The HR suggested a lower risk of severe and moderate exacerbations (0.80 [95% CI 0.69–0.93] and 0.80 [95% CI 0.74–0.87], respectively) and a marginally non-significant decreased risk of pneumonia (0.85 [95% CI 0.70–1.02]) associated with fluticasone/umeclidinium/vilanterol.
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Comparative effectiveness and safety of fluticasone-based versus beclometasone-based single-inhaler triple therapies in patients with chronic obstructive pulmonary disease: a population-based cohort study.
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