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

Latanoprost Demo

Active Ingredient:
Latanoprost
Origin:
EU

Latanoprost Demo (Latanoprost)

Latanoprost, the active ingredient in Latanoprost Demo, 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. By enhancing fluid outflow from the eye, it helps preserve visual function and delay disease progression.

GNH India supplies Latanoprost Demo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our distribution network ensures consistent quality and regulatory compliance across EU and global markets.

Manufacturer / TM Owner

Demo Abee

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Indications & Clinical Uses

Latanoprost is a prostaglandin analog used to manage conditions characterized by elevated intra‑ocular pressure.

  • Open-angle glaucoma: reduces intra‑ocular pressure to slow optic nerve damage and preserve visual field.
  • Ocular hypertension: lowers eye pressure to prevent progression to glaucoma.
  • Secondary glaucoma (e.g., pseudoexfoliative): improves aqueous outflow to control pressure and reduce risk of optic nerve injury.

How It Works

  • Latanoprost binds to prostaglandin F (FP) receptors on the ciliary muscle, activating a cascade that remodels extracellular matrix and increases uveoscleral outflow of aqueous humor. This enhanced outflow lowers intra‑ocular pressure, helping to protect the optic nerve from pressure‑related damage.

Side Effects

Latanoprost may cause ocular and systemic adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Eye redness: mild conjunctival hyperemia.
  • Increased eyelash growth: longer, thicker lashes.
  • Darkening of iris: gradual brownish pigmentation.
  • Eye irritation: transient stinging or burning sensation.

Serious or Rare Side Effects

  • Inflammatory eye conditions: uveitis or iritis.
  • Corneal edema: swelling of the cornea.
  • Allergic reaction: severe eye swelling or rash.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Monitor intra‑ocular pressure: check pressure regularly after initiation.
  • Assess for ocular infections: avoid use if active eye infection is present.
  • Evaluate for hypersensitivity: discontinue if allergic reaction occurs.
  • Use with caution in patients with corneal disease: may exacerbate existing conditions.
  • Avoid concurrent use with other prostaglandin analogs: increased risk of side effects.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Latanoprost can interact with other ocular or systemic agents, requiring attention to potential effects.

Major Interactions (Avoid)

  • Concomitant use with other intra‑ocular pressure‑lowering eye drops (e.g., beta‑blockers) may cause excessive pressure reduction.
  • Use with non‑steroidal anti‑inflammatory eye drops may increase risk of ocular inflammation.

Moderate Interactions (Monitor Closely)

  • Systemic prostaglandin analogs (e.g., misoprostol) could potentiate systemic effects.
  • Anticholinergic agents may affect tear production, influencing drug tolerance.
  • CYP450 inducers are not known to affect latanoprost, but monitor for unexpected efficacy changes.

Frequently Asked Questions

Latanoprost Demo is used to lower intra‑ocular pressure in patients with open‑angle glaucoma or ocular hypertension. By improving fluid outflow from the eye, it helps to protect the optic nerve and preserve visual function.

Latanoprost activates prostaglandin F (FP) receptors in the eye, which remodels extracellular matrix in the ciliary body and increases uveoscleral outflow of aqueous humor. This enhanced outflow reduces intra‑ocular pressure.

The prescribed dose is determined by the treating clinician. Typically, one drop is instilled into the affected eye(s) once daily in the evening, but exact dosing and timing should 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 any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

Enquiries can be submitted on the product page at gnhindia.com, specifying the required quantity. GNH India supplies 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 intra‑ocular pressure reduction with once‑daily dosing compared with beta‑blockers such as timolol. It is often preferred for its efficacy and convenient dosing, though individual response may vary.

Latanoprost eye drops should be stored at room temperature, below 25 °C, in the original container. Protect the product from light and moisture, and keep the cap tightly closed when not in use.

The medication is administered as an ophthalmic solution. The patient should instill one drop into the prescribed eye(s) as directed, typically in the evening, avoiding contact with the eyelid or eyelashes.

Serious adverse events, though rare, include inflammatory eye conditions such as uveitis or iritis, corneal edema, and severe allergic reactions that may cause significant eye swelling or systemic rash. Prompt medical attention is required if these occur.

Latanoprost should not be used by individuals with known hypersensitivity to the drug or any of its components, and it is contraindicated in eyes with active infections or severe inflammation. Patients with certain corneal disorders should use it only under close supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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