Coronavirus

"When all we have been fed are lies upon lies, how can one reason and come to logical conclusions within that sea of lies."

The logical conclusion (as you point out) is that other peoples' observations frequently include lies.

Other peoples' observations are their conscious brains reaction to lies they have been fed. In the meantime you have at your disposal something called the Law of your Being described as a Law that cannot err. Now your conscious mind errs all the time so no part of the Law of your Being incorporates any portion of your conscious mind. What then does this Law operate on?

Since you (your conscious) errs non-stop and you have no way to perfect the end product (thought and action) why not just continue to err knowing anything you do, say or think is going to contain faults?

The only way to not err is to think, say or do nothing at all. By so doing Ziero you shall have achieved PERFECTION!

Thank God this spigot of mass harm and killing will be in off position very soon.

__________________________________________________ _________

https://vaticancatholic.com/nih-dire...ht-to-justice/

NIH Director Calls For COVID Conspiracists To Be “Brought To Justice”


infowars.comDecember 7, 2021

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National Institutes of Health (NIH) Director Francis Collins has angrily called for anyone who spreads “misinformation” about COVID-19 online to be “brought to justice.”

“Conspiracies are winning here. Truth is losing. That’s a really serious indictment of the way in which our society seems to be traveling,” Collins told the Washington Post.

Citing an onslaught of angry messages directed at Dr. Anthony Fauci, who Collins appears to believe is above criticism, the bureaucrat demanded that those responsible for such behavior should be identified and “brought to justice.”

The article cited one such example of “misinformation” being Fauci’s involvement in barbaric experiments conducted on dogs by the National Institute of Allergy and Infectious Diseases (NIAID), despite the fact that such cruelty factually occurred under Fauci’s leadership.

While Collins didn’t specify precisely what he meant by “brought to justice,” Pfizer CEO Albert Bourla previously asserted that individuals who spread false information about COVID vaccines are “criminals” who “have literally cost millions of lives.”

It seems likely that whatever the National Institutes of Health, Anthony Fauci or Pfizer deem to be “misinformation” will become the standard.

As we previously highlighted, efforts to brand those who question the safety and efficacy of products manufactured by pharmaceutical corporations that have been plagued by a myriad of historical scandals are also underway in the UK.

The Online Safety Bill, described as “the flagship legislation to combat abuse and hatred on the internet,” will apparently include a provision that jails “antivaxers spreading false information that they know to be untrue” for a period of two years.

(Please see original posting for highlighting and hyperlinks.)

https://jamesfetzer.org/2021/12/jack...nley-us-hr-wv/

Jack Mullen, OPEN LETTER TO REPRESENTATIVE DAVID MCKINLEY US HR WV

December 7, 2021 James Fetzerblog

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Jack Mullen

Dear Congressman McKinley:

I am disgusted to see that you and 79 other “Republicans” voted in support, and along with the Democrats, to pass the Immunization Infrastructure Modernization Act (H.R.550) This bill, if passed in the Senate and signed into law, would fund a computerized database that records immunization doses, violating medical privacy laws and wasting $400 million in taxpayer money.

I already know that you were sent a notification printed and mailed by Cole Publishing of Wisconsin regarding the fraudulent nature of the Covid-19 scam and the use of a manufactured biological weapon mislabeled and marketed as a “vaccine” (violating FTC statutes on fraudulent marketing of untested medical treatments) which is now being injected into most Americans including children.

Congressman McKinley, you also already know that this vaccine is killing tens of thousands of people in the United States and untold numbers around the world and furthermore the deaths and damages are massively under reported through official sources.

You were also told that Fauci has lied before Congress at least two times regarding Covid-19. Lying before congress is a felony and can result in up to five years in jail.

Anthony Fauci lied before Congress and the American public when he claimed during a congressional hearing that he has not funded gain-of-function research being conducted by the Wuhan Institute of Virology. (Bioweapon research) This lie has already been exposed by Newsweek magazine which reported that the National Institute for Allergy and Infectious Diseases (NIAID), a Fauci led organization, funded scientists at the Wuhan Institute of Virology and other institutions for work on gain-of-function research on bat coronaviruses.

