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   DIR Return to: Covid Treatments
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       #Post#: 2530--------------------------------------------------
       FDA revokes Emergency Use Authorizations for 4 Covid-19
       treatments
   DIR By: Steve
       Date: December 23, 2024, 1:20 pm
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       SUMMARY - The Food and Drug Administration (FDA) in the United
       States has revoked the emergency use authorization for four
       COVID-19 antibody-based drugs: bebtelovimab, Evusheld,
       sotrovimab & REGEN-COV. The reasons for the revocations are that
       the shelf life of those drugs had expired and that the drugs are
       not effective against the strains of Covid-19 currently
       circulating. There are no plans by the companies who make those
       drugs to re-apply for emergency use authorizations in the United
       States.
       LINK -
  HTML https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-revokes-authorization-five-covid-treatments-2024-12-23/
  HTML https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-revokes-authorization-five-covid-treatments-2024-12-23/<br
       />
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