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Protecting Patients from Deceptive Drug Ads Act

S. 652 Sen. Richard Durbin (D-IL) In committee
  1. Introduced Feb 20
  2. Committee Feb 20
  3. Passed Senate Next
  4. Passed House Not yet
  5. To President Not yet
  6. Law Not yet
Where it stands
In committee, Feb 20, 2025Next: Senate vote
614d ago Feb 20, 2025: Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text: CR S1129-1130)
Final votes
No roll callsNo recorded vote on this bill yet
Lobbying
2companies, 7 filings
Member trades
2trades in the last 90 days
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Companies lobbying on this bill

2 companies
Companies by sector
Biotech & Pharma 1Medical Devices & Healthcare 1
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Summary

Protecting Patients from Deceptive Drug Ads Act

Full summary5 paragraphs

This bill establishes civil penalties for false or misleading communications about prescription drugs by certain entities on social media. It also requires additional disclosures and reporting relating to drug advertisements on social media or via telehealth.

The bill’s civil penalties apply when social media influencers or health care providers make communications regarding prescription drugs, using social media platforms, from which they financially benefit that (1) are made knowingly or recklessly and are false or inaccurate, or (2) fail to include the brief summary information (i.e., side effects, contraindications, effectiveness) required in drug advertisements. The Food and Drug Administration (FDA) must issue guidance and publish notice of such enforcement actions. The FDA may notify drug manufacturers when such communications fail to include the brief summary information.

The bill also requires telehealth providers (i.e., entities that use telecommunications to bring together patients and drug prescribers or dispensers) to include the brief summary information in prescription drug advertisements.

Also, payments from drug manufacturers to health care providers or social media influencers, or from health care providers to influencers, for communications promoting prescription drugs must be reported in accordance with anti-kickback laws for federal health care programs.

Additionally, the FDA may conduct market surveillance regarding prescription drug promotion on social media, including analyzing communications and establishing a task force with the Federal Trade Commission.

Library of Congress summary, Feb 20, 2025

Summary versions
  • Introduced in SenateFeb 20, 2025

Official record from Congress.gov, the House Clerk and the Senate; lobbying from Lobbying Disclosure Act filings. Updated Oct 27, 2026.