Originally published on Trial Site News. On August 23, 2021, the US Food and Drug Administration (FDA) granted approval (or licensure) to the first ever COVID-19 mRNA gene therapy product by Pfizer/BioNTech, which from the onset was misbranded as a ‘vaccine.’
Nice article, Sonia. These CDC and FDA criminals need to pay for lying about the safety concerns associated with these "vaccines." They should all go to jail and be stripped of all of their wealth.
One of the main things I remember from the October 2020 meeting was the similarities and differences between the FDA's adverse event slide and the CDC's Shimabukuro's slide. The CDC had covid listed as an adverse event while the FDA did not. When I saw that it told everyone what they needed to know. Period. Game over.
Sonia, Thank you for the great article. From what I've read, only the EUA product is available to the public. This way Pfizer and Moderna are protected legally. The FDA product is not available to the public and was only licensed so that these products could be mandated by employers and universities. From what I understand, this was a bait and switch strategy? If the licensed product had been administered, the pharmaceutical companies like Pfizer would have exposed themselves to potential litigation due to injuries and deaths.
Great summary. But you're missing a key piece of info, perhaps for another story.
The licensed product has NEVER been used in even one patient in the United States. Not once. And Pfizer made it clear when the fact that the shot contents differed from the licensed product that they had no plans to use the licensed formula in the U.S.
Combine that with the fact that Pfizer was operating under a DoD contract. And patents exist for the virus itself at least two decades ago, and the "vaccine" contents circa 2017 by Moderna, who was hired to do this by... drum roll.... DoD.
Nice article, Sonia. These CDC and FDA criminals need to pay for lying about the safety concerns associated with these "vaccines." They should all go to jail and be stripped of all of their wealth.
Sonia,
Never have so many owed so much to so few; as you.
Thank you for your great courage, clarity, charity, commitment, and sacrifice.
I continue to be amazed by findings. Keep up tge good work.
One of the main things I remember from the October 2020 meeting was the similarities and differences between the FDA's adverse event slide and the CDC's Shimabukuro's slide. The CDC had covid listed as an adverse event while the FDA did not. When I saw that it told everyone what they needed to know. Period. Game over.
Sonia, Thank you for the great article. From what I've read, only the EUA product is available to the public. This way Pfizer and Moderna are protected legally. The FDA product is not available to the public and was only licensed so that these products could be mandated by employers and universities. From what I understand, this was a bait and switch strategy? If the licensed product had been administered, the pharmaceutical companies like Pfizer would have exposed themselves to potential litigation due to injuries and deaths.
All the while they have been touting it as "safe and effective."
This is the biggest crime against humanity in all of human history, by far!
Great summary. But you're missing a key piece of info, perhaps for another story.
The licensed product has NEVER been used in even one patient in the United States. Not once. And Pfizer made it clear when the fact that the shot contents differed from the licensed product that they had no plans to use the licensed formula in the U.S.
Combine that with the fact that Pfizer was operating under a DoD contract. And patents exist for the virus itself at least two decades ago, and the "vaccine" contents circa 2017 by Moderna, who was hired to do this by... drum roll.... DoD.
So, what do you think? Innocent "mistakes?"
Excellent writeup