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

Lataxin

Active Ingredient:
Timolol Maleate, Latanoprost
Origin:
EU

Lataxin (Timolol Maleate, Latanoprost)

Timolol maleate and latanoprost, the active ingredients in Lataxin, are a beta‑blocker and a prostaglandin analog presented as an ophthalmic solution for ocular use. They lower intra‑ocular pressure in patients with primary open‑angle glaucoma or ocular hypertension.
GNH India supplies Lataxin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Doc Generici S.R.L.

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Indications & Clinical Uses

Lataxin is used in glaucoma therapy to reduce intra‑ocular pressure through complementary mechanisms.

  • Primary open‑angle glaucoma: provides sustained IOP reduction to prevent optic nerve damage.
  • Ocular hypertension: lowers elevated IOP to reduce the risk of progression to glaucoma.
  • Pseudoexfoliative glaucoma: helps control IOP where single‑agent therapy is insufficient.

How It Works

  • Timolol maleate non‑selectively blocks β‑adrenergic receptors in the ciliary body, decreasing aqueous humor production. Latanoprost, a prostaglandin F2α analog, remodels the extracellular matrix of the uveoscleral pathway, enhancing outflow of aqueous humor. The combined actions result in a greater overall reduction of intra‑ocular pressure than either agent alone.

Side Effects

Lataxin may cause ocular and systemic adverse reactions.

Common Side Effects

  • Eye irritation or burning sensation.
  • Blurred vision shortly after instillation.
  • Conjunctival hyperemia (redness).
  • Itching or mild allergic eyelid dermatitis.
  • Dry eye or foreign‑body sensation.
  • Transient increase in IOP after initial dosing.

Serious or Rare Side Effects

  • Severe allergic reaction with swelling of the eyelid or periorbital tissues.
  • Persistent worsening of glaucoma despite therapy.
  • Systemic beta‑blocker effects such as bradycardia, hypotension, or bronchospasm.
  • Irreversible darkening of the iris or periorbital fat atrophy.
  • Corneal edema or ulceration.
  • Acute angle‑closure glaucoma precipitated by pupillary dilation.

Precautions & Warnings

Before prescribing Lataxin, clinicians should consider patient‑specific factors and monitor for adverse events.

  • Cardiovascular disease: assess for bradycardia, heart block, or heart failure.
  • Respiratory conditions: avoid in patients with asthma or severe COPD.
  • Pregnancy and lactation: use only if potential benefit justifies the risk, as safety data are limited.
  • Contact lens wear: advise removal before and after instillation to prevent lens discoloration.
  • Concomitant ocular medications: evaluate for additive IOP‑lowering effects.
  • Store at room temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Lataxin can interact with systemic and ocular agents, altering efficacy or safety.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers: may cause additive bradycardia or hypotension.
  • Other prostaglandin analog eye drops: risk of excessive uveoscleral outflow and ocular irritation.
  • Sympathomimetic agents (e.g., epinephrine eye drops): may reduce IOP‑lowering effect.

Moderate Interactions (Monitor Closely):\n- Topical anesthetics: may increase corneal toxicity when used together.

  • Anticholinergic eye drops: monitor for additive dry‑eye symptoms.
  • Systemic carbonic anhydrase inhibitors: watch for enhanced IOP reduction and electrolyte changes.

Frequently Asked Questions

Lataxin is prescribed for primary open‑angle glaucoma and ocular hypertension. By lowering intra‑ocular pressure, it helps prevent optic nerve damage and reduces the risk of vision loss associated with these conditions.

Timolol maleate blocks β‑adrenergic receptors in the eye, decreasing aqueous humor production. Latanoprost mimics prostaglandin F2α, increasing uveoscleral outflow of aqueous humor. Together they provide a complementary reduction in intra‑ocular pressure.

The dosing regimen for Lataxin is determined by the prescribing clinician based on the patient’s IOP level, response to therapy, and overall health status. Patients should follow the specific instructions provided by their eye‑care professional.

Safety data for Lataxin in pregnancy and lactation are limited. It should only be used if the potential benefit outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare provider.

To order Lataxin, 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.

Lataxin combines a beta‑blocker and a prostaglandin analog, offering dual mechanisms of action in a single formulation. This can provide greater IOP reduction than single‑agent drops, potentially improving adherence compared with using two separate products.

Lataxin should be stored at room temperature, below 25 °C, in its original packaging. Keep the bottle tightly closed, protect it from light and moisture, and discard any solution that appears discolored or contains particles.

Lataxin is applied as an ophthalmic solution. The patient instills one drop into the affected eye(s) as directed by the prescriber, typically once daily in the evening, and avoids touching the dropper tip to any surface.

Serious risks include severe allergic reactions, worsening of glaucoma despite treatment, systemic beta‑blocker effects such as bradycardia or bronchospasm, and irreversible changes in iris color or periorbital fat. Patients should seek immediate medical attention if these occur.

Lataxin 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 bradycardia, or second‑degree or third‑degree atrioventricular block without a pacemaker.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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