Extreme Warning Information on the Bivalent Boosters - and their strange promotion by the FDA
#FriendsDontLetFriendsInject
BS”D
This is a very important article for you to share with any friends or family who may be planning on getting the new, bivalent “boosters”, which are likely to be exceedingly dangerous for a number of reasons. As we have already discussed:
•Every additional covid injection dose has been shown to worsen health outcomes - i.e. the more doses, the more likely one is to experience serious adverse effects or death, (and the more rapidly, as well.)
•All the 10 mice in the Moderna bivalent trial became infected when challenged with the virus after vaccination.
•The 8 mice in the Pfizer bivalent trial displayed wildly varying levels of Omicron antibodies. The highest level was 73x higher than the lowest. Having antibody levels on steroids is likely a portender of serious adverse effects.
•These new bivalent shots WERE NOT TESTED ON ANY HUMAN BEINGS AT ALL.
Now, I’m bringing you new information from Dr. Meryl Nass, MD, that demonstrates the sheer lunacy of the bivalent rollout.
But first - make no mistake, the FDA is heavily promoting the boosters, despite all the awful data emerging in clear daylight about the inefficacy of all the covid shots, and the injuries and deaths resulting from them. It’s so strange - it’s like there are two alternate worlds going on and they don’t cross.
See the FDA’s weird ads for the bivalent boosters:
Kathryn Huwig, who writes a substack called “Beyond the Data”, posted those ads in an article yesterday titled “Since when did the FDA add marketing for pharmaceutical companies to its mission?”
She wrote:
The FDA has put up some pretty crazy tweets over the last few days. At first I thought they were memes, but no, they’re real and can be seen in their feed here: https://twitter.com/US_FDA
I’m grateful that Kathryn led me to the FDA site. I found this one on there, now, too. Talk about mis-/dis-/ and malinformation. 😰
Here’s more of the thread:
These tweets endanger people. They directly contradict the actual data now available, from the British Office of National Statistics and other sources, which show increased risk of illness and death in vaccinated individuals, with the risks increasing more with every additional dose of the covid injections.
(I have included some of this data in previous articles, but I have additional excellent information which, G-d willing, I hope to write up today.)
It really seems that no matter what safety or efficacy data emerges, the government agencies will always continue their narrative promoting these shots.
Back to the special dangers of the new boosters. You may have seen what I posted last week, with Igor Chudov’s research.
Here, I’m bringing more information, from Dr. Meryl Nass, MD. She wrote a guest column last week on Michael Capuzzo’s substack, Rescue. Michael noted:
Editor’s Note: This is a must-read dispatch from Dr. Meryl Nass, a renowned Maine physician, anthrax and bioterrorism expert, and leading covid doctor and researcher who helped FLCCC.net develop long-haul treatment protocols. ~ M.C.
Here are excerpts from Dr. Nass’s article. The link to her original article is at the end.
The High-Speed, Bivalent Covid Boosters Are Here
Watch out. There is nothing good about them, and we should be worried about why they are being used.
By Dr. Meryl Nass MD
On Wednesday, August 31, the FDA issued emergency use authorizations for new Pfizer and Moderna mRNA booster vaccines for covid. The next day, September 1, the CDC’s advisory committee and CDC Director approved the immediate rollout of the new vaccines. They will be administered in the US starting this week.
Fastest vaccine rollout in world history
Surprisingly, more than a month before either agency had given its okay to the entirely new formulation, the federal government ordered 105 million doses from Pfizer and 66 million doses from Moderna.
The desired composition of the vaccine had only been formally determined by FDA after its advisory committee had met on June 24, 2022. The vaccines contain a mix of the old, original Wuhan strain vaccine mRNA (now also referred to as the ancestral vaccine) and a new omicron BA.4/5 mRNA coding for the omicron spike protein.
The total amount of mRNA for the Pfizer and Moderna booster vaccines is the same as before: 30 mcg for Pfizer and 50 mcg for Moderna. Each is composed of 50 percent omicron mRNA and 50 percent ancestral mRNA, and they are termed bivalent vaccines. The new vials and their boxes do not list the dose, hinting that the decision regarding how much to use was made very recently. Even the members of the CDC’s advisory committee did not know the dosage of the new bivalent vaccines until their September 1 meeting.
