABSCESS ( 8 FDA reports)
ABDOMINAL WALL ABSCESS ( 8 FDA reports)
ABORTION ( 8 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 8 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
ACUTE PSYCHOSIS ( 8 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 8 FDA reports)
ALTERNARIA INFECTION ( 8 FDA reports)
AMYLOIDOSIS ( 8 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 8 FDA reports)
ANEURYSM RUPTURED ( 8 FDA reports)
AORTIC BYPASS ( 8 FDA reports)
AORTIC CALCIFICATION ( 8 FDA reports)
ARTERITIS ( 8 FDA reports)
ARTHRITIS INFECTIVE ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 8 FDA reports)
ATROPHY ( 8 FDA reports)
BIOPSY ( 8 FDA reports)
BLEPHARITIS ( 8 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BLOOD PH INCREASED ( 8 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 8 FDA reports)
BURSITIS INFECTIVE ( 8 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 8 FDA reports)
CATARACT NUCLEAR ( 8 FDA reports)
CATHETER PLACEMENT ( 8 FDA reports)
CEREBRAL THROMBOSIS ( 8 FDA reports)
CEREBROVASCULAR SPASM ( 8 FDA reports)
CHOREA ( 8 FDA reports)
CHORIORETINOPATHY ( 8 FDA reports)
CLUMSINESS ( 8 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 8 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 8 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 8 FDA reports)
ENCEPHALITIS VIRAL ( 8 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 8 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 8 FDA reports)
EROSIVE DUODENITIS ( 8 FDA reports)
ERYTHEMA NODOSUM ( 8 FDA reports)
EXCITABILITY ( 8 FDA reports)
EXTRADURAL ABSCESS ( 8 FDA reports)
EXTRAVASATION ( 8 FDA reports)
FLUID INTAKE REDUCED ( 8 FDA reports)
FOLLICULITIS ( 8 FDA reports)
FOOD ALLERGY ( 8 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 8 FDA reports)
GINGIVAL INFECTION ( 8 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 8 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 8 FDA reports)
GOUTY ARTHRITIS ( 8 FDA reports)
HEPATIC HAEMATOMA ( 8 FDA reports)
HYDROCELE ( 8 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 8 FDA reports)
ILEAL PERFORATION ( 8 FDA reports)
ILEOSTOMY ( 8 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 8 FDA reports)
INFECTED SKIN ULCER ( 8 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 8 FDA reports)
INJECTION SITE IRRITATION ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 8 FDA reports)
INTESTINAL RESECTION ( 8 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 8 FDA reports)
LARYNGITIS ( 8 FDA reports)
LEFT VENTRICULAR FAILURE ( 8 FDA reports)
LEUKAEMIA ( 8 FDA reports)
LIGAMENT INJURY ( 8 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 8 FDA reports)
LINEAR IGA DISEASE ( 8 FDA reports)
LIPOHYPERTROPHY ( 8 FDA reports)
LOOP ELECTROSURGICAL EXCISION PROCEDURE ( 8 FDA reports)
MENOPAUSAL SYMPTOMS ( 8 FDA reports)
METABOLIC ALKALOSIS ( 8 FDA reports)
METABOLIC ENCEPHALOPATHY ( 8 FDA reports)
METASTASES TO ADRENALS ( 8 FDA reports)
METASTATIC NEOPLASM ( 8 FDA reports)
METRORRHAGIA ( 8 FDA reports)
MUCOUS MEMBRANE DISORDER ( 8 FDA reports)
MUSCLE NECROSIS ( 8 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 8 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 8 FDA reports)
NASAL SEPTUM DEVIATION ( 8 FDA reports)
NECROSIS ISCHAEMIC ( 8 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 8 FDA reports)
OSTEOCHONDROSIS ( 8 FDA reports)
OVARIAN MASS ( 8 FDA reports)
PANCREATIC CARCINOMA ( 8 FDA reports)
PANCREATIC NEOPLASM ( 8 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 8 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 8 FDA reports)
PERITONITIS BACTERIAL ( 8 FDA reports)
PERSECUTORY DELUSION ( 8 FDA reports)
PRESBYOPIA ( 8 FDA reports)
PRODUCT QUALITY ISSUE ( 8 FDA reports)
ABDOMINAL HERNIA ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ACQUIRED HAEMOPHILIA ( 7 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 7 FDA reports)
AFFECT LABILITY ( 7 FDA reports)
ALVEOLAR OSTEITIS ( 7 FDA reports)
AMAUROSIS ( 7 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 7 FDA reports)
ANOXIC ENCEPHALOPATHY ( 7 FDA reports)
ANTIBODY TEST POSITIVE ( 7 FDA reports)
ANTITHROMBIN III DECREASED ( 7 FDA reports)
ARACHNOID CYST ( 7 FDA reports)
ARTERIAL THROMBOSIS ( 7 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 7 FDA reports)
ASTROCYTOMA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
BACTERIA URINE IDENTIFIED ( 7 FDA reports)
BILE DUCT NECROSIS ( 7 FDA reports)
BIOPSY GINGIVAL ( 7 FDA reports)
BIPOLAR II DISORDER ( 7 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 7 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 7 FDA reports)
BLOOD PH DECREASED ( 7 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 7 FDA reports)
BLOOD PRESSURE ABNORMAL ( 7 FDA reports)
BLOOD SODIUM INCREASED ( 7 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 7 FDA reports)
BLOOD TEST ABNORMAL ( 7 FDA reports)
BODY HEIGHT DECREASED ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
BONE MARROW NECROSIS ( 7 FDA reports)
BONE MARROW OEDEMA ( 7 FDA reports)
CACHEXIA ( 7 FDA reports)
CANDIDA TEST POSITIVE ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CAROTID BRUIT ( 7 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 7 FDA reports)
CEREBRAL ARTERY STENOSIS ( 7 FDA reports)
CHIMERISM ( 7 FDA reports)
CHOKING ( 7 FDA reports)
CHONDROMALACIA ( 7 FDA reports)
COAGULATION FACTOR DECREASED ( 7 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 7 FDA reports)
CORONARY ARTERY RESTENOSIS ( 7 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 7 FDA reports)
DIABETIC NEPHROPATHY ( 7 FDA reports)
DRY THROAT ( 7 FDA reports)
DYSPHORIA ( 7 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 7 FDA reports)
ENDOCARDITIS BACTERIAL ( 7 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 7 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 7 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 7 FDA reports)
EPIDERMAL NECROSIS ( 7 FDA reports)
EROSIVE OESOPHAGITIS ( 7 FDA reports)
EYE INFLAMMATION ( 7 FDA reports)
FACIAL BONES FRACTURE ( 7 FDA reports)
FEMALE STERILISATION ( 7 FDA reports)
FEMORAL ARTERY OCCLUSION ( 7 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 7 FDA reports)
GASTRODUODENITIS ( 7 FDA reports)
GASTROENTERITIS SALMONELLA ( 7 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 7 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 7 FDA reports)
GESTATIONAL HYPERTENSION ( 7 FDA reports)
GINGIVAL HYPERPLASIA ( 7 FDA reports)
GLARE ( 7 FDA reports)
GLOMERULONEPHROPATHY ( 7 FDA reports)
HAEMANGIOMA OF SKIN ( 7 FDA reports)
HAEMATOMA INFECTION ( 7 FDA reports)
HAEMOGLOBIN ABNORMAL ( 7 FDA reports)
HEPATIC INFARCTION ( 7 FDA reports)
HEPATITIS A ( 7 FDA reports)
HEPATITIS VIRAL ( 7 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 7 FDA reports)
HUMERUS FRACTURE ( 7 FDA reports)
HYDROPNEUMOTHORAX ( 7 FDA reports)
HYPERSOMNIA ( 7 FDA reports)
HYPERTRICHOSIS ( 7 FDA reports)
HYPOPERFUSION ( 7 FDA reports)
ILLUSION ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
INCREASED APPETITE ( 7 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 7 FDA reports)
INJECTION SITE EXTRAVASATION ( 7 FDA reports)
INJECTION SITE ULCER ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
INTRACARDIAC THROMBUS ( 7 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
JUGULAR VEIN DISTENSION ( 7 FDA reports)
KIDNEY RUPTURE ( 7 FDA reports)
KLEBSIELLA TEST POSITIVE ( 7 FDA reports)
LAPAROTOMY ( 7 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 7 FDA reports)
LIFE EXPECTANCY SHORTENED ( 7 FDA reports)
LISTERIOSIS ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LOW TURNOVER OSTEOPATHY ( 7 FDA reports)
LYMPH NODE PAIN ( 7 FDA reports)
LYMPHANGITIS ( 7 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 7 FDA reports)
MACULAR DEGENERATION ( 7 FDA reports)
MALIGNANT MELANOMA IN SITU ( 7 FDA reports)
MARROW HYPERPLASIA ( 7 FDA reports)
MEGACOLON ( 7 FDA reports)
METHAEMOGLOBINAEMIA ( 7 FDA reports)
MONOPARESIS ( 7 FDA reports)
MOTION SICKNESS ( 7 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
MYELOPATHY ( 7 FDA reports)
NEOPLASM RECURRENCE ( 7 FDA reports)
NERVE COMPRESSION ( 7 FDA reports)
NERVE INJURY ( 7 FDA reports)
NEUROMYOPATHY ( 7 FDA reports)
ORAL NEOPLASM ( 7 FDA reports)
OVARIAN CANCER ( 7 FDA reports)
OVARIAN NEOPLASM ( 7 FDA reports)
PALATAL OEDEMA ( 7 FDA reports)
PANCREATIC NECROSIS ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
PCO2 INCREASED ( 7 FDA reports)
PERICARDIAL CYST ( 7 FDA reports)
PERITONEAL HAEMORRHAGE ( 7 FDA reports)
PIGMENTATION DISORDER ( 7 FDA reports)
PLASMACYTOSIS ( 7 FDA reports)
POLYDIPSIA ( 7 FDA reports)
POSTURING ( 7 FDA reports)
PROTEUS INFECTION ( 7 FDA reports)
PROTHROMBIN TIME SHORTENED ( 7 FDA reports)
PSYCHIATRIC SYMPTOM ( 7 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 7 FDA reports)
PULMONARY HILUM MASS ( 7 FDA reports)
PYODERMA ( 7 FDA reports)
PYOTHORAX ( 7 FDA reports)
RAYNAUD'S PHENOMENON ( 7 FDA reports)
RED MAN SYNDROME ( 7 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 7 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 7 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 7 FDA reports)
RENAL HYPERTROPHY ( 7 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 7 FDA reports)
RESPIRATORY MONILIASIS ( 7 FDA reports)
RESPIRATORY RATE DECREASED ( 7 FDA reports)
RETINAL INFARCTION ( 7 FDA reports)
SCEDOSPORIUM INFECTION ( 7 FDA reports)
SCRATCH ( 7 FDA reports)
SICCA SYNDROME ( 7 FDA reports)
SIMPLE PARTIAL SEIZURES ( 7 FDA reports)
SKIN GRAFT ( 7 FDA reports)
SKIN MASS ( 7 FDA reports)
SMALL FOR DATES BABY ( 7 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 7 FDA reports)
SOCIAL PROBLEM ( 7 FDA reports)
SPLEEN DISORDER ( 7 FDA reports)
SPUTUM INCREASED ( 7 FDA reports)
STENOTROPHOMONAS INFECTION ( 7 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 7 FDA reports)
TEARFULNESS ( 7 FDA reports)
THYROID ADENOMA ( 7 FDA reports)
TRANSFUSION ( 7 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 7 FDA reports)
UMBILICAL CORD ABNORMALITY ( 7 FDA reports)
UNDERDOSE ( 7 FDA reports)
UPPER MOTOR NEURONE LESION ( 7 FDA reports)
URETERAL NECROSIS ( 7 FDA reports)
URETERITIS ( 7 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 7 FDA reports)
VAGINAL DISCHARGE ( 7 FDA reports)
VASCULAR GRAFT COMPLICATION ( 7 FDA reports)
VASOSPASM ( 7 FDA reports)
VENOUS STENOSIS ( 7 FDA reports)
VIRAL DNA TEST POSITIVE ( 7 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
PURULENCE ( 6 FDA reports)
QUADRIPARESIS ( 6 FDA reports)
RADIATION PNEUMONITIS ( 6 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 6 FDA reports)
RENAL CANCER ( 6 FDA reports)
RETINAL VASCULITIS ( 6 FDA reports)
RHEUMATOID FACTOR INCREASED ( 6 FDA reports)
ROSACEA ( 6 FDA reports)
SCAB ( 6 FDA reports)
SCLERITIS ( 6 FDA reports)
SEASONAL ALLERGY ( 6 FDA reports)
SENSATION OF FOREIGN BODY ( 6 FDA reports)
SENSORIMOTOR DISORDER ( 6 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SKIN ATROPHY ( 6 FDA reports)
SKIN CANCER ( 6 FDA reports)
SKIN STRIAE ( 6 FDA reports)
SKIN TIGHTNESS ( 6 FDA reports)
SPINAL DECOMPRESSION ( 6 FDA reports)
SPLENIC ARTERY ANEURYSM ( 6 FDA reports)
SPONDYLOLYSIS ( 6 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 6 FDA reports)
STENOTROPHOMONAS SEPSIS ( 6 FDA reports)
STREPTOCOCCAL SEPSIS ( 6 FDA reports)
SUBDURAL HAEMORRHAGE ( 6 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 6 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
TEMPERATURE INTOLERANCE ( 6 FDA reports)
TENDON CALCIFICATION ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
TENSION HEADACHE ( 6 FDA reports)
THROMBOCYTHAEMIA ( 6 FDA reports)
TINEA CRURIS ( 6 FDA reports)
TONIC CLONIC MOVEMENTS ( 6 FDA reports)
TONSIL CANCER ( 6 FDA reports)
TONSILLAR HYPERTROPHY ( 6 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
TRICHOSPORON INFECTION ( 6 FDA reports)
TRIGEMINAL NEURALGIA ( 6 FDA reports)
UMBILICAL HERNIA ( 6 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 6 FDA reports)
