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

ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMA ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC CANCER STAGE II ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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