
Should the FDA have eased mRNA vaccine regulations during the pandemic and what are the safety consequences of regulatory delays?
We will discuss the third major issue related to DNA contamination with residual bacterial plasmids and truncated mRNA from the manufacturing process.
We introduce the inflammatory response to the spike protein and one of its subunit proteins and how they may contribute to serious adverse events.
We will now discuss how the LNPs are constructed and how they behave in the body.
The regulatory authorities knew about the adverse events found in animals by January 2021, but the vaccines were permitted to go forward in humans.
Despite lack of adequate safety testing for the first mRNA “vaccine” for humans, the FDA granted authorization and assured the public that the product was safe.
Should the FDA have eased mRNA vaccine regulations during the pandemic and what are the safety consequences of regulatory delays?
We will discuss the third major issue related to DNA contamination with residual bacterial plasmids and truncated mRNA from the manufacturing process.
We introduce the inflammatory response to the spike protein and one of its subunit proteins and how they may contribute to serious adverse events.
We will now discuss how the LNPs are constructed and how they behave in the body.
The regulatory authorities knew about the adverse events found in animals by January 2021, but the vaccines were permitted to go forward in humans.
Despite lack of adequate safety testing for the first mRNA “vaccine” for humans, the FDA granted authorization and assured the public that the product was safe.