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Eliciting adverse effects data from participants in clinical trials
BACKGROUND: Analysis of drug safety in clinical trials involves assessing adverse events (AEs) individually or by aggregate statistical synthesis to provide evidence of likely adverse drug reactions (ADR). While some AEs may be ascertained from physical examinations or tests, there is great reliance...
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| 出版年: | Cochrane Database Syst Rev |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley & Sons, Ltd
2018
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| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7098080/ https://ncbi.nlm.nih.gov/pubmed/29372930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.MR000039.pub2 |
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