In an unsurprising move slammed by critics as “unjustified” and “unethical,” and in blatant disregard of the recommendations against administration of so-called Covid booster shots to the general population by their respective safety oversight committees, the FDA and CDC have both signed off on Pfizer 3rd dose injections for anyone in the general population whose job is deemed a ‘high risk’ workplace or who reside in ‘close living conditions’, effectively giving the green light to Biden’s 3rd dose booster rollout plan and opening the door for booster use among the entire adult population under the guise of ‘limited’ authorization.
https://twitter.com/RobertKennedyJr/status/1441201716997681156
- RobertKennedyJr
The FDA’s vaccine advisory committee had previously and unexpectedly voted overwhelmingly against Pfizer’s request for approval of a 3rd dose of its experimental injection for the general population, in a 16-2 decision, voting only to authorize use among those aged 65 and older and limited ‘at risk’ populations, those with specific underlying conditions. This decision followed an 8 hour safety meeting held on September 17 which featured presentations given by a number of experts, and the reason for rejecting the Pfizer/Fauci/Biden plan for general population booster use was that the risk of harm outweighed any potential benefits, and the committee also cited extremely limited available data on 3rd dose safety and efficacy.
Nevertheless, the FDA extended its emergency authorization of Pfizer’s experimental injections last Wednesday to include single 3rd dose booster use not only for those 65 and older and limited ‘at risk’ populations, but also workers deemed to be at ‘high risk’ of exposure, so pretty much anyone in any public service industry, a move deemed by Dr. Robert Malone to be “regulatory overreach on the part of the FDA and the commissioner.”
“After considering the totality of the available scientific evidence and the deliberations of our advisory committee of independent, external experts, the FDA amended the EUA for the Pfizer-BioNTech COVID-19 Vaccine to allow for a booster dose in certain populations such as healthcare workers, teachers and daycare staff, grocery workers and those in homeless shelters or prisons, among others,” Dr. Janet Woodcock, acting FDA commissioner said in a statement.
Similarly, the FDA’s Center for Biologics Evaluation and Research director, Dr. Peter Marks, said in a statement that: “The FDA considered the committee’s input and conducted its own thorough review of the submitted data to reach today’s decision.”
The “available scientific evidence” and “submitted data” the FDA overviewed before making this decision in contravention of its own advisory committee tasked with issuing the agency guidance related to safety, clearly indicates that the risks do indeed far outweigh the benefits; with all of the available evidence demonstrating that the Pfizer injections (first 2 doses) harm more people than they save, killing at least 2 people for every person they allegedly save. This is demonstrated by Pfizer’s own trial data, real world US and Israeli data, VAERS reports, and has been confirmed by at least four independent analyses which have come to the very same conclusions based on data in other parts of the world.
Extensive documentation that the harm from these injections definitively far outweigh any alleged benefits can be found in my last post on the subject, including evidence from several medical studies and that which was presented at the safety advisory meeting:
In an email to the Children’s Health Defense, Dr. Meryl Nass explained that Pfizer had requested licensing of a 3rd dose of its injection based on “unconvincing data,” as its phase 1 trial for boosters was extremely small and limited, the company didn’t test a booster in anybody who was actually at risk, while one of the 300 participants also had a heart attack, and it contained no control group data as it was entirely unblinded; the participants of the original Phase 1 trial who had initially been given a placebo, from which the small selection of subjects included in the booster study were selected, were later given the injections; with at least 93% of Pfizer trial participants in the placebo arm and at least 98% of placebo recipients in Moderna’s trial now vaccinated.
“As a result, the FDA’s vaccine advisory committee voted against approving the third booster dose for the general population. And that was the only question they had been asked to vote on. However, the FDA was unwilling to take that as its final answer.
“So suddenly the FDA created a new question for the committee: Would it approve (i.e., license) boosters for those over 65 and /or immune compromised? In a transparent attempt to give Pfizer a consolation prize, the committee voted ‘Yes.’”
