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      <constitutionalAuthorityStatementText>&lt;pre&gt;[Congressional Record Volume 169, Number 33 (Friday, February 17, 2023)][House]From the Congressional Record Online through the Government Publishing Office [&lt;a href="https://www.gpo.gov"&gt;www.gpo.gov&lt;/a&gt;]By Ms. MATSUI:H.R. 1092.Congress has the power to enact this legislation pursuantto the following:Article 1, Section 8 of the United States ConstitutionThe single subject of this legislation is:To strengthen the use of patient-experience data within thebenefit-risk framework for approval of new drugs.[Page H856]&lt;/pre&gt;</constitutionalAuthorityStatementText>
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        <fullName>Rep. Yakym, Rudy [R-IN-2]</fullName>
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        <fullName>Rep. Cleaver, Emanuel [D-MO-5]</fullName>
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        <lastName>Cleaver</lastName>
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        <fullName>Rep. Cárdenas, Tony [D-CA-29]</fullName>
        <firstName>Tony</firstName>
        <lastName>Cárdenas</lastName>
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        <fullName>Rep. Harder, Josh [D-CA-9]</fullName>
        <firstName>Josh</firstName>
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        <fullName>Rep. Fitzpatrick, Brian K. [R-PA-1]</fullName>
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        <fullName>Rep. Thanedar, Shri [D-MI-13]</fullName>
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        <fullName>Rep. Higgins, Brian [D-NY-26]</fullName>
        <firstName>Brian</firstName>
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        <fullName>Del. Norton, Eleanor Holmes [D-DC-At Large]</fullName>
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        <fullName>Rep. Phillips, Dean [D-MN-3]</fullName>
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        <fullName>Rep. Cole, Tom [R-OK-4]</fullName>
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        <state>OK</state>
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        <fullName>Rep. Gottheimer, Josh [D-NJ-5]</fullName>
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        <fullName>Rep. Van Drew, Jefferson [R-NJ-2]</fullName>
        <firstName>Jefferson</firstName>
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        <fullName>Rescom. González-Colón, Jenniffer [R-PR-At Large]</fullName>
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        <fullName>Rep. LaMalfa, Doug [R-CA-1]</fullName>
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        <fullName>Rep. Lawler, Michael [R-NY-17]</fullName>
        <firstName>Michael</firstName>
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        <fullName>Rep. Thompson, Glenn [R-PA-15]</fullName>
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        <fullName>Rep. James, John [R-MI-10]</fullName>
        <firstName>John</firstName>
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        <fullName>Rep. Wasserman Schultz, Debbie [D-FL-25]</fullName>
        <firstName>Debbie</firstName>
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        <fullName>Rep. Tonko, Paul [D-NY-20]</fullName>
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        <fullName>Rep. Balderson, Troy [R-OH-12]</fullName>
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        <fullName>Rep. Grothman, Glenn [R-WI-6]</fullName>
        <firstName>Glenn</firstName>
        <lastName>Grothman</lastName>
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        <actionDate>2023-02-17</actionDate>
        <actionDesc>Introduced in House</actionDesc>
        <updateDate>2023-06-22T13:17:09Z</updateDate>
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          <text>&lt;p&gt;&lt;b&gt;Better Empowerment Now to Enhance Framework and Improve Treatments Act of 2023 or the BENEFIT Act of &lt;/b&gt;&lt;b&gt;2023&lt;/b&gt;&lt;/p&gt; &lt;p&gt;This bill requires the Food and Drug Administration (FDA) to consider relevant patient experience data in the risk-benefit assessment framework used in the process for approving new drugs.&lt;/p&gt; &lt;p&gt;After a new drug application has been approved, the FDA's public statement about how it used patient experience data shall include a description of how such data was considered in the risk-benefit assessment framework. &lt;/p&gt;</text>
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    <title>BENEFIT Act of 2023</title>
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        <title>To strengthen the use of patient-experience data within the benefit-risk framework for approval of new drugs.</title>
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