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)

Latanoprost and Timolol, the active ingredients in Latanoprost/Timolol Viatris, are a prostaglandin analog/beta‑blocker combination presented as eye drops for ocular use. They lower intra‑ocular pressure in patients with open‑angle glaucoma or ocular hypertension.

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

Manufacturer / TM Owner

Viatris Limited

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Indications & Clinical Uses

Latanoprost/Timolol is used in the management of ocular conditions that require reduction of intra‑ocular pressure.

  • Open‑angle glaucoma: reduces intra‑ocular pressure to slow disease progression.
  • Ocular hypertension: lowers eye pressure to prevent development of glaucoma.
  • Glaucoma (any type) where pressure reduction is needed: provides additive pressure‑lowering effect when monotherapy is insufficient.

How It Works

  • Latanoprost, a prostaglandin F2α analogue, increases uveoscleral outflow of aqueous humor by remodeling extracellular matrix in the ciliary body. Timolol maleate, a non‑selective β‑adrenergic antagonist, decreases aqueous humor production by blocking β‑receptors in the ciliary epithelium. The combined actions result in additive lowering of intra‑ocular pressure.

Side Effects

The following adverse reactions have been reported with Latanoprost/Timolol eye drops.

Common Side Effects

  • Eye irritation or burning sensation.
  • Blurred vision.
  • Conjunctival hyperemia (redness).
  • Increased eyelash growth.
  • Darkening of the iris.
  • Ocular discomfort or foreign body sensation.

Serious or Rare Side Effects

  • Severe allergic reaction (e.g., angio‑edema, anaphylaxis).
  • Exacerbation of asthma or chronic obstructive pulmonary disease.
  • Bradycardia or hypotension.
  • Systemic beta‑blocker effects such as fatigue or depression.
  • Corneal ulceration or keratitis.
  • Persistent intra‑ocular pressure reduction leading to hypotony.

Precautions & Warnings

Before prescribing Latanoprost/Timolol, clinicians should consider the following precautions.

  • Assess beta‑blocker contraindications: avoid in patients with asthma, COPD, severe bradycardia, or heart block.
  • Monitor intra‑ocular pressure: ensure adequate pressure reduction without causing hypotony.
  • Evaluate for sulfonamide allergy if preservative contains sulfonamide.
  • Do not instill other eye medications within 5 minutes of this product to prevent wash‑out.
  • Store at room temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Latanoprost/Timolol may interact with other medicines; relevant interactions are grouped below.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers (e.g., propranolol): risk of additive bradycardia and hypotension.
  • Sympathomimetic eye drops (e.g., epinephrine): may diminish intra‑ocular pressure‑lowering effect.
  • Other ocular hypotensive agents used concurrently: risk of excessive pressure reduction (hypotony).

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

  • Anticholinergic eye drops: potential effect on pupil size and accommodation.
  • Topical anesthetics: increased risk of corneal toxicity when used together.

Frequently Asked Questions

Latanoprost/Timolol is indicated for the reduction of intra‑ocular pressure in patients with open‑angle glaucoma and ocular hypertension. By lowering eye pressure, it helps to prevent optic nerve damage and preserve visual field.

Latanoprost is a prostaglandin F2α analogue that increases uveoscleral outflow of aqueous humor. It remodels extracellular matrix in the ciliary body, allowing more fluid to drain from the eye, which lowers intra‑ocular pressure.

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

The pregnancy category for this combination is unknown. It should only be used during pregnancy or lactation if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

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 and any necessary import documentation.

Compared with single‑agent therapy, the combination provides additive intra‑ocular pressure reduction because Latanoprost increases outflow while Timolol decreases production. This often achieves target pressure with fewer drops than using two separate agents.

Store at room temperature, preferably below 25 °C. Keep the bottle in its original packaging, protect it from light, and avoid exposure to moisture. Do not freeze the product.

The medication is supplied as sterile eye drops. The patient should wash their hands, tilt the head back, pull down the lower eyelid, and place one drop into the conjunctival sac of each prescribed eye, avoiding contact between the tip and the eye.

Serious risks include severe allergic reactions, exacerbation of asthma or COPD, marked bradycardia or hypotension, and excessive lowering of intra‑ocular pressure leading to hypotony, which can cause vision loss if untreated.

Patients with known hypersensitivity to either component, those with severe asthma, chronic obstructive pulmonary disease, sinus bradycardia, second‑ or third‑degree heart block, or uncontrolled heart failure should avoid this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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