This was weeks before the rollouts began.
This is slide 16 from their presentation.
Proof they knew there could be the worst possible adverse reactions before they granted Emergency Use Authorisation (EUA).
And do any of these adverse reactions sound familiar to those you’re hearing about?
True, they have to look at potential risks before granting EUA, but why did they think any of these risks were worth it for a disease with a survivability rate of 99.9X%? Not to mention when there were known – albeit censored and massively suppressed – cures.
How can a handful of people make this choice and play Russian roulette with the lives of the rest of the population?
Specifically, it was the Vaccines and Related Products Advisory Committee of CBER (Center for Biologics Evaluation and Research) within the FDA that met.
This is a link to their presentation including Slide 16.
And this is the link a video of the virtual meeting held on 22 Oct 2020.
Disclaimer: The meeting is about 9 hours long. So no, I haven’t watched all of it.
I’ve seen enough.