I invite @c_drosten to a public scientific debate with @DrJBhattacharya and @MartinKulldorff rather than trying to discredit them in German on Twitter. Grown up professionals conduct face to face scientific discourse. Thatโs how adulthood is done. I have guesses why not.
@JordanSchachtel Also once itโs actually available it would become illegal to give any more emergency use authorized therapies for cov. Moderna, j&j, astrozenica, and Pfizer would have to destroy all the previous lots.
Moderna's FDA approved Spikevax also remains unavailable to Americans. Neither company has announced any plans to make the product available to Americans. The CDC currently says the products are "not orderable at this time."
This is one of the more powerful videos Iโve seenโผ๏ธโผ๏ธ
This is Dr. Bill Deagle a decade foretelling of the New World Order via biopharmaceutical enslavementโ๐ง๐๐๐
I am seeing quite a number of patients who are just now getting their first shots so they can travel. How does this make any sense from a medical perspective? We heard the Pfizer CEO himself say his product has no benefit against omicron.
As well as all the heart-breaking suffering due to the war in ๐บ๐ฆ we're also witnessing more and more corporate & political opportunism. Politicians & lobbyists alike are exploiting the war to push through things like blocking any reductions in the use of pesticides and fertiliser
@sugarpetals72@BobVanWagner1 *Caution should be used with Paxlovid for Covid in those who got the Vx. It is a protease inhibitor which could exacerbate further Vx related blood clot issues. -Protease inhibitor patients at higher risk of thrombosis? https://t.co/9rro5DNMLP
Biden & his new FDA commiss @DrCaliff_FDA (under pressure from Pharma) should insist on a vote by FDA's external experts before authorizing 4th doses. Public health confidence has been signif eroded. Bypassing the expert vote to push 4th doses will make it worse. Science>politics
Is this following the science?? FDA will authorize 4th doses this week by bypassing the typical voting process of their external experts. FDA will then convene them after the authoriz to "discuss". It's like a judge issuing a verdict and then having lawyers make their arguments.