the voice of the natural health consumer

Adverse Event Reporting

FDA Accepting Comments on Adverse Event Reporting

Washington, D.C., October 15, 2007 - Today the FDA released  and is accepting comments on its guidance on requirements for the reporting of serious adverse events under the Dietary Supplement and Nonprescription Drug Consumer Protection Act. 


AER Bill Passes: A Victory for Consumers and the Natural Products Community!

Washington, D.C.—December 9, 2006—Thousands upon thousands of faxes and e-mails from Citizens for Health members, along with leadership and support from the Natural Products Association and the Council for Responsible Nutrition (CRN), led to victory: the passage of the Dietary Supplement and Non-Prescription Drug Consumer Protection Act (the "AER bill"), S. 3546.


Drug Maker Recalls Acetaminophen Caplets Due to Metal Contamination

Perrigo Co., a major manufacturer of store-brand acetaminophen, recalled 11 million bottles of the pain-relieving pills after discovering some were contaminated with metal fragments.


Dietary supplements are safe. Senate Bill 3546 makes them even safer.

Citizens for Health commends Senators Orrin Hatch (R-Utah), Tom Harkin (D-Iowa) and Richard Durbin (D-Ill.) for introducing Senate Bill 3546, the “Dietary Supplement and Nonprescription Drug Consumer Act,” a bill that will require manufacturers to notify the FDA of all serious adverse events (AEs) for over-the-counter (OTC) drugs and dietary supplements reported to them.

Send a letter to your Senators in support of this bill today!


Ephedra Ban Overturned

Court Overturns One Year Old FDA Ephedra Ban

Low Doses of 5000 Year Old Herb Not Proved Dangerous
Congressional Democrats Attack Decision

Opinion & Analysis
by Jim Turner, Chairman of Citizens for Health

What do Tom Delay, Ted Kennedy and Henry Waxman have in common?   When the federal courts go against them they threaten retaliation.

On April 13, 2005 Judge Tina Campbell of the United States District Court of Utah threw out the part of the sweeping FDA ban of the herb ephedra that prohibited sale of products yielding less than 10 mg of ephedrine alkaloids (ephedra) per day.


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