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

METABOLIC ACIDOSIS ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
CONFUSIONAL STATE ( 12 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 12 FDA reports)
DIARRHOEA ( 11 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
HYPOMAGNESAEMIA ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
VOMITING ( 7 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
TORSADE DE POINTES ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
BACK PAIN ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
KUSSMAUL RESPIRATION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SHORT-BOWEL SYNDROME ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GRIEF REACTION ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OVARIAN ABSCESS ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHRENIC NERVE PARALYSIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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