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

DIARRHOEA ( 9 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
DEATH ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OBESITY ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
THROMBOANGIITIS OBLITERANS ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
COMA ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERLIPASAEMIA ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RETINAL DISORDER ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
TERMINAL STATE ( 3 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URINE LEUKOCYTE ESTERASE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ECHOCARDIOGRAM ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANOXIA ( 1 FDA reports)
APPENDIX DISORDER ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCUMCISION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHROLEUKAEMIA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GASTRIC VARICES ( 1 FDA reports)
GASTROINTESTINAL BACTERIAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MIXED INCONTINENCE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRICUSPID VALVE REPAIR ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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