Further, you already know that no virus has ever been genetically sequenced or scientifically identified as Sars Cov-2 and you already know that Covid-19 is not a virus but rather a collection of symptoms and that Sars Cov-2 is the infection for which no vaccine conveying immunity exists.

The Covid-19 epidemic continues to rage, especially in countries that have been unable or unwilling to institute strong public health measures. A return to normality has increasingly come to rely on the success of vaccines to prevent disease and, we hope, limit further spread of infection. However, this hope has been tempered by several unknowns. No existing vaccines have been shown to be effective against infection with any betacoronavirus, the family that includes SARS-CoV-2, which causes Covid-19. New England Journal of Medicine Dec 2020.

You also know that spiked proteins (s1) are created in the human body after injection of what is legally defined as a gene therapy mislabeled a vaccine and further that these spiked proteins cause the disease which match the symptoms of Covid-19 – including death, heart disease, stroke, cancers, respiratory failures and more.

Let’s start back in 1990. And you heard what I said correctly. 1990 Pfizer filed the first Coronavirus vaccine patent on canine Coronavirus vaccine 1990. And you know what that vaccine was? The S1 spike protein. Has anybody heard of the S1 spike protein? before anybody, anybody, anybody? Yes, that is a bio weapon. And it turns out that it’s a protein sequence derived from the model of Coronavirus, and it is a bio weapon, it is not a pathogen, it’s a weapon. And we need to start using the correct language because you know what a parent won’t do. – Dr David Martin

Therefore supporting a “vaccine” database can only be useful if the plans are to use the information obtained as a “[…] a legislative tool to enforce vaccine mandates and force their Orwellian rules onto those who do not comply” – Republican Congresswoman Mary Miller.

Congressman McKinley you and all of those continuing to support and play along with the false narrative that claims a worldwide coronavirus pandemic exists and is killing millions of people and an experimental gene therapy must be injected into each and every American before we can be safe from that virus are liable to charges of genocide.

You were sent absolute proof of a murder and conspiracy to commit murder crime in progress by those responsible for the Covid-19 lies and the deaths and damages caused by a gene-therapy fraudulently labeled and advertised as a vaccine.

You are also being served notice here, now, that members of congress that do not intervene and demand an investigation into the crimes of the men and women, government agencies, universities (University of North Carolina for example), pharmaceutical corporations, and officials of federal government and state governments who, after having been fully informed, willfully assisted in distribution of a biological weapon fraudulently called a vaccine will be charged with the appropriate crimes, including treason and put on trial.

To be clear, the Biological Weapons Convention, known as the biological warfare anti-terrorism Act of 1989 with legislation and treaty passing unanimously by both houses of the United States Congress, and signed into law by President George Bush Senior with the approval of the United States Department of Justice in 1989 is applicable to the Covid-crimes mentioned above.

Ҥ 175. Prohibitions with respect to biological weapons
“(a) IN GENERAL.—Whoever knowingly develops, produces, stockpiles, transfers, acquires, retains, or possesses any biological agent, toxin, or delivery system for use as a weapon, or knowingly assists a foreign state or any organization to do so, shall be fined under this title or imprisoned for life or any term of years, or both.

Have no doubt – these crimes are being exposed and with only one grand jury indictment and subsequent conviction from just one of the 50 states and over 3000 counties we can begin to round up and imprison those responsible.

The Centers for Disease Control and Prevention released new data late Monday [11-29-2021] showing a total of 913,268 adverse events following COVID vaccines were reported between Dec. 14, 2020, and Nov. 19, 2021, to the Vaccine Adverse Event Reporting System (VAERS). VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 19,249 reports of deaths — an increase of 396 over the previous week — and 143,395 reports of serious injuries, including deaths, during the same time period — up 4,269 compared with the previous week. – The Defender

I urge you now to revisit the documentation sent to you regarding this most egregious ongoing crime and to take a stand on the side of the people that voted you into office. Retract your position on H.R. 550 and speak out against the medical/pharmaceutical mafia that now controls the media and future of all Americans.

Sincerely,

Jack Mullen

7 December 2021

Young Lives Destroyed by COVID Vaccines

Excerpt

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666 Cases of Heart Disease in 12 to 17-Year-Olds After COVID Shots – Less than 2 Cases Per Year Following All Vaccines for Past 30+ Years

December 7, 2021 James Fetzerblog

Brian Shilhavy
Editor, Health Impact News

The COVID-19 shots cause heart disease, mainly myocarditis and pericarditis, which is destroying the health of our young people.

