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

PAIN ( 25 FDA reports)
RENAL FAILURE ( 24 FDA reports)
INJURY ( 23 FDA reports)
ANXIETY ( 22 FDA reports)
FEAR ( 16 FDA reports)
UNEVALUABLE EVENT ( 16 FDA reports)
EMOTIONAL DISTRESS ( 15 FDA reports)
RENAL INJURY ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
STRESS ( 13 FDA reports)
ANHEDONIA ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
DEATH ( 11 FDA reports)
ANAEMIA ( 6 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
QUALITY OF LIFE DECREASED ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 4 FDA reports)
UNRESPONSIVE TO STIMULI ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
ENZYME ABNORMALITY ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMOTHORAX ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPOKALAEMIC SYNDROME ( 2 FDA reports)
INTESTINAL ULCER ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
MASS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY HEIGHT BELOW NORMAL ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GROWTH HORMONE DEFICIENCY ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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