After using RESTASIS® for 2 months, 85% of patients planned to continue using RESTASIS® Ophthalmic Emulsion. (n=1,868 )
Data on file, Allergan, Inc.
Only 5 out of 293 patients in clinical trials discontinued RESTASIS® due to burning and stinging
Sall K, Stevenson OD, Mundorf, Reis BL, and the CsA Phase 3 Study Group. Two multicenter, randomized studies of the efficacy and safety of cyclosporine ophthalmic emulsion in moderate to severe dry eye disease. Ophthalmology. 2000;107(4):631-639.
Chronic Dry Eye is the most common patient complaint in the ophthalmologist's office
Stevenson D, Tauber J, Reis BL, and The Cyclosporin A Phase 2 Study Group. Efficacy and safety of cyclosporin A ophthalmic emulsion in the treatment of moderate-to-severe dry eye disease: a dose-ranging, randomized trial. Ophthalmology. 2000;107:967-974.
While estimates vary, at least 3.2 million women in the U.S. suffer from Chronic Dry Eye
Schaumberg DA, Sullivan DA, Buring JE, Dana MR. Prevalence of dry eye syndrome among US women. Am J Ophthalmol. 2003;136:2318-2326.
Patients may have already tried several brands of artificial tears.
Multi-Sponsor Surveys, Inc. The 2008 Gallup Study of Dry Eye Sufferers. Summary Volume. July 2008.
97.9% of patients with commercial insurance have reimbursement coverage for their RESTASIS® prescriptions.