VAGINAL CANDIDIASIS ( 6 FDA reports)
VARICOSE VEINS VULVAL ( 6 FDA reports)
VENOUS THROMBOSIS LIMB ( 6 FDA reports)
VERTEBRAL COLUMN MASS ( 6 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 6 FDA reports)
WOUND NECROSIS ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ABSCESS INTESTINAL ( 6 FDA reports)
ACCIDENT AT WORK ( 6 FDA reports)
AKINESIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
ALCOHOL USE ( 6 FDA reports)
AMMONIA INCREASED ( 6 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 6 FDA reports)
AMPUTATION ( 6 FDA reports)
ANAL FISTULA ( 6 FDA reports)
ANASTOMOTIC STENOSIS ( 6 FDA reports)
ANGIOGRAM PERIPHERAL ABNORMAL ( 6 FDA reports)
APHAGIA ( 6 FDA reports)
APHAKIA ( 6 FDA reports)
ARACHNOIDITIS ( 6 FDA reports)
ARRESTED LABOUR ( 6 FDA reports)
ARTERIAL HAEMORRHAGE ( 6 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 6 FDA reports)
BACTERIAL TEST POSITIVE ( 6 FDA reports)
BACTEROIDES INFECTION ( 6 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BILIARY DILATATION ( 6 FDA reports)
BLADDER CATHETERISATION ( 6 FDA reports)
BLADDER PAIN ( 6 FDA reports)
BLOOD MAGNESIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 6 FDA reports)
BONE METABOLISM DISORDER ( 6 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
BRAIN SCAN ABNORMAL ( 6 FDA reports)
BREAST ABSCESS ( 6 FDA reports)
BREAST CANCER IN SITU ( 6 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 6 FDA reports)
BRONCHOSCOPY ( 6 FDA reports)
BUNION ( 6 FDA reports)
CAMPYLOBACTER INFECTION ( 6 FDA reports)
CANDIDURIA ( 6 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CASTLEMAN'S DISEASE ( 6 FDA reports)
CATHETERISATION CARDIAC ( 6 FDA reports)
CD4 LYMPHOCYTES ( 6 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 6 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 6 FDA reports)
CEREBRAL FUNGAL INFECTION ( 6 FDA reports)
CITROBACTER INFECTION ( 6 FDA reports)
COCCIDIOIDOMYCOSIS ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 6 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 6 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DENTAL OPERATION ( 6 FDA reports)
DERMAL CYST ( 6 FDA reports)
DISORDER OF ORBIT ( 6 FDA reports)
DISSOCIATION ( 6 FDA reports)
DROOLING ( 6 FDA reports)
DRUG LEVEL FLUCTUATING ( 6 FDA reports)
DRUG SCREEN POSITIVE ( 6 FDA reports)
EMBOLIC STROKE ( 6 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 6 FDA reports)
ENDOMETRIOSIS ( 6 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 6 FDA reports)
EYE INFECTION FUNGAL ( 6 FDA reports)
FAMILY STRESS ( 6 FDA reports)
FEEDING DISORDER ( 6 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 6 FDA reports)
FINGER DEFORMITY ( 6 FDA reports)
FISTULA REPAIR ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FOETAL GROWTH RESTRICTION ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
FOOT AMPUTATION ( 6 FDA reports)
FRACTURE NONUNION ( 6 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 6 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 6 FDA reports)
GINGIVAL ERYTHEMA ( 6 FDA reports)
GLOMERULOSCLEROSIS ( 6 FDA reports)
GRAFT INFECTION ( 6 FDA reports)
GRAFT ISCHAEMIA ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 6 FDA reports)
GRAVITATIONAL OEDEMA ( 6 FDA reports)
GYNAECOMASTIA ( 6 FDA reports)
HAEMOGLOBINURIA ( 6 FDA reports)
HEPATIC CONGESTION ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HOSPITALISATION ( 6 FDA reports)
HYPERAMYLASAEMIA ( 6 FDA reports)
HYPOCHROMIC ANAEMIA ( 6 FDA reports)
HYPOMANIA ( 6 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 6 FDA reports)
INCISIONAL HERNIA REPAIR ( 6 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 6 FDA reports)
INTESTINAL ANASTOMOSIS ( 6 FDA reports)
IRIS ADHESIONS ( 6 FDA reports)
IRON BINDING CAPACITY UNSATURATED INCREASED ( 6 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 6 FDA reports)
JEJUNAL PERFORATION ( 6 FDA reports)
JOINT TUBERCULOSIS ( 6 FDA reports)
KERATITIS ( 6 FDA reports)
KNEE ARTHROPLASTY ( 6 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 6 FDA reports)
LEG AMPUTATION ( 6 FDA reports)
LEUKAEMIA PLASMACYTIC ( 6 FDA reports)
LEUKODYSTROPHY ( 6 FDA reports)
LIFE SUPPORT ( 6 FDA reports)
LIGAMENT SPRAIN ( 6 FDA reports)
LIPOMATOSIS ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LUNG TRANSPLANT ( 6 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 6 FDA reports)
LYMPHOHISTIOCYTOSIS ( 6 FDA reports)
MADAROSIS ( 6 FDA reports)
MALIGNANT TUMOUR EXCISION ( 6 FDA reports)
MASTOCYTOSIS ( 6 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 6 FDA reports)
MENINGITIS TUBERCULOUS ( 6 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
METASTATIC PAIN ( 6 FDA reports)
MIGRAINE WITH AURA ( 6 FDA reports)
MOYAMOYA DISEASE ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
MUSCLE CRAMP ( 6 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 6 FDA reports)
MYOGLOBINURIA ( 6 FDA reports)
NEPHROSTOMY ( 6 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 6 FDA reports)
NOSOCOMIAL INFECTION ( 6 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 6 FDA reports)
OCCULT BLOOD POSITIVE ( 6 FDA reports)
OROANTRAL FISTULA ( 6 FDA reports)
OVERWORK ( 6 FDA reports)
PANCREATIC ABSCESS ( 6 FDA reports)
PANIC REACTION ( 6 FDA reports)
PARKINSON'S DISEASE ( 6 FDA reports)
PELVIC ABSCESS ( 6 FDA reports)
PEMPHIGOID ( 6 FDA reports)
PERICARDIAL HAEMORRHAGE ( 6 FDA reports)
PHARYNGEAL ERYTHEMA ( 6 FDA reports)
PLATELET COUNT ABNORMAL ( 6 FDA reports)
PLEOCYTOSIS ( 6 FDA reports)
POISONING ( 6 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 6 FDA reports)
PRE-ECLAMPSIA ( 6 FDA reports)
PREMATURE DELIVERY ( 6 FDA reports)
PRODUCT CONTAMINATION ( 6 FDA reports)
PROTEIN TOTAL INCREASED ( 6 FDA reports)
ABNORMAL DREAMS ( 5 FDA reports)
ACCELERATED HYPERTENSION ( 5 FDA reports)
ACCIDENT AT HOME ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
ACID FAST BACILLI INFECTION ( 5 FDA reports)
ACINETOBACTER BACTERAEMIA ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 5 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 5 FDA reports)
ADIPOSIS DOLOROSA ( 5 FDA reports)
ADRENAL NEOPLASM ( 5 FDA reports)
ANAEMIA MEGALOBLASTIC ( 5 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 5 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANAL FISSURE EXCISION ( 5 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 5 FDA reports)
ANOPLASTY ( 5 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 5 FDA reports)
AORTIC ANEURYSM RUPTURE ( 5 FDA reports)
AORTIC THROMBOSIS ( 5 FDA reports)
APPENDICECTOMY ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
BACTERIAL PYELONEPHRITIS ( 5 FDA reports)
BACTERIAL TOXAEMIA ( 5 FDA reports)
BASAL GANGLION DEGENERATION ( 5 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 5 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 5 FDA reports)
BIOPSY LIVER ABNORMAL ( 5 FDA reports)
BIOPSY THYMUS GLAND ABNORMAL ( 5 FDA reports)
BLADDER IRRITATION ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLAST CELL CRISIS ( 5 FDA reports)
BLOOD ALBUMIN INCREASED ( 5 FDA reports)
BLOOD CALCIUM INCREASED ( 5 FDA reports)
BLOOD CREATININE ABNORMAL ( 5 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 5 FDA reports)
BLOOD IRON DECREASED ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BONE LESION EXCISION ( 5 FDA reports)
BRADYARRHYTHMIA ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BREAST CELLULITIS ( 5 FDA reports)
BRONCHITIS ACUTE ( 5 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 5 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 5 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 5 FDA reports)
CATHETER SITE INFECTION ( 5 FDA reports)
CATHETER SITE RELATED REACTION ( 5 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 5 FDA reports)
CEREBRAL CALCIFICATION ( 5 FDA reports)
CEREBRAL MICROANGIOPATHY ( 5 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 5 FDA reports)
CHEST WALL OPERATION ( 5 FDA reports)
CHOLANGITIS SUPPURATIVE ( 5 FDA reports)
CHRONIC FATIGUE SYNDROME ( 5 FDA reports)
COLON CANCER METASTATIC ( 5 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 5 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 5 FDA reports)
CONJUNCTIVAL OEDEMA ( 5 FDA reports)
CONNECTIVE TISSUE DISORDER ( 5 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 5 FDA reports)
CSF TEST ABNORMAL ( 5 FDA reports)
CULTURE WOUND POSITIVE ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
CYSTITIS VIRAL ( 5 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 5 FDA reports)
DEAFNESS UNILATERAL ( 5 FDA reports)
DIABETIC COMA ( 5 FDA reports)
DIABETIC MICROANGIOPATHY ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRUG-INDUCED LIVER INJURY ( 5 FDA reports)
DURAL FISTULA ( 5 FDA reports)
DYSHIDROSIS ( 5 FDA reports)
DYSPLASTIC NAEVUS SYNDROME ( 5 FDA reports)
DYSPNOEA EXACERBATED ( 5 FDA reports)
EAR DISORDER ( 5 FDA reports)
ENCEPHALOMALACIA ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
ENTEROBACTER SEPSIS ( 5 FDA reports)
ENTEROVESICAL FISTULA ( 5 FDA reports)
EPIDIDYMITIS ( 5 FDA reports)
EPIGLOTTITIS ( 5 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 5 FDA reports)
EXTREMITY NECROSIS ( 5 FDA reports)
EYELID DISORDER ( 5 FDA reports)
EYES SUNKEN ( 5 FDA reports)
FACIAL SPASM ( 5 FDA reports)
FALLOPIAN TUBE OPERATION ( 5 FDA reports)
FAT EMBOLISM ( 5 FDA reports)
FLAT AFFECT ( 5 FDA reports)
FOOD INTOLERANCE ( 5 FDA reports)
FOREIGN BODY ( 5 FDA reports)
FOREIGN BODY TRAUMA ( 5 FDA reports)
FRACTURE DELAYED UNION ( 5 FDA reports)
FURUNCLE ( 5 FDA reports)
GALLBLADDER ENLARGEMENT ( 5 FDA reports)
GASTROINTESTINAL OEDEMA ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 5 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 5 FDA reports)
GOUTY TOPHUS ( 5 FDA reports)
GROWTH HORMONE DEFICIENCY ( 5 FDA reports)
HAIR DISORDER ( 5 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 5 FDA reports)
HEMIANOPIA HOMONYMOUS ( 5 FDA reports)
HEPATIC ARTERY ANEURYSM ( 5 FDA reports)
HEPATIC HAEMORRHAGE ( 5 FDA reports)
HEPATOCELLULAR INJURY ( 5 FDA reports)
HYPOGONADISM ( 5 FDA reports)
HYPOPITUITARISM ( 5 FDA reports)
IIIRD NERVE PARALYSIS ( 5 FDA reports)
INADEQUATE ANALGESIA ( 5 FDA reports)
INCISION SITE PAIN ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFECTIVE TENOSYNOVITIS ( 5 FDA reports)
INJECTION SITE BURNING ( 5 FDA reports)
INJECTION SITE HAEMATOMA ( 5 FDA reports)
INJECTION SITE NECROSIS ( 5 FDA reports)
INJECTION SITE STINGING ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INTERNAL HERNIA ( 5 FDA reports)
INTESTINAL DILATATION ( 5 FDA reports)
INTRACRANIAL HAEMATOMA ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 5 FDA reports)
INTUBATION ( 5 FDA reports)
JOINT CONTRACTURE ( 5 FDA reports)
KERATOMILEUSIS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
LATENT TUBERCULOSIS ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
LUNG HYPERINFLATION ( 5 FDA reports)
LYMPHATIC DUCT RUPTURE ( 5 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 5 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 5 FDA reports)
MANTLE CELL LYMPHOMA STAGE IV ( 5 FDA reports)
MAXILLOFACIAL OPERATION ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEAN CELL VOLUME DECREASED ( 5 FDA reports)
MEDIASTINAL CYST ( 5 FDA reports)
MELANOMATOUS MENINGITIS ( 5 FDA reports)
MENINGITIS BACTERIAL ( 5 FDA reports)
METASTASES TO KIDNEY ( 5 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 5 FDA reports)
MICROCYTIC ANAEMIA ( 5 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 5 FDA reports)
MUCOUS STOOLS ( 5 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 5 FDA reports)
MYCOTIC ANEURYSM ( 5 FDA reports)
MYELITIS ( 5 FDA reports)
MYOCLONIC EPILEPSY ( 5 FDA reports)
MYOPERICARDITIS ( 5 FDA reports)
NAIL OPERATION ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA ( 5 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 5 FDA reports)
NEUTROPHILIA ( 5 FDA reports)
OLIGODENDROGLIOMA ( 5 FDA reports)
