“We should stop trying to prevent all symptomatic infections in healthy, young people.”
Posted BY: | NwoReport
Dr. Paul Offit, a member of the U.S. FDA’s vaccine advisory committee, has written in the New England Journal of Medicine, the world’s top medical journal, calling for an end to the mass vaccination of anyone at low risk from the virus.
In an op-ed titled “Bivalent COVID-19 Vaccines – A Cautionary Tale”, Dr. Offit writes that Covid boosters are “probably best reserved for the people most likely to need protection against severe disease”.
“I believe we should stop trying to prevent all symptomatic infections in healthy, young people by boosting them with vaccines containing mRNA from strains that might disappear a few months later,” he writes.
Dr. Offit, who is a Professor of Vaccinology and Professor of Paediatrics at the University of Pennsylvania, goes through in detail the process that led to bivalent vaccines being recommended in the U.S. for everyone over five years of age with no relevant data from humans. He is clearly very unhappy about it.
Trending: Dr. Malone shares dire warning: mRNA vaccines are being injected into our food supply…
On June 28th 2022, researchers from Pfizer-BioNTech and Moderna presented data on their bivalent vaccines to the FDA’s Vaccines and Related Biological Products Advisory Committee (of which I am a member). The results were underwhelming. Bivalent boosters resulted in levels of neutralising antibodies against BA.1 that were only 1.5 to 1.75 times as high as those achieved with monovalent boosters. Previous experience with the companies’ vaccines suggested that this difference was unlikely to be clinically significant. Safety data were reassuring. At the time of the FDA presentation, BA.1 was no longer circulating in the United States, having been replaced by more immune-evasive and contagious Omicron subvariants. But winter was around the corner. The FDA advisory committee, sensing the urgency of responding to these immune-evasive strains, voted to authorise bivalent vaccines with an understanding that they would target Omicron subvariants BA.4 and BA.5, which at the time had accounted for more than 95% of circulating strains.
A series of rapid-fire policy decisions followed. On June 29th 2022, the day after the advisory committee meeting, the Biden administration agreed to purchase 105 million doses of Pfizer-BioNTech’s bivalent vaccine containing BA.4 and BA.5 mRNA. One month later, on July 29th 2022, the administration agreed to purchase 66 million doses of Moderna’s bivalent vaccine, intending to offer both vaccines in the fall and winter. On September 1st 2022, the FDA withdrew its emergency use authorisation for monovalent vaccine boosters and the CDC recommended bivalent vaccine boosters for everyone 12 years of age or older. On October 12th 2022, the CDC extended this recommendation to include everyone five years of age or older. At that point, no data from humans, including immunogenicity data, were available for comparing the relative capacities of the monovalent and bivalent vaccines to protect against BA.4 and BA.5.
On October 24th 2022, David Ho and colleagues released the results of a study examining levels of neutralizing antibodies against BA.4 and BA.5 after receipt of a monovalent or bivalent booster dose. They found “no significant difference in neutralisation of any SARS-CoV-2 variant”, including BA.4 and BA.5, between the two groups. One day later, Dan Barouch and colleagues released the results of a similar study, finding that “BA.5 [neutralising-antibody] titers were comparable following monovalent and bivalent mRNA boosters”. Barouch and colleagues also noted no appreciable differences in CD4+ or CD8+ T-cell responses between participants in the monovalent-booster group and those in the bivalent-booster group. Neither research group found the bivalent boosters to elicit superior immune responses. The results are now published in the Journal.
The likely reason the bivalent vaccines failed is immune imprinting, Dr. Offit explains.
The immune systems of people immunised with the bivalent vaccine, all of whom had previously been vaccinated, were primed to respond to the ancestral strain of SARS-CoV-2. They therefore probably responded to epitopes shared by BA.4 and BA.5 and the ancestral strain, rather than to new epitopes on BA.4 and BA.5.
When epidemiological data did become available, they showed very poor protection.
