FDA Approves Emergency Use of Remdesivir for COVID-19

By Robin Foster and E.J. Mundell
HealthDay Reporters

MONDAY, May well 4, 2020 (HealthDay Information) — As the U.S. coronavirus dying toll neared 65,000 on Friday, the U.S. Meals and Drug Administration authorized crisis use of the initially drug that seems to raise recovery between COVID-19 patients.

Remdesivir, Gilead Sciences’ intravenous antiviral treatment, is to be made use of for hospitalized patients with “extreme condition,” these kinds of as those who want supplemental oxygen or ventilators to breathe, the Associated Press reported.

“This was lightning speed in terms of having something authorized,” Food and drug administration Commissioner Stephen Hahn mentioned throughout a media briefing Friday, calling the drug “an significant scientific advance.”

The company based its final decision on the success of a governing administration research that confirmed remdesivir shortened the time to recovery by 31% for COVID-19 patients in the clinic, the AP reported.

All those supplied the drug

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