December 24, 2020 (American Thinker) — There are ongoing reports of the COVID-19 vaccine causing severe allergic reactions in recipients throughout the world. There is information that suggests that such allergic reactions, along with other dangers, were known to be associated with the COVID-19 vaccines but were covered up or wrongly downplayed prior to and during the emergency use authorization process.
Before providing that information, one should be reminded of what “Emergency Use Authorization” means. Another COVID-19 vaccine has received Emergency Use Authorization by the U.S. Food and Drug Administration (FDA). Much of the mainstream media and many public health officials are wrongly portraying the COVID-19 vaccines as “FDA-approved.” That is not true. Emergency Use Authorization is not FDA approval. In the FDA’s own words:
In the event an [Emergency Use Authorization] is issued for this product, it would still be considered unapproved and would continue under further investigation (under an Investigational New Drug Application). (page 8, emphasis added)
A person who receives one of the two COVID-19 vaccines authorized for emergency use should consider himself in the realm of guinea pigs and human research subjects. (Note also: Public health and pharmaceutical officials are mostly immune to liability if one is injured or
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