bepotastine
bepotastine
(be-poe-tass-teen) bepotastine,Bepreve
(trade name)Classification
Therapeutic: ocular agentsPharmacologic: antihistamines
Indications
Action
Therapeutic effects
Pharmacokinetics
Time/action profile (antihistaminic activity)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
ophth | within 15 min | 1–2 hr† | 12 hr |
Contraindications/Precautions
Adverse Reactions/Side Effects
Central nervous system
- headache
Ear, Eye, Nose, Throat
- nasopharyngitis
Gastrointestinal
- taste in mouth following instillation (most frequent)
Interactions
Drug-Drug interaction
None noted.Route/Dosage
Availability
Nursing implications
Nursing assessment
- Assess signs and symptoms of allergic conjunctivitis (redness, itching, watering) periodically during therapy.
Potential Nursing Diagnoses
Deficient knowledge, related to medication regimen (Patient/Family Teaching)Implementation
- Ophthalmic: Instill 1 drop into affected eyes twice daily. See for administration guidelines.
Patient/Family Teaching
- Instruct patient to instill bepotastine drops as directed. Do not touch dropper to eye or to any surface.
- Advise patient to remove contact lens prior to instillation. Do not use bepotastine for treatment of irritation related to contact lens. Do not wear contact lens if eyes are red. Contact lens may be reinserted 10 min following instillation.
- Advise female patient to notify health care professional if pregnancy is planned or suspected or if breastfeeding.
Evaluation/Desired Outcomes
- Decrease in ocular itching due to allergic conjunctivitis.