FDA & Government News

RSV Vaccine Eligibility Expands

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  • 1

    FDA expands Arexvy approval to adults 18-49 at increased risk for RSV.

  • 2

    Prior approval was only for those 60+ years and 50-59 with risk factors.

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    21 million under 50 have RSV risk factors in the US.

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    Phase 3b trial showed noninferior immune response in younger adults.

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    Common adverse events include injection site pain and fatigue.

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    RSV may exacerbate chronic conditions like COPD and asthma.

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    Vaccine has global approvals and shows safety consistency from trials.

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