BUSTED: Scripted Covid propaganda reveals how nearly all American doctors are just puppets of the corrupt American Medical Association and the Vaccine Industrial Complex

Image: BUSTED: Scripted Covid propaganda reveals how nearly all American doctors are just puppets of the corrupt American Medical Association and the Vaccine Industrial Complex

Here’s a section from the document, entitled, “COVID-19 Language Swaps”

SEE: https://www.ama-assn.org/system/files/2021-02/covid-19-vaccine-guide-english.pdf

BY S.D. WELLS

SEE: https://www.naturalnews.com/2021-09-07-covid-propaganda-reveals-american-doctors-just-puppets-ama-big-pharma.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) You haven’t seen anything until you’ve seen the AMA’s “Interview Response Formula” and “Controlled Response” script specifically written to train all the puppet MDs in America how to brainwash everyone into getting toxic, spike-protein bioweapon injections for the lab-made China Flu. This absolutely corrupt, complete propaganda-ridden guide to “Covid-19 Language Swaps” tells doctors EXACTLY what to say, word for word, in order to con vaccine skeptics into getting billions of spike proteins injected, so they too can infect and damage their blood and organs, permanently. Clients for life is what they call it in the sick care industry of America, and this is not a joke or a hoax. This is the AMA.

The AMA has doctored an “interview response formula” so doctors never have to think for a second how to answer tough questions to which the AMA does NOT want Americans getting proper answers. Brilliant doctors who survived eight years of medical school plus residencies are forced to “swap” lies for actual answers and to swap propaganda and buzz words for facts in order to trick Americans into full pandemic submission, loss of their civil liberties, and loss of all personal medical choice and rights, forever.

The truth would shock everyone nearly to death. This is planned. This is a controlled and coordinated response. This is communism and medical tyranny hosted by the American Medical Association. This is criminal. This is the AMA Covid-19 Guide for promoting misinformation about all things vaccine-related, included social media posts, memes, questions in private groups, and even lies about clinical trials and safety.

Doctors are instructed in writing by the AMA to lump in every single hospitalization as part of total “death rates” from Covid

Using results from a conducted poll, the AMA believes if they force medical doctors to use certain diction, they can distort the thinking of people who are doubting vaccines, and lessen their (severe) “perceived partisanship” in order to get more skeptics (people who know better) shot up with billions of heart-straining spike proteins.

Instead of doctors referring to illegal home quarantining as a “lockdown,” doctors should use propaganda and refer to it as a “stay-at-home order.” When speaking or writing anything about unconstitutional provisions like Covid orders, controls, directives, or mandates, the AMA tells doctors to say “Covid protocols” instead. This is how the AMA gets millions of Americans to comply with medical tyranny and mass experimentation, with minimal resistance.

That’s just the beginning. Doctors are now supposed to substitute the word ‘pandemic’ for anything that talks about ‘Coronavirus’ or ‘Covid-19.’ They are to call hospitalization rates deaths — and that’s blatantly lying about hospitalization rates as opposed to death rates. That would mean that every person who checks into a hospital anywhere in the USA is now a Covid death statistic. Hospitalization rates are NOT the same thing as death rates, and “death” rates aren’t even the same as Covid death rates, so it’s lies piled on top of lies.

Remember, these are instructions for doctors using language swaps as propaganda to spread the fear-based pandemic and sell everyone possible on getting dangerous, dirty vaccines. No doubt every American doctor (and most hospital staff) must sit through long training seminars and ‘continued education’ for the Nazi-style plandemic and proper propaganda use, as the following AMA guide spells out in clear, concise language.

This propaganda guide is called “best practices” by the AMA and is to be used by every American doctor when providing guidance or media commentary for Covid-19

The insidious AMA is literally, in writing, telling doctors that these lies and propaganda-based “Covid-19 language swaps” can be “leveraged for interviews and other external engagements.” This is their new interview response formula. Doctors are told to “stay on message” and practice these lies ahead of time. They are to “speak slowly, clearly” in order to make the lies sound real as if they were organizing thoughts of their own.

All of the American doctors are also instructed by the AMA to take credit for all work, discoveries, and research by any doctors and scientists around the world, by swapping the phrase “the world’s leading experts” to “America’s leading experts.”

Instead of “operation warp speed” call it a “standard process” to un-Trump it and falsely make this mass medical experiment somehow sound safe.

Instead of science-based, fact-based or medicine-based, call all things Covid “fact-based,” because if anyone looks at the science, they’ll know the doctors are lying, and that PCR tests are fake, masks cause bacterial infections, and the vaccines cause blood clotting and ADE (compromised immunity and autoimmune disorders).

According to the AMA, this is all to “mitigate perceived partisanship” in Covid-19 messaging and conversations. In other words, make it look like we’re all in this together, even when most doctors quietly refuse vaccines, chemotherapy, and prescription medications for themselves (but that’s all quickly coming to an end also under the AMA/Biden Tyranny).

The American Medical Association does not want any doctors thinking for themselves and going “off the record,” meaning off-script. If the answer to a question is not already scripted by the AMA, then doctors are instructed to reply, “no comment” (that’s the #2 language swap instruction under ‘DON’Ts.’

The AMA also instructs doctors to utilize scare tactics as “calls to action,” including warning people who refuse vaccines that they can suffer from acute liver injury, disabilities, and septic shock, and to use imagery to strengthen this fear-based propaganda. Yet, the Covid vaccines themselves cause disabilities and liver injury, as billions of spike proteins invade cleansing organs, the lungs, the heart, and the brain, by causing damage to endothelial and epithelial tissues inside blood vessels.

Corrupt AMA instructs American doctors to polish their social profiles and actively solicit positive reviews

The AMA says the best way to bury negative reviews is to drown them in (fake) positive ones that are drummed up through solicitation. This is part of the “game plan” for doctors and their staff because the pandemic is like a game, where the losers all take the blood-clotting bioweapon jabs, while the winners laugh in back rooms and at training seminars that teach them how to sling propaganda and lies about Covid.

When doctors get horrible reviews on a business page or Facebook, the AMA says just simply flip reviews on or off, accordingly, while establishing “boilerplate responses” (standard, pre-scripted lies and language swaps) for all staff members who manage doctor profiles. That’s why no American should ever trust the AMA, FDA, or CDC, because they all have scripted lies for selling America on a plandemic that pushes dangerous, blood-clotting, contaminated inoculations as “vaccinations.”

Tune your truth news dial to Pandemic.news for updates on the war against dirty vaccines and socialism, and how to keep your family happy, healthy, and safe.

Sources for this article include:

AMA.assn.org

Pandemic.news

NaturalNews.com

TruthWiki.org

NaturalNews.com

Top FDA vaccine officials RESIGN to avoid prosecution for crimes against humanity as White House, CDC commit GENOCIDE~Red Cross issues warning to stop blood plasma donations from vaccinated people

Red Cross issues warning to stop blood plasma donations from vaccinated people 

SEE: https://www.naturalnews.com/2021-09-02-red-cross-stop-blood-plasma-donations-vaccinated.html

EXCERPTS:

(Natural News) If you took a Wuhan coronavirus (Covid-19) “vaccine,” the American Red Cross will not accept blood plasma donations from you due to the inherent toxicity issues caused by the injection.

As it turns out, convalescent plasma should only be collected from the unvaccinated who still have clean blood that has not been contaminated with deadly spike proteins and other chemicals that threaten to kill those who receive blood transfusions.

Thanks to “Operation Warp Speed,” there is now a massive shortage of pure blood in the United States that has not been tainted with genetic modifications and other damage. Mass vaccination, in other words, is effectively killing people who desperately need unvaccinated blood but cannot find it.

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ALSO: https://www.naturalnews.com/2021-09-02-top-fda-vaccine-officials-resign-to-avoid-prosecution-for-crimes-against-humanity-as-white-house-cdc-commit-genocide.html

(Natural News) It’s fascinating that two senior FDA officials who have overseen decades of mass vaccinations have now finally reached the end of their tolerance for crimes against humanity. They resigned earlier this week, citing the astonishing fact that the White House, CDC and UN have conspired to lock the FDA out of vaccine approval decisions, bypassing FDA regulatory authority and pushing vaccines for political reasons that have no scientific basis. (FDA director Woodcock is on board with the crimes, of course, which is why she’s fraudulently issuing personal letters to “approve” vaccines, bypassing the rest of the FDA’s regulatory process.)

Apparently, the outrageous vaccine fraud now being committed by the Biden regime was too much for even lifelong FDA vaccine advocates.

Now, Dr. Marion Gruber, director of the U.S. Food and Drug Administration’s vaccines office, and her deputy, Dr. Philip Krause have both resigned, accusing the White House and CDC of pushing booster shots without supporting data. But a more informed analysis of the timing of their resignations arrives at the conclusion that they know about the criminal indictments that are coming against the genocidal vaccine mass murderers, and they want no part in the post-vaccine “Nuremberg 2.0” trials that will indict and prosecute hundreds of former government officials for their role in crimes against humanity.

After the Nuremberg trials following World War II, several scientists and doctors were sentenced to death for their role in the coordinated mass murder of six million Jews. Today, the CDC, White House, UN and vaccine makers are trying to mass murder billions of human beings.

 

Famous Doctor Exposes FDA Ivermectin Lies

"...if we look at COVID numbers in countries that give ivermectin, the number of cases is 134.4 per 100,000, and the number of deaths is 2.2 per 100,000"

Source: https://biblescienceforum.com/2021/08/28/tokyos-medical-association-chairman-recommends-ivermectin/

Also: https://www.lifesitenews.com/news/breaking-japanese-medical-association-chairman-tells-doctors-to-prescribe-ivermectin-for-covid/

BY RENEE NAL

SEE: https://rairfoundation.com/bam-famous-doctor-exposes-fda-ivermectin-lies/;

republished below in full unedited for informational, educational & research purposes:

“Sadly, anything that might possibly work against the virus is opposed by those in power…” – TheBlaze Senior Editor Daniel Horowitz

Robert W. Malone, MD, the inventor of mRNA Vaccines, slammed the Food and Drug Administration (FDA) for discouraging the use of ivermectin as a potential treatment or prophylaxis for the coronavirus.

A viral Tweet from the FDA condescendingly portrayed Ivermectin only as a drug for animals, and therefore unacceptable for human consumption. “You are not a horse. You are not a cow. Seriously, y’all. Stop it,” read the Tweet, which linked to a completely unsourced article posted at the FDA’s website.

Dr. Malone took issue with the “childish” messaging from the FDA, stating in part that the message contradicts a current government-sponsored outpatient ivermectin clinical trial. Later, he tweeted an image of the ivermectin used for horses versus the ivermectin used for people.

“Ivermectin – one form is for horses, the other for humans. Simple stuff. Making it easy to understand. Is that sufficiently clear?,” he said.

“The FDA has not reviewed data to support the use of ivermectin in COVID-19 patients to treat or to prevent COVID-19; however, some initial research is underway,” the article at the FDA website article concedes.

The move by the FDA is only the latest to discourage promising coronavirus treatments. As Dr. Joseph Mercola has stated:

“While the list of crimes committed by authorities during the COVID-19 pandemic is a long one, perhaps the biggest crime of all is the purposeful suppression of safe and effective treatments.”

TheBlaze Senior Editor Daniel Horowitz also took issue with the FDA’s obnoxious statement. “For the assholes at the FDA claiming ivermectin, which could save millions, is only for horses, here is the readout from the Nobel Prize Assembly on ivermectin,” he said.

Horowitz also linked to an article which goes into detail about how ivermectin has been beneficial for humans, not horses. “Sadly, anything that might possibly work against the virus is opposed by those in power,” Horowitz states in part.

Please see a newly-surfaced video clip of the chairman of the Tokyo Medical Association Haruo Ozaki praising ivermectin during a press conference Feb. 9, 2021:

Brighteon: FDA gaslights the world with FAKE “approval” of Pfizer vaccine

We now know the FDA “approval” of the Pfizer covid vaccine is a bold, treacherous gaslighting campaign involving media lies, fake science and criminal conduct at the FDA itself. Issuing two letters on Monday, the FDA actually extended the EUA for the Pfizer vaccine while granting approval to a different vaccine called “Comirnaty” which does not exist in the marketplace and isn’t even in production.

Read more at https://www.naturalnews.com/2021-08-25-fda-gaslights-the-world-with-fake-approval-of-pfizer-vaccine.html

FDA gaslights the world with FAKE “approval” of Pfizer vaccine while Biden’s fake presidency collapses

BY MIKE ADAMS

SEE: https://www.naturalnews.com/2021-08-25-fda-gaslights-the-world-with-fake-approval-of-pfizer-vaccine.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) We now know the FDA “approval” of the Pfizer covid vaccine is a bold, treacherous gaslighting campaign involving media lies, fake science, and criminal conduct at the FDA itself. Issuing two letters on Monday, the FDA actually extended the EUA for the Pfizer vaccine while granting approval to a different vaccine called “Comirnaty” which does not exist in the marketplace and isn’t even in production.

Through carefully crafted weasel words, the FDA has attempted to conflate the two vaccines to try to gaslight America into thinking the Pfizer covid vaccine now has full approval, all while making sure Pfizer still has legal immunity under the EUA for all the injuries and deaths caused by its vaccine. The media has played along, fraudulently reporting that the Pfizer vaccine now has “full approval” even though no such thing actually occurred.

