COVID-19 Vaccine Associated Parkinson's Disease, A Prion Disease Signal in the UK Yellow Card Adverse Event Database

J. Classen
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引用次数: 3

Abstract

Many have argued that SARS-CoV-2 spike protein and its mRNA sequence, found in all COVID-19 vaccines, are priongenic. The UK’s Yellow Card database of COVID-19 vaccine adverse event reports was evaluated for signals consistent with a pending epidemic of COVID vaccine induced prion disease. Adverse event reaction rates from AstraZeneca’s vaccine were compared to adverse event rates for Pfizer’s COVID vaccines. The vaccines employ different technologies allowing for potential differences in adverse event rates but allowing each to serve as a control group for the other. The analysis showed a highly statistically significant and clinically relevant (2.6-fold) increase in Parkinson’s disease, a prion disease, in the AstraZeneca adverse reaction reports compared to the Pfizer vaccine adverse reaction reports (p= 0.000024). These results are consistent with monkey toxicity studies showing infection with SARS-CoV-2 results in Lewy Body formation. The findings suggest that regulatory approval, even under an emergency use authorization, for COVID vaccines was premature and that widespread use should be halted until full long term safety studies evaluating prion toxicity has een complete. Alternative vaccines like the Measles Mumps Rubella (MMR) vaccine should be explored for those desiring immunization against COVID-19.Many have argued that SARS-CoV-2 spike protein and its mRNA sequence, found in all COVID-19 vaccines, are priongenic. The UK’s Yellow Card database of COVID-19 vaccine adverse event reports was evaluated for signals consistent with a pending epidemic of COVID vaccine induced prion disease. Adverse event reaction rates from AstraZeneca’s vaccine were compared to adverse event rates for Pfizer’s COVID vaccines. The vaccines employ different technologies allowing for potential differences in adverse event rates but allowing each to serve as a control group for the other. The analysis showed a highly statistically significant and clinically relevant (2.6-fold) increase in Parkinson’s disease, a prion disease, in the AstraZeneca adverse reaction reports compared to the Pfizer vaccine adverse reaction reports (p= 0.000024). These results are consistent with monkey toxicity studies showing infection with SARS-CoV-2 results in Lewy Body formation. The findings suggest that regulatory approval, even under an emergency use authorization, for COVID vaccines was premature and that widespread use should be halted until full long term safety studies evaluating prion toxicity has been complete. Alternative vaccines like the Measles Mumps Rubella (MMR) vaccine should be explored for those desiring immunization against COVID-19.
COVID-19疫苗相关帕金森病,英国黄卡不良事件数据库中的朊病毒疾病信号
许多人认为,在所有COVID-19疫苗中发现的SARS-CoV-2刺突蛋白及其mRNA序列是朊病毒原性的。对英国的COVID-19疫苗不良事件报告黄卡数据库进行了评估,以寻找与即将发生的COVID疫苗诱导的朊病毒疾病流行相一致的信号。将阿斯利康疫苗的不良事件反应率与辉瑞COVID疫苗的不良事件发生率进行比较。这些疫苗采用不同的技术,考虑到不良事件发生率的潜在差异,但允许每种疫苗作为另一种疫苗的对照组。分析显示,与辉瑞疫苗不良反应报告相比,阿斯利康疫苗不良反应报告中帕金森病(一种朊病毒疾病)的发生率有高度统计学意义和临床相关性(2.6倍)的增加(p= 0.000024)。这些结果与猴子毒性研究一致,表明感染SARS-CoV-2导致路易体形成。研究结果表明,监管部门批准COVID - 19疫苗,即使是在紧急使用授权下,也为时过早,在评估朊病毒毒性的全面长期安全性研究完成之前,应停止广泛使用。对于那些希望免疫COVID-19的人,应探索麻疹、腮腺炎、风疹(MMR)疫苗等替代疫苗。许多人认为,在所有COVID-19疫苗中发现的SARS-CoV-2刺突蛋白及其mRNA序列是朊病毒原性的。对英国的COVID-19疫苗不良事件报告黄卡数据库进行了评估,以寻找与即将发生的COVID疫苗诱导的朊病毒疾病流行相一致的信号。将阿斯利康疫苗的不良事件反应率与辉瑞COVID疫苗的不良事件发生率进行比较。这些疫苗采用不同的技术,考虑到不良事件发生率的潜在差异,但允许每种疫苗作为另一种疫苗的对照组。分析显示,与辉瑞疫苗不良反应报告相比,阿斯利康疫苗不良反应报告中帕金森病(一种朊病毒疾病)的发生率有高度统计学意义和临床相关性(2.6倍)的增加(p= 0.000024)。这些结果与猴子毒性研究一致,表明感染SARS-CoV-2导致路易体形成。研究结果表明,监管部门批准COVID - 19疫苗,即使是在紧急使用授权下,也为时过早,在评估朊病毒毒性的全面长期安全性研究完成之前,应停止广泛使用。对于那些希望免疫COVID-19的人,应探索麻疹、腮腺炎、风疹(MMR)疫苗等替代疫苗。
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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