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I authorize Regeneron Pharmaceuticals, Inc., [the maker of EYLEA® (aflibercept) Injection,] together with its collaborators, affiliates, representatives, agents, and contractors (collectively, “Regeneron”), to provide me with educational and promotional information, materials, and services. Regeneron may de-identify information I provide and use it in performing research, education, business analytics, marketing studies, or for other commercial purposes. Additionally, I understand that Regeneron may use my information (1) to help improve, develop, and evaluate products, services, materials, and programs related to my condition and treatment; and (2) as otherwise described in the Regeneron Privacy Policy.

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See More Important Safety Information and Indications
  • CONTRAINDICATIONS: EYLEA® (aflibercept) Injection is contraindicated in patients with ocular or periocular infections, active intraocular inflammation, or known hypersensitivity to aflibercept or to any of the excipients in EYLEA.
Important Safety Information and Indications INDICATIONS

EYLEA® (aflibercept) Injection 2 mg (0.05 mL) is indicated for the treatment of patients with Neovascular (Wet) Age-related Macular Degeneration (AMD), Macular Edema following Retinal Vein Occlusion (RVO), Diabetic Macular Edema (DME), and Diabetic Retinopathy (DR).

Please see the full Prescribing Information for EYLEA.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit, or call 1-800-FDA-1088.

The information provided in this site is intended for U.S. Doctors of Optometry.