Dec 29, 2022
Seventy-five years. That’s how long Pfizer and the FDA tried to hide the Pfizer documents from public view — long after just about everyone affected is dead. It wasn’t until renowned attorney Aaron Siri led a FOIA case against the FDA that a federal judge ordered the documents to be released in 108 days, the same amount of time it took the FDA to approve the Covid-19 injections.
Dr. Chris Flowers, MBBS, FRCR, FSBI, is a retired Associate Professor of Radiology at the University of South Florida [is] an extraordinary member of the Pfizer documents volunteer team [investigating those court-ordered released documents]. It was he who broke the story that Pfizer and the FDA knew, months ahead of time, that 35 teens suffered heart damage within a week of receiving the C19 shots before any U.S. government agency issued a press release warning the risks of myopericarditis to parents. He is also an author and a retired scientific paper reviewer for multiple radiology journals.
He writes: “As you know, endlessly on TV, all the pundits, all the bigwigs, they were all telling us we had to get the vaccine, and it was “perfectly safe.” But it’s getting more and more clear, as we spend time going through the documents, that the safety aspects of any vaccine trial were basically ignored. And I found out even more disturbing things coming out of the European Medicines Agency (think of as Europe’s FDA) in that they don’t even require the safety testing. They don’t even require the distribution and excretion of a vaccine to be approved for use in patients.”
Dr. Flowers came to this conclusion from a paper by Hélène Banoun, biological pharmacist, PhD: “The anti-Covid mRNA vaccines aren’t subject to biodistribution and excretion studies, and this is according to the regulations of the health agencies.”
“The same product may or may not be classified as a gene product depending on whether or not it is qualified as a vaccine against an infectious disease. In the latter case, it may be exempted from these studies.”