FDA: Crimes Against Humanity

Attached is a petition that is fully-explained with evidence and references, against the approval of Pfizer's mRNA formula as a COVID19 vaccine. As explained, this approval of an experimental injection violates the Nuremberg Code, and thus is a crime against humanity.

Among the issues referred to:Omission of critical phases in the research (e.g. animal testing)**Ignoring of side effects, illness and deaths, and lack or poor recording of vaccinated people's reportsManufacturers' Exemption from liability**Ignoring the troubling results in animals, from preceding mRNA technology researches*Ignoring of information and statements brought by well-known experts, including the mRNA technology inventor; experts that have served in senior positions for Pfizer, Nobel prize winners, and more.

This petition will be used to address the ICC (International Criminal Court) by email, requesting they open an investigation on crimes against humanity performed by FDA.

======hTO: [email protected]

Information and Evidence Unit

Office of the Prosecutor

Post Office Box 19519

==========ן 

Dear Sir/Madame,

We, the undersigned, civilians of the world, would like to file an urgent complaint and request a formal investigation

concerning crimes against humanity that are being perpetrated by the FDA (U.S. Food and Drug Administration).

On the 23-AUG-2021, we saw publications, stating that the FDA has provided full approval, or extended the EUA (Emergency Use Approval), to the experimental COVID19 mRNA vaccine formula, where the first option indicates wrongly that it is no longer experimental:

https://www.fda.gov/media/150386/download?fbclid=IwAR0zn-Ojtd7EXtTUaOaP8eQbD7-5gj6wvPFeeX47B40ahFoJXiNXapl6iiQ

Note: even if FDA provided “only” an extended EUA (Emergency Use Approval) for the above formula – it is still to be investigated as crimes against humanity, according to the information provided below.

Providing Pfizer or Moderna COVID19 mRNA formula, with any type of FDA approval as a “vaccine” – whether EUA or full approval - is a mis-representation, and thus forgery…… According to USA law, Forgery is: making, using, altering, or possessing a false document with the intent to commit fraud. Forgery can be the creation of a false document, or changing an authentic one. Forgery is a crime that is classified as a felony in all fifty states and by the federal government.

https://www.legalmatch.com/law-library/article/forgery-laws.html

The following examples indicate that the COVID19 mRNA formula experimental phases have not been completed properly, and thus cannot have been approved by the regulatory authority, not even for Emergency Use!:

1. Ignored evidences and no stable recording of side effects, including illness and death Example evidences:
   • Many social media groups
   • According to the FDA approval itself, there is a risk of Myocarditis, vaccine associated Enhanced Disease over time, etc. https://www.fda.gov/media/144245/download
   • French scientists and researchers: the COVID19 vaccines have created an un-precedent rate of deaths! https://blogs.mediapart.fr/laurent-mucchielli/blog/300721/la-vaccination-covid-l-epreuve-des-faits-2eme-partie-une-mortalite-inedite

2. Ignored horrific safety history of the mRNA technology: The mRNA technology has a history of alerting safety problems. Some examples:
   • Stopped an mRNA project: Alexion Pharmaceuticals “…Moderna’s treatment would never be safe enough for humans” https://en.m.wikipedia.org/wiki/Moderna
   • Animal studies: Preceding researches …, indicating the animals got very sick and died when re-exposed to the virus. Examples:
     • https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0035421
     • https://www.jstage.jst.go.jp/article/jvms/60/1/60_1_49/_article
     • https://pubmed.ncbi.nlm.nih.gov/22536382/
     • https://pubmed.ncbi.nlm.nih.gov/17194199/

3. Ignored information brought by well-known scientists and Doctors:g.:
   • Robert Mallon (inventor of mRNA technology): https://www.knowheretoknow.com/post/%D7%9E%D7%9E%D7%A6%D7%99%D7%90-%D7%98%D7%9B%D7%A0%D7%95%D7%9C%D7%95%D7%92%D7%99%D7%99%D7%AA-%D7%94-mrna-%D7%90%D7%99%D7%9F-%D7%A9%D7%A7%D7%99%D7%A4%D7%95%D7%AA-%D7%9C%D7%92%D7%91%D7%99-%D7%94%D7%A1%D7%99%D7%9B%D7%95%D7%A0%D7%99%D7%9D-%D7%9E%D7%94%D7%97%D7%99%D7%A1%D7%95%D7%9F-%D7%93-%D7%A8-%D7%A8%D7%95%D7%91%D7%A8%D7%98-%D7%9E%D7%90%D7%9C%D7%95
   • Sucharit Bhakdi, Microbiologist and Virologist https://rumble.com/vlm3zs-prof-sucharit-bhakdi.html rappeh.org.il
   • Mike Yeadon, Pfizer's former Vice President and Chief Scientist: about 100 childrean per million will die from this “vaccination” https://www.facebook.com/benny.bargig/videos/820204218681713
   • Duchi, BMJ: Does the FDA think these data justify the first full approval of a covid-19 vaccine? https://blogs.bmj.com/bmj/2021/08/23/does-the-fda-think-these-data-justify-the-first-full-approval-of-a-covid-19-vaccine/
   • Many other doctors and researchers, and civil investigation groups of scientists and lawyers, such as America Frontline Doctors, Israel people committee, and many more.

