Product image of Latanoprost Teva Sante (Latanoprost) supplied by GNH India

Latanoprost Teva Sante

Active Ingredient:
Latanoprost
Origin:
EU

Latanoprost Teva Sante (Latanoprost)

Latanoprost, the active ingredient in Latanoprost Teva Sante, is a prostaglandin analog presented as eye drops for ocular use. It lowers intra‑ocular pressure and is indicated for the management of open‑angle glaucoma and ocular hypertension in adult patients. The drug increases uveoscleral outflow of aqueous humor, thereby reducing intra‑ocular pressure.

GNH India supplies Latanoprost Teva Sante as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established quality‑assured distribution channels across the EU and other regulated markets.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

  • Latanoprost is a prostaglandin analog used to lower intra‑ocular pressure in glaucoma and ocular hypertension.
  • Open-angle glaucoma: reduces intra‑ocular pressure to slow disease progression.
  • Ocular hypertension: lowers pressure to prevent conversion to glaucoma.
  • Secondary open-angle glaucoma: helps control pressure in pseudoexfoliative or pigmentary forms.

How It Works

  • Latanoprost binds to prostaglandin F (FP) receptors in the ciliary muscle, activating a cascade that remodels extracellular matrix and enhances uveoscleral outflow of aqueous humor. This increased drainage lowers intra‑ocular pressure, addressing the primary pathogenic factor in open‑angle glaucoma and ocular hypertension.

Side Effects

Latanoprost may cause ocular and systemic reactions.

Common Side Effects

  • Eye redness or hyperemia.
  • Increased eyelash length and density.
  • Darkening of the iris or peri‑ocular skin.
  • Mild eye irritation or foreign‑body sensation.

Serious or Rare Side Effects

  • Severe allergic reaction (e.g., angio‑edema, anaphylaxis).
  • Ocular inflammation such as uveitis.
  • Paradoxical increase in intra‑ocular pressure.
  • Corneal edema or keratitis.
  • Vision loss due to optic nerve compromise.

Precautions & Warnings

  • Before initiating therapy, clinicians should evaluate ocular health and baseline intra‑ocular pressure.
  • Assess baseline IOP: confirm elevated pressure before treatment.
  • Monitor IOP regularly: check pressure after the first week and periodically thereafter.
  • Avoid use with active ocular infection: postpone treatment until infection resolves.
  • Caution in patients with a history of uveitis: monitor for inflammation.
  • Do not wear contact lenses during treatment: lenses may trap medication.
  • Store at room temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Latanoprost can interact with other ocular or systemic agents.

Major Interactions (Avoid)

  • Concurrent use with other prostaglandin analogs: risk of additive ocular effects.
  • Use with non‑steroidal anti‑inflammatory eye drops: may diminish efficacy.
  • Combination with systemic carbonic anhydrase inhibitors: potential excessive IOP reduction.

Moderate Interactions (Monitor Closely)

  • Co‑administration with beta‑blocker eye drops: additive pressure‑lowering effect.
  • Use alongside corticosteroid eye drops: steroids may counteract latanoprost's action.
  • Combination with ocular anesthetic drops: possible increased ocular irritation.

Frequently Asked Questions

Latanoprost Teva Sante is prescribed to lower intra‑ocular pressure in adults with open‑angle glaucoma or ocular hypertension. By reducing pressure, it helps prevent optic nerve damage and preserves visual field loss associated with these conditions.

Latanoprost activates prostaglandin F (FP) receptors in the eye, triggering remodeling of the extracellular matrix in the ciliary body. This enhances uveoscleral outflow of aqueous humor, leading to a reduction in 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 must follow the prescriber’s instructions.

Safety data for latanoprost in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

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

Latanoprost belongs to the prostaglandin analog class, which generally offers once‑daily dosing and strong IOP‑lowering efficacy. Compared with beta‑blockers such as timolol, latanoprost often has a more favorable systemic safety profile but may cause ocular pigmentation changes.

Store the eye‑drop bottle at room temperature, preferably below 25 °C, in its original packaging. Protect it from light and moisture, and keep the cap tightly closed when not in use to maintain stability.

The medication is applied as a single drop into the conjunctival sac of the affected eye(s) in the evening. The patient should wash their hands before use, avoid touching the tip of the bottle to the eye or any surface, and gently close the eye after instillation.

Serious risks include severe allergic reactions such as angio‑edema, ocular inflammation (uveitis), paradoxical increase in intra‑ocular pressure, and corneal edema. Any sudden vision changes, pain, or intense redness should prompt immediate medical evaluation.

Patients with active ocular infections, known hypersensitivity to latanoprost or any component of the formulation, or those who have experienced severe ocular inflammation with prostaglandin analogs should avoid using this product. A clinician should assess suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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