Then again, this entire plandemic has been nothing but fraud from the very start, so it’s no surprise that the fraud remains firmly in place at the highest levels of the criminally-run FDA, which functions as nothing more than the monopoly marketing enforcers for Big Pharma.

The result of all this is that Big Pharma, Big Media, and Big Tech are gaslighting America like never before, faking like the Pfizer mRNA vaccine has been “fully approved” by the FDA and using that as an excuse to demand full vaccine compliance.

But it isn’t even a vaccine. Even the CDC’s own director Walensky admits this “vaccine” doesn’t halt transmission and doesn’t prevent infections. It merely reduces symptoms, which allows infected people to become superspreaders because they appear to be asymptomatic while they actually carry a far higher viral load. (See this important article by Dr. Peter McCullough for full details on why this happens.)

What the vaccine does accomplish, however, is the mass death of the vaccinated via blood clots, autoimmune disorders, and more. A website called The Covid Blog is documenting many of these shocking, disturbing deaths, including a recent case of a woman whose skin began to rot off her face after she took the covid jab. (Warning: Extremely graphic photos in that story.)

Get more details on all this in today’s Situation Update podcast, below.

Fake pandemic, fake “approval” of a vaccine, and a fake president, too

Meanwhile, the Imposter-In-Chief Joe Biden is watching his approval ratings absolutely plunge in the aftermath of the Afghanistan catastrophe (which isn’t even over) that saw the transfer of tens of billions of dollars in military equipment to the Taliban while tens of thousands of Americans were deliberately stranded behind enemy lines. (This is all by design, of course, and has long been the plan of the Obiden administration.)

USA Today is now reporting that Biden’s approval has plunged to 41%. If you strip away the polling bias and deliberately dishonest lying by USA Today, in truth Biden’s support numbers are now in the low-30s.

With Biden’s popularity having now plunged into the low-30s, he’s going to be removed rather soon. Regime change is coming, and Kamala isn’t going to be the one sitting in the Oval Office once the chaos settles.

Be prepared for all possibilities: Total financial collapse, civil war, secession, military martial law, invasion by UN troops, collapse of supply lines, grid-down scenarios, and more. Anyone who isn’t prepared is at risk of not surviving the next 18 months. And anyone taking the spike protein bioweapons injections is probably already a goner unless they’re pursuing very specific nutritional strategies to block the spike protein.

Full details in today’s podcast:

Brighteon.com/30271ddf-2931-4142-b5c1-012c775ed8cb

FDA Approval Illegal! Doctor Reveals Pfizer Insert Proves Criminal Regulation Violations!

FDA Approval may give lawyers more ammunition to fight mandates and the Pfizer injections from being pushed onto your kids! The package insert reveals "criminal action", according to Dr. Jane Ruby, who joins Stew Peters to discuss the unprecedented action taken by the FDA.

BUT- That's not a story. It's a lie. The FDA only approved a name change. The product is still only emergency-use authorized. The emergency use has been extended, no full approval. The communists call it full approval to dupe more sheeple & lemmings into getting jabbed.

As I understand it, full approval cannot be obtained before 2023.

 

FDA vaccine “approval” leads blue states to order the mass slaughter of teachers, workers and first responders

BY MIKE ADAMS

SEE: https://www.naturalnews.com/2021-08-24-fda-vaccine-approval-leads-blue-states-to-order-the-mass-slaughter-of-workers.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) The FDA’s fraudulent “approval” of the failing Pfizer covid vaccine is all that leaders of blue cities and states needed to order the mass slaughter of their own employees. In mere hours after the FDA’s announcement yesterday, the State of New Jersey ordered the mass slaughter of all NJ teachers and state workers via spike protein injections, a “clot shot” that has already killed an estimated 500,000 Americans (and counting).

The NY Dept. of Education announced a similar vaccine slaughter campaign for all education workers statewide, including teachers, school administrators, janitors and food prep workers. Los Angeles also chimed in, ordering the vaccine slaughter of its 60,000 employees, including firefighters, law enforcement officers and other first responders.

Many other blue cities and states have joined the mass executions, demanding total compliance to an experimental, deadly vaccine — yes, it’s still a medical experiment, even according to the FDA’s own “approval” letter — despite the total lack of animal trials, bio-distribution studies and long-term safety data. In essence, these blue cities and states are committing vaccine suicide, leading to a scenario in the not-too-distant future where many of these Democrat-run cities will be collapsed ghost towns.

I cover this in a 13-minute emergency podcast update that you’ll find here:

Brighteon.com/a8c4746f-b4de-4da5-938b-d15594889cb3

Governments unleash total war against the human population with vaccines, starvation and death camps

The coming collapse of blue cities and states isn’t the end of this medical horror, however: In collusion with Big Pharma criminals, governments around the world have now declared total war against the human population, and they’ve initiated vaccine slaughter, engineered starvation and the construction of covid death camps in order to carry out their global depopulation agenda.

Their goal is to reduce the current human population by 90%. This means killing around 7 billion people. Vaccines are only part of the “final solution” to achieve this since only around 2.5 billion people have been vaccinated on the planet so far. The rest of the deaths are being engineered to come from starvation (deliberate food collapse), violence, lawlessness, and government-run death camps where vaccine-hesitant people are rounded up and thrown into covid death camps to be exterminated en masse, Holocaust-style. The CDC has publicly announced this plan on its own website, calling the covid death camps “green zones” and claiming they will meet “minimum humanitarian standards.” The CDC’s covid camp plans offer no description for how healthy people might one day leave those camps, by the way.

Keep in mind that engineered financial events will also contribute to the mass death and destitution across the planet as humanity is plunged into End Times scenarios by satanic forces.

Ultimately, by the way, we believe Satan’s forces will be defeated and humanity will prevail. While the depopulation globalists are trying to mass murder 7 billion people, we hope the damage can be limited to just one billion. But it all depends on how quickly humanity rises up against the evil and demands the arrest and prosecution of the criminals running the covid plandemic bioweapons scheme.

Today’s Situation Update podcast provides a lot more details:

Brighteon.com/a864d1b4-320b-4692-a755-24ea6bab6488

Children’s Health Defense to Challenge Full Approval of Pfizer COVID Vaccine

BY RAVEN CLABOUGH

SEE: https://thenewamerican.com/childrens-health-defense-to-challenge-full-approval-of-pfizer-covid-vaccine/;

republished below in full unedited for informational, educational & research purposes:

Children’s Health Defense (CHD) is challenging the Food and Drug Administration’s “premature, arbitrary, and capricious” approval of the Pfizer-BioNTech COVID vaccine for people aged 16 and up.

On Monday, the FDA announced the Pfizer-BioNTech COVID-19 vaccine will be marketed as Comirnaty, protecting against COVID for those aged 16 and up. Individuals between ages 12 and 15 may continue to get the vaccine, but it remains approved only under emergency use authorization currently.

Immediately following this announcement, CHD announced it intended to challenge the agency’s decision. CHD president Mary Holland accused the agency of putting the interests of the pharmaceutical industry over Americans.

“With over 13,000 reported deaths from COVID shots, we are deeply concerned about the impact on health, both short- and long-term,” she said. “We intend to challenge this approval and licensure. We do not believe that this approval will significantly affect the trajectory of the pandemic, as we know that these shots are less than 50% effective against the variant in circulation now.”

According to LifeSite News, the 13,000-plus deaths following the COVID vaccination are “more deaths than all [post-vaccination] deaths reported during the entire 30-year history of the federal reporting system.”

In Ottawa, Canada, burial costs will be covered by the government for individuals who’ve died after receiving federally approved vaccines, underscoring the prevalence of the vaccine-related deaths.

Internal medicine physician and vaccine expert Meryl Nass, M.D. asserts that deaths related to the COVID vaccinations have not been explained or addressed by the FDA or the Centers for Disease Control and should have been enough to stop the FDA from granting a license to the Pfizer vaccine.

Beyond the recorded deaths related to the vaccine, the Vaccine Adverse Event Reporting System (VAERS) shows more than 595,000 adverse events following the COVID vaccine as of August 13.

And because VAERS relies on self-reporting, it should be assumed that all of these figures are likely higher than what’s reflected in the numbers.

Meanwhile, the level of protection afforded by the vaccines does not justify the health risks they pose, as data now show that vaccine-related immunity begins to fade within months. According to Israel’s minister of health, vaccine protection has dropped to 39 percent.

Doctors with CHD are also raising concerns over the COVID “booster” vaccines, which are shown to provide even less protection.

“While the US government has said it will begin booster doses of mRNA vaccines the week of September 20, there is actually no evidence that Covid-19 boosters will provide increased protection against infection, or that they are effective against the delta variant or other new variants,” according to Nass. “For other vaccines, such as mumps and pertussis, there is no evidence that booster doses after the initial course add measurable protection.”

“CHD opposes vaccine mandates on principle; all humans are biologically unique, and one-size-fits-all medicine is simply not scientific, given what we know about individual risk and vaccine injury,” said Holland.

Children’s Health Defense has been a leading opponent of vaccine mandates and has been calling out what many say are less-than-honorable interests behind the push to vaccinate Americans. Just last week, CHD, along with 18 students, sued Rutgers University over its COVID vaccine mandate, calling it “an affront to human dignity and personal freedom because it violates our basic right to control our bodies.” Rutgers was the first major college in the United States to require students to receive the vaccine, according to LifeSite News.

According to the lawsuit, Rutgers is working with all three of the vaccine manufacturers — Pfizer, Moderna, and Johnson & Johnson — to study and develop their vaccines in on-going clinical trials. As such, Rutgers will benefit financially if more people are required to take the shots.

“The Rutgers mandate stems from the financial relationship the university has with the vaccine makers which is clearly a conflict of interest,” said New Jersey attorney Julio Gomez, who represents the students.

“Unjustified fear and insatiable greed drive the vaccine industry, especially now, during the pandemic,” Gomez added. “This has created an opportunity for manufacturers to bring to market expensive, novel and patentable drugs, vaccines, biologics, treatments and medical devices that will reap huge profits.”

Rutgers student Peter Cordi, a plaintiff in the lawsuit, said Rutgers is driven by “greed and ties to Big Pharma” and is putting its own financial interests over the lives of its students.

CHD reports that Pfizer expects to pull in $33.5 billion in COVID vaccine revenue this year alone, and, along with Moderna, locked up COVID vaccine supply agreements worth more than $60 billion in sales for 2021 and 2022. These agreements include the two doses of the vaccine as well as potential boosters.

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ALSO SEE: https://childrenshealthdefense.org/

NUREMBERG 2.0: Biden’s corrupt DOJ just declared experimental vaccine mandates LEGAL; forced experimental injections will now commence

Image: NUREMBERG 2.0: Biden’s corrupt DOJ just declared experimental vaccine mandates LEGAL… forced experimental injections will now commence

BY ETHAN HUFF

SEE: https://www.naturalnews.com/2021-07-30-bidens-doj-vaccine-mandates-legal-force-employees.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) Fake “president” Joe Biden has decided that it is perfectly legal for the government and private businesses to force employees against their will to get injected with experimental gene modification chemicals for the Wuhan coronavirus (Covid-19).

Biden’s Justice Department concluded in a new opinion that there is no federal law barring either the public or private sector from requiring people to get jabbed with the drugs, which currently hold “emergency use authorization” (EUA) from the U.S. Food and Drug Administration (FDA).

The decision came about after the U.S. Department of Veterans Affairs, the state of California, and New York City all decided to require that some of their workers either get “vaccinated” for Chinese Germs or agree to weekly testing for the rest of their lives.

Veterans Affairs, ironically enough, was the first federal agency to mandate the lethal injections, negating the brave efforts of actual veterans who fought overseas in years past – and some of them paid the ultimate price with their lives – to stop this type of medical fascism from ever encroaching on our borders.

The Office of Legal Counsel at the Department of Justice (DOJ) issued a letter stating that because access to Fauci Flu shots is now widespread, “numerous educational institutions, employers, and other entities across the United States” have chosen to mandate Chinese Virus shots as a condition of staying employed.

“For instance,” the letter reads, “certain schools will require vaccination in order for students to attend class in person, and certain employers will require vaccination as a condition of employment.”

Wuhan Flu shots shouldn’t even have EUA in the first place, but Biden’s Justice Department couldn’t care less

It is important to note that since other remedies for the University of North Carolina, Chapel Hill Virus already exist, there was never any legal precedent in the first place for the FDA to grant EUA to Pfizer-BioNTech, Moderna, and Johnson & Johnson (J&J) for their respective injections.

If the Justice Department was really devoted to pursuing justice, it would be shouting this fact from the rooftops and calling on the FDA to immediately revoke all EUAs for the Fauci Flu shot. Instead, the agency under China Joe says there is nothing to “prohibit public or private entities from imposing vaccine requirements, even when the only vaccines available are those authorized under EUAs.”

By giving this green light, the expectation is that other federal agencies will soon follow suit, along with at least some segments of the private sector. Institutions of “higher learning” all seem to be falling right in line as well, requiring their students to undergo experimental gene therapy in order to get an education this fall.

