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

THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
GASTRITIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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