April 15, 2024

FDA Wants 55 years to Process FOIA Request Over Vaccine Data


In this November 19, 2021 article for Reuters, Jenna Greene reports on the response put out by the Food and Drug Administration (FDA) regarding a Freedom of Information Act (FOIA) request.

A group of scientists has filed a FOIA request to the federal government asking it to share the data used by the FDA to license Pfizer’s COVID vaccine. The FDA says that it needs to review all the vaccine-related documents it possesses, but that it needs 55 years (and beyond) to be able to do so.

The plaintiffs are a group of more than 30 professors and scientists from universities including Yale, Harvard, UCLA, and Brown. They say, releasing the information would reassure vaccine skeptics that indeed, the shots are “safe and effective and, thus, increase confidence in the Pfizer vaccine”.

The lawyers representing the FDA, however, note that there are at least 329,000 pages of documents included in the FOIA request. “The records must be reviewed to redact “confidential business and trade secret information of Pfizer or BioNTech and personal privacy information of patients who participated in clinical trials”, they said.

The plaintiffs assert that the government must grant their request by March 3, 2022, saying “This 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer’s COVID-19 vaccine”.

The plaintiffs were represented by Aaron Siri of Siri & Glimstad in New York and John Howie of Howie Law in Dallas in court papers [Siri has figured in a number of important lawsuits lately, see Know Your Right, a Law Firm Fighting Mandatory COVID-19 Vaccine and CDC: No Record of Naturally Immune Transmitting COVID-19].

Editor’s Note: We stand in awe of the brazenness of the FDA. Are the courts also corrupted that they can grant such a request?

We agree with the plaintiffs, if the FDA can approve the Pfizer vaccine in just a few days despite the more than 329,000 they have to sort through, they will definitely be able to produce the data needed to peer review their decision to approve the experimental vaccine for general use.

It is clear that the FDA is only buying time. Citizens should pay close attention to this case as the release of such data give conclusive proof that the COVID vaccines are dangerous [Covid Vaccines are Bioweapons for Mass Genocide, Scientists Sound Alarm: Vaccines Will Kill Millions].

Though we have to say, it’s not as if we need any more confirmations. The data alone speaks of the truth, see New study: Vaccines are the likely cause of adverse effects and deaths following vaccination, W.H.O’s VigiAccess Shows More than Two Million Adverse Events Following COVID Vaccination, Majority of Covid-19 Deaths and Hospitalizations in Scotland are Fully Vaccinated, Norway Study Finds ZERO Vaccine Effectiveness Against Death for Covid Hospital Patients].

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