Product image of Laventair Ellipta (Umeclidinium Bromide, Vilanterol) supplied by GNH India

Laventair Ellipta

Active Ingredient:
Umeclidinium Bromide, Vilanterol
Origin:
EU

Laventair Ellipta (Umeclidinium Bromide, Vilanterol)

Umeclidinium bromide / Vilanterol, the active ingredients in Laventair Ellipta, are a Long‑acting muscarinic antagonist (LAMA) and Long‑acting β2‑agonist (LABA) combination presented as a 62.5 µg umeclidinium bromide / 25 µg vilanterol dry powder inhaler (Ellipta device) for inhalation use. It treats chronic obstructive pulmonary disease (COPD) and asthma as maintenance therapy in adults.

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

Manufacturer / TM Owner

Glaxosmithkline Trading Services Limited

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Indications & Clinical Uses

Laventair Ellipta is indicated for maintenance bronchodilation in chronic airway diseases.

  • Chronic obstructive pulmonary disease (COPD): improves lung function, reduces exacerbation frequency, and enhances exercise tolerance.
  • Asthma (maintenance therapy): provides long‑term bronchodilation and helps achieve better symptom control.
  • Chronic bronchitis (as part of COPD): maintains airway patency and reduces cough severity.

How It Works

  • Umeclidinium bromide selectively blocks muscarinic M3 receptors on airway smooth muscle, preventing acetylcholine‑mediated bronchoconstriction. Vilanterol activates β2‑adrenergic receptors, stimulating adenylate cyclase, increasing intracellular cAMP, and causing relaxation of bronchial smooth muscle. The combined LAMA/LABA action produces sustained bronchodilation and improves airflow in the lower respiratory tract.

Side Effects

Common Side Effects

  • Cough or throat irritation: mild irritation after inhalation.
  • Headache: transient, often resolves without intervention.
  • Dry mouth: reduced salivation due to anticholinergic activity.
  • Nasopharyngitis: upper respiratory tract infection symptoms.
  • Upper respiratory tract infection: mild viral‑like symptoms.

Serious or Rare Side Effects

  • Paradoxical bronchospasm: sudden worsening of breathing requiring immediate medical attention.
  • Tachycardia or arrhythmia: rapid or irregular heart rhythm.
  • Severe hypersensitivity reactions: rash, swelling, or anaphylaxis.
  • Angioedema: swelling of lips, tongue, or throat.
  • Cardiovascular events: chest pain or myocardial ischemia in susceptible patients.

Precautions & Warnings

Before prescribing Laventair Ellipta, consider the following precautions:

  • Cardiovascular assessment: evaluate patients with known heart disease for potential tachycardia.
  • COPD severity monitoring: watch for worsening symptoms or frequent exacerbations.
  • History of paradoxical bronchospasm: avoid use if previously experienced.
  • Hepatic impairment: use with caution in severe liver disease.
  • Known hypersensitivity: do not administer to patients allergic to either component.
  • Store at room temperature: keep in original blister, protect from moisture and heat.

Avoid Interactions

Laventair Ellipta may interact with other medicines. Review patient medication lists carefully.

Major Interactions (Avoid)

  • Beta‑blockers: may diminish bronchodilator effect and increase risk of bronchospasm.
  • Other long‑acting muscarinic antagonists: additive anticholinergic effects can lead to dry mouth, urinary retention, or glaucoma.

Moderate Interactions (Monitor Closely)

  • Diuretics: may exacerbate dry mouth and dehydration.
  • Theophylline: vilanterol can increase plasma theophylline levels, requiring dose adjustment.
  • Anticholinergic eye drops: may increase systemic anticholinergic load, leading to blurred vision or urinary retention.

Frequently Asked Questions

Laventair Ellipta is prescribed as a maintenance inhaler for adults with chronic obstructive pulmonary disease (COPD) and for long‑term control of asthma. It helps keep the airways open, reduces the frequency of exacerbations, and improves overall breathing stability.

Umeclidinium bromide blocks muscarinic M3 receptors, preventing acetylcholine‑induced bronchoconstriction. Vilanterol stimulates β2‑adrenergic receptors, increasing cyclic AMP and causing smooth‑muscle relaxation. Together they provide sustained bronchodilation, improving airflow in the lungs.

The prescribed dose of Laventair Ellipta is determined by the treating physician based on the patient’s disease severity and response to therapy. The inhaler delivers a fixed combination of 62.5 µg umeclidinium bromide and 25 µg vilanterol per inhalation.

Safety data for Laventair Ellipta in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

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.

Laventair Ellipta combines a LAMA (umeclidinium) and a LABA (vilanterol) in a single inhaler, offering the convenience of dual bronchodilation. Compared with single‑component inhalers, it may provide greater symptom control and fewer devices for patients, though individual response varies.

Store the inhaler at room temperature, below 25 °C, in its original packaging. Keep it away from moisture, direct sunlight, and excessive heat to maintain dose integrity and device functionality.

Laventair Ellipta is a dry‑powder inhaler. The patient opens the Ellipta device, exhales fully away from the inhaler, places the mouthpiece in the mouth, and inhales forcefully and deeply. The inhaler is then closed to protect the dose until the next use.

Serious risks include paradoxical bronchospasm, which can worsen breathing suddenly, and cardiovascular events such as tachycardia or arrhythmia. Severe hypersensitivity reactions, including anaphylaxis and angioedema, also require immediate medical attention.

Patients with a known hypersensitivity to umeclidinium, vilanterol, or any excipients in the inhaler should avoid use. It is also contraindicated in individuals who have experienced a paradoxical bronchospasm with similar bronchodilators.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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