“Public sector entities need to move as quickly as possible,” shouted New York City Mayor Bill de Blasio, who eagerly announced his own citywide mandate that all public sector workers will need to either get jabbed or submit to weekly testing with fraudulent PCR tests.

“This DOJ decision is important,” de Blasio added. “I think that will be helpful. We have got to put pressure on this situation.”

Up until this point, the federal government has limited its involvement with the plandemic to targeting travel and public transportation, both of which are still restricted to masked people only. De Blasio would seem to want that involvement to now extend to compulsory Fauci Flu injections.

“We need to rise up and say enough is enough,” wrote one frustrated commenter at The Epoch Times.

“What is it going to take to get Americans riled up enough to demand this communistic taking away of freedoms day-by-day to stop? It is shocking what we are tolerating.”

The latest news about Beijing Biden’s Wuhan coronavirus (Covid-19) tyranny can be found at ChemicalViolence.com.

Sources for this article include:

TheEpochTimes.com

PGurus.com

NaturalNews.com

NaturalNews.com

CDC, FDA prepare mass distribution of a Merck/Sanofi six-in-one vaccine for kids, turning blind eye to safety signals

SEE: https://www.naturalnews.com/2021-06-26-cdc-fda-prepare-mass-distribution-merck-sanofi-vaccine.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) Since the mid-1980s, the number of childhood shots on the Centers for Disease Control and Prevention (CDC) vaccine schedule has more than quadrupled. When parents express reluctance about turning their little ones into perpetual pin cushions, drug makers and doctors have a ready answer — combination vaccines that “simplify” the schedule by decreasing the number of injections administered.

(Article republished from ChildrensHealthDefense.org)

This month marks the U.S. launch of the Merck/Sanofi joint-venture vaccine, Vaxelis, a six-in-one (hexavalent) combination vaccine that contains diphtheria, tetanus and acellular pertussis (DTaP) components as well as components said to protect against polio, Haemophilus influenzae type b (Hib) and hepatitis B.

Public health officials optimistically believe that bundling all of these components into one shot will help close noncompliance loopholes and increase the likelihood that children will complete “all recommended vaccinations.”

Though Vaxelis is the nation’s first hexavalent injection, it joins other four- or five-in-one vaccines already on the CDC schedule. The U.S. Food and Drug Administration (FDA) approved Vaxelis in late 2018 — as a three-dose series for 2-, 4- and 6-month-old infants — but it is only now, two-and-a-half years later, that the shot is being readied for widespread distribution.

There are numerous warning signs that potent all-in-one vaccines are too much for immature immune systems to handle. Concerning safety signals have emerged not just for hexavalent but also pentavalent (five-in-one) vaccines.

In Europe, where infants have been given hexavalent vaccines for some years (including Vaxelis since 2016), the formulations have produced many troubling reports of sudden infant death.

Absurdly, none of the clinical studies assessing Vaxelis safety and efficacy conducted fair comparisons against an inert placebo. Instead, in the two U.S. clinical trials for Vaxelis, not only did investigators compare infants receiving Vaxelis to babies who received Sanofi’s five-in-one Pentacel — but babies in both groups also received rotavirus and pneumococcal vaccines at the same time!

In this context, the CDC’s sales pitch to the public — and its claims that side effects are “usually mild” — cannot be considered credible.

Here are some of the other facts missing from the CDC’s communications:

  • In the two U.S. trials six infants died (slide #27) in the Vaxelis group (some after receiving just one dose); one infant also died in the “control” group that received five-in-one vaccines.
  • All six Vaxelis recipients died within six weeks of vaccination. This timing matches other published accounts of infant deaths “clustering” following hexavalent vaccination.
  • The reported causes of death for the infants who received Vaxelis included asphyxia, sepsis, fluid in the brain and sudden infant death syndrome (SIDS). These outcomes correspond to the types of adverse events reported following hexavalent vaccination in Europe.
  • Package inserts for other vaccines on the CDC schedule list similar causes of death, suggesting these fatal Vaxelis outcomes are plausibly associated with vaccination.
  • In the clinical trials, the rate of fever was notably higher in Vaxelis recipients even when compared to children receiving five-in-one vaccines (47% vs. 34%).

Juicing vaccine sales

In the no-liability context enjoyed by vaccine makers in the U.S., combination vaccines are already quite popular. In fact, market watchers and health economists praise the jumbo shots as being a catalyst for positive industry trends and a “key to commercial success.”

Thus, financial analysts expect Vaxelis to “garner significant patient share following its [U.S.] launch” — predicting that it will account for almost a third of U.S. DTaP vaccinations by 2028 — or $841 million in annual sales.

These predictions represent good news for Merck and Sanofi, two of the “big four” pharma giants that dominate the childhood vaccine market in the United States. Merck is already doing a booming vaccine business, recently reporting annual sales growth of 14.8% for its pneumococcal vaccine (Pneumovax 23) and 5.4% for its human papillomavirus (HPV) vaccine Gardasil-9.

However, Merck also faces proliferating Gardasil-related lawsuits — including legal actions alleging that the company knew about and ignored life-changing adverse events from the get-go, many of which (when not fatal) have involved autoimmunity and chronic pain. In fact, before the advent of emergency use COVID vaccines (responsible for an alarming escalation of vaccine-related adverse events), Gardasil had had “more side effects reported than all other vaccines combined.”

Sanofi, too, is embroiled in thousands of lawsuits worldwide — notably for its disastrous and sometimes fatal dengue vaccine. As with Merck, this has not dampened overall vaccine sales growth, which continues its strong upward trajectory, likely to be further strengthened by the U.S. Vaxelis rollout.

Although Sanofi has not been a front-runner in the COVID vaccine race, the company is currently running clinical trials for messenger RNA (mRNA) vaccines for both COVID and seasonal influenza.

Aluminum secrecy and grandfathered ingredients

Merck’s proprietary, “super-powered” aluminum adjuvant — amorphous aluminum hydroxyphosphate sulfate (AAHS) — which is believed to play a significant role in Gardasil’s risk profile, is also present in Vaxelis.

After Merck developed AAHS, it began to “preferentially” feature AAHS in its vaccines even though, as Danish scientists outlined last year, the company appears to have disregarded procedures ordinarily required for approval of new adjuvants.

According to the Danes, at the time AAHS appeared, it represented a “new type of aluminium adjuvant with excipients that [had] not been used earlier in [European Medicines Agency] authorized vaccines.” It should have been — but apparently was not — tested against an inert placebo. For this and other reasons, the Danish scientists question the ethical underpinnings of the Gardasil clinical trials.

In noting that Merck also “seems to have prevented independent studies of AAHS,” the Danes repeated a critique aired by world-famous aluminum expert Christopher Exley in 2018. In an extensive discussion of different aluminum-based adjuvants and their immunological mechanisms of action, Exley and co-authors emphasized the importance of studying aluminum adjuvants one by one, as each is “chemically and biologically dissimilar with concomitantly potentially distinct roles in vaccine-related adverse events.”

Concerningly, the Vaxelis liquid suspension is adjuvanted onto not just AAHS, but also another aluminum adjuvant — aluminum phosphate). The package insert disingenuously shorthands the combination of adjuvants as “aluminum salts.”

How this double whammy of aluminum (319 micrograms per vaccine dose) interacts with the vaccine’s six antigens, or Vaxelis’s numerous other ingredients, or the heavy aluminum load in other childhood vaccines is largely unknown.

According to the Vaxelis package insert, the vaccine also includes: polysorbate 80 (an ingredient flagged for its propensity to induce hypersensitivity reactions); glutaraldehyde and formaldehyde (problematic chemicals deemed necessary to inactivate pertussis toxin); bovine serum albumin (often harvested from bovine fetuses when female cows are found to be pregnant at slaughter); three different antibiotics (neomycin, streptomycin and polymyxin B); ammonium thiocyanate (also a rust inhibitor, weedkiller and defoliant); and yeast protein (associated, notably in hepatitis B vaccines, with autoimmune reactions).

Regulatory loopholes allow manufacturers to “grandfather” ingredients into new vaccines if the components are already present in other licensed vaccines — regardless of how inadequate the original safety testing may have been.

Thus, Merck and Sanofi perceived no need to test Vaxelis for DNA-damaging or cancer-causing effects and conducted no studies of the ingredients’ pharmokinetics (i.e., how the substances move “into, through, and out of the body”).

The main cautionary note sounded in the meager Vaxelis patient information sheet is to not give Vaxelis to children if they are “allergic to any of the ingredients.”

For thee and thee … but not for me?

The CDC seems to be particularly interested in ensuring that poor and non-white children get Vaxelis. The agency began laying the groundwork to offer Vaxelis through the Vaccines for Children (VFC) Program — the agency’s vaccine program for the poor — over two years ago, in March 2019.

In September of that year, the CDC followed up with an affirmative vote. Public health departments have been promoting Vaxelis to participating VFC providers since early June 2021.

At its September 2019 meeting, CDC outlined another topic deemed important for discussion in the near future — raising the issue of whether Vaxelis should be “preferentially recommended” for the American Indian/Alaskan Native (AI/AN) pediatric population.

The tenuous rationale, according to the meeting notes, was because, “in the pre-vaccine era” (more than 35 years ago), “Hib disease occurred at a younger age among the AI/AN population compared to the general population.”

Wave of the future?

Judging from its website, the CDC perceives combination vaccines to be the wave of the future, and has signaled its strong endorsement of Vaxelis by incorporating the new vaccine into its 2021 vaccine schedule.

As if exposure to six antigens were not enough, FDA and CDC also say it is okay for healthcare providers to administer the six-in-one shot at the same time as other vaccines.

These agencies’ characterization of the Vaxelis safety profile as “acceptable” indicates they have either not done their due diligence, or are willing to accept a high level of collateral damage in exchange for the “convenience” of six-in-one shots.

However, as the “overwhelmed by guilt” parents of COVID-vaccine-injured teens are increasingly finding out, convenience is poor consolation for life-changing or life-threatening adverse outcomes.

Read more at: ChildrensHealthDefense.org

Absolutely NOT safe and NOT effective: FDA and CDC lied about vaccine efficacy to obtain ’emergency authorized use’ (EAU) for highly-suspect human medical experiment using mRNA

BY S.D. WELLS

SEE: https://www.naturalnews.com/2021-06-01-fda-cdc-lied-about-vaccine-efficacy.html#;

republished below in full unedited for informational, educational & research purposes:

(Natural News) As they say, the proof is in the pudding. COVID-19 shots have been the deadliest inoculations ever documented, by far, and that’s according to the CDC’s very own data. More people have died from Covid vaccines (approaching 5,000 now) than all vaccine deaths totaled since the 1950s. No wonder why. They couldn’t even reach the EAU (emergency authorized use) 50 percent efficacy threshold for approval, and that is pretty sad, but worst of all, these ‘treatments’ are super dangerous and haphazard.

Safety thresholds have been thrown out the window with all of these Covid jabs from all three manufacturers. They always assume that none of us can remember what happened last month or last year, but some of us can (the unvaccinated) and do, and we review the data and the findings too. Investigative journalists who support clean living and healthy living must expose the truth to the masses, or the “fence riders” (those not sure whether to vax-up or not) have no chance at all.

Scamdemic Alert: Gene-tampering Covid jabs offer ZERO safety or effectiveness proof while causing blood clots around the world

In the summer of 2020, the FDA’s commissioner stated that in order for the vaccine manufacturers to even get just emergency authorized use, they had to cross the minimum threshold of 50 percent efficacy, that’s according to their own documented standard, and even if they did, that would only be considered a medical experiment, not some mass campaign to inoculate more than 70 percent of the world’s populace in less than 6 months. So how did they even get 50 percent efficacy, when the shots haven’t proven that ANYBODY at all is yet immune to Covid? Easy. Fake the research. Fake the results. Fake everything.

All Covid vaccines are actually a crime right now because none of them even meet the EAU threshold. FDA testing reveals more than half of the test-subject participants came down with Covid-19 within 7 days post-vaccination, but the symptoms were labeled “reactogenicity” to alter the results in order to gain emergency approval. In other words, the FDA/CDC created a gray area where they say symptoms of Covid overlap with symptoms and adverse reactions or “side effects” of the inoculations.

So what did the vaccine manufacturers do to solve this little dilemma, and in their favor? They never bothered to verify whether those test subjects (human guinea pigs) even had Covid, they just chalked up all the symptoms they had as common reactogenicity.

They simply never checked to see if the vaccinated sheeple really caught Covid, because they didn’t want those results (and records), as they would demolish their chances of reaching the 50 percent EAU acceptable medical experiment threshold. And when will the worldwide “test” of vaccine “efficacy” cross the blood clot threshold of 50 percent?

Reactogenicity is the inflammatory response to vaccination, now used as a cover story for “safety and efficacy” of dangerous, deadly Covid vaccines

Chronic inflammation is the root of nearly all ill-health problems. The CDC tries their best to convince the worried, “hesitant” populace that all the horror stories are fake and that the only side effects from inoculations are slight pain at the injection site, fatigue and a low-grade fever. That’s only the tip of the iceberg, and they know it, but most Americans never look any deeper than that.

