I have no idea where you got the idea that I supported mandated vaccinations. One would think that the anti-vaxxers would appreciate knowing that once these vaccines are approved they can be mandated.
Ha! Sure, you don’t.
And, contridict yourself much? (A: Yes.) Why on God’s green Earth would anyone who questions these unproven, experimental agents appreciate ‘knowing these shots could be mandated’????
Lets refresh your memory, FRVP....
DugwayDeepState said....
...Pfizer has completed the lengthy part of the process. Thousands participated in the phase 1/2/3 trials. Hundreds of thousands of doses have been administered. The data clearly shows the vaccines are safe and effective. Pfizer/Moderna are about to submit their applications for full Approval. It’s been estimated that full Approval might be granted in six months.
(WRONG-O....and, you were corrected by ransomnote, and SEVERAL others, on that fib, McGee.)
Now, here’s why that could be upsetting to the anti-vaxxer crowd.
First, it would take away one of their more effective arguments.
Second, once the vaccines are fully Approved, then governments can mandate vaccination.....
https://freerepublic.com/focus/news/3955432/posts?page=32#32
Upsetting to the ‘anti-vaxxer’ crowd. (Only, many have told you, REPEATEDLY, that we’re not anti-vax....only anti-EXPERIMENTAL AGENT).
Take away one of our more effective arguments??? Geez, troll, can’t have that...even if it’s the TRUTH, can we??
Lastly, you saying “once the vaccines are fully Approved, then governments can mandate vaccination” sure reeks of supporting mandated fake vaccines. You sound down-right giddy, in that post.
Even one your fellow FRVPs chimed in to say that THEY were, at least, against mandated, fake vaccines.
Now, run along, DS FRVP, we’ve seen your true colors and you can no longer push your fibs.
Jane Long wrote: “Upsetting to the ‘anti-vaxxer’ crowd. (Only, many have told you, REPEATEDLY, that we’re not anti-vax....only anti-EXPERIMENTAL AGENT).”
You should be happy to learn that these vaccines might be fully approved within six months because then the vaccines will no longer be ‘EXPERIMENTAL’ and you can get vaccinated with an ‘APPROVED’ vaccine. Only an anti-vaxxer would react negatively to this great news.
Jane Long wrote: “(WRONG-O....and, you were corrected by ransomnote, and SEVERAL others, on that fib, McGee.)”
None of those are experts in the vaccine approval process so no one provided a credible correction.
Jane Long wrote: “(WRONG-O....and, you were corrected by ransomnote, and SEVERAL others, on that fib, McGee.)”
As I said: “...Pfizer has completed the lengthy part of the process. Thousands participated in the phase 1/2/3 trials. Hundreds of thousands of doses have been administered. The data clearly shows the vaccines are safe and effective. Pfizer/Moderna are about to submit their applications for full Approval. It’s been estimated that full Approval might be granted in six months.”
https://www.contagionlive.com/view/pfizer-biontech-covid-19-vaccine-91-percent-effective-6-months
“The first US Food & Drug Administration (FDA) marketing approval for a COVID-19 vaccine may be imminent.”
“Pfizer and BioNTech intend to submit the six-month data for publication in a scientific peer-reviewed journal. The data will also be included in a BLA submission to the FDA, which has currently granted EUA to 3 COVID-19 vaccines, but marketing approval to none.”
“These data confirm the favorable efficacy and safety profile of our vaccine and position us to submit a Biologics License Application to the U.S. FDA,” Albert Bourla, chairman and chief executive officer of Pfizer, said in a statement. “The high vaccine efficacy observed through up to six months following a second dose and against the variant prevalent in South Africa provides further confidence in our vaccine’s overall effectiveness.”
And this:
https://www.nuventra.com/resources/blog/submitting-your-fda-marketing-application/
“Current FDA performance goals under the Prescription Drug User Fee Act (PDUFA) stipulate that FDA intends to review and act on 90% of standard NDA and BLA submissions within 10 months of the filing date. The goal for priority review applications is 6 months.Jun 5, 2019”