Why did the FDA suppress all evidence of vaccine injuries?

Written by A Midwestern Doctor on October 14, 2025. Posted in Current News

Many individuals I’ve spoken to believe Peter Marks is the government official most directly responsible for the entire Covid catastrophe, and those I know who directly interacted with him despise him

For that reason, six months ago, I published a detailed exposé of his conduct throughout the pandemic, both to highlight the systemic issues within our healthcare bureaucracy that must be fixed and to disincentivize other health officials from following in his footsteps.

Since that time:

•Despite immense industry pushback, he was replaced with MAHA appointee Vinay Prasad

•Marks has made statements on the national media which display either a profound degree of ignorance of vaccines or a cult-like devotion to them, such as telling CBS the MMR vaccine absolutely does not cause encephalitis—despite this specific injury being one of the only vaccine injuries the Federal Government acknowledged as real and eligible for compensation when it created the the National Childhood Vaccine Injury Act of 1986.

Note: the primary reason DMSO (a safe and affordable substance with remarkable therapeutic applications against a wide range of “incurable” ailments) never entered mainstream medical practice was because the FDA, feeling DMSO’s broad therapeutic potential threatened their control of American medicine, waged a multi-decade war against it despite widespread opposition from the public, Congressmen, scientists and physicians across the country. One journalist who interviewed the successive FDA commissioners throughout this saga was struck by how “lacking [they were] in solid information about the most spectacular and controversial drug of our time” and how often they simply quoted nonsensical misinformation the FDA had previously put out about the drug without a basic understanding of it—something I would argue also applies to Peter Marks.

•Yesterday, it was announced that Peter Marks had started working with Eli Lilly, where he will oversee molecule discovery and infectious diseases at Lilly. While his salary has not been publicly announced, the AI systems I queried said given the existing precedent, he would likely get 2-6 million this year (a big upgrade from his roughly $200,000.00 FDA salary)—and possibly much more (e.g. 10-15 million).

This understandably enraged the vaccine injured parties who directly interacted with Marks over the last four years, so I felt it was important to revisit exactly what Marks did and discuss the broader revolving door in regulatory medicine.

Note: last year, the FDA approved Eli Lilly’s anti-amyloid monoclonal antibody for the treatment of Alzheimer’s disease (granting the application Fast Track, Priority Review, and Breakthrough Therapy designations). I showed in last weekend’s article, that these costly drugs do close to nothing (they may slightly slow the progression of Alzheimer’s disease) while simultaneously creating a variety of severe symptoms including giving over a quarter of recipients brain bleeds and brain swelling—yet remarkably, safer and much more effective Alzhemier’s therapies have languished in obscurity.

Sociopathic Structuring

A frequent criticism of corporations (which I believe also applies to governmental bureaucracies) is that their organizational structure encourages sociopathic behavior.

This is because members of these entities are shielded from legal or personal accountability for their actions, with any wrongdoings being attributed to the corporation as a whole.

In contrast, the main form of accountability most members face is the pressure to advance the institution’s mission (e.g., make more money), leading to the proliferation of increasingly unethical methods to achieve that goal.

To illustrate, consider this quote from Peter Rost, a former executive at Pfizer and one of the few pharmaceutical leaders to speak out against the industry:

It is scary how many similarities there are between this industry and the mob. The mob makes obscene amounts of money, as does this industry. The side effects of organized crime are killings and deaths, and the side effects are the same in this industry.

The mob bribes politicians and others, and so does the drug industry … The difference is, all these people in the drug industry look upon themselves – well, I’d say 99 percent, anyway – look upon themselves as law-abiding citizens, not as citizens who would ever rob a bank …

However, when they get together as a group and manage these corporations, something seems to happen … to otherwise good citizens when they are part of a corporation. It’s almost like when you have war atrocities; people do things they don’t think they’re capable of.

When you’re in a group, people can do things they otherwise wouldn’t, because the group can validate what you’re doing as okay.

In looking through what went awry with the COVID-19 response, while Fauci was commonly blamed for all that went amiss, I kept running into another less-known individual who, while hidden within the FDA bureaucracy, I believe was directly responsible for many of the mishaps that happened.

This was because Peter Marks was:

•The primary person who covered up the reports of COVID vaccine injuries (and instead repeatedly told the world they were “safe and effective”).

•Kept on pushing the FDA’s chief vaccine scientists (who were very pro-vaccine) to accelerate and condense the approval timelines for the COVID vaccines (as those approvals were needed to legally implement Biden’s vaccine and booster mandates).

Eventually, Gruber and Krause reported their were no more corners they could cut to further accelerate the COVID vaccine approvals, at which point they were removed from the COVID vaccine approval process and Marks took it over (at which point the unjustifiable approvals and mandates quickly followed).

As such, I felt Marks should not be in the agency and put together a detailed summary of his gross malfeasance at the FDA throughout COVID-19 in the hopes his abhorrent conduct could become widely known.

Shortly after, Marks announced his resignation in a spiteful letter that concluded with:

I was willing to work to address the Secretary’s concerns regarding vaccine safety and transparency…However, it has become clear that truth and transparency are not
desired by the Secretary, but rather he wishes subservient confirmation of his misinformation and lies.

This, in turn, prompted Robert Redfield (Trump’s 2018-2021 CDC director) to make a Twitter account to state:

Secretary Kennedy and Commissioner Marty Makary have the responsibility to build their own team at the FDA to move our nation forward. It was extremely disappointing to see Dr Peter Marks’ vindictive comments towards Secretary Robert Kennedy Jr. in his resignation letter.

I firmly believe RFK will be the most consequential Health Secretary in our nation’s history.

Note: Redfield, to my knowledge, is the only CDC director who went into private practice (he treats long COVID) after leaving the CDC (whereas in contrast most directors accept lucrative or prestigious positions following their tenure).

Following Mark’s resignation (which many news outlets claimed was forced), many news outlets attempted to paint him as saint and a victim of RFK’s “war against science”.

This gushing coverage of Marks, in turn, I would argue was due to his background.

Specifically:

•Prior to joining the FDA, Marks was an academic hematologist and oncologist with an “average and unimpressive publication history” (none of which related to vaccines, but one of which extensively discussed the global need for fully informed consent and stated “those that have only pretended to move [towards informed consent] will have the greatest difficulty”).

•Prior to joining the FDA, he’d also worked for several years the pharmaceutical industry (although oddly, no information exists online as to which companies he worked for—although one was likely Novartis).

•While at the FDA, he prioritized pushing through extremely expensive gene therapies (22 in total—most of which cost over half a million dollars), including some highly questionable ones (e.g., he overruled three FDA review teams and two top officials to push through a failed muscular dystrophy treatment which subsequently killed a patient).

Note: Robert Malone recently showed that Peter Marks was not qualified to be a senior regulator and had minimal knowledge or background in molecular biology, immunology or vaccinology (and worse still, repeatedly chose to overrule the FDA scientists who did).

•Marks was seen as a global leader in commercializing this field (e.g., he helped direct Germany’s national program to develop gene therapies, his resignation shook the entire sector, and following his resignation, large drops occurred in the stocks of key gene therapy companies).

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