[Sooner or later]

And this pile of waist deep crap that I waded into.

Originally Posted by javadog

https://www.americanthinker.com/articles/2021/08/the_fda_has_authorized_an_early_covid_treatment_pr otocol.html

"After nearly a year-and-a-half and over 618,000 recorded COVID-related deaths in the U.S. alone, the FDA has finally released an emergency use authorization for REGEN-COV, a new drug that was being tested in 2020 (pre Biden)"




My response to the pack of friggin lies.

Originally Posted by Sooner or later

It has had an EUA authentication since Nov 2020. In July, 2021 the EUA was expanded.

"After nearly a year-and-a-half and over 618,000 recorded COVID-related deaths in the U.S. alone, the FDA has finally released an emergency use authorization for REGEN-COV, a new drug that was being tested in 2020 (pre-Biden). Primary care physicians can now use it as an early treatment option."

Regeneron's press release from November 21st, 2020.
https://investor.regeneron.com/news-releases/news-release-details/regenerons-regen-cov2-first-antibody-cocktail-covid-19-receive/
TARRYTOWN, N.Y., November 21, 2020 – Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that the antibody cocktail casirivimab and imdevimab administered together (formerly known as REGN-COV2 or REGEN-COV2), a therapy currently being investigated for use in COVID-19, has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA). Casirivimab and imdevimab administered together are authorized for the treatment of mild to moderate COVID-19 in adults, as well as in pediatric patients at least 12 years of age and weighing at least 40 kg, who have received positive results of direct SARS-CoV-2 viral testing and are at high risk for progressing to severe COVID-19 and/or hospitalization. The clinical evidence from Regeneron’s outpatient trial suggests that monoclonal antibodies such as casirivimab and imdevimab have the greatest benefit when given early after diagnosis and in patients who have not yet mounted their own immune response or who have high viral load.


The July expanded EUA
https://investor.regeneron.com/index.php/news-releases/news-release-details/fda-expands-authorized-use-regen-covtm-casirivimab-and-imdevimab

And here we have the standard fabrication on the PCR test.

"Coincidentally with its approving a new drug, the CDC is finally pulling the plug on the PCR test for COVID-19. The PCR test often gave false positives and can misidentify the seasonal flu as COVID-19 (although it will remain in use through the end of 2021)."

Why should I continue to open and read the crap sources you post?