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

PAIN ( 13 FDA reports)
MULTIPLE INJURIES ( 12 FDA reports)
DIZZINESS ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
CHEST PAIN ( 10 FDA reports)
ANXIETY ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
FALL ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
ECONOMIC PROBLEM ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
VOMITING ( 8 FDA reports)
ANAEMIA ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
MITRAL VALVE INCOMPETENCE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
ATELECTASIS ( 5 FDA reports)
COUGH ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
VITREOUS DETACHMENT ( 5 FDA reports)
VITREOUS HAEMORRHAGE ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CARDIAC FAILURE CHRONIC ( 4 FDA reports)
CYSTOCELE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEAR ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEART RATE ABNORMAL ( 4 FDA reports)
HIP FRACTURE ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INJURY ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RETINAL TEAR ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
STRESS URINARY INCONTINENCE ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC VALVE DISEASE ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DRUG DOSE OMISSION ( 3 FDA reports)
DYSLIPIDAEMIA ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
LIMB INJURY ( 3 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
RETINAL HAEMORRHAGE ( 3 FDA reports)
URGE INCONTINENCE ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
AMENORRHOEA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HEART INJURY ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
STRESS ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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