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

INTENTIONAL OVERDOSE ( 4 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
ALOPECIA ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)

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