Patients’ Right to Know Their Medication Act of 2025
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Summary
This bill amends the Federal Food, Drug, and Cosmetic Act to require the FDA to establish regulations mandating that prescription drugs include standardized, printed patient medication information (PMI) with each dispensed prescription. The regulations must specify the content, format, language, graphics, and dissemination of this information, which must be scientifically accurate, use plain language, and include safety warnings, contraindications, adverse reactions, drug interactions, and manufacturer contact information. Failure to provide the required printed PMI would constitute misbranding under federal law.
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