Johnson & Johnson Seeks F.D.A. Approval for Covid Booster

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

The corporate mentioned {that a} second shot of its vaccine about two months after the primary considerably boosts safety, to 94 %, in opposition to average 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 knowledgeable advisory committee subsequent week to debate the problem.

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