Product image of Lenigron (Timolol Maleate, Bimatoprost) supplied by GNH India

Lenigron

Active Ingredient:
Timolol Maleate, Bimatoprost
Origin:
EU

Lenigron (Timolol Maleate, Bimatoprost)

Timolol maleate and bimatoprost, the active ingredients in Lenigron, are a beta‑adrenergic antagonist and a prostaglandin F2α analog presented as an ophthalmic solution for ocular use. The combination lowers intra‑ocular pressure and is indicated for patients with open‑angle glaucoma or ocular hypertension, and is commonly prescribed by ophthalmologists.

GNH India supplies Lenigron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution through its extensive network of certified partners.

Manufacturer / TM Owner

Pharmathen S.A.

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Indications & Clinical Uses

Lenigron, a combination beta‑adrenergic antagonist and prostaglandin analog, is used to manage conditions that involve elevated intra‑ocular pressure.

  • Open-angle glaucoma: reduces intra‑ocular pressure to slow visual field loss.
  • Ocular hypertension: lowers intra‑ocular pressure to prevent progression to glaucoma.
  • Pseudoexfoliative glaucoma: assists in pressure control where exfoliative material increases outflow resistance.
  • Secondary open-angle glaucoma: provides additional pressure reduction when monotherapy is insufficient.

How It Works

  • Timolol maleate blocks β1 and β2 adrenergic receptors in the ciliary body, decreasing aqueous humor production. Bimatoprost activates prostaglandin F2α receptors in the uveoscleral pathway, enhancing outflow of aqueous humor. This combined effect is maintained with once‑daily dosing, providing consistent pressure control throughout the day.

Side Effects

Lenigron may cause ocular and systemic adverse reactions; they are categorized by frequency.

Common Side Effects

  • Eye irritation: mild burning or stinging upon instillation.
  • Blurred vision: transient visual disturbance after dosing.
  • Conjunctival hyperemia: redness of the eye.
  • Itching: localized pruritus around the eye.
  • Dry eye: decreased tear production leading to discomfort.
  • Headache: mild headache reported by some patients.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling, rash, or difficulty breathing.
  • Uveitis: inflammation of the uveal tract requiring medical attention.
  • Macular edema: fluid accumulation in the macula affecting vision.
  • Decreased visual acuity: sudden loss of sharpness.
  • Systemic beta‑blocker effects: bradycardia, hypotension, or bronchospasm.

Precautions & Warnings

Before prescribing Lenigron, clinicians should evaluate patient history and monitor for specific risks.

  • Pregnancy: safety not established; use only if benefits outweigh risks.
  • Breastfeeding: caution as drug may be excreted in milk.
  • Respiratory disease: avoid in patients with severe asthma or COPD due to beta‑blockade.
  • Cardiac disease: monitor for bradycardia or heart block in patients with conduction disorders.
  • Systemic beta‑blocker therapy: assess for additive hypotensive or cardiac effects.
  • Store at ambient temperature: keep below 25 °C, protect from light and moisture in original container.

Avoid Interactions

Lenigron can interact with other medications; some combinations require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers: may cause excessive bradycardia or hypotension.
  • Other prostaglandin analog eye drops: increase risk of ocular inflammation.
  • Monoamine oxidase inhibitors (MAOIs): potential for severe bronchospasm when combined with timolol.

Moderate Interactions (Monitor Closely)

  • Anticholinergic eye drops: may reduce intra‑ocular pressure‑lowering efficacy.
  • Topical corticosteroids: can counteract pressure‑lowering effect and raise IOP.
  • Sympathomimetic agents (e.g., epinephrine): may diminish timolol’s effect on aqueous production.

Frequently Asked Questions

Lenigron is a prescription ophthalmic solution that combines timolol maleate and bimatoprost to lower intra‑ocular pressure. It is indicated for the treatment of open‑angle glaucoma and ocular hypertension, helping to prevent optic nerve damage and preserve visual function.

Timolol maleate is a non‑selective β‑adrenergic blocker that reduces the production of aqueous humor by inhibiting β‑receptors in the ciliary body. This decrease in fluid formation contributes to lower intra‑ocular pressure when used together with bimatoprost.

The dosing regimen for Lenigron is determined by the prescribing eye‑care professional. Typically, one drop is instilled in the affected eye(s) once daily, but the exact dose and frequency are individualized based on the patient’s response and clinical judgment.

Safety data for Lenigron in pregnancy and lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To order Lenigron, 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.

Lenigron combines a beta‑blocker (timolol) and a prostaglandin analog (bimatoprost) in a single formulation, offering a dual mechanism that can achieve greater pressure reduction than monotherapy. Compared with single‑agent drops, it may simplify regimens but requires careful monitoring for additive side effects.

Lenigron should be stored at ambient temperature, preferably below 25 °C, in its original container. Protect the bottle from light and moisture, and keep it out of reach of children. Do not freeze the solution, and discard any product that appears discolored or contaminated.

Lenigron is applied as an eye drop. The patient should wash hands, tilt the head back, pull down the lower eyelid to create a small pocket, and place one drop into the conjunctival sac. Close the eye gently for a few seconds and avoid blinking excessively.

Serious risks include severe allergic reactions (e.g., swelling, rash, difficulty breathing), uveitis, macular edema, and systemic beta‑blocker effects such as bradycardia, hypotension, or bronchospasm. Any sudden vision changes or systemic symptoms should prompt immediate medical evaluation.

Lenigron should be avoided in patients with known hypersensitivity to timolol, bimatoprost, or any excipients, as well as in individuals with severe asthma, chronic obstructive pulmonary disease, sinus bradycardia, heart block, or uncontrolled heart failure. Consultation with a physician is essential before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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