Product image of Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord (Montelukast) supplied by GNH India

Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord

Active Ingredient:
Montelukast
Origin:
EU

Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord (Montelukast)

Montelukast, the active ingredient in Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord, is a leukotriene receptor antagonist presented as an oral dosage form for oral use. It is used to manage asthma and allergic rhinitis in children aged 6 to 14 years.
GNH India supplies Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Montelukast is a leukotriene receptor antagonist indicated for respiratory allergic conditions.

  • Asthma: improves long‑term control and reduces the frequency of bronchospasm in pediatric patients.
  • Allergic rhinitis: relieves nasal congestion, sneezing, and itching caused by seasonal or perennial allergens.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing triggered by physical activity in children.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotrienes from binding and triggering bronchoconstriction, vascular permeability, and inflammatory cell recruitment. By inhibiting this pathway, it reduces airway inflammation and hyper‑responsiveness associated with asthma and allergic rhinitis.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate pain often reported.
  • Abdominal pain: discomfort or cramps in the stomach area.
  • Nausea: feeling of queasiness without vomiting.
  • Cough: occasional dry cough.
  • Dizziness: transient light‑headedness.
  • Fatigue: unusual tiredness or lack of energy.

Serious or Rare Side Effects

  • Allergic reactions: rash, urticaria, or angioedema.
  • Neuropsychiatric events: mood changes, anxiety, or suicidal thoughts.
  • Hepatic enzyme elevation: abnormal liver function tests.
  • Hematologic effects: neutropenia or eosinophilia.
  • Stevens‑Johnson syndrome: severe skin blistering.
  • Anaphylaxis: rapid, life‑threatening allergic response.

Precautions & Warnings

Before prescribing Montelukast, clinicians should consider several safety aspects.

  • Assess asthma control: ensure baseline therapy is optimized.
  • Monitor neuropsychiatric symptoms: watch for mood changes or suicidal ideation.
  • Use caution in hepatic impairment: adjust therapy if liver disease is present.
  • Avoid in patients with known hypersensitivity to montelukast or any component of the formulation.
  • Review concomitant medications: consider potential interactions.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Montelukast may interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir): may increase montelukast plasma levels.
  • CYP3A4 inducers (e.g., phenobarbital, rifampicin): may lower therapeutic concentrations.

Moderate Interactions (Monitor Closely)

  • Warfarin: monitor INR as montelukast can affect anticoagulation.
  • Other leukotriene modifiers (e.g., zafirlukast): additive effects may increase risk of side effects.
  • Beta‑agonists: no direct pharmacokinetic interaction, but clinical response should be observed.

Frequently Asked Questions

Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord is a leukotriene receptor antagonist indicated for maintenance treatment of asthma, relief of allergic rhinitis symptoms, and prevention of exercise‑induced bronchoconstriction in children aged 6 to 14 years.

Montelukast blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotrienes from causing bronchial smooth‑muscle contraction, airway edema, and inflammatory cell recruitment. This inhibition reduces airway narrowing and inflammation associated with asthma and allergic rhinitis.

The specific dose of Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord is determined by the prescribing healthcare professional based on the child’s age, weight, and clinical condition. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Montelukast in pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against any possible risks before prescribing to pregnant or nursing mothers, and discuss alternative options when appropriate.

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 offers an oral, once‑daily option that targets leukotriene‑mediated inflammation, unlike inhaled corticosteroids which act on broader inflammatory pathways. It is often used as an add‑on therapy or when inhaled treatments are unsuitable, providing a complementary mechanism of action.

Montelukast 6–14-Vuotiaille Pediatrisille Potilaille Accord should be stored at room temperature, below 25 °C, in its original packaging to protect from moisture and light. Do not store in extreme heat or humidity.

The medication is taken orally, usually as a tablet or chewable form, once daily in the evening as directed by the prescriber. It should be swallowed whole with water unless the formulation specifies otherwise.

Serious risks include rare neuropsychiatric events such as mood changes or suicidal thoughts, severe allergic reactions like anaphylaxis or Stevens‑Johnson syndrome, and liver enzyme abnormalities. Patients should seek immediate medical attention if any of these symptoms appear.

Montelukast is contraindicated in individuals with known hypersensitivity to the drug or any of its excipients. It should also be used with caution in patients with severe hepatic impairment or those who have experienced serious neuropsychiatric reactions to leukotriene modifiers.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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