The Conspiracy Theorists were correct again. Now the dust is settling, it's very clear that the jabs weren't properly tested and that known severe side effects were concealed.
In recent months, two Pfizer officials have bragged about moving vaccine science forward at a speed that disallows proper scientific protocols from being followed, and the release of reformulated mRNA COVID boosters without testing is now the norm.
In November 2022, recently retired head of vaccine R&D at Pfizer, Kathrin Jansen, said "we flew the aeroplane while we were still building it. We couldn't wait for data, we had to do so much at risk." Pfizer compressed its vaccine development timeline from 10 years to a mere nine months by simultaneously developing and testing the product in human trials.
Pfizer and other COVID jab makers hid side effects by eliminating the control groups long before the studies were over
Vaccine makers are readying to release other mRNA shots, many of which are being fast-tracked and predicted to receive authorization in months rather than years. Moderna is working on a three-in-one shot for COVID, flu and RSV (respiratory syncytial virus), and they seem to expect releasing it before clinical trials are finished
Pfizer quoted and relied on data from Israel when it sought approval from the FDA, and as it turns out, the Israeli government hid information about side effects. It didn't even implement its surveillance system until a year after the shots rolled out, and when the data were analyzed, researchers concluded there were causative links between certain side effects and the jabsPfizer's primary focus was to create a shot that minimized the symptoms of infection, but aside from that, there was no time to assess side effects or long-term drawbacks of the technology, such as antibody-dependent enhancement, myocarditis, or spontaneous abortions.
This is probably why Pfizer and the other COVID jab makers all decided to eliminate the control groups long before the studies were even over. This way, side effects could be hidden, and we see the effects of that decision now.
Myocarditis, blood clots, lethal heart attacks, strokes, cancer and sudden death are all skyrocketing, but since there's no official control group to compare with, those trends are written off as either normal or coincidental. You've probably seen that heart attacks are now blamed on everything from hot weather and cold showers to soil microbes in your garden, climate change and loud noises.
We know warp speed is the new norm because of a decision made by the U.S. Food and Drug Administration this past summer. During its June 28, 2022, Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting, they approved a bivalent COVID shot for fall 2022.3
With that vote, they sneaked in a whole new policy, a new framework, under which reformulated COVID shots will be treated as biologically similar to existing shots and therefore be allowed to skip clinical trials.
During that meeting, they were originally scheduled to vote on the Future Framework policy question of whether reformulated shots should be treated as new molecular entities subject to formal review. They never addressed that policy question and instead skipped right to the vote on a bivalent COVID shot for the fall.
By approving it, knowing there would be no time for testing and data gathering, they replaced the old evidence-based system through a sleight of hand. The bivalent shots received emergency use authorization (EUA) at the end of August 2022, based on the antibody levels in eight mice.