Dr. Wodarg and Dr. Yeadon request the stop of all corona vaccination studies and call for the petition to be signed.
Dr. Wodarg and Dr. Yeadon demand that the studies - to protect the life and health of the test subjects - only be continued when a study concept is available that is suitable to address the considerable safety concerns that are being expressed by more and more well-known scientists against the vaccine and the study design taken into account.
On the one hand, the petitioners demand that, because of the known lack of accuracy of the PCR test, a serious study must use what is known as Sanger sequencing. This is the only way to make reliable statements about the effectiveness of a vaccine against Covid-19. On the basis of the many different PCR tests of very different quality, neither the disease risk nor a possible vaccine benefit can be determined with the necessary certainty, which is why testing the vaccine on humans is per se unethical.
Furthermore, they demand that it must be excluded e.g. by means of animal experiments that risks known from previous studies, some of which arise from the nature of the corona viruses, can be realized. The concerns focus on the following points in particular:
The formation of so-called “non-neutralizing antibodies” can lead to an excessive immune reaction, especially if the test person is confronted with the real, “wild” virus after the vaccination. This so-called antibody dependent enhancement, ADE, is e.g. long known from experiments with corona vaccines in cats. 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 raise antibodies against the 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 excluded that a vaccine against SARS-CoV-2 triggers an immune reaction against syncytin-1, as otherwise infertility of indefinite duration in vaccinated women could result.
BioNTech / Pfizer mRNA vaccines contain polyethylene glycol (PEG). 70% of people develop antibodies against this substance - this means that many people can develop allergic, possibly fatal reactions to the vaccination.
The far too short duration of the study does not permit a realistic assessment of the long-term effects. As in the narcolepsy cases after the swine flu vaccination, a planned emergency approval with subsequent observation of long-term consequences would possibly expose millions of healthy people to an unacceptable risk.
Nevertheless, BioNTech / Pfizer apparently submitted an application for emergency approval on December 1, 2020.
CALL FOR HELP: Dr. Wodarg and Dr. Yeadon ask that as many EU citizens as possible sign their petition by sending the email prepared here to the EMA.
Please send e mail to:
example: Dear Sir or Madam, I am hereby co-signing the petition of Dr. Wodarg to support his 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 can be found here:
I hereby respectfully request that EMA act on the petition of Dr. Wodarg immediately.
The EFVV (European Forum for Vaccine Vigilance) is an alliance of member-organisations and individual members from 25 European countries. Our member-organisations consist of consumer groups and pro-choice groups whose members in turn include medical professionals and scientists. Their combined memberships exceed 100,000. We call on all Europeans to stand together in a demand for a united vaccination policy based on freedom of choice and informed consent. We believe that mandatory vaccination is not only a serious risk but a violation of human rights and dignity. We therefore demand transparency and caution as well as recognition and concern for the many vaccine-injured in Europe and beyond.