Product image of Latafor (Timolol Maleate, Latanoprost) supplied by GNH India

Latafor

Active Ingredient:
Timolol Maleate, Latanoprost
Origin:
EU

Latafor (Timolol Maleate, Latanoprost)

Timolol maleate and latanoprost, the active ingredients in Latafor, are a beta‑blocker and prostaglandin analog combination presented as eye drops for ocular use. They reduce intra‑ocular pressure by decreasing aqueous humor production and increasing outflow, treating open‑angle glaucoma and ocular hypertension in adult patients.

GNH India supplies Latafor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory‑approved batches to qualified healthcare institutions.

Manufacturer / TM Owner

Omnivision Gmbh

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Indications & Clinical Uses

Latafor is prescribed for ocular conditions that require reduction of intra‑ocular pressure, primarily within the glaucoma and ocular hypertension therapeutic area.

  • Open‑angle glaucoma: lowers intra‑ocular pressure to slow optic nerve damage.
  • Ocular hypertension: reduces elevated eye pressure to prevent progression to glaucoma.
  • Pseudoexfoliative glaucoma: helps control pressure in this secondary form of open‑angle glaucoma.

How It Works

  • Timolol maleate acts as a non‑selective beta‑adrenergic antagonist, blocking β1 and β2 receptors in the ciliary body to decrease aqueous humor production. Latanoprost is a prostaglandin F2α analog that binds to FP receptors in the iris‑ciliary body, remodeling extracellular matrix and enhancing uveoscleral outflow of aqueous humor. Through the combined actions, the net reduction of intra‑ocular pressure is achieved.

Side Effects

Latafor may cause ocular and systemic adverse reactions; reported events are categorized by frequency.

Common Side Effects

  • Eye irritation or burning sensation: transient discomfort after instillation.
  • Blurred vision: temporary visual disturbance.
  • Conjunctival hyperemia: mild redness of the eye.
  • Eyelash changes: increased length or thickness.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling, itching, or rash requiring medical attention.
  • Persistent ocular inflammation: uveitis or iritis.
  • Systemic bradycardia or hypotension: unusually low heart rate or blood pressure.

Precautions & Warnings

Before prescribing Latafor, clinicians should evaluate patient history and follow specific safety measures.

  • Assess cardiovascular status: avoid use in patients with severe bradycardia or heart block.
  • Monitor respiratory conditions: caution in asthma or COPD due to beta‑blocker effect.
  • Evaluate ocular surface: discontinue if severe eye irritation or allergic response occurs.
  • Check for hypersensitivity: avoid in individuals allergic to timolol, latanoprost, or any excipients.
  • Use with caution in pregnancy: limited data, risk‑benefit assessment required.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Latafor can interact with other medications; awareness of major and moderate interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Non‑selective beta‑blockers (oral): additive systemic beta‑blockade may cause bradycardia.
  • Sympathomimetic agents (e.g., epinephrine eye drops): antagonistic effect reducing efficacy.

Moderate Interactions (Monitor Closely)

  • Carbonic anhydrase inhibitors: may enhance intra‑ocular pressure lowering effect.
  • Anticholinergic eye drops: potential for reduced aqueous outflow.
  • Systemic antihypertensives: monitor blood pressure for additive hypotensive effect.

Frequently Asked Questions

Latafor is an ophthalmic solution indicated for the reduction of intra‑ocular pressure in adults with open‑angle glaucoma or ocular hypertension. By lowering eye pressure, it helps prevent optic nerve damage and visual field loss associated with these conditions.

Timolol maleate blocks beta‑adrenergic receptors in the ciliary body, reducing aqueous humor production. Latanoprost, a prostaglandin F2α analog, binds to FP receptors and increases uveoscleral outflow. The complementary mechanisms produce a greater overall decrease in intra‑ocular pressure than either agent alone.

The dosing regimen for Latafor is determined by the prescribing clinician. Typically, one drop is instilled in the affected eye(s) once daily, but the exact frequency and duration depend on individual patient response and therapeutic goals.

Safety data for Latafor in pregnancy and lactation are limited. Clinicians should weigh potential benefits against risks and consider alternative therapies when possible. Women who are pregnant, planning pregnancy, or breastfeeding should discuss use with their healthcare provider.

To request Latafor, 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 and any necessary import documentation.

Latafor combines a beta‑blocker and a prostaglandin analog, offering dual mechanisms in a single eye‑drop bottle. Compared with monotherapy agents, it may achieve comparable pressure reduction with fewer administrations, but individual response varies and some patients may prefer separate agents based on tolerance or cost.

Store Latafor at room temperature, below 25 °C, in the original packaging. Protect the bottle from direct sunlight, moisture and extreme temperatures. Keep the container tightly closed when not in use to maintain sterility.

Latafor is applied as an eye drop. The patient should wash hands, tilt the head back, pull down the lower eyelid to form a pocket, and instill one drop without touching the tip to the eye. Close the eye gently for a few minutes to aid absorption.

Serious risks include severe allergic reactions such as swelling, itching or rash, persistent ocular inflammation (uveitis or iritis), and systemic effects like marked bradycardia or hypotension. Any sudden visual changes, eye pain or systemic symptoms should prompt immediate medical evaluation.

Latafor is contraindicated in patients with known hypersensitivity to timolol, latanoprost, or any excipients, and in individuals with severe sinus bradycardia, second‑ or third‑degree heart block, or uncontrolled asthma. Caution is also advised for patients with severe COPD or those taking non‑selective beta‑blockers systemically.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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