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Abelson MB, Gomes P, Crampton HJ, Schiffman RM, Bradford RR, Whitcup, SM. Efficacy and tolerability of ophthalmic epinastine assessed using the conjunctival antigen challenge model in patients with a history of allergic conjunctivitis. Clin Ther. 2004:26(1):35-47.

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Data on file, Allergan, Inc.; Adult Ocular Allergy Attitudes Evaluation, December 2003.
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Data on file, Inspire Pharmaceuticals, Inc.
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ELESTAT® Prescribing Information.
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Friedlaender M, Scharf L, Brashears D. Control of ocular allergy symptoms by epinastine HCl 0.05% in a conjunctival antigen challenge evaluation. Poster presented at: 8th Winter Refractive Surgery Meeting of the European Society of Cataract and Refractive Surgeons; January 23-25, 2004; Barcelona, Spain.
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Kamei C, Akagi M, Mio M, et al. Antiallergic effect of epinastine (WAL 801 CL) on immediate hypersensitivity reactions: (I). Elucidation of the mechanism for histamine release inhibition. Immunopharmacol Immunotoxicol. 1992;14(1-2):191-205.
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©2006 Inspire Pharmaceuticals, Inc., Durham, NC 27703 ® Marks owned by Allergan, Inc. Inspire and the Inspire logo are registered trademarks of Inspire Pharmaceuticals, Inc. ELESTAT® is licensed from Boehringer Ingelheim Pty. Ltd., Ingelheim, Germany.



ELESTAT® ophthalmic solution is indicated for the prevention of ocular itching associated with allergic conjunctivitis.

Important Safety Information:
ELESTAT® ophthalmic solution is contraindicated in those patients who have shown hypersensitivity
to epinastine or to any of the other ingredients.

Patients should be advised not to wear a contact lens if their eye is red. ELESTAT® ophthalmic solution should not be used to treat contact lens related irritation. The preservative in ELESTAT®, benzalkonium chloride, may be absorbed by soft contact lenses.Contact lenses should be removed prior to instillation of ELESTAT® ophthalmic solution and may be reinserted after 10 minutes following its administration.

The most frequently reported ocular adverse events occuring in approximately 1% to 10% of patients were burning sensation in the eye, folliculosis, hyperemia, and pruritus. The most frequently reported nonocular adverse events were infection (cold symptoms and upper respiratory infections), seen in approximately 10% of patients, and headache, rhinitis, sinusitis, increased cough, and pharyngitis seen in approximately 1% to 3% of patients. Some of these events were similar to the underlying disease being studied.

Please see prescribing information for ELESTAT®.