Los Angeles Times

FDA revokes authorization for key anti-COVID-19 drug, a blow for vulnerable Americans

Eureva Walker, director of pharmacy at Stroger Hospital, shows off Evusheld injection, a new COVID-19 treatment that people can take before becoming symptomatic, in Chicago on Friday, Feb. 4, 2022.

The Food and Drug Administration has withdrawn its provisional support for the use of Evusheld, a medication that was once a valuable tool for preventing patients with weakened immune systems from becoming severely ill with COVID-19.

With new viral variants increasingly adept at defeating Evusheld, the FDA said the biological drug should no longer be used.

The FDA decision marks the end — at least for now — of a medication that had helped restore some normalcy to the lives of cancer patients, transplant recipients and others who either could — 7.2 million adults — is thought to have immune deficiencies that put them at risk of becoming severely ill or dying if they are infected with the pandemic virus.

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