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

MULTI-ORGAN FAILURE ( 11 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
ENGRAFT FAILURE ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
INFECTION ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
NEUTROPENIC SEPSIS ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 2 FDA reports)
GASTROENTERITIS NOROVIRUS ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRICHOSPORON INFECTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHIMERISM ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INFUSION SITE REACTION ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)

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