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

THROMBOCYTOPENIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
COMA ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ASCITES ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
CHILLS ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
APLASIA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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