No Covid-19 urgent vaccine approval
Stop ongoing vaccination studies
Stop the ongoing vaccination studies
https://www.wodarg.com/impfen/1.12.2020 Together with Dr. Michael Yeadon, ex-Pfizer Head of Research, I filed an application with the EMA, the European Medicine Agency responsible for EU-wide drug approval, on December 1, 2020 for the immediate suspension of all SARS-CoV-2 vaccine studies, in particular the BioNtech / Pfizer study on BNT162b (EudraCT number 2020-002641-42)....
1.12.2020 Together with the ex-Pfizer research director Dr. Michael Yeadon I will have one at the EMA, the European Medicine Agency, which is responsible for EU-wide drug approval, on December 01st, 2020 Application for the immediate suspension of all SARS-CoV-2 vaccine studies, in particular the study by BioNtech / Pfizer on BNT162b (EudraCT number 2020-002641-42).
We demand that the studies - to protect the life and health of the test persons - are only 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, To take into account.
As petitioners, we demand, on the one hand, that because of the known lack of accuracy of the PCR test in a serious study, so-called Sanger sequencing must be used. 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 risk of the disease nor a possible vaccination benefit can be determined with the necessary certainty. For this reason alone, such tests of vaccines on humans are per se unethical.
Furthermore, we demand that it must be ruled out beforehand that risks already known from previous studies, some of which arise from the nature of the corona viruses, could have dangerous effects. Our concerns focus on the following points in particular:
- The formation of so-called “non-neutralizing antibodies” can lead to an excessive immune reaction, especially when test subjects are confronted with the real, “wild” virus after vaccination. This so-called antibody dependent enhancement, ADE, has long been known from experiments with corona vaccines in cats. In the course of these studies, all cats that initially tolerated the vaccination well died after being infected with real coronaviruses. This overreaction is further promoted by active enhancers.
- The vaccinations are expected to raise antibodies against the spike proteins of SARS-CoV-2. But also contain spike proteins among other things Syncytin-homologous proteinswhich in mammals, such as humans, are essential for the formation of the placenta. It must be absolutely ruled out that a vaccine against SARS-CoV-2 triggers an immune reaction against syncytin-1, otherwise Infertility of indefinite duration this could result in vaccinated women.
- In the mRNA vaccines from BioNTech / Pfizer is Polyethylene glycol (PEG) contain. 70% of people develop antibodies against this substance - that means many people can allergic, possibly fatal reactions to develop vaccination.
- The far too short duration of the study does not allow a realistic assessment of the long-term effects. As with the narcolepsy cases after the swine flu vaccination, long-term consequences would only be observed in the event of a planned emergency approval when it is already too late for millions of people who have been vaccinated. Governments plan to expose millions of healthy people to unacceptable risks and force them to vaccinate through discriminatory restrictions on those who are not vaccinated.
- Nevertheless, BioNTech / Pfizer apparently submitted an application for emergency approval on December 01st, 2020. Scientific responsibility forces us to take this action.