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RESPIRATORY SYSTEM › DRUGS FOR OBSTRUCTIVE AIRWAY DISEASES › ADRENERGICS, INHALANTS › Adrenergics in combination with anticholinergics incl. triple combinations with corticosteroids
vilanterol and umeclidinium bromide
R03AL03
Forms & Strengths
- Inhalation powder: umeclidinium 62.5 mcg / vilanterol 25 mcg per actuation
Adult Dosing
- Chronic Obstructive Pulmonary Disease (COPD): 1 inhalation (62.5 mcg/25 mcg) once daily orally at the same time of day
Pediatric Dosing
- Safety and efficacy in pediatric patients (<18 years) have not been established; not indicated for use in children
Indications
- Long-term, once-daily, maintenance treatment of airflow obstruction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and/or emphysema
- Reduction of COPD exacerbations
Mechanism of Action
- Umeclidinium is a long-acting muscarinic antagonist (LAMA) that inhibits the muscarinic M3 receptor on airway smooth muscle, causing bronchodilation
- Vilanterol is a long-acting beta2-adrenergic agonist (LABA) that stimulates intracellular adenylate cyclase, increasing cyclic AMP and causing smooth muscle relaxation and bronchodilation
Contraindications
- Hypersensitivity to umeclidinium, vilanterol, or any component of the formulation
- Severe hypersensitivity to milk proteins (contains lactose)
Adverse Reactions
- Nasopharyngitis
- Upper respiratory tract infection
- Headache
- Cough
- Paradoxical bronchospasm
- Worsening of narrow-angle glaucoma
- Urinary retention
Drug Interactions
- Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir): May increase systemic exposure to vilanterol, increasing cardiovascular adverse effects; use with caution
- Beta-blockers: May antagonize the therapeutic effects of vilanterol and produce severe bronchospasm in COPD patients; cardioselective beta-blockers should be used only if medically necessary
- Other anticholinergic agents: Concomitant use may potentiate anticholinergic adverse effects such as dry mouth, constipation, and urinary retention
Curated Content: Needs Vetting Before Put to Clinical Use