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

TRANSPLANT REJECTION ( 20 FDA reports)
FEBRILE NEUTROPENIA ( 17 FDA reports)
PYREXIA ( 13 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
DIARRHOEA ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
LEUKOPENIA ( 9 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
BRONCHIECTASIS ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 5 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PNEUMONIA FUNGAL ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GRAFT LOSS ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 4 FDA reports)
HYPERVOLAEMIA ( 4 FDA reports)
KAPOSI'S SARCOMA ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PARANASAL SINUS DISCOMFORT ( 4 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
RHINITIS HYPERTROPHIC ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SARCOMA METASTATIC ( 4 FDA reports)
SINUSITIS ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
TONSILLAR HYPERTROPHY ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DRUG CLEARANCE DECREASED ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INCISION SITE CELLULITIS ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
APLASIA ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG RESISTANCE ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERPARATHYROIDISM ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LYMPHOCYTIC INFILTRATION ( 2 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOYAMOYA DISEASE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERITONEAL EFFUSION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA HERPES VIRAL ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RECTAL POLYP ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SPINAL LAMINECTOMY ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VIRAL LOAD INCREASED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL OBESITY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENCEPHALITIS ALLERGIC ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART-LUNG TRANSPLANT REJECTION ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPYREXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
MALACOPLAKIA GASTROINTESTINAL ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS FUNGAL ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONITIS SCLEROSING ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SPLENIC VEIN THROMBOSIS ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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