Ex-Pfizer Doctor Yeadon and Lung Specialist Doctor Wodarg file for suspension of all SARS CoV2 Vaccine Studies-Sign their Petition

On December 1, 2020, the ex-Pfizer head of respiratory research Dr. Michael Yeadon and the lung specialist and former head of the public health department Dr. Wolfgang Wodarg filed an application with the EMA, the European Medicine Agency responsible for EU-wide drug approval, for the immediate suspension of all SARS CoV 2 vaccine studies, in particular the BioNtech/Pfizer study on BNT162b (EudraCT number 2020-002641-42).

Dr. Wodarg and Dr. Yeadon demand that the studies – for the protection of the life and health of the volunteers – should not be continued until a study design is available that is suitable to address the significant safety concerns expressed by an increasing number of renowned scientists against the vaccine and the study design.

On the one hand, the petitioners demand that, due to the known lack of accuracy of the PCR test in a serious study, a so-called Sanger sequencing must be used. This is the only way to make reliable statements on the effectiveness of a vaccine against Covid-19. On the basis of the many different PCR tests of highly varying quality, neither the risk of disease nor a possible vaccine benefit can be determined with the necessary certainty, which is why testing the vaccine on humans is unethical per se.

Furthermore, they demand that it must be excluded, e.g. by means of animal experiments, that risks already known from previous studies, which partly originate from the nature of the corona viruses, can be realized. The concerns are directed in particular to the following points:

  • The formation of so-called “non-neutralizing antibodies” can lead to an exaggerated immune reaction, especially when the test person is confronted with the real, “wild” virus after vaccination. This so-called antibody-dependent amplification, ADE, has long been known from experiments with corona vaccines in cats, for example. In the course of these studies all cats that initially tolerated the vaccination well died after catching the wild virus.
  • The vaccinations are expected to produce antibodies against spike proteins of SARS-CoV-2. However, spike proteins also contain syncytin-homologous proteins, which are essential for the formation of the placenta in mammals such as humans. It must be absolutely ruled out that a vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1, as otherwise infertility of indefinite duration could result in vaccinated women.
  • The mRNA vaccines from BioNTech/Pfizer contain polyethylene glycol (PEG). 70% of people develop antibodies against this substance – this means that many people can develop allergic, potentially fatal reactions to the vaccination.
  • The much too short duration of the study does not allow a realistic estimation of the late effects. As in the narcolepsy cases after the swine flu vaccination, millions of healthy people would be exposed to an unacceptable risk if an emergency approval were to be granted and the possibility of observing the late effects of the vaccination were to follow. Nevertheless, BioNTech/Pfizer apparently submitted an application for emergency approval on December 1, 2020.

CALL FOR HELP: Dr. Wodarg and Dr. Yeadon ask as many EU citizens as possible to co-sign their petition by sending the e-mail prepared here to the EMA.

Nachtrag: Wegen teilweiser Überlastung der Server hier der Inhalt der E-Mail und die Kontaktadressen zum späteren Selbst-Versenden: 

An: press@ema.europa.eu; petitionEMA@corona-ausschuss.com

Betreff: Co-signing the petition of Dr. Wodarg, Germany, and Dr. Yeadon, UK (submitted on 1-Dec-2020)

Dear Sir or Madam, I am hereby co-signing the petition of Dr. Wodarg and Dr. Yeadon to support their urgent request to stay the Phase III clinical trial(s) of BNT162b (EudraCT Number 2020-002641-42) and other clinical trials. The full text of the petition of Dr. Wodarg and Dr. Yeadon can be found here: https://www.scribd.com/document/487135032/Wodarg-Yeadon-EMA-Petition-Pfizer-Trial-FINAL-01DEC2020-en-Unsigned-With-Exhibits I hereby respectfully request that EMA act on the petition of Dr. Wodarg and Dr. Yeadon immediately. Regards 

9 Comments

  1. Dr Wodarg led the Council of Europe investigation into the WHO’s Swine Flu ‘pandemic’ caught them faking it, red-handed, ten years ago…. “fool me once. Thanks to Thom Forester

    European Parliament to Investigate WHO and “Pandemic” Scandal
    by F. William Engdahl

    The Council of Europe member states will launch an inquiry in January 2010 on the influence of the pharmaceutical companies on the global swine flu campaign, focusing especially on extent of the pharma’s industry’s influence on WHO. The Health Committee of the EU Parliament has unanimously passed a resolution calling for the inquiry.

    The step is a long-overdue move to public transparency of a “Golden Triangle” of drug corruption between WHO, the pharma industry and academic scientists that has permanently damaged the lives of millions and even caused death.

