Sasha Latypova has a background in pharmaceutical research and development. She has worked for over 60 pharmaceutical companies including Pfizer and Johnson and Johnson.
1.Pfizer’s program did not include a comprehensive end-to-end test of all components of the final approved product. The studies included in the approval package were for a variety of versions of the product with no comparability assessments, thus no comprehensive assessment of product safety can be made.
2. The toxicity of the vaccine’s mRNA active ingredient was never studied!
3. Pfizer claimed absence of potential for “vaccine-elicited disease enhancement” based on studies of an animal species that does not get sick from Sars-Cov-2.
4. CDC, FDA and Pfizer lied about “vaccine staying in the injection site”
5. Pfizer skipped major categories of safety testing altogether.
6. Pfizer used dishonest and self-serving interpretation of regulatory guidelines to avoid routine safety testing.
7. Both FDA and Pfizer knew about major toxicities associated with gene therapy class of medicines, and therefore cannot claim lack of anticipatory knowledge of these risks. This points to intentional fraud and collusion between Pfizer and the regulators to push this untested dangerous product on the market.
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