Product image of Montelucaste Azevedos (Montelukast) supplied by GNH India

Montelucaste Azevedos

Active Ingredient:
Montelukast
Origin:
EU

Montelucaste Azevedos (Montelukast)

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

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

Manufacturer / TM Owner

Laboratórios Azevedos - Indústria Farmacêutica, S.A.

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Indications & Clinical Uses

Montelukast acts on the leukotriene pathway to reduce airway inflammation and bronchoconstriction.

  • Asthma (maintenance therapy): improves long‑term control and reduces exacerbations.
  • Allergic rhinitis: alleviates nasal congestion, sneezing and itching.
  • Exercise‑induced bronchoconstriction: prevents airway narrowing triggered by physical activity.

How It Works

  • Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1, preventing leukotrienes from binding and triggering bronchoconstriction, mucus secretion, and inflammatory cell recruitment. By inhibiting this pathway, it reduces airway edema and hyperresponsiveness, contributing to better respiratory function in asthma and allergic conditions.

Side Effects

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

Common Side Effects

  • Headache: mild to moderate intensity.
  • Abdominal pain: occasional discomfort.
  • Cough: transient irritation.
  • Fever: low‑grade elevations.
  • Sore throat: mild irritation.
  • Nausea: occasional upset stomach.

Serious or Rare Side Effects

  • Angioedema: swelling of face, lips or tongue.
  • Allergic reactions: rash, urticaria, or anaphylaxis.
  • Mood changes: depression, anxiety, or suicidal thoughts.
  • Hepatic injury: rare elevation of liver enzymes.
  • Severe bronchospasm: paradoxical worsening of breathing.
  • Stevens‑Johnson syndrome: rare severe skin reaction.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety aspects.

  • Assess asthma control: ensure patient is stable on current regimen.
  • Monitor for allergic reactions: watch for rash or swelling after first doses.
  • Evaluate liver function: consider baseline tests in patients with hepatic disease.
  • Caution in psychiatric history: monitor mood and suicidal ideation.
  • Avoid in known hypersensitivity: discontinue if severe reaction occurs.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Montelukast may interact with other medicines, requiring attention to dosage and monitoring.

Major Interactions (Avoid)

  • Rifampin, phenobarbital, carbamazepine: strong CYP3A4 inducers that markedly reduce montelukast exposure.
  • St. John's wort: herbal inducer that may diminish therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Fluconazole, ketoconazole: CYP3A4 inhibitors that can increase montelukast plasma levels.
  • SSRIs or SNRIs: may heighten risk of neuropsychiatric events.
  • NSAIDs: concurrent use may increase bronchospasm risk in sensitive individuals.
  • Warfarin: occasional reports of altered INR; monitor coagulation if combined.

Frequently Asked Questions

Montelucaste Azevedos contains montelukast, which is prescribed for maintenance therapy of asthma, relief of allergic rhinitis symptoms, and prevention of exercise‑induced bronchoconstriction. It helps control airway inflammation and reduces the frequency of asthma attacks and allergy‑related nasal symptoms.

Montelukast selectively blocks the cysteinyl leukotriene receptor CysLT1. By preventing leukotrienes from binding, it stops the cascade that leads to bronchoconstriction, mucus production, and airway inflammation, thereby improving breathing and reducing allergic responses.

The specific dose of Montelucaste Azevedos is determined by the prescribing healthcare professional based on the patient’s age, condition severity, and response to therapy. 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 weigh potential benefits against unknown risks before prescribing it to pregnant or nursing individuals. Patients should discuss their situation with a qualified clinician.

To request Montelucaste Azevedos, submit an enquiry on the product page at gnhindia.com, indicating 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. It is especially useful for patients with aspirin‑sensitive asthma or those who prefer a non‑inhaled maintenance option, though it may be less potent for severe persistent asthma.

Montelucaste Azevedos should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain its stability and potency.

Montelucaste Azevedos is taken orally, usually once daily, with or without food, as directed by the prescriber. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed.

Serious risks include rare but severe allergic reactions such as angioedema, mood alterations including depression or suicidal thoughts, and hepatic injury. Patients should seek immediate medical attention if they experience swelling, rash, severe mood changes, or signs of liver dysfunction.

Montelucaste Azevedos is contraindicated in individuals with known hypersensitivity to montelukast or any of the tablet’s excipients. It should also be avoided in patients who have experienced severe allergic reactions to leukotriene‑modifying agents.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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