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CYTOMEGALOVIRUS INFECTION ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
ADENOVIRUS INFECTION ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 3 FDA reports)
CYSTITIS VIRAL ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ANGIOSARCOMA ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CAMPYLOBACTER TEST POSITIVE ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTION REACTIVATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
PARAINFLUENZAE VIRAL LARYNGOTRACHEOBRONCHITIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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