The number of participants that experienced at least one, and the total number of genitourinary (GU) and laboratory adverse events<sup>*</sup> by treatment group, initiation day of AE, and association with study product.
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资源简介：
N = number of women with at least one finding; TN = total number of findings. *Adverse events that did not occur are not listed. †Includes 11 events on Day 22 and one each on Days 23 and 24.
创建时间：
2011-01-20
