FDA authorizes Moderna’s coronavirus vaccine

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The Food and Drug Administration on Friday authorized Moderna’s coronavirus vaccine for emergency use — the second to clear that bar in the United States.

The Moderna decision comes a week after FDA authorized the use of a Covid-19 vaccine by Pfizer, and five days after the nation launched the most urgent and ambitious vaccination campaign in its history.

On Thursday, an independent FDA advisory panel endorsed use of the shot for people over 18, based on clinical trial data that found the vaccine to be 94 percent effective with largely mild side effects.



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