FDA Withdraws Emergency Use Authorization For AstraZeneca Drug Evusheld

They need to do the same for all of them. The other shots are just as bad and ineffective. FDA has a lot to answer for with these authorizations.

"Evusheld, which is made by British-Swedish pharmaceutical and biotechnology company, AstraZeneca, was first authorized in December 2021 as pre-exposure prophylaxis against the virus for those who are immunocompromised and less likely to generate antibodies from vaccination."

"However, the FDA said the medication does not neutralize several omicron subvariants including BQ.1, BQ.1.1, BF.7, BF.11, BA.5.2.6, BA.4.6, BA.2.75.2, XBB and XBB.1.5."
https://abcnews.go.com/Health/fda-withdraws-authorization-covid-drug-effective-new-variants/story?id=96715718

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