This is the fastest rollout of a new vaccine in world history. How did it happen? Instead of this being a tale of human grit and ingenuity, it is a tale of human weakness and recklessness. Let me ask again: how did such a rapid vaccine rollout occur?
It occurred the only way it could possibly occur: by bending the rules, creating a new regulatory playbook, and failing to obtain any human data for the new vaccines. The manufacturers did not have to go through months-long trials, and FDA did not have to pore over any human trial data, because there weren’t any. Let that sink in: the new BA.4/5 bivalent vaccines have only been tested in mice, not humans.
Unexpected international coordination
Here is an amazing fact: On the same day that the CDC gave its approval to start the vaccine program, September 1, health agencies in Canada, Switzerland and the European Union’s FDA (the European Medicines Association) also rolled out new, bivalent booster shot programs. Almost simultaneously, the UK authorized two different bivalent boosters on August 15 and September 3.
The UK has told people to expect the largest rollout in history for the new bivalent boosters. And it has started the program by promising large bonuses to doctors if they manage to vaccinate every single resident of a nursing home by October 23.
These other countries are using an earlier omicron mRNA as the template for their omicron-ancestral bivalent vaccines, while the US is using the mRNA code for the later omicron variant BA.4/5 spike.
How can you get complete information on these boosters?
How are the mainstream media telling this story? With their usual spin, avoiding the sticky parts. Instead of helping you understand what just happened, the New York Times asks, “When should you get yours?” Not should you get it, just when should you get it. The Herald Tribune tells you why you should get it. STAT News says it answers your questions, but it never asks the relevant questions about why such a rapid, unprecedented rollout occurred—especially when we are at practically historic lows for deaths and ICU stays due to covid.
The Associated Press did slightly better, at least posing the question of whether you should get a new booster. But then its answers don’t dig any deeper than its fellow media outlets.
It looks like you won’t be getting the information you need to understand the boosters and the process by which they were ushered in from the major media. So the Defender has reviewed FDA documents, attended the all day CDC advisory committee meeting on September 1, studied a review of the boosters published in the New England Journal of Medicine on August 31, and evaluated a study of omicron boosters that were tested in non-human primates by Dr. Fauci's Vaccine Research Center. We will provide you real science.
What did FDA say about its Emergency Use Authorization for the new boosters?
FDA did not convene its advisory committee before issuing the authorizations, and it is not hard to guess why. Last year, its advisors voted against authorizing the ancestral boosters, because the data they were given indicated the old vaccines were continuing to work well. Two top officials at FDA who disagreed with the 2021 booster rollout resigned, hinting that the decision to issue boosters had been imposed on the FDA.
This year, FDA’s VRBPAC (Vaccine and Related Biological Products Advisory Committee) members have been complaining about being given less and less data as they are asked to sign off on vaccine programs for younger and younger ages. VRBPAC member Dr. Paul Offit, a professor of pediatric infectious diseases at the University of Pennsylvania and coinventor of a Rotavirus vaccine said last month that “the fix was in,” implying that the committee’s deliberations were a sham, because the White House announced it was purchasing the vaccine right after the meeting ended.
Dr. Offit was quoted last week as saying the mouse data were not sufficient to roll out the new boosters. So FDA chose not to give him and the other members a public venue where they would predictably complain about FDA’s laxity—what some might call recklessness, insubordination, or even gross malfeasance. After all, according to the FDA’s mission statement, FDA “is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices.” Not rubber-stamping untested vaccines.
The FDA justified its authorizations using language that was probably intended to confuse the public. Here are several examples:
Everyone knows the term “safe and effective,” which is an official FDA stamp of approval for licensed drugs and vaccines. However, by law the term cannot be used by FDA to refer to unlicensed, experimental products, which is what all emergency use authorized drugs and vaccines are. So FDA tried to hint at the desired terminology without using it. In its press release on the new boosters, FDA used almost, but not quite identical terminology, quoting Dr. Peter Marks, the director of FDA’s vaccine center: “We have worked closely with the vaccine manufacturers to ensure the development of these updated boosters was done safely and efficiently.”
Dr. Marks also said, “The public can be assured that a great deal of care has been taken by the FDA to ensure that these bivalent COVID-19 vaccines meet our rigorous safety, effectiveness and manufacturing quality standards for emergency use authorization.” Again, ‘safe and effective’ is implied but not exactly stated.
What Dr. Marks expects the public to miss is the fact that there are no quality standards for emergency use authorizations (EUAs). The statute authorizing EUAs simply requires that the known and expected benefits outweigh the known and expected risks of the product. There are no quality requirements at all, and FDA is not even required to inspect the factories where EUA products are manufactured, as it must do for licensed products. Nor is it required to inspect the final product. So the FDA is fooling us when it claims the standards are rigorous. Furthermore, Dr. Marks and the FDA know that all EUA products have been granted an extremely broad waiver of liability that covers Dr. Marks, the FDA, CDC, HHS, the manufacturers, distributors, doctors, pharmacists, and everyone involved in the vaccine program. So they can tell us anything, because the public has no recourse to the courts to bring suit when an EUA product is involved.
FDA justifies its assessment that the untested vaccines are safe using the following argument: “The safety data accrued with the bivalent vaccine (original and omicron BA.1) and with the monovalent Moderna COVID-19 Vaccine are relevant to the Moderna COVID-19 Vaccine, Bivalent because these vaccines are manufactured using the same process.”
This is the same as claiming that almond butter is safe, so peanut butter is safe, too, because it is manufactured using the same process. Is that really the best excuse for failing to perform its regulatory functions that FDA can offer?
What happened at the CDC ACIP (Advisory Committee on Immunization Practices) meeting on September 1?
CDC knew that it would have a hard time convincing the public to take these vaccines, since almost everyone has already had covid, the earlier vaccine benefits were overpromised, the disease has become milder, the vaccines do not prevent infection or transmission, and the fearfulness around covid is mostly gone. Therefore, CDC needed to employ new strategies.
One strategy was to invoke the ‘bandwagon effect.’ You try to convince the public that everyone else is getting the shot, so they too should jump on the bandwagon. A poll was presented at the ACIP meeting that claimed that 72 percent of people that were eligible planned to get the new boosters. How likely is that to be true? Only 33 percent of the population has already gotten a first booster, while 67 percent have said, ‘No thanks.’ And the interest in covid jabs is way down. Under 5 percent of preschoolers have received a covid vaccine in the three months since they were authorized.
CDC implied to the ACIP that 49 percent of the public had been boosted, while its own statistics in the New York Times say the actual number is 33 percent. Here is how CDC performed the calculation to make it appear the boosters are more popular than they are: 67 percent of the public is ‘fully vaccinated’ according to the CDC. 49 percent of those 67 percent (those who are fully vaccinated) is 33 percent.
The federal government allocated a billion dollars to buy advertising and guarantee positive news coverage (and suppress bad news) to push the earlier covid vaccines. One wonders how much will be spent to push the new boosters.
CDC says that 224 million Americans are ‘fully vaccinated.’ The ACIP members were told that of this number, 210 million are already eligible for the new boosters. The government has bought 171 million bivalent booster doses so far (105 million from Pfizer and 66 million from Moderna) which can be used for those aged twelve and up.
FDA and CDC have yet to allow the rollout of new bivalent boosters for children under twelve, who have in the past received lower dose covid vaccines than adults. But the agencies said they plan to do so within weeks.
Another testy issue for the ACIP committee was the question of how long these boosters will work, and how frequently they will be recommended. The ACIP members are responsible for giving advice on all vaccines, and they don’t want the covid vaccines to sour the public on other vaccines.
Although a recommendation to give the bivalent boosters four months after an earlier dose had once been floated, the ACIP committee was asked to approve the boosters when at least two months had passed since a prior dose. CDC’s Dr. Twentyman said that CDC is no longer counting the total number of doses. She said that even if a person has received four or five prior covid vaccinations, a new bivalent booster “should not be denied,” as long as two months have passed since the last dose.
How long will it work?
