Bayer Access Programs

IMPORTANT CHANGE to the Eylea® (aflibercept) 2mg Patient Access Program

From 28th February 2026, the Eylea 2mg Patient Access Program will be managed directly by Bayer Australia. For resupplies for Eylea 2mg, send your resupply request form to medaffairs.anz@bayer.com .

For more information, please contact your Bayer representative or email medaffairs.anz@bayer.com .

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Bayer Australia Ltd, ABN 22 000 138 714,
875 Pacific Highway, Pymble, NSW 2073.

MA-AFL_8mg-AU-0024-4 Date of Prep February 2026

PBS Information: EYLEA 8 mg: Authority required for the treatment of wet age-related macular degeneration and diabetic macular oedema. EYLEA 2 mg: Authority required for the treatment of wet age-related macular degeneration, diabetic macular oedema, central retinal vein occlusion and branch retinal vein occlusion, myopic choroidal neovascularisation. Refer to PBS schedule for full Authority Required

Please review the product information before prescribing Eylea.
available here.

Adverse Event

To report an adverse event, relevant safety event or quality complaint, please email Atlantis Health on orders.eylea@atlantishealth.com within 1 business day of awareness. See Resources called Adverse Event Reporting for definitions of adverse event, relevant safety event and quality complaint.

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2mg 6-month Patient Review

Continuing supply – Please continue the ongoing supply of Eylea (aflibercept) Required field

Discontinuing supply – Please discontinue the ongoing supply of Eylea (aflibercept) Required field

From 1st October 2024, Eylea 8mg (aflibercept) is available on the Pharmaceutical Benefits Scheme (PBS).

Please contact your patients as soon as possible to transition them to PBS supply.

If you have any questions, please contact Atlantis Health on 1800 460 150 or email orders.eylea@atlantishealth.com.

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