On November 22nd 2022, the CDC published data on the effectiveness of the BA.4 and BA.5 mRNA vaccines for preventing symptomatic infection within two months after receipt of the booster dose. For people who had received a monovalent vaccine two to three months earlier, the extra protection associated with the bivalent booster dose ranged from 28% to 31%. For those who had received a monovalent vaccine more than eight months earlier, the extra protection ranged from 43% to 56%. Given the results of previous studies, it’s likely that this moderate increase in protection against probably generally mild disease will be short lived.
The bivalent vaccine had very poor take-up and the variants it was targeted against were quickly gone.
As of November 15th 2022, only about 10% of the population for whom the bivalent vaccine had been recommended had received it. By December 2022, the BA.4 strain was no longer circulating, and BA.5 accounted for less than 25% of circulating SARS-CoV-2 strains, having been partially replaced by more immune-evasive strains, such as BQ.1, BQ.1.1, BF.7, XBB, and XBB.1.
It’s welcome that Dr. Offit is breaking ranks and expressing dismay about the poor process and the lack of data, and calling for the end of the mass vaccination campaign. The intervention is particularly significant because it denotes a failure of the central U.S. biosecurity strategy of trying to use fast-track mRNA vaccines to provide a lightning response to an emerging biological threat. It is thus likely that his conclusions will be strongly resisted by those who are invested – financially, psychologically and politically – in this strategy.
That Dr. Offit is only doing so now, and not with any recognition of any safety problems, is less welcome, of course. Still, he will likely not be thanked by his paymasters, and it is in the right direction, so he should receive credit for that.
We still await the acknowledgment that the benefit of these vaccines was never favorable for people at low risk from the virus, who never needed them, and that their safety profile is far worse than the companies and regulators have led the public to believe.
Stop Press: CNN reports that Dr. Offit is “angry” that Moderna failed to include unfavorable infection data in its submission to the FDA last year. “I was angry to find out that there was data that was relevant to our decision that we didn’t get to see,” Dr. Offit said. According to CNN: “The data that was not presented to the experts looked at actual infections: who caught COVID-19 and who did not. It found that 1.9% of the study participants who received the original booster became infected. Among those who got the updated bivalent vaccine – the one that scientists hoped would work better – a higher percentage, 3.2%, became infected.” Does it make you wonder what else they’re not telling you, Dr. Offit?
Is this the same FDA vaccine committee that unanimously voted to vaccinate infants 5 and up, basically giving pharmaceutical companies permanent immunity from liability for adverse effects to the death jabs?
Without specifying where “here” is – babies 6 months old and up. So how do you communicate with a 6 month old baby that cannot communicate verbally with you, to tell it the vaccines you are injecting into it are safe and are going to save it from a Covid virus patented by Moderna in 2013 along with 4 other Covid Patents at the same time – oh, hang on a moment – the Chinese were responsible for Covid, so how come Moderna has the patents and not the Chinese?
is this just before their recommended hangings
I suggest you have a look at Christine’s substack on Steve Kirsch’s substack which he owns and runs – Christine has a pretty good overall view of what is going on here and you can believe or disbelieve her take on things as you please.
Her substack is free and if you offered to pay, I dare say she would tell you clearly and succinctly what you could do with your money and where to put it – so rather than chatting here – why not there instead?