But this “consolation prize” won by the FDA in its last minute ‘change of request’ wasn’t good enough for Pfizer, and not being good enough for Pfizer, it wasn’t good enough for the FDA. Who works for who here should be readily apparent, as if it wasn’t already made clear enough back when FDA issued its first premature approval to Pfizer’s injection on August 23, despite data indicating both a higher rate of harm and far lower efficacy in the Pfizer injection than in Moderna’s similar mRNA shot. This higher rate of injury is also evidenced in VAERS reports and especially pronounced among child injuries, with 90% of deaths (18 out of 20), 99% of anaphylactic reactions and myocarditis, and all blood clotting disorders reported following injection attributed to Pfizer.
In fact, it would appear that the criminal organization managed to create the deadliest of all of the four major Covid ‘vaccines’ (trial data showing 5 deaths for each life saved among the vaccinated) - no small task considering all of these experimental Covid injections are exponentially more dangerous than any previous vaccine ever made - and still somehow pulled off both the first ‘full’ approval and first ‘booster’ authorization!
Immediately following the unexpected advisory committee decision to vote against general population use, Dr. Fauci and his boss NIH director Francis Collins both took to the airwaves to assure media outlets that Biden’s plan would still likely go forward, and booster use for the general population was all but assured; Fauci explaining that it might just take a little time, he and Collins both acting as if the committee vote was nothing but a minor speed bump on the path to widespread booster use by all but perhaps children.
As I noted at the time: “Whether or not the FDA approves the ‘boosters’ for the general population or not will reveal just how sold out to Big Pharma the so-called regulatory agency really is.”
It turns out the agency is indeed fully sold out to both Pfizer and Biden’s political mandavaxx agenda, which is in actuality Anthony Fauci’s and Bill Gates’ agenda, and the president is but a useful political puppet. The advisory committee’s guidance is meant to be followed by the FDA, not ignored in favor of pre-planned, profit-driven political agendas decided in advance of any safety or efficacy data even becoming available. And FDA standard procedure is to follow its advisory committee guidance, but nothing has been standard or normal about government or medical operations since the rise of Covid Clown World in January, 2020.
Now readily apparent, the FDA is in no way truly a regulatory agency, but rather a revolving door for Big Pharma, doing the bidding of criminal pharmaceutical cartels and serving globalist political agendas with complete disregard for the safety and efficacy of the products being authorized and approved. They are as complicit in this crime against humanity as the perpetrators, and their true colors and the true colors of this vaccination campaign are showing more clearly now than ever before. More deaths and injuries will occur as a result of this criminal fraud, likely at a higher rate than during the 2 dose regimen, as the evidence shows that risk of ‘vaccine’ harm and severity of adverse reactions only compounds with each additional injection.
The CDC must approve any FDA authorization, however, before public use can begin, and the agency’s advisory committee can amend FDA recommendations on boosters; and indeed it did, rejecting the broad use among the general population authorized by the FDA, voting only for use among the elderly “and some with medical conditions that put them at higher risk of severe COVID-19,” following the guidance of the FDA’s advisory committee. And just like the FDA, the CDC director likewise overruled her agency’s own vaccine advisory committee, and expanded the agency’s backing of the FDA authorization to include, along with those over 65 and adults with underlying medical conditions, “adults in high-risk working and institutional settings,” Reuters reported
https://twitter.com/ggreenwald/status/1441399817045958657
- ggreenwald
According to CDC director Walensky, her decision was ostensibly to “provide access” to communities who have “already been hardest hit” by the so-called pandemic, those in ‘close living conditions’ and who work in what are being deemed ‘high risk’ jobs - “our frontline workers, essential workers, and those in congregate settings.” The reality, however, is that the latest FDA and CDC decisions open up access to these ‘booster’ shots to any and all adults, and as such they effectively serve as a de-facto authorization of the shot for the entire general population, a back-door approval of Biden’s original plan to begin ‘booster’ distribution to the entire general population on September 20.
