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

ASTHENIA ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
JAUNDICE ( 8 FDA reports)
COMA ( 6 FDA reports)
DIARRHOEA ( 5 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
APNOEA ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
PARANOIA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
RALES ( 3 FDA reports)
RASH ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
MALAISE ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
THROMBIN TIME PROLONGED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
AGITATION ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use