The Blind Spot in COVID-19 Vaccination Policies: Under-Reported Adverse Events

P. Provost
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引用次数: 1

Abstract

Case reports involving two academic researchers suggest that adverse events (AEs) to COVID-19 messenger RNA (mRNA) vaccination are largely underreported due to numerous clinical, systemic, political and media factors. The lack of proper analysis and consideration of the reported AEs also suggests that these injections are not as safe as widely purported. The resulting biased risk-benefit assessment may only produce misinformed public health recommendations and misguided political decisions, thereby exposing the population to an underestimated risk, in possible violation of the precautionary principle and of the right to a free and informed consent. The possible mechanisms underlying AEs to COVID-19 vaccination raise serious concerns regarding the new vaccine application of the mRNA technology that need to be addressed before expanding it to other infectious diseases. The legal considerations of AE underreporting are also discussed, and recommendations are formulated. AEs to mRNA injections are a reality and need to be better assessed than heretofore, diagnosed and reported to public health authorities for follow-up investigation in order to inform policy decisions and updates to physician guidelines in an objective, scientifically based, independent, and transparent manner.
COVID-19疫苗接种政策的盲点:未报告的不良事件
涉及两名学术研究人员的病例报告表明,由于众多临床、系统、政治和媒体因素,COVID-19信使RNA (mRNA)疫苗接种的不良事件(ae)在很大程度上被低估了。对报道的不良反应缺乏适当的分析和考虑,也表明这些注射并不像广泛声称的那样安全。由此产生的有偏见的风险-利益评估可能只会产生错误的公共卫生建议和错误的政治决定,从而使民众面临被低估的风险,可能违反预防原则和自由知情同意的权利。COVID-19疫苗接种产生不良反应的可能机制引发了对mRNA技术在新疫苗应用方面的严重担忧,在将其推广到其他传染病之前,需要解决这一问题。本文还讨论了AE低报的法律考虑,并提出了建议。mRNA注射的不良反应是一个现实,需要比以往更好地评估、诊断并报告给公共卫生当局进行后续调查,以便以客观、科学、独立和透明的方式为政策决定和医生指南的更新提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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