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Respiratory products

Please find a list of our respiratory products below.

Trelegy Ellipta (fluticasone furoate/umeclidinium/vilanterol inhalation powder)

Prescribing Information

Trelegy Ellipta (92/55/22 micrograms inhalation powder) is a combination of inhaled corticosteroid, long-acting muscarinic receptor antagonist and long-acting beta2-adrenergic agonist (ICS/LAMA/LABA) and is indicated for maintenance treatment in adult patients with moderate to severe COPD who are not adequately treated by a combination of an ICS and a LABA or a combination of a LAMA and a LABA. 

Anoro Ellipta (umeclidinium / vilanterol inhalation powder)

Prescribing information

Anoro Ellipta (55 micrograms/22 micrograms inhalation powder) is a long-acting muscarinic receptor antagonist/long-acting beta2-adrenergic agonist (LAMA/LABA) and is indicated as a maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD).

Incruse Ellipta (umeclidinium inhalation powder)

Prescribing information

Incruse Ellipta (55 micrograms inhalation powder) is a long acting muscarinic receptor antagonist and is indicated as a maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease.

Relvar Ellipta (fluticasone furoate/vilanterol inhalation powder)

Relvar 184/22 mcg Prescribing information

Relvar 92/22 mcg summary of product characteristics

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

Relvar Ellipta (92/22mcg inhalation powder) 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.

Nucala (mepolizumab)

Prescribing information

Nucala is indicated as an add-on treatment for severe refractory eosinophilic asthma in adults, adolescents and children aged 6 years and older.
The recommended dose of Nucala is 100mg SC once every 4 weeks in adults and adolescents 12 years and older, available in pre-filled pen, pre-filled syringe or as a lyophilised powder.
The pre-filled formulations are not indicated in 6-11 year olds.

Seretide Accuhaler and Evohaler devices

Seretide (salmeterol xinafoate / fluticasone propionate)

Seretide 50/100, 50/250, 50/500 Diskus

Prescribing information

Asthma

Seretide is indicated in the regular treatment of asthma where use of a combination product (long- acting β2 agonist and inhaled corticosteroid) is appropriate:

  • patients not adequately controlled with inhaled corticosteroids and 'as needed' inhaled short-acting β2 agonist

or

  • patients already adequately controlled on both inhaled corticosteroid and long-acting β2 agonist

Note: Seretide 50 microgram /100 microgram strength is not appropriate in adults and children with severe asthma.

Seretide 500/50 Diskus

Chronic Obstructive Pulmonary Disease (COPD)

Seretide is indicated for the symptomatic treatment of patients with COPD, with a FEV1 <60% predicted normal (pre-bronchodilator) and a history of repeated exacerbations, who have significant symptoms despite regular bronchodilator therapy.

Seretide 25/50, 25/125, 25/250 Evohaler

Prescribing information

Asthma

Seretide is indicated in the regular treatment of asthma where use of a combination product (long-acting β2 agonist and inhaled corticosteroid) is appropriate:

  • patients not adequately controlled with inhaled corticosteroids and 'as needed' inhaled short- acting β2 agonist

or

  • patients already adequately controlled on both inhaled corticosteroid and long-acting β2 agonist

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.