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

TORSADE DE POINTES ( 10 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
HYPOMAGNESAEMIA ( 9 FDA reports)
VENTRICULAR TACHYCARDIA ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
EXTRASYSTOLES ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 4 FDA reports)
HEPATITIS B ( 3 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
PNEUMONIA ASPERGILLUS ( 2 FDA reports)
PERIANAL ABSCESS ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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