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

ECONOMIC PROBLEM ( 24 FDA reports)
ASTHENIA ( 18 FDA reports)
ATRIAL FIBRILLATION ( 17 FDA reports)
MULTIPLE INJURIES ( 14 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 13 FDA reports)
CORONARY ARTERY DISEASE ( 12 FDA reports)
HYPOTENSION ( 11 FDA reports)
INJURY ( 11 FDA reports)
ANXIETY ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
HYPERTENSION ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
PAIN ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
BRADYCARDIA ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HIATUS HERNIA ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
MITRAL VALVE STENOSIS ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
INFECTED SKIN ULCER ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOVEMENT DISORDER ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OPEN ANGLE GLAUCOMA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SURGERY ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CATARACT CORTICAL ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL MICROANGIOPATHY ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEPHRITIS ( 2 FDA reports)
NODULE ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CHOKING ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEAR ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALO VISION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT ATRIAL HYPERTROPHY ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)

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