灰瑞mRNA实验把严重副作用的都算成与疫苗无关的
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辉瑞将试验不良反应归类为与注射无关
06/21/22
辉瑞将COVID疫苗试验期间几乎所有严重不良事件归类为"与注射无关"
美国食品和药物管理局6月1日发布的辉瑞临床试验文件中包含的病例报告揭示了辉瑞将几乎所有不良反应，特别是严重不良反应，都分类为与疫苗"无关"。
https://childrenshealthdefense.org/defender/pfizer-covid-vaccine-trials-adverse-events-shots-fda-eua-documents/
SSRN2022年6月1日
https://papers.ssrn.com/sol3/papers.cfm?abstract_id=4125239
二○二二年六月二十二日
在辉瑞针对COVID-19注射的临床试验中，该制药公司将几乎所有严重不良事件归类为与注射"无关"，并宣布注射是安全的。
FDA于2022年6月1日发布了80,000页的试验文件中的一些，仔细阅读它们显示"在3期试验期间持续严重不良副作用的参与者的无数实例。 这些参与者中的一些人退出了试验，一些人被丢弃，一些人死亡"。
许多不良副作用与心脏问题有关，如心包炎，肺栓塞和血栓形成，但没有一个被列为mRNA注射的结果。 事实上，有许多严重的不良反应，辩护人说，包括六人死亡，都没有详细描述，因为他们被确定与研究无关。
在2022年6月1日的一份SSRI期刊报告中，外部调查人员指出，"在辉瑞和Moderna试验中，安慰剂组的COVID-19住院的风险低于mRNA疫苗实验组！”
Pfizer Classified Trial Adverse Reactions as Not Related to the Shots
06/21/22
Pfizer Classified Almost All Severe Adverse Events During COVID Vaccine Trials ‘Not Related to Shots’
The case reports included in Pfizer clinical trial documents, released June 1 by the U.S. Food and Drug Administration, reveal a trend of classifying almost all adverse events — and in particular severe adverse events — as being “not related” to the vaccine.
https://childrenshealthdefense.org/defender/pfizer-covid-vaccine-trials-adverse-events-shots-fda-eua-documents/
SSRN June 1, 2022
https://papers.ssrn.com/sol3/papers.cfm?abstract_id=4125239
June 22, 2022
In the Pfizer clinical trials for the COVID-19 shots, the drug company classified almost all serious adverse events to “not related” to the injections, and announced the shots were safe.
The FDA released some of the 80,000 pages of trial documents June 1, 2022, and a close reading of them shows “numerous instances of participants who sustained severe adverse events during Phase 3 trials. Some of these participants withdrew from the trials, some were dropped and some died,” according to The Defender and Children’s Health Defense.
Many of the adverse events were related to heart problems such as pericarditis, pulmonary embolism and thrombosis, but none was listed as a red flag against the shots. In truth, there were many serious adverse events, The Defender says — including six deaths, which were not described in detail as they were determined to not being related to the study.
In an SSRI journal report June 1, 2022, outside investigators noted that “The excess risk of serious adverse events of special interest surpassed the risk reduction for COVID-19 hospitalization relative to the placebo group in both Pfizer and Moderna trials.”
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