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TRELEGY Ellipta addresses undertreated bronchoconstriction in asthma¹

Single-inhaler Triple Therapy that delivers the additional benefit of LAMA along with ICS/LABA for adult asthma patients uncontrolled on ICS/LABA, significantly improving lung function and enabling more patients to achieve asthma control vs. an ICS/LABA (FF/VI).1,2 These are the three components that make up TRELEGY Ellipta:

Fluticasone furoate

Inhaled corticosteroid (ICS)

fluticasone

Vilanterol

Long-acting β2-adrenergic agonist (LABA)

vilanterol

Umeclidinium

Long-acting muscarinic antagonist (LAMA)

umeclidinium

TRELEGY Ellipta – Triple Therapy that opens the airways and keeps them open¹

triple therapy

A maintenance treatment for asthma that has three complementary modes of action

Watch how the ICS, LABA and LAMA in TRELEGY Ellipta address both inflammation and bronchoconstriction in asthma

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Trelegy Succinct Safety Information:

Contraindications: Hypersensitivity to the active substances or to any of the excipients (lactose monohydrate and magnesium stearate) or patients with severe milk-protein allergy. Warnings & Precautions: Asthma: Should not be used to treat acute asthma symptoms or an acute exacerbation in COPD for which a short-acting bronchodilator is required. COPD: Should not be used to treat an acute exacerbation in COPD for which a short-acting bronchodilator is required. Patients should not stop therapy with Trelegy Ellipta, in asthma or COPD, without physician supervision since symptoms may recur after discontinuation. Discontinue Trelegy if paradoxical bronchospasm occurs and institute alternative therapy if necessary. Cardiovascular effects, such as cardiac arrhythmias e.g. atrial fibrillation and tachycardia, may be seen after the administration of muscarinic receptor antagonists or sympathomimetics, use with caution in patients with unstable or life-threatening cardiovascular disease. Monitor patients with moderate to severe hepatic impairment for systemic corticosteroid-related adverse reactions and the 100/62.5/25 micrograms dose should be used. Systemic effects may occur, particularly at high doses for long periods, but much less likely than with oral corticosteroids. Possible systemic effects include HPA suppression, decrease in bone mineral density, cataract, glaucoma, central serous chorioretinopathy and more rarely, a range of psychological or behavioural effects including psychomotor hyperactivity, sleep disorders, anxiety, depression or aggression. Use with caution in patients with urinary retention, narrow angle glaucoma, pulmonary tuberculosis or with chronic or untreated infections. hyperglycaemia and severe hepatic impairment. Consider risk factors for pneumonia in patients with COPD before prescribing, and re-evaluate treatment if pneumonia occurs. Adverse Reactions: Very Common: Nasopharyngitis. Common: Urinary tract infection, sinusitis, pharyngitis, upper respiratory tract infection, headache, cough, oropharyngeal pain, dysphonia, constipation, pneumonia, bronchitis, rhinitis, influenza, candidiasis of mouth and throat, arthralgia, back pain, viral respiratory tract infection. Uncommon: dry mouth, dysgeusia, atrial fibrillation, supraventricular tachyarrythmia, tachycardia, fractures.

Version number: GDS12/IPI13a(SI)

Footnotes

FF, fluticasone furoate; GINA, Global Initiative for Asthma; ICS, inhaled corticosteroid; LABA, long-acting β₂-adrenergic agonist; LAMA, long-acting muscarinic antagonist; VI, vilanterol

TRELEGY Ellipta is indicated for the maintenance treatment of asthma in patients aged 18 years and older who are not adequately controlled with a combination of a LABA and ICS.2

References

  1. Pavord I et al. Abstract 785. J Allergy Clin Immunol 2020; 145:AB241.
  2. TRELEGY Ellipta Singapore Prescribing Information GDS12/IPI13a (SI).
  3. Global Initiative for Asthma. Global Strategy for Asthma Management and Prevention, 2023. Available at: www.ginasthma.org (Accessed February 2024).

Adverse events should be reported. For reporting of adverse events, please write to sg.drugsafety@gsk.com

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PM-SG-FVU-WCNT-240017 | April 2024