Guest Post by Steve Kirsch
It’s all about liability. It will magically become available when the vaccine for children is fully approved, not before.
The reason Comirnaty isn’t available is because those shots would expose the company to liability since the fully-licensed product doesn’t have the liability waiver of the EUA product.
But once the Pfizer vaccine is fully approved in kids, then Pfizer gets liability waiver on all age groups due to a “feature” in federal law for child vaccines (NCVIA). At that time, they are done. They can market the COVID vaccine products under full approval for all age groups and face no liability when it kills or disables you.
This is why they are focused on the kids. This is why there is a reformulation at a 1/3 dose and they changed the buffer and the storage conditions (low temperatures not required). All of these will weaken the protection, but result in a safer vaccine (since it is ineffective).
But for the clinical trials on the 5-11 year olds, they did not use the formulation they approved in the meeting. This is known as bait and switch. So they used a more effective vaccine to show efficacy (in the trials they completed), then they get the FDA to approve the drug but with a change in formulation, then the product product with the new buffer will go out to the public with the lower efficacy, but better safety. This is because they don’t want to jeopardize any adverse events happening until they are fully approved. So they basically use formula 1 for safety, get approval for formula 2 (safer, less effective), then roll out formula 2 under EUA.
They also arrange with the FDA and CDC to make sure no early treatment drugs get approved or recommended. This is why there is no movement on fluvoxamine, ivermectin, etc. since that would blow the EUA. Fluvoxamine is the best drug ever for COVID with a mortality reduction of 12X when taken early. It’s the best drug to date for COVID, but the CDC and NIH are deliberately burying it until the vaccines are fully approved. Then they’ll say, “ok, we have all the data.”
So at the end, Pfizer gets a fully approved vaccine with full liability protection. At that time, then the NIH can recognize other treatments.
This is how it is wired to go. Let’s be honest about it.
This is why nobody wants to debate our team about what is going on.
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Comirnaty, it’s got electrolytes !
” Under the cover of vaccinating people, we are really preparing to tag and track people. The once free nations of the West are testing a new authoritarian system of total control under the guise of public health. Just look at Australia or New Zealand or Canada or Italy to see how basic civil rights have been suspended indefinitely and a pseudo-medical tyranny has been installed. The Great Reset is being implemented with the lie that it’s all about “protecting your health.” Our military and intelligence agencies are not confronting China — they’re copying China. A totalitarian nightmare is being imported into free countries through surveillance technologies.
You don’t have to be a Christian to understand that such technology will be used to build a global surveillance state. The vaccine mandates have already led to vaccine passports. The vaccine passports are basically QR codes to track you by connecting to your smartphone. This will inevitably lead very soon to biometric ID embedded into your body. You won’t be able to enter restaurants or buy groceries or go to work without it. As the Bible says: no one will be able to buy or sell anything except those that have the mark. You will know the mark by its name, which is the name of the beast: the enemy of all mankind who, before he fell, was an angel of light named Lucifer. That’s why “Luciferase” should send a chill down your spine.”
https://emeralddb3.substack.com/p/what-is-luciferase
Speaking of Italy :
https://www.zerohedge.com/markets/italian-institute-health-drastically-reduces-its-official-covid-death-toll-number
This was news last year. I posted an article saying this same thing, whilst MyGirl and Chris Martenson were running around screaming for the government to do something otherwise we’re all going to die. The truth is slow to seep into the craniums of the agenda driven profiteers and the less astute.
Why have so many coronavirus patients died in Italy?
The country’s high death toll is due to an ageing population, overstretched health system and the way fatalities are reported
By
Sarah Newey,
GLOBAL HEALTH SECURITY CORRESPONDENT
23 March 2020 • 4:55pm
A study in JAMA this week found that almost 40 per cent of infections and 87 per cent of deaths in the country have been in patients over 70 years old.
And according to modelling by Imperial College, London the majority of this age group are likely to need critical hospital care – including 80 per cent of 80-somethings – putting immense pressure on the health system.
But Prof Ricciardi added that Italy’s death rate may also appear high because of how doctors record fatalities.
https://www.telegraph.co.uk/global-health/science-and-disease/have-many-coronavirus-patients-died-italy/
Comirnaty, it’s got electrolytes !
LOL
The Immune System Mutilator!
This junk isn’t the mark of the beast but it is a great trial run to indoctrinate the people to obey without question. I always wondered why people would take the mark mentioned in Revelation but I now see the virtue signaler will fight to be first in line. Idiots all. As my final thought, never argue with an idiot. They will drag you down to their level and beat you with experience.
If comirnasty gets approval for use inside the US, modernasty and J&J are out of the vaccine biz on day 1
Rest assured that key individuals in Congress, the NIH, and the CDC will be long Pfizer stock, and short Moderna and J&J stock in the days leading up to that announcement.
The corruption, collusion, and propaganda mechanisms in play here are nothing new to the FDA-Pharma joint-venture. All of these same things happened just recently in the Oxycontin mass murders.
Multiple legal cases are still in the system that should have illuminated the deep criminal dysfunction (or function, depending on your perspective) of the FDA as anything but a regulatory capture and bizdev arm of pharma. The opiates story was finally unfolding right as covid was conjured and yet the public consciousness was sent warp-speed into a deep coma of FDA-Pharma greatness with the whole not-vaccine fraud.
The entirety of the media was not only derelict in failing to bring light to the evil Oxy roll-out but then doubled-down to sanctify these evil institutions as our one and only savior from certain covid death. The FDA-Pharma cabal should have been at the hangman’s noose but instead was made into the alter of holy moral sacrament where now we are to place our children.
The lies are stacked so deep and the corruption so codified there is no way to investigate and prosecute these crimes against humanity in such a way to bring any lasting change or redress for the masses of dead, injured, and otherwise subjected to this web of lies. Especially in light of at the same obvious patterns in the Oxy crime syndicate being adjudicated on the heels of this arguably more egregious and obvious crime.
The facts to keep in mind. Pharma is the largest money source in media advertising. Pharma is the largest money source in political lobbying in the US. Pharma is largely a “self-regulating” industry in which the FDA’s core functions are to facilitate product development, not to protect citizens from harm. Remedies and enforcement are all after harm has been done. And largely a function of financial negotiation.
The only way to change any of this is to put faces on the crimes, top to bottom, and “prosecute “. Another sea of lawyers and file boxes will do nothing. Just as Oxy still rages and our people still die every day from the long war on our way of life. This is all bigger than mere trickery and greed.
any parent that allows their kid to be vaxxed isguilty of homicide.
Thank you for this enlightening article.
Question..
In your statement above
“So they basically use formula 1 for safety, get approval for formula 2 (safer, less effective), then roll out formula 2 under EUA.” – shouldn’t this be “so they basically use formula 1 for EFFICACY, …”?
“This is because they don’t want to jeopardize any adverse events happening until they are fully approved. So they basically use formula 1 for safety, get approval for formula 2 (safer, less effective), then roll out formula 2 under EUA.” – so the vaccines that the public is now getting (under EUA) are less effective but safer – this is done to have as fewer adverse events as possible (for full approval)? But once the vaccines are fully approved, they will use formula 1 again – not safer but more effective as they are not concerned any more about safety because they now face zero liability?
What are the pros and cons of using formula 1 and formula 2 (for pharma and the general public) after the vaccines have been fully approved?
Thank you for clarifying.
Richard Sia