Nonprofit Sues HHS to Immediately Stop Emergency Use of COVID Vaccines

America’s Frontline Doctors, a nonprofit, filed a motion on July 19 seeking immediate injunctive relief to stop the emergency use authorization (EUA) of COVID-19 vaccines for three groups of Americans: anyone under the age of 18, anyone who has recovered from COVID-19, and those who haven’t given informed consent as defined by federal law.

The motion was filed against Xavier Becerra, Secretary of the Department of Health and Human Services (HHS), and other defendants in a federal district court in the Northern District of Alabama.

The emergency declaration and its multiple renewals are illegal,” the complaint (pdf) alleges.

According to the Federal Food, Drug, and Cosmetic Act, when the HHS secretary declares that an emergency use is appropriate, the FDA (Food and Drug Administration) may then authorize unapproved use or EUA of a vaccine.

On Feb. 4, 2020, then-HHS Secretary Alex Azar declared a public health emergency, saying that existing circumstances justify the EUA.

The complaint alleges that the legal requirements to issue and maintain COVID-19 vaccine EUAs aren’t being met.

First, there’s no underlying emergency and no “serious or life-threatening disease or condition,” the complaint states.

According to the defendants’ data, the CCP virus has an overall survivability rate of 99.8 percent globally, “on a par with the seasonal flu.

However, the defendants’ data is deliberately inflated, the complaint alleges. It claims that HHS has changed the rules applicable to people responsible for writing death certificates and requires them to make cause of death determinations primarily attributable to COVID-19. From last March, death certificates indicated “COVID-19 [as] being the underlying cause more often than not.

The way in which COVID-19 is diagnosed, using magnified values from PCR tests that were also authorized for emergency use, guarantees “an unacceptably high number of false-positive results,” the complaint states.

Second, COVID-19 vaccines aren’t effective in diagnosing, treating, or preventing a disease or condition, which fails another requirement for issuing and maintaining EUAs.

The complaint cites data from the Centers for Disease Control and Prevention (CDC) that says a total of 10,262 CCP virus breakthrough infections (detection of SARS-COV-2 within 14 or more days after receiving required dosages of a COVID-19 vaccine) were reported between Jan. 1 and April 30.

It is important to note that the vaccines were only shown to reduce symptoms—not block transmission,” the complaint reads.

Third, the benefits don’t outweigh the known and potential risks of each vaccine. Those risks are especially increased in reproductive health, potential death, neurological damage, more virulent strains, and others.

And lastly, there are adequate, approved, and available alternatives to the vaccines, such as Ivermectin, Budesonide, Hydroxychloroquine, and others.

Not Adequately Informed

The plaintiffs also allege that health care professionals and vaccine candidates aren’t being adequately informed about the vaccines, as the federal law requires.

No one ever provided me with any information regarding possible adverse reactions, nor did they provide me with any information regarding alternative treatments. I did not understand this was gene therapy rather than a traditional vaccine. Again, I also did not understand that the vaccines were not ‘approved’ by the FDA,” plaintiff Angelia Deselle said in a declaration included in the lawsuit.

The Vaccine Adverse Event Reporting System (VAERS) was established to provide information regarding adverse events potentially caused by vaccines. The complaint states that VAERS isn’t accurate and that the federal government is failing to provide data from other sources, such as the military, Medicare, and Medicaid.

According to the complaint, a patient can’t give informed consent without an understanding of the risks.

Under-18 Age Group and Those Recovered From COVID-19

CDC data indicates that children under 18 have a 99.998 percent COVID-19 recovery rate with no treatment,” the complaint reads. “Injecting this under-18 subpopulation with the Vaccines threatens them with immediate, potentially life-threatening harm.

Last month, the CDC said that more than 1,200 cases of heart inflammation in adolescents and young adults were reported following the administration of Pfizer’s or Moderna’s two-dose vaccines.

There is no public interest in subjecting children to experimental vaccination programs, to protect them from a disease that does not threaten them,” Dr. Angelina Farella, a pediatrician who has actively practiced for over 25 years, said in a statement. Farella is an expert for America’s Frontline Doctors.

The complaint also asserts that Americans who have recovered from COVID-19 shouldn’t get vaccinated.

It cites a recent Cleveland Clinic study that demonstrates that natural immunity through prior infection is stronger than any benefit conferred by a COVID-19 vaccine. Another study, published in the New England Journal of Medicine, shows that of those with preexisting COVID-19 immunity, 89 percent reported adverse side-effects after receiving the first vaccine injection.

COVID recovered patients are at extremely high risk to a vaccine,” plaintiffs’ expert Dr. Richard Urso said in a statement. “They have all the requisite components of immune memory. Vaccination may activate a hyperimmune response leading to a significant tissue injury and possibly death.

Whistleblower Testimony: 45,000 Deaths Following Vaccinations

Jane Doe, a computer programmer with expertise in the health care data analytics field, filed a sworn statement indicating that the actual number of deaths following the COVID-19 vaccination is about 45,000.