This is a fact that is no longer in dispute, as even the CDC admits this, as their most recent report states:

As of November 24, 2021, VAERS has received 1,949 reports of myocarditis or pericarditis among people ages 30 and younger who received COVID-19 vaccine. Most cases have been reported after mRNA COVID-19 vaccination (Pfizer-BioNTech or Moderna), particularly in male adolescents and young adults. (Source.)

The only debatable points are, 1, whether or not these cases are “rare,” and 2, if the benefits of COVID-19 mass vaccination of young people outweigh the risk for heart disease.

And it is on these two points that the CDC is lying to the public, as I will conclusively prove in this article.

The second point is actually very easily debunked, by simply looking at publicly available statistics on COVID-19 deaths for this age group.

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SNIP

https://www.statista.com/statistics/...vid-by-age-us/
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Dachsie comment:

Anyone who has followed the information in this thread for the last two years has begun to question viruses, vaccines and virology, and what determines the ethics of science and the medical profession IN GENERAL.

Many, probably tens of thousands, people who have taken the regular vaccines, other than the recent COVID vaccine have a myriad of auto-immune conditions for which they take steroid medications the rest of their life. There really is no diagnosis for these chronic auto-immune conditions and just about the only way to get by and keep functioning is to take these steroid medications. And often, among this untold number of cases, the official "auto-immune" phrase is not recorded on the patient's record if the patient's lab test results are just barely within the normal values range.

I remember Dr. Russell Blaylock M.D. said years ago on a radio show that he recommended that children not take combination vaccines, such as the DPT vaccine but rather take each part of this coverage separately and appropriately spaced in time. Today, it is most likely impossible to find a doctor who will provide that. It is extremely difficult for parents to choose not to have their child get the 60-plus number of prescribed infant and childhood vaccines today. The real track record for vaccines in general is NOT GOOD and the TRUST IS GONE.

Now, under the guise of a "pandemic" of a mysterious pathogen and meaningless PCR test and Emergency Use Authorization EUA of unknown chemical and device ? make-up, even age 5 to 11 year old children are being injected and soon we will see the death and severe adverse effect of that debacle.
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It were better for him, that a millstone were hanged about his neck, and he cast into the sea, than that he should scandalize one of these little ones.
Luke 17:2

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Fired for Freedom - Press Conference
LeeVlietMD Published December 6, 2021 829 Views


https://www.truthforhealth.org/2021/...ss-conference/

1:35:06 video runtime

DrLee4America, General News, Legal, News, Vaccine News
Fired for Freedom Press Conference
by Dr. Lee Vlietupdated on December 7, 2021
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Fired for Freedom - Press Conference
LeeVlietMD Published December 6, 2021 829 Views )



(LifeSiteNews) — On this 80th anniversary of the surprise attack on freedom at Pearl Harbor that launched America into World War II to preserve life and liberty against evil, join this powerful press conference to hear from courageous doctors and nurses who were “Fired For Freedom” doing the right thing to protect patients.

In 1941, Pearl Harbor galvanized a nation to unite against evil, defend freedom with the American spirit and resolve to defeat the enemy against overwhelming odds. In 2020, America faced a surprise attack of an invisible virus that divided our nation, kept Americans in fear, assaulted our liberty, and blocked people from accessing truthful medical information and effective early treatment, as well as imposing the tyranny of mandatory experimental COVID shots.

Fired For Freedom will be livestreamed at 12 NOON ET on Tuesday, December 7 by LifeSiteNews, alongside multiple other livestream platforms. To participate and join the press conference, please save this link OR email info@TruthForHealth.org. The conference will also be streamed live on the homepage of LifeSiteNews.com

Elizabeth Lee Vliet, MD, President and CEO of the Truth for Health Foundation, moderates this press conference which features speakers willing to share their stories and expose the outright manipulation, intimidation, and cover-up of deaths in hospitals and medical facilities across America. LifeSite co-founder John-Henry Westen and Archbishop Carlo Maria Vigano present a crucial Biblical perspective on our God-given right to bodily integrity.