Forget about “hesitancy.” It’s gone way beyond that. The skeptics of vaccines have much more to worry about than a slight fever or some numb pain called reactogenicity. If the CDC and the FDA were honest, or even if someone somehow was keeping them honest, they would have to disclose right now that the jabs are causing blood clots around the world.

Now, the CDC is targeting young teens. Pfizer wants 12-year-olds to get the vaccine, even though there’s nary a case of death on Earth for anyone that young, and if there is, it’s probably faked too (they probably died in a car wreck or drowned, and then tested positive for Covid proteins – and those are fake tests too).

Meanwhile, the vaccine industry is busy collaborating with the CDC and the tech giants, shutting down all talk (and literature) about natural remedies and indigenous cures that have worked against these viruses for millennia. The scamdemic also reveals that the PCR tests are fundamentally invalid and fraudulent.

The vaccines don’t prevent infection, but rather cause blood clots and hyper-inflammatory responses that are very dangerous to the immune system and can even cause mad cow disease in humans through the uncontrollable creation of prions thanks to mRNA “technology.”

Tune your internet frequency to Pandemic.news for updates on how to prepare for the upcoming VACCINE PANDEMIC and communist apocalypse.

Sources for this article include:

Pandemic.news

NaturalNews.com

TheLibertyLoft.com

FDA document reveals 86% of children who participated in Pfizer covid vaccine trial experienced adverse reactions

BY MIKE ADAMS

SEE: https://www.naturalnews.com/2021-05-27-fda-document-pfizer-covid-vaccine-trial-adverse-reactions.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) A publicly-available FDA “fact sheet” document reveals that 86% of children who participated in a Pfizer covid vaccine trial reported adverse reactions ranging from “mild” to “serious.”

As part of the vaccine experiments, children aged 12 to 15 are being injected with mRNA sequences that take control of their cells, causing them to churn our spike proteins in their blood. Spike proteins cause vascular disease and blood clots. Even the Jonas Salk Institute conclusively identifies spike proteins as the culprit behind vascular disease and blood clots.

This is all openly admitted by the FDA, which has published extremely disturbing reports of adverse reactions experienced by children in a Pfizer covid vaccine “fact sheet” labeled 144413. See the original FDA document here (PDF).

In case the FDA removes this sheet, we have archived it at Natural News servers here (PDF).

FDA admits mRNA vaccines cause adverse reactions in 86% of children, but calls it “safe” anyway

This Pfizer page at the FDA provides links to all the fact sheets and press releases where the FDA celebrates expanding its emergency use authorization to children aged 12 to 15.

That fact sheet contains the following table that details the alarming rate of side effects and damage experienced by 12 – 15-year-olds (i.e. children) who were given the mRNA injections:

Table 5: Study 2 – Frequency and Percentages of Adolescents With Solicited Local Reactions, by Maximum Severity, Within 7 Days After Each Dose – Adolescents 12 Through 15 Years of Age

As you can see from the table, 1127 children were given the first dose of the vaccine, and 1097 children received the second dose. What happened to the 30 children who didn’t show up for the second dose? Did they die? Why were they removed from the second dose?

Among those children injected with the mRNA vaccine medical experiment:

  • A shocking 86% experienced side effects.
  • Nearly 44% suffered “moderate” side effects defined as “interfering with activity.”
  • 66% of the children experienced fever.
  • 65% suffered headaches.
  • Other side effects experienced by these children as part of these medical experiments include chills, vomiting, diarrhea, fever, muscle pain and even joint pain.
  • Even after 86% of children experienced such side effects after being injected with the first dose, researchers continued to inject the children with a second dose.

The FDA claims this is all about “protecting” children while pushing more vaccine sales to generate billions of dollars in profits for Pfizer

The FDA claims in its celebratory press release that expanding Pfizer’s experimental vaccine to 12 to 15-year-olds is a kind of breakthrough, not a crime against children:

“The FDA’s expansion of the emergency use authorization for the Pfizer-BioNTech COVID-19 Vaccine to include adolescents 12 through 15 years of age is a significant step in the fight against the COVID-19 pandemic,” said Acting FDA Commissioner Janet Woodcock, M.D. “Today’s action allows for a younger population to be protected from COVID-19, bringing us closer to returning to a sense of normalcy and to ending the pandemic. Parents and guardians can rest assured that the agency undertook a rigorous and thorough review of all available data, as we have with all of our COVID-19 vaccine emergency use authorizations.”

In other words, the FDA is admitting they are fully aware of the 86% side effect rate when it comes to injecting children with experimental mRNA “vaccines.”

Vaccine medical experiments are harming children in the name of Big Pharma profits

When it comes to mRNA vaccine trials in the USA, when serious reactions such as facial paralysis are identified in the vaccinated group, the FDA (and presumably, the researchers) dismiss them as coincidence. From the FDA’s own document:

Bell’s palsy (facial paralysis) was reported by four participants in the Pfizer-BioNTech COVID-19 Vaccine group. Onset of facial paralysis was Day 37 after Dose 1 (participant did not receive Dose 2) and Days 3, 9, and 48 after Dose 2. No cases of Bell’s palsy were reported in the placebo group. Currently available information is insufficient to determine a causal relationship with the vaccine.

Thus, no matter what horrific side effects are caused by the vaccine experiment, they are dismissed and ignored. After all, there are billions of dollars to be earned from authorizing vaccines for widespread use in children. (It’s a whole new demographic market to target.)

This FDA document even admits the vaccine is not approved and may cause serious injury or even death:

FDA has authorized the emergency use of the Pfizer-BioNTech COVID-19 Vaccine, which is not an FDA-approved vaccine.

Adverse Reactions in Clinical Trials

Adverse reactions following the Pfizer-BioNTech COVID-19 Vaccine that have been reported in clinical trials include injection site pain, fatigue, headache, muscle pain, chills, joint pain, fever, injection site swelling, injection site redness, nausea, malaise, and lymphadenopathy (see Full EUA Prescribing Information).

Adverse Reactions in Post Authorization Experience

Severe allergic reactions, including anaphylaxis, and other hypersensitivity reactions (e.g., rash, pruritus, urticaria, angioedema), diarrhea, vomiting, and pain in extremity (arm) have been reported following administration of the Pfizer-BioNTech COVID-19 Vaccine outside of clinical trials. Additional adverse reactions, some of which may be serious, may become apparent with more widespread use of the Pfizer-BioNTech COVID-19 Vaccine.

The FDA also admits that life-threatening anaphylactic shock may occur following the vaccine, or that vaccine recipients may lose consciousness:

Appropriate medical treatment used to manage immediate allergic reactions must be immediately available in the event an acute anaphylactic reaction occurs following the administration of Pfizer-BioNTech COVID-19 Vaccine.

Syncope (fainting) may occur in association with the administration of injectable vaccines, in particular in adolescents. Procedures should be in place to avoid injury from fainting.

Any rational person, after reading this “fact sheet” from the FDA, would express serious concern over the continued recruitment and exploitation of children as human guinea pigs in vaccine medical experiments.

This is why we continue to sound the alarm on such practices.

_______________________________________________________

SEE ALSO:

Covid vaccine spike proteins attack male fertility, too

https://www.naturalnews.com/2021-05-27-covid-vaccine-bioweapons-attack-male-fertility-too.html

PRO-VAX DOC: “I CAN NO LONGER RECOMMEND THE VACCINE TO ANY INDIVIDUAL”

Jim Meehan, MD, has a candid “doctor to doctor” discussion with Professor of Medicine, Peter McCullough, MD, about why he changed his mind on recommending the Covid vaccine to his patients, especially if they have already recovered from #Covid19.

Doctors, Parents File Motion to Stop FDA Authorization of COVID Vaccines for Children

Doctors, Parents File Motion to Stop FDA Authorization of COVID Vaccines for Children

BY RAVEN CLABOUGH

SEE: https://thenewamerican.com/doctors-parents-file-motion-to-stop-fda-authorization-of-covid-vaccines-for-children/;

republished below in full unedited for informational, educational & research purposes:

America’s Frontline Doctors (AFLDS) has filed a motion in federal court seeking a temporary restraining order to “prevent the expansion of the FDA’s Emergency Use Authorization (EUA) for COVID-19 vaccines to include children under the age of 16,” the group announced in a statement this weekend.  

Life Site News reports the motion was filed in the U.S. District Court for the Northern District of Alabama and is directed against Secretary Xavier Becerra and the Department of Health and Human Services.

“There is no public interest in subjecting children to an inoculation program, in order to protect them from a disease that simply does not threaten them,” stated attorney Lowell H. Becraft, Jr. “Children are inherently incapable of providing informed consent. Neither the children nor their parents can possibly give informed consent to these vaccines since the DHHS Secretary has failed to make even the minimum statutory disclosures regarding risks and alternative treatments.” 

According to concerned doctors with the group, the risks associated with the COVID-19 vaccine far outweigh any benefits of protecting children from a virus that causes minimal, if any, symptoms.

“We’ve never seen this level of side effects for any vaccine without the FDA taking action,” stated Dr. Angelina Farella, AFLDS Pediatric Medical Director. “The Rotavirus vaccine was pulled for 15 cases of non-lethal side effects and the Swine Flu vaccine was pulled for 25 deaths. But now, by the CDC’s own data, we are seeing a 12,000 percent increase in deaths with these vaccines and they’re still talking about giving this to our kids.”

The latest side effect of the COVID-19 vaccine, it seems, is myocarditis, an inflammation of the heart muscle, which has been reported in teens and young adults within days of receiving a second dose of the Moderna and Pfizer vaccines.

“Our children should never be the experiment,” she continued. “No additional authorizations or mandates should be granted. We want to preserve the previously established safety standards.”

In addition to AFLDS, plaintiffs on the motion include individual doctors and parents of minor children.  

“I’ve done my research and know that there is essentially zero percent risk for young people dying of COVID-19 and fiercely oppose the use of an untested product that has not been fully approved for use in healthy children,” said plaintiff Matt Schweder, a parent of minor children.

Because of the minimal risks for children of dying of COVID-19, the plaintiffs contend the defendants will be unable to make “science-based” arguments that assert “preserving the status quo will create any hardship for them or for the public.” After all, the survivability rate for COVID-19 for individuals under the age of 20 is 99.997 percent, according to statistics cited by the plaintiffs.

The motion reads, “EUA requires that an intervention address a serious or life-threatening condition, and for known and potential benefits of the intervention to be balanced against the known and potential harms.” But, “[t]here is not even a pretense of a factual basis that COVID-19 represents a serious or life-threatening condition for children under 16, since the CDC acknowledges they face 0% risk of mortality from COVID-19 statistically.”

Meanwhile, the risks associated with the vaccine have been well-documented since their rollout. The plaintiffs note there have been more than 4,000 deaths tied to the COVID-19 vaccines in the last four months, far surpassing the 1,500 total in the previous 10 years for all vaccines.

Likewise, researchers have voiced concerns that spike proteins from the vaccines cross the blood-brain barrier and can potentially increase autoimmune disorders, which are far more harmful than COVID-19 for young people.

In addition to fighting against the use of vaccines for minor children, the plaintiffs also strongly discourage the vaccines for healthy populations between the ages of 20 and 69, the motion reads.

Sadly, the government’s COVID agenda has prompted decision-makers at all levels, as well as much of the medical community and average citizens, to look the other way when it comes to the dangers of the COVID vaccines. Typically, the plaintiffs note, experimental vaccine rollout is paused by the government when there are 25 unexplained deaths associated with the shot. Yet 4,000 deaths have failed to prompt any action.

The plaintiffs contend their motion includes arguments that will make clear to the court that the EUAs should never have been granted and should be immediately revoked, and that the injections are more dangerous than the virus itself. The motion also asserts that numerous laws have been broken in the process of granting the EUAs and the efforts to push the vaccines out. The motion includes assurances that the plaintiffs will be bringing suit “in the near future” against the EUAs.

“We all would like to put COVID-19 behind us, but we must be responsible about it as physicians, parents and as a nation. People are being misled here and we need to ensure that we don’t rob our children of their future because of a rush to administer a vaccine that has not been fully tested and approved,” stated Dr. Teryn Clarke, executive communications director for America’s Frontline Doctors. 

The group contends the best approach to COVID-19 should protect both physicians and citizens from government overreach, preserve Constitutional freedoms, and remove threats of “medical ‘cancel culture’ and media censorship.” More successful ways to stop the virus, according to the motion, include expanding COVID-19 treatment options for all Americans and providing over-the-counter COVID preventative and early treatment options to all Americans who need them. The group rejects mandatory government lockdowns and restrictions unsupported by science, instead asserting the best care focuses on the nation’s “at-risk” population.  

 

Two young mothers paralyzed after receiving Pfizer’s COVID vaccine~FDA inspectors document horrific conditions at J&J COVID-19 vaccine plant~NIH established a “public health emergency” loophole, enabling Chinese scientists to exploit moratorium on gain-of-function coronavirus research

Image: BOMBSHELL: FDA inspectors document horrific conditions at J&J COVID-19 vaccine plant

SEE: https://www.naturalnews.com/2021-05-16-mothers-paralyzed-after-receiving-pfizers-covid-vaccine.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) A woman in Nashville is the second person to describe how she became paralyzed within hours of taking a Pfizer coronavirus vaccine.

