Judge Orders FDA to go Back to The Future where it Reveals Pfizer’s Covid-19 Vaccine Killed over 1200 in first 90 days of EUA use starting in 2020
In response to a Freedom of Information Act (FOIA) request for vaccine records submitted by Pfizer to obtain an FDA Emergency Use Authorization (EUA) for their Covid-19 shot, the Biden Department of Justice argued for 55 years in order for the FDA to comply. That would put them in the year 2076!
This FDA’ counter offer to the FOIA request for over 329,000 documents was made on the basis of what can only be described as ‘hardship’. In citing the need to exclude sensitive information exempted from a FOIA, such as trade secrets, the FDA complained that their ‘review and redact’ department only had 10 employees. The best they could do, presumably with sleeves rolled up, was to release 500 pages per month.1
This JFK-like sealed records approach to transparency would have their progeny answering to our progeny.
Apparently, however, there is at least one Federal Judge who still owns a DeLorean. That judge ordered the FDA to go back to the future and return with the FOIA, in full.2 Perhaps the judge reasoned that if the Biden administration could hire 80 thousand new IRS agents to monitor the minuscule financial transactions of 320 million Americans, somebody could approve some overtime at the FDA.3
Reportedly, the reason for the Biden administration’s obstruction to the FOIA can already be found in some numbers released by the FDA, as they comply with the original order.
In the first 90 days of jabbing with the Pfizer vaccine under the FDA’s Emergency Use Authorization, there were 1223 reported fatalities.4 While we are still searching for overall vaccine numbers to arrive at an actual percentage of deaths per vaccinated, the idea that this vaccine can be mandated over an individual’s right to make an informed consent to receive the jab is hereby tragically shown to be criminal.
The extent to which the Biden administration can be held responsible for mandating Americans to their deaths is something for future litigation to determine, but a more immediate slew of actions might now be brought against Pfizer. If it can be proved that Pfizer conspired with the FDA, and was helped by Biden’s DOJ, to cover up known reactions, including death, caused by their vaccine, they may have broken their ‘shield’.
Operating under the FDA’s Emergency Use Authorization shielded Pfizer form lawsuits arising from adverse reactions to their vaccine. That shield prevented victims and victims’ survivors from suing for damages. This could be huge. Even the adverse reactions report cited above notes that “Reports are submitted voluntarily, and the magnitude of underreporting is unknown.”5
[Editor’s Note: Due to current reporting methods and lack of verification measures, adverse reactions, including fatalities, resulting from the Covid-19 vaccines are difficult to quantify. The Centers for Disease Control (CDC) maintains The Adverse Event Reporting System (VAERS). While VARES encourages health care providers, manufacturers, and the public to report vaccine events, they are completely voluntary, and the means to definitively verify them does not exist at this time. Conversely, at least one study has suggested that the actual instances where reports are submitted to VARES may represent only 1% of actual vaccine reactions, in some cases. The European counterpart to the FDA is the European Medicines Agency (EMA) with its EudaVigilance (EV) for vaccine event reporting. The EV cites similar constraints in being able to assess and verify submitted data. To date, VARES has published figures for Covid-19 fatalities as high as 19,532 total events, and the EMA’s EV has reported 30,551 fatalities. While these numbers are made available by these agencies to the public, the numbers are scarcely reported in the media, in part, due to the difficulties cited above. It is critical to note that the vaccines administered when these numbers were obtained for VARES are the ones, such as Pfizer-BioNTech Covid-19, that were authorized for use under the FDA’s Emergency Use Authorization (EUA). This EUA status was reaffirmed in the FDA’s letter approving the biologics license application (BLA) for the, as yet unavailable, COMERNATY vaccine, dated August 23, 2021 (original), and as conceded in DOE et al v. AUSTIN et al, case number 3:21-cv-01211, 12 NOV 21, US District Court for the Northern District of Florida.]
Notes:
- “FDA Requesting 55 years to Process FOIA Request For COVID Vaccine Data,” Legal Insurrection. November 21, 2021. https://legalinsurrection.com/2021/11/fda-requesting-55-years-to-process-foia-requestfor-covid-vaccine-data/
2. “Court Orders FDA To Comply With FOIA and Release Information On Pfizer Vaccine – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS,” Gateway Pundit, By Julian Conradson, Published December 2, 2021 at 7:00am
- “Biden plan to hire 80K IRS agents will backfire, letting wealthy dodge taxes, expert warns,” The Washington Times. November 11, 2021. https://www.washingtontimes.com/news/2021/nov/11/tax-expert-bidens-plan-hire-80k-irs-agents-will-ba/
4 – 5. Cumulative Analysis of Post-authorization Adverse Event Reports, CONDFIDENTIAL, page 7, 5. https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
