RESTASIS

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Starting and Managing Patients for Maximum Success

This section is designed to help you help your patients start right and get the most out of RESTASIS® therapy. The information and tools below should prove useful in ensuring maximum success with RESTASIS® (cyclosporine ophthalmic emulsion) 0.05%.

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Allergan, Inc.

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RESTASIS® Ophthalmic Emulsion is indicated to increase tear production in patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca. Increased tear production was not seen in patients currently taking topical anti-inflammatory drugs or using punctal plugs.

Important Safety Information:

RESTASIS® is contraindicated in patients with active ocular infections and has not been studied in patients with a history of herpes keratitis.

The most common adverse event was ocular burning (upon instillation) – 17%. Other events reported in 1% to 5% of patients included conjunctival hyperemia, discharge, epiphora, eye pain, foreign body sensation, pruritus, stinging, and visual disturbance (most often blurring).

Please see full prescribing information for RESTASIS® (cyclosporine ophthalmic emulsion) 0.05%.