There were no COVID-19 vaccines close to approval on August 27, 2020. In fact, the Pfizer/BioNTech vaccine trial phase 2/3 had only started a month earlier on July 27.The first contract, with General Dynamics, is dated August 27, 2020. It outlines a series of services the company was to provide to the CDC pursuant to the “anticipated increase” in VAERS reports due to the COVID-19 vaccines. It certainly appears that by August, 2020, the impending emergency use authorization of at least one COVID-19 vaccine was a foregone conclusion. BioNTech CEO Ugur Sahin says that his mRNA vaccines rolled out in January this year (2021): Link here: https://www.ibtimes.sg/fact-check-biontech-ceo-ugur-sahin-refuses-take-pfizer-covid-19-vaccine-due-safety-concerns-61652 but by August 27, 2020 – The first contract, with General Dynamics, is dated August 27, 2020 had been let and the contract states that they were expecting up to 1,000 VAERS reports to be filed per day, with up to 40% of the reports being serious in nature and the CDC was already anticipating that the COVID vaccines might generate nearly seven times as many reports as all other vaccines combined (a 600% increase), The amounts paid out under the contracts with General Dynamics were redacted. But according to this site, the initial amount paid was $9.45 million, with $4.4 million added in late February, and then an additional $16.3 million tacked on in early March. In March of 2022 there was an additional $5.2 million added (increases in deaths and injuries beyond the initial contracts)
The Contracts 23 00099 General Dynamics Information Te..https://substack.com/redirect/dac78dc8-9d2d-4280-a390-218d47bb331d?j=eyJ1IjoibjFlaXcifQ.OkComRnvTz45cW2ospKdwvhGbhkMepFwvepUF91fYF023 00099 Eagle Health Analytics, Llhttps://substack.com/redirect/bcba05ff-1dce-4b15-a6a7-0f59f3cb115a j=eyJ1IjoibjFlaXcifQ.OkComRnvTz45cW2ospKdwvhGbhkMepFwvepUF91fYF0 Grand total? $35,425,642 The Vaccine Adverse Event Reporting System (VAERS) records 1% of all reports:
VAERS updated its numbers showing a staggering 1,481,226 reports of adverse events (x41 to arrive at December 2022 numbers) following COVID-19 vaccines were submitted between Dec. 14, 2020, and Dec. 9, 2022. …The above information posted by Josh Guetzkow
BioNTech CEO Ugur Sahin says that his mRNA vaccines rolled out in January this year (2021): Link here: https://www.ibtimes.sg/fact-check-biontech-ceo-ugur-sahin-refuses-take-pfizer-covid-19-vaccine-due-safety-concerns-61652 but by August 27, 2020 – The first contract, with General Dynamics, is dated August 27, 2020 had been let and the contract states that they were expecting up to 1,000 VAERS reports to be filed per day, with up to 40% of the reports being serious in nature and the CDC was already anticipating that the COVID vaccines might generate nearly seven times as many reports as all other vaccines combined (a 600% increase), with a rate of serious adverse events that could be up to 8 times higher, (bearing in mind that VAERS represents only 1% of all injuries and deaths recorded and multiplying the numbers given by 41 (x41) gives a much better appreciation of just how many American’s were being injured or had died, after vaccinations began in early 2021), on a daily basis: The Vaccine Adverse Event Reporting System (VAERS) Friday updated its numbers showing a staggering 1,481,226 reports of adverse events (x41) following COVID-19 vaccines were submitted between Dec. 14, 2020, and Dec. 9, 2022, so for 100% x41 = 60,730,266 dead or injured Americans so far and it does not include the numbers your governments are inflicting on you, if you don’t live in America.
See Electron Microscope studies of blood at cellular level and the nanotechnology to be found there: https://www.drrobertyoung.com/post/the-mindset-of-dr-robert-young-on-blood-clots-pleomorphism-the-jibby-jab-t-cruzi-h-vulgaris?postId=3704e561-ae34-4a1b-98f5-ded468531d93&utm_campaign=5003d1c8-c42a-4ec7-837d-42a0d74c29a2&utm_source=so&utm_medium=mail&utm_content=ca364f20-ac6e-41bf-9814-33ce0b02ff77&cid=8bec1d4c-3773-415a-83c2-1694daa095a4
The US Department of Defense (US DoD) has had a dominant role in the response to the SARS-CoV-2 virus and the US DoD took charge of the Covid vaccine funding, development and testing from the very start of the perceived threat in early 2020 and in the development, and distribution of the Covid 19 vaccines, a fact hidden from the general public. In those processes many standard steps and procedures, otherwise required for pharmaceutical products, were omitted or circumvented.
The US FDA’s website (FDA, 2020) reveals that the United States Department of Defence (DoD) has been in full control of the Covid Vaccine development program since its beginning. The DoD has been responsible for development, manufacturing, clinical trials, quality assurance, distribution and administration, since that time (FDA, 2020; Rees and Latypova, 2022; KEI, 2022; Medical Defense Consortium, 2022; Rees, 2022). The major pharmaceutical companies have been involved as “Project Coordination Teams” effectively performing as subcontractors to the DoD. The Chief Operating Officer for (Trump’s) Warp Speed vaccine program is the US Department of Defence, and the Chief Science Advisor is the US Department of Health and Human Services (HHS).
