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Press Releases:

» (10/2/08 ) FDA Should Ban Over-the-Counter Cough and Cold Medicines For All Children Under 12, Public Citizen Testifies » (7/8/08 ) FDA Must Do More to Warn Patients Taking Flouroquinolone Antibiotics of Possible Tendon Ruptures » (2/27/08 ) Congress Must Act Quickly to Address Growing Crisis At the Food and Drug Administration » (2/15/08 ) FDA Proposal on the Promotion of Off-Label Uses Highlights Drug Agency’s Recklessness » (2/8/08 ) FDA's Botox Warning Falls Short » (1/24/08 ) Stricter Warnings Needed for Botox, Myobloc Injections » (6/21/07 ) FDA Should Give Oral Presentations at All Advisory Committee Meetings, Public Citizen Tells Agency » (5/22/07 ) FDA Knew of Avandia’s Dangers Nearly Five Years Ago, Memo Shows » (5/4/07 ) Eliminate FDA’s Dependency on Drug Industry Money, Public Citizen Tells Congress » (3/30/07 ) FDA Should Not Have Approved Tegaserod (Zelnorm); Public Citizen Warned of Dangers When Drug Was Considered in 2001 » (11/17/06 ) Silicone Gel Breast Implants: Most Defective Medical Device Ever Approved by the FDA » (8/24/06 ) FDA’s Delay on Plan B Contraceptive Pill Is Another Black Mark Against Troubled Watchdog Agency » (7/20/06 ) Survey Confirms Long-Standing Problems at FDA That Stem From Lack of Congressional Oversight and Massive Drug Industry Funding of the Agency » (7/13/06 ) Public Citizen Sues FDA Over Secrecy on Blood Substitute Meeting; Move to Hold Closed Advisory Meeting on Proposal to Test Blood Substitute Product on Civilian Trauma Patients Is Unlawful » (6/27/06 ) FDA Fails to Protect Americans from Dangerous Drugs & Unsafe Food, Watchdog Groups Say » (6/27/06 ) The 100th Anniversary of the FDA: The Sleeping Watchdog Whose Master is Increasingly the Regulated Industries » (6/22/06 ) Companies Must Stop Fraudulently Promoting Laser Therapy as a Treatment to Quit Smoking, Public Citizen Tells FDA » (5/24/06 ) New Harris Poll on Public Perception of FDA Shows That People Understand Systemic Problems at Drug Agency » (3/3/06 ) FDA Report Highlights Poor Enforcement of Post-Marketing Follow-Up; Statement of Peter Lurie, Deputy Director, Public Citizen’s Health Research Group » (9/14/05 ) Potentially Harmful Medical Devices Should Be Recalled When Safer Alternatives Are Developed, Public Citizen Tells FDA >> more press releases ...

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