美国食品和药物管理局(FDA)从冠状病毒(COVID-19)的教训中得出的“任何速度都不安全”的想法仍然适用

Bennett C, Martin L
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引用次数: 0

摘要

版权所有:©2020 Bennett C, et al。由诺贝尔研究出版社出版。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。关于美国食品和药物管理局(FDA)在批准治疗冠状病毒(covid - 19)的药物和预防病毒的疫苗,同时确保药物安全方面的作用,已经有了广泛的新闻报道。COVID-19治疗最初侧重于羟氯喹,现在已改为瑞德西韦。冠状病毒疫苗的开发现在是一个竞争和合作的行业项目,美国总统唐纳德·特朗普将其命名为“曲速行动”。FDA的目标是尽快批准临床治疗方法,并在年底前大规模生产疫苗,但安全性很可能再次被忽视。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lessons for the coronavirus (COVID-19) “not safe at any speed” thinking for the United States Food and Drug Administration (FDA) still applies
Copyright: © 2020 Bennett C, et al. Published by NobleResearch Publishers. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. There has been extensive news coverage about the USA Food and Drug Administration’s (FDA’s) role in approving medications to treat the coronavirus (COVID19) and vaccines to prevent the virus while at the same time, ensuring medication safety. COVID-19 treatment was initially focused on hydroxychloroquine and now has changed to remdesivir. Coronavirus vaccination development is now a competitive and collaborative 14industry program that USA President Donald Trump has named “Operation Warp Speed”. With the goals of having FDA approved treatments in the clinic as soon as possible and vaccines in mass production by the end of the year, safety is likely to be overlooked—again.
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