Speakers are fearless nurses and doctors, including world-renown Dr. Paul Marik, co-founder of Front Line Covid Critical Care Alliance, US Attorneys Tom Renz, Todd Callender, Lauren Martel, and Australia’s Charles Kovess to present the efforts being made every day to bring help and hope to people who have lost loved ones due to treatments denied, or have seen family and friends injured or dead following experimental vaccines and drugs like remdesivir.

Truth for Health Foundation, a 501(c)3 public charity, presents the seventh press conference featuring the courageous volunteer medical freedom fighters who have paid a high price to defend your rights to safe and effective early treatments free of coercion. Their names will go down in history books for standing in the gap to save lives and preserve freedom, just as Americans did in 1941.

The stories shared will inspire and encourage you to stand against tyranny and protect the freedoms with which we are endowed by our Creator, and that are enshrined in the founding documents of America, Canada, and many other Western nations.

"
Truth for Health Foundation, a 501(c)3 public charity"

501(c)3....code for TREASURY AGENT

https://blog.nomorefakenews.com/2021...eloved-expert/

Smoking gun: Fauci states COVID PCR test has fatal flaw; confession from the “beloved” expert of experts

Dec 8, 2021
by Jon Rappoport

The COVID PCR test is a complete fraud

by Jon Rappoport

December 8, 2021

(To join our email list, click here.)

As my readers know, I’ve been proving for well over a year that the SARS-CoV-2 virus doesn’t exist.

Therefore, any test for it would be absurd.

However, I frequently put on my hazmat suit and enter the crazy world where all “the experts” claim the virus is real. I make these forays to show that, even within their fantasy bubble, and by their own standards, the pros are fatally contradicting themselves and lying constantly.

That’s what I’m doing in this article. I’ve got my hazmat suit on and I’m exploring the crazy landscape. I’ve published this piece several times, but I want to make sure people understand how the test has been used to manufacture the false appearance of a pandemic.

OK, here we go. Smoking gun. Jackpot.

Right from the horse’s mouth. Right from the man we’re told is the number-one COVID expert in the nation. What Fauci says is golden truth.

Well, how about THIS?

July 16, 2020, podcast, “This Week in Virology”: Tony Fauci makes a point of saying the PCR COVID test is useless and misleading when the test is run at “35 cycles or higher.” A positive result, indicating infection, cannot be accepted or believed.

Here, in techno-speak, is an excerpt from Fauci’s key quote (starting at about the 4-minute mark): “…If you get [perform the test at] a cycle threshold of 35 or more…the chances of it being replication-competent [aka accurate] are miniscule…you almost never can culture virus [detect a true positive result] from a 37 threshold cycle…even 36…”

Each “cycle” of the test is a quantum leap in amplification and magnification of the test specimen taken from the patient.

Too many cycles, and the test will turn up all sorts of irrelevant material that will be wrongly interpreted as relevant.

That’s called a false positive.

What Fauci failed to say on the video is: the FDA, which authorizes the test for public use, recommends the test should be run up to 40 cycles. Not 35.

Therefore, all labs in the US following the FDA guideline are knowingly or unknowingly participating in fraud. Fraud on a monstrous level, because…

Millions of Americans are being told they are infected with the virus on the basis of a false positive result, and…

The total number of COVID cases in America—which is based on the test—is a gross falsity.

The lockdowns and other restraining measures are based on these fraudulent case numbers.

Let me back up and run that by you again. Fauci says the test is useless when it’s run at 35 cycles or higher. The FDA says run the test up to 40 cycles, in order to determine whether the virus is there. This is the crime in a nutshell.

“Hello, America, you’ve been tricked, lied to, conned, and taken for a devastating ride. On the basis of fake science, the country was locked down.”

If anyone in the Congress has a few brain cells operating, pull Fauci into a televised hearing and, in ten minutes, make mincemeat out of the fake science that has driven this whole foul, stench-ridden assault on the global economy and its 8 billion citizens.

All right, here are two chunks of evidence for what I’ve written above. First, we have a CDC quote on the FDA website, in a document titled: “CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel For Emergency Use Only.” This document is marked, “Effective: 07/13/20.” That means, even though the virus is being referred to by its older name, the document is still relevant as of July 2020. “For Emergency Use Only” refers to the fact that the FDA has certified the PCR test under a traditional category called “Emergency Use Authorization.”

