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

CORONARY ARTERY STENOSIS ( 140 FDA reports)
CORONARY ARTERY DISEASE ( 108 FDA reports)
VENTRICULAR FIBRILLATION ( 54 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 51 FDA reports)
HAEMOGLOBIN DECREASED ( 48 FDA reports)
CARDIAC FAILURE ( 46 FDA reports)
MYOCARDIAL INFARCTION ( 43 FDA reports)
ATRIAL FIBRILLATION ( 40 FDA reports)
CARDIAC ARREST ( 34 FDA reports)
MYOCARDIAL ISCHAEMIA ( 31 FDA reports)
PULMONARY OEDEMA ( 30 FDA reports)
CHEST PAIN ( 28 FDA reports)
EJECTION FRACTION DECREASED ( 27 FDA reports)
CORONARY ARTERY OCCLUSION ( 26 FDA reports)
HYPOTENSION ( 23 FDA reports)
THROMBOCYTOPENIA ( 23 FDA reports)
ANGINA UNSTABLE ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 20 FDA reports)
DYSPNOEA ( 20 FDA reports)
CARDIOGENIC SHOCK ( 19 FDA reports)
HAEMATOCRIT DECREASED ( 19 FDA reports)
DIZZINESS ( 18 FDA reports)
BRADYCARDIA ( 17 FDA reports)
PROCEDURAL COMPLICATION ( 17 FDA reports)
HAEMATOMA ( 16 FDA reports)
POST PROCEDURAL COMPLICATION ( 16 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 15 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 15 FDA reports)
HAEMATEMESIS ( 15 FDA reports)
ISCHAEMIA ( 14 FDA reports)
MITRAL VALVE INCOMPETENCE ( 14 FDA reports)
VENTRICULAR TACHYCARDIA ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 13 FDA reports)
CORONARY ARTERY THROMBOSIS ( 13 FDA reports)
ANGINA PECTORIS ( 12 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
BRONCHOPNEUMONIA ( 12 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 12 FDA reports)
RENAL IMPAIRMENT ( 12 FDA reports)
DILATATION VENTRICULAR ( 11 FDA reports)
INTRACARDIAC THROMBUS ( 11 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
VENTRICULAR HYPOKINESIA ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
FALL ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
LEFT VENTRICULAR FAILURE ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
PRODUCTIVE COUGH ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 8 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
DILATATION ATRIAL ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
RALES ( 8 FDA reports)
VENTRICULAR DYSFUNCTION ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
CARDIAC ANEURYSM ( 7 FDA reports)
DISEASE RECURRENCE ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
INJECTION SITE HAEMORRHAGE ( 7 FDA reports)
MULTI-ORGAN FAILURE ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
THROMBOSIS IN DEVICE ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ATRIAL FLUTTER ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 6 FDA reports)
HYPERCHOLESTEROLAEMIA ( 6 FDA reports)
ISCHAEMIC STROKE ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MALLORY-WEISS SYNDROME ( 6 FDA reports)
PALLOR ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ACUTE CORONARY SYNDROME ( 5 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
CORONARY ARTERY SURGERY ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MYOCARDIAL RUPTURE ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
STENT OCCLUSION ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
TROPONIN I INCREASED ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
AORTIC DISORDER ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CAROTID SINUS SYNDROME ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
WOUND INFECTION ( 4 FDA reports)
AKINESIA ( 3 FDA reports)
ANEURYSM ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BREAST PAIN ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATHETER SITE HAEMATOMA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
CORONARY OSTIAL STENOSIS ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERTENSIVE CRISIS ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
HYPOVOLAEMIC SHOCK ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IATROGENIC INJURY ( 3 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AV DISSOCIATION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ANGIOPLASTY ( 2 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 2 FDA reports)
CORONARY ARTERY ANEURYSM ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LIVER INDURATION ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PUNCTURE SITE REACTION ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RECTAL CANCER ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 2 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 2 FDA reports)
SCAR ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR BYPASS GRAFT ( 2 FDA reports)
VENTRICULAR DYSKINESIA ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WOUND NECROSIS ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIODYSPLASIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL INJURY ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIAC VENTRICULOGRAM ABNORMAL ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY DISSECTION ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE CORONARY ARTERY ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS NON-A NON-B ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST NEGATIVE ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERICARDIAL FIBROSIS ( 1 FDA reports)
PERICARDITIS ADHESIVE ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELLS URINE ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
SPIROMETRY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
THROMBOLYSIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICLE RUPTURE ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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