Prediction: The Bivalent Boosters Will Become the New Primary Two-Dose Series
What does that mean?
The FDA is holding yet another “Vaccines and Related Biological Products Advisory Committee” (VRBPAC) virtual meeting on January 26th, 2023. The intent of the committee is “to discuss the future vaccination regimens addressing COVID-19.”1 (Emphasis added)
Link to live video and details here.
I, along with a few others, predict that the current Bivalent boosters will become the new primary two-dose series. Here’s why…
Currently, the original monovalent’s are no longer in production.
Whether they are out of stock or simply outdated… it doesn’t change the fact that you cannot find the monovalent version in any U.S. pharmacy.
Why does this matter?
Well, consider for a moment that you’ve made it this long without injecting yourself with mRNA but your employer is demanding that you get “vaccinated.” How would even you start? The primary series is not available. You would have to start with the boosters. There is no other option. I just checked with my local pharmacy last week. The following photo is all they had:
Note: This is a Bivalent booster. It is for the Original and Omicron BA.4/BA.5. It’s still only available under Emergency Use Authorization.
What is the Primary Series?
Simply put, it’s the two dose regimen before the boosters. Here’s what the CDC says about the Primary Series Vaccination
Primary series vaccination
For primary series vaccination, three monovalent COVID-19 vaccines (listed in alphabetical order by manufacturer), are recommended: Moderna, Novavax, and Pfizer-BioNTech.
Bivalent mRNA vaccines are not authorized at this time for primary series doses with the following exception: children ages 6 months–4 years who receive 2 primary series doses of a monovalent Pfizer-BioNTech vaccine should receive a bivalent Pfizer-BioNTech vaccine as their third primary series dose.
Vaccine products made by the same manufacturer should be used for all doses of the primary series (see Interchangeability of COVID-19 vaccine products)
Right.
Two things should stand out:
The monovalent (that no longer exist) are still the primary series.
Bivalent mRNA vaccines are not authorized for primary series “at this time.”
USG and DoD Contracts
The same government that illegally mandated the use of these unlicensed EUA injections is the same government that is spending billions on procurement.
The U.S. Government (USG) and Dept of Defense (DoD) spent a combined $4.94 billion (summer 2022) on 170 million mRNA booster doses, with option to procure up to 600 million to meet demand.
Here’s the DoD Press Release:
Links: DoD Press Release ; HHS Press Release
A couple things should stand out.
Up to 600 million doses to meet demand? The current U.S. population sits at about 331 million. Why in the world would we need 600 million boosters? How many times does the administration think people are going to line up for the bivalent booster?
Unless of course the plan is to make the bivalents the new primary two-dose series… then the math adds up.
Also look at that last paragraph. Who is leading the effort? The Executive Office for Chemical, Biological, Radiological, and Nuclear Defense (CBRND) in partnership with HHS’s Biomedical Advanced Research and Development Authority (BARDA).
Rather than explain these agencies in depth (I am working on a separate article for that), I am going to show you how they are all connected:
PHEMC stands for The Public Health Emergency Medical Countermeasures Enterprise.2 It was established in 2006 by Public Law 109-417.
The PHEMCE is a coordinated, interagency effort led by the ASPR; it includes three HHS internal agencies, the NIH, FDA, and CDC, as well as ex officio participation of other HHS agencies and Federal interagency partners, particularly DHS, the Department of Defense (DOD), and the the Department of Veterans Affairs (VA). BARDA (previously OPHEMC) manages PHEMCE operations in support of this mission.
The mission of PHEMCE is to coordinate research, development, acquisition and deployment of medical countermeasures for public emergencies (hence the need to continue to renew the emergency) that are, “naturally occurring, deliberately induced, or accidental events.”3 Their current goals can be found here.
Long story short, the Covid “vaccines” are part of the PHEMCE acquisitions and deployment program, therefore it makes sense that the vaccines are purchased by USG and DoD. Especially since the “vaccines” are still unlicensed EUA. Only the government can purchase medical countermeasures that are EUA.
What doesn’t make sense is how the FDA can arbitrarily can turn the boosters into the primary series, unless of course you understand what’s truly happening and the relationships established by PHEMCE. The FDA is part of the PHEMCE umbrella alongside the CDC, NIH and DoD.
Continued Covid Emergency
On January 11th, 2023, the HHS Secretary renewed the Covid Emergency Declaration for the 12th time. The Emergency Declaration is the legal basis that is required in order to grant emergency use authorizations.
With USG and DoD spending nearly $5 billion on 170 million mRNA doses under emergency use authorization, it is hardly a surprise that the emergency declaration continues to this day.
By the way, the January 11th declaration is the 2nd time HHS renewed the emergency since the press release announcing the bivalent purchase in July 2022.
Until a “licensed” product is produced the emergency declarations will continue.
Conclusion
The monovalent vaccines are no longer being produced in the U.S.
HHS/DoD purchased 170 million bivalent EUA doses (up to 600 million) for $4.94 billion.
HHS continues to renew the emergency declarations for covid as the legal basis to keep pushing the EUA products.
There are no licensed vaccines available in the U.S.
The Bivalent boosters will replace the monovalent as the original primary two-dose series.
