Interesting...the phases.
Phase 4 reads
"Phase IV clinical trials happen after the FDA has approved medication. This phase involves thousands of participants and can last for many years."
https://www.healthline.com/health/clinical-trial-phases#phase-iv
When did these vaccines get approved by the FDA? (yes, that is a loaded question).
So essentially, all you could get back to me with, was proof that the vaccines were administered to our population after by passing our normal procedures.
Because, these vaccines did not follow the established route.
Notably,
70% of medications move on to phase II 33% of medications move to phase III 28% of medications move to phase IV.
Meaning if you have 1,000 experimental vaccines, 700 will make it to phase II. Out of which only 231 will make it to phase III. Out of which 64 will make it to phase IV.
Phase II "Investigators monitor participants for several months or years"
Phase III "this phase can last for several years."
all of these procedures...down the drain.
The answer you’re looking for is “we don’t have time for established routes as there is a pandemic occurring and the planet would collapse if we stuck to current established routes”
Standard practice is 10 years and uber safe. However we don’t have 10 years for this one particular vaccine, but we do have many years of studies on the effects of similar variants.
Pitting the known risks of the mRNA vaccines against the known risk of the COVID virus, the vaccines win by orders of magnitude in terms of calculated risk.
If you have concerns, put numbers on them.
So what you are saying, is that is fine that we did not follow standard practice given the circumstances? Right?
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