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ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
RASH ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HYPOTENSION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
CORYNEBACTERIUM SEPSIS ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA REPAIR ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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