Product image of Latanoprost Agepha (Latanoprost) supplied by GNH India

Latanoprost Agepha

Active Ingredient:
Latanoprost
Origin:
EU

Latanoprost Agepha (Latanoprost)

Latanoprost, the active ingredient in Latanoprost Agepha, is a prostaglandin analog presented as an ophthalmic solution for ocular use. It lowers intra‑ocular pressure and is employed in the management of glaucoma and ocular hypertension in adult patients.

GNH India supplies Latanoprost Agepha as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches to meet global demand. Customers benefit from reliable logistics, comprehensive documentation, and responsive technical support throughout the supply chain.

Manufacturer / TM Owner

Agepha Pharma S.R.O

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Indications & Clinical Uses

Latanoprost is used to reduce intra‑ocular pressure in conditions affecting the eye’s fluid dynamics.

  • Primary open‑angle glaucoma: reduces intra‑ocular pressure to slow optic nerve damage.
  • Ocular hypertension: lowers elevated eye pressure to prevent progression to glaucoma.
  • Secondary open‑angle glaucoma: helps control pressure when caused by other ocular conditions.
  • Pseudoexfoliative glaucoma: decreases pressure associated with exfoliative material accumulation.
  • Angle‑closure glaucoma (post‑laser iridotomy): may be used adjunctively to control pressure.

How It Works

  • Latanoprost is a synthetic analogue of prostaglandin F₂α that binds to FP receptors on the ciliary muscle and scleral tissue. Activation of these receptors remodels the extracellular matrix, enhancing uveoscleral outflow of aqueous humor. The increased drainage lowers intra‑ocular pressure without affecting aqueous production, providing sustained pressure reduction after once‑daily topical administration. The effect begins within hours and can be maintained for 24 hours, allowing convenient once‑daily dosing.

Side Effects

Latanoprost may cause ocular and systemic reactions, most of which are mild and transient.

Common Side Effects

  • Eye redness: transient hyperemia of the conjunctiva.
  • Increased eyelash growth: longer, thicker lashes may develop.
  • Iris pigmentation: gradual darkening of the iris color.
  • Eye irritation: burning or stinging sensation after instillation.
  • Blurred vision: temporary reduction in visual clarity.
  • Foreign body sensation: feeling of something in the eye.

Serious or Rare Side Effects

  • Increased intra‑ocular pressure: paradoxical rise requiring medical attention.
  • Uveitis: inflammation of the uveal tract that may threaten vision.
  • Corneal edema: swelling of the cornea leading to visual disturbance.
  • Severe allergic reaction: swelling, itching, or rash around the eye.
  • Persistent eye pain: may indicate underlying complication.
  • Vision loss: rare but requires immediate evaluation.

Precautions & Warnings

Before prescribing Latanoprost, clinicians should evaluate patient history and monitor ocular response.

  • Monitor intra‑ocular pressure: assess IOP regularly after initiation.
  • Assess for ocular infection: avoid use in active conjunctivitis or keratitis.
  • Use with caution in patients with a history of uveitis: may exacerbate inflammation.
  • Avoid in patients with known hypersensitivity to prostaglandin analogues.
  • Pregnancy and lactation: safety not established; weigh benefits and risks.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Latanoprost can interact with other ophthalmic agents and systemic medications that affect intra‑ocular pressure.

Major Interactions (Avoid)

  • Concurrent use of other prostaglandin analog eye drops: additive effect may increase side‑effects.
  • Ocular surgery performed shortly after initiation: may impair wound healing.

Moderate Interactions (Monitor Closely)

  • Topical beta‑blockers: combined therapy may enhance pressure‑lowering effect; monitor IOP.
  • Systemic carbonic anhydrase inhibitors: additive IOP reduction; adjust dosing as needed.
  • Topical corticosteroids: may reduce efficacy of Latanoprost; observe pressure control.

Frequently Asked Questions

Latanoprost Agepha is indicated for the reduction of elevated intra‑ocular pressure in patients with primary open‑angle glaucoma, ocular hypertension, and related glaucomatous conditions. By lowering eye pressure, it helps to slow or prevent optic nerve damage and visual field loss associated with these disorders.

Latanoprost is a synthetic prostaglandin F₂α analogue that binds to FP receptors in the ciliary body and scleral tissue. This binding remodels extracellular matrix proteins, increasing uveoscleral outflow of aqueous humor. The enhanced drainage reduces intra‑ocular pressure, providing a sustained therapeutic effect after once‑daily topical application.

The dosing regimen for Latanoprost Agepha is determined by the prescribing clinician. In clinical practice the medication is typically administered as one drop in the affected eye(s) once daily in the evening, but the exact dose and timing should follow the prescriber’s instructions and the patient’s individual response.

Safety data for Latanoprost in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. Healthcare providers should weigh potential benefits against possible risks and consider alternative therapies when treating pregnant or nursing patients.

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

Latanoprost belongs to the prostaglandin analogue class, which generally offers greater IOP reduction with once‑daily dosing compared with beta‑blockers such as timolol. It is often preferred for its efficacy and convenient dosing, although individual response and side‑effect profiles may lead clinicians to select alternative agents or combination therapy.

Latanoprost Agepha should be stored at room temperature, preferably below 25 °C, in its original packaging. Protect the product from direct light, excessive heat and moisture. Do not freeze the solution, and keep the container tightly closed when not in use to maintain stability.

Latanoprost is applied topically as an ophthalmic solution. The patient should wash their hands, tilt the head back, pull down the lower eyelid to create a small pocket, and instill one drop into the conjunctival sac. Close the eye gently for a few seconds without blinking excessively, and avoid touching the dropper tip to any surface.

Serious adverse events, although rare, include a paradoxical increase in intra‑ocular pressure, uveitis (inflammation of the uveal tract), corneal edema, and severe allergic reactions that may present with swelling, redness or pain. Patients should seek immediate medical attention if they experience sudden vision changes, intense eye pain, or signs of infection.

Latanoprost should be avoided in individuals with known hypersensitivity to latanoprost or any prostaglandin analogue, those with active ocular infections, recent ocular surgery (unless cleared by the surgeon), and patients with a history of severe uveitis. Clinicians should also exercise caution in pregnant or nursing women due to limited safety data.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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