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

MUCOSAL INFLAMMATION ( 13 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 11 FDA reports)
GRAFT VERSUS HOST DISEASE ( 11 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
PNEUMONIA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
SEPSIS ( 3 FDA reports)
PNEUMONIA ASPERGILLUS ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
INFECTION ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DELAYED ENGRAFTMENT ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
GROWTH ACCELERATED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
BLOOD GONADOTROPHIN INCREASED ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
SECONDARY SEXUAL CHARACTERISTICS ABSENCE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)

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