From Sp1r0 Sk0uras: https://bit.ly/2KhNIUV
The Pfizer C0V1D V_XXC1NE is already being administered to the public in the UK and the first doses have been given in the US ahead of a mass vaccination campaign on a global scale.
It is important to recognize that the Pfizer C0V1D V_XXC1NE has not been approved by the FDA. It has only received Emergency Use Authorization (EUA) meaning the V_XXC1NE has not gone through the standard process to get official approval from the regulatory agency.
Now Moderna’s experimental C0V1D V_XXC1NE is set to get the same Emergency Use Authorization allowing the shot to be distributed to millions of people.
We have already witnessed short term adverse events (side effects) from the Pfizer V_XXC1NE. Truth is, nobody knows what the long term effects could be and it appears the public is being subjected to an experiment on a global scale.
In this report, we examine discrepancies in the FDA Moderna report that was voted on by an advisory panel. The panel voted 20-0 recommending EUA.
Some of the discrepancies include cherry picked trial participants to achieve the desired results to gain EUA. As well as 13 total deaths in the trials, 6 in the vaccinated group and 7 in the placebo. Something the media refuses to address.
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