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AMMONIA INCREASED ( 6 FDA reports)
DEATH ( 6 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
AGITATION ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CATHETER SITE RELATED REACTION ( 2 FDA reports)
COMA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMINO ACID LEVEL DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
ORNITHINE TRANSCARBAMOYLASE DEFICIENCY ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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