FDA announces limits on who can receive Johnson & Johnson COVID-19 vaccine

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The reason is a rare, but serious risk of blood clots.

In December, the Centers for Disease Control and Prevention prioritizing Moderna and Pfizer shots over J&J's because of its safety issues. Previously, U.S. officials had treated all three vaccines similarly because they'd each been shown to offer strong protection.

Under the new FDA instructions, J&J's vaccine could still be given to people who had a severe allergic reaction to one of the other vaccines and can't receive an additional dose. J&J's shot could also be an option for people who refuse to receive the mRNA vaccines from Pfizer and Moderna, and therefore would otherwise remain unvaccinated, the agency said.

The FDA based its decision on"our safety surveillance systems and our commitment to ensuring that science and data guide our decisions."

 

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