Assess and address
How can patient perceptions of asthma control affect disease management?
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Relvar contains a unique combination of long-lasting molecules – fluticasone furoate and vilanterol.1 This means that once-daily dosing with Relvar provides continuous 24-hour efficacy with no drop in effectiveness towards the end of the 24-hour dosing interval.1–3
This graph has been reprinted by permission of the publisher Informa UK Limited trading as Taylor & Francis Ltd, http://www.tandfonline.com. The original graph was published in David I Bernstein, Eric D Bateman, Ashley Woodcock, William T Toler, Richard Forth, Loretta Jacques, Carol Nunn, Paul M O'Byrne. Fluticasone furoate (FF)/vilanterol (100/25 mcg or 200/25 mcg) or FF (100 mcg) in persistent asthma. Journal of Asthma 2015;52:1073–1083.
Fluticasone furoate and vilanterol are not licensed as monotherapies for patients with asthma in all markets. Relvar is not indicated for the relief of acute bronchospasm.
Reprinted from Respiratory Medicine, Vol 119, Braithwaite I, et al, Randomised, double-blind, placebo-controlled, cross-over single dose study of the bronchodilator duration of action of combination fluticasone furoate/vilanterol inhaler in adult asthma, pp115–121, Copyright © 2016, with permission from Elsevier. The same results were first published in Braithwaite I, et al. Respir Med 2016;119:115–121.
Fluticasone furoate and vilanterol are not licensed as monotherapies for patients with asthma in all markets. Relvar is not indicated for the relief of acute bronchospasm.
Abbreviations
AE, adverse event; CI, confidence interval; FEV1, forced expiratory volume in one second; LS, least square.
Relvar Safety Information4
Contraindications
Hypersensitivity to the active substances or to any of the excipients.
Undesirable effects
Very Common: Headache, Nasopharyngitis.
Common: Infections and infestations, Oropharyngeal pain, Sinusitis, Pharyngitis, Rhinitis, Cough, Dysphonia, Abdominal pain, Arthralgia, Back pain, Fractures, Muscle spasms and Pyrexia.
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Department of Pharmacovigilance & Drug Information |
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PM-RCH-FFV-WCNT-250001 Date of preparation: July 2025