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

MYOCARDIAL INFARCTION ( 36 FDA reports)
ANGINA PECTORIS ( 27 FDA reports)
RHABDOMYOLYSIS ( 23 FDA reports)
CHEST PAIN ( 18 FDA reports)
MELAENA ( 16 FDA reports)
CARDIAC FAILURE ( 15 FDA reports)
CEREBRAL INFARCTION ( 15 FDA reports)
DRUG INTERACTION ( 15 FDA reports)
ERYSIPELAS ( 14 FDA reports)
PALPITATIONS ( 13 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
ATRIAL FIBRILLATION ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
CORONARY ARTERY OCCLUSION ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
GASTRIC ULCER ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 6 FDA reports)
DEATH ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
HELICOBACTER INFECTION ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CAROTID ARTERY STENOSIS ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MUSCLE FATIGUE ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
RASH ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
SINUS ARRHYTHMIA ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
AKATHISIA ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
DYSPRAXIA ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUROMYOPATHY ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PROSTATISM ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
COUGH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE ABNORMAL ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POSTOPERATIVE INFECTION ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TROPONIN T INCREASED ( 2 FDA reports)
VESTIBULAR NEURONITIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INCLUSION BODY MYOSITIS ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC ATROPHY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
RECTAL POLYP ( 1 FDA reports)
REGURGITATION OF FOOD ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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