Product image of Laberon (Beclometasone Dipropionate, Formoterol Fumarate Dihydrate) supplied by GNH India

Laberon

Active Ingredient:
Beclometasone Dipropionate, Formoterol Fumarate Dihydrate
Origin:
EU

Laberon (Beclometasone Dipropionate, Formoterol Fumarate Dihydrate)

Beclometasone dipropionate, the active ingredient in Laberon, is a combination corticosteroid and long‑acting β2‑agonist presented as an inhalation formulation for inhalation use. It treats asthma and chronic obstructive pulmonary disease (COPD) in adults and children as prescribed.

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

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Laberon is a combination inhaled corticosteroid and long‑acting β2‑agonist used to manage chronic airway diseases.

  • Asthma: improves symptom control and reduces the frequency of exacerbations.
  • Chronic obstructive pulmonary disease (COPD): enhances lung function and decreases dyspnoea during daily activities.
  • Exercise‑induced bronchoconstriction (in patients with asthma): provides prophylactic bronchodilation to maintain airway patency during physical activity.

How It Works

  • Beclometasone dipropionate binds to intracellular glucocorticoid receptors, modulating gene transcription to suppress airway inflammation. Formoterol fumarate selectively stimulates β2‑adrenergic receptors on bronchial smooth muscle, increasing cyclic AMP levels and producing prolonged bronchodilation. The combined actions reduce inflammatory cell infiltration while maintaining airway calibre, supporting long‑term control of asthma and COPD.

Side Effects

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

Common Side Effects

  • Throat irritation or soreness.
  • Hoarseness of voice.
  • Oral candidiasis (thrush).
  • Headache.

Serious or Rare Side Effects

  • Paradoxical bronchospasm.
  • Adrenal suppression with prolonged high‑dose use.
  • Severe allergic reactions such as anaphylaxis.
  • Cardiac arrhythmias or tachycardia.
  • Pneumonia, particularly in patients with COPD.

Precautions & Warnings

Before prescribing Laberon, clinicians should consider several safety aspects.

  • Infection risk: monitor for signs of respiratory infection, especially in COPD patients.
  • Growth monitoring: assess growth velocity in children receiving long‑term therapy.
  • Discontinuation: avoid abrupt cessation; taper if high‑dose corticosteroid therapy is used.
  • Administration technique: advise use of a spacer and mouth‑rinse after inhalation to reduce local effects.
  • Concomitant steroids: limit total systemic corticosteroid exposure.
  • Store at room temperature: keep in the original container, protect from moisture and direct heat.

Avoid Interactions

Laberon can interact with other medicines that affect cardiovascular or steroid pathways.

Major Interactions (Avoid)

  • Non‑selective β‑blockers: may diminish bronchodilator response and precipitate bronchospasm.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir): can increase systemic exposure to beclometasone.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance the risk of hypokalaemia when combined with β2‑agonists.
  • Other inhaled or systemic corticosteroids: increase risk of systemic steroid effects.
  • Monoamine oxidase inhibitors (MAOIs): may potentiate cardiovascular effects of formoterol.
  • Anticholinergic bronchodilators: monitor for additive bronchodilation and potential tachycardia.

Frequently Asked Questions

Laberon is prescribed for the long‑term management of asthma and chronic obstructive pulmonary disease (COPD). It helps control symptoms, reduce exacerbations, and improve lung function when used regularly as part of a maintenance therapy plan.

Beclometasone dipropionate acts as an inhaled corticosteroid that binds glucocorticoid receptors to suppress airway inflammation. Formoterol fumarate is a long‑acting β2‑agonist that activates β2‑adrenergic receptors, causing sustained bronchodilation. Together they provide anti‑inflammatory and bronchodilatory effects.

The dose of Laberon is individualized by the prescribing healthcare professional based on disease severity, patient age, and response to therapy. Patients should follow the specific instructions provided by their prescriber and the product label.

Safety data for Laberon in pregnancy and lactation are limited. The prescriber should weigh the potential benefits against any possible risks to the fetus or infant. If treatment is necessary, it should be used under close medical supervision.

To request Laberon, 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 (including any cold‑chain requirements) and import documentation.

Laberon combines an inhaled corticosteroid with a long‑acting β2‑agonist in a single device, offering convenience over separate inhalers. Compared with monotherapy agents, the combination provides both anti‑inflammatory and bronchodilator actions, which can improve adherence and overall disease control in asthma and COPD.

Laberon should be stored at room temperature, below 25 °C, in its original packaging. Keep the inhaler away from moisture, direct sunlight, and excessive heat to maintain product integrity.

Laberon is delivered by inhalation using a dry‑powder inhaler or similar device. Patients should inhale a full dose as instructed, use a spacer if recommended, and rinse their mouth after each use to reduce the risk of local side effects.

Serious risks include paradoxical bronchospasm, adrenal suppression with prolonged high‑dose use, severe allergic reactions such as anaphylaxis, and cardiac effects like tachycardia or arrhythmias. Patients should seek immediate medical attention if they experience these symptoms.

Laberon is contraindicated in patients with known hypersensitivity to beclometasone, formoterol, or any excipients in the inhaler. It should also be avoided in individuals who have experienced a severe allergic reaction to other inhaled corticosteroids or long‑acting β2‑agonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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