“The CDC on Thursday told its advisers that there would be no requirements to submit documentation to prove that people have the underlying conditions or work in at-risk settings,” Reuters reported.
A number of experts see this move for what it clearly looks to be, an open invitation for any adult seeking a 3rd dose to get one, and this has in fact been cited as one of the reasons the CDC vaccine advisory committee voted to amend the FDA authorization to restrict distribution to the elderly and those with verifiable underlying conditions.
SVB Leerink analyst Geoffrey Porges said he expects many of the "worried well" to seek booster shots in the coming weeks because of the CDC's loose requirement on who is eligible.
"That literally means anyone can show up and say I’m at an increased risk of getting re-infected," Porges said.
Dr. Paul Offit, director of the Vaccine Education Center and professor of pediatrics in the Division of Infectious Diseases at the Children’s Hospital of Philadelphia, also sees the CDC director’s decision as a de facto green-lighting of the Biden Administration rollout plan for the general population under the guise of a more conservative ‘limited’ authorization.
“That was a hole that you could drive a truck through, that essentially what we were doing was basically what the [Biden] administration initially asked — to just have a vaccine for the general population, because obviously the pharmacists aren’t going to figure out whether you’re working in a grocery store or hospital,” Offit said.
Not only does this move effectively open the door for distribution of 3rd dose injections to the entire adult population, it also paves the way for employer and government mandates alike requiring boosters for large swaths of the population, many millions of Americans. Every aspect and every step of this vaccination coercion campaign has from its inception and continues to be strategically coordinated to facilitate universal forced injection of the entire population; as mandatory vaccination for all has always been the goal of this campaign since even before it was first launched at the end of last year, and we are now seeing that clearly with the current accelerated march of mandavaxx madness, as the mask is ripped off from the facade that this was ever about ‘personal choice’.
Walgreens and Walmart both had doses waiting and ready to go on Friday, and if they aren’t already by now a week later, they will soon be available at vaccination stations and pharmacies all across the country. Biden acted on the CDC approval immediately, announcing that his administration would begin delivering shots right away, feigning reliance on the science when in fact the entire process was highly politically motivated and involved ignoring all of the relevant science, hundreds of thousands of safety signals, and the specific recommendations of two regulatory vaccination oversight committees, not to mention dozens of experts who spoke out against the move, in favor of his orchestrated plan.
“We have the tools to beat Covid if we come together as a country and use the tools we have," Biden said in a speech Friday. "This week we took a step in protecting the vaccinated with booster shots. I've made clear all along ... the decision of which booster shot to give and who will get them is left to the scientists and the doctors."
Biden’s victory statement is absolutely false and misleading, as the decision of who will get the shots is being left entirely up to the people choosing to get them, with the CDC specifically opting to forego requirements to prove ‘at risk’ status, while doctors, scientists, and decisions by safety oversight committees were all summarily ignored to reach this approval.
Meanwhile the notion of ‘protecting’ the vaccinated (the ‘protected’) is nonsensical, and illuminates the ineffective nature of these experimental injections. If you have to ‘protect’ the ‘protected’, then there is a serious problem with the ‘protection’ that more of it simply won’t be able to fix, as has been demonstrated on so many levels in so many different medical studies. Piling bandaids on a gaping wound is pointless, and additional doses of an injection that is entirely incapable of stopping transmission and infection of a ‘virus’ won’t stop its spread, especially when that ‘protection’ has been repeatedly shown to be powerless against a host of ‘vaccine resistant’ variants we are told are now driving disease, if the variant narrative is not in fact simply a cover for ‘vaccine’-induced disease and/or a shot that is simply ineffective as a tool in the fight against ‘Covid19’.
