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COMPLICATIONS OF BONE MARROW TRANSPLANT ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
NOCARDIOSIS ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
THYROID CANCER ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ADENOVIRUS INFECTION ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
MELAENA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
APLASIA ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
PARESIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IIIRD NERVE PARESIS ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEROMA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)

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