(Article by Celeste McGovern republished from LifeSiteNews.com)

“This has been a nightmare,” Brandy McFadden told WSMV-TV’s News 4 Program in Nashville as she fought tears. “I got my shot, just trying to do due diligence. I never expected this to happen, at all.”

The day Brandy McFadden got her second dose of the Pfizer/BioNTech vaccine on April 16, she “just started not feeling great,” she told the local news station.

By the following afternoon, McFadden said she couldn’t walk and had excruciating neck pain. “It just started progressively getting worse and I just started screaming in pain at the top of my lungs.”

McFadden’s husband took her to the emergency room at Vanderbilt University Medical Center. Six days later, the local news stations interviewed her at the hospital where she had undergone a CT scan, MRI, EMG, and blood work, all of which were unrevealing about what was happening to her. “As far as to answers as to why this happened, they don’t know,” McFadden told News4.

She had regained movement in her arms and could wiggle her toes one week following her shot.

A similar case in Pittsburgh

McFadden was in touch with a woman in Pittsburgh who had a similar experience. Rachel Cecere, 33, told WPXI-TV news that she woke up paralyzed from the neck down 12 hours after her first dose of Pfizer’s COVID-19 vaccine.  “It was the scariest thing in the world to go to sleep completely fine, to wake up 1:30 in the morning and not be able to move at all,” the woman told Channel 11.

Cecere was moved from her local hospital to the Cleveland Clinic where tests ruled out Guillain Barré Syndrome, a neurological disease linked to the pandemic 1976 swine flu vaccine, which caused about 450 people to be paralyzed.

“There is just nothing they can find wrong with me. No underlying conditions, I have nothing in my history and they are basically telling me, ‘You’re healthy and we can’t figure out why this is going on,’” the woman told her local news channel.

Nearly three weeks after Cecere was hospitalized she told WPXI that she is doing occupational and physical therapy at Jefferson Hospital but still had no feeling in either leg and can only move the left one. She was given a prosthetic brace and knee support to keep her leg straight. The single mother had regained strength in her upper body, she told the news station, but still felt weakness in her left hand and was unable to lift her daughter.

“It’s discouraging not having the feeling or sensation in my legs. It’s just difficult for me to grasp and understand,” Cecere said.

“I was told multiple times that the diagnosis was an acute distress to the nervous system brought on by the COVID-19 vaccine Pfizer,” Cecere told Channel 11, but her discharge papers did not mention her COVID-19 vaccine.

“It doesn’t sound like they are willing to attribute it to the vaccine or any specific medical diagnosis,” local infectious disease doctor Dave Weber told the news channel.

Reports of paralysis 

However, the Centers for Disease Control and Preventions Vaccine Adverse Event Reporting System (VAERS) has received 1,619 reports of events following COVID-19 vaccination that include paralysis or paralyzing conditions such as Guillain Barré Syndrome, transverse myelitis, acute disseminated encephalomyelitis, and Bell’s Palsy, a condition that causes face muscles to paralyze, marked frequently by a drooping mouth and inability to close one eye. Of those reports, 794 relate to Pfizer’s COVID vaccine, including 131 reports of paralysis among patients aged 30-39 years old as of April 30. The CDC stresses that VAERS reports do not establish a causal link between a vaccine and an adverse event.

Just as public health agencies say that vaccines cannot be counted on to provide full protection within two weeks of shots because the immune system has not fully responded, immune system adverse events can take time to build as the body produces antibodies.

Among the dozens of reports among those aged 18 to 29 was a physician report of a 21-year-old in Michigan who received a first dose of Moderna’s vaccine in March and subsequently began experiencing “ascending paralysis” nine days later.

The young man’s condition “rapidly escalated requiring intubation and mechanical ventilation” according to the VAERS report. He was treated for Guillain-Barré Syndrome, the report stated, and had “flaccid paralysis and lost his ability to protect his airway.” The report stated that he would likely need a tracheostomy – a surgical opening in the neck to allow air to enter the lungs via a tube.

Another physician report to VAERS described a 26-year-old who received her first dose of Pfizer’s vaccine in March and three days later began feeling numbness in her toes that spread to her legs. Five days later she noticed numbness in her fingers and her mouth and weakness in her arms. A few days after that, she noticed that her face was dropping on the right side and she went to the emergency departments where a lumbar puncture (spinal tap) test indicated Guillain-Barré Syndrome and she was started on IV immune globulin treatment.

McFadden had already been infected with the coronavirus, something Pennsylvania immunologist Hooman Noorchashm has warned about as a potential for catastrophic immune events following vaccination. He has advised people to defer vaccination if they have previously been infected or tested positive for the coronavirus.

Read more at: LifeSiteNews.com

__________________________________________________________

SEE: https://www.naturalnews.com/2021-05-16-fda-inspectors-document-horrific-conditions-jj-covid19-vaccine-plant.html;

republished below in full unedited for informational, educational & research purposes:

(Natural News) Over 15 million doses of Covid-19 vaccines were halted and trashed after FDA inspectors found ingredients from other vaccines in the Johnson & Johnson jabs, and discovered ‘brown residue’ all over the floors and walls, and open bags of medical waste being dragged around the facility. Talk about dirty vaccines, this is beyond all comprehension. This sounds like some (fast food) chicken processing plant, where the animals wallow in their own feces, infected with pathogens and then end up in everybody’s mouths, except in this case it’s dirty vaccines that end up killing people. No wonder some vaccines list E. coli and urea as “ingredients.”

So much for ‘safety and efficacy’ — vaccine ‘science’ is now just dirty and dangerous

This Baltimore factory for J&J Covid-19 vaccine manufacturing was documented by FDA inspectors as being in total disregard for procedures set in place for safety and efficacy. Too bad all these mask-loving Americans can’t watch the video footage of their beloved vaccine scientists and doctors dragging around open bags of medical waste right where they’re concocting the inoculations. Talk about germ paranoia.

FDA inspectors also noted peeling paint, inadequate cleaning, and employees contaminating areas by not following procedures. So far, nothing created at this septic plant has been injected into sheeple arms, yet (doesn’t mean they won’t sell those dirty vaccines to another country). No worries here though, because the eight million doses of the J&J vaccine given to Americans came from Europe, though there’s no telling how many open bags of biomedical waste they’re dragging around in their vaccine dungeons, with feces spread all over the floors and walls.

Somehow, Johnson & Johnson’s lab ‘managers’ even managed to cross-contaminate their own shot’s ingredients with those of AstraZeneca’s toxic jab. Now how on earth could that have happened? Why are they even in the same place? Are they just working on them both side by side, with open beakers and overflowed toilets everywhere?

Is any of the inspection information redacted or undisclosed, because for the FDA to even release this, and for mass media (yes, this came from CBS news themselves) to publish is beyond fathomable.

Dirty labs, dirty vaccines and dirty politics

It’s all dirty, the whole American medical establishment. The FDA is dirty. The CDC is dirty. The vaccine manufacturers – dirty. Now they’re all playing the dirty game of trying to con all of the pro-science, pro-natural health enthusiasts into getting the jabs. They’re using propaganda and coercion tactics (think vaccine passports) to force us to inject dirty vaccines into our blood and tissue. Vaccines that are dirty with pathogens. Vaccines that are dirty with mRNA that create protein ‘prions’ that cause blood clots and dementia.

Welcome to the New World Order, again. They want your health and your money. They want your land and your guns. They want your human rights obliterated. They want you diseased and dying. That’s communism.

This has been going on for half a century in the USA. Even the polio vaccine was dirty. The inventor had no idea what he was doing, just incubating different combinations of polio strains in monkey tissue. It’s all been a con game since the outset, and the wool has definitely been pulled over the Sheeple’s eyes. The mRNA vaccine is the dirtiest of them all because it controls your immune system function and can shut it down with the flip of a switch (the second and third round of Covid jabs).

Tune your internet frequency to ChemicalViolence.com for updates on how vaccines ARE the pandemic.

__________________________________________________

SEE ALSO: https://www.naturalnews.com/2021-05-16-nih-established-loophole-exploiting-moratorium-gain-of-function-coronavirus-research.html

Rumble — More conservatives are joining Sen. Rand Paul in questioning Dr. Anthony Fauci’s credibility. One America’s John Hines caught up with Sen. Roger Marshall from Kansas and has more from Capitol Hill.

 

Sickening E-mails Surface: FDA, NIH Buying Aborted Human Fetal Parts for Experiments

BY ANNALISA PESEK

SEE: https://thenewamerican.com/sickening-e-mails-surface-fda-nih-buying-aborted-human-fetal-parts-for-experiments/;

republished below in full unedited for informational, educational & research purposes:

It was just a matter of time — though it took nearly 100 years — before Planned Parenthood would cancel its own founder, the suddenly “problematic” Margaret Sanger (1879–1966).

In an April 17 New York Times op-ed, Planned Parenthood President and CEO Alexis McGill Johnson admitted that “Up until now, Planned Parenthood has failed to own the impact of our founder’s actions. We have defended Sanger as a protector of bodily autonomy and self-determination while excusing her association with white supremacist groups and eugenics as an unfortunate ‘product of her time.’”

Sanger’s vision for limiting America’s black population through the championing of birth control and “healthcare services” is seamlessly outlined in her 1939 initiative “The Negro Project.” Sanger herself wrote about speaking at a Ku Klux Klan meeting in her autobiography and publicly supported the 1927 Supreme Court ruling Buck v. Bell, permitting the sterilization of “unfit” people without their consent. But Johnson is careful not to rush to judgment: “Whether our founder was a racist is not a simple yes or no question. Our reckoning is understanding her full legacy and its impact. Our reckoning is the work that comes next.”

But while the organization conducts its “woke” investigation, and this trivia makes the national news, the nefarious evils of America’s largest abortion provider remain buried.

Planned Parenthood faces ongoing investigations by U.S. House and Senate committees into their involvement in human fetal tissue trafficking — a federal felony — and illegal profiting from transfers of organs harvested from aborted human fetuses, yet, it’s clear abortion alone does not satisfy the agency. So it’s not surprising they would have come up with other ways to turn a profit.   

A harrowing report from Judicial Watch, published April 1, reveals that the U.S. Food and Drug Administration (FDA) has paid tens of thousands of taxpayer dollars to obtain human fetal tissue from the California-based “procurement” firm Advanced Bioscience Resources (ABR), undoubtedly supplied by abortion providers such as Planned Parenthood.

According to the report, the fetal tissue was used in a sort of Frankenstein project to create “humanized mice” to test “biologic drug products.” To this day, research continues unimpeded on these lifeless, preborn babies, as no one can provide consent for medical experimentation on an aborted fetus — certainly, the mother would not object, as she is not concerned about what happens to her aborted child.

Now the pro-abortion side would say that fetal experimentation is a complete myth concocted by “anti-choice” activists stirring the pot over a “trivialized harm.” Yet records of tissue purchases between ABR and government agencies prove the reality is far from being all in our minds.

Judicial Watch has acquired communications from January 2011 to April 2018 between ABR procurement manager Perrin Larton and FDA research veterinary medical official Dr. Kristina Howard, confirming the purchase of organs from aborted human fetuses.

In an e-mail dated September 27, 2012, Howard submitted an application to Larton for “tissue purchases” in the amount of $12,000. The contract reportedly requested tissue from an aborted fetus with a gestational age of 16 to 24 weeks and “One set of tissue (thymus/liver) approx. twice monthly.”

Instructions stated that the tissues were to be shipped “fresh; on wet ice.”

Judicial Watch President Tom Fitton, whose watchdog group has released two previous sets of records exposing unlawful transactions between ABR and the FDA, had these remarks on the findings:

These fetal organ trafficking documents shock the conscience and show potentially illegal use of tax dollars to purchase organs of the unborn killed through abortion.

According to 42 U.S. Code § 289g–2 — prohibitions regarding human fetal tissue, the purchase of human fetal tissue is “unlawful for any person who knowingly acquires, receives, or otherwise transfers any human fetal tissue for valuable consideration if the transfer affects interstate commerce.”

In March 2019, Judicial Watch moved forward with a Freedom of Information Act (FOIA) lawsuit against Health and Human Services (HHS), of which the FDA is a part (Judicial Watch v. U.S. Department Health and Human Services (No. 1:19-cv-00876). Additional records secured by the group demonstrate the National Institutes of Health (NIH) purchased aborted fetal parts for HIV research, paying “at least $18,100 between December 2016 and August 2018 to ABR for livers and thymuses from second-trimester aborted fetuses.”

Judicial Watch reported that “ABR has been the subject of criminal referrals from House and Senate committees investigating whether Planned Parenthood or any other entity was illegally profiting from the handling of fetal tissue from aborted babies.”

However, in March 2018, government agency officials determined that purchasing human fetal tissue for research purposes was not protected by federal regulations.

An “overview” supplied by ABR describes the firm as a “non-profit corporate foundation … devoted to providing services in connection with the procurement of human organs and tissues for medical and scientific research.”

Yet such a statement is deceptive, as ABR is most certainly capitalizing on abortions performed every few seconds in this country. Meanwhile, Planned Parenthood rakes in triple the amount of money from one abortion, selling livers, brains, eyes, hearts — really whatever organs they can salvage. And now it’s up to the courts, and so far many judges have been complicit in continuing this evil, though they hold the power to stop it.