It is my professional estimate that VAERS database, while extremely useful, is under-reported by a conservative factor of at least 5. On July 9, 2021, there were 9,048 deaths reported in VAERS,” Jane Doe said in her statement (pdf). “I queried data from CMS medical claims with regard to vaccines and patient deaths, and have assessed that the deaths occurring within 3 days of vaccination are higher than those reported in VAERS by a factor of at least 5. This would indicate the true number of vaccine-related deaths was at least 45,000.

Jane Doe noted that the swine flu vaccine was taken off the market because of 53 deaths reported following vaccination.

The evidence makes it irrefutable that Plaintiffs and others in the public will suffer irreparable injury … if this motion is denied,” the plaintiffs asserted. “Finally, the evidence tilts the balance of hardships and public interest … decisively in favor of Plaintiffs.

In an email to The Epoch Times, HHS declined to comment on the lawsuit, saying, “As a matter of policy, we do not comment on pending litigation.

President Joe Biden has praised the vaccines as safe and effective.

You know, some people have questions about how quickly the vaccines were developed. They say they’ve been developed so quickly, they can’t be that good. Well, here’s what you need to know: Vaccines were developed over a decade of research in similar viruses, and they’ve gone through strict FDA clinical trials,Biden said last month. “The bottom line is this—I promise you: They are safe. They are safe. And even more importantly, they’re extremely effective.

The Biden administration announced earlier this month that it would begin a door-to-door outreach campaign in targeted communities to boost COVID-19 vaccination rates.

See more here: theepochtimes.com

Header image: Technology Record

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Comments (4)

  • Avatar

    sir_isO

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    And I ruled against AFD for peddling non-essential, toxic big pharma products such as HCQ and ivermectin while conveniently ignoring essential, more easily addressed factors.

    Sure, they’re not as bad as the CDC, but at least the CDC helped point them out as subversive, undermining industrial agents peddling the fundamental fraud of pasteur methodology.

    Reply

    • Avatar

      sir_isO

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      The reason say, Merck, isn’t promoting their ivermectin is to inflate prices (essentially artificial scarcity for a non-essential product, though it has some benefits in that it completely fucks up the damage signature that is classified as covid. Every peddled virus btw, is essentially damage signature from underlying problems relating to toxicity and defciiency) WHILE there’s capitalization on vaccinations. You see, those vaccines you pay for are really super expensive. What, you don’t know that you pay for them? Are you kidding me? Tax, monetary inflation, resulting problems that “need” more pharma.

      If they didn’t want you to know about ivermectin or HCQ, it wouldn’t have been projected at you. Practically everything projected AT you,, is subversion. You know, like Goebbels said “I want everyone to have a radio”. Well, shit, they have smartphones instead, WAAAAY more damaging and indoctrinating.

      In the mean time, in America, apparently cysteine, a pretty important precursor, amino acid is, for a rather important antioxidant factor, glutathione being marginalized (like sunlight, iodine, and other essential factors) and apparently being sort of outlawed. Glutathione apparently, being quite implicated with symptoms you’d associate with things like covid, respiratory issues. I wonder why those super health promoters don’t mention those sort of essential things and always seem to promote unessential, expensive toxins.

      Hey, just think of all those “recalls” and attempted demonizations of fresh fruit, vegetables, etc regarding trivial laughable and easily disproven issues, relatively…you know, so as to promote more homogenized, processed, toxified products involving say GMO roundup/atrazine/chlorpyrifos/etc sort of monopolized degenerate “food”.

      Reply

      • Avatar

        Andrew Pilkington

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        You always have some interesting points to make in your comments and yes I’ve checked some things out, time permitting. Many thanks.

        Still, I say “Best of Luck” to them on this one, more for the sake of our kids, but yes, for all our sakes, too.

        The 1st job is for AFD to get them Stopped, other things are being dealt with elsewhere and, if they fired Every Covid-related Topic at the Courts, it would take Months if not Years, to Stop these Internationally Illegal Human DNA Experiments? The kids don’t have that long, infact none of us have?
        I mean, AFD are covering a variety of connected issues as it is, but if they say, included the Graphene Oxide Nanotech from the Muzzles, Nasal “Test” Swabs, Injections and Chemtrails, into the equation, their chance of success would plummet?

        ALL the Conspiracies are interconnected and the odds are Heavily stacked against us. We can’t trust Anyone at this stage and, sadly, sometimes that includes Ourselves.

        We need Mainstream Media Silenced, to bring this Demonic House of Cards tumbling down. A “They Live” broadcast hack would help? 🙂

        All the best.

        Reply

  • Avatar

    Doug Harrison

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    I think it is now a given that the vaccines were “perfected” as far back as 2010. So much for the speed of development. The problem was they didn’t have a disease that they could be used against. Cometh the hour cometh the man: Tony Fauci steps up with his gain of function spike protein and away we go.

    Reply

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