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

HYDROCEPHALUS ( 10 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
CATHETER RELATED COMPLICATION ( 8 FDA reports)
GASTROINTESTINAL NECROSIS ( 8 FDA reports)
INTESTINAL ISCHAEMIA ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
THROMBOSIS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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