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

Latira

Active Ingredient:
Timolol Maleate, Latanoprost
Origin:
EU

Latira (Timolol Maleate, Latanoprost)

Timolol maleate and latanoprost, the active ingredients in Latira, are a beta‑blocker and a prostaglandin analog presented as sterile ophthalmic eye drops for ocular use. They work together to lower intra‑ocular pressure by reducing aqueous humor production and increasing uveoscleral outflow, providing effective control in adults diagnosed with open‑angle glaucoma or ocular hypertension.

GNH India supplies Latira as a licensed, GDP‑compliant international pharmaceutical supplier, adhering to stringent quality standards and regulatory requirements. The company serves hospitals, pharmacies, and clinics worldwide, providing reliable access to this prescription ophthalmic medication for qualified healthcare professionals.

Manufacturer / TM Owner

Ratiopharm Gmbh

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Indications & Clinical Uses

Latira combines a beta‑blocker and a prostaglandin analog to manage conditions characterized by elevated intra‑ocular pressure.

  • Open‑angle glaucoma: reduces intra‑ocular pressure to slow optic nerve damage.
  • Ocular hypertension: lowers eye pressure to prevent progression to glaucoma.
  • Post‑surgical intra‑ocular pressure control: helps maintain target pressure after ocular surgery.

How It Works

  • Timolol maleate non‑selectively blocks β‑adrenergic receptors in the ciliary body, decreasing aqueous humor production. Latanoprost, a prostaglandin F2α analogue, binds to FP receptors, remodeling the extracellular matrix and enhancing uveoscleral outflow of aqueous humor. The combined actions result in a net reduction of intra‑ocular pressure, addressing the primary pathogenic factor in glaucoma and ocular hypertension. This dual mechanism provides complementary pressure‑lowering effects throughout the 24‑hour cycle.

Side Effects

Like all ophthalmic medications, Latira may cause local and systemic adverse reactions.

Common Side Effects

  • Blurred vision
  • Eye irritation or burning sensation
  • Redness of the conjunctiva
  • Dry eye or foreign body sensation

Serious or Rare Side Effects

  • Severe allergic reaction (e.g., eyelid swelling, rash)
  • Paradoxical increase in intra‑ocular pressure
  • Corneal ulcer or keratitis
  • Systemic beta‑blocker effects such as bradycardia or bronchospasm

Precautions & Warnings

Before prescribing Latira, clinicians should consider several safety factors.

  • Cardiovascular assessment: evaluate heart rate and blood pressure before initiating therapy.
  • Respiratory caution: avoid use in patients with severe asthma or chronic obstructive pulmonary disease.
  • Concomitant beta‑blockers: monitor for additive systemic beta‑blockade.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit evaluation.
  • Contact lens wear: remove lenses before instillation and wait before reinserting.
  • Store at room temperature: keep bottle tightly closed, protect from light and moisture.

Avoid Interactions

Latira may interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers (e.g., propranolol): may cause excessive bradycardia or hypotension.
  • Topical adrenergic agonists (e.g., epinephrine): can diminish timolol’s intra‑ocular pressure‑lowering effect.
  • Other prostaglandin analog eye drops: increase risk of ocular inflammation.

Moderate Interactions (Monitor Closely)

  • Carbonic anhydrase inhibitor eye drops (e.g., dorzolamide): additive IOP reduction may require monitoring.
  • Anticholinergic ophthalmic agents: may affect pupil size and comfort.
  • Systemic antihypertensive drugs: monitor for enhanced hypotensive response.

Frequently Asked Questions

Latira is a prescription ophthalmic eye drop that combines timolol maleate and latanoprost to lower intra‑ocular pressure. It is indicated for the treatment of open‑angle glaucoma and ocular hypertension, helping to prevent optic nerve damage and preserve visual function.

Timolol maleate is a non‑selective beta‑adrenergic blocker. In the eye it reduces the production of aqueous humor by blocking β‑receptors in the ciliary body, which leads to a decrease in intra‑ocular pressure.

The dosing regimen for Latira is determined by the prescribing clinician based on the patient’s condition, response, and tolerance. Typically, one drop is instilled in the affected eye(s) once daily, but the exact schedule should follow the prescriber’s instructions.

The safety of Latira in pregnancy or while breastfeeding has not been definitively established. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To order Latira, 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.

Latira combines two mechanisms—beta‑blockade and prostaglandin‑mediated outflow enhancement—offering complementary pressure‑lowering effects. Compared with single‑agent drops, the combination can achieve greater IOP reduction in a single daily dose, potentially improving adherence while maintaining a safety profile similar to its individual components.

Latira should be stored at room temperature, below 25 °C. Keep the bottle tightly closed, protect it from light and moisture, and avoid freezing. Do not refrigerate unless specifically instructed by the product label.

Latira is applied as a sterile eye drop. 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. The eye should be closed gently for a few seconds to aid absorption.

Serious risks, though uncommon, include severe allergic reactions such as eyelid swelling or rash, paradoxical increase in intra‑ocular pressure, corneal ulceration, and systemic beta‑blocker effects like bradycardia or bronchospasm. Any of these symptoms require immediate medical attention.

Latira is contraindicated in patients with known hypersensitivity to timolol, latanoprost, or any excipients, as well as those with severe asthma, chronic obstructive pulmonary disease, sinus node dysfunction, or advanced heart block without a pacemaker. It should also be avoided in patients with active ocular infections.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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