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

ASPARTATE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
FATIGUE ( 5 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EPISTAXIS ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAIN ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISCERAL ARTERIAL ISCHAEMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use