Product image of Latanoprost Actavis (Latanoprost) supplied by GNH India

Latanoprost Actavis

Active Ingredient:
Latanoprost
Origin:
EU

Latanoprost Actavis (Latanoprost)

Latanoprost, the active ingredient in Latanoprost Actavis, is a prostaglandin analog presented as an ophthalmic solution for ocular use. It is employed to lower intra‑ocular pressure in patients with open‑angle glaucoma or ocular hypertension, helping to preserve visual function.

GNH India supplies Latanoprost Actavis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches for global distribution. Clients benefit from reliable logistics, comprehensive documentation, and responsive technical support throughout the supply chain.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Latanoprost is a prostaglandin analog used to manage conditions that involve elevated intra‑ocular pressure.

  • Open‑angle glaucoma: reduces intra‑ocular pressure to slow disease progression.
  • Ocular hypertension: lowers eye pressure to prevent development of glaucoma.
  • Secondary open‑angle glaucoma: helps control pressure when caused by other ocular conditions.

How It Works

  • Latanoprost binds to prostaglandin F‑type receptors (FP receptors) in the ciliary muscle and scleral tissue, activating a cascade that remodels extracellular matrix and enhances uveoscleral outflow of aqueous humor. The increased outflow reduces intra‑ocular pressure, providing therapeutic benefit in glaucoma and ocular hypertension. This effect is dose‑dependent and persists with once‑daily administration, offering sustained pressure control without systemic absorption. The drug’s high ocular bioavailability is achieved through its lipophilic ester form, which is hydrolyzed to the active acid after penetration.

Side Effects

Latanoprost may cause ocular and systemic reactions; most are mild and reversible.

Common Side Effects

  • Eye redness: transient hyperemia of the conjunctiva.
  • Eye irritation: burning or stinging sensation after instillation.
  • Increased eyelash growth: longer, thicker lashes.
  • Darkening of iris: gradual increase in brown pigmentation.
  • Blurred vision: temporary focusing changes.
  • Foreign body sensation: feeling of grit in the eye.

Serious or Rare Side Effects

  • Severe eye inflammation: uveitis or iritis requiring medical attention.
  • Allergic reaction: swelling, itching, or rash around the eye.
  • Vision loss: sudden decrease in visual acuity.
  • Ocular infection: bacterial or fungal infection at the application site.
  • Systemic hypotension: rare drop in blood pressure.

Precautions & Warnings

When prescribing Latanoprost, clinicians should consider several safety measures to minimize risks.

  • Assess baseline intra‑ocular pressure: ensure appropriate indication before initiating therapy.
  • Monitor iris color changes: inform patients that permanent darkening may occur.
  • Avoid use in active ocular infection: postpone treatment until infection resolves.
  • Caution in patients with asthma: prostaglandin analogs can rarely trigger bronchospasm.
  • Discontinue if severe ocular inflammation develops: seek ophthalmologic evaluation.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Latanoprost can interact with other ocular or systemic agents, affecting efficacy or safety.

Major Interactions (Avoid)

  • Concurrent use of other intra‑ocular pressure‑lowering eye drops (e.g., timolol, dorzolamide): may cause excessive pressure reduction.
  • Systemic non‑steroidal anti‑inflammatory drugs (NSAIDs): can diminish prostaglandin‑mediated outflow enhancement.

Moderate Interactions (Monitor Closely)

  • Topical corticosteroids: may counteract IOP‑lowering effect.
  • Anticholinergic eye drops: may affect pupil size and drug distribution.
  • Contact lens wear: may reduce drug absorption; advise removal before instillation.
  • Beta‑blocker eye drops: monitor for additive hypotensive effect.

Frequently Asked Questions

Latanoprost Actavis is indicated for the reduction of intra‑ocular pressure in patients with open‑angle glaucoma and ocular hypertension. By lowering eye pressure, the medication helps to slow disease progression and protect visual function.

Latanoprost acts as a prostaglandin F‑type receptor agonist in the eye. Activation of these receptors remodels extracellular matrix in the ciliary body, increasing uveoscleral outflow of aqueous humor and thereby reducing intra‑ocular pressure.

The dosing regimen for Latanoprost Actavis is determined by the prescribing ophthalmologist. Typically, a single drop is instilled in the affected eye(s) once daily, but the exact dose and timing should follow the prescriber’s instructions.

Safety data for Latanoprost in pregnancy and lactation are limited. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by the treating physician.

To order, 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.

Latanoprost belongs to the prostaglandin analog class, which generally provides greater IOP reduction with once‑daily dosing compared with beta‑blockers such as timolol. It also has a different side‑effect profile, notably changes in iris color and eyelash growth, which may influence choice.

Latanoprost Actavis should be stored at ambient temperature, protected from light and moisture, and kept in its original container. Do not freeze the product, and discard any solution that appears discolored or cloudy.

Instill one drop of Latanoprost into the affected eye(s) once daily, preferably in the evening. Avoid touching the tip of the bottle to the eye or any surface, and remove contact lenses before application if possible.

Serious risks include severe eye inflammation (uveitis or iritis), allergic reactions around the eye, sudden loss of visual acuity, and rare ocular infections. Patients should seek immediate medical attention if they experience any of these symptoms.

Latanoprost should not be used by individuals with known hypersensitivity to the drug or any component of the formulation, and it is contraindicated in eyes with active infection or inflammation until the condition is resolved.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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