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Real-life effectiveness and safety of salbutamol Steri-Neb™ vs. Ventolin Nebules® for exacerbations in patients with COPD: Historical cohort study

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  • David B Price
  • Eran Gefen
  • Gokul Gopalan
  • Rosie McDonald
  • Vicky Thomas
  • Simon Wan Yau Ming
  • Emily Davis

Abstract

Introduction: Ventolin Nebules® (reference product; GlaxoSmithKline) was the first licensed nebulizer solution containing the rapid-onset, short-acting β2-agonist salbutamol. Salbutamol Steri-Neb™ (comparator; Teva Pharmaceuticals, Inc.) has the same chemical composition as the reference product. This study evaluated whether the effectiveness of the comparator is non-inferior to the reference product alongside concomitant medications during real-life clinical management of COPD exacerbations. Safety in terms of adverse events (AEs) was also examined. Methods: This matched (1:1) historical cohort study evaluated data from 2 UK primary care databases on patients prescribed the salbutamol comparator or reference. The study included a 1-year baseline period, starting 1 year before the index prescription date, and 1-year outcome period. Cohorts were matched for baseline COPD respiratory medications. The primary outcome was analysis of non-inferiority for the comparator versus reference product for the rate of moderate and severe COPD exacerbations. Non-inferiority was satisfied if the 95% confidence interval (CI) upper limit for mean differences in proportions between treatments was

Suggested Citation

  • David B Price & Eran Gefen & Gokul Gopalan & Rosie McDonald & Vicky Thomas & Simon Wan Yau Ming & Emily Davis, 2018. "Real-life effectiveness and safety of salbutamol Steri-Neb™ vs. Ventolin Nebules® for exacerbations in patients with COPD: Historical cohort study," PLOS ONE, Public Library of Science, vol. 13(1), pages 1-18, January.
  • Handle: RePEc:plo:pone00:0191404
    DOI: 10.1371/journal.pone.0191404
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