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

CHRONIC GRAFT VERSUS HOST DISEASE ( 13 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 12 FDA reports)
DIARRHOEA ( 11 FDA reports)
GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
NAUSEA ( 9 FDA reports)
PNEUMONIA ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
INFECTION ( 7 FDA reports)
LEUKAEMIA RECURRENT ( 7 FDA reports)
MALAISE ( 7 FDA reports)
VOMITING ( 7 FDA reports)
CONVULSION ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
TRANSPLANT FAILURE ( 6 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
ENCEPHALITIS VIRAL ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BK VIRUS INFECTION ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GRAFT LOSS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RASH ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOVENOUS FISTULA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLORECTAL CANCER METASTATIC ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANEL-REACTIVE ANTIBODY INCREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERITONEAL HAEMATOMA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VULVOVAGINITIS ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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