FDA: “…a specimen is considered positive for 2019-nCoV [virus] if all 2019-nCoV marker (N1, N2) cycle threshold growth curves cross the threshold line within 40.00 cycles ([less than] 40.00 Ct).”

Naturally, testing labs reading this guideline would conclude, “Well, to see if the virus is there in a patient, we should run the test all the way to 40 cycles. That’s the official advice.”

Then we have a New York Times article (August 29/updated September 17, 2020) headlined: “Your coronavirus test is positive. Maybe it shouldn’t be.” Here are money quotes:

“Most tests set the limit at 40 [cycles]. A few at 37.”

“Set-the-limit” would mean, We’re going to look all the way to 40 cycles, to see if the virus is there.

The Times: “This number of amplification cycles needed to find the virus, called the cycle threshold, is never included in the results sent to doctors and coronavirus patients.”

Boom. That’s the capper, the grand finale. Labs don’t or won’t reveal their collusion in this crime.

Get the picture?

I hope so.

If a lawyer won’t go to court with all this, or if a judge won’t pay attention and see the light, they should be stripped of their jobs and sent to the Arctic to sell snow.

2021 CODA: Recently, Florida, a state which has remained far more open and free from COVID restrictions and mandates than most other states, is reporting very low COVID case numbers. Why?

Because as of December 3, 2020, the state of Florida started doing something unheard of. It demanded that labs report the number of cycles (“cycle threshold”) for every test they run.

Here is the relevant wording in a release from the Florida governor, Ron DeSantis, and the state Department of Health:

“Cycle threshold (CT) values and their reference ranges, as applicable, must be reported by laboratories to FDOH via electronic laboratory reporting or by fax immediately.”

“If your laboratory is not currently reporting CT values and their reference ranges, the lab should begin reporting this information to FDOH within seven days of the date of this memorandum.”

We can assume there is only one reason for this order. The Florida governor and the Department of Health are aware that tests run at 35 cycles or higher are useless and misleading, creating a mountain of false-positives, and they want to stop this crime.

And with the Governor’s recent appointment of a new state Surgeon General, who is well aware of certain aspects of the COVID fraud, the requirement for labs to start telling the truth is taking hold.

Hence, lower case numbers.

SOURCES:

(forthcoming)

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PANNICCCKKKKKK - Everybody PAAANNNIICCCKKK by Katie Hopkins

Watch
https://www.bitchute.com/video/BRrcUw4QEHLh/

First published at 14:50 UTC on November 30th, 2021.

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2:56 video runtime
Jim Fetzer

8480 subscribers

BRILLIANT and HILARIOUS statement by the great Katie Hopkins regarding the continual scaring of the public by phony "variant" fear-propaganda.

https://www.bitchute.com/video/W0oYQblMVuzT/
Katie Hopkins: https://www.katiehopkins.co.uk/index…

New VAERS Data as of Nov 26th, 2021 (posted Dec 3)

21,154 Deaths and 997,322 Adverse Events

19,532 Pfizer / Moderna and 1,622 J&J Deaths PLUS 927,740 Pfizer / Moderna and 69,582 J&J Adverse Events

https://vaxxter.com/the-fda-and-pfiz...ces-to-murder/


The FDA and Pfizer: Accomplices to Murder
TOPICS:Coronaviruscovid vaccineCOVID19


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Posted By: Fed Up Texas Chick 12/06/2021

by Fed Up Texas Chick

The FDA has turned a simple and straightforward Freedom of Information Act (FOIA) request for Pfizer-BioNTech COVID-19 vaccine records into a 50+-year waiting game. To put it in perspective, Elon Musk would reach Mars way, way before the FDA would ever finish this task.
What was requested?

A Freedom of Information Act (FOIA) lawsuit was filed for documents tied to the approval of the Pfizer-BioNTech COVID-19 vaccine. The FOIA process gives the American public the right to request access to records from any federal agency. The law was put into place in 1967 to ensure that citizens remain informed about their government. Federal agencies must comply with the law by disclosing the requested information unless it compromises things like personal privacy or national security. There are nine exemption categories in all.

On an interesting side note, FOIA also requires federal agencies to post frequently requested information online, again unless it compromises one of the nine exemption categories.
Who requested the information?

