Data from EMA (European Medicines Agency) - Curated by EPG Health - Last updated 23 August 2018

Indication(s)

- Relvar Ellipta 92 micrograms/22 micrograms inhalation powder, pre-dispensed

Asthma
Relvar Ellipta is indicated for the regular treatment of asthma in adults and adolescents aged 12 years and older where use of a combination medicinal product (long-acting beta2-agonist and inhaled corticosteroid) is appropriate:
• patients not adequately controlled with inhaled corticosteroids and 'as needed' inhaled short acting beta2-agonists.
• patients already adequately controlled on both inhaled corticosteroid and long-acting beta2-agonist.

COPD (Chronic Obstructive Pulmonary Disease)
Relvar Ellipta is indicated for the symptomatic treatment of adults with COPD with a FEV1<70% predicted normal (post-bronchodilator) with an exacerbation history despite regular bronchodilator therapy.



- Relvar Ellipta 184 micrograms/22 micrograms inhalation powder, pre-dispensed

Asthma
Relvar Ellipta is indicated for the regular treatment of asthma in adults and adolescents aged 12 years and older where use of a combination medicinal product (long-acting beta2-agonist and inhaled corticosteroid) is appropriate:
• patients not adequately controlled with inhaled corticosteroids and 'as needed' inhaled short acting beta2-agonists.
• patients already adequately controlled on both inhaled corticosteroid and long-acting beta2-agonist.

Full Prescribing information

Learning Zones

An epgonline.org Learning Zone (LZ) is an area of the site dedicated to providing detailed self-directed medical education about a disease, condition or procedure.

Chronic Obstructive Pulmonary Disease (COPD)

Chronic Obstructive Pulmonary Disease (COPD)

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Moderate to severe asthma

Moderate to severe asthma

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Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis

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More information

Category Value
Agency product number EMEA/H/C/002673
Orphan designation No
Date First Approved 13-11-2013
Type Medicinal product subject to medical prescription
Marketing authorisation holder Glaxo Group Ltd
Warnings This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions