August 23, 2021 |
As expected the FDA announces today that Pfizer has been granted Biologic License Application approval for their COVID-19 vaccine. [Press release Here] and you can find the Approval Letter at the following LINK HERE. The vaccine will now be known as “Comirnaty”, and is approved for individuals 16 years of age and older.
Two key issues stick in my mind about the COVID vaccines that make me pretty firm in opposition:
(1) The fact that vaccine makers would abandon the clinical trial control group is a big red flag. The fact that vaccine makers could not abandon the clinical trial control group without authorization from the FDA, CDC and NIH is an even bigger red flag. {Go Deep}
The clinical trial was assembled to produce only one result. THAT is not science. THAT is sketchy and points to an ulterior motive. That is not science, that’s political science.
(2) The fact that data shows the vaccine provides no benefit is another big red flag. Specifically, the equal hospitalization rate of vaxxed and non-vaxxed patients. Almost every study I can find with data on COVID hospitalized cases that includes the vaccination status (not many), shows an equal percentage of vaccinated/hospitalized people to the vaccinated population in general. {Go Deep}
[ex. If 75% of the regional population is vaccinated, then 75% of the hospitalized COVID patients are vaccinated.] This statistic demonstrates the vaccine doesn’t stop serious illness.
Put both of those issues together, and overlay the demonstrably collapsed institutional credibility, and I am not comfortable with this specific vaccine.
Spike Proteins In Immune Cells - Dr. Bruce Patterson Discusses COVID Long Haul
1:24:33
With Pfizer Likely to Get FDA Approval Monday It’s Worth Remembering Pfizer and Moderna Lost The Clinical Trial Control Group Testing Vaccine Efficacy and Safety
August 23, 2021
According to the New York Times and multiple media outlets, Pfizer is expected to get full FDA approval today. “The move would make it the first Covid vaccine to go from emergency use authorization to full FDA approval.” (read more) With that in mind, it is worth a reminder that both Pfizer and Moderna stopped the clinical trials the FDA was using in their review:
The Moderna and Pfizer vaccine tests were conducted, as customary, with a control group; a group within the trial who were given a placebo and not the test vaccine. However, during the trial -and after the untested vaccines were given emergency use authorization- the vaccine companies conducting the trial decided to break protocol and notify the control group they were not vaccinated. Almost all the control group were then given the vaccine.
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