TrainsOfDisney
Well-Known Member
It was “expedited”You claiming it was rushed is the lie.
It was “expedited”You claiming it was rushed is the lie.
They aren’t approved. If that’s not signiciyto you that’s fine but it’s a fact.You repeatedly make posts questioning the safety of the vaccine based on lies, be it by pushing that they are not approved and refusing to explain that significance or by claiming that the testing was rushed. The safety testing was not expedited. Full approval does not require more safety testing. That you keep pushing these ideas is the lie.
The test phases weren't expedited AT ALL.It was “expedited”
Yeah agreed on this.
Disney is too committed. I HIGHLY doubt you will see any changes.
The testing of people was not even "expedited" we had to wait for results. Thanks for a raging pandemic we got them fast. Clearing hurdles on other aspects did happen, but testing was soundIt was “expedited”
Repeating lies it doesn't make it true.They aren’t approved. If that’s not signiciyto you that’s fine but it’s a fact.
The testing was “expedited” - that’s a fact.
Lack of approval is a meaningless fact unless you are pushing the lie that safety is unknown, which you seem to be doing.They aren’t approved. If that’s not signiciyto you that’s fine but it’s a fact.
The testing was “expedited” - that’s a fact.
My endgame at the moment is I’m scared I’ll end up with nerve damage... or a blood clot although since I’m not a woman I have less of a chance with that one.What is your end game here with this?
How long it takes for a reaction to occur has been explained repeatedly. “Long term side effects” are an anti-vaxxer lie that you have bought into and in the process are now repeating more anti-vaxxer lies.My endgame at the moment is I’m scared I’ll end up with nerve damage... or a blood clot although since I’m not a woman I have less of a chance with that one.
You need to work to get over these fears. I almost started freaking out when I first read about heart inflammation among teen boys (my oldest hadn't had his second shot yet, and heart issues run in the family), so I understand being afraid.My endgame at the moment is I’m scared I’ll end up with nerve damage... or a blood clot although since I’m not a woman I have less of a chance with that one.
What did I say that was a lie?in the process are now repeating more anti-vaxxer lies.
56,000 people go to the ER each year from this DEADLY FDA APPROVED MEDICINE. Is it in your home? Click here to find out:You can have an unknown adverse reaction to Advil and die. It's all about you evaluating your risk threshold.
But of course the very same agenda and click driven media that will scold everyone to get a shot, is also the first group lining up to sensationalize the second Mrs. Smith in Peoria has an bad reaction to the vaccine.
You can say this as many times as you want and that still won’t make it true.It was “expedited”
Are you vaccinated?My endgame at the moment is I’m scared I’ll end up with nerve damage... or a blood clot although since I’m not a woman I have less of a chance with that one.
That the testing was “expedited” is a lie. Without you explaining otherwise, repeating the importance of approval pushes a lie.What did I say that was a lie?
Would you rather end up on a ventilator that you never come off of?My endgame at the moment is I’m scared I’ll end up with nerve damage... or a blood clot although since I’m not a woman I have less of a chance with that one.
“You can say this as many times as you want and that still won’t make it true.
Of course not. But my chances of that are also very low and even lower if I stay locked in my basement!Would you rather end up on a ventilator that you never come off of?
Yes. With J&J. Hence my extra concern over this report. Yes I know it’s rare but that still worries me!Are you vaccinated?
The paperwork process was faster. Not the testing. Two totally different things.“
Pharmacy Times® interviewed Chad Landmon, JD, chair of intellectual property and FDA practice groups at Axinn, Veltrop & Harkrider, on the FDA’s emergency use authorization (EUA) process for COVID-19 vaccines, such as the expedited process for the recently authorized Johnson & Johnson COVID-19 vaccine.
Alana Hippensteele: So, Chad, how does the EUA process expedite the FDA’s normal approval procedures?
Chad Landmon: Sure, thanks for having me today. So, the EUA process at a basic level is expedited, and basically the way this works is it starts with an emergency declaration by the HHS secretary.
“
- https://www.pharmacytimes.com/view/how-the-fda-s-expedited-eua-process-works
How long ago?Yes. With J&J. Hence my extra concern over this report. Yes I know it’s rare but that still worries me!
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