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Anti-VEGF agent (intravitreal)

Aflibercept 2mg/0.05mL Intravitreal Injection (Eylea)

Brand names: Eylea

Aflibercept is an intravitreal anti-VEGF agent (a recombinant fusion protein) used for neovascular (wet) age-related macular degeneration, diabetic macular oedema, diabetic retinopathy and retinal vein occlusion.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It acts as a soluble decoy receptor that binds VEGF-A, VEGF-B and placental growth factor, preventing their interaction with native receptors and thereby reducing pathological retinal vascular leakage and neovascularisation.

Prescribing in practice

  • Endophthalmitis is the most serious risk of intravitreal injection, so administer under strict aseptic technique and warn patients to report eye pain, increasing redness or vision loss urgently.
  • Measure and manage intraocular pressure, as transient rises can occur after injection.
  • Avoid in patients with active ocular or periocular infection or active intraocular inflammation.

Monitoring

Monitor visual acuity, intraocular pressure and the retina (including optical coherence tomography) before and after injections to guide ongoing treatment.

Counselling the patient

  • Seek urgent ophthalmic review for new eye pain, marked redness, increased floaters or sudden reduced vision after an injection.
  • Do not drive until vision has recovered after the procedure.
  • Attend all scheduled injection and review appointments, as treatment is given on an ongoing basis.

Evidence & guidelines

NICE recommends aflibercept across several retinal vascular indications, supported by the VIEW trials in neovascular AMD.

Reference: NICE TA294 (wet AMD); NICE TA509 (DMO); Eylea SPC; Confirm identity and dosing against the manufacturer SPC (eMC) and NICE. Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.