Product image of Latanox (Latanoprost) supplied by GNH India

Latanox

Active Ingredient:
Latanoprost
Origin:
EU

Latanox (Latanoprost)

Latanoprost, the active ingredient in Latanox, is a prostaglandin analog presented as an eye drop for ocular use. It lowers intra‑ocular pressure and is prescribed for patients with open‑angle glaucoma or ocular hypertension. Latanox is supplied in a sterile ophthalmic solution suitable for once‑daily administration.

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

Manufacturer / TM Owner

Jadran-Galenski Laboratorij D.D.

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Indications & Clinical Uses

Latanox belongs to the prostaglandin analog class and is used to manage conditions that involve elevated intra‑ocular pressure.

  • Open‑angle glaucoma: reduces intra‑ocular pressure to prevent optic nerve damage.
  • Ocular hypertension: lowers pressure to reduce the risk of developing glaucoma.
  • Secondary ocular hypertension: helps control pressure when caused by other ocular conditions.

How It Works

  • Latanoprost is a synthetic analogue of prostaglandin F2α that binds to FP receptors in the ciliary muscle. Activation of these receptors remodels the extracellular matrix, enhancing uveoscleral outflow of aqueous humor, which results in a sustained reduction of intra‑ocular pressure.

Side Effects

Latanox may cause a range of ocular and systemic reactions.

Common Side Effects

  • Eye redness: mild conjunctival hyperemia.
  • Increased eyelash growth: longer, thicker lashes.
  • Iris pigmentation: gradual darkening of eye color.
  • Eye irritation: burning or stinging sensation.
  • Blurred vision: transient visual disturbance.
  • Foreign body sensation: feeling of grit in the eye.

Serious or Rare Side Effects

  • Uveitis: inflammation of the uveal tract.
  • Macular edema: swelling of the central retina.
  • Severe allergic reaction: swelling, itching, or rash.
  • Ocular pain: persistent discomfort.
  • Vision loss: sudden decrease in visual acuity.
  • Systemic hypersensitivity: fever, chills, or malaise.

Precautions & Warnings

Before prescribing Latanox, clinicians should evaluate patient history and monitor for ocular changes.

  • Baseline intra‑ocular pressure assessment: establish starting pressure values.
  • Monitor iris color changes: document any pigmentation over time.
  • Avoid use in active ocular infection: risk of worsening infection.
  • Caution in patients with a history of uveitis: may precipitate inflammation.
  • Do not combine with other prostaglandin analog eye drops: risk of hypotony.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Latanox can interact with other ocular or systemic agents, affecting pressure control or ocular health.

Major Interactions (Avoid)

  • Concurrent prostaglandin analog eye drops: additive IOP lowering may cause hypotony.
  • Systemic carbonic anhydrase inhibitors: may enhance pressure reduction beyond desired levels.
  • Ocular NSAIDs: increased risk of corneal complications.

Moderate Interactions (Monitor Closely)

  • Beta‑blocker eye drops: additive effect on IOP reduction, monitor pressure.
  • Topical corticosteroids: may diminish Latanox efficacy, assess response.
  • Systemic antihistamines: possible impact on ocular surface, observe for dryness.

Frequently Asked Questions

Latanox is an ophthalmic solution containing Latanoprost, prescribed to lower intra‑ocular pressure in patients with open‑angle glaucoma or ocular hypertension. By reducing pressure, it helps prevent optic nerve damage and progression of visual field loss.

Latanoprost mimics prostaglandin F2α and activates FP receptors in the eye’s ciliary body. This activation remodels extracellular matrix proteins, increasing uveoscleral outflow of aqueous humor, which leads to a sustained decrease in intra‑ocular pressure.

The dosing regimen for Latanox is determined by the prescribing clinician. Typically, one drop is instilled into the affected eye(s) once daily in the evening, but the exact dose and timing should follow the prescriber’s instructions.

The safety of Latanox in pregnancy or while breastfeeding has not been definitively established. Healthcare providers should weigh potential benefits against unknown risks and consider alternative treatments if appropriate.

To order Latanox, 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 necessary import documentation.

Latanox belongs to the prostaglandin analog class, which generally offers once‑daily dosing and strong IOP‑lowering efficacy. Compared with beta‑blocker or carbonic anhydrase inhibitor eye drops, prostaglandin analogues often achieve greater pressure reduction with a convenient dosing schedule.

Latanox should be stored at room temperature, away from direct sunlight and moisture. Keep the bottle tightly closed when not in use and protect it from freezing. Do not use the product if the solution becomes discolored or cloudy.

Latanox is applied as a single drop into the conjunctival sac of the affected eye(s) once daily, preferably in the evening. The patient should avoid touching the tip of the bottle to the eye or any other surface to maintain sterility.

Serious risks include uveitis, macular edema, and severe allergic reactions that may affect vision. Patients should seek immediate medical attention if they experience eye pain, sudden vision loss, or signs of systemic hypersensitivity such as rash or fever.

Latanox should be avoided in patients with active ocular infections, known hypersensitivity to Latanoprost or any component of the formulation, and those who are currently using other prostaglandin analog eye drops without medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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