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GRAFT VERSUS HOST DISEASE ( 12 FDA reports)
NEUTROPENIA ( 8 FDA reports)
FUNGAL INFECTION ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
SEPSIS ( 6 FDA reports)
STEM CELL TRANSPLANT ( 5 FDA reports)
SUDDEN CARDIAC DEATH ( 5 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
SHOCK ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMOCONCENTRATION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MOUTH PLAQUE ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RETCHING ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL PROSTHESIS USER ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS BRAIN STEM ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ASPERGILLUS ( 1 FDA reports)
PROPIONIBACTERIUM INFECTION ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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