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

RENAL FAILURE ( 101 FDA reports)
HYPOTENSION ( 51 FDA reports)
POST PROCEDURAL COMPLICATION ( 50 FDA reports)
MULTI-ORGAN FAILURE ( 41 FDA reports)
RESPIRATORY FAILURE ( 39 FDA reports)
RENAL FAILURE ACUTE ( 37 FDA reports)
CEREBROVASCULAR ACCIDENT ( 35 FDA reports)
RENAL IMPAIRMENT ( 34 FDA reports)
MYOCARDIAL INFARCTION ( 30 FDA reports)
SEPSIS ( 29 FDA reports)
ANXIETY ( 28 FDA reports)
DEATH ( 28 FDA reports)
INTRACARDIAC THROMBUS ( 27 FDA reports)
THROMBOSIS ( 27 FDA reports)
CARDIAC ARREST ( 25 FDA reports)
PAIN ( 25 FDA reports)
FEAR ( 24 FDA reports)
HAEMORRHAGE ( 23 FDA reports)
PULMONARY EMBOLISM ( 23 FDA reports)
STRESS ( 23 FDA reports)
UNEVALUABLE EVENT ( 23 FDA reports)
INJURY ( 22 FDA reports)
EMOTIONAL DISTRESS ( 21 FDA reports)
DEEP VEIN THROMBOSIS ( 20 FDA reports)
PULMONARY OEDEMA ( 20 FDA reports)
HEPATIC FAILURE ( 19 FDA reports)
RENAL INJURY ( 19 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 18 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 18 FDA reports)
PULMONARY HYPERTENSION ( 18 FDA reports)
VENTRICULAR FAILURE ( 18 FDA reports)
CARDIOGENIC SHOCK ( 16 FDA reports)
DEPRESSION ( 16 FDA reports)
ILEUS ( 16 FDA reports)
DIALYSIS ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
PROCEDURAL COMPLICATION ( 15 FDA reports)
ANHEDONIA ( 14 FDA reports)
AORTIC THROMBOSIS ( 14 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 14 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 14 FDA reports)
RIGHT VENTRICULAR FAILURE ( 14 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
EMBOLISM ( 13 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
SEPTIC SHOCK ( 12 FDA reports)
THROMBOCYTOPENIA ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
SHOCK ( 11 FDA reports)
BRADYCARDIA ( 10 FDA reports)
SPLENIC INFARCTION ( 10 FDA reports)
THROMBOSIS IN DEVICE ( 10 FDA reports)
URETEROSTOMY SITE DISCOMFORT ( 10 FDA reports)
ATRIAL THROMBOSIS ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
INTESTINAL ISCHAEMIA ( 9 FDA reports)
NEUROLOGICAL SYMPTOM ( 9 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
ANAEMIA ( 8 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
CORONARY ARTERY THROMBOSIS ( 8 FDA reports)
FUNGAL SEPSIS ( 8 FDA reports)
MYOCARDIAL ISCHAEMIA ( 8 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 8 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 7 FDA reports)
COAGULOPATHY ( 7 FDA reports)
DILATATION VENTRICULAR ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
VENA CAVA THROMBOSIS ( 7 FDA reports)
VENTRICULAR HYPOKINESIA ( 7 FDA reports)
CARDIAC DEATH ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
DEVICE ALARM ISSUE ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
HAEMOLYSIS ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
SURGICAL PROCEDURE REPEATED ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
WOUND DEHISCENCE ( 6 FDA reports)
WOUND SECRETION ( 6 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
ASPERGILLOSIS ( 5 FDA reports)
ASTHENIA ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
CATHETER RELATED COMPLICATION ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
EMBOLISM VENOUS ( 5 FDA reports)
GRAFT THROMBOSIS ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 5 FDA reports)
HEPATIC INFARCTION ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TUMOUR HAEMORRHAGE ( 5 FDA reports)
URINE OUTPUT DECREASED ( 5 FDA reports)
VASCULAR GRAFT OCCLUSION ( 5 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEPATIC CONGESTION ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATOCELLULAR DAMAGE ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
IATROGENIC INJURY ( 4 FDA reports)
ILEUS PARALYTIC ( 4 FDA reports)
ISCHAEMIA ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 4 FDA reports)
PROCEDURAL PAIN ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
RESPIRATORY ACIDOSIS ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SPUTUM CULTURE POSITIVE ( 4 FDA reports)
THERAPY NON-RESPONDER ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DIFFICULT TO WEAN FROM VENTILATOR ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC ENZYME ABNORMAL ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
ILIAC ARTERY THROMBOSIS ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL EMBOLISM ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SHUNT OCCLUSION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
THORACOTOMY ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
AIR EMBOLISM ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE ABNORMAL ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CEREBRAL PALSY ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
COLON GANGRENE ( 2 FDA reports)
COLON NEOPLASM ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
FIBRINOLYSIS ABNORMAL ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FOOT AMPUTATION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC ARTERY STENOSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POST PROCEDURAL CELLULITIS ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RENAL CORTICAL NECROSIS ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART TRANSPLANT ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
NEGATIVE CARDIAC INOTROPIC EFFECT ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROMUSCULAR BLOCKADE ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PERICARDIAL DISEASE ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PLATELET AGGREGATION INCREASED ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PNEUMATOSIS ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL DEPIGMENTATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VASCULAR INJURY ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use