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

PNEUMONIA ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
ACANTHAMOEBA KERATITIS ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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