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

URINE OUTPUT DECREASED ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
RENAL ARTERIOSCLEROSIS ( 6 FDA reports)
NEPHROCALCINOSIS ( 6 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
INFECTIOUS PERITONITIS ( 3 FDA reports)
HEADACHE ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ADENOVIRAL HEPATITIS ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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