辉瑞论文：辉瑞危害人类罪[有声读物]

English | ASIN: B0DGVN1TMD | 2024 | MP3@64 kbps | ~16:01:00 | 440 MB

The WarRoom/DailyClout Pfizer Documents Analysts, Naomi Wolf, Amy Kelly, Laura Darrell (Narrator), "The Pfizer Papers: Pfizer's Crimes Against Humanity"

The Pfizer Papers features new reports written by WarRoom/DailyClout research volunteers, which are based on the primary source Pfizer clinical trial documents released under court order and on related medical literature. The book shows in high relief that Pfizer’s mRNA COVID-19 vaccine clinical trial was deeply flawed and that the pharmaceutical company knew by November 2020 that its vaccine was neither safe nor effective. The reports detail vaccine-induced harms throughout the human body, including to the reproductive system; show that women suffer vaccine-related adverse events at a 3:1 ratio; expose that vaccine-induced myocarditis is not rare, mild, or transient; and, shockingly, demonstrate that the mRNA vaccines have created a new category of multi-system, multi-organ disease, which is being called “CoVax Disease.”

Despite the fact that Pfizer committed in its own clinical trial protocol to follow the placebo arm of its trial for twenty-four months, Pfizer vaccinated approximately 95 percent of placebo recipients by March 2021, thus eliminating the trial’s control group and making it impossible for comparative safety determinations to be made.

Just as importantly, The Pfizer Papers makes it clear that the US Food and Drug Administration knew about the shortfalls of Pfizer’s clinical trial as well as the harms caused by the company’s mRNA COVID vaccine product, thus highlighting the FDA’s abject failure to fulfill its mission to “[protect] the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices.”

The Pfizer Papers offers an in-depth look at how Big Pharma, the US government, and healthcare entities stand protected behind the broad legal immunity provided by the Public Readiness and Emergency Preparedness Act (PREP Act) when creating, prescribing, and administering vaccines; and, under that shield of protection, do what is best for their bottom lines rather than for the health and well-being of Americans.

中文|亚洲：B0DGVN1TMD | 2024 |MP3@64kbps|~16:01:00|440 MB《作战室/日报》辉瑞文件分析师Naomi Wolf、Amy Kelly、Laura Darrell（旁白），“辉瑞文件：辉瑞的反人类罪行” 辉瑞论文以WarRoom/DailyClout研究志愿者撰写的新报告为特色，这些报告基于根据法院命令发布的辉瑞临床试验文件的主要来源和相关医学文献。该书高度欣慰地表明，辉瑞公司的mRNA新冠肺炎疫苗临床试验存在严重缺陷，该制药公司在2020年11月之前就知道其疫苗既不安全也不有效。这些报告详细介绍了疫苗对整个人体的危害，包括对生殖系统的危害；表明女性遭受疫苗相关不良事件的比例为3:1；暴露疫苗诱导的心肌炎并不罕见、轻微或短暂；令人震惊的是，mRNA疫苗创造了一种新的多系统、多器官疾病，被称为“CoVax疾病” 尽管辉瑞公司在其自己的临床试验方案中承诺在24个月内遵循其试验的安慰剂组，但到2021年3月，辉瑞公司为大约95%的安慰剂接种者接种了疫苗，从而消除了试验的对照组，使得无法进行比较安全性测定。 同样重要的是，辉瑞论文明确指出，美国食品和药物管理局知道辉瑞临床试验的不足以及该公司mRNA新冠疫苗产品造成的危害，从而突显了美国食品和药品管理局未能履行其“通过确保人用和兽药、生物制品和医疗器械的安全性、有效性和安全性来保护公众健康”的使命 辉瑞论文深入探讨了大型制药公司、美国政府和医疗保健实体在创建、处方和管理疫苗时，如何在《公共准备和应急准备法案》（PREP法案）提供的广泛法律豁免权背后受到保护；而且，在这种保护之下，做对他们的底线最好的事情，而不是为了美国人的健康和福祉。

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