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Ex-Pfizer Exec Demands EU Halt COVID-19 Vaccine Studies Over 'Indefinite Infertility' And Other Health Concerns
Ex-Pfizer Exec Demands EU Halt COVID-19 Vaccine Studies Over 'Indefinite Infertility' And Other Health Concerns by Tyler Durden Sun, 12/06/2020 - 11:35
Former Pfizer vice president and scientific director Dr. Michael Yeadon and German lung specialist and parliamentarian Dr. Wolfgang Wodarg have filed an urgent application with the European Medicine Agency calling for the immediate suspension of all SARS-CoV-2 vaccine studies - particularly the BioNtech/Pfizer study on BNT162b (EudraCT number 2020-002641-42).
Yeadon and Wodarg say the studies should be halted until a design study is available which addresses a host of serious safety concerns expressed by a growing body of renowned scientists who are skeptical of how quickly the vaccines are being developed, according to Germany's 2020 News.
Zitat 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. -2020 News
The pair also point to concerns raised in previous studies involving other coronaviruses - including (via 2020 News):
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.
Dr. Yeadon made headlines last month when he said "There is no science to suggest a second wave should happen," and that false positive results from inherently flawed COVID-19 tests are being used to 'manufacture' a second wave.
As Ralph Lopez write at HubPages, Yeadon warns that half or even "almost all" of tests for COVID are false positives. Dr. Yeadon also argues that the threshold for herd immunity may be much lower than previously thought, and may have been reached in many countries already.
In an interview last month (see below) Dr. Yeadon was asked:
Zitat "we are basing a government policy, an economic policy, a civil liberties policy, in terms of limiting people to six people in a meeting...all based on, what may well be, completely fake data on this coronavirus?"
Dr. Yeadon answered with a simple "yes."
He then lamented the lives lost as a result of lockdown policies, and of the "savable" countless lives which will be further lost, from important surgeries and other healthcare deferred, should lockdowns be reimposed.
Why a pandemic flu shot caused narcolepsy By Gretchen Vogel Jul. 1, 2015 , 2:15 PM
The 2009 H1N1 influenza pandemic left a troubling legacy in Europe: More than 1300 people who received a vaccine to prevent the flu developed narcolepsy, an incurable, debilitating condition that causes overpowering daytime sleepiness, sometimes accompanied by a sudden muscle weakness in response to strong emotions such as laughter or anger. The manufacturer, GlaxoSmithKline (GSK), has acknowledged the link, and some patients and their families have already been awarded compensation. But how the vaccine might have triggered the condition has been unclear.
In a paper in Science Translational Medicine (STM) this week, researchers offer a possible explanation. They show that the vaccine, called Pandemrix, triggers antibodies that can also bind to a receptor in brain cells that help regulate sleepiness. The work strongly suggests that Pandemrix, which was given to more than 30 million Europeans, triggered an autoimmune re action that led to narcolepsy in some people who are genetically at risk.
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Their search turned up a suspect: a piece of a receptor for hypocretin resembles part of the H1N1 influenza nucleoprotein—which binds to the virus genome and plays a key role in its replication. “That was really an ‘Aha’ moment,” says Ahmed, who is now at GSK, which bought part of Novartis’s vaccine division. The flu vaccine is designed to trigger antibodies to influenza’s surface proteins, but if it elicits antibodies to the nucleoprotein as well, those might well latch on to the hypocretin receptor, and eventually lead to death of the cells, the researchers thought.