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

CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
HEADACHE ( 5 FDA reports)
DYSPEPSIA ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
RASH ( 4 FDA reports)
ULCER HAEMORRHAGE ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACALCULIA ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
GASTRIC DILATATION ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TENSION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
AURA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NODULE ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)

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