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

RHABDOMYOLYSIS ( 7 FDA reports)
MYALGIA ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
ALOPECIA ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CREATININE URINE INCREASED ( 4 FDA reports)
CYSTIC LYMPHANGIOMA ( 4 FDA reports)
DIABETIC FOOT ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
GOUT ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPERTENSIVE CRISIS ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
NEUROMYOPATHY ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
REFRACTORY ANAEMIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
DERMATITIS PSORIASIFORM ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
POLYMYOSITIS ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE ATROPHY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DENTAL IMPLANTATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMPLANT SITE PAIN ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)

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