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

SEPTIC SHOCK ( 4 FDA reports)
PYREXIA ( 3 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
COMA ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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