The vaccine become the third approved for use in the United States.
The Food and Drug Administration on Saturday announced it had approved the Johnson & Johnson COVID-19 vaccine for emergency use throughout the country.
In a press release announcing the decision, the agency said it had “determined that the [vaccine] has met the statutory criteria” for an emergency authorization.
“After a thorough analysis of the data, the FDA’s scientists and physicians have determined that the vaccine meets the FDA’s expectations for safety and effectiveness appropriate for the authorization of a vaccine for emergency use,” Peter Marks, the director of the FDA’s Center for Biologics Evaluation and Research, said in the announcement.
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