) has authorized the use of a non-vaccine therapy to prevent COVID-19 infections in immunocompromised people.
The Food and Drug Administration issued an emergency use authorization for AstraZeneca’s Evusheld on Wednesday. The AstraZeneca logo is pictured with a syringe in the forefront in this picture taken on November 17, 2020."Vaccines have proven to be the best defense available against COVID-19," Dr. Patrizia Cavazzoni, director of the FDA's Center for Drug Evaluation and Research, said in a.
Evusheld is administered as two intramuscular injections, given in immediate succession, and may be effective at preventing COVID-19 infections for up to six months. Thel that formed the basis of the therapy's authorization found that it was 83 percent effective in preventing infections among mostly high-risk participants.
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