According to this week’s NEJM article:
“Increased neutralizing antibody titers, as well as clinical effectiveness, have been shown to wane by four months after a third messenger RNA immunization. After a fourth messenger RNA immunization, protection against infection with SARS-CoV-2 omicron has been reported to wane after just four weeks, although protection against severe disease lasts longer. Hybrid immunity from both vaccination and infection provides greater and more durable protection than either alone.”
Four weeks! Antibody titers sink four weeks after the fourth dose. No wonder CDC is allowing, and may encourage, such frequent boosters.
The covid vaccinators have coined a new term, hybrid immunity, riffing off hybrid electric cars. It refers to the improved immunity a vaccinated person has if they also got the disease! As if being vaccinated but getting the disease anyway is to be normalized as desirable. After CDC spent two years denying that natural immunity—the kind people get after infection—even exists, CDC is now trying to take a lemon vaccine, add natural immunity, call it hybrid immunity, and make lemonade!
How was this rollout justified?
Omicron variants have been present since last November, and it was soon discovered that both vaccine-induced and natural immunity due to earlier variants were very limited for omicron variants, because they are so different from the ancestral strain. The health agencies and manufacturers have been testing omicron vaccine prototypes for up to nine months. Most of those tests involved BA.1 and BA.2 omicron strains. However, 90 percent of current cases are caused by Omicron BA.5, which is genetically far from BA.1 and BA.2.
But there was some human data (involving a few hundred subjects each) for several of the earlier omicron vaccine prototypes, so the health agencies decided to simply pretend that mRNA designed for BA.1 and BA.2 was close enough to BA.5 that the data were comparable.
Since 50 percent of the vaccine contents would be the old vaccine, FDA claimed it had already established the safety and efficacy of that half. Then, to round things out, there were data from mice, which generated comparable antibody levels to the new vaccines as they had to older vaccines. And of course, we can rely on mice to behave exactly like people, right? After all, they have been ‘humanized’ to contain a human ACE-2 receptor.
No, we cannot rely on mice. We cannot even rely on nonhuman primates as a model for vaccines, as every species reacts uniquely and unpredictably to infections and to vaccinations. But mice data do bulk up FDA’s authorization ‘package’ so it looks like FDA did a more thorough review.
Having discussed how long this booster might last, one needs to ask how well it might work.
Predictions from Nature magazine and Dr. Fauci’s NIAID Vaccine Research Center at the NIH are that the new vaccines will not improve on the old vaccines.
According to the VRC, “a study in nonhuman primates showed that an omicron specific messenger RNA vaccine was not better than the original messenger RNA-1273 [ancestral Moderna] vaccine for protection against omicron challenge.”
Nature notes, “an analysis [posted August 26] suggests that updated boosters seem to offer much the same protection as an extra dose of the older vaccines—particularly when it comes to keeping people out of hospital.”
Neither of these studies was discussed at the ACIP meeting. No discussion was provided regarding why and how the bivalent vaccines were chosen.
The reason why the omicron vaccines won’t stimulate a good omicron response is attributed by the NIAID VRC authors to antigenic priming, also known as original antigenic sin. This means that the immune system has been programmed to respond over and over again to the first coronavirus infection or vaccine it encountered, even when it encounters different coronavirus antigens later.
How well did the old vaccine work? The CDC slide below, presented by CDC’s Dr. Link-Gelles, is not well labeled, but it shows that whether you got two or three doses of the old vaccine, during the omicron period efficacy in all age groups was under 40 percent at three months. By six months it hovered around zero efficacy (no benefit), and after that it was negative (harmful) for most ages.
Negative efficacy means that the vaccinated are more prone to being infected with covid than the unvaccinated. This is consistent with what we are seeing from the UK and some other countries: the vaccinated become more likely to get covid. And it is this effect that the public health agencies are probably trying to stave off, or hide, with perpetual boosters.
It appears the public here and in many other countries is being misled to receive an untested (or in other countries a BA. 1 or 2 minimally tested) shot on the false promise it will be so much better than the older vaccine. The regulators know it is unlikely to be better, but their public relations engines are revved up to convince us otherwise.
