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

HYPOTENSION ( 9 FDA reports)
ABASIA ( 8 FDA reports)
ANAEMIA ( 8 FDA reports)
ARTHRITIS ( 8 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
DELIRIUM ( 8 FDA reports)
FALL ( 8 FDA reports)
MUSCULOSKELETAL PAIN ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
SINUSITIS ( 8 FDA reports)
TEMPERATURE INTOLERANCE ( 8 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
WRIST FRACTURE ( 8 FDA reports)
ANHEDONIA ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
AZOTAEMIA ( 7 FDA reports)
BLINDNESS UNILATERAL ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
CONSTIPATION ( 7 FDA reports)
DEAFNESS ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
EAR DISCOMFORT ( 7 FDA reports)
ECONOMIC PROBLEM ( 7 FDA reports)
EXCORIATION ( 7 FDA reports)
FEELING ABNORMAL ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
MENTAL STATUS CHANGES ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
CAROTID ARTERY OCCLUSION ( 6 FDA reports)
CAROTID BRUIT ( 6 FDA reports)
CONDUCTION DISORDER ( 6 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 6 FDA reports)
EYE INJURY ( 6 FDA reports)
FEELING COLD ( 6 FDA reports)
MULTIPLE INJURIES ( 6 FDA reports)
PAIN ( 6 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DIVERTICULUM ( 5 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
SINUS BRADYCARDIA ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
WEIGHT FLUCTUATION ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DIASTOLIC DYSFUNCTION ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NOCTURIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
VASCULAR CALCIFICATION ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INJURY ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
PERIDIVERTICULITIS ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
COMA ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PULMONARY CALCIFICATION ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
STRESS URINARY INCONTINENCE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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