Overall summary of 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.bAs determined by the investigator.cElevation of aspartate aminotransferase and/or alanine aminotransferase ≥3 × upper limit of normal combined with elevated total bilirubin ≥2 × upper limit of normal at the same visit.dAsthma worsening.AE, adverse event.Overall summary of adverse events (treated set).
创建时间：
2015-12-03
