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

DYSPEPSIA ( 5 FDA reports)
SOMNOLENCE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
MANIA ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FISTULA ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
OVARIAN TORSION ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
APHASIA ( 1 FDA reports)
RETCHING ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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