4. Research Methodological errors, and failure to comply with “vaccine” definition: The approval procedure ignores and violates the regulations of the FDA itself: omission of animal testing phase, reduction of experiment duration (thus preventing any ability to investigate long term effects), eliminating the control (Placebo) group by giving them the actual formula, etc. Examples:
   • Eliminating the placebo control group: https://www.bloomberg.com/news/articles/2020-12-14/pfizer-may-offer-shots-to-trial-volunteers-who-received-placebo
   • Ignoring deaths: Prof Dolores Kahil indicates that in the past formula researches, appearance of 50 deaths brought to halt of the research, and the formula declared as dangerous: https://t.me/worlddoctorsalliance/6527 YET, in the COVID19 mRNA formula research, thousands of deaths reported are still ignored by FDA, which extends formula approval! Below is an example screen shot from the VAERS system, indicating deaths following the COVID19 “vaccine”:

• Research follow-up: Where is the follow-up on the people participating in the experiment? In fact – it seems that some of them have mysteriously “disappeared”.
  • https://www.medrxiv.org/content/10.1101/2021.07.28.21261159v1.full.pdf
  • Duchy, associate editor at the BMJ (British Medical Journal): https://blogs.bmj.com/bmj/2021/01/04/peter-doshi-pfizer-and-modernas-95-effective-vaccines-we-need-more-details-and-the-raw-data/ The Pfizer research included 1594 “suspected for Covid” that were omitted from the study. If they were to be included, the efficiency would be reduced dramatically.
  • Dr Duchi: The Pfizer research omitted 311 participants from the vaccinated group (and only 60 from the Placebo group), due to protocol deviation. No indication has been done regarding the nature of the deviation, and why the vaccine group is 5 times larger.

5. Political pressure to provide approval, and conflict of interests: There have been publications, indicating political pressure to approve the vaccine, including threatening FDA officials that they will be fired if they do not approve the vaccine by a specific date:: https://www.cnbc.com/2020/12/11/white-house-threatens-to-fire-fda-chief-unless-covid-vaccine-oked-friday-report.html In addition, conflict of interests have been seen. For example: SCOTT GOTTLIEB, previously an FDA commissioner, is now a Pfizer Director(!): https://www.pfizer.com/people/leadership/board-of-directors/scott_gottlieb-md https://www.fda.gov/about-fda/fda-leadership-1907-today/scott-gottlieb
6. Indication of DNA alteration: Tal Zaks, Moderna’s clinical manager in Israel, admits that the mRNA may alter the DNA: https://israel-news.co.il/archives/25085

7. Research Duration: Even according to the FDA itself, the research phase was to be completed by 2023, thus the indication that the research testing phase has been completed, if indeed a full approval was granted, is misleading, https://clinicaltrials.gov/ct2/show/NCT04368728 https://www.reuters.com/article/factcheck-vaccines-trials-idUSL1N2L71IT

Notes:

• We the people, did not get sufficient information about the method and place of the isolation of the virus, the proof it is related to the specific illness, and the method and labs identifying specific variants.
• We the people demand that vaccinated people perform d-dimer tests to check for clotting.
• We the people demand that autopsies are performed in vaccinated casualties, with the presence of experts from our behalf at the site and during autopsy itself, where the autopsy is done according to our representative demands.
• The formula has been defined as a vaccine even in the previous FDA EUA. We the people, claim that this formula cannot be defined as a vaccine, as there is no proof it reduces infection. The FDA is the one that needs to ensure such poof exists. Otherwise, the document indicating this mRNA formula is “vaccine” is forgery.
• The vaccine manufacturers have taken no responsibility for any damages caused by the vaccines.

This forged FDA approval, claiming wrongly and thus misleading, that this experimental matter is safe – even if “only” for emergency use – as well as the statement that it is a “vaccine”, resulted in nations performing mass vaccination, mis-interpreting the meaning of EUA to the public, thus violating the Nuremberg Code. The resulting deaths around the world, reported ever since starting to vaccinate the population, are shocking. We do not understand how anyone involved can sleep at nights.

These above claims are supported by huge numbers of evidences and facts, and serve as preliminary statements, to initiate an urgent investigation to IMEDIATELY STOP and prevent any additional crimes against humanity.

Thank you for your assistance.

kind regards,

From the people who promised to forgive but never forget, identifying similar procedures prior to the rise of Nazism.=======h

עצומה נגד אישור חיסוני פייזר ע"י ה-FDA========ימובאת בפניכם עצומה מנומקת היטב נגד אישור החומר הניסיוני של פייזר כחיסון לקורונה, אישור המהווה פשע נגד האנושות. בין שאר הנימוקים:*דילוג על שלבי מחקר קריטיים (כגון ניסוי בבעח)*התעלמות מתופעות הלואי ורישום רשלני אם בכלל*פטירת היצרניות מאחריות*התעלמות מתוצאות מחקרי עבר בטכנולוגיית mRNA בבעלי חיים*התעלמות מחוות דעת מומחים ידועי שם, כולל ממציא הטכנולוגיה, בכירים לשעבר בפייזר, זוכי פרס נובל, ועוד

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