AAPS: FDA DELAYS ON HYDROXYCHLOROQUINE OUTPATIENT APPROVAL ARE CAUSING DEATHS DAILY

SEE: https://www.technocracy.news/aaps-fda-delays-on-hcq-outpatient-approval-are-causing-deaths-daily/;

republished below in full unedited for informational, educational & research purposes:
The venerable Association of American Physicians and Surgeons is calling on the FDA to immediately release HCQ for outpatient treatment to save thousands of needless deaths from COVID-19. The FDA’s blatant hypocrisy in failing to do sos should outrage all Americans. ⁃ TN Editor

20,000 more Americans have died while the FDA has delayed since July 1 a new emergency use approval for outpatient use of hydroxychloroquine (HCQ) for COVID-19.

On July, 1 Henry Ford Hospital physicians and researchers in Detroit filed an urgent request to FDA Commissioner Dr. Stephen Hahn for a new outpatient Emergency Use Authorization (EUA) for FDA approval of HCQ to be used in early treatment for COVID-19. Baylor Scott & White Heart and Vascular Institute in Dallas, issued an urgent appeal supporting the Henry Ford EUA application, based on their clinical study of prophylactic use of HCQ in their own medical workers. Baylor cardiologists emphasized there were no adverse cardiac outcomes in their own or the Ford study.

Henry Ford’s new clinical trial found an impressive 51% reduction in deaths if HCQ was begun within 24 hours of admission to hospital. An outpatient primary care study by Dr. Vladimir Zelenko, using HCQ, azithromycin and zinc given within less than 7 days of COVID-19 symptoms, showed approximately 80% decrease in deaths, and less than 1% of his patients needed to be admitted to hospital. These U.S. early intervention studies extraordinary results show how many lives can be saved with early HCQ treatment.

If the FDA had acted quickly on the Henry Ford and Baylor approval request for HCQ, we can reasonably consider that 16,000 lives could have been saved since July 1.

EUA applications do not have to take long to approve, when well documented rationale and supporting research is presented as Henry Ford team and Baylor cardiologists did.

HCQ is already an FDA-approved drug, unlike remdesivir, which had almost an immediate compassionate use authorization granted that has now been expanded for early use despite severe side effects. The former director of the FDA subagency BARDA, Rick Bright, Ph.D., submitted an EUA for HCQ approval for hospital use at 11:30 pm on March 28, 2020. Dr. Hahn’s approval was granted a little after midnight, March 29, 2020. Approval in about 30 minutes.

We have been waiting almost 30 days for Dr. Hahn to issue approval of the Henry Ford EUA application for outpatient use. Dr. Hahn has stated that we need more data. Henry Ford and Baylor doctors have already provided research documentation stronger than in Rick Bright’s March application, and included current COVID-19 studies from the U.S. and other countries.What amount of “data” will ever satisfy Dr. Hahn?

Let THIS sink in: Laboratory studies published by the National Institutes of Health 15 years ago (2005) showed potent antiviral effects of chloroquine against SARS-CoV-1 to block the infection at the earliest stage. Anthony Fauci, who was working at NIH at that time, has to have known for the last 15-18 years that chloroquine and hydroxychloroquine are effective against SARS-Co-V-1, which shares 79% of the viral genome with SARS-CoV-2, the cause of COVID-19 disease.

It is appalling that so many more Americans have died, while the physician who is head of the FDA has dawdled on approving HCQ for an urgent new use in this pandemic. Dr. Hahn knows full well the 65-year track record of safety worldwide in patients of all ages, all ethnic groups, and even pregnant women and nursing mothers.

Doctors who are treating COVID-19 patients see lives being saved by cheap, safe, FDA-approved medicines—hydroxychloroquine, azithromycin, doxycycline.

It is crucial to start HCQ early, during days 1-7 of symptoms, for these key reasons:

  • Early treatment is when HCQ works best two ways: to stop viral entry into our cells, and block the virus from multiplying using the cell’s machinery.
  • The viral load explodes by day 6, and then can trigger an exaggerated inflammatory response called Cytokine Storm, which severely damages critical organs: lungs, kidneys, heart, brain, liver and intestines. This severe complication doesn’t occur in all COVID-19 patients, but often is fatal when it does.
  • Early treatment keeps infected people from spreading the virus to others.
  • Early treatment is crucial to keep people out of hospitals and off ventilators.
  • Availability of early treatment is urgently needed to safely re-open businesses, schools, and churches, and help relieve public anxiety and fear.

Front-line doctors have been pleading with the FDA and State officials since March to open access to early treatment with HCQ. The supply of HCQ has been ramped up to handle its use in early treatment of COVID. The Strategic National Stockpile has millions of doses deteriorating in government warehouses that are not being distributed because doctors are prevented from prescribing for outpatients with COVID-19. FDA’s misleading statements about HCQ have led to dangerous, unprecedented restrictions on physicians’ off-label prescribing rights imposed by state governors, medical boards and pharmacy boards.

Generic HCQ with azithromycin or doxycycline plus zinc is taken by mouth.Total treatment cost is about $25-$30 cash price for the 5-7 day course used in COVID-19.

Remdesivir must be given intravenously to patients in hospital, at a cost of about $3,500. Its serious side effects include respiratory failure, the very condition it is supposed to treat. It has shown limited success: it shortened hospital stays by only 4 days and has not been clearly shown to reduce deaths.

Baylor’s study showing prophylactic benefits for hospital workers is profoundly important, not only for front-line medical workers, but also for law enforcement officers, paramedics, clergy, dentists/dental hygienists, truck drivers, food-processing workers, teachers, behavioral health professionals, factory and grocery store workers, flight attendants, and many others.

HCQ is a safe, effective outpatient treatment we have NOW. Physicians and patients need freedom to use it. Delays waiting for the “magic bullet” of a vaccine inevitably mean more deaths. Even IF we have a vaccine that works, we still need therapeutics, such as HCQ.

Testing is inaccurate and often unavailable, and HCQ dispensing must not be limited to persons with a positive test. Such limits also prevent prophylactic use. Governors and other officials must not be allowed to arbitrarily restrict life-saving HCQ treatment.

Continued shutdowns of businesses, schools, churches, and mandatory mask edicts are not controlling the epidemic. Meanwhile, these orders have eroded our constitutional freedoms, and devastated our economic, psychological, physical, and spiritual well-being.

Dr. Hahn’s FDA is costing more lives with its delay in removing the obstructions it created to prescribing safe, effective early HCQ treatment: deaths directly from COVID-19 and indirectly by destroying livelihoods and distributions of foods, goods and services required to sustain our lives.

Dr. Hahn, America needs you to act NOW.

Read full story here…

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The Great Technocrat War Against Hydroxychloroquine

BY:  STEVEN HATFIL VIA REALCLEARPOLITICS

SEE: https://www.technocracy.news/the-great-technocrat-war-against-hydroxychloroquine/;

republished below in full unedited for informational, educational & research purposes:
It is Technocrats like Anthony Fauci who originally fomented the war against HCQ and they blocked its use at every turn. All testimony by MDs and scientists supporting HCQ is summarily ridiculed and dismissed.Tens of thousands of people have needlessly died because of these mean-spirited policies by Big Pharma to protect the deployment of their expensive drugs and vaccines. ⁃ TN Editor

On Friday, July 31, in a column ostensibly dealing with health care “misinformation,” Washington Post media critic Margaret Sullivan opened by lambasting “fringe doctors spouting dangerous falsehoods about hydroxychloroquine as a COVID-19 wonder cure.”

Actually, it was Sullivan who was spouting dangerous falsehoods about this drug, something the Washington Post and much of the rest of the media have been doing for months. On May 15, the Post offered a stark warning to any Americans who may have taken hope in a possible therapy for COVID-19. In the newspaper’s telling, there was nothing unambiguous about the science — or the politics — of hydroxychloroquine: “Drug promoted by Trump as coronavirus game-changer increasingly linked to deaths,” blared the headline. Written by three Post staff writers, the story asserted that the effectiveness of hydroxychloroquine in treating COVID-19 is scant and that the drug is inherently unsafe. This claim is nonsense.

Biased against the use of hydroxychloroquine for COVID-19 — and the Washington Post is hardly alone — the paper described an April 21, 2020, drug study on U.S. Veterans Affairs patients hospitalized with the illness. It found a high death rate in patients taking the drug hydroxychloroquine. But this was a flawed study with a small sample, the main flaw being that the drug was given to the sickest patients who were already dying because of their age and severe pre-existing conditions. This study was quickly debunked. It had been posted on a non-peer-reviewed medical archive that specifically warns that studies posted on its website should not be reported in the media as established information.

Yet, the Post and countless other news outlets did just the opposite, making repeated claims that hydroxychloroquine was ineffective and caused serious cardiac problems. Nowhere was there any mention of the fact that COVID-19 damages the heart during infection, sometimes causing irregular and sometimes fatal heart rhythms in patients not taking the drug.

To a media unrelentingly hostile to Donald Trump, this meant that the president could be portrayed as recklessly promoting the use of a “dangerous” drug. Ignoring the refutation of the VA study in its May 15 article, the Washington Post cited a Brazil study published on April 24 in which a COVID trial using chloroquine (a related but different drug than hydroxychloroquine) was stopped because 11 patients treated with it died. The reporters never mentioned another problem with that study: The Brazilian doctors were giving their patients lethal cumulative doses of the drug.

On and on it has gone since then, in a circle of self-reinforcing commentary. Following the news that Trump was taking the drug himself, opinion hosts on cable news channels launched continual attacks on both hydroxychloroquine and the president. “This will kill you!” Fox News Channel’s Neil Cavuto exclaimed. “The president of the United States just acknowledge that he is taking hydroxychloroquine, a drug that [was] meant really to treat malaria and lupus.”

Washington Post reporters Ariana Cha and Laurie McGinley were back again on May 22, with a new article shouting out the new supposed news: “Antimalarial drug touted by President Trump is linked to increased risk of death in coronavirus patients, study says.” The media uproar this time was based on a large study just published in the Lancet. There was just one problem. The Lancet paper was fraudulent and it was quickly retracted.

However, the damage from the biased media storm was done and it was long-lasting. Continuing patient enrollment needed for early-use clinical trials of hydroxychloroquine dried up within a week. Patients were afraid to take the drug, doctors became afraid to prescribe it, pharmacies refused to fill prescriptions, and in a rush of incompetent analysis and non-existent senior leadership, the FDA revoked its Emergency Use Authorization for the drug.

Read full story here…

 
 

DR. JOHN BERGMAN: SURVIVING IN A TIME OF CRISIS

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THE WAR ON HYDROXYCHLOROQUINE

BY DENNIS BEHREANDT

SEE: https://www.thenewamerican.com/print-magazine/item/36249-the-war-on-hydroxychloroquine;

republished below in full unedited for informational, educational & research purposes:

As strange as it may sound, a propaganda and demonization campaign is being waged against hydroxychloroquine so that globalism and U.S. socialism can make headway.

President Donald Trump several times has lauded the drug hydroxychloroquine (HCQ) as a potential cure for COVID-19, even saying that he was taking it himself to ward off the disease, and he ordered his administration to make it readily available. Recently, however, the U.S. Food and Drug Administration revoked its Emergency Use Authorization (EUA) for using hydroxychloroquine to fight COVID-19, saying, in essence, it doesn’t seem to treat COVID-19 and is dangerous. Doctors, though, can still prescribe it for off-label use.

Yet researchers writing a review of COVID-19 treatments for the Journal of the American Medical Association (JAMA) summarized the safety of chloroquine (CQ) treatment for COVID-19: “Chloroquine and hydroxychloroquine are relatively well tolerated as demonstrated by extensive experience in patients with SLE and malaria,” the researchers wrote, noting that in some cases there have been “rare and serious adverse effects.” Still, of the safety of the drugs in the context of COVID-19, they wrote: “No significant adverse effects have been reported for chloroquine at the doses and durations proposed for COVID-19. Use of chloroquine and hydroxychloroquine in pregnancy is generally considered safe. A review of 12 studies including 588 patients receiving chloroquine or hydroxychloroquine during pregnancy found no overt infant ocular toxicity.”

As well, peer-reviewed studies and anecdotal evidence show that the drug works to treat COVID-19.

So what is happening here? The answer: There is a war going on for your mind.

Prior to the election of Donald Trump, the war was somewhat hidden. Though a subset of Americans had noticed the gradual increase in statist, internationalist, and socialist propaganda over the years, most Americans remained unaware of the trend. The election of Donald Trump, however, was a wake-up call, and the statists, or “deep statists” if you will, began a concerted campaign to remove the president from office. Still, nasty as this was, for most Americans this was just political theater. 

The war broke furiously into the open with COVID-19, though, and has accelerated, and grown more vicious still, with the wave of violent terrorist riots that have struck the nation’s cities. With COVID-19, the nation’s petty tyrants in state government took the opportunity presented by the crisis to revoke the rights and freedoms of the American people and impose mass house arrest. The next phase of the war immediately followed in the form of the terrorist riots that have resulted in widespread property destruction and the sowing of intense fear among the law-abiding, who are increasingly left to their own devices in defending themselves against the tide of violence. In total, the entire campaign is aimed at forcibly limiting what Americans do, say, and even think — trying to make social controls “the new norm.”

