Product image of Montelukast Eg (Montelukast) supplied by GNH India

Montelukast Eg

Active Ingredient:
Montelukast
Origin:
EU

Montelukast Eg (Montelukast)

Montelukast, the active ingredient in Montelukast Eg, is a leukotriene receptor antagonist presented as an oral dosage form for oral use. It is used to manage asthma, allergic rhinitis, and exercise‑induced bronchoconstriction in patients who require maintenance therapy.

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

Manufacturer / TM Owner

Eg S.P.A.

1
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Indications & Clinical Uses

Montelukast acts on the leukotriene pathway to control chronic respiratory conditions.

  • Asthma: provides maintenance therapy that reduces the frequency of exacerbations and improves lung function.
  • Allergic rhinitis: relieves nasal congestion, sneezing and itching associated with seasonal or perennial allergies.
  • Exercise‑induced bronchoconstriction: prevents bronchospasm triggered by physical activity, allowing better exercise tolerance.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotriene D4 from binding. This inhibition reduces leukotriene‑mediated bronchoconstriction, vascular permeability, and inflammatory cell recruitment in the airways, thereby improving respiratory function and decreasing allergic inflammation.

Side Effects

Montelukast is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate pain often resolves without intervention.
  • Abdominal pain: discomfort in the stomach area, usually transient.
  • Cough: occasional irritation of the throat.
  • Nausea: feeling of queasiness, may improve with food.
  • Dizziness: light‑headed sensation, typically short‑lived.
  • Fatigue: mild tiredness.

Serious or Rare Side Effects

  • Allergic reactions: rash, angioedema, or anaphylaxis requiring immediate medical attention.
  • Mood changes: depression, anxiety, or suicidal thoughts, especially in children.
  • Liver enzyme elevation: abnormal liver function tests, monitor if symptomatic.
  • Stevens‑Johnson syndrome: severe skin reaction, rare but requires urgent care.

Precautions & Warnings

Before initiating therapy, consider the following safety measures.

  • Assess liver function: monitor patients with existing hepatic disease.
  • Review psychiatric history: observe for mood alterations or depressive symptoms.
  • Use caution in pregnancy: discuss potential risks with the prescriber.
  • Avoid in known hypersensitivity: discontinue if allergic reaction occurs.
  • Adjust in severe renal impairment: consider dose evaluation.
  • Store below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Montelukast may interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Rifampin: induces metabolism, reducing montelukast levels.
  • Phenobarbital: increases hepatic clearance, lowering effectiveness.
  • Carbamazepine: accelerates metabolism, potentially decreasing therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Ketoconazole: may increase montelukast concentrations.
  • Oral contraceptives: montelukast may reduce contraceptive efficacy, requiring additional protection.

Frequently Asked Questions

Montelukast Eg is prescribed for the long‑term management of asthma, relief of symptoms associated with allergic rhinitis, and prevention of exercise‑induced bronchoconstriction. It helps reduce airway inflammation and bronchospasm, improving breathing and quality of life for patients with these respiratory conditions.

Montelukast works by selectively blocking the cysteinyl leukotriene receptor CysLT1. This prevents leukotriene D4 from binding, which in turn reduces bronchoconstriction, mucus production, and inflammatory cell recruitment in the airways, leading to improved airflow and decreased allergic inflammation.

The appropriate dose of Montelukast Eg is determined by the prescribing healthcare professional based on the patient’s age, condition severity, and clinical response. Dosage instructions are individualized and should be followed exactly as written on the prescription label.

The safety of Montelukast during pregnancy and lactation has not been definitively established. Healthcare providers weigh potential benefits against possible risks, and the decision to use the medication should be made in consultation with a qualified prescriber.

To place an order, 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.

Montelukast belongs to the leukotriene receptor antagonist class, offering an oral alternative to inhaled corticosteroids and long‑acting beta‑agonists. It is particularly useful for patients with aspirin‑exacerbated respiratory disease or those who prefer a non‑inhaled maintenance option, though it may be used in combination with other therapies for optimal control.

Montelukast Eg should be stored below 25 °C in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the tablet’s stability and potency throughout its shelf life.

Montelukast Eg is taken orally, usually once daily in the evening, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed by a healthcare professional.

Serious risks, though rare, include severe allergic reactions such as rash, angioedema, or anaphylaxis, and neuropsychiatric events like depression, anxiety, or suicidal thoughts. Patients should seek immediate medical attention if they experience any of these symptoms.

Montelukast Eg should be avoided in individuals with known hypersensitivity to montelukast or any of its excipients. It is also contraindicated in patients who have experienced severe allergic reactions to the drug in the past.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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