The FOIA request was originally made by a group of doctors and scientists known as the Public Health and Medical Professionals for Transparency (PHMPT) group. PHMPT comprises an esteemed group of over 30 scientists and physicians, including Yale professor Harvey Risch, who has been a consistent voice of common sense during the pandemic. After the FDA denied the original request to expedite record release, PHMPT filed a lawsuit. Here’s the link to that lawsuit if you want to review it.

Like any federal agency, the FOIA mandate states that agencies should rarely withhold information unless it violates one of the aforementioned nine areas, or if for some reason disclosure of such records is prohibited by law. Federal agencies should always consider partial disclosure. In the case of the FDA’s holdings of Pfizer records, neither of these special cases applies.
Did FDA Comply with the FOIA request?

Well…sort of. While the FDA has no choice but to comply with the law and release these records to the American public, that doesn’t mean the agency wouldn’t try to use other tactics or perhaps slow roll the effort. And sure enough, that is what happened. The Department of Justice (DOJ) Office of Information Policy is in charge of FOIA and issues guidance to all other federal agencies.

As such, DOJ lawyers representing the FDA asked a federal judge to allow until 2076 to fully release the FOIA-requested documents. With the request, the FDA is effectively sealing the records. The agency’s defense is that 330,000 pages of material were requested, and they simply do not have the resources to fill the request in a timely manner. At a proposed rate of 500 pages per month, it will take 55 years, until 2076, to fulfill the request. Yes, you read that right. 2 0 7 6; the FDA will squeak in right under the deadline – 55 years from now.

As you can imagine, outrage ensued over the FDA’s “shameless effort to bury the information.”

Are 500 pages per month really too taxing for the FDA? The equivalent is Harry Potter books 1 and 2, so the FDA would have to review, redact exempt material, and copy the equivalent of two Harry Potter books each month. The FDA defended its position in their court filing, explaining that the 500-page-per-month rate is consistent with the pace of other federal agencies.

PHMPT attorney Aaron Siri isn’t buying the stall tactic, saying that “the FDA’s promise of transparency is, to put it mildly, a pile of illusions.”

By comparison, the FDA only took 108 days to license the Pfizer vaccine. In the FDA’s own words, the agency described the effort as “an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure.” Yet the agency is asking for more than 20,000 days to now make these documents publicly available.

PHMPT lawyers are asking for the FDA records by March 3, 2022, which is the same 108-day period it took to achieve the far more complex task of actually approving the vaccine. The argument was that FDA could conduct the same robust and intense document analysis this time around. If they did it for the actual vaccine, they should be able to easily do it to release those same records. The legal team continued by saying the records are important because the ability of Americans to participate in civil society is largely now contingent on receiving the COVID-19 vaccine.

According to the Epoch Times, “as of November 14, more than 256 million doses of Pfizer’s COVID-19 vaccine have been administered in the United States.”
What is the FDA hiding?

Pfizer has whistleblowers, and one of them told the British Medical Journal (BMJ), one of the oldest medical journals in the world, that the Pfizer clinical trials were fraught with issues. Whistleblower Brook Jackson worked for Ventavia Research Group which operated several of Pfizer’s clinical trial sites during the latter part of 2020. Jackson claimed that the trial issues included, among other issues, the falsification of data. At the time Jackson alerted the FDA, he was fired within hours of doing so. The BMJ now reports that the FDA never inspected Ventavia’s trial sites even after Jackson alerted them to the problems. The FDA told the Epoch Times that it nevertheless has “full confidence” in the trial data.

As if data falsification is not a big issue, there may be an even bigger elephant in the room. While the federal budget pays 55% ($3 billion) of the FDA budget, the remaining 45% ($2.4 billion) comes from industry user fees paid by manufacturers being regulated. Yes, you read that right – nearly half of the FDA funding comes from the companies it regulates.

Since its inception in 1938 as a new authority to protect Americans from unsafe food, medication and cosmetics manufacturing methods, the FDA was entirely taxpayer-funded.

The FDA has had some very public success stories, such as its refusal to approve thalidomide, a treatment for morning sickness that caused debilitating birth defects. The thalidomide-era FDA was driven by data, not by corporate interests. Then-President John F. Kennedy applauded their decision.

