コーパス検索結果 (left1)
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1 16 (9%) of
184 patients had a serious adverse event related to treatment wit
2 Across both trials, 38 (
20%)
patients had a serious adverse event during the first 48 week
3 19 (8%) of
249 patients had a serious adverse event related to treatment wit
4 e GP2013-CVP group had an adverse event and 71 [23%] of
312 patients had a serious adverse event; 288 [91%] of 315 patien
5 Four (
33%)
patients had a serious adverse event, and 12 (100%) patients
6 Four of 73 (5.
5%)
patients had a serious adverse event in the placebo group, te
7 -up period of 26 months (interquartile range, 20-30 mo),
no patients had a serious adverse event or relapse of vasculitis
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