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

Latanoprost/Timolol Viatris

Active Ingredient:
Timolol Maleate, Latanoprost
Origin:
EU

Latanoprost/Timolol Viatris (Timolol Maleate, Latanoprost)

Timolol maleate, the active ingredient in Latanoprost/Timolol Viatris, is a beta blocker presented as an ophthalmic solution for ocular use. It reduces intra‑ocular pressure in patients with open‑angle glaucoma or ocular hypertension. Combined with Latanoprost, a prostaglandin analog, the formulation targets both aqueous humor production and outflow to achieve better pressure control.

GNH India supplies Latanoprost/Timolol Viatris as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation to support global distribution.

Manufacturer / TM Owner

Upjohn Eesv

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Indications & Clinical Uses

Latanoprost/Timolol is indicated for conditions affecting intra‑ocular pressure within the glaucoma disease family.

  • Open-angle glaucoma: lowers intra‑ocular pressure to prevent optic nerve damage
  • Ocular hypertension: reduces elevated eye pressure to lower risk of glaucoma development
  • Secondary open-angle glaucoma: helps control pressure when caused by other ocular conditions

How It Works

  • Latanoprost acts as a prostaglandin F2α analog, increasing uveoscleral outflow of aqueous humor, while Timolol maleate non‑selectively blocks beta‑adrenergic receptors in the ciliary body, decreasing aqueous humor production. The combined actions result in a net reduction of intra‑ocular pressure, helping to preserve optic nerve function.

Side Effects

Common Side Effects

  • Eye irritation or burning sensation
  • Blurred vision shortly after instillation
  • Redness of the conjunctiva
  • Itching or mild allergic reaction on the eyelid
  • Dry eye or foreign‑body sensation
  • Increased pigmentation of the iris

Serious or Rare Side Effects

  • Severe allergic reaction with swelling of the eyelid or face
  • Unexpected rise in intra‑ocular pressure (rebound effect)
  • Systemic beta‑blocker effects such as bradycardia, hypotension, or bronchospasm
  • Chest pain or signs of heart failure
  • Acute angle‑closure glaucoma
  • Vision loss

Precautions & Warnings

Before initiating therapy, evaluate patient-specific risk factors and monitor for adverse events.

  • Assess cardiovascular status: avoid in patients with severe bradycardia, heart block, or decompensated heart failure
  • Monitor respiratory function: caution in asthma or chronic obstructive pulmonary disease
  • Check for sulfonamide or prostaglandin allergy: discontinue if hypersensitivity occurs
  • Avoid abrupt discontinuation: may cause rebound intra‑ocular pressure elevation
  • Pregnancy and lactation: use only if potential benefit justifies potential risk to the fetus or infant
  • Store at room temperature: keep in original container, protect from light and moisture

Avoid Interactions

Latanoprost/Timolol may interact with other systemic or ocular agents; review concomitant medications.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers (e.g., propranolol): additive bradycardia or hypotension
  • Other ocular hypotensive agents (e.g., carbonic anhydrase inhibitors): excessive IOP lowering
  • Sympathomimetic eye drops (e.g., epinephrine): antagonistic effect reducing efficacy

Moderate Interactions (Monitor Closely):\n- Calcium channel blockers: may influence ocular blood flow and IOP response

  • Anticholinergic ophthalmic drops: possible alteration of pupil dynamics
  • Systemic antihypertensives: monitor blood pressure for additive lowering

Frequently Asked Questions

Latanoprost/Timolol Viatris is a prescription ophthalmic solution used to lower intra‑ocular pressure in patients with open‑angle glaucoma or ocular hypertension. By reducing pressure, it helps prevent optic nerve damage and progression of visual field loss associated with these conditions.

Timolol maleate is a non‑selective beta‑adrenergic blocker that reduces the production of aqueous humor by inhibiting beta receptors in the ciliary body. This decrease in fluid formation contributes to lower intra‑ocular pressure when combined with Latanoprost.

The dosing regimen for Latanoprost/Timolol Viatris is determined by the prescribing ophthalmologist. Typically, one drop is instilled into the affected eye(s) once daily in the evening, but the exact dose and timing should follow the prescriber’s instructions.

Safety data for Latanoprost/Timolol in pregnancy and lactation are limited. The product should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com with 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.

Compared with monotherapy agents, the Latanoprost/Timolol combination offers dual mechanisms—enhanced outflow and reduced production—resulting in greater IOP reduction. It may be preferred when a single agent does not achieve target pressure, but individual patient response and tolerance guide therapy choice.

Store the ophthalmic solution at room temperature, preferably below 25 °C. Keep the bottle tightly closed, protect it from light and moisture, and do not freeze. Once opened, discard any remaining product after the period indicated on the label.

Latanoprost/Timolol is administered as a single drop into the conjunctival sac of the affected eye(s) once daily, usually in the evening. Patients should avoid touching the tip of the bottle to the eye or any other surface to maintain sterility.

Serious risks include severe allergic reactions, a sudden increase in intra‑ocular pressure (rebound), systemic beta‑blocker effects such as bradycardia, hypotension, bronchospasm, and rare cases of acute angle‑closure glaucoma. Prompt medical attention is required if any of these occur.

Patients with known hypersensitivity to either component, severe sinus bradycardia, second‑ or third‑degree heart block, decompensated heart failure, or uncontrolled asthma/COPD should avoid this medication. Contraindications should be confirmed by the prescribing clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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