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

PYREXIA ( 9 FDA reports)
ANAEMIA ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
BREAST CANCER METASTATIC ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS A ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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