Demonstration device
Demonstration device for healthcare professionals to show patients how to use the Ellipta device correctly. Visit resources page to order.
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Dosing | The recommended and maximum dose is one inhalation of Trelegy Ellipta 92/55/22 micrograms once daily, at the same time each day. If a dose is missed the next dose should be inhaled at the usual time the next day.4
See below to compare critical errors of commonly used devices
Adapted from Van der Palen J et al. 2016
Open label, placebo inhaler, crossover comparison in patients naïve to Ellipta and the comparator inhaler (p<0.001 for all comparisons)
This study assessed critical errors in the most common type of MDI where shaking prior to use is required. The most common critical error with an MDI was poor actuation and inhalation coordination. *Defined as errors that are likely to result in no, or minimal medication being delivered to the lungs
In another phase IV, randomised, open label, multicentre effectiveness study the percentage of patient at week 24 with >1 critical error in inhaler technique was 6% in the Trelegy treatment group and 3% in the non-Ellipta MITT group. Odds ratio: 1:99; p=0.103(NS)10
Where patients are using several classes of inhalers and poor inhaler technique is identified with once device, the DPI class should be prioritised if the patient is able to use these safely.7
This figure does not represent all inhalers of all possible combinations. Trademarks are the property of their perspective owners.
A single inhaler triple therapy
See how easy it is for patients to use the Ellipta inhaler device as part of daily life.
Trelegy Ellipta Prescribing Information (pdf)
Seretide Accuhaler Prescribing Information (pdf)
Incruse Ellipta Prescribing information (pdf)
Relvar Ellipta Prescribing Information (pdf)
Trelegy Ellipta OD is indicated for maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (COPD) who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting β2-agonist or a combination of a long-acting β2-agonist and a long-acting muscarinic antagonist.4
Seretide accuhaler is indicated for symptomatic treatment of patients with COPD with a FEV1 <60% predicted normal (prebronchodilator) and a history of repeated exacerbations, who have significant symptoms despite regular bronchodilator therapy5
Relvar Ellipta OD is indicated for the symptomatic treatment of adults with COPD with a FEV1<70% predicted normal (post-bronchodilator) and an exacerbation history despite regular bronchodilator therapy.8
Incruse Ellipta OD is indicated for maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD)9
ICS, inhaled corticosteroid; LABA, long-acting β2-agonist; LAMA, long-acting muscarinic antagonist; DPI, dry powder inhaler; MDI, metered-dose inhaler; pMDI, pressurised metered-dose inhaler, OD, once daily.
References
Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/ or search for MHRA Yellowcard in the Google Play or Apple App store. Adverse events should also be reported to GlaxoSmithKline on 0800 221 441.
August 2022 | PM-GB-FVU-WCNT-200008 (V4.0)