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

CYTOMEGALOVIRUS INFECTION ( 10 FDA reports)
GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
FASCIAL INFECTION ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GLOMERULONEPHRITIS ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BALLISMUS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE GRAFT ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 1 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROTEIN S DECREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENIC INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VESTIBULITIS ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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