By Liberty Counsel —— Bio and Archives--July 27, 2023
WASHINGTON, D.C. – The U.S. Food and Drug Administration (FDA) last week fully approved a second-generation anthrax vaccine meant to treat adults ages 18 to 65 only after anthrax exposure, even though it must be administered together with other antibacterial drugs. The two-dose vaccine is called Cyfendus, and its ingredient list contains known toxic substances such as aluminum, formaldehyde, and benzethonium chloride, and may cause serious side effects according to the vaccine’s package insert.
The ingredient list also names CPG 7909, a largely unexplained synthetic DNA molecule. Except for this synthetic ingredient, Cyfendus contains the same ingredients as its predecessor Biothrax, which was FDA approved in 2016 and is meant to be taken before anthrax exposure.
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By Wayne on 2023 07 28
they need a blanket party
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