Product image of Mynzepli (Aflibercept) supplied by GNH India

Mynzepli

Active Ingredient:
Aflibercept
Origin:
EU

Mynzepli (Aflibercept)

Aflibercept, the active ingredient in Mynzepli, is a VEGF inhibitor presented as a solution for intravitreal injection use. It treats neovascular age‑related macular degeneration, diabetic macular edema and macular edema secondary to retinal vein occlusion in adult patients.

GNH India supplies Mynzepli as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Advanz Pharma Limited

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Indications & Clinical Uses

Aflibercept is an anti‑VEGF agent used to manage ocular conditions driven by abnormal vascular growth and leakage.

  • Neovascular age‑related macular degeneration: reduces fluid accumulation and can stabilize or improve visual acuity.
  • Diabetic macular edema: decreases retinal swelling and helps preserve vision.
  • Macular edema secondary to retinal vein occlusion: limits edema and supports visual function.

How It Works

  • Aflibercept is a recombinant fusion protein that combines the extracellular domains of VEGF receptors 1 and 2 with the Fc portion of human IgG1. By binding VEGF‑A, VEGF‑B and placental growth factor with high affinity, it prevents these ligands from activating endothelial VEGF receptors, thereby inhibiting angiogenesis, vascular permeability and the formation of abnormal retinal vessels.

Side Effects

Intravitreal administration of aflibercept may be associated with ocular and systemic adverse reactions.

Common Side Effects

  • Conjunctival hemorrhage: minor bleeding on the eye surface.
  • Increased intraocular pressure: transient rise after injection.
  • Floaters: visual disturbances from vitreous particles.
  • Eye pain: mild discomfort at injection site.

Serious or Rare Side Effects

  • Endophthalmitis: severe intraocular infection requiring urgent treatment.
  • Retinal detachment: separation of retinal layers, a vision‑threatening emergency.
  • Vitreous hemorrhage: bleeding into the vitreous cavity.
  • Uveitis: inflammation of the uveal tract.

Precautions & Warnings

Before using aflibercept intravitreal injections, clinicians should consider several safety and handling precautions.

  • Patient assessment: evaluate for active ocular infection or inflammation before injection.
  • Anticoagulant therapy: assess bleeding risk and coordinate with managing physician.
  • Prior ocular surgery: allow appropriate healing interval before administration.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Monitoring: schedule follow‑up examinations to detect intraocular pressure changes or inflammation.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Aflibercept may interact with other agents that affect ocular healing or systemic vascular processes.

Major Interactions (Avoid)

  • Intravitreal steroids: combined use may increase risk of elevated intraocular pressure.
  • Systemic anti‑VEGF therapies: concurrent use can amplify systemic VEGF inhibition and related adverse events.

Moderate Interactions (Monitor Closely)

  • Anticoagulants/antiplatelet drugs: may raise risk of intraocular hemorrhage.
  • Ocular hypotensive agents: monitor pressure changes when used together.
  • Systemic hypertension medications: watch for blood pressure fluctuations.

Frequently Asked Questions

Mynzepli contains aflibercept and is indicated for the treatment of neovascular age‑related macular degeneration, diabetic macular edema, and macular edema secondary to retinal vein occlusion. These conditions involve abnormal blood‑vessel growth and fluid leakage in the retina, and the drug is administered by intravitreal injection to help preserve or improve visual function.

Aflibercept is a fusion protein that binds VEGF‑A, VEGF‑B and placental growth factor with high affinity. By sequestering these ligands, it blocks their interaction with VEGF receptors on endothelial cells, thereby reducing angiogenesis and vascular permeability that contribute to retinal swelling and neovascularization.

The dose and injection schedule for Mynzepli are determined by the prescribing ophthalmologist based on the specific indication, disease severity, and individual patient response. Clinicians follow approved labeling and clinical guidelines to decide the volume and frequency of intravitreal administration.

Safety data for aflibercept in pregnant or nursing women are limited. Use is generally reserved for situations where the potential benefit outweighs any possible risk to the fetus or infant. The decision should be made by the treating physician in consultation with the patient.

To request Mynzepli, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain handling) and any necessary import documentation.

Mynzepli (aflibercept) has a broader binding profile, targeting VEGF‑A, VEGF‑B and placental growth factor, whereas agents such as ranibizumab bind only VEGF‑A. Clinical studies suggest comparable efficacy in improving visual acuity, with

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GNH India Pharmaceuticals Limited

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Last updated:

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