How safe are the new vaccines?
That is anybody’s guess, because you cannot assess human safety from animal models, since they don’t predict the human response. What was done to evaluate the safety of the bivalent vaccines?
An ACIP member asked whether the Jynneos monkeypox vaccine, which can also induce myocarditis, could be given together with the new bivalent vaccines? Would this increase the myocarditis risk? The surprising response was, “Read the briefing book,” which may have meant that this was not to be discussed in public.
Speaking of what could be discussed in public, any discussion of pregnancy and covid vaccination was forbidden at the ACIP meeting. Multiple committee members asked for information on pregnancy, but the briefers steadfastly refused to provide any. Nothing on hospitalizations, deaths, fetal outcomes. The ACIP members were told they would be briefed on this at a future meeting. Dr. Miller, representing Moderna, said they were in the process of enrolling a total of 800 pregnant women in a study. Which would someday be completed. The only conclusion I can draw is that the CDC doesn’t like the results they have now. And they plan to delay providing them to the public for as long as possible.
Yet CDC established a pregnancy registry for the covid vaccines nearly eighteen months ago. CDC and FDA must have data on many thousands of pregnancies. Every woman who receives a covid vaccine dose must provide information on whether she is pregnant before she can be vaccinated, and CDC collects all this information. Furthermore, there are thousands of VAERS reports on adverse pregnancy outcomes.
FDA required Pfizer/BioNTech to study the effect of the vaccine in pregnancy when it issued a license for Comirnaty on August 23, 2021. FDA also required additional vaccine safety studies in children and additional studies of myocarditis at the same time. The problem is that these studies won’t be completed for up to five years, long after billions of doses have been given and the vaccines will be long out of date. It is difficult to justify why FDA would ask for these studies to take so long. Was FDA requesting such long study durations in order to delay its vaccine safety assessment until after the vaccines are no longer in use?
The only conclusion I can draw is that FDA and CDC don’t like the safety results they already have. And they plan to withhold the bad news for as long as possible.
Long covid
The committee was also interested in long covid. Might the vaccines prevent this dread complication? CDC was mum. The CDC briefer claimed that CDC does not have “systematic data” on long covid. Nor has CDC developed a case definition for long covid. Why has CDC delayed investigating this critically important complication?
The New York Times revealed in February 2022 that CDC conceals the bulk of the public health data it collects. According to the Times, “Much of the withheld information could help state and local health officials better target their efforts to bring the virus under control.”
You are not going to find a more public indictment from the Times of our Centers for Disease Control than that.
Does vaccination fail to prevent long covid? Does it cause long covid? FLCCC founder and esteemed intensive care physician Dr. Paul Marik has postulated that both long covid and many covid vaccine injuries are due to the same thing: the prolonged presence of spike proteins in the circulation. If true, there may be considerable overlap between the symptoms and pathology of long covid and vaccine injuries, and CDC may be trying to conceal this, or perhaps be seeking a way to claim that all the vaccine injuries are due to covid.
FDA revoked all Pfizer and Moderna emergency use authorizations for the old boosters on August 31.
This was sudden and unexpected. Appointments had to be cancelled, because starting on August 31 the old vaccines were limited to use in only young children or for the initial series. The FDA did not withdraw or recall the licensed Comirnaty and Spikevax vaccines, which have also been approved as a booster dose. Is this a tacit acknowledgement that there is no licensed Comirnaty or Spikevax available in the US?
Might the FDA have rolled out the new vaccines so quickly to justify removing most of the old vaccines from use, soon after reports began circulating about their contents containing undisclosed and possibly harmful materials?
••••
End of excerpted article by Dr. Meryl Nass.
Link to original below.
Link to Kathryn Huwig’s article:
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IMHO, Meryl Nass says it all in this paragraph: "... there are no quality standards for emergency use authorizations (EUAs). The statute authorizing EUAs simply requires that the known and expected benefits outweigh the known and expected risks of the product. There are no quality requirements at all, and FDA is not even required to inspect the factories where EUA products are manufactured, as it must do for licensed products. Nor is it required to inspect the final product. So the FDA is fooling us when it claims the standards are rigorous. "