Definition of these vaccines as “countermeasures” rather than therapeutic agents has permitted their expedited progression to emergency use authorisation and widespread rollouts. Many adverse consequences have been the outcome of this secret military response to a public health matter. Excepts From: Phillip Altman’s Essay he is Pharmacologist and Clinical trial and drug regulatory affairs consultant in Melbourne, Australia and Brownstone Institute
Synthetic mRNA vaccines – they were never, ever, intended to kill Covid anything, because viral infections attack your breathing apparatus, which is your FIRST closed system in itself and the mRNA vaccines injected into your blood which kid the brain blood barrier into thinking they are safe, is your SECOND closed system too – so taking anything by mouth – well that goes down into your stomach acid, where it is broken down into its elements, which your body does not need and expelled in your piss and shit is your THIRD closed system, too and they all interact to give us life, while not having internal access to each other and interact in the body, but differently – which is why cures taken by mouth, are just another way to skim you for your money and more mumbo jumbo.
The obvious question then is, for the vaccinated – is what to do about the installed nanotechnology which is far ahead of our technical ability – how to explain that.
So let’s go with aircraft engines:
Up to the end of World War 2 (1939-1945) all aircraft were powered by piston engine technology and it was only towards the end of World War 2 (1944) that the jet engine was invented, in its infancy and because it delivered more thrust, provided faster speeds, took up less space, than piston engine aircraft – it eventually became our main mode of aircraft propulsion.
So with the nanotechnology in 2023 – we are at the beginning of World War 2 as above and the vaccines are to become jet engines, way beyond our understanding or mechanical ability to create in now, because we didn’t have the specialized equipment, or the engineering capability to create them and won’t reach that level of capability for at least 10 years forwards from today, let’s see 2033 and here we have them being injected with the Pfizer’s (and other vaccines) from January 2021 – do you see the conundrum?
Bottom line: The CDC set American’s up to be exterminated at over 1,000 per day, although the records show in Feb and March 2021, the deaths and injury rates were far higher than previously forecast and this does not take into account their impact on those countries outside America. Injured read should have, but next time around finish the job
So, on the one hand we have the vaccines way to save life, which exterminate with documented facts confirming this and the CDC’s expectation of that happening – so obviously – we need some other way which works 100% and had injured or killed nobody that I know of, so far that is really easy to do and which the poorest person to the richest can do with simple materials to hand – I sent a copy of the below cure to President Trump before he introduced the vaccines:
30 years never had a virus or bacteria infection = never ill: Mix one heaped teaspoon of salt in a mug of clean warm water – cup a hand and in stages, sniff or snort the mugful up your nose spitting out anything which comes down into your mouth. If burning sensation, you have a virus and the salt solution is disinfecting it, so wait 2-3 minutes until burning sensation goes away, then blow out your nose on toilet paper and flush away, washing your hands afterwards. Do my free salt water cure morning, noon, night or more often if you want, until it feels like you are flushing with water only – job done. 3 minutes idea to job done – simple. No virus, no Covid or Long Covid in your head possible. You cannot catch Covid, you have to catch a Coronavirus first and let it become Covid in the nasal passages of your head, later transported down into your body in the one liter of snot, or mucus, we each produce daily – the engine oil of the body. Vaccines – what for – I never have any. My method is like using a fire hose to put out a fire. It takes 3 minutes to prepare and do with salt and clean water and over the 30 years I and others have been doing it, it has NOT killed or injured ONE PERSON, unlike those synthetic mRNA vaccines, ALSO verified by Alberta Medical University – Canada. Do it – you will be amazed at how quickly it destroys colds and flu in the nasal passages of your head. No infection, no Covid possible. Spread the word to everyone please. Neti pots are like using a garden sprinkler to put out a house fire. your life, your choice!! AND free!!