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

RENAL FAILURE ACUTE ( 10 FDA reports)
BICYTOPENIA ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
DEHYDRATION ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
ASTHMA ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
DIARRHOEA ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ARTERIAL INJURY ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DEATH ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
VASCULAR ENCEPHALOPATHY ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SKIN FISSURES ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
AGITATION ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTERIOVENOUS FISTULA OCCLUSION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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