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FDA Authorizes Merck’s COVID Pill For Early, At Home Treatment

The action comes after the agency authorized a Pfizer pill Wednesday

Merck & Co Inc/via Reuters, FILE

From ABC.go.com…

The Food and Drug Administration on Thursday authorized Merck’s COVID-19 pill for certain adults.

The authorization for molnupiravir is limited to adults over 18 who have a high risk of severe illness and “for whom alternative FDA-authorized treatment options are not accessible or medically appropriate,” the FDA said in a press release Thursday. It’s not recommended for use in pregnant people.

 

This is the second COVID-19 treatment in pill form after Pfizer’s pill, Paxlovid, was authorized Wednesday. Paxlovid is authorized for a slightly larger pool of people — anyone over 12 and at high risk of severe illness.

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