FDA takes actions to expand use of treatment for outpatients with mild to moderate COVID-19

FDA

21 January 2022 - Today, the U.S. FDA took two actions to expand the use of the antiviral drug Veklury (remdesivir) to certain non-hospitalised adults and paediatric patients for the treatment of mild-to-moderate COVID-19 disease. 

This provides another treatment option to reduce the risk of hospitalisation in high-risk patients. 

Previously, the use of Veklury was limited to patients requiring hospitalisation.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , COVID-19