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

CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
DYSPNOEA ( 7 FDA reports)
GOUT ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
HYPERLIPIDAEMIA ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
OSTEOARTHRITIS ( 5 FDA reports)
BACK DISORDER ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DUODENITIS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ACROCHORDON ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHRONIC FATIGUE SYNDROME ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
GASTRIC DISORDER ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERPLASIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
NEOPLASM PROSTATE ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PAPILLOMA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 3 FDA reports)
PROSTATITIS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SKIN DEGENERATIVE DISORDER ( 3 FDA reports)
SNORING ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BRONCHIAL HYPERACTIVITY ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYST ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
FEAR ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE REPAIR ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
OBESITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPINAL CORD HAEMORRHAGE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
ULCER ( 1 FDA reports)

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