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Vaccine FAILURE, on every level.

Well not there not even waiting to test on people before releasing to people

Omicron Boosters Are Coming, But They Weren’t Tested on People. Here’s What You Need to Know​

Not surprising... they already allowed other shots based on opinions and politics!
 
My job finally stopped the weekly testing, so I've got that going for me. Which is nice.
My wife's finally told them yesterday they no longer needed weekly tests as well. I was waiting to not get my contract renewed/fired also but the state mandate for healthcare providers was finally changed. I had been just ignoring the bad boy emails that I needed to be be vaxxed and boosted for the last year. Good thing for lazy government workers I guess.
 
Not surprising... they already allowed other shots based on opinions and politics!
heard rumblings about a monkeypox vaccine being out and available
ain't that shit only like 5mo old?
Very rigorous testing, I'm sure
 
Well not there not even waiting to test on people before releasing to people

Omicron Boosters Are Coming, But They Weren’t Tested on People. Here’s What You Need to Know​

Somewhere over the last year or two, I remember a clip, might of been Gates. Where it was stated (paraphrased) “once the mrna platform was approved. They wouldn’t need trials for future variants because the necessary changes were just a line of code”

Scared yet?
 
Just another friendly reminder when you hear 'authorized' they still mean emergency use only. If you still think this is an emergency, go take part in the experiment.

That was the shit about any jab or lose your job talk. The real vaccine wasn't even out there to be offered to keep your job.
 
Somewhere over the last year or two, I remember a clip, might of been Gates. Where it was stated (paraphrased) “once the mrna platform was approved. They wouldn’t need trials for future variants because the necessary changes were just a line of code”

Scared yet?
Just wait until they figure out how to make vaccines transmittable from person to person.
 
Just another friendly reminder when you hear 'authorized' they still mean emergency use only. If you still think this is an emergency, go take part in the experiment.

That was the shit about any jab or lose your job talk. The real vaccine wasn't even out there to be offered to keep your job.

Do you (or anybody) know if the actual Comirnaty / approved one is even distributed yet, or are they still running on the version that carries no liability under the EUA?
 

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Do you (or anybody) know if the actual Comirnaty / approved one is even distributed yet, or are they still running on the version that carries no liability under the EUA?
the comirnaty one was never produced for distribution, and will not be, probably because it would be throwing away the ridiculous protections given by the EUA

the biontech one "is totally approved really we actually tested it this time guys we need to fill the cave with molten lead I'm super cereal"
I don't think its FDA approval affects their immunity from litigation on that one though.
 
I have read many articles on that. It’s truly scary. Who knows, the latest boosters could be a trial for just that.
Is what they mean by "vaccine shedding"? I never wrapped my head around that one. Sounded a little out there.
 
And one more with the line “to help protect naive populations”

 
A friend of mine went into the ER for shortness of breath and trouble breathing last week. Ended up in the icu for blood clots. I know he got the first round, he posted the card online when he did. He’s out now and doing better but still can’t walk very far without getting winded.
 
There is a second wave of "the vid " (or whatever) currently making its way through our shop/office. Everyone that is catching it has had the jab.
We think the wife had it (mild symtoms, no test)... She's got the first jab...
Just sayin'..
 
Every person I have talked to in real life that has been jabbed says they don't plan on any more boosters.
I ask why and their answers are all the same. Because even after the jab, they still got it so they feel it simply doesn't work and there is no point.
 
Do you (or anybody) know if the actual Comirnaty / approved one is even distributed yet, or are they still running on the version that carries no liability under the EUA?
I researched it a couple weeks ago and they are claiming it's the same even though the bottles don't say it. So more BS

A lot of different links make the same claim. This one is rich:
"[1] The licensed vaccine has the same formulation as the EUA-authorized vaccine and the products can be used interchangeably to provide the vaccination series without presenting any safety or effectiveness concerns. The products are legally distinct with certain differences that do not impact safety or effectiveness."

...Since the branded and unbranded vials of vaccines are chemically identical, despite being legally distinct.....




You asked, we answered: Are Pfizer's Comirnaty and BioNTech COVID-19 vaccines the same or different?


.Question:I've heard that the U.S. Food and Drug Administration (FDA) said Pfizer's Comirnaty and BioNTech formulas are distinctly different in their vaccine approval letter. Is that true?Answer from infectious diseases pharmacist Bryan Alexander, PharmD:No. In terms of what is contained inside the vial of each they are identical. Pfizer and BioNTech simply formally "branded" or named their vaccine Comirnaty. BioNTech is the German biotechnology company that partnered with Pfizer in bringing this COVID-19 vaccine to market. "Pfizer Comirnaty" and "Pfizer BioNTech COVID-19 vaccine" are biologically and chemically the same thing.The confusion stems from this section of the FDA's Comirnaty Vaccine Information for Recipients and Caregivers sheet: "[1] The licensed vaccine has the same formulation as the EUA-authorized vaccine and the products can be used interchangeably to provide the vaccination series without presenting any safety or effectiveness concerns. The products are legally distinct with certain differences that do not impact safety or effectiveness."The FDA desires to have a single, combined Vaccine Information Sheet. A single sheet keeps things simple for the people administering and receiving the vaccines. Since the branded and unbranded vials of vaccines are chemically identical, despite being legally distinct, this information must be included.The FDA's approval letter outlines rules Pfizer and BioNTech must follow to maintain full approval for people ages 16 and older. It also explains how the companies can earn full FDA approval for people 16 and under. These rules include completing a series of studies focusing on people under age 16 to obtain full approval in this population. These studies are already underway. The companies must also maintain post-approval studies for those over 16 to monitor the vaccine's safety and efficacy. These studies are a standard part of the post-approval process that most drugs must go through to maintain full FDA approval. This list of required studies does not mean the vaccine is not fully approved. Why is the name just showing up now?Medications often have a scientific name or number throughout the research and development process and are given a brand name upon FDA approval.In a joint media statement released by Pfizer and BioNTech on Dec. 21, 2020, the companies explained, "The vaccine will be marketed in the EU under the brand name COMIRNATY, which represents a combination of the terms COVID-19, mRNA, community and immunity, to highlight the first authorization of a messenger RNA (mRNA) vaccine…"Pfizer and BioNTech received permission to market the vaccine as Comirnaty in the United States within the FDA's recent approval. The FDA's approval letter states, "You may label your product with the proprietary name, Comirnaty, and market it in 2.0 mL glass vials, in packages of 25 and 195 vials."Comirnaty, also commonly referred to as the Pfizer COVID-19 vaccine, received final FDA approval for people age 16 and older on Aug. 23.
 
The product is the same. One is FDA approved (consumer use). One is FDA authorized (emergency use). The legal/regulatory treatment of the product is different between those two designations.
 
The product is the same. One is FDA approved (consumer use). One is FDA authorized (emergency use). The legal/regulatory treatment of the product is different between those two designations.
It can't be. The extent of the damage caused and recorded in VAERS would keep the vax from being FDA approved. That is why it continues to be authorized for emergency use only.
 
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