What is transpiring here is transparent for all to see, who are but willing to step outside of the establishment illusion and look at the mechanisms behind the launching of this long-planned 3rd dose rollout and just how this latest installment of a never-ending vaccination campaign came to fruition. But not only are the authorities ignoring all of the evidence overwhelmingly suggesting these injections cause far more harm than they prevent, they are at the same time ignoring and suppressing the very injuries being caused and the injured victims seeking help and treatment for their serious conditions.
All this for one purpose; to increase ‘vaccine’ uptake, discourage ‘vaccine hesitancy’, and get as many shots in arms as possible at any and all costs. It is an agenda that has been transparent from the very beginning, and has nothing to do with ‘public health’ and everything to do with Big Pharma profit and the enslavement of the human race by an emerging global technocratic world order.
As the FDA director herself and representatives of every government health and regulatory agency out there have made absolutely clear to Danice Hertz, a physician who was immediately injured and has been “horribly ill” and effectively incapacitated since the day she got her first Pfizer injection in December, the authorities are not interested in hearing about or researching any of the ‘vaccine’ injuries it has admittedly been aware of since the clinical trials. Her story of being injured and then completely ignored and denied care, a story shared by thousands of fellow ‘vaccine’-injured victims of this coercion campaign the world over, can be heard in a video recording at CV19 Vax Reactions.
The NIH, FDA and CDC have acknowledged that they are aware of the large scale of injuries, but the ‘vaccine’-injured are given the run around, and promised follow up always falls through, while the media will not cover their stories as they are prohibited from publishing or airing any coverage of ‘vaccine’ injuries.
“The NIH is aware of what is happening but publicly has been dismissive of vaccine adverse reactions,” Hertz said in a recent interview with the Defender detailing her saga of being sidelined by the health agencies which are supposed to be tracking and researching adverse reactions, but are instead suppressing and ignoring them.
https://twitter.com/RobertKennedyJr/status/1441155868318310402
- RobertKennedyJr
Dr. Peter Marks of the FDA has promised that a member of the pharmacovigilance program would contact her, but to date it has never happened, nor has the CDC ever contacted her to follow up on her VAERS report, nor has Pfizer responded to her letters, nor has the NIH promise to present her case (along with the other 1,000 or more known similar neurological adverse reactions to the scientific community) ever been acted upon. Many others have reported having to file VAERS reports two or three times before they are even accepted into the CDC-run system, and hundreds of people in similar situations seeking acknowledgement and help have all been similarly ignored in dystopian manner.
Doctors and hospitals are for the most part absolutely unwilling to diagnose any symptoms as adverse ‘vaccine’ reactions, often diagnosing severe debilitating neurological damage as mere anxiety, and referring the patients to psychologists or releasing them without care, having no idea how to treat these unprecedented syndromes being caused specifically by these experimental injections. Many of the adverse reactions are unfamiliar even to seasoned vaccine injury researchers.
It is clear that the FDA, CDC, and NIH, although fully aware of the scale of injury being caused by these injections, are unwilling to publicly acknowledge them, let alone track and research them as pharmacovigilance programs are created to do. They do not wish to collect data or research the thousands of ‘vaccine’ injuries, for to do so would be to acknowledge their reality, and that would create ‘vaccine hesitancy’, which is not an acceptable option for those driving this sick, tyrannical agenda. Not only is this travesty of justice a great disservice to the many compliant ‘vaccine’ victims who were just dutifully ‘doing their part’ in the ‘war on Covid’, it also ensures that no prospective ‘vaccine’ recipients are capable of giving truly informed consent before getting their injections.
The uniform response to all of these adverse events by the whole of the medical, political and media establishments is a coordinated suppression effort being used to deny the right of informed consent to all injection recipients, past, present and future.
The thousands of ‘vaccine’ injuries are publicly discounted as a ‘conspiracy’ by the very same authorities which privately acknowledge their reality.
