Thursday, May 19, 2022
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The FDA on Thursday issued an emergency use authorization for Merck’s molnupiravir

On Thursday, the US Food and Drug Administration (FDA) authorized the use of molnupiravir, an oral antiviral pill developed by…


The FDA on Thursday issued an emergency use authorization for Merck’s molnupiravir

On Thursday, the US Food and Drug Administration (FDA) authorized the use of molnupiravir, an oral antiviral pill developed by Merck to treat COVID-19 in select adults ages 18 and older who are experiencing mild-to-moderate symptoms and are at risk for “progression to severe COVID-19.”

The FDA on Thursday authorized Merck’s antiviral Covid pill for adults who are vulnerable to becoming severely ill and for whom alternative treatment options are “not accessible or clinically appropriate.”

The FDA cleared a second Covid pill, developed by Merck, offering another treatment for high-risk adults as the Omicron variant surges.

What people are saying?

LustrousGem FDA approving anything. It will take 75 years to release data on COVID vaccine to the public. But it took FDA 108 days to approve vaccine. Not against vaccine but this is weird.

basically This adds to the fact that there is NO justification for mandated Covid vaccines & vaccine passports (especially when what’s being called a vaccine is in fact not a vaccine at all.. it does not prevent Covid whatsoever. On the contrary).

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