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

WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FALL ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
DIZZINESS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)

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