Product image of Nexotrav (Timolol, Travoprost) supplied by GNH India

Nexotrav

Active Ingredient:
Timolol, Travoprost
Origin:
EU

Nexotrav (Timolol, Travoprost)

Timolol and Travoprost, the active ingredients in Nexotrav, are a beta‑blocker and prostaglandin analog presented as eye drops for ocular use. They treat open‑angle glaucoma and ocular hypertension in adult patients.
GNH India supplies Nexotrav as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Davi Ii - Farmacêutica, S.A.

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Indications & Clinical Uses

  • Nexotrav is indicated for conditions affecting intraocular pressure within the glaucoma disease family.
  • Open‑angle glaucoma: lowers intraocular pressure to slow disease progression.
  • Ocular hypertension: reduces pressure to prevent development of glaucoma.
  • Elevated intraocular pressure in patients at risk of glaucoma: helps maintain target pressure and protect optic nerve health.

How It Works

  • Timolol acts as a non‑selective beta‑adrenergic antagonist, decreasing aqueous humor production by the ciliary body. Travoprost is a prostaglandin F2α analog that enhances uveoscleral outflow of aqueous humor. The combined actions result in a net reduction of intraocular pressure, addressing the primary pathogenic factor in open‑angle glaucoma and ocular hypertension.

Side Effects

Nexotrav may cause ocular and systemic adverse reactions.

Common Side Effects

  • Eye irritation or burning sensation.
  • Redness (hyperemia) of the conjunctiva.
  • Blurred vision shortly after instillation.
  • Itching or mild allergic conjunctivitis.
  • Increased eyelash growth.
  • Dry eye sensation.

Serious or Rare Side Effects

  • Severe allergic reaction with swelling of the eyelid or face.
  • Sudden loss of vision or acute ocular pain.
  • Systemic beta‑blocker effects such as bradycardia, hypotension, or bronchospasm.
  • Persistent corneal edema or ulceration.
  • Worsening of pre‑existing respiratory conditions.

Precautions & Warnings

  • Before prescribing Nexotrav, clinicians should evaluate patient-specific risk factors.
  • Assess cardiovascular status: timolol may lower heart rate and blood pressure.
  • Screen for asthma or COPD: beta‑blockade can precipitate bronchospasm.
  • Monitor intraocular pressure response after initiation.
  • Avoid use in patients with known hypersensitivity to any component.
  • Consider pregnancy and lactation: safety not established; use only if benefit outweighs risk.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Nexotrav can interact with systemic and ocular medications.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers: additive bradycardia or hypotension.
  • Other prostaglandin analog eye drops: increased risk of ocular side effects.
  • Sympathomimetic ocular agents (e.g., phenylephrine): may reduce IOP‑lowering efficacy.

Moderate Interactions (Monitor Closely):\n- Anticholinergic eye drops: may affect pupil size and comfort.

  • Topical anesthetics: potential for increased corneal toxicity.
  • Systemic carbonic anhydrase inhibitors: additive intraocular pressure reduction.

Frequently Asked Questions

Nexotrav is a prescription ophthalmic solution indicated for the treatment of open‑angle glaucoma and ocular hypertension. By lowering intraocular pressure, it helps prevent optic nerve damage and visual field loss associated with these conditions.

Timolol reduces the production of aqueous humor by blocking beta‑adrenergic receptors in the ciliary body, while Travoprost increases uveoscleral outflow by mimicking prostaglandin F2α. The dual action results in a net decrease in intraocular pressure.

The dosing regimen for Nexotrav is determined by the prescribing clinician. Typically, one drop is instilled in the affected eye(s) once daily, but the exact frequency and duration are individualized based on patient response and clinical judgment.

Safety of Nexotrav during pregnancy or lactation has not been established. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

To place an order, submit an enquiry on the Nexotrav 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.

Nexotrav combines a beta‑blocker and a prostaglandin analog, offering a two‑mechanism approach in a single formulation. Compared with monotherapy agents, it may achieve greater intraocular pressure reduction with fewer drops, potentially improving adherence while maintaining a safety profile similar to its individual components.

Store Nexotrav at room temperature, below 25 °C, in the original packaging. Protect the bottle from light and moisture, and keep the cap tightly closed when not in use to maintain sterility and potency.

Instill one drop of Nexotrav into the conjunctival sac of the prescribed eye(s) as directed by the healthcare provider, typically once daily in the evening. Avoid touching the tip of the bottle to the eye or any surface to prevent contamination.

Serious adverse events include severe allergic reactions (e.g., eyelid swelling, facial rash), sudden vision loss, acute ocular pain, and systemic beta‑blocker effects such as marked bradycardia, hypotension, or bronchospasm. Patients should seek immediate medical attention if any of these occur.

Nexotrav is contraindicated in patients with known hypersensitivity to timolol, travoprost, or any excipients, as well as those with severe asthma, chronic obstructive pulmonary disease, or certain cardiac conduction disorders where beta‑blockade is unsafe.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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