Dr. Robert Malone, the inventor of the mRNA vaccine technology, joined Bannon’s War Room on Tuesday to discuss the Covid vaccine’s FDA ‘approval status.’
According to Dr.Malone, it appears that the Pfizer vaccine is not fully approved and they were only issued an extension under the Emergency Use Authorization (EUA), which grants them full liability protection.
The FDA approval of the Biologics License Application (BLA) is actually in regards to the Comirnaty vaccine that is “substantially similar, but not necessarily identical,” and has yet to be manufactured.
“It’s [Comirnaty] absolutely not available. So, the little trick that they’ve done here is, they have issued two separate letters for two separate vaccines. The Pfizer vaccine which is what is currently available, is still under emergency use authorization.” – Dr. Malone said on War Room
The FDA deceptively sent out two letters regarding the separate jabs, confusing the public and aiding in the fake-news media’s manipulation.
The Pfizer letter explains how, rather than granting full approval to both, they are extending the EUA so Pfizer’s vaccine can be supplied when there is ‘limited or no supply’ of the Comirnaty vaccine.
From the Pfizer Letter (Full document):
On August 23, 2021, having concluded that revising this EUA is appropriate to protect the public health or safety under section 564(g)(2) of the Act, FDA is reissuing the August 12, 2021 letter of authorization in its entirety with revisions incorporated to clarify that the EUA will remain in place for the Pfizer-BioNTech COVID-19 vaccine for the previously-authorized indication and uses, and to authorize use of COMIRNATY (COVID-19 Vaccine, mRNA) under this EUA for certain uses that are not included in the approved BLA.
Comirnaty (BioNTech) is an almost identical product to the Pfizer vaccine, but differs in legality. Since the Comirnaty was given full FDA approval it assumes legal responsibilities that may arise, this differs from the Pfizer vaccine which is still listed under EUA providing them with legal immunity.
So why not just get the FDA approved Comirnaty jab?
Well first of all, it’s not available. Like mentioned above, the product has not been manufactured, and now with Pfizer being granted the extended EUA, they will still be using the Pfizer jab in place of the nonexistent Comirnaty shot.
See the bait and switch there? This is all just a front to get you to take unapproved Pfizer shot, while shielding the company from legal responsibility.
“It’s called Comirnaty… and its not yet available, they haven’t started manufacturing it or labeling it, and that’s the one that the liability waiver will no longer apply to. So the one that’s actually licensed is not yet available, and when it does become available it will no longer have the liability shield. In the interim, the one that does have the liability shield is the Pfizer product and that’s what is currently available – and its still under emergency use authorization.” – Dr. Malone added.
If you are thinking of waiting for a fully approved Covid vaccine, don’t hold your breath…
Why would Big Pharma spend the money to manufacture and distribute another vaccine, that could easily get them into legal trouble, when they can keep jabbing you with Pfizer shot that is legally protected? (Especially when the bootlicking media deceives the public by propagating it as being FDA approved.)
The scumbags at Pfizer and BioNTech don’t care about protecting you against the China virus in the least. According to what Dr. Malone has found, unless they are given full immunity, they will not supply the vaccine at all.
“That [Emergency use authorization] will keep Pfizer indemnified because that’s something that Pfizer has been seeking in all of their worldwide contracts with other governments – is full indemnification. They will not sell you vaccine, unless you waive liability if you are a government head of state.”
If you need another reason to hold off on the jab, look no further. According to the COMIRNATY letter, multiple clinical studies that need to be conducted for full approval won’t be completed for up to five years. The FDA also acknowledges the increased risks of adverse reactions such as Myocarditis, requiring a 5 year follow up report from the company.
Dr Malone also graciously took the time to put together a concise 2 page outline on the letters that goes over them in detail.
Take a look here:
Here is the Video of Dr. Malone’s interview on Steve Bannon’s War Room:
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