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

THROMBOTIC MICROANGIOPATHY ( 10 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
STOMATITIS ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 6 FDA reports)
CAPILLARY LEAK SYNDROME ( 6 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 6 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 6 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 6 FDA reports)
ENGRAFT FAILURE ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
XERODERMA ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA RECURRENT ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
DEATH ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use