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Jay Hsu mark this message contains true information
originally written by Jay Hsu
兩個醫生,兩位都是台大的,其中一個有到美國哈佛修碩士。
然後一堆"帳號"不做功課就說這些是假的。
s蛋白的問題早在2020年日本人就有研究報告。
Rumble也只是一個影音平台。youtube的大老闆是疫苗廠的投資人,所以他們早就制定規則,要求影音內容創作者不得討論疫苗缺點,他們表面的假理由是:擴大疫苗猶豫,實際上是為了片更多人去打無效、不安全的新冠實驗疫苗。

1. https://academic.oup.com/ofid/article/10/6/ofad209/7131292
DOI: 10.1093/ofid/ofad209
世界第二名的醫院Cleveland Clinic 5萬1千人的研究報告:有打更危險。

2. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10125209/
doi: 10.1016/j.isci.2023.106733
University of Southern Denmark, Odense, Denmark全世界排名約261的大學,發現,mRNA試驗組和對造組死亡率相當。不防死亡(既然不防死亡,我們當然可以合理懷疑其實根本也不防重症)(藥廠的研究也顯示:實驗組死亡人數更多)

3. https://pubmed.ncbi.nlm.nih.gov/36055877/
DOI: 10.1016/j.vaccine.2022.08.036
(BMJ)主編Peter Doshi博士團隊發現,新冠疫苗:有打更危險。

4. https://www.medrxiv.org/content/10.1101/2022.02.25.22271454v1
doi: https://doi.org/10.1101/2022.02.25.22271454
NY Study 證明1個半月內,12-17歲疫苗有效率從66%變51%。5-11歲疫苗(對感染)有效率從68%變12%。ARR(絕對風險減少值)低於50%,則是無效疫苗。也就是說5-17歲人口注射新冠疫苗,大約在1個半月內失效。代表需要重複施打(加強針?)但是每打一針,副作用的機率就會增高,另外會造成免疫印記的問題(Cleveland Study可以證明)。所以這個針不能重複施打,而且打了2針(完整接種)後,約1.5個月就失效。

5. https://onlinelibrary.wiley.com/doi/10.1111/eci.13998
DOI: 10.1111/eci.13998
Batch-dependent safety 丹麥研究發現:每位注射者回報3種不良反應。

6. https://phmpt.org/wp-content/uploads/2022/04/reissue_5.3.6-postmarketing-experience.pdf
BNT file

7. https://www.thelancet.com/journals/ebiom/article/PIIS2666-5247(21)00069-0/fulltext?fbclid=IwAR0fh1DF8bsd2mQA7n7zynjO6QiuVFdDFSYNIWXL6HNLQ5AdoNBxTZbklvo#
DOI: 10.1016/S2666-5247(21)00069-0
ARR, RRR"絕對風險減少值"與"相對風險減少值"的問題。
根據WHO,有效的疫苗是50%ARR(絕對風險減少值)。
但是新冠疫苗廠商使用的是RRR(相對風險減少值)。
真實的ARR值為:
1·3% for the AstraZeneca–Oxford,
1·2% for the Moderna–NIH,
1·2% for the J&J,
0·93% for the Gamaleya, and
0·84% for the Pfizer–BioNTech vaccines.

References

https://academic.oup.com/ofid/article/10/6/ofad209/7131292
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10125209/
https://pubmed.ncbi.nlm.nih.gov/36055877/
https://www.medrxiv.org/content/10.1101/2022.02.25.22271454v1
https://onlinelibrary.wiley.com/doi/10.1111/eci.13998

Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults - PubMed

The excess risk of serious adverse events found in our study points to the need for formal harm-benefit analyses, particularly those that are stratified according to risk of serious COVID-19 outcomes.

https://pubmed.ncbi.nlm.nih.gov/36055877/

Effectiveness of the BNT162b2 vaccine among children 5-11 and 12-17 years in New York after the Emergence of the Omicron Variant

Importance There is limited evidence on the effectiveness of the BNT162b2 vaccine for children, particularly those 5-11 years and after the Omicron variant’s emergence. Objective To estimate BNT162b2

https://www.medrxiv.org/content/10.1101/2022.02.25.22271454v1

Effectiveness of the BNT162b2 vaccine among children 5-11 and 12-17 years in New York after the Emergence of the Omicron Variant

Importance There is limited evidence on the effectiveness of the BNT162b2 vaccine for children, particularly those 5-11 years and after the Omicron variant’s emergence. Objective To estimate BNT162b2

https://doi.org/10.1101/2022.02.25.22271454

Serious adverse events of special interest following mRNA COVID-19 vaccination in randomized trials in adults - PubMed

The excess risk of serious adverse events found in our study points to the need for formal harm-benefit analyses, particularly those that are stratified according to risk of serious COVID-19 outcomes.

https://pubmed.ncbi.nlm.nih.gov/36055877/

Effectiveness of the BNT162b2 vaccine among children 5-11 and 12-17 years in New York after the Emergence of the Omicron Variant

Importance There is limited evidence on the effectiveness of the BNT162b2 vaccine for children, particularly those 5-11 years and after the Omicron variant’s emergence. Objective To estimate BNT162b2

https://www.medrxiv.org/content/10.1101/2022.02.25.22271454v1

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