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

CARDIAC ARREST ( 11 FDA reports)
ECONOMIC PROBLEM ( 11 FDA reports)
PAIN ( 11 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BACK PAIN ( 7 FDA reports)
EMOTIONAL DISORDER ( 7 FDA reports)
MALAISE ( 7 FDA reports)
MUSCLE SPASMS ( 7 FDA reports)
NECK PAIN ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
SOCIAL PROBLEM ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
ATRIAL TACHYCARDIA ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
INJURY ( 5 FDA reports)
MULTIPLE INJURIES ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
PARTNER STRESS ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
FALL ( 3 FDA reports)
FAMILY STRESS ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
HYPOVOLAEMIA ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
COMA ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RENAL MASS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VASCULAR GRAFT OCCLUSION ( 2 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CERVICOBRACHIAL SYNDROME ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)

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