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
- Conjunctival hemorrhage (up to 25%)
- Serious side effects:
- Intraocular inflammation
- Endophthalmitis
- Elevated intraocular pressure
- Retinal detachment
- Intraocular inflammation
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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