Johnson & Johnson Asks FDA to Authorize Covid-19 Booster


Johnson & Johnson has requested U.S. well being regulators to authorize a booster dose for its Covid-19 vaccine, citing research exhibiting it improved safety amongst adults who beforehand obtained a single shot.

The Meals and Drug Administration may resolve on J&J’s request inside weeks. The company has scheduled an Oct. 15 assembly of an advisory panel to review the proof of the necessity for a booster, and to suggest whether or not the company ought to authorize one. | Johnson & Johnson Asks FDA to Authorize Covid-19 Booster


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