Aspartame, the controversial artificial sweetener that is broken down to methanol and formaldehyde, has prompted thousands of reports to the FDA about adverse reactions, including Dr. Russell Blalock’s 1994 book Excitotoxins. In some people, aspartame, which is found in over 4,000 consumer products, causes symptoms ranging from headaches to dizziness, vomiting, fatigue and diarrhea.
There’s an old adage, “Any publicity is good publicity,” but the exposure of four New Jersey lawmakers on the front page of the New York Times was anything but good news for them. The article reported that Menaflex, a medical device that reinforces damaged knee tissue, was approved only after the two senators and two […]
The New York Times reports that Judge Jeffrey S. White of Federal District Court in San Francisco has overturned U.S. approval of Monsanto’s GMO sugar beet sold as “Roundup Ready.” White ruled that the USDA Animal and Plant Health Inspection Service violated environmental law by failing to assess whether the beets would eventually share their […]
The National Organic Standards Board (NOSB) has announced a meeting of the board to take place November 3-5 at the Washington Plaza Hotel. In anticipation of this meeting, the Board will be accepting written comments and requests to present in person at the meeting until October 19. We would like to encourage all of you […]
Natural health and integrative medicine recently won a court victory, and it is worth taking a bit of time to understand what it means.
In the US, preparations for Swine Flu center entirely on a new and untested vaccine along with anti-viral drugs that don’t work very well and have serious side effects. The Canadian government by contrast is willing to consider some other, common sense alternatives.
ANH-USA has filed three lawsuits against the FDA in recent weeks. In each case, we have been joined as plaintiffs by dietary supplement formulators Durk Pearson and Sandy Shaw and the Coalition to End FDA and FTC Censorship. We are being represented by the law firm of Emord & Associates.
We have learned that Time-Cap Labs, producer of a generic version of the brand name drug Armour, a natural and bioidentical thyroid replacement, has been ordered by the FDA to stop production. The FDA has decided to classify the company’s product, available for over a century, as an unapproved new drug. Since the new drug […]
The Senate’s “Food Safety” bill is better than the House’s in some important respects. For example, it drops the draconian jail sentences and fines for vague infractions including paperwork errors. But it includes a Codex provision that absolutely must be removed by amendment in order to protect free choice about supplements. Please take action to […]
Thank you to our 801 advocates who used AAHF’s Action Center to submit comments in response to Docket Number FDA-200-N-0247, letting the Food and Drug Administration’s Transparency Task Force know that you support increased transparency at the FDA. On August 6, AAHF proudly hand-delivered 801 letters to the FDA’s Division of Docket Management. These comments […]