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

MYOCARDIAL INFARCTION ( 45 FDA reports)
HYPERTENSION ( 33 FDA reports)
CORONARY ARTERY DISEASE ( 30 FDA reports)
PAIN ( 24 FDA reports)
CEREBROVASCULAR ACCIDENT ( 22 FDA reports)
DEPRESSION ( 20 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 19 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 19 FDA reports)
CHEST PAIN ( 16 FDA reports)
ANXIETY ( 15 FDA reports)
SLEEP APNOEA SYNDROME ( 13 FDA reports)
GASTRIC DISORDER ( 12 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
ARTHROPATHY ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
HIATUS HERNIA ( 11 FDA reports)
BRADYCARDIA ( 10 FDA reports)
DYSPEPSIA ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
BACK PAIN ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
PULMONARY CONGESTION ( 9 FDA reports)
THROMBOSIS ( 9 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 9 FDA reports)
VENTRICULAR FIBRILLATION ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
FALL ( 8 FDA reports)
HYPERSENSITIVITY ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
ADVERSE EVENT ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
ARTERIAL RESTENOSIS ( 7 FDA reports)
BACTERIAL INFECTION ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PANIC ATTACK ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
BARRETT'S OESOPHAGUS ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
EMOTIONAL DISTRESS ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
INFECTION ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
PULMONARY EMBOLISM ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
VENTRICULAR DYSFUNCTION ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
AORTIC DILATATION ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
ERUCTATION ( 5 FDA reports)
GENERALISED ANXIETY DISORDER ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
JOINT EFFUSION ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
LOCAL SWELLING ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
RETINAL ISCHAEMIA ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
TONGUE HAEMORRHAGE ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
CORONARY ARTERY OCCLUSION ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
GASTRIC CANCER ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HERNIA ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
MENISCUS LESION ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
VENTRICULAR HYPERTROPHY ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
EYE INFECTION ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MITRAL VALVE PROLAPSE ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OPTIC DISC DRUSEN ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROSTATIC DISORDER ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUDDEN CARDIAC DEATH ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
AXILLARY VEIN THROMBOSIS ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIGAMENT DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIPHERAL EMBOLISM ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
READING DISORDER ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARANASAL SINUS DISCOMFORT ( 1 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLYP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PYURIA ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
SCAR ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THORACIC CAVITY DRAINAGE TEST ABNORMAL ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use