OPERATIVE HAEMORRHAGE ( 5 FDA reports)
OSTEOGENESIS IMPERFECTA ( 5 FDA reports)
OSTEOMA ( 5 FDA reports)
PANCREATIC INSUFFICIENCY ( 5 FDA reports)
PANCREATITIS NECROTISING ( 5 FDA reports)
PANIC DISORDER ( 5 FDA reports)
PARTNER STRESS ( 5 FDA reports)
PELVIC MASS ( 5 FDA reports)
PERFORMANCE STATUS DECREASED ( 5 FDA reports)
PERIRENAL HAEMATOMA ( 5 FDA reports)
PHARYNGEAL INFLAMMATION ( 5 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 5 FDA reports)
PHOTOPSIA ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
PLACENTAL DISORDER ( 5 FDA reports)
PLASTIC SURGERY ( 5 FDA reports)
PNEUMONIA LIPOID ( 5 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 5 FDA reports)
PO2 INCREASED ( 5 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 5 FDA reports)
POSTPARTUM HAEMORRHAGE ( 5 FDA reports)
POTENTIATING DRUG INTERACTION ( 5 FDA reports)
POVERTY OF THOUGHT CONTENT ( 5 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 5 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 5 FDA reports)
PROCEDURAL HYPOTENSION ( 5 FDA reports)
PROCEDURAL SITE REACTION ( 5 FDA reports)
PROCTOCOLECTOMY ( 5 FDA reports)
PROLAPSE REPAIR ( 5 FDA reports)
PULMONARY EOSINOPHILIA ( 5 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 5 FDA reports)
PULMONARY MYCOSIS ( 5 FDA reports)
PULMONARY SEPSIS ( 5 FDA reports)
PULMONARY VASCULITIS ( 5 FDA reports)
PYONEPHROSIS ( 5 FDA reports)
RADIATION SKIN INJURY ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RENAL ABSCESS ( 5 FDA reports)
RENAL NECROSIS ( 5 FDA reports)
RENAL VEIN OCCLUSION ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
RETINAL HAEMORRHAGE ( 5 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 5 FDA reports)
RETINITIS ( 5 FDA reports)
RETROPERITONEAL HAEMATOMA ( 5 FDA reports)
RHEUMATOID NODULE ( 5 FDA reports)
RHINOPLASTY ( 5 FDA reports)
SALMONELLOSIS ( 5 FDA reports)
SCLERODERMA ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SEPSIS SYNDROME ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SIGMOIDITIS ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SKIN OEDEMA ( 5 FDA reports)
SPINAL CORD COMPRESSION ( 5 FDA reports)
STARING ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
TOE AMPUTATION ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
TONIC CONVULSION ( 5 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
UTERINE CANCER ( 5 FDA reports)
UTERINE DISORDER ( 5 FDA reports)
UTERINE PROLAPSE REPAIR ( 5 FDA reports)
VAGINAL INFECTION ( 5 FDA reports)
VEIN DISORDER ( 5 FDA reports)
VOCAL CORD DISORDER ( 5 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 5 FDA reports)
WAXY FLEXIBILITY ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
WOUND COMPLICATION ( 5 FDA reports)
WOUND DECOMPOSITION ( 5 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 4 FDA reports)
PSEUDOFOLLICULITIS BARBAE ( 4 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 4 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 4 FDA reports)
PSOAS ABSCESS ( 4 FDA reports)
PSYCHOLOGICAL TRAUMA ( 4 FDA reports)
PULMONARY CAVITATION ( 4 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
RECTAL LESION ( 4 FDA reports)
RECTAL POLYP ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
RED BLOOD CELL ABNORMALITY ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE ABNORMAL ( 4 FDA reports)
REFRACTORY ANAEMIA ( 4 FDA reports)
RENAL ANEURYSM ( 4 FDA reports)
RESPIRATORY ALKALOSIS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 4 FDA reports)
RESUSCITATION ( 4 FDA reports)
RETICULOCYTE COUNT DECREASED ( 4 FDA reports)
RETICULOCYTE COUNT INCREASED ( 4 FDA reports)
RETROPERITONEAL ABSCESS ( 4 FDA reports)
SALIVARY HYPERSECRETION ( 4 FDA reports)
SCHIZOTYPAL PERSONALITY DISORDER ( 4 FDA reports)
SECONDARY HYPERTENSION ( 4 FDA reports)
SECRETION DISCHARGE ( 4 FDA reports)
SINUS OPERATION ( 4 FDA reports)
SJOGREN'S SYNDROME ( 4 FDA reports)
SKELETAL INJURY ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN FISSURES ( 4 FDA reports)
SKIN IRRITATION ( 4 FDA reports)
SKIN PLAQUE ( 4 FDA reports)
SMALL CELL CARCINOMA ( 4 FDA reports)
SOLITARY KIDNEY ( 4 FDA reports)
SPINAL SHOCK ( 4 FDA reports)
SPLENECTOMY ( 4 FDA reports)
SPLENIC RUPTURE ( 4 FDA reports)
SPLENIC VEIN THROMBOSIS ( 4 FDA reports)
STAPHYLOCOCCAL MEDIASTINITIS ( 4 FDA reports)
STENT PLACEMENT ( 4 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 4 FDA reports)
STRESS INCONTINENCE ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
SUPERINFECTION ( 4 FDA reports)
SUPPORTIVE CARE ( 4 FDA reports)
SYSTEMIC SCLEROSIS ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 4 FDA reports)
THYROID GLAND ABSCESS ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONSILLAR DISORDER ( 4 FDA reports)
TONSILLECTOMY ( 4 FDA reports)
TOOTH INJURY ( 4 FDA reports)
TORULOPSIS INFECTION ( 4 FDA reports)
TRACHEAL ULCER ( 4 FDA reports)
TRANSFUSION MICROCHIMERISM ( 4 FDA reports)
TRAUMATIC BRAIN INJURY ( 4 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 4 FDA reports)
TRIGEMINAL NERVE DISORDER ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TUBERCULOUS PLEURISY ( 4 FDA reports)
TUMOUR INVASION ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
ULCERATIVE KERATITIS ( 4 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 4 FDA reports)
URACHAL ABSCESS ( 4 FDA reports)
UREAPLASMA INFECTION ( 4 FDA reports)
URETERIC CANCER ( 4 FDA reports)
URINARY SEDIMENT PRESENT ( 4 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE TRANSITIONAL CELLS PRESENT ( 4 FDA reports)
UTERINE POLYP ( 4 FDA reports)
VAGINITIS BACTERIAL ( 4 FDA reports)
VASCULAR HEADACHE ( 4 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 4 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 4 FDA reports)
VIRAL HEPATITIS CARRIER ( 4 FDA reports)
VIRAL MYOCARDITIS ( 4 FDA reports)
VIRAL TEST POSITIVE ( 4 FDA reports)
VISCERAL LEISHMANIASIS ( 4 FDA reports)
VITAMIN B12 DEFICIENCY ( 4 FDA reports)
VITH NERVE PARALYSIS ( 4 FDA reports)
VON WILLEBRAND'S FACTOR ACTIVITY INCREASED ( 4 FDA reports)
VON WILLEBRAND'S FACTOR ANTIGEN INCREASED ( 4 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 4 FDA reports)
WEIGHT BEARING DIFFICULTY ( 4 FDA reports)
WOUND EVISCERATION ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL SEPSIS ( 4 FDA reports)
ABNORMAL FAECES ( 4 FDA reports)
ABSCESS BACTERIAL ( 4 FDA reports)
ADENOMA BENIGN ( 4 FDA reports)
ADHESION ( 4 FDA reports)
ADNEXA UTERI MASS ( 4 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 4 FDA reports)
AEROMONA INFECTION ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ALOPECIA EFFLUVIUM ( 4 FDA reports)
ALPHA TUMOUR NECROSIS FACTOR INCREASED ( 4 FDA reports)
ANAL FISSURE ( 4 FDA reports)
ANKLE DEFORMITY ( 4 FDA reports)
ANO-RECTAL STENOSIS ( 4 FDA reports)
ANORECTAL STENOSIS ( 4 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 4 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
AORTIC VALVE REPLACEMENT ( 4 FDA reports)
APATHY ( 4 FDA reports)
APHONIA ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 4 FDA reports)
ASPERGILLOMA ( 4 FDA reports)
ASTIGMATISM ( 4 FDA reports)
AUTOIMMUNE DISORDER ( 4 FDA reports)
B-LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
BACTERIA URINE ( 4 FDA reports)
BEHCET'S SYNDROME ( 4 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 4 FDA reports)
BILE ACID MALABSORPTION ( 4 FDA reports)
BILIARY DRAINAGE ( 4 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 4 FDA reports)
BLOOD ARSENIC INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 4 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 4 FDA reports)
BLOOD UREA ABNORMAL ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 4 FDA reports)
BRAIN MASS ( 4 FDA reports)
BREAST DISORDER ( 4 FDA reports)
BRONCHIAL CARCINOMA ( 4 FDA reports)
BRONCHIAL DISORDER ( 4 FDA reports)
BRONCHIAL SECRETION RETENTION ( 4 FDA reports)
BRONCHIOLITIS ( 4 FDA reports)
BRONCHOPLEURAL FISTULA ( 4 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CALCULUS BLADDER ( 4 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 4 FDA reports)
CARTILAGE ATROPHY ( 4 FDA reports)
CATHETER RELATED COMPLICATION ( 4 FDA reports)
CATHETER SEPSIS ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CELL DEATH ( 4 FDA reports)
CENTRAL OBESITY ( 4 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 4 FDA reports)
CEREBROSPINAL FISTULA ( 4 FDA reports)
CERVIX DISORDER ( 4 FDA reports)
CHOLECYSTITIS INFECTIVE ( 4 FDA reports)
CHOLESTATIC LIVER INJURY ( 4 FDA reports)
CHOREOATHETOSIS ( 4 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 4 FDA reports)
CHRONIC GRANULOMATOUS DISEASE ( 4 FDA reports)
CHYLOTHORAX ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
COLON POLYPECTOMY ( 4 FDA reports)
COMPULSIVE SHOPPING ( 4 FDA reports)
CONCENTRIC SCLEROSIS ( 4 FDA reports)
CONJUNCTIVAL PALLOR ( 4 FDA reports)
CONTRAST MEDIA REACTION ( 4 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 4 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 4 FDA reports)
CRACKLES LUNG ( 4 FDA reports)
CRYOFIBRINOGENAEMIA ( 4 FDA reports)
CRYOGLOBULINAEMIA ( 4 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 4 FDA reports)
CSF GRANULOCYTE COUNT ABNORMAL ( 4 FDA reports)
CULTURE POSITIVE ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CULTURE THROAT POSITIVE ( 4 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 4 FDA reports)
CYTOMEGALOVIRUS DUODENITIS ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DERMATITIS ATOPIC ( 4 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 4 FDA reports)
DIABETIC COMPLICATION ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 4 FDA reports)
DISTRIBUTIVE SHOCK ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DRUG THERAPY ( 4 FDA reports)
DRY GANGRENE ( 4 FDA reports)
DYSGRAPHIA ( 4 FDA reports)
DYSPNOEA AT REST ( 4 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 4 FDA reports)
ENTEROCOLITIS FUNGAL ( 4 FDA reports)
ENTEROCUTANEOUS FISTULA ( 4 FDA reports)
EOSINOPHILIC LEUKAEMIA ( 4 FDA reports)
EOSINOPHILIC PNEUMONIA ( 4 FDA reports)
EPENDYMOMA ( 4 FDA reports)
EPIDERMOLYSIS BULLOSA ( 4 FDA reports)
EXCESSIVE EYE BLINKING ( 4 FDA reports)
EXTRACORPOREAL MEMBRANE OXYGENATION ( 4 FDA reports)
EYE INFECTION TOXOPLASMAL ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
EYELID PAIN ( 4 FDA reports)
FASCIITIS ( 4 FDA reports)
FAT NECROSIS ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FIBROUS HISTIOCYTOMA ( 4 FDA reports)
FIBULA FRACTURE ( 4 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 4 FDA reports)
FOETAL HEART RATE ABNORMAL ( 4 FDA reports)
FRACTURE DISPLACEMENT ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 4 FDA reports)
FUNGAL TEST POSITIVE ( 4 FDA reports)
GALLBLADDER INJURY ( 4 FDA reports)
GASTRIC ULCER PERFORATION ( 4 FDA reports)
GASTRITIS BACTERIAL ( 4 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 4 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 4 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL TOXICITY ( 4 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 4 FDA reports)
GENITAL NEOPLASM MALIGNANT FEMALE ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GLIOBLASTOMA ( 4 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HEART INJURY ( 4 FDA reports)
HELICOBACTER SEPSIS ( 4 FDA reports)
HELLP SYNDROME ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 4 FDA reports)
HEPATIC VEIN OCCLUSION ( 4 FDA reports)
HEPATIC VEIN STENOSIS ( 4 FDA reports)
HEPATITIS C RNA INCREASED ( 4 FDA reports)
HEPATITIS C RNA POSITIVE ( 4 FDA reports)
HERPES ZOSTER DISSEMINATED ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HIP SURGERY ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HODGKIN'S DISEASE STAGE II ( 4 FDA reports)
HOMICIDE ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYPERCHLORAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 4 FDA reports)
HYPEROXALURIA ( 4 FDA reports)
HYPERTONIC BLADDER ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
HYPOPNOEA ( 4 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 4 FDA reports)