    The parliament motion was introduced by Dr. Wolfgang Wodarg, former SPD Member of the German Bundestag and now chairman of the Health Committee of PACE (Parliamentary Assembly of the Council of Europe). Wodarg is a medical doctor and epidemiologist, a specialist in lung disease and environmental medicine, who considers the current “pandemic” Swine Flu campaign of the WHO to be “one of the greatest medicine scandals of the Century.”1][1]

    The text of the resolution just passed by a sufficient number in the Council of Europe Parliament says among other things, “In order to promote their patented drugs and vaccines against flu, pharmaceutical companies influenced scientists and official agencies, responsible for public health standards to alarm governments worldwide and make them squander tight health resources for inefficient vaccine strategies and needlessly expose millions of healthy people to the risk of an unknown amount of side-effects of insufficiently tested vaccines. The “bird-flu”-campaign (2005/06) combined with the “swine-flu”-campaign seem to have caused a great deal of damage not only to some vaccinated patients and to public health-budgets, but to the credibility and accountability of important international health-agencies.”1][2]

    https://healthcare-in-europe.com/en/news/european-parliament-to-investigate-who-pandemic-scandal.html

  2. The vital interaction that mRNA has with our DNA has made selling mRNA vaccine technology extremely difficult for those who believe it’s the future of human medicine. The fact that it will alter the function of your DNA in your body has made many people suspicious of what unexpected horrors could arise through mass use of this new and experimental technique.

    Unsurprisingly, the people marketing the vaccines have tried to downplay the aggressive and genetically manipulative nature of the treatment. In fairness, trying to explain the workings of such a complex new technology in plain English is exceedingly difficult. This is apparent when one listens to representatives of the mainstream media, who are often mealy mouthed when describing the biological processes that will take place when you receive the mRNA vaccine. But inability to articulate the technology isn’t surprising when you consider that part of your DNA, after breaking in two through a natural process, will then be combined with the experimental mRNA in a way that seems esoteric to many of us. It’s almost impossible to imagine such a process taking place in one’s own vulnerable biological system, in one’s DNA, the most precious building blocks of life that define your very existence.” – Johnny Vedmore

    https://unlimitedhangout.com/2020/11/reports/pfizers-experimental-covid-19-vaccine-what-youre-not-being-told/?fbclid=IwAR05W6MOF4a80b1wZtvmCrai-wpwRdTGaUmPcYLXlcxGWH1u-WC-i40r3Zg

  3. Thank you for this enlightening post! Readers may be interested in the Emergency Injunctions issues by an International Tribunal against such COVID vaccinations – SEE: Judgment of the Tribunal in the matter of
    Genocidal Technologies Pandemic
    CITATION: https://exopolitics.blogs.com/international_criminal_co/2020/12/judgment-of-the-tribunal-in-the-matter-of-genocidal-technologies-pandemic-on-the-indictment-genocide-crimes-against-human.html

    TRIBUNAL PRESS RELEASE
    International Tribunal Indicts Pandemic defendants that distribute COVID vaccines and rollout 5G installations that allegedly cause DNA damage and EMF/vaccine genocide
    https://newsinsideout.com/2020/11/international-tribunal-indicts-pandemic-defendants-that-distribute-covid-vaccines-and-rollout-5g-installations-that-allegedly-cause-dna-damage-and-emf-vaccine-genocide/

    On the Indictment:
    Genocide & Crimes against Humanity by 5G-Pandemic Perpetrators
    https://exopolitics.blogs.com/international_criminal_co/2020/11/indictment-hearing-genocide-crimes-against-humanity-by-5g-pandemic-perpetrators-parts-1-to-3.html

    Legal Standing of the Natural and Common Law Tribunal for Public Health and Justice – A Summary
    https://exopolitics.blogs.com/international_criminal_co/2020/12/legal-standing-of-the-natural-and-common-law-tribunal-for-public-health-and-justice-a-summary.html

  4. Fantastic work Alfred, you’re one of few high quality investigative journalists unafraid to dive deep into all topics. Thank you. We do have your website in our links list too.

    1. https://evolvetoecology.org/2020/12/15/dr-kory-recommends-ivermectin-a-powerful-anti-viral-drug-for-early-treatment-for-covid-patients/

      Lawyer Robert F Kennedy Jr stated on Instagram –

      ”The published peer reviewed medical literature supports Ivermectin as a miraculously effective treatment for COVID-19. The drug’s scientifically proven success creates a new dilema for Anthony Fauci and his 20 billion dollar vaccine enterprise. If FDA approves Ivermectin as a treatment, none of Dr. Faucie’s mischievous vaccines will be eligible for Emergency Use Authorisation. All of them would be measured against a new standard of care against which none of them can complete. And widespread use of Ivermectin will mean the disappearance of the pandemic as infection fatalities drop below mortality rates for seasonal flu.

      These considerations drove Dr. Fauci’s fraudulent and genocidal campaign against hydroxychloroquine last Spring. His current posture towards Ivermectin is to ignore it for the moment-and let patients die-while rushing his vaccines in to saturate the market so that he can claim credit when death rates drop. Then they will stop the PCR testing and the pandemic will miraculously disappear. The Medical Cartel will attribute COVID’s abolition to lockdowns, masks, surveillance and vaccines. The elites will declare Dr. Fauci a ”human rights hero”, and we will all be stuck genuflecting to Big Pharma, its totalitarian controls and its infernal boondoggles for eternity. I hope I am wrong, but I’ve known Dr Fauci for decades. I’ve seen all his homicidal filmflams and swindles. He is Boss Bunco Artist for the Medical Cartel and we are all his pigeons (Read my upcoming biography of Dr. Fauci, ”Teflon Tony-Big Pharma’s Coup against Democracy”. Published this coming February 2021 by Skyhourse/CHD)”- R.F.Kennedy Jr

      https://evolvetoecology.org/2020/12/15/dr-kory-recommends-ivermectin-a-powerful-anti-viral-drug-for-early-treatment-for-covid-patients/

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