Frequency of cardiac adverse events (treated set).
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aPatients were randomised 2:2:1 to the tiotropium Respimat 5 μg, tiotropium Respimat 2.5 μg and placebo Respimat groups, respectively.
bOne event from each category occurred in a single patient prior to Day 59.
Frequency of cardiac adverse events (treated set).
创建时间：
2015-04-20
