FDA issues emergency use authorization for Johnson & Johnson COVID-19 vaccine

Lincoln Wylie

On Saturday, the U.S. Foods and Drug Administration issued an unexpected emergency use authorization for the Johnson & Johnson vaccine for the prevention of COVID-19.

The EUA allows the Johnson & Johnson Janssen COVID-19 vaccine to be dispersed in the U.S for people eighteen decades of age and older. 4 million doses are anticipated to go out subsequent week and 20 million doses by the finish of March.

WHY THIS Matters

Approval signifies there are now three COVID-19 vaccines for use in the United States, to velocity up the vaccination course of action.

The Janssen COVID-19 vaccine has the reward of remaining administered as a solitary dose. The present Pfizer and Moderna vaccines remaining administered require two doses. 

Its success is a lot less than that of the Pfizer and Moderna vaccines, which each individual claimed at minimum a ninety four.5% helpful level.

Johnson & Johnson is at minimum 66%

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