FDA Wants 55 Years to Release COVID Jab Reaction Data
Analysis by Dr. Joseph MercolaFact Checked

December 02, 2021
STORY AT-A-GLANCE

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

It 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?

It took the U.S. Food and Drug Administration 108 days to review all the data Pfizer/BioNTech submitted in order to gain FDA approval for its Comirnaty COVID shot, which was licensed August 3, 2021.

Considering the agency claims there are 329,000 pages of data, the fact that they were able to read, analyze and draw conclusions about its safety and effectiveness in just 108 days — about 80,000 pages a month — is no small miracle. They must employ some very efficient speed readers.

And that is why the FDA’s claim that it now needs half a century to review the documents before they can release them to the public doesn’t seem very credible. Even Reuters has expressed shock, and its former CEO is on the board of Pfizer.1

Expedited FOIA Request for Comirnaty 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.

This includes safety and effectiveness data, adverse reaction reports and lists of active and inactive ingredients. Approximately 400 additional FOIA requests by other individuals for all or part of this information have also been filed.2

In their FOIA application, the PHMPT asked the agency to expedite release of the documents — a reasonable request, considering we have no raw data and the shots are being pushed on children as young as 5.

FOIA guidelines include two conditions upon which a request may be expedited. One is “if the lack of expedited treatment could reasonably be expected to pose a threat to someone’s life or physical safety,” which one could easily argue is the case here.

The second condition is “if there is an urgency to inform the public about an actual or alleged federal government activity, if made by a person who is primarily engaged in disseminating information.” This too is clearly applicable.

“During a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, and the military, the public has an urgent and immediate need to have access to this data,” the PHMPT said in its request.3

More at this link:https://articles.mercola.com/sites/articles/archive/2021/12/02/vaccine-reaction-data.aspx?

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Thank You GeorgeE for this very important post above, this information is vital and must be used to stop this insane mandate.

It is insane, pushing the clot shot is done by those that are insane!

Many Blessings,
CrystalRiver