IMMOBILE ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFARCTION ( 4 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 4 FDA reports)
INFLAMMATORY MARKER INCREASED ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INJECTION SITE INFLAMMATION ( 4 FDA reports)
INJECTION SITE RASH ( 4 FDA reports)
INTESTINAL GANGRENE ( 4 FDA reports)
INTESTINAL STENOSIS ( 4 FDA reports)
INTRAUTERINE INFECTION ( 4 FDA reports)
INTUSSUSCEPTION ( 4 FDA reports)
JOINT LOCK ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LARYNGOSPASM ( 4 FDA reports)
LEFT VENTRICLE OUTFLOW TRACT OBSTRUCTION ( 4 FDA reports)
LEUKOENCEPHALOMYELITIS ( 4 FDA reports)
LEUKOPLAKIA ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 4 FDA reports)
LUNG INJURY ( 4 FDA reports)
LUNG LOBECTOMY ( 4 FDA reports)
LUNG NEOPLASM SURGERY ( 4 FDA reports)
LUNG OPERATION ( 4 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 4 FDA reports)
LYMPHORRHOEA ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
MASTOIDITIS ( 4 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 4 FDA reports)
METAL POISONING ( 4 FDA reports)
METASTASES TO BONE MARROW ( 4 FDA reports)
METASTASES TO HEART ( 4 FDA reports)
METASTASES TO PELVIS ( 4 FDA reports)
METASTASES TO SPLEEN ( 4 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 4 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 4 FDA reports)
MONOCYTE COUNT DECREASED ( 4 FDA reports)
MONOCYTE COUNT INCREASED ( 4 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
MUCOEPIDERMOID CARCINOMA ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
NEONATAL HYPONATRAEMIA ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEPHROSCLEROSIS ( 4 FDA reports)
NEUROCRYPTOCOCCOSIS ( 4 FDA reports)
NEUROTRANSMITTER LEVEL ALTERED ( 4 FDA reports)
NEUTROPHIL MORPHOLOGY ABNORMAL ( 4 FDA reports)
NICOTINE DEPENDENCE ( 4 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 4 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIB ( 4 FDA reports)
OESOPHAGEAL ULCER ( 4 FDA reports)
OLIGOHYDRAMNIOS ( 4 FDA reports)
ONYCHOLYSIS ( 4 FDA reports)
OPHTHALMOPLEGIA ( 4 FDA reports)
OPTIC ATROPHY ( 4 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
OVARIAN CANCER METASTATIC ( 4 FDA reports)
OVARIAN GERM CELL CANCER STAGE III ( 4 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 4 FDA reports)
PAIN OF SKIN ( 4 FDA reports)
PALMAR ERYTHEMA ( 4 FDA reports)
PALPABLE PURPURA ( 4 FDA reports)
PANCREATIC CYST ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 4 FDA reports)
PARENTERAL NUTRITION ( 4 FDA reports)
PAROTID GLAND ENLARGEMENT ( 4 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 4 FDA reports)
PAST-POINTING ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PENIS DISORDER ( 4 FDA reports)
PERIORBITAL OEDEMA ( 4 FDA reports)
PERIPANCREATIC FLUID COLLECTION ( 4 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 4 FDA reports)
PERITONEAL ADHESIONS ( 4 FDA reports)
PERITONITIS SCLEROSING ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PHAEHYPHOMYCOSIS ( 4 FDA reports)
PHONOPHOBIA ( 4 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 4 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 4 FDA reports)
PLATYBASIA ( 4 FDA reports)
PLEURAL DISORDER ( 4 FDA reports)
PLEURAL HAEMORRHAGE ( 4 FDA reports)
PNEUMONECTOMY ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
POLYCHONDRITIS ( 4 FDA reports)
POLYTRAUMATISM ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 4 FDA reports)
POST PROCEDURAL FISTULA ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
POST PROCEDURAL INFECTION ( 4 FDA reports)
POST THROMBOTIC SYNDROME ( 4 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 4 FDA reports)
PRIMARY EFFUSION LYMPHOMA ( 4 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA ( 4 FDA reports)
PROSTATE INFECTION ( 4 FDA reports)
PROSTATITIS ( 4 FDA reports)
ABDOMINAL ADHESIONS ( 3 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 3 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 3 FDA reports)
ADRENAL MASS ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
AGEUSIA ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 3 FDA reports)
ALOPECIA TOTALIS ( 3 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 3 FDA reports)
ANAL ULCER ( 3 FDA reports)
ANASTOMOTIC COMPLICATION ( 3 FDA reports)
ANGIODYSPLASIA ( 3 FDA reports)
ANGIOSARCOMA METASTATIC ( 3 FDA reports)
ANION GAP DECREASED ( 3 FDA reports)
ANISOCYTOSIS ( 3 FDA reports)
ANKLE OPERATION ( 3 FDA reports)
ANOSMIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
AORTIC EMBOLUS ( 3 FDA reports)
AORTIC RUPTURE ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APOPTOSIS ( 3 FDA reports)
APPENDICITIS PERFORATED ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
ARTERIAL BYPASS OPERATION ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTERITIS INFECTIVE ( 3 FDA reports)
ARTHRITIS FUNGAL ( 3 FDA reports)
ASPERGILLUS TEST ( 3 FDA reports)
ASPERGILLUS TEST POSITIVE ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
ATRIAL THROMBOSIS ( 3 FDA reports)
AUTOIMMUNE PANCREATITIS ( 3 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
AUTOMATIC BLADDER ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIAL CULTURE POSITIVE ( 3 FDA reports)
BASOPHIL COUNT INCREASED ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BILE DUCT CANCER ( 3 FDA reports)
BILIARY CYST ( 3 FDA reports)
BILIARY SPHINCTEROTOMY ( 3 FDA reports)
BILIARY TRACT INFECTION ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIOPSY KIDNEY ( 3 FDA reports)
BIOPSY LUNG ABNORMAL ( 3 FDA reports)
BLOOD BICARBONATE INCREASED ( 3 FDA reports)
BLOOD CORTISOL DECREASED ( 3 FDA reports)
BLOOD CREATININE DECREASED ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD OSMOLARITY INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
BONE TRIMMING ( 3 FDA reports)
BOWEN'S DISEASE ( 3 FDA reports)
BRACHIAL PLEXOPATHY ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BRAIN HYPOXIA ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BREAST CANCER STAGE I ( 3 FDA reports)
BREAST TENDERNESS ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHIAL OBSTRUCTION ( 3 FDA reports)
BRONCHIAL ULCERATION ( 3 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 3 FDA reports)
CALCULUS URETHRAL ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CAPILLARY DISORDER ( 3 FDA reports)
CARBON DIOXIDE ABNORMAL ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARCINOID TUMOUR ( 3 FDA reports)
CARDIAC ASTHMA ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 3 FDA reports)
CARDITIS ( 3 FDA reports)
CATARACT SUBCAPSULAR ( 3 FDA reports)
CATHETER SITE ERYTHEMA ( 3 FDA reports)
CATHETER SITE NECROSIS ( 3 FDA reports)
CATHETER SITE OEDEMA ( 3 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBRAL VASOCONSTRICTION ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CHROMOSOMAL DELETION ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COLD TYPE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 3 FDA reports)
COMPLEMENT FACTOR DECREASED ( 3 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CONDYLOMA ACUMINATUM ( 3 FDA reports)
CONJUNCTIVAL IRRITATION ( 3 FDA reports)
COR PULMONALE ACUTE ( 3 FDA reports)
CORNEAL PERFORATION ( 3 FDA reports)
CRYSTAL URINE PRESENT ( 3 FDA reports)
CSF PRESSURE INCREASED ( 3 FDA reports)
CYSTITIS BACTERIAL ( 3 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 3 FDA reports)
CYTOTOXIC OEDEMA ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 3 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 3 FDA reports)
DIZZINESS POSTURAL ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DRUG TOLERANCE INCREASED ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 3 FDA reports)
EMBOLISM ARTERIAL ( 3 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 3 FDA reports)
ENTEROBACTER BACTERAEMIA ( 3 FDA reports)
ENTEROBACTER TEST POSITIVE ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYE ROLLING ( 3 FDA reports)
FACTOR VIII DEFICIENCY ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FEMORAL HERNIA, OBSTRUCTIVE ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GALLBLADDER PERFORATION ( 3 FDA reports)
GASTRIC CANCER STAGE IV ( 3 FDA reports)
GASTRIC MUCOSAL LESION ( 3 FDA reports)
GASTRITIS ATROPHIC ( 3 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 3 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 3 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 3 FDA reports)
GENITAL LESION ( 3 FDA reports)
GESTATIONAL DIABETES ( 3 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 3 FDA reports)
GROIN ABSCESS ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMOPHILUS INFECTION ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HAIR GROWTH ABNORMAL ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEMISENSORY NEGLECT ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 3 FDA reports)
HENOCH-SCHONLEIN PURPURA NEPHRITIS ( 3 FDA reports)
HEPATIC ARTERY EMBOLISM ( 3 FDA reports)
HEPATIC ARTERY OCCLUSION ( 3 FDA reports)
HEPATIC INFECTION ( 3 FDA reports)
HEPATITIS INFECTIOUS ( 3 FDA reports)
HEPATOSPLENIC T-CELL LYMPHOMA ( 3 FDA reports)
HERPES SEPSIS ( 3 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 3 FDA reports)
HIRSUTISM ( 3 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE UNSPECIFIED ( 3 FDA reports)
HYPERMAGNESAEMIA ( 3 FDA reports)
HYPERPROTEINAEMIA ( 3 FDA reports)
HYPERSEXUALITY ( 3 FDA reports)
HYPERSPLENISM ACQUIRED ( 3 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 3 FDA reports)
HYPOAESTHESIA FACIAL ( 3 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 3 FDA reports)
HYPOPYON ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
ILIAC ARTERY STENOSIS ( 3 FDA reports)
ILIAC ARTERY THROMBOSIS ( 3 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPLANT SITE REACTION ( 3 FDA reports)
IMPLANT SITE URTICARIA ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INCISION SITE HAEMORRHAGE ( 3 FDA reports)
INFECTIVE SPONDYLITIS ( 3 FDA reports)
INFESTATION ( 3 FDA reports)
INFUSION SITE THROMBOSIS ( 3 FDA reports)
INGUINAL MASS ( 3 FDA reports)
INTESTINAL FISTULA ( 3 FDA reports)
INTRACRANIAL HYPOTENSION ( 3 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 3 FDA reports)
IRIDOCYCLITIS ( 3 FDA reports)
IRON DEFICIENCY ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
JOINT CREPITATION ( 3 FDA reports)
KERATITIS HERPETIC ( 3 FDA reports)
KERATOSIS FOLLICULAR ( 3 FDA reports)
KNEE OPERATION ( 3 FDA reports)
KOUNIS SYNDROME ( 3 FDA reports)
LANGERHANS' CELL GRANULOMATOSIS ( 3 FDA reports)
LARYNGEAL OBSTRUCTION ( 3 FDA reports)
LENTIGO ( 3 FDA reports)
LEUKAEMOID REACTION ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
LOSS OF EMPLOYMENT ( 3 FDA reports)
LUNG CANCER METASTATIC ( 3 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 3 FDA reports)
LUNG VOLUME REDUCTION SURGERY ( 3 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 3 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MASTOID DISORDER ( 3 FDA reports)
MEDIASTINITIS ( 3 FDA reports)
MENINGITIS HERPES ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
METASTASES TO THORAX ( 3 FDA reports)
MICROSPORIDIA INFECTION ( 3 FDA reports)
MIDDLE EAR EFFUSION ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOSAL ULCERATION ( 3 FDA reports)
MULTIPLE ALLERGIES ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MUSCLE ABSCESS ( 3 FDA reports)
MYELOCYTE COUNT INCREASED ( 3 FDA reports)
MYELOFIBROSIS ( 3 FDA reports)
MYOCARDIAC ABSCESS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NASAL OEDEMA ( 3 FDA reports)
NASOPHARYNGEAL DISORDER ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 3 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 3 FDA reports)
NEPHROURETERECTOMY ( 3 FDA reports)
NEUROGENIC BLADDER ( 3 FDA reports)
NEUROPATHIC PAIN ( 3 FDA reports)
NOCTURNAL DYSPNOEA ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OCCIPITAL NEURALGIA ( 3 FDA reports)
OCCULT BLOOD ( 3 FDA reports)
