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

Lenigron

Active Ingredient:
Timolol, Bimatoprost
Origin:
EU

Lenigron (Timolol, Bimatoprost)

Timolol and Bimatoprost, the active ingredients in Lenigron, are a beta‑blocker and a prostaglandin analog presented as eye drops for ocular use. They are indicated for the management of primary open‑angle glaucoma and ocular hypertension, helping to lower intra‑ocular pressure and protect the optic nerve.
GNH India supplies Lenigron as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Pharmathen S.A.

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Indications & Clinical Uses

Lenigron is used in ophthalmology to control intra‑ocular pressure in glaucoma‑related conditions.

  • Primary open‑angle glaucoma: lowers intra‑ocular pressure to prevent optic‑nerve damage.
  • Ocular hypertension: reduces pressure to decrease the risk of progression to glaucoma.
  • Secondary open‑angle glaucoma: assists in achieving target pressure when other therapies are insufficient.

How It Works

  • Timolol blocks non‑selective β‑adrenergic receptors in the ciliary body, decreasing aqueous humor production. Bimatoprost, a prostaglandin F2α analogue, enhances uveoscleral outflow of aqueous humor. The combined actions result in a greater reduction of intra‑ocular pressure than either agent alone.

Side Effects

Lenigron may cause ocular and systemic adverse reactions.

Common Side Effects

  • Eye redness: mild conjunctival hyperemia.
  • Eye irritation: burning or stinging sensation.
  • Blurred vision: temporary visual disturbance.
  • Eyelash growth: increased length and thickness.
  • Darkening of iris: gradual pigmentation change.
  • Foreign body sensation: feeling of grit in the eye.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling, rash, or difficulty breathing.
  • Increased intra‑ocular pressure: paradoxical rise requiring medical attention.
  • Persistent eye pain: may indicate corneal involvement.
  • Corneal edema: swelling of the cornea affecting vision.
  • Uveitis: inflammation of the uveal tract.
  • Systemic beta‑blocker effects: bradycardia, hypotension, or bronchospasm.

Precautions & Warnings

Before prescribing Lenigron, clinicians should consider patient‑specific factors and monitor for adverse events.

  • Cardiovascular assessment: evaluate for bradycardia or heart block.
  • Respiratory status: avoid in patients with asthma or severe COPD.
  • Intra‑ocular pressure monitoring: check pressure after initiation and periodically.
  • Concurrent ocular surgery: discontinue before and after procedures as advised.
  • Use with other beta‑blockers: monitor for additive systemic effects.
  • Store at room temperature: keep bottle tightly closed, protect from light and moisture.

Avoid Interactions

Lenigron can interact with other medications that affect ocular pressure or systemic beta‑adrenergic activity.

Major Interactions (Avoid)

  • Systemic non‑selective beta‑blockers (e.g., propranolol): may cause excessive bradycardia.
  • Other ocular beta‑blocker drops: risk of over‑suppression of aqueous production.
  • Topical adrenergic agonists (e.g., phenylephrine): may reduce the IOP‑lowering effect.

Moderate Interactions (Monitor Closely):\n- Carbonic anhydrase inhibitor eye drops: additive IOP‑lowering effect, monitor pressure.

  • Topical corticosteroids: may increase risk of cataract or glaucoma.
  • Antihistamine eye drops: possible reduced efficacy of prostaglandin component.

Frequently Asked Questions

Lenigron is an ophthalmic eye‑drop containing Timolol and Bimatoprost that is prescribed to lower intra‑ocular pressure in patients with primary open‑angle glaucoma or ocular hypertension, helping to prevent optic‑nerve damage.

Timolol reduces aqueous humor production by blocking β‑adrenergic receptors in the ciliary body, while Bimatoprost increases uveoscleral outflow as a prostaglandin F2α analogue. Together they achieve a greater reduction in intra‑ocular pressure than either agent alone.

The dosing regimen for Lenigron is determined by the prescribing eye‑care professional based on the individual’s condition and response. Typically, one drop is instilled in the affected eye(s) once daily, but the exact schedule should follow the prescriber’s instructions.

Safety data for Lenigron in pregnancy and lactation are limited. It should only be used 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 Lenigron, submit an enquiry 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 required import documentation.

Lenigron combines a beta‑blocker (Timolol) with a prostaglandin analogue (Bimatoprost), offering dual mechanisms of action. Compared with single‑agent drops, this combination often provides greater intra‑ocular pressure reduction, potentially reducing the need for multiple separate medications.

Lenigron should be stored at room temperature, below 25 °C, in its original container. Keep the bottle tightly closed, protect it from light and moisture, and discard any solution that appears discolored or contains particles.

Lenigron is applied as a topical eye‑drop. The patient should wash hands, tilt the head back, pull down the lower eyelid to form a pocket, and instill one drop into each prescribed eye. Close the eye gently for a few seconds without blinking excessively.

Serious risks include severe allergic reactions, paradoxical increase in intra‑ocular pressure, corneal edema, uveitis, and systemic beta‑blocker effects such as bradycardia, hypotension, or bronchospasm. Any of these symptoms require immediate medical attention.

Lenigron is contraindicated in patients with known hypersensitivity to Timolol, Bimatoprost, or any excipients, as well as those with severe asthma, chronic obstructive pulmonary disease, sinus bradycardia, or second‑ or third‑degree heart block without appropriate cardiac monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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