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April 14, 2021 (Common Ground) – Canadians are not being told the truth about the COVID vaccine products which have only been given emergency use authorization. Those lining up to participate in this human experiment are not given sufficient information to make an informed decision.
Here are the facts
On November 20, 2020, Pfizer submitted an Emergency Use Authorization (EUA) request to the US Food and Drug Administration (FDA) for an investigational product intended to prevent COVID-19. This information was the basis upon which the FDA permited emergency use authorization of their product in the general population.
The Pfizer vaccine includes ingredients never before used in licenced vaccines, and functions unlike any previous vaccine to date. This treatment is more accurately a medical device and includes synthetic genetic technology based on a computer generated “spike glycoprotein antigen encoded by RNA and formulated in lipid nanoparticles.”
The information below is taken directly from the Pfizer Emergency Use Authority request and a meeting of the Vaccines and Related Biological Products Advisory Committee.
Under Section 6.2: Unknown Benefits/Data Gaps
Duration of protection
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