OCULAR ICTERUS ( 3 FDA reports)
OCULOGYRIC CRISIS ( 3 FDA reports)
OEDEMATOUS PANCREATITIS ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OESOPHAGEAL SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
OOPHORITIS ( 3 FDA reports)
OPSOCLONUS MYOCLONUS ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
ORAL SOFT TISSUE DISORDER ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 3 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 3 FDA reports)
OTORRHOEA ( 3 FDA reports)
OVARIAN EPITHELIAL CANCER ( 3 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PAPILLARY THYROID CANCER ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PARANASAL SINUS DISCOMFORT ( 3 FDA reports)
PARANASAL SINUS MUCOSAL HYPERTROPHY ( 3 FDA reports)
PARANEOPLASTIC SYNDROME ( 3 FDA reports)
PARAOESOPHAGEAL ABSCESS ( 3 FDA reports)
PARESIS CRANIAL NERVE ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 3 FDA reports)
PELVIC KIDNEY ( 3 FDA reports)
PERICARDIAL DISEASE ( 3 FDA reports)
PERIRECTAL ABSCESS ( 3 FDA reports)
PERITONEAL EFFUSION ( 3 FDA reports)
PERSONALITY DISORDER ( 3 FDA reports)
PHAEOCHROMOCYTOMA ( 3 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 3 FDA reports)
PLATELET DESTRUCTION INCREASED ( 3 FDA reports)
PLEURISY VIRAL ( 3 FDA reports)
PNEUMONIA HERPES VIRAL ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
POOR SUCKING REFLEX ( 3 FDA reports)
POST CONCUSSION SYNDROME ( 3 FDA reports)
POST INFLAMMATORY PIGMENTATION CHANGE ( 3 FDA reports)
POSTRENAL FAILURE ( 3 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 3 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 3 FDA reports)
PSEUDALLESCHERIA INFECTION ( 3 FDA reports)
PULMONARY BULLA ( 3 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 3 FDA reports)
PULMONARY NECROSIS ( 3 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 3 FDA reports)
QUALITY OF LIFE DECREASED ( 3 FDA reports)
RADIATION FIBROSIS - LUNG ( 3 FDA reports)
RASH FOLLICULAR ( 3 FDA reports)
REGRESSIVE BEHAVIOUR ( 3 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL NEOPLASM ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 3 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 3 FDA reports)
RETICULOCYTOPENIA ( 3 FDA reports)
RETINAL LASER COAGULATION ( 3 FDA reports)
RETINOPATHY HYPERTENSIVE ( 3 FDA reports)
RHINITIS HYPERTROPHIC ( 3 FDA reports)
SARCOMA METASTATIC ( 3 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 3 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 3 FDA reports)
SCLERODACTYLIA ( 3 FDA reports)
SCROTAL OEDEMA ( 3 FDA reports)
SENSATION OF PRESSURE IN EAR ( 3 FDA reports)
SENSE OF OPPRESSION ( 3 FDA reports)
SENSITIVITY OF TEETH ( 3 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 3 FDA reports)
SEPTIC EMBOLUS ( 3 FDA reports)
SEXUAL DYSFUNCTION ( 3 FDA reports)
SHOULDER OPERATION ( 3 FDA reports)
SKIN DEPIGMENTATION ( 3 FDA reports)
SKIN GRAFT REJECTION ( 3 FDA reports)
SLEEP TALKING ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 3 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPINAL PAIN ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STRESS CARDIOMYOPATHY ( 3 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 3 FDA reports)
SUBDURAL EMPYEMA ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
SYSTOLIC HYPERTENSION ( 3 FDA reports)
T-LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
TACHYPHRENIA ( 3 FDA reports)
TARSAL TUNNEL SYNDROME ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
TETANY ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 3 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 3 FDA reports)
THROAT LESION ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TIBIA FRACTURE ( 3 FDA reports)
TIC ( 3 FDA reports)
TOBACCO USER ( 3 FDA reports)
TRACHEITIS ( 3 FDA reports)
TRACHEOBRONCHITIS VIRAL ( 3 FDA reports)
TRACHEOMALACIA ( 3 FDA reports)
TRAUMATIC FRACTURE ( 3 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 3 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 3 FDA reports)
TRICHOMONIASIS ( 3 FDA reports)
TUMOUR FLARE ( 3 FDA reports)
TUMOUR ULCERATION ( 3 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 3 FDA reports)
TYPE I HYPERSENSITIVITY ( 3 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 3 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
URETERIC ANASTOMOSIS COMPLICATION ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
VAGINAL PROLAPSE ( 3 FDA reports)
VASCULAR INSUFFICIENCY ( 3 FDA reports)
VASCULAR STENT INSERTION ( 3 FDA reports)
VASCULITIS NECROTISING ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VITREOUS DISORDER ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
VULVAL CANCER ( 3 FDA reports)
VULVAL DISORDER ( 3 FDA reports)
VULVOVAGINAL PRURITUS ( 3 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 3 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 3 FDA reports)
WHITE BLOOD CELL DISORDER ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
WISDOM TEETH REMOVAL ( 3 FDA reports)
WOUND TREATMENT ( 3 FDA reports)
YAWNING ( 3 FDA reports)
PSEUDOCYST ( 2 FDA reports)
PUBIC PAIN ( 2 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 2 FDA reports)
PULMONARY FISTULA ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
RADIATION INJURY ( 2 FDA reports)
REACTION TO DRUG EXCIPIENT ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 2 FDA reports)
RELAPSING FEVER ( 2 FDA reports)
REMOVAL OF FOREIGN BODY ( 2 FDA reports)
RENAL ARTERY FIBROMUSCULAR DYSPLASIA ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CANCER RECURRENT ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL VASCULITIS ( 2 FDA reports)
RESECTION OF RECTUM ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETROPERITONEAL EFFUSION ( 2 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 2 FDA reports)
RHABDOID TUMOUR OF THE KIDNEY ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIGHT AORTIC ARCH ( 2 FDA reports)
ROTAVIRUS INFECTION ( 2 FDA reports)
SACRAL PAIN ( 2 FDA reports)
SALPINGOSTOMY ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
SCROTAL ERYTHEMA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEBORRHOEA ( 2 FDA reports)
SEBORRHOEIC DERMATITIS ( 2 FDA reports)
SECONDARY HYPOGONADISM ( 2 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 2 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
SECONDARY SEXUAL CHARACTERISTICS ABSENCE ( 2 FDA reports)
SECONDARY SYPHILIS ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SENSITISATION ( 2 FDA reports)
SERRATIA TEST POSITIVE ( 2 FDA reports)
SHRINKING LUNG SYNDROME ( 2 FDA reports)
SHUNT INFECTION ( 2 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SINUS RHYTHM ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKIN DYSTROPHY ( 2 FDA reports)
SKIN GRAFT FAILURE ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SKIN INJURY ( 2 FDA reports)
SKIN SWELLING ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SOFT TISSUE MASS ( 2 FDA reports)
SOMATOFORM DISORDER CARDIOVASCULAR ( 2 FDA reports)
SPIDER NAEVUS ( 2 FDA reports)
SPINAL CORD INFARCTION ( 2 FDA reports)
SPINAL VASCULAR DISORDER ( 2 FDA reports)
SPIROMETRY ABNORMAL ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
SPLEEN PALPABLE ( 2 FDA reports)
SPLINT APPLICATION ( 2 FDA reports)
SPONDYLITIS ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STENT REMOVAL ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STOMATITIS NECROTISING ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
STROKE VOLUME DECREASED ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SUDDEN HEARING LOSS ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SYMPTOM MASKED ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
SYNOSTOSIS ( 2 FDA reports)
T-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TENSION ( 2 FDA reports)
TESTICULAR CYST ( 2 FDA reports)
TESTICULAR SWELLING ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THOUGHT BLOCKING ( 2 FDA reports)
THYMOMA ( 2 FDA reports)
THYMUS DISORDER ( 2 FDA reports)
THYROXINE FREE INCREASED ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TONGUE CANCER METASTATIC ( 2 FDA reports)
TRACHEAL FISTULA ( 2 FDA reports)
TRANSIENT PSYCHOSIS ( 2 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 2 FDA reports)
TRICHOPHYTIC GRANULOMA ( 2 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 2 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UNEMPLOYMENT ( 2 FDA reports)
URACHAL ABNORMALITY ( 2 FDA reports)
URAEMIC ENCEPHALOPATHY ( 2 FDA reports)
URETERAL DISORDER ( 2 FDA reports)
URETERAL STENT INSERTION ( 2 FDA reports)
URETERIC PERFORATION ( 2 FDA reports)
URETHRITIS ( 2 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
URINARY TRACT PAIN ( 2 FDA reports)
URINE ABNORMALITY ( 2 FDA reports)
URINE AMYLASE INCREASED ( 2 FDA reports)
URINE CYTOMEGALOVIRUS ( 2 FDA reports)
VAGINAL INFLAMMATION ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASCULAR STENOSIS ( 2 FDA reports)
VASCULITIS GASTROINTESTINAL ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VASOPLEGIA SYNDROME ( 2 FDA reports)
VEILLONELLA INFECTION ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VIRUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
VIRUS URINE TEST POSITIVE ( 2 FDA reports)
VITAMIN D DECREASED ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITREOUS ABSCESS ( 2 FDA reports)
VITRITIS ( 2 FDA reports)
VULVA CYST ( 2 FDA reports)
WEIGHT ABNORMAL ( 2 FDA reports)
WEIGHT DECREASE NEONATAL ( 2 FDA reports)
WHIPLASH INJURY ( 2 FDA reports)
WHOLE BLOOD TRANSFUSION ( 2 FDA reports)
WOUND DEBRIDEMENT ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 2 FDA reports)
ABDOMINAL RIGIDITY ( 2 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 2 FDA reports)
ABDOMINAL WALL DISORDER ( 2 FDA reports)
ACANTHOLYSIS ( 2 FDA reports)
ACCIDENTAL NEEDLE STICK ( 2 FDA reports)
ACHOLIA ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACUTE CHEST SYNDROME ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 2 FDA reports)
ADENOVIRAL HEPATITIS ( 2 FDA reports)
ADRENAL HAEMORRHAGE ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
ADRENOCORTICAL STEROID THERAPY ( 2 FDA reports)
ALBUMINURIA ( 2 FDA reports)
ALDOLASE INCREASED ( 2 FDA reports)
ALKALOSIS ( 2 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 2 FDA reports)
ANAEMIA NEONATAL ( 2 FDA reports)
ANAESTHESIA ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 2 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-THYROID ANTIBODY ( 2 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
AORTITIS ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
ARTERIAL RUPTURE ( 2 FDA reports)
ARTERIOPATHIC DISEASE ( 2 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 2 FDA reports)
ARTERITIS CORONARY ( 2 FDA reports)
ARTERY DISSECTION ( 2 FDA reports)
ARTHRITIS SALMONELLA ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASBESTOSIS ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ATONIC SEIZURES ( 2 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BACILLUS TEST POSITIVE ( 2 FDA reports)
BACTERIURIA ( 2 FDA reports)
BALANOPOSTHITIS ( 2 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 2 FDA reports)
BED REST ( 2 FDA reports)
BILIARY ANASTOMOSIS ( 2 FDA reports)
BILIARY SEPSIS ( 2 FDA reports)
BILOMA ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BIOPSY BREAST ( 2 FDA reports)
BIOPSY SKIN ABNORMAL ( 2 FDA reports)
BLADDER CANCER STAGE 0, WITH CANCER IN SITU ( 2 FDA reports)
BLADDER CATHETER REMOVAL ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD PARATHYROID HORMONE DECREASED ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BODY HEIGHT BELOW NORMAL ( 2 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 2 FDA reports)
BONE CALLUS EXCESSIVE ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE NEOPLASM ( 2 FDA reports)
BONE TUBERCULOSIS ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BREAST MICROCALCIFICATION ( 2 FDA reports)
BREAST NEOPLASM ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIAL ANASTOMOSIS COMPLICATION ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
