Geronimo
Member
- Joined
- May 11, 2020
- Messages
- 346
After the widespread administration of the vaccine and reading in the news about it, I think it will be helpful to replace the word "despite" with "because of".
Follow along with the video below to see how to install our site as a web app on your home screen.
Note: This feature may not be available in some browsers.
Click Here if you want to upgrade your account
If you were able to post but cannot do so now, send an email to admin at raypeatforum dot com and include your username and we will fix that right up for you.
Any chance this monoclonal antibody trial might have been sabotaged so that ongoing vaccine trials would be favoured (especially since those are not going too well)? Trump spoke positively about Regeneron.
The company didn’t say what happened , let’s guess, it was a "pre existing genetic condition" of the inferior human we selected.
Any chance this monoclonal antibody trial might have been sabotaged so that ongoing vaccine trials would be favoured (especially since those are not going too well)? Trump spoke positively about Regeneron. We all saw what the cabal did when he voiced support for hydroxychloroquine. Within weeks they had a fraudulent study published in the Lancet claiming a causative relationship between HCQ and heart failure in covid patients (of course this study was fairly quickly retracted, but not before every HCQ proponent in the western world had been labelled a quack).
...aaannnd now the FDA has granted "emergency" use authorization (EUA) to the treatment despite the health risks. Given the safety issues, the treatment was probably doomed if submitted through the regular approval process, so now it basically gets to be administered to patients as "emergency" (which implies acceptance of the risks) but the company is exempt from liability as most other EUA interventions are.
FDA okays Lilly's antibody treatment for Covid-19 - CNN
@Drareg @tankasnowgod
...aaannnd now the FDA has granted "emergency" use authorization (EUA) to the treatment despite the health risks. Given the safety issues, the treatment was probably doomed if submitted through the regular approval process, so now it basically gets to be administered to patients as "emergency" (which implies acceptance of the risks) but the company is exempt from liability as most other EUA interventions are.
FDA okays Lilly's antibody treatment for Covid-19 - CNN
@Drareg @tankasnowgod
Thalidomide is back.I have to wonder...... what other incredibly dangerous treatments can be brought back under emergency use? Vioxx? Thalidomide? Mercury diuretics? Hey, AZT was considered far too dangerous a chemotherapy drug for cancer patients, so Fauci & Co. just approved it for use in "treating" AIDS patients back in the late 80's. No reason they won't try the same model again.
Vioxx
I think Vioxx is back, or about to be very soon.
https://www.medpagetoday.com/blogs/revolutionandrevelation/72647