FDA funding changed in the AIDS era. When the first HIV case was identified 1981, it spread rapidly and affected many people, including well-known celebrities, so the disease was very visible to Americans. People were angry about how long it was taking to get medication treatments to the market, so in 1992, Congress passed the Prescription Drug User Fee Act which was signed into law by President George H.W. Bush.

This law provided the FDA with funding from prescription drug user fees that manufacturers paid when submitting applications to the FDA for new drugs. Companies pay annual fees, prorated per the number of approved drugs they have on the market. (You can only imagine how much money Pfizer pays the FDA). Over time, fees for generic drugs, over-the-counter drugs, medical devices, and even veterinary drugs were added to help fill FDA’s coffers, and today, nearly half of the funding comes from the industries it regulates.

Fee negotiations also occur between the FDA and manufacturers for performance measures. In other words, the FDA gets paid more if they do a better job for the drug companies. The most important performance measure is the time between the drug new submission and the time it takes FDA to get the product approved and to market. The FDA is also measured on how quickly the agency responds to meeting requests and other requests.

The FDA stands behind the fees, saying the funding allows them to much more rapidly approve new products. The agency says it is only fair to charge the manufacturers these user fees. After all, the manufacturers stand to make a lot of money from the approval and sale of these drugs, and the fees are a small “carving out” that provides viable relief for the FDA’s financial burden, and ultimately relief to the taxpayer.

Sounds pretty good, doesn’t it?

Indeed, the FDA has better performance with the fees, as the FDA now takes 10 months for approval (2018 data), an improvement from the 29-month timeframe in 1987. The FDA also states that these funds helped them respond to the COVID-19 emergency use authorization in a matter of weeks rather than months or even years.

However, even though the FDA has more rapidly approved more drugs, the number of drugs with serious safety issues after FDA approval has also increased. Today about 27% of drugs have issues (called black box warnings) or have been removed from the market, up from 21% before the user fee was initiated. As an example, here is Pfizer’s black box warning for its drug Celebrex.

It is critical that the American public understand how FDA is funded. Does the public benefit, or does patient safety take a back seat to corporate profits? By the way, Congress must reauthorize these user fee programs every five years; the next occurrence is September 2022.
Has the FDA released any of these FOIA records yet?

As a matter of fact, the FDA has released the first tranche of Pfizer records after being ordered by the court to comply with the FOIA release. First reported by the Gateway Pundit, the initial release is a bombshell.

In the first 90 days after the Pfizer vaccine Emergency Use Authorization (EUA) rollout, from December 2020 to February 2021, tens of thousands of adverse events were reported including 1,200 deaths. Here is the full report.

Furthermore, the report only included researcher-deemed serious cases, meaning thousands more adverse events were not included in the data. To put it a different way, there were so many spontaneous adverse events reported for the Pfizer product that the team had to prioritize the serious cases. Furthermore, the report only includes recorded events, so the number of actual adverse events is likely far, far greater.

The FDA says it best: “(Adverse event) reports are submitted (to VAERS) voluntarily, and the magnitude of underreporting is unknown.”

Worldwide, the number of adverse events over the first 90-day period totaled more than 42,000, with about 13,000 adverse event reports within the US and the UK, repectively. Women were three times more likely to experience a reaction than men, and just to reiterate, 1,223 fatal reactions (DEATHS) were reported within the first 90 days. The report goes on to elaborate on thousands of “special interest conditions” that could possibly develop after a person takes the vaccine. The Gateway Pundit list is astonishingly nine pages long – single-spaced.

Even more astonishing is that after the FDA review of the first 90 days of data, they concluded the data was satisfactory to move forward to release the EUA for the Pfizer vaccine.

Naturally, this begs the question: Why did the FDA not immediately pull this product? Why have they still not done it?

And there are 329,500 pages to go. Let that sink in. What else will this report reveal?

By the way, Pfizer is projected to make $36 billion in profit in 2021 from the vaccine alone. This amounts to $1,000 per second in profit.

Let that sink in too.

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Fed Up Texas Chick is a contributing writer for Vaxxter. She’s a rocket scientist turned writer, having worked in the space program for many years. She is a seasoned medical writer and researcher who is fighting for medical freedom for all of us through her work.