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

PYREXIA ( 13 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
PROSTATE CANCER ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CARDIAC PACEMAKER INSERTION ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
SICK SINUS SYNDROME ( 6 FDA reports)
SINUS ARREST ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
COUGH ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
INFECTION ( 5 FDA reports)
MYOGLOBINURIA ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONJUNCTIVAL DISORDER ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
RASH ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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