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Topic: Janssen COVID-19 Vaccine

President Joe Biden’s statement on Emergency Use Authorization of the Johnson & Johnson COVID-19 Vaccine

 

The White HouseWashington, D.C. – After a rigorous, open, and objective scientific review process, the Food and Drug Administration issued an emergency use authorization for a third safe and effective vaccine to help us defeat the COVID-19 Coronavirus pandemic — the Janssen COVID-19 (Johnson & Johnson) vaccine.

This is exciting news for all Americans, and an encouraging development in our efforts to bring an end to the crisis.

United States President Joe Biden.

United States President Joe Biden.

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FDA Issues Emergency Use Authorization for Janssen COVID-19 Vaccine

 

U.S. Food and Drug Administration (FDA)Silver Spring, MD – Today, February 27th, 2021,  the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for the third vaccine for the prevention of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The EUA allows the Janssen COVID-19 Vaccine to be distributed in the United States for use in individuals 18 years of age and older.

COVID-19 Coronavirus Vaccine

COVID-19 Coronavirus Vaccine

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