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

INITIAL INSOMNIA ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
MIDDLE INSOMNIA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE DISORDER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
BINGE EATING ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPOD STING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
IRITIS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
STRESS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)

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