Countless serious adverse reactions are censored from Google search results, denying information to prospective recipients attempting to research the possible side effects before getting their shot, while innumerable stories from the thousands of ‘vaccine’-injured are indiscriminately censored from Big Tech Big Tech social media platforms platforms as ‘misinformation’ and simultaneously all but ignored by mainstream outlets - always reported as ‘extremely rare’ side effects when they are even reported at all. Recipients are not warned of a great many of the known risks by doctors, nurses and pharmacists encouraging and administering the injections, the CDC blatantly lies about the frequency and seriousness of the known risks it does acknowledge (such as myocarditis), political and media talking heads continue to endlessly repeat the mantra that these injections are proven to be ‘totally safe and effective and effective’, symptoms following injection are frequently misreported or not reported at all, and all the while there are more and more new injuries each and every day that that this injection campaign continues.
The misreporting or failure to report suspected adverse reactions is a crime, particularly when it comes to symptoms observed in clinical trials, that can be prosecuted in a court of law; and, in the case of the Pfizer trial for 12-15 year olds in which young Maddie de Geray’s paralysis was reported as “abdominal pain,” with the myriad of other persistent symptoms never reported and her debilitating symptoms diagnosed as “anxiety,” the FDA has failed to investigate this trial fraud. This is not “collecting data,” this is criminal fraud.
The right of informed consent has been denied to every single recipient of these experimental injections outside of clinical trials, with only those who go out of their way to find the vast amount of highly suppressed information on the known risks able to give truly informed consent, with the majority of these people who have done the required extensive research to be adequately informed among the ‘vaccine hesitant’, only coerced into accepting the injection, if they are, against their will by tyrannical and unjust mandates.
This coordinated denial of the universal right of informed consent is in and of itself a crime against humanity, the crime that much greater when bribes and mandates are additionally employed to coerce the unwilling into compliance.
“This is evil, this is evil at the highest level,” nurse and DHHS whistleblower Jodie O’ Malley noted in an an interview on Project Veritas last month; “you have the FDA, you have the CDC, that are both supposed to be protecting us, but they are under the government, and everything we have done so far is unscientific.” I’d say the recent FDA and CDC actions have proved her assessment to be spot on.
Meanwhile Pfizer has announced that its trial of 5-11 year olds showed its experimental injections were ‘safe and effective’ for these younger children, and said it plans to soon request FDA emergency authorization, with a senior Vice President saying that he feels “a sense of urgency” and FDA officials said it could authorize the injections just weeks within the request submission. A number of experts question the trial data findings, particularly because of previous coverups of adverse reactions and limited trial size, and are “concerned that the risk of taking this new technology injection is higher than the benefits for children in the 5-11 age group.”
Since the benefits are zilch, with healthy children in this age group at zero risk of death or hospitalization from ‘Covid19’, even the smallest risk would outweigh the benefits, and the mad rush to vaccinate the child population with these injections is both unethical and insane, as are the methods of bribery and coercion being used towards that end.
https://twitter.com/FreundMirjam/status/1442103919602245634
- FreundMirjam
https://m.theepochtimes.com/dr-scott-atlas-on-vaccine-mandates-for-children-natural-immunity-and-floridas-covid-19-surge_4013490.html/amp
Given the FDA’s recent decisions to fast-track Pfizer injections over the past several weeks, the company looks to be on track for yet another imminent authorization, regardless of the weight of the evidence for or against such an authorization.
In other news, Johnson & Johnson has also recently announced that its researchers found a 2nd dose of its own injection given just 2 months following initial injection boosted waning efficacy and ‘protection’. For comparison, Pfizer’s 3rd dose booster has been authorized for use at 6 months following 2nd dose.
https://twitter.com/Timcast/status/1440292780010455045
- Timcast
The world is being indoctrinated into a dangerous cult, one of its primary goals is perpetual forced injections for all, and they are coming for our children. As recent history has shown, this march of mandavaxx madness will never end until We The People stand up and make it stop.