FDA panel endorses booster shot for Johnson & Johnson COVID-19 vaccine


WASHINGTON (AP) — A panel of U.S. well being advisers endorsed booster doses of Johnson & Johnson’s single-shot COVID-19 vaccine Friday, saying they need to be provided a minimum of two months after immunization.

J&J has requested the Meals and Drug Administration for flexibility with its booster, arguing the additional dose provides necessary safety as early as two months after preliminary vaccination — however that it’d work higher if folks wait till six months later.

The FDA’s advisory panel voted unanimously {that a} booster must be provided with out setting a agency time. The advisers cited rising fear that recipients of J&J’s vaccination appear to be much less protected than individuals who received two-dose Pfizer or Moderna choices — and that the majority received that single dose many months in the past.

The FDA isn’t sure by the vote however its final choice may assist develop the nation’s booster marketing campaign.

The federal government says all three U.S. vaccines proceed to supply robust safety in opposition to hospitalization and dying from COVID-19, and that the precedence is getting first pictures to the unvaccinated. However there’s a rising push to shore up safety in opposition to “breakthrough” infections and the extra-contagious delta variant of the coronavirus.

Booster doses of Pfizer’s vaccine started final month for folks at excessive danger of COVID-19, and the FDA advisory panel has really helpful the identical strategy for Moderna recipients. | FDA panel endorses booster shot for Johnson & Johnson COVID-19 vaccine


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