“Original and Omicron BA.4/BA.5”
Afterthought
If there were any questions regarding the integrity and autonomy of the FDA, you can put them out of your head with ease. Do you recall the two FDA regulators who resigned during summer of 2021?
Let me refresh your memory. If you search for “Two Top FDA Vaccine Regulators Resign” you’ll find various reputable news outlets reporting on Marion Gruber’s and Phil Krause’s untimely departure.
Marion Gruber was the director of the FDA’s Office of Vaccines Research and Review.
Phil Krause was the deputy director.
These are positions at FDA’s Center for Biologics Evaluations and Research (CBER). CBER is the center within FDA that regulates biological products for human use under applicable federal laws, including the Public Health Service Act and the Federal Food, Drug and Cosmetic Act.4
Reason for resignation? Biden’s booster plan:
“The administration’s booster plan; it wasn’t the FDA’s booster plan,” University of Pennsylvania infectious disease expert Paul Offit, who serves on the FDA’s vaccine advisory committee, told Politico. “The administration has kind of backed themselves up against the wall a little bit here.”
There are no shortage of these types of quotes from inside sources. Here’s another one:
the two officials were at odds with the FDA’s top vaccine official, Peter Marks, and were discontented over the roles of the Centers for Disease Control and Prevention…
And one more for good measure:
Some public health experts have said the administration’s booster shot announcement, which did include a caveat that the F.D.A. would first have to authorize such shots, undermined the agency’s responsibility to make that assessment on its own schedule, led by career scientists. Since Mr. Biden took office in January, the White House has made a point of saying it would not influence the F.D.A.’s work.
If and when the FDA approves the bivalent boosters as the primary doses, it simply means one thing and something we’ve known all along: The FDA is no longer a regulatory agency. Rather, they are a front organization doing the bidding of BigPharma and the Executive Branch under the protection of the PHEMC Enterprise.
If you read nothing about the resignations, at least read the following:
Officials within the FDA were stunned by the news that Gruber and Krause were leaving the agency. One described it as a “big loss” for the FDA and noted that it caught leadership off guard. CNN has reported that morale at the agency, which still has no permanent leadership, has been eroded by the intense workload brought on by the pandemic.
Though Biden’s political aides have stressed their booster rollout plan relies entirely on decisions by the FDA and CDC, there is concern that they are publicly pre-judging the determination before all the data has been thoroughly reviewed. The announcement in mid-August that was tied to a specific date baffled multiple government health officials.
Zients defended the Biden administration’s decision, however, citing the involvement of Woodcock in the decision.
“The booster decision, which you referenced, as we’ve talked about – that decision was made by and announced by the nation’s leading public health officials including Dr. Walensky, Dr. Fauci, Surgeon General Vivek Murthy, Dr. Janet Woodcock, the FDA Acting Commissioner, Dr. Francis Collins, Dr. Kessler and others,” he said.
Source: https://www.cnn.com/2021/08/31/health/fda-vaccine-officials-step-down/index.html
https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-january-26-2023-meeting-announcement
https://www.medicalcountermeasures.gov/BARDA/documents/bioshieldannualreport2006.pdf
https://www.medicalcountermeasures.gov/BARDA/documents/bioshieldannualreport2006.pdf
https://www.fda.gov/about-fda/fda-organization/center-biologics-evaluation-and-research-cber
just in case you thought viruses exist. our ancestors knew 150 years ago. we've been so dumbed down.
NEVER in the history of mankind has injecting poisons into your body given you better health.Quite the opposite. They’ve ALL maimed and killed. Read and learn the history of this barbaric act:
The Poisoned Needle: Suppressed Facts About Vaccinations https://a.co/d/cfvx9Q6 https://rumble.com/v1wxx5q-nephrologist-dr-suzanne-humphries-vaccines-have-never-been-safe.html
Dissolving Illusions: Disease, Vaccines, and The Forgotten History https://a.co/d/coVuit4
- George William Winterburn, PhD, MD, The Value of Vaccination: A Non-partisan Review of Its History and Results, 1886 https://archive.org/details/64940640R.nlm.nih.gov
- History and Pathology of Vaccination, Edgar R. Crookshank, 1889 https://archive.org/details/historypathology02crooiala
- Charles Creighton, Jenner and Vaccination. A Strange Chapter of Medical History, 1889 https://archive.org/details/b21357067
There are many others, they’re just a few.Finding the truth isn’t that hard.But you do have to get off your butt and turn off the tube and read.
We’ve known for well over 150 years the concept of vaccination is a fraud concept.And the criminals that pose as our elected officials are in on the take and are raking in millions, and will NEVER stop the madness that is called vaccination.And neither will doctors who are being PAID handsomely for jabbing and lying to their trusting patients.If you’ve been jabbed then your death will be influenced by and/or directly caused by said jab.People should quit thinking it’s coincidence. That’s propaganda talk.And yet the populace of today (being dumbed down by design) have their heads buried in the sand/phones and believe the corrupt media’s story of blaming these deaths on everything else under the sun except the obvious. What a pity.
If you avoided the vaxx til now, good for you. They've made it near impossible to "catch up", even if you wanted.
And yes, it's now a permanent "emergency".