EYLEA® (English Alternative) 2mg/0.05ml

Tier

Packs Discount (%) For Each
1 - 3 $1,599.00
4 - 10 6.25 % $1,499.00
11 - 20 6.88 % $1,489.00
21+ 7.5 % $1,479.00

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Product description

Eylea® is an ophthalmic medication commonly prescribed by eye specialists for managing retinal conditions associated with abnormal blood vessel growth and fluid buildup in the eye. It is primarily used for wet age-related macular degeneration (AMD), a condition that can affect central vision, as well as retinal swelling caused by vascular blockages. By targeting the underlying processes that contribute to excess fluid leakage in the retina, Eylea® helps support vision preservation and is an established treatment option in the field of retinal care.

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FAQ

EYLEA® (aflibercept) is a prescription-only, intravitreal injectable medication designed for the treatment of various retinal vascular diseases. It is a recombinant fusion protein that acts as a VEGF inhibitor, targeting vascular endothelial growth factor-A (VEGF-A), VEGF-B, and placental growth factor (PlGF) to reduce abnormal blood vessel growth and fluid leakage in the eye. EYLEA® is indicated for conditions such as wet age-related macular degeneration (wAMD), macular edema following retinal vein occlusion (RVO), diabetic macular edema (DME), diabetic retinopathy (DR), and retinopathy of prematurity (ROP). It is administered via intravitreal injection by a trained ophthalmologist.

EYLEA® must be administered by an eye care professional via intravitreal injection under aseptic conditions. The protocol varies depending on the indication.

  • wAMD: 2 mg every month for the first 3 months, followed by 2 mg every 2 months.
  • RVO: 2 mg monthly injections until visual and anatomic improvement is achieved.
  • DME/DR: 2 mg monthly for 5 doses, then once every 2 months.
  • ROP: 0.4 mg administered intravitreally in neonates.

EYLEA® is indicated for multiple retinal conditions but has specific contraindications and potential adverse effects.

Indications:

  • Wet Age-related Macular Degeneration (wAMD)
  • Macular edema following RVO
  • Diabetic macular edema (DME)
  • Diabetic retinopathy (DR)
  • Retinopathy of prematurity (ROP)

Contraindications:

  • Ocular or periocular infections
  • Hypersensitivity to aflibercept or formulation components

Potential Side Effects:

  • Common: Conjunctival hemorrhage, eye pain, vitreous floaters
  • Serious: Endophthalmitis, retinal detachment, increased intraocular pressure

EYLEA® contains the following:

  • Active ingredient: Aflibercept 40 mg/mL
  • Inactive ingredients: Polysorbate 20, sodium phosphate monobasic, sodium phosphate dibasic, sodium chloride, sucrose, and water for injection

Each 0.05 mL intravitreal dose delivers 2 mg of aflibercept.

The EYLEA® package includes all necessary components for administration:

  • 1 pre-filled sterile syringe (single-use)
  • Each syringe contains 0.1 mL of solution, allowing extraction of a 0.05 mL dose
  • Packaged in protective blister or tray, depending on region

Yes, EYLEA® has a range of potential side effects, mostly related to the intravitreal administration route.

  • Common side effects:

    • Conjunctival hemorrhage (up to 25%)
    • Eye pain or discomfort
    • Vitreous detachment or floaters
  • Serious side effects:

    • Intraocular inflammation
    • Endophthalmitis
    • Elevated intraocular pressure
    • Retinal detachment

Proper storage of EYLEA® is critical to maintain efficacy and safety.

  • Storage temperature: 2°C to 8°C (refrigerated)
  • Do not freeze
  • Keep in original packaging to protect from light
  • Shelf life: Refer to expiry date on packaging
  • Single-use only – discard unused portion immediately after administratio

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