Radical transparency in post-market oversight of medicine safety
Author:
Publisher
BMJ
Subject
General Engineering
Reference13 articles.
1. Development Times, Clinical Testing, Postmarket Follow-up, and Safety Risks for the New Drugs Approved by the US Food and Drug Administration
2. The impact of serious adverse drug reactions: a population-based study of a decade of hospital admissions in New South Wales, Australia
3. Trends in emergency hospital admissions in England due to adverse drug reactions: 2008-2015
4. Percentage of Patients with Preventable Adverse Drug Reactions and Preventability of Adverse Drug Reactions – A Meta-Analysis
5. Characterization and corroboration of safety signals identified from the US Food and Drug Administration Adverse Event Reporting System, 2008-19: cross sectional study
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Regulatory judgments for toxicity signals of medicinal products: in search of accountability;BMJ;2022-11-03
2. Transparency and robustness of safety signals;BMJ;2022-11-03
3. Personal reflective practice can lead to change;BMJ;2022-10-06
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