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

Latanoprost/Timolol Teva

Active Ingredient:
Timolol Maleate, Latanoprost
Origin:
EU

Latanoprost/Timolol Teva (Timolol Maleate, Latanoprost)

Latanoprost and Timolol Maleate, the active ingredients in Latanoprost/Timolol Teva, are a prostaglandin analog and beta‑blocker combination presented as eye drops for ocular (topical) use. It treats open‑angle glaucoma and ocular hypertension in adult patients, reducing intra‑ocular pressure through dual mechanisms.

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

Manufacturer / TM Owner

Teva Santé

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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 slow optic nerve damage.
  • Ocular hypertension: reduces elevated eye pressure to prevent progression to glaucoma.
  • Secondary glaucoma (e.g., pseudoexfoliative): provides pressure control when monotherapy is insufficient.

How It Works

  • Latanoprost binds to prostaglandin F receptors in the ciliary body, increasing uveoscleral outflow of aqueous humor. Timolol maleate non‑selectively blocks β1 and β2 adrenergic receptors in the ciliary epithelium, decreasing aqueous humor production. The combined actions result in a synergistic reduction of intra‑ocular pressure.

Side Effects

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

Common Side Effects

  • Ocular hyperemia: redness of the eye.
  • Eye irritation or burning sensation.
  • Blurred vision shortly after instillation.
  • Increased eyelash growth (hypertrichosis).
  • Darkening of the iris color.
  • Foreign body sensation.

Serious or Rare Side Effects

  • Severe allergic reaction (e.g., angio‑edema, anaphylaxis).
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Marked bradycardia or heart block.
  • Bronchospasm or worsening of asthma.
  • Systemic beta‑blocker effects such as hypotension.
  • Ocular infection or corneal ulceration.

Precautions & Warnings

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

  • Cardiovascular assessment: evaluate for bradycardia, heart block, or heart failure.
  • Respiratory evaluation: avoid in patients with asthma or severe chronic obstructive pulmonary disease.
  • Intra‑ocular pressure monitoring: ensure adequate pressure reduction after initiation.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk, as safety data are limited.
  • Storage: Store at room temperature: keep bottle in original packaging, protect from light and moisture.

Avoid Interactions

Latanoprost/Timolol may interact with other medicines; awareness of the interaction level helps guide clinical decisions.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers: additive bradycardia and hypotension.
  • Inhaled or oral β‑agonists (e.g., albuterol): may reduce bronchodilator efficacy.
  • Other ocular beta‑blockers: risk of excessive intra‑ocular pressure lowering.

Moderate Interactions (Monitor Closely)

  • Carbonic anhydrase inhibitors (e.g., dorzolamide): may further lower intra‑ocular pressure.
  • Systemic antihypertensives (e.g., calcium channel blockers): monitor for additive blood pressure effects.
  • Prostaglandin analogs used concurrently: assess for cumulative ocular surface changes.

Frequently Asked Questions

Latanoprost/Timolol is a prescription eye‑drop combination used to lower intra‑ocular pressure in adults with open‑angle glaucoma or ocular hypertension, helping to prevent optic nerve damage and preserve vision.

Latanoprost increases the outflow of aqueous humor through the uveoscleral pathway, while Timolol blocks β‑adrenergic receptors to reduce aqueous humor production. Together they provide a synergistic pressure‑lowering effect.

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

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

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 required import documentation.

Compared with monotherapy agents, the combination offers dual mechanisms—enhanced outflow and reduced production—often achieving greater pressure reduction with a single drop, which can improve adherence versus using two separate eye‑drops.

Store the eye‑drop bottle at room temperature, away from direct sunlight and moisture. Keep it in the original container, and discard any product that appears discolored or has been opened beyond the recommended period.

The patient should wash their hands, tilt the head back, pull down the lower eyelid to form a pocket, and place one drop into the conjunctival sac. Close the eye gently and avoid blinking excessively for a few seconds.

Serious risks include severe allergic reactions, bronchospasm in susceptible individuals, marked bradycardia or heart block, and rare ocular complications such as corneal ulceration or Stevens‑Johnson syndrome. Prompt medical attention is required if these occur.

Patients with known hypersensitivity to either component, severe asthma or chronic obstructive pulmonary disease, sinus bradycardia, heart block, or uncontrolled heart failure should avoid this medication unless a physician determines it is essential.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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