FDA wants to hide COVID vaccine reaction data

In September 2021, a group called Public Health and Medical Professionals for Transparency (PHMPT) filed a Freedom of Information Act (FOIA) request with the FDA to obtain the documentation used to approve Comirnaty. When, after a month, the FDA had not replied, the PHMPT sued
    I
t took the U.S. Food and Drug Administration 108 days to “thoroughly and completely” review the 329,000 pages of data Pfizer/BioNTech submitted to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021
   
The FDA now claims it needs 55 years to release those same pages to the public (at a rate of 500 pages per month), as each page must be reviewed and sensitive information redacted 

The FDA has so far only released 91 pages. These documents show that within the first 2.5 months of the Pfizer shot’s rollout, Pfizer received 42,086 reports of adverse events, including 1,223 fatalities
   
While Pfizer admits it received such a large number of spontaneous adverse event reports that they had to hire a redacted number of additional full-time personnel to handle the additional data entry, they claim that “The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.” If they expected this volume of injuries, why were they short-staffed — and why does the FDA think the number of new hires is proprietary information?

Read the full analysis by Dr. Mercola

 

 

George W. Bush: The terrorists want to change our lifestyle