Patients’ Right to Know Their Medication Act of 2023
Referred to the Subcommittee on Health.
Congressional Research Service
Official summary
Version 00 · Introduced in House · Feb 24, 2023
Patients' Right to Know Their Medication Act of 2023
This bill establishes requirements relating to the form, content, and distribution of patient safety labels for prescription drugs.
Specifically, the Food and Drug Administration must issue regulations with requirements relating to the authorship, content, format, color, printing, and dissemination of such patient safety information. The regulations must require labels to include the drug's approved uses, known interactions with other drugs or substances, contact information for the drug's manufacturer, and other specified information relating to patient safety. The information must be in plain, neutral language and must be given in printed form with each prescription.
No related bills are listed in this snapshot. This does not establish whether the proposal has appeared in earlier Congresses.
Source last updated: Nov 2, 2024. Consult Congress.gov for the current record.
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