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warnings and cautions
5 WARNINGS AND PRECAUTIONS To minimize the risk of contamination, do not touch dropper tip to any surface. Keep bottle tightly closed when not in use. ( 5.1 ) BEPREVE™ should not be used to treat contact lens-related irritation. ( 5.2 ) Remove contact lenses prior to instillation of BEPREVE™ . ( 5.2 ) 5.1 Contamination of Tip and Solution To minimize contaminating the dropper tip and solution, care should be taken not to touch the eyelids or surrounding areas with the dropper tip of the bottle. Keep bottle tightly closed when not in use. 5.2 Contact Lens Use Patients should be advised not to wear a contact lens if their eye is red. BEPREVE™ should not be used to treat contact lens-related irritation. BEPREVE™ should not be instilled while wearing contact lenses. Remove contact lenses prior to instillation of BEPREVE™. The preservative in BEPREVE™, benzalkonium chloride, may be absorbed by soft contact lenses. Lenses may be reinserted after 10 minutes following administration of BEPREVE™. 5.3 Topical Ophthalmic Use Only BEPREVE™ is for topical ophthalmic use only.
6 ADVERSE REACTIONS The most common reported adverse reaction occurring in approximately 25% of subjects was a mild taste following instillation. Other adverse reactions occurring in 2-5% of subjects were eye irritation, headache, and nasopharyngitis. The most common adverse reaction occurring in approximately 25% of patients was a mild taste following instillation. Other adverse reactions which occurred in 2-5% of subjects were eye irritation, headache, and nasopharyngitis. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact ISTA Pharmaceuticals, Inc. at 1-877-788-2020, or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.