GNH USA

Europe — EMA

Laventair Ellipta

GNH USA supplies Laventair Ellipta (Umeclidinium/Vilanterol), a LAMA/LABA bronchodilator for COPD and asthma maintenance therapy.

Umeclidinium Bromide, Vilanterol

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

What is Umeclidinium Bromide, Vilanterol used for?

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.

What are the side effects of Umeclidinium Bromide, Vilanterol?

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.

What precautions apply to Umeclidinium Bromide, Vilanterol?

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.

What does Umeclidinium Bromide, Vilanterol interact with?

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

What conditions is Laventair Ellipta used for?+
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.
How do the active ingredients umeclidinium bromide and vilanterol work?+
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.
What is the usual dose of Laventair Ellipta?+
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.
Is Laventair Ellipta safe to use during pregnancy or breastfeeding?+
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.
How do I order Laventair Ellipta from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Laventair Ellipta compare with other COPD inhalers?+
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.
What are the storage requirements for Laventair Ellipta?+
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.
How is Laventair Ellipta administered?+
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.
What are the most serious risks associated with Laventair Ellipta?+
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.
Who should not use Laventair Ellipta?+
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.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Umeclidinium Bromide, Vilanterol
Route
Inhalation Use
Manufacturer
Glaxosmithkline Trading Services Limited
Origin
EU

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