Recommendations to improve adverse event reporting in clinical trial publications: a joint pharmaceutical industry/journal editor perspective.
نویسندگان
چکیده
and introduction [Abstract] 4. Avoid use of overly general text descriptions for adverse events, including in abstracts. Abstracts should include a phrase or sentence summarizing the most clinically relevant adverse event data with frequency percentages consistent with those presented in the main text of the publication. [Abstract and introduction] “(1, 2) If the study collected data on harms and benefits, the title or abstract, and introduction, should so state.”
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عنوان ژورنال:
- BMJ
دوره 355 شماره
صفحات -
تاریخ انتشار 2016