Start With EYLEA. Stay With EYLEA.1

TRUST ≈8 YEARS OF EXTENSIVE CLINICAL EXPERIENCE AND THE INTEGRITY OF DATA FROM LARGE, WELL–CONTROLLED TRIALS1

EYLEA is the #1 prescribed anti–VEGF FDA approved for Wet AMD, DME, and MEfRVO*

*IBM Truven MarketScan data: Number of injections administered from Q4 2017 through Q3 2018; data on file.

The Established Experience of EYLEA1,2
  • ≈8 years of real–world experience1
  • An estimated ≈9 million doses administered to ≈790,000 eyes since launch (and counting)1,2
  • 8 phase 3 clinical trials including more than 3000 EYLEA–treated patients across all approved indications1

EYLEA 2 mg (0.05 mL) Dosing Schedule1

EYLEA dosing for Macular Edema following Retinal Vein Occlusion: 2 mg every 4 weeks. EYLEA dosing for Macular Edema following Retinal Vein Occlusion: 2 mg every 4 weeks.
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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 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 www.fda.gov/medwatch, or call 1-800-FDA-1088.

The information provided in this site is intended only for healthcare professionals in the United States. The products discussed herein may have different product labeling in different countries.

References
  1. EYLEA® (aflibercept) Injection full U.S. Prescribing Information. Regeneron Pharmaceuticals, Inc. August 2019.
  2. Data on file. Regeneron Pharmaceuticals, Inc.