Product image of Montelukast Accord Healthcare Ireland (Montelukast) supplied by GNH India

Montelukast Accord Healthcare Ireland

Active Ingredient:
Montelukast
Origin:
EU

Montelukast Accord Healthcare Ireland (Montelukast)

Montelukast, the active ingredient in Montelukast Accord Healthcare Ireland, is a leukotriene receptor antagonist presented as an oral tablet for oral use. It treats asthma, allergic rhinitis and exercise‑induced bronchoconstriction in adults and children as prescribed.

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

Manufacturer / TM Owner

Accord Healthcare Ireland Limited

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Indications & Clinical Uses

Montelukast is a leukotriene receptor antagonist used to manage respiratory allergic conditions.

  • Asthma: Improves control of chronic asthma and reduces frequency of exacerbations.
  • Allergic rhinitis: Relieves nasal congestion, sneezing and itching associated with seasonal or perennial allergic rhinitis.
  • Exercise‑induced bronchoconstriction: Prevents airway narrowing triggered by physical activity.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor type 1 (CysLT1) on airway smooth‑muscle cells, mast cells and eosinophils. By antagonising this receptor, it prevents leukotriene D4‑mediated bronchoconstriction, mucus secretion and inflammatory cell recruitment, thereby reducing airway hyper‑responsiveness, vascular permeability and edema in the respiratory mucosa.

Side Effects

Montelukast may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Upper respiratory tract infection: sore throat or nasal congestion.
  • Abdominal pain: stomach discomfort.
  • Diarrhoea: loose stools.

Serious or Rare Side Effects

  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Mood changes: depression, anxiety, or suicidal thoughts.
  • Hepatotoxicity: elevated liver enzymes or hepatitis.
  • Angioedema: swelling of lips, tongue or face.

Precautions & Warnings

When prescribing Montelukast, clinicians should consider several safety precautions to minimise risk.

  • Assess asthma control: ensure patient’s asthma is adequately managed before initiating therapy.
  • Monitor for mood changes: watch for signs of depression or suicidal ideation.
  • Evaluate liver function: consider baseline hepatic assessment in patients with liver disease.
  • Use with caution in the elderly: adjust monitoring due to potential comorbidities.
  • Avoid in known hypersensitivity: discontinue if allergic reaction occurs.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Phenobarbital, carbamazepine, rifampin: strong enzyme inducers that may reduce montelukast plasma levels.
  • Ritonavir or other potent CYP3A4 inhibitors: may increase montelukast exposure and risk of adverse effects.

Moderate Interactions (Monitor Closely)

  • Warfarin: possible alteration of anticoagulant effect; monitor INR.
  • Theophylline: additive bronchodilator effects; observe for increased side effects.
  • Antidepressants (e.g., fluoxetine): potential for enhanced central nervous system effects.

Frequently Asked Questions

Montelukast is prescribed to manage chronic asthma, relieve symptoms of allergic rhinitis, and prevent exercise‑induced bronchoconstriction. By targeting leukotriene‑mediated inflammation, it helps reduce airway narrowing and nasal congestion in patients with these respiratory conditions.

Montelukast works by selectively blocking the cysteinyl leukotriene receptor CysLT1. This inhibition prevents leukotriene D4 from binding, thereby reducing bronchoconstriction, mucus production, and inflammatory cell recruitment that contribute to asthma and allergic airway disease.

The dose of Montelukast is determined by the prescribing clinician based on the patient’s age, condition and response to therapy. Healthcare professionals follow approved labeling and clinical guidelines to select the appropriate strength and dosing schedule.

Safety data for Montelukast in pregnancy and lactation are limited. Prescribers weigh the potential benefits against any unknown risks and may choose alternative therapies if concerns arise. Women should discuss their specific situation with a healthcare provider.

To 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 or long‑acting beta‑agonists for asthma control. While inhaled steroids target broader inflammation, Montelukast specifically blocks leukotriene pathways, which can be advantageous for patients with aspirin‑exacerbated respiratory disease or those preferring oral therapy.

Montelukast tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture and direct sunlight to maintain stability throughout the shelf life.

Montelukast is taken orally as a tablet, swallowed whole with or without food. The exact timing (e.g., evening dosing) is guided by the prescriber and may depend on the specific indication.

Serious adverse events include allergic reactions such as rash, swelling or anaphylaxis, mood alterations like depression or suicidal thoughts, and rare liver injury. Patients should seek immediate medical attention if they experience any of these symptoms.

Montelukast is contraindicated in individuals with known hypersensitivity to the drug or any of its excipients. Caution is also advised for patients with severe liver impairment or those who have experienced serious psychiatric side effects while on the medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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