BRONCHIAL WALL THICKENING ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BRUGADA SYNDROME ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
BURKITT'S LYMPHOMA ( 2 FDA reports)
BURSA REMOVAL ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 2 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC INDEX DECREASED ( 2 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 2 FDA reports)
CARDIAC VALVE ABSCESS ( 2 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CARPUS CURVUS ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 2 FDA reports)
CELLS IN URINE ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CEREBRAL SARCOIDOSIS ( 2 FDA reports)
CERVICITIS ( 2 FDA reports)
CERVIX DYSTOCIA ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHOLANGIOGRAM ABNORMAL ( 2 FDA reports)
CHOLANGITIS ACUTE ( 2 FDA reports)
CHOLANGITIS CHRONIC ( 2 FDA reports)
CHOLESTEROSIS ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHORIORETINAL ATROPHY ( 2 FDA reports)
CHORIORETINAL DISORDER ( 2 FDA reports)
CHORIORETINITIS ( 2 FDA reports)
CHROMOSOME ABNORMALITY ( 2 FDA reports)
CHRONIC HEPATITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COLD EXPOSURE INJURY ( 2 FDA reports)
COLONIC FISTULA ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMA SCALE ABNORMAL ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATION OF DEVICE REMOVAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CONUS MEDULLARIS SYNDROME ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CORNEAL GRAFT REJECTION ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIAL NERVE PARALYSIS ( 2 FDA reports)
CRANIOCEREBRAL INJURY ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CSF CULTURE POSITIVE ( 2 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
CUTANEOUS SARCOIDOSIS ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYANOSIS CENTRAL ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 2 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 2 FDA reports)
CYTOMEGALOVIRUS SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS TEST ( 2 FDA reports)
CYTOTOXIC CARDIOMYOPATHY ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELAYED ENGRAFTMENT ( 2 FDA reports)
DELUSION OF GRANDEUR ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DERMOID CYST ( 2 FDA reports)
DIABETIC AUTONOMIC NEUROPATHY ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 2 FDA reports)
DISLOCATION OF VERTEBRA ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG INTERACTION POTENTIATION ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DUODENOGASTRIC REFLUX ( 2 FDA reports)
DURAL TEAR ( 2 FDA reports)
DWARFISM ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
DYSPRAXIA ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
ENCEPHALITIS ALLERGIC ( 2 FDA reports)
ENCEPHALITIS AUTOIMMUNE ( 2 FDA reports)
ENDOMETRIAL CANCER ( 2 FDA reports)
ENDOMETRITIS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 2 FDA reports)
ENTEROBACTER PNEUMONIA ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 2 FDA reports)
ETHANOL GELATION TEST POSITIVE ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
EXTRAVASATION BLOOD ( 2 FDA reports)
EXTRAVASCULAR HAEMOLYSIS ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYELIDS PRURITUS ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FACTOR IX DEFICIENCY ( 2 FDA reports)
FACTOR V LEIDEN MUTATION ( 2 FDA reports)
FACTOR XI DEFICIENCY ( 2 FDA reports)
FACTOR XII DEFICIENCY ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FAILED INDUCTION OF LABOUR ( 2 FDA reports)
FASCIAL OPERATION ( 2 FDA reports)
FIBRILLARY GLOMERULONEPHRITIS ( 2 FDA reports)
FIBRIN ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FUNGAL DNA TEST POSITIVE ( 2 FDA reports)
FUSARIUM INFECTION ( 2 FDA reports)
GALLBLADDER ABSCESS ( 2 FDA reports)
GALLBLADDER OEDEMA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GANGLION ( 2 FDA reports)
GASTRECTOMY ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTRITIS FUNGAL ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOBULINS DECREASED ( 2 FDA reports)
GLOSSECTOMY ( 2 FDA reports)
GRAFT HAEMORRHAGE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
GRANULOCYTOSIS ( 2 FDA reports)
GRANULOMA SKIN ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
HAEMANGIOMA REMOVAL ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMOGLOBINAEMIA ( 2 FDA reports)
HAEMOPERFUSION ( 2 FDA reports)
HAEMORRHAGIC CYST ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HEAD LAG ABNORMAL ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 2 FDA reports)
HEPATIC ATROPHY ( 2 FDA reports)
HEPATIC INFECTION BACTERIAL ( 2 FDA reports)
HEPATIC INFECTION FUNGAL ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATITIS GRANULOMATOUS ( 2 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 2 FDA reports)
HEPATOBILIARY SCAN ABNORMAL ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HERPES ZOSTER MULTI-DERMATOMAL ( 2 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 2 FDA reports)
HLA MARKER STUDY POSITIVE ( 2 FDA reports)
HODGKIN'S DISEASE RECURRENT ( 2 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERLACTACIDAEMIA ( 2 FDA reports)
HYPERMETROPIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERURICOSURIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPERVISCOSITY SYNDROME ( 2 FDA reports)
HYPOCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOCHROMASIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 2 FDA reports)
IATROGENIC INFECTION ( 2 FDA reports)
IIIRD NERVE DISORDER ( 2 FDA reports)
ILEOCOLOSTOMY ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPLANT SITE EFFUSION ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INFECTIOUS DISEASE CARRIER ( 2 FDA reports)
INFECTIVE ANEURYSM ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE MASS ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
INTENTION TREMOR ( 2 FDA reports)
INTERCOSTAL RETRACTION ( 2 FDA reports)
INTERTRIGO ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL MASS ( 2 FDA reports)
INTESTINAL POLYP ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTRANASAL FUNGAL INFECTION ( 2 FDA reports)
IRITIS ( 2 FDA reports)
ISCHAEMIC ULCER ( 2 FDA reports)
JAUNDICE NEONATAL ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KABUKI MAKE-UP SYNDROME ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LARGE CELL LUNG CANCER STAGE IV ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LARYNGEAL GRANULOMA ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEGIONELLA INFECTION ( 2 FDA reports)
LEGIONELLA TEST ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LIMB ASYMMETRY ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP BLISTER ( 2 FDA reports)
LIPODYSTROPHY ACQUIRED ( 2 FDA reports)
LISTERIA ENCEPHALITIS ( 2 FDA reports)
LISTERIA SEPSIS ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LYMPHADENECTOMY ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
LYMPHOMA TRANSFORMATION ( 2 FDA reports)
MACULAR CYST ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MACULE ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASS EXCISION ( 2 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MEDIASTINAL MASS ( 2 FDA reports)
MEDICAL DIET ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENINGEAL NEOPLASM ( 2 FDA reports)
MENINGITIS CANDIDA ( 2 FDA reports)
MENINGITIS ENTEROCOCCAL ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
MENINGORADICULITIS ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 2 FDA reports)
MESENTERIC HAEMORRHAGE ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASES TO NECK ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
METASTATIC CARCINOID TUMOUR ( 2 FDA reports)
MICROSCOPIC POLYANGIITIS ( 2 FDA reports)
MICTURITION DISORDER ( 2 FDA reports)
MINERAL METABOLISM DISORDER ( 2 FDA reports)
MISCARRIAGE OF PARTNER ( 2 FDA reports)
MITOCHONDRIAL MYOPATHY ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
MONONEUROPATHY ( 2 FDA reports)
MONONEUROPATHY MULTIPLEX ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUTISM ( 2 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 2 FDA reports)
MYCOPLASMA INFECTION ( 2 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 2 FDA reports)
MYELOID LEUKAEMIA ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL CYST ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NECK INJURY ( 2 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 2 FDA reports)
NECROTISING RETINITIS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROFIBROMA ( 2 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 2 FDA reports)
NEUTROPENIC COLITIS ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NOCARDIA SEPSIS ( 2 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCULAR MYASTHENIA ( 2 FDA reports)
OCULOMOTOR STUDY ABNORMAL ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OESOPHAGEAL ACHALASIA ( 2 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
ORGAN TRANSPLANT ( 2 FDA reports)
ORTHOPEDIC PROCEDURE ( 2 FDA reports)
OSTEOMALACIA ( 2 FDA reports)
OSTEOMYELITIS CHRONIC ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PAIN EXACERBATED ( 2 FDA reports)
PANCREATECTOMY ( 2 FDA reports)
PANCREATIC ENZYMES ABNORMAL ( 2 FDA reports)
PANCREATIC PSEUDOCYST ( 2 FDA reports)
PANIC DISORDER WITH AGORAPHOBIA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARAPROTEINAEMIA ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
PELVIC CONGESTION ( 2 FDA reports)
PELVIC POUCH PROCEDURE ( 2 FDA reports)
PERICARDITIS INFECTIVE ( 2 FDA reports)
PERINEAL PAIN ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 2 FDA reports)
PHAGOCYTOSIS ( 2 FDA reports)
PLACENTAL HYPERTROPHY ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PLATELET TRANSFUSION ( 2 FDA reports)
PLEURODESIS ( 2 FDA reports)
PLEUROPERICARDITIS ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOCOCCAL INFECTION ( 2 FDA reports)
PNEUMONIA INFLUENZAL ( 2 FDA reports)
PNEUMONIA MYCOPLASMAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 2 FDA reports)
POOR VENOUS ACCESS ( 2 FDA reports)
POROKERATOSIS ( 2 FDA reports)
PORTAL VEIN OCCLUSION ( 2 FDA reports)
PORTAL VEIN STENOSIS ( 2 FDA reports)
POSITIVE ROMBERGISM ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
POSTOPERATIVE ABSCESS ( 2 FDA reports)
PRECANCEROUS SKIN LESION ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PRESSURE OF SPEECH ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PROCEDURAL HYPERTENSION ( 2 FDA reports)
PROCTOCOLITIS ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
PROSTATE CANCER METASTATIC ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABDOMINAL WALL INFECTION ( 1 FDA reports)
ABNORMAL LABOUR ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABORTION MISSED ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACETABULUM FRACTURE ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACQUIRED PHIMOSIS ( 1 FDA reports)
ACTH STIMULATION TEST ABNORMAL ( 1 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 1 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ALEXIA ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
ALPERS' DISEASE ( 1 FDA reports)
ALPHA-1 ACID GLYCOPROTEIN INCREASED ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
AMNESTIC DISORDER ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANCER METASTATIC ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL EROSION ( 1 FDA reports)
ANAL NEOPLASM ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOGRAM CEREBRAL ABNORMAL ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANTERIOR SPINAL ARTERY SYNDROME ( 1 FDA reports)
ANTI-HBS ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-SS-A ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTICOAGULANT THERAPY ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APGAR SCORE ABNORMAL ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE INFLAMMATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ARTERIAL ANEURYSM REPAIR ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL INSUFFICIENCY ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 1 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 1 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ARTHRODESIS ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
