Johnson & Johnson seeks F.D.A. authorization for its booster shot.

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Johnson & Johnson on Tuesday morning requested federal regulators to authorize a booster shot for adults, turning into the third coronavirus vaccine producer to take action.

The corporate stated {that a} second shot of its vaccine about two months after the primary considerably boosts safety, to 94 %, in opposition to reasonable to extreme illness.

The corporate submitted its findings in a request to the Meals and Drug Administration to amend emergency use authorization of its vaccine to incorporate a second injection. The company has known as a gathering of its skilled advisory committee subsequent week to debate the difficulty.

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