Figure 3From: Safety and tolerability of once-daily umeclidinium/vilanterol 125/25 mcg and umeclidinium 125 mcg in patients with chronic obstructive pulmonary disease: results from a 52-week, randomized, double-blind, placebo-controlled studyOn-treatment AEs and SAEs. On-treatment AEs reported by ≥4% of patients in any treatment group and SAEs reported by ≥1% of patients in any treatment group in the ITT population. AE, adverse event; COPD, chronic obstructive pulmonary disease; ITT, intent-to-treat; SAE, serious AE; UMEC, umeclidinium; VI, vilanterol. Patient numbers are indicated above bars.Back to article page