ASPIRATION BIOPSY ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
AURICULAR PERICHONDRITIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
B PRECURSOR TYPE ACUTE LEUKAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
BACILLARY ANGIOMATOSIS ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA TISSUE SPECIMEN IDENTIFIED ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BARTONELLOSIS ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BENIGN BONE NEOPLASM ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BIFASCICULAR BLOCK ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BIOPSY CHORIONIC VILLOUS ABNORMAL ( 1 FDA reports)
BIOPSY SITE UNSPECIFIED ABNORMAL ( 1 FDA reports)
BIOPSY SKIN ( 1 FDA reports)
BIOPSY VOCAL CORD ( 1 FDA reports)
BITE ( 1 FDA reports)
BLADDER CALCULUS REMOVAL ( 1 FDA reports)
BLADDER DYSFUNCTION ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLADDER NEOPLASM SURGERY ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLADDER TAMPONADE ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE NORMAL ( 1 FDA reports)
BLOOD AMYLASE ABNORMAL ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD KETONE BODY PRESENT ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BLUNTED AFFECT ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BORDETELLA INFECTION ( 1 FDA reports)
BOWEL PREPARATION ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BRAIN STEM ISCHAEMIA ( 1 FDA reports)
BREAST CANCER STAGE II ( 1 FDA reports)
BREAST CANCER STAGE IV ( 1 FDA reports)
BREAST INFLAMMATION ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREECH DELIVERY ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS FUNGAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOGRAM ABNORMAL ( 1 FDA reports)
BRUCELLOSIS ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE IV ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURNING MOUTH SYNDROME ( 1 FDA reports)
BURNOUT SYNDROME ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
C-REACTIVE PROTEIN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CAFE AU LAIT SPOTS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CAPILLARY FRAGILITY INCREASED ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 1 FDA reports)
CARBOHYDRATE TOLERANCE DECREASED ( 1 FDA reports)
CARDIAC ANEURYSM ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC INDEX INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIOPLEGIA ( 1 FDA reports)
CARDIOPULMONARY BYPASS ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
CD4 LYMPHOCYTES ABNORMAL ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CELLULITIS ENTEROCOCCAL ( 1 FDA reports)
CELLULITIS GANGRENOUS ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL PAIN SYNDROME ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMOSIDERIN DEPOSITION ( 1 FDA reports)
CEREBRAL MICROHAEMORRHAGE ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX CARCINOMA STAGE III ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHILD NEGLECT ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 1 FDA reports)
CHORIORETINAL SCAR ( 1 FDA reports)
CHOROIDAL DETACHMENT ( 1 FDA reports)
CHOROIDITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMOBLASTOMYCOSIS ( 1 FDA reports)
CHROMOSOMAL MUTATION ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CITROBACTER TEST POSITIVE ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION DISORDER NEONATAL ( 1 FDA reports)
COAGULATION TIME ABNORMAL ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC ARTERY STENOSIS ( 1 FDA reports)
COGNITIVE DETERIORATION ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLD AGGLUTININS ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLITIS EROSIVE ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
COLORECTOSTOMY ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPLICATED MIGRAINE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONGENITAL ANOMALY IN OFFSPRING ( 1 FDA reports)
CONGENITAL CYSTIC LUNG ( 1 FDA reports)
CONGENITAL HYDRONEPHROSIS ( 1 FDA reports)
CONGENITAL MUSCULOSKELETAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL ABSCESS ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORNEAL LIGHT REFLEX TEST ABNORMAL ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CRANIAL NERVE OPERATION ( 1 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CRANIOPHARYNGIOMA ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
CRYSTAL NEPHROPATHY ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYST ASPIRATION ABNORMAL ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYTAPHERESIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN ( 1 FDA reports)
CYTOMEGALOVIRUS MUCOCUTANEOUS ULCER ( 1 FDA reports)
DEATH OF COMPANION ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DENGUE FEVER ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DEVELOPMENTAL COORDINATION DISORDER ( 1 FDA reports)
DEVICE EXPULSION ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC EYE DISEASE ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC GASTROPARESIS ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 1 FDA reports)
DIFFUSE MESANGIAL SCLEROSIS ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DILUTIONAL COAGULOPATHY ( 1 FDA reports)
DIPHTHERIA ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIRECT INFECTION TRANSMISSION ( 1 FDA reports)
DIVERTICULAR HERNIA ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRESSLER'S SYNDROME ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL CHANGED ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ECZEMA WEEPING ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROLYTE DEPLETION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOCRINE NEOPLASM MALIGNANT ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOSCOPY LARGE BOWEL ABNORMAL ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTERAL NUTRITION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ENTEROCOLITIS VIRAL ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
ENTHESOPATHY ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPINEPHRINE ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
ERYTHEMA MARGINATUM ( 1 FDA reports)
ERYTHROID MATURATION ARREST ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EWING'S SARCOMA METASTATIC ( 1 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 1 FDA reports)
EXPOSURE VIA SEMEN ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EXTRANODAL NK/T-CELL LYMPHOMA, NASAL TYPE ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
EXTRASKELETAL OSTEOSARCOMA ( 1 FDA reports)
EYE ABSCESS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE MUSCLE OPERATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTOR IX INHIBITION ( 1 FDA reports)
FACTOR XIII DEFICIENCY ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FALLOPIAN TUBE DISORDER ( 1 FDA reports)
FAMILIAL HAEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ( 1 FDA reports)
FEAR OF PREGNANCY ( 1 FDA reports)
FEEDING DISORDER OF INFANCY OR EARLY CHILDHOOD ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FELTY'S SYNDROME ( 1 FDA reports)
FEMORAL PULSE DECREASED ( 1 FDA reports)
FIBRINOLYSIS ABNORMAL ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOLLICLE CENTRE LYMPHOMA, FOLLICULAR GRADE I, II, III ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL CYSTITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL RHINITIS ( 1 FDA reports)
FUSOBACTERIUM INFECTION ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAS GANGRENE ( 1 FDA reports)
GASTRIC INFECTION ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GASTROINTESTINAL SURGERY ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ( 1 FDA reports)
GENITAL ABSCESS ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GENITOURINARY TRACT INFECTION ( 1 FDA reports)
GILBERT'S SYNDROME ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
GOODPASTURE'S SYNDROME ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUN SHOT WOUND ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMATOMA EVACUATION ( 1 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMODILUTION ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HASHIMOTO'S ENCEPHALOPATHY ( 1 FDA reports)
HBV DNA INCREASED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE CALCIFICATION ( 1 FDA reports)
HEMIPLEGIA TRANSIENT ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 1 FDA reports)
HEPATIC CANCER METASTATIC ( 1 FDA reports)
HEPATIC CYST INFECTION ( 1 FDA reports)
HEPATIC ENZYME ( 1 FDA reports)
HEPATIC INFILTRATION EOSINOPHILIC ( 1 FDA reports)
HEPATIC MASS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATIC RUPTURE ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B VIRUS ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOPULMONARY SYNDROME ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES SIMPLEX HEPATITIS ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HIGH FREQUENCY ABLATION ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HODGKIN'S DISEASE REFRACTORY ( 1 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 1 FDA reports)
HOSPICE CARE ( 1 FDA reports)
HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE I INFECTION ( 1 FDA reports)
HUNTINGTON'S CHOREA ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDROURETER ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERCORTICOIDISM ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPALLAESTHESIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMEGALY ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHONDRIASIS ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
ILEAL ULCER ( 1 FDA reports)
ILIAC ARTERY EMBOLISM ( 1 FDA reports)
ILIUM FRACTURE ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE EXTRAVASATION ( 1 FDA reports)
IMPLANT SITE INFLAMMATION ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION OF WOUND ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INSULIN RESISTANT DIABETES ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERLEUKIN-2 RECEPTOR INCREASED ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL MUCOSAL HYPERTROPHY ( 1 FDA reports)
INTESTINAL STOMA ( 1 FDA reports)
INTESTINAL STOMA COMPLICATION ( 1 FDA reports)
INTESTINAL ULCER PERFORATION ( 1 FDA reports)
INTRA-AORTIC BALLOON PLACEMENT ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRADUCTAL PAPILLOMA OF BREAST ( 1 FDA reports)
IODINE ALLERGY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JEJUNOSTOMY ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT FLUID DRAINAGE ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KARYOTYPE ANALYSIS ABNORMAL ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KERATOCONUS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LEUKODERMA ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN MYXOEDEMATOSUS ( 1 FDA reports)
LICHENIFICATION ( 1 FDA reports)
LIGHT CHAIN DISEASE ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPASE ABNORMAL ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIVE BIRTH ( 1 FDA reports)
LIVER AND PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
LIVER AND SMALL INTESTINE TRANSPLANT ( 1 FDA reports)
LIVER TENDERNESS ( 1 FDA reports)
LORDOSIS ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER MOTOR NEURONE LESION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOID TISSUE HYPERPLASIA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MACROPHAGES INCREASED ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT TRANSFORMATION ( 1 FDA reports)
MARBURG'S VARIANT MULTIPLE SCLEROSIS ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEGAKARYOCYTES ( 1 FDA reports)
MELANOSIS COLI ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA BENIGN ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERITIS ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
