FDA OKs Moderna, J&J boosters, along with 'mix and match' approach

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FDA OKs Moderna, J&J boosters, along with 'mix and match' approach
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The move will greatly expand access to booster shots.

The authorizations and increased flexibility on which vaccine people can receive as a booster will increase access to the shots, experts say.

Cohn gave the example of a women in her 30s who may have received the Johnson & Johnson shot before it was discovered the vaccine was linked to a small but increased risk for. A mix-and-match approach would allow that woman, Cohn said, to choose a different type of vaccine for her booster. For people who initially got Johnson & Johnson, a booster is authorized for all adults 18 and up at least two months after their first dose.The FDA previously authorizedfor the latest coverage on the coronavirus outbreak.

“The whole notion of a booster is to reduce moderate and mild disease," Poland said. While boosters may lower the risk of severe illness,"the efficacy of the primary series of vaccine is already so high that you’re only adding to that a modicum."It will be up to the CDC to clarify who is eligible for which shot, a job that could be tricky given the existing criteria for people.

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