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FDA OKs mixing and matching COVID-19 vaccines; backs Moderna, J&J boosters – Pittsburgh, Pennsylvania

Pittsburgh, Pennsylvania 2021-10-20 17:45:00 –

U.S. regulators approved the extension of the COVID-19 booster to Americans vaccinated with Moderna or Johnson & Johnson on Wednesday, giving anyone eligible for additional doses a brand different from the one originally received. Said it was available. Food and Drug Administration decision mark A major step towards expanding the US booster campaign that began with the additional dose of Pfizer vaccine last month. But before more people roll up their sleeves, the Centers for Disease Control and Prevention will consult an expert panel later this week before finalizing official recommendations on who should get boosters and when. .. The latest move has expanded the number of Americans targeted for boosters by tens of millions and officially allows “mixing and matching” of shots. In particular, the FDA has had side effects from one brand, but specifically, the FDA has addressed elderly people and other people who are at high risk for COVID-19 due to health problems, work, or living conditions. We approved a third Moderna injection 6 months after the last injection. One big change: Moderna boosters are half the dose used for the first two shots. This is based on company data showing that it was enough to boost immunity again. Administer at least 2 months after the first vaccination. FDA decisions differ due to different vaccine manufacturing methods and dosing schedules. In addition, the J & J vaccine has consistently shown lower levels of efficacy than the two-shot Moderna and Pfizer vaccines. This is a developing story. Check for the latest information. ___ AP writer Mike Stobbe contributed to this story from New York. The Associated Press’s Department of Health Sciences is supported by the Department of Science Education at the Howard Hughes Medical Institute. AP is solely responsible for all content.

U.S. regulators approved the extension of the COVID-19 booster to Americans vaccinated with Moderna or Johnson & Johnson on Wednesday, giving anyone eligible for additional doses a brand different from the one originally received. Said it was available.

The Food and Drug Administration’s decision marks a major step towards expanding the US booster campaign, which began with an additional dose of Pfizer vaccine last month. But before more people roll up their sleeves, the Centers for Disease Control and Prevention will consult an expert panel later this week before finalizing official recommendations on who should get boosters and when. ..

The latest move has expanded the number of Americans targeted for boosters by tens of millions and officially allows “mixing and matching” of shots. In particular, there were some brand side effects, but still proven protection of vaccination.

Specifically, the FDA has issued a third Moderna six months after the last shot to elderly people and other people at high risk of COVID-19 due to health problems, work, or living conditions. Approved the shot. One big change: Moderna’s booster will be half the dose used for the first two shots, based on company data showing that it was enough to boost immunity again.

For J & J’s one-shot vaccine, the FDA stated that all US recipients should receive a second dose at least two months after the first vaccination.

FDA decisions differ due to different vaccine manufacturing methods and dosing schedules. In addition, the J & J vaccine has consistently shown lower levels of efficacy than the two-shot Moderna and Pfizer vaccines.

This is a developing story. Please check for updates.

___

AP writer Mike Stobbe contributed to this story from New York.

___

The Associated Press’s Department of Health Sciences is supported by the Department of Science Education at the Howard Hughes Medical Institute. AP is solely responsible for all content.

FDA OKs mixing and matching COVID-19 vaccines; backs Moderna, J&J boosters Source link FDA OKs mixing and matching COVID-19 vaccines; backs Moderna, J&J boosters

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