FDA Authorizes Convalescent Plasma As Emergency Treatment For COVID-19

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FDA Authorizes Convalescent Plasma As Emergency Treatment For COVID-19
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President Trump announced that the Food and Drug Administration granted emergency use authorization to treat COVID-19 patients with plasma from people who have recovered from the virus, based on 'promising' results.

President Donald Trump, left, FDA Commissioner Stephen Hahn, right, and Health and Human Services Secretary Alex Azar, center, announced at a news conference on Sunday that the FDA issued emergency use authorization for convalescent plasma as a COVID-19 treatment.

Convalescent plasma, Hahn explained, is the liquid portion of the blood that contains the antibodies an individual develops in response to an infection and can be given to patients currently fighting that virus. He said this treatment has long been a part of the infectious disease arsenal. "We dream, in drug development, of something like a 35% mortality reduction," Azar said."This is a major advance in the treatment of patients."

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