15 Dec Sonia Elijah – FDA’s forced hand drops Pfizer’s Bombshell Safety Document
We don’t know Ms. Elijah, but her report is an example of throwback journalism. We doubt a reader could discern Ms. Elijah’s political views. She’s actually read the very few documents released by Pfizer, carefully analyzed them, and offered reasoned observations. The article is probably a little too technical for most tastes, so we haven’t reproduced it within this post (you can read it by clicking on the link above). But the first paragraph of her conclusion jumps off the page:
While this author strives to remain as objective and unbiased as humanly possible, a thorough review of this one report suggests that the FDA and Pfizer have appeared to conceal the full extent of the Pfizer-BioNTech vaccine side effects from the public. If this assumption is in fact true, then the ‘Gold Standard’ regulatory agency and the prestigious multinational pharmaceutical company have thrown the entire concept of informed consent out the window.
“…thrown the entire concept of informed consent out the window“…and so the question is why?
And anyone with an ounce of common sense knows the reason why. Which is, that if the full extent of adverse side effects from the vaccines (the data they want to withhold from public view for 75 years) were known and evaluated objectively in relation to a disease which the CDC itself indicates has a 99+% recovery rate for almost everyone, many reasonable people would say ‘no thanks’ to the vaccines. Which would kill Big Pharma’s cash cow and derail any other agenda behind ‘vaccine mandates’.
The scale and breadth of corruption in Big Pharma and Big Public Health is starting to dawn on millions of people, worldwide. That can be a good thing. Time will tell.