MICROCYTOSIS ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MITOCHONDRIAL TOXICITY ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONEURITIS ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MORPHOEA ( 1 FDA reports)
MOTOR NEURONE DISEASE ( 1 FDA reports)
MUCOCUTANEOUS ULCERATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUSCLE HYPERTROPHY ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MUSCULAR DYSTROPHY ( 1 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYCOBACTERIUM KANSASII PNEUMONIA ( 1 FDA reports)
MYCOBACTERIUM MARINUM INFECTION ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYELOID MATURATION ARREST ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCARDITIS MYCOTIC ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
N-TELOPEPTIDE URINE DECREASED ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NASAL SINUS CANCER ( 1 FDA reports)
NASAL TURBINATE ABNORMALITY ( 1 FDA reports)
NATURAL KILLER CELL COUNT INCREASED ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NECROTIC PRESERVATION INJURY OF GRAFT ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEONATAL TACHYPNOEA ( 1 FDA reports)
NEPHRITIS ALLERGIC ( 1 FDA reports)
NEPHROBLASTOMA ( 1 FDA reports)
NERVE BLOCK ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROBLASTOMA RECURRENT ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEUROFIBROMATOSIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NONINFECTIVE BRONCHITIS ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OEDEMA DUE TO HEPATIC DISEASE ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGITIS BACTERIAL ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ORAL ALLERGY SYNDROME ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
ORBITAL APEX SYNDROME ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL NEOPLASM ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSMOLAR GAP ABNORMAL ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OSTEOSARCOMA LOCALISED ( 1 FDA reports)
OTOTOXICITY ( 1 FDA reports)
OVARIAN ADENOMA ( 1 FDA reports)
OVARIAN ATROPHY ( 1 FDA reports)
OVARIAN HAEMORRHAGE ( 1 FDA reports)
OVERLAP SYNDROME ( 1 FDA reports)
PACEMAKER COMPLICATION ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PAGET'S DISEASE OF THE BREAST ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREAS LIPOMATOSIS ( 1 FDA reports)
PANCREAS TRANSPLANT ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC FISTULA ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PAPILLARY MUSCLE DISORDER ( 1 FDA reports)
PARANASAL SINUS BENIGN NEOPLASM ( 1 FDA reports)
PARANEOPLASTIC CEREBELLAR DEGENERATION ( 1 FDA reports)
PARANEOPLASTIC DERMATOMYOSITIS ( 1 FDA reports)
PARASITIC TEST POSITIVE ( 1 FDA reports)
PARATHYROIDECTOMY ( 1 FDA reports)
PARKINSONIAN GAIT ( 1 FDA reports)
PASSIVE SMOKING ( 1 FDA reports)
PASTEURELLA INFECTION ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PELVIC PERITONEAL ADHESIONS ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PERIARTICULAR DISORDER ( 1 FDA reports)
PERICARDIAL EXCISION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERICARDITIS FUNGAL ( 1 FDA reports)
PERICARDITIS RHEUMATIC ( 1 FDA reports)
PERIDIVERTICULAR ABSCESS ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)
PERIODONTAL INFECTION ( 1 FDA reports)
PERIORBITAL DISORDER ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL NERVE DESTRUCTION ( 1 FDA reports)
PERIPHERAL NERVE INJURY ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL CANCER STAGE UNSPECIFIED ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGOLARYNGEAL ABSCESS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PHOTODYNAMIC THERAPY ( 1 FDA reports)
PHOTOSENSITIVE RASH ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PIGMENTATION BUCCAL ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLASMABLASTIC LYMPHOMA ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLATELET MORPHOLOGY ABNORMAL ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL NEOPLASM ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA TOXOPLASMAL ( 1 FDA reports)
PNEUMONITIS CRYPTOCOCCAL ( 1 FDA reports)
PNEUMORETROPERITONEUM ( 1 FDA reports)
POIKILODERMA ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POLYP COLORECTAL ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
POOR WEIGHT GAIN NEONATAL ( 1 FDA reports)
PORTAL VENOUS GAS ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST POLIO SYNDROME ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST PROCEDURAL DRAINAGE ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL URINE LEAK ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTICTAL PARALYSIS ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 1 FDA reports)
POSTURAL REFLEX IMPAIRMENT ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PRE-ENGRAFTMENT IMMUNE REACTION ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREGNANCY TEST POSITIVE ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMARY ADRENAL INSUFFICIENCY ( 1 FDA reports)
PRIMARY HYPOTHYROIDISM ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROLONGED EXPIRATION ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PROSTATE TENDERNESS ( 1 FDA reports)
PROSTATIC CALCIFICATION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROSTHESIS IMPLANTATION ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PSEUDO LYMPHOMA ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOPARALYSIS ( 1 FDA reports)
PSEUDOPOLYPOSIS ( 1 FDA reports)
PSYCHIATRIC EVALUATION ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY ARTERY WALL HYPERTROPHY ( 1 FDA reports)
PULMONARY FUNCTION CHALLENGE TEST ABNORMAL ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY VALVE CALCIFICATION ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VEIN OCCLUSION ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
PYOMYOSITIS ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
RADIAL NERVE PALSY ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADICULAR SYNDROME ( 1 FDA reports)
RADICULITIS LUMBOSACRAL ( 1 FDA reports)
RADIOTHERAPY TO BRAIN ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH DECREASED ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL AGENESIS ( 1 FDA reports)
RENAL AND PANCREAS TRANSPLANT ( 1 FDA reports)
RENAL AND PANCREAS TRANSPLANT REJECTION ( 1 FDA reports)
RENAL ARTERITIS ( 1 FDA reports)
RENAL ARTERY OCCLUSION ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE I ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE II ( 1 FDA reports)
RENAL DYSPLASIA ( 1 FDA reports)
RENAL HAEMANGIOMA ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL INTERSTITIAL FIBROSIS ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL PAPILLARY NECROSIS ( 1 FDA reports)
RENAL SALT-WASTING SYNDROME ( 1 FDA reports)
RENAL SCAN ABNORMAL ( 1 FDA reports)
RENAL TUBERCULOSIS ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL TEAR ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
ROSEOLOVIRUS TEST POSITIVE ( 1 FDA reports)
SACCADIC EYE MOVEMENT ( 1 FDA reports)
SALMONELLA TEST POSITIVE ( 1 FDA reports)
SALPINGO-OOPHORITIS ( 1 FDA reports)
SARCOMA ( 1 FDA reports)
SCAR PAIN ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCHNITZLER'S SYNDROME ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERODERMA RENAL CRISIS ( 1 FDA reports)
SCROTAL MASS ( 1 FDA reports)
SEGMENTED HYALINISING VASCULITIS ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF-INJURIOUS IDEATION ( 1 FDA reports)
SENSATION OF BLOCK IN EAR ( 1 FDA reports)
SERUM FERRITIN ABNORMAL ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN DEGENERATIVE DISORDER ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
SMOOTH MUSCLE CELL NEOPLASM ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOCIAL PHOBIA ( 1 FDA reports)
SOFT TISSUE NECROSIS ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
SOPOR ( 1 FDA reports)
SPASTIC PARAPLEGIA ( 1 FDA reports)
SPERMATOCELE ( 1 FDA reports)
SPINAL MENINGIOMA BENIGN ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLINTER HAEMORRHAGES ( 1 FDA reports)
SPONDYLOLISTHESIS ACQUIRED ( 1 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEREOTYPY ( 1 FDA reports)
STERNAL WIRING ( 1 FDA reports)
STERNOTOMY ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STILL'S DISEASE ADULT ONSET ( 1 FDA reports)
STOMATOCOCCAL INFECTION ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBSTANCE-INDUCED PSYCHOTIC DISORDER ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURFACTANT PROTEIN INCREASED ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNOVIAL FLUID ANALYSIS ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL PRESENT ( 1 FDA reports)
SYNOVIAL RUPTURE ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
T-LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THERAPEUTIC ASPIRATION ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYMECTOMY ( 1 FDA reports)
THYMIC CANCER METASTATIC ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TINEA CAPITIS ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE ERUPTION ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOTAL LUNG CAPACITY ABNORMAL ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TOXIC OPTIC NEUROPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRANSFUSION WITH INCOMPATIBLE BLOOD ( 1 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRANSPLANT ABSCESS ( 1 FDA reports)
TRANSURETHRAL BLADDER RESECTION ( 1 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TRICHOPHYTOSIS ( 1 FDA reports)
TRIGEMINAL NERVE ABLATION ( 1 FDA reports)
TRISOMY 18 ( 1 FDA reports)
TROPICAL SPASTIC PARESIS ( 1 FDA reports)
TROPONIN I ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULOSIS LIVER ( 1 FDA reports)
TUBERCULOSIS OF INTRATHORACIC LYMPH NODES ( 1 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS AND UVEITIS SYNDROME ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
TUMOUR PERFORATION ( 1 FDA reports)
TUMOUR RELATED COMPLICATION ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
ULNA FRACTURE ( 1 FDA reports)
ULNAR NEURITIS ( 1 FDA reports)
ULTRASONIC ANGIOGRAM ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
ULTRASOUND UTERUS ABNORMAL ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 1 FDA reports)
URETERAL STENT REMOVAL ( 1 FDA reports)
URETERIC FISTULA ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL FISTULA ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY BLADDER SARCOMA ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY SYSTEM X-RAY ABNORMAL ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE CYTOMEGALOVIRUS POSITIVE ( 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 SODIUM INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
URTICARIA CHRONIC ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE ATONY ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE INFECTION ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL EROSION ( 1 FDA reports)
VAGINAL FISTULA ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VARICOCELE ( 1 FDA reports)
VASCULAR ACCESS COMPLICATION ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR NEOPLASM ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENTOUSE EXTRACTION ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBRAL INJURY ( 1 FDA reports)
VESTIBULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
VESTIBULAR NEURONITIS ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL SINUSITIS ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VISUAL EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VITAMIN B6 DECREASED ( 1 FDA reports)
VITAMIN C DECREASED ( 1 FDA reports)
VITAMIN C DEFICIENCY ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOLVULUS OF BOWEL ( 1 FDA reports)
VOMITING NEONATAL ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VOMITING PSYCHOGENIC ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
XERODERMA ( 1 FDA reports)
YERSINIA INFECTION ( 1 FDA reports)