As an integral part of this “new norm,” the elitists who desire total power have devised another strategem: institute a vaccine program — ostensibly to safeguard us against coronavirus — that will allow elites to track us at all times and control the lives and activities of people around the world. The scheme has been heavily promoted by Bill Gates and the controlled international menagerie of NGOs and world government bodies. (See the article “Bill Gates: Philanthropist or Scoundrel?”)

Anything that gets in the way of this effort is demonized by the leftist mainstream media. Case in point: Trump’s promotion of hydroxychloroquine to fight COVID-19. Why? Because if a simple and effective treatment for the pandemic disease exists and is readily available, the overarching need for a vaccine is diminished or eliminated.

Within this framework, the motivation behind the media and Democratic politicians’ unceasing attacks on hydroxychloroquine becomes understandable. Though the science is not yet settled and important studies are ongoing, some research and plenty of clinical anecdotal evidence continue to point to the drug as a useful treatment for COVID-19. If it is, then the need for a vaccine forced on the world’s population is diminished or even eliminated, and with that, the plan to track everyone via a digital vaccine ID has had a stake firmly planted in its heart.

Thus, we have an all-out campaign of demonization waged against the drug, convincing Americans to abandon hope of a non-vaccine treatment.

A Chorus of Lies and Calumnies

The Washington Post, one of the key organs of the statist propaganda machine, exemplifies the “coverage” given to HCQ by mainstream-media organs.

In a “Fact Checker” analysis, the paper first quoted President Trump, who said on March 19 about the drug that “it’s looking like it’s having some good results. That would be a phenomenal thing.” Then the newspaper criticized one of the French studies that had found potential value in HCQ. It said about the study by Didier Raoult, et al.: “Scientists have since discredited the trial, pointing to major flaws in the way it was conducted. The journal that published the study announced on April 3 that it did not meet its standards.”

The study was not retracted, and the journal in question did not call the paper’s findings into question; it merely cast aspersions on portions of how the study was conducted with regard to study participants. The study, the journal’s board said, did not meet the “expected standard, especially relating to the lack of better explanations of the inclusion criteria and the triage of patients to ensure patient safety.” Again, this was not a criticism of the results reported. Moreover, the journal said its peer-review process was followed. “Despite some suggestions online as to the reliability of the article’s peer review process, the process did adhere to the industry’s peer review rules,” the statement said.

But from the Post’s coverage, readers will get the impression that the entire study was dubious.

The online Daily Beast published a hit piece on Dr. Raoult calling him a “B.S. Artist,” along with attempting to shame him as a “climate denier” and a “coronavirus truther.” The Daily Beast even criticized him for having long hair and a beard, saying it made him look like “a latter day Wild Bill Hickok, albeit in a medical researcher’s white coat.” And he has bad taste too, they claimed: “He wears a biker ring and adorns the walls of his office with schlock paintings of, among others, an imposing Poseidon, god of the seas.”

According to the statists, you shouldn’t believe anything this man says because he is obviously a crackpot. Except this “crackpot” has many other scientific collaborators — he has 17 co-authors joining him on the paper criticized by the Post. This “B.S. Artist,” by the way, has authored or co-authored more than 3,000 peer-reviewed papers during his scientific career. He has collaborated on these with more than 6,000 other scientists, and his peer-reviewed papers have been cited more than 110,000 times by other scientists.

FDA Follies

Perhaps being persuaded by President Trump, or perhaps having actually taken the early results from hydroxychloroquine seriously, in March the Food and Drug Administration authorized emergency use of hydroxychloroquine to make it more available for study and use in the early days of the pandemic’s spread in the United States. The authorization made it possible for large donations of chloroquine and hydroxychloroquine from the companies Bayer and Novartis, respectively, “to be distributed and prescribed by doctors to hospitalized teen and adult patients with COVID-19, as appropriate.”

This earned positive commentary from Health and Human Services Secretary Alex Azar at the time. “President Trump is taking every possible step to protect Americans from the coronavirus and provide them with hope,” Secretary Azar said, according to an agency press release.

Since then, in the wake of ongoing demonization of the drugs, the FDA backtracked and revoked its EUA.

In a letter discussing the revocation of the EUA for the drugs, FDA chief scientist Denise Hinton said the agency no longer found the drugs likely to be effective in treating COVID-19. “We now believe that the suggested dosing regimens for CQ and HCQ as detailed in the Fact Sheets are unlikely to produce an antiviral effect,” Hinton said in the letter. “Earlier observations of decreased viral shedding with HCQ or CQ treatment have not been consistently replicated and recent data from a randomized controlled trial assessing probability of negative conversion showed no difference between HCQ and standard of care alone,” she continued.

The agency concluded, Hinton wrote, that “it is no longer reasonable to believe that oral formulations of HCQ and CQ may be effective in treating COVID-19, nor is it reasonable to believe that the known and potential benefits of these products outweigh their known and potential risks.”

Treatment Strategy Ignored

The claim that hydroxychloroquine use to fight COVID-19 infection lacks merit is a dubious assertion. Notably missing from the FDA’s statement pulling its Emergency Use Authorization is the fact that successful treatment protocols using the drug for COVID-19 have relied on hydroxychloroquine being part of a multi-drug treatment provided early in the course of a SARS-CoV-2 infection, not used alone and given in late stages of the disease.

One doctor who says he has had significant success with a combination treatment that includes hydroxychloroquine is Dr. Vladimir Zelenko.

Practicing in a community on the outskirts of New York City, the epicenter of the pandemic outbreak in the United States, Dr. Zelenko gained fame for his work in treating COVID-19 patients with a three-drug treatment consisting of hydroxychloroquine, azithromycin, and zinc. Heavily promoted early on by Trump, but panned by the mainstream media and politicized almost to extinction in the United States, the treatment as administered by Dr. Zelenko seems to have had noteworthy success.

In an interview with The New American’s Christian Gomez, Dr. Zelenko described how he decided on the course of treatment, as well as why and how he believes it has proven effective in saving lives. “I started studying the basic science of how this virus works,” Dr. Zelenko said in the video interview made available on YouTube.

“So it turns out that zinc, it’s well-known that it inhibits viral replication and specifically in the cytoplasm, in the inside of the cell there is an enzyme … and it’s used by the virus to make copies of its genetic material so that it makes more virus,” Zelenko said. “So this enzyme is essential to viral growth. Turns out that zinc inhibits that enzyme, it deactivates the enzyme and so it makes it very difficult if not impossible for the virus to grow. The problem that we have with zinc is that it doesn’t get into the cell…. So even though zinc is effective against the viral growth, it cannot get into the place where the virus is. So what does hydroxychloroquine do? In this case, it’s nothing more than opening a door, a channel, a zinc transport channel, it’s called a zinc ionophore, and it allows for zinc to go from outside the cell to the cytoplasm, to inside the cell. That’s all it does.”

Initially because of his claims of success in treating COVID-19, Zelenko was increasingly targeted by anti-Trump partisans eager to smear anyone who seemed to be providing evidence that supported the president’s contention that hydroxychloroquine might be useful in treating the disease.

Still, Dr. Zelenko pressed onward, seemingly eager to participate in a study that would clarify the usefulness of his course of treatment. Word of Zelenko’s work reached FDA commissioner Dr. Stephen Hahn, formerly the chief medical executive at the University of Texas MD Anderson Cancer Center, who reached out to Dr. Zelenko to offer insights into how to support the study.

This seems a completely innocent and understandable thing to do in the midst of a pandemic. Why wouldn’t a medical doctor and high-ranking federal official inquire into helping another medical doctor set up a study to investigate what seems a promising treatment? Failure to do so, if the opportunity existed, would seem a cold-hearted dereliction of duty. But the mainstream media, eager to create a controversy where none exists in order to harm Trump, presented the situation as a “gotcha, caught you red-handed” moment.

In a breathless report positioned as one intended to reveal a new administration “scandal,” Vanity Fair reported that it had obtained a series of text messages between Zelenko and Hahn. How scandalous!

Here’s what Vanity Fair said it had uncovered:

Two days after that first phone call, in a series of text messages obtained by Vanity Fair, Zelenko returned to Hahn for help setting up a clinical trial of some 750 outpatients at St. Francis Hospital in Roslyn, New York. “The Catholic Health System (St. Francis Hospital) / Dr Zelenko COVID-19 trial is ready to go,” Zelenko wrote to Hahn, copying one of the hospital’s doctors involved in the trial. “We need ASAP 1. Hydroxychloroquine 200mg. 10000 pills 2. Azithromycin 500mg 5000 pills 3. Zinc sulfate 220 mg 5000 pills. This treatment will be deployed in outpatient primary care.”

Hahn responded, “Not sure what the ask of FDA is.” To which Zelenko replied, “We need the medication to run the study.” Hahn then asked, “Do you have IRB approval?” This referred to an institutional review board that hospitals use to oversee clinical trials and research. The doctor answered, “Hopefully this week.”

“Congratulations,” Hahn offered. “Really well done.” He then advised the doctor to reach out to the Federal Emergency Management Agency (FEMA) to obtain hydroxychloroquine from the Strategic National Stockpile, a federal cache of emergency equipment and supplies managed by the Department of Health and Human Services (HHS). When the doctor expressed uncertainty over how to do that, Hahn offered, “I’ll send you the contact.”

That’s some smoking gun, right there. If anything it proves that there is at least one federal official who is willing to try to help people solve problems.

Subsequently, the left-wing establishment attacked the doctor. Yet, despite the bombast of Vanity Fair and the mainstream media in general, the study exists and is legitimate. Details about the study, entitled “Hydroxychloroquine and Zinc With Either Azithromycin or Doxycycline for Treatment of COVID-19 in Outpatient Setting,” are available at ClinicalTrials.gov. 

The study is currently recruiting participants with a goal of enrolling 750 for the research. The study is expected to be completed by December 31.

The study is being led by Dr. Avni Thakore, a cardiologist, who said, according to WLNY, the CBS affiliate in New York, “What we know about the mechanism of action of the drugs suggests they could be helpful early in the course of a viral infection.” “We know zinc is an anti-viral. We know that hydroxychloroquine can help reduce an immune response that can get out of control.”

While we have to wait until the end of the year, at the earliest, to find out the results of this trial, a similar study has already reported results.

The study, conducted by researchers affiliated with the New York University School of Medicine and New York University Langone Health, has found that the combination of zinc with hydroxychloroquine may, in fact, prevent COVID-19 from progressing to serious illness. The researchers noted:

The main finding of this study is that after adjusting for the timing of zinc therapy, we found that the addition of zinc sulfate to hydroxychloroquine and azithromycin was found to associate with a decrease in mortality or transition to hospice among patients who did not require ICU level of care.

A Real Bogus Study

Promising findings such as this one and others are ignored by the mainstream media, but negative studies get loads of publicity. Their over-the-top propaganda campaign to discredit hydroxychloroquine reached a fever pitch with the publication in the prestigious medical journal The Lancet of a study that called the drug ineffective and unsafe.

The study, entitled “Hydroxychloroquine or chloroquine with or without a macrolide for treatment of COVID-19: a multinational registry analysis,” was led by Dr. Mandeep R. Mehra, a cardiologist and medical director of the Brigham and Women’s Hospital Heart and Vascular Center in Boston. 

Using data sourced from a small company called Surgisphere, the study’s authors, which also included Sapan Desai, the founder of Surgisphere, reached an alarming conclusion: “We were unable to confirm a benefit of hydroxychloroquine or chloroquine, when used alone or with a macrolide, on in-hospital outcomes for COVID-19.” “Each of these drug regimens was associated with decreased in-hospital survival and an increased frequency of ventricular arrhythmias when used for treatment of COVID-19.”

The statist mainstream media latched onto this finding with all due haste and breathlessly reported its conclusions in most, if not all, mainstream outlets. The results were touted as the final straw that would end hydroxychloroquine once and for all. This gambit almost worked.

Shocked by the study’s conclusion, researchers conducting or contemplating clinical trials involving hydroxychloroquine began to reevaluate their efforts based on worries that patients included in such studies might be harmed. “The World Health Organization and a number of national governments have changed their Covid-19 policies and treatments on the basis” of the study, The Guardian newspaper reported. One of the studies halted was the COPCOV study, a very large international study from Oxford University in the U.K. That study has now been restarted, and its principal investigators have indicated that they are anxious to further understand the potential of HCQ in prevention and early treatment of COVID-19. (For full coverage of the restart of COPCOV, see TNA online here: www.thenewamerican.com/hcq-study)

But almost immediately after the Lancet study was published, other researchers began to notice disquieting elements in the work. So troubling were the flaws that no less than the left-wing mouthpiece New York Times was forced to report on the situation. “Critics were quick to point out anomalies … including implausible findings that should have been detected during the peer review process — like the … apparent inclusion of a large number of Covid-19 cases very early on in the pandemic, even in Africa, where few hospitals have electronic health records,” the Times reported.

The Times continued: “Many researchers were astonished to find out that such a database could exist, or that the gathering and analysis of tens of thousands of medical records on multiple continents could have been carried out so quickly.”

