FDA Withholding Autopsy Results on People Who Died After Getting COVID-19 Vaccines

Above image: FDA Commissioner Robert Califf

The FDA has refused a Freedom of Information Act request from a news organization, using a spurious excuse, according to an FDA advisor, that the reports would violate the medical privacy of the subjects.

Kim Witczak, a drug safety advocate who advises the FDA as part of the Psychopharmacologic Drugs Advisory Committee, said that the reports could be easily be released with personal information blacked out.

The Epoch Times reported on September 29, 2022:

The U.S. Food and Drug Administration (FDA) is refusing to release the results of autopsies conducted on people who died after getting COVID-19 vaccines.

The FDA says it is barred from releasing medical files, but a drug safety advocate says that it could release the autopsies with personal information redacted.

The refusal was issued to The Epoch Times, which submitted a Freedom of Information Act for all autopsy reports obtained by the FDA concerning any deaths reported to the Vaccine Adverse Event Reporting System following COVID-19 vaccination.

Kim Witczak told the Times via email:

“The personal information could easily be redacted without losing the potential learnings from [the] autopsy….Autopsies can be an important part of postmortem analysis and should be done especially with increased deaths following COVID-19 vaccination,” 

The FDA refusal takes place after a number of pathologists in different countries have concluded firmly that the COVID vaccines, which are still in phase III adult clinical trials, are the direct cause of many of the unexpected deaths being reported post-vaccination, to databases such as the CDC’s Vaccine Adverse Event Reporting System (VAERS,) which was set up as an “early warning system that monitors the safety of vaccines after they are authorized or licensed for use by the U.S. Food and Drug Administration (FDA).

The VAERS “early warning system,” the CDC’s words, was set up to indicate when the distribution of a drug must be terminated so that it can be studied further for safety issues.

To date the CDC’s VAERS has registered an unprecedented number of safety signals, including over 7,000% more deaths for the COVID vaccines than for all other vaccines combined, per year. For nearly 30 years since the system’s inception, about 200 deaths per year have been reported to VAERS for all vaccines combined. For COVID vaccines alone, over 30,000 deaths have been reported in just under two years.

(click for larger image below)

In September of 2021, two German pathologists, Professor Arne Burkhardt, MD, and Professor Walter Lang, MD, presented autopsy findings at a conference at the Pathological institute in Reutlingen, Germany, entitledCause of death after COVID-19 vaccination & Undeclared components of the COVID-19 vaccines video below. The conference was the first of a series.

September 20th, 2021, Conference at Pathological institute in Reutlingen, Germany, “Cause of death after COVID-19 vaccination & Undeclared components of the COVID-19 vaccines (view at Bitchute)

For the entire conference series and the work of other pathologists see “Autopsies Show Direct Causal Link Between Unexpected Deaths and COVID Vaccines.”

 The COVID vaccines are unprecedented for bypassing the normal one to three years of animal safety trials in vaccine and drug development which are typical before a new drug ever enters a human, in human clinical trials. The average time for bringing any new drug or vaccine to general use is 10 years.

Phase III adult clinical trials for both the Pfizer and Moderna injections are still ongoing. Moderna’s data is scheduled to be complete in December 2022, and Pfizer’s in February 2024. As such, both drugs are still in experimental stages. FDA authorization of a novel drug before clinical trials are complete is unprecedented.

Below: Cover sheet for Pfizer adult clinical trials protocol submitted to FDA, “Study to Describe the Safety, Tolerability, Immunogenicity, and Efficacy of RNA Vaccine Candidates Against COVID-19 in Healthy Individuals”

The current commissioner of the FDA is Robert Califf, first nominated and confirmed under Obama in 2015, then again in 2021 under Biden. Califf’s ties to the pharmaceuticals industry caused Democratic Senator Bernie Sanders to vote against his 2021 renomination.

According to The Hill, Califf owns millions of dollars of stock in drug companies. High FDA officials are also allowed to owns parts of patents on the very drugs they are charged with regulating, and can keep up to $150,000 per year in royalties, for life.

The Epoch Times reported on September 22, 2021, on the first pathology conference at the Pathological institute in Reutlingen (click on Google translate from German to English):

“The doctors suspect autoimmune phenomena, reduction in immune capacity, acceleration of cancer growth, vascular damage “endothelitis”, vasculitis, perivasculitis and erythrocyte “clumping” as further corona vaccination side effects with potential fatal consequences…Burkhardt described it as “extreme” that among the ten deceased examined, three very rare autoimmune diseases were found, namely Sjögren’s syndrome, leukoclasic vasculitis of the skin and Hashimoto’s disease.”

Dr. Arne Burkhardt has taught at the Universities of Hamburg, Berne and Tübingen, and has published more than 150 scientific articles in German and international scientific journals. Burkhardt has audited and certified institutes of pathology in Germany.

For perspective, the issue of pharmaceuticals companies and the FDA hiding data is a sore spot with some people like former Blackrock investment guru Ed Dowd, who says that the moment data is hidden the worst must be assumed by the responsible investment manager exercising “due diligence” (video below.)

The FDA receives 45% of its budget from the pharmaceuticals companies it regulates.

 Interview: Former Blackrock Portfolio Manager Ed Dowd on Vaccine Deaths and Pfizer Safety Trials Fraud (view at Kristi Leigh channel on Rumble)



Feature: Non-Partisan Guide to What You Can do to Prevent Election Fraud in November: Demand Full Local Signature-Matching of Mail-In Ballots, with Observers Present


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