Posted on 12/25/2023 10:21:58 AM PST by Angelino97
Are you that stupid or do you just play a fool on FR?
Fauci, is this you?
I must admit, most people did Nat Zee that coming.
AndyJackson wrote: “Fauci, is this you?”
Don’t you get tired of being played the fool by the anti-vaxxers?
I am sure the folks tried for violating the Nuremburg code after WWII should have tried your “not international law” defense.
Lol.
“The COVID vaccines are fully approved”
What in the world is that supposed to mean?
Mengele “fully approved” all of his “cures” as well.
“Fauci, is this you?”
He sounds vaccinated.
cgbg wrote: “What in the world is that supposed to mean?”
Fully approved as in no longer under an Emergency Use Authorization.
Emergency Use Authorization Vs. Full FDA Approval: What’s the Difference?
BY CARRIE MACMILLAN MARCH 7, 2022
A primer on the two and why it matters, especially when it
comes to COVID-19 vaccines.
What does the normal full FDA approval process entail?
The FDA’s full approval process varies depending on the product. For vaccines and therapeutics (a treatment, therapy, or drug), companies file what is called a “biologics license application”—or a BLA.
But before filing an application for a vaccine BLA, development and testing must follow a standard set of steps. Here is the typical process:
Research and discovery stage: Scientists conduct laboratory research—often in animals—to test their vaccine candidate.
Pre-clinical stage: Researchers perform additional lab testing in animals to gather information on how the vaccine works and whether it’s likely to be safe and perform well in humans.
Clinical development stage: When studies are ready to begin in humans, the company compiles results of their pre-clinical testing and information about the manufacturing technology, and submits them to the FDA for assessment. If all looks good, the FDA green-lights clinical trials, which include four phases:
Phase I: Small groups of volunteers receive the trial vaccine to gather safety data. Generally, this involves about 20 to 100 volunteers.
Phase II: If there are no safety concerns from Phase I, more people (in the hundreds), with varying health statuses and from different demographic groups, are given various dosages.
Phase III: The vaccine is given to thousands of people and tested for efficacy (the percentage reduction of disease in people who received the trial vaccine versus those who received a placebo), safety, and immune response.
Phase IV: Monitoring trials (more below)
Assessment of manufacturing stage: While clinical trials are being conducted, FDA investigators review the manufacturing processes. This step includes visits to the facility to ensure it operates in compliance with FDA regulations.
Seeking approval stage: Once clinical trials are completed—and if the manufacturing process in place demonstrates that the vaccine can be produced reliably and consistently—the company submits its BLA, containing all the data from steps above, to the FDA.
Full approval granted stage: If the vaccine is approved (or licensed, as it is also known), the company can market it for use in the population for which it was approved.
To decide on approval, FDA scientists evaluate all of the data and information in the BLA. Sometimes, the agency seeks input from its Vaccines and Related Biological Products Advisory Committee (VRBPAC)—a group of outside, independent experts from scientific and public health fields. (The FDA considers input from the committee, but is not bound by its recommendations.
Continued oversight stage: After approving a vaccine, the FDA continues to oversee its production and monitor its safety. This includes periodic facility inspections. There are also Phase IV trials, which are optional, ongoing studies to identify uncommon adverse events and long-term complications, as well as to monitor effectiveness. Vaccines are also monitored by various surveillance systems, including the Vaccine Adverse Event Reporting System (VAERS), which accepts and analyzes reports of possible health problems after vaccination.
https://www.yalemedicine.org/news/what-does-eua-mean
IOW, it is inappropriate to call a fully approved vaccine experimental.
Why drag Menegle into this?
You trust “authority figures”.
I do not.
Mengele was an authority figure for his regime.
“Approval” means nothing—when those who give the approval are corrupt and evil.
Experimental emergency use authorization isn’t the same as “approved”.
cgbg wrote: “You trust “authority figures”. I do not.”
Instead, you trust grifters like Malone, Mercola, RFKjr, McCullough, etc.
DesertRhino wrote: “Experimental emergency use authorization isn’t the same as “approved”.”
Who said it was? The vaccines are fully approved. The EUA is past history.
Pfizer CEO condemns Pisser CEOs.
No. He doesn't "trust" them. He works for them.
The best thing to do with paid shills is to ignore them. He might as well be a bot.
The hypocrisy—it burns.
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