A key element of science in general and scientific studies in particular is the idea of reproducibility. In scientific writing, it is expected and required that researchers provide sufficient details in a “materials and methods” section or sections of a paper so that other researchers can reproduce the described experiment. Such reproduction allows other researchers to evaluate the methods and data described while allowing them to derive the conclusions — or not — for themselves. This is the central feedback loop in scientific publishing that prevents fraud and ensures accuracy of results.

This was a central failing of the studies (there were two in total) that were based on the Surgisphere data. After such concerns were raised, the authors of the paper who were not affiliated with Surgisphere arranged for an independent review of the data. That review could not be completed because Surgisphere “would not transfer the full dataset, client contracts, and the full ISO audit report to their servers for analysis,” a group of the study’s original authors pointed out.

Ultimately, The Lancet was forced to retract the study. Speaking to Tucker Carlson of Fox News, Dr. Marc Siegel said the study was simply political in nature. “Political,” he said, “we know this is a political hit job.”

More Work Remains

It seems fairly clear at this point, despite the controversy, that lives have been saved by the careful use of hydroxychloroquine and that continued investigation of the drug and continued use by physicians treating COVID-19 patients should not be stopped.

One example of a life likely saved is the story of Margaret Novins, 53, who tested positive for COVID-19 in March. “I couldn’t breathe,” she said of her fight with the disease, according to Forbes.

Very quickly her doctors prescribed hydroxychloroquine, and she experienced improvement in her condition in just one day, according to Forbes. She credited the drug, sold under the brand name Plaquenil, with her recovery. “From my notes it is clear that my fevers and horrible chills I fought hard from 3/8-3/18 turned the corner the day I started Plaquenil 3/19,” she said.

Others, including doctors, have said that they, a family member, or someone they know have used and needed hydroxychloroquine during the pandemic. The aforementioned Dr. Siegel is one of these.

Again speaking to Fox News host Tucker Carlson, Siegel shared a personal story. “Tucker, I want to tell you about a 96-year-old man in Florida who said one night, ‘I don’t think I’m going to make it. I feel very weak. The end is coming. I’m coughing, I’m short of breath, I can’t get up from the couch,’” Siegel said. “The next day he was on hydroxychloroquine and antibiotics, per his cardiologist, he got up the next day, he was fine.” That man was Siegel’s father.

Congressman Roger Marshall (R-Kan.), an obstetrician, commenting on President Trump’s use of HCQ, has said that his family, too, has taken hydroxychloroquine. According to Newsweek, Marshall said “that he, his siblings, his parents and his wife are taking the drug ‘prophylactically’” — to ward off the disease.

Even a Michigan Democratic lawmaker, Karen Whitsett (D-Mich.), told Fox host Laura Ingraham that the drug saved her when she was suffering from COVID-19. “I really want to say that you have to give this an opportunity,” she said. “For me, it saved my life.”

One expert who believes hydroxychloroquine should not be taken off the table is Harvey A. Risch, professor of epidemiology at the Yale School of Public Health and Yale School of Medicine. Risch argued in favor of early treatment of COVID-19 with a combination of hydroxychloroquine and azithromycin.

“Five studies, including two controlled clinical trials, have demonstrated significant major outpatient treatment efficacy,” Risch observed in an article for the American Journal of Epidemiology. “Hydroxychloroquine+azithromycin has been used as standard-of-care in more than 300,000 older adults with multicomorbidities, with estimated proportion diagnosed with cardiac arrhythmias attributable to the medications 47/100,000 users, of which estimated mortality is <20%, 9/100,000 users, compared to the 10,000 Americans now dying each week. These medications need to be widely available and promoted immediately for physicians to prescribe.”

Clearly, despite bureaucratic resistance, the potential benefits of hydroxychloroquine seem significant enough to continue additional research, as well as to provide a foundation for doctors working with patients to continue, if they deem necessary, to utilize the drug, either alone or in combination with other drugs and supplements such as zinc.

Attempts by federal and state health agencies, bolstered by mainstream media propaganda, to restrict usage of hydroxychloroquine is, at its base, an effort to supplant individual physician expertise with blanket control of healthcare by government bureaucrats. It stands to reason that effective healthcare is delivered by skilled doctors and other healthcare staff working with patients directly, and that one-size-fits-all, politically motivated dictates from government bureaucrats put patients at significantly increased risk of poor outcomes.

The effort to discredit HCQ continues, but is on shaky ground because propaganda ultimately must fail when it is opposed by the truth.

Indeed, if COVID-19 is to be countered effectively, and lives are to be saved, then, as always, freedom is the cure. Government must get its nose out of the business of science and let researchers and doctors — the actual experts — conduct their life-saving research and work unencumbered by government regulation.

 

ALLERGY RISKS INCREASE AS FDA CHANGES FOOD LABELING REQUIREMENTS DURING COVID-19 PANDEMIC

BY CAROLYN HENDLER, J.D.

SEE: https://thevaccinereaction.org/2020/06/allergy-risks-increase-as-fda-changes-food-labeling-requirements-during-covid-19-pandemic/;

republished below in full unedited for informational, educational & research purposes:
Allergy Risks Increase as FDA Changes Food Labeling  Requirements During COVID-19 Pandemic

Opinion | On May 22, 2020, the U.S. Food and Drug Administration (FDA) issued a public comment providing new guidance that will relax the labeling requirements on packaged food to allow food companies more flexibility during the COVD-19 pandemic. Companies selling food are now allowed to make minor changes to the formulation of food products without being required to change the product label, raising the risks for serious food allergies.

FDA Made Change Without Public Comment

The FDA’s stated goal of changing food labeling requirements is to minimize the effects of food supply chain disruption and meet consumer demand.1 A departure from the standard practice of first taking public comment before issuing new guidance to companies selling products that carry health risks, this guidance by the FDA took effect immediately without public comment.2

The FDA is the oldest U.S. government consumer protection agency.3 The Federal Food, Drug, Cosmetic Act granted the FDA the authority to protect consumers from unsafe products by requiring that most prepared and packaged foods be accurately labeled by the manufacturer.4

The FDA states;

Consumers use the ingredient list to make purchasing decisions and determine whether a food contains an ingredient they want (e.g., whole grains) or ones they do not want (e.g., due to allergies). Without this ingredient information, consumers would not be able make nutrition-based food decisions, as well as avoid ingredients for health or other reasons.5

Protecting Food Company Profits But What About Safety?

However, during the coronavirus pandemic, it appears that the FDA has shifted its responsibility from protecting consumers to helping food companies protect their profits from any lost business stemming from potential disruption of the food supply chain.6

The guidelines provide that manufacturers may substitute a minor ingredient in a recipe without changing the label when the substituted ingredient:

  1. is not known to cause adverse health effects such as food allergens, gluten, sulfites;
  2. is generally less than 2 percent of the product weight;
  3. is not be a major product ingredient;
  4. is not a characterizing ingredient;
  5. does not affect the nutrient content or health claims on the product label; and does not have a significant impact on the finished product.7

A label does not need to be changed, for example, when certain oils that contain a similar type of fat have been substituted in a recipe, such as canola oil for sunflower oil, or when an oil is highly refined and does not pose a risk for an allergic reaction according to the FDA.8 However, many people have allergic reactions to highly refined products derived from one of the top eight allergens such as such as peanut oil or soy lecithin.9

The FDA guidance provides that minor formulation changes may be made as long as the substituted ingredient,

does not cause adverse health effect “(including food allergens, gluten, sulfites, or other foods known to cause sensitivities in some people, for example, glutamates).10

The FDA does not define what ingredients are considered to cause an “adverse health effect.”11 Food allergies are unique in that an individual may react to ingredients the FDA does not consider allergens. According to the Food Allergy Research and Education (FARE) more than 170 foods have been reported to cause allergic reactions.12

Cross Contamination A Safety Issue

The guidance states that food companies must continue to list the top 8 allergens including peanuts, tree nuts, milk, eggs, soy, wheat, fish, and crustacean shellfish on the package ingredient list. However, there is still cause for concern for those allergic to the top eight allergens even when other ingredients are substituted because of cross-contamination.

Take the example of a milk chocolate bar that carries the advisory statement: “Made on equipment that also processes almonds.” If the manufacturer decides to substitute peanut flour for almond flour in another product in the same line, that advisory statement may be rendered incorrect or incomplete.13

Manufacturers are not required to list the substituted ingredients of their food products on labels, or on their website or a central FDA website. The only way to find out if an ingredient was substituted and what it was substituted for is to call the manufacturers for every food product.14

32 Million Americans With Food Allergies

Approximately 32 million American live with a food allergy.15 In 2018, it was estimated that eight percent or one in 13 children and 1 in 10 adults had a food allergy.16 According to the CDC, food allergies increased 50 percent between 1997 to 2011. Between 1997 and 2008, peanut and tree nut allergies have tripled in children in the U.S.17

Food allergy reactions range from mild such as a few hives to life threatening anaphylactic reactions. In the U.S each year, allergic reactions to food send 200,000 people to seek emergency medical care.18

Allergic Reactions Are Life Threatening

Life threatening allergic reactions require the immediate use of an epi-pen within minutes of the start of symptoms of a reaction. Medical professionals instruct that anyone having an anaphylactic reaction immediately inject an epi-pen and then go to the hospital. While going to the hospital after an allergic reaction is always a cause for concern, it is an even more frightening experience during the COVID-19 crisis.

In order to protect their children from the risk of an allergic reaction, food allergy parents know exactly what packaged food their child can eat and what ingredients they need to stay away from. Many families have learned the hard way to have a list of safe snacks and not to vary their food choices. Even a small change in the type of spice or kind of oil used in a recipe could cause a child to react negatively or even go into anaphylactic shock.

Food Allergies of Special Concern in Autism Community

Food allergies are of special concern for parents of very young children or non-verbal children with autism, who may not be able to effectively communicate that they are having an allergic reaction.

These new guidelines will particularly affect the autism community. One in 54 children in the United States have autism. Studies have shown that children with autism are five times as likely as other children to have difficult eating habits such as only eating a narrow range of food items.19

Children with autism have an increased risk of food allergies.20 According to a study, 11.25 percent of children with autism had a food allergy compared to 4.25 percent of children without autism.21 22

Substituting ingredients in products without making corresponding changes to the label is especially concerning with nonverbal children on the autism spectrum, who may not be able to effectively communicate a reaction to foods they were once able to tolerate.

New Food Labeling Guidelines Could Remain in Effect Long Term

The FDA has stated that the new guidelines were issued in response to the COVD-19 pandemic. However, there is no set end date and these changes may be extended or renewed by the Secretary of Health and Human Services if food companies say they need additional time to restock supply chains.

Although the new guidelines went into effect immediately, without first taking public comments, public comments may be submitted at any time for FDA’s consideration.

The FDA provides,

… upon termination of the public health emergency, FDA intends to consider and publicly communicate regarding whether an extension, in whole or in part, is warranted, based on comments received to this guidance and our experience with its implementation.23

Submitting Written Comments to FDA on Food Labeling

You can submit written comments to the Dockets Management Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Submit electronic comments to https://www.regulations.gov. All comments should be identified with the docket number FDA-2020-D-1139 and complete title of the guidance in the request.24

Note: This commentary provides referenced information and perspective on a topic related to vaccine science, policy, law or ethics being discussed in public forums and by U.S. lawmakers.  The websites of the U.S. Department of Health and Human Services (DHHS) provide information and perspective of federal agencies responsible for vaccine research, development, regulation and policymaking.

References:

1 U.S. Food and Drug Administration. FDA Announces Temporary Flexibility Policy Regarding Certain Labeling Requirements for Foods for Humans During COVID-19 Pandemic. May 22, 2020.
2 FDA. Temporary Policy Regarding Nutrition Labeling of Certain Packaged Food During the COVID-19 Public Health Emergency. March 2020.
3 FDA. The History of FDA’s Fight for Consumer Protection and Public Health. June 29, 2018.
4 FDA. FDA: Foods Must Contain What Label SaysFeb. 24, 2013.
5 FDA. Temporary Policy Regarding Certain Food Labeling Requirements During the COVID-19 Public Health Emergency: Minor Formulation Changes and Vending Machines. May 2020.
6 FDA. FDA Fundamentals.
7 See Footnote 1.
8 Ibid.
9 Bloom D. The FDA Has Relaxed Labeling Requirements Under COVID-19. What it Means for the Food Allergy Community. SnackSafely.com May 4, 2020.
10 See Footnote 5.
11 Ibid.
12 Food Allergy Research & Research. The Food Allergy Epidemic. 2020.
13 See Footnote 9.
14 Ibid.
15 See Footnote 12.
16 U.S. Centers for Disease Control and Prevention. Healthy Schools Food Allergies. May 29, 2019.
17 See Footnote 12.
18 Asthma and Allergy Foundation of America. Allergy Facts & Figures. 2018.
19 Autism and Food Aversions: Seven Ways to Help a Picky EaterAutism Speaks Oct. 9, 2018.
20 TVR Staff. Autism Numbers Increase by 10 Percent in U.S.The Vaccine Reaction May 24, 2020.
21 Gordon S. Allergies More Common in Kids With AutismWebMD June 8, 2018.
22 MacReady N. ASD Tied to Excess Risk for Food AllergyMedscape June 8, 2018.
23 See Footnote 5.
24 See Footnote 2.

 
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