The proposed budget of the US Food and Drug Administration (FDA) is worrying the Democrats. They are concerned that FDA’s annual increases in industry user fees—$828 million from manufacturers of medical and food products, including hundreds of millions drug manufacturers pay annually to help speed the review of new medicines—might compromise the agency’s independence.
Sen. Mike Enzi (R-WY) announced that the Senate HELP Committee has approved President Obama’s nomination of Dr. Margaret A. Hamburg, a former New York City health commissioner, as the next commissioner of the Food and Drug Administration. The approval process now moves to the full Senate.
We have an update to an article we published in last week’s issue of Pulse of Heath Freedom. A judge has now ruled that Daniel Hauser, a 13-year-old boy from Sleepy Eye, Minnesota, must receive conventional medical treatment for Hodgkin’s lymphoma—over his parents’ objections.
As we have reported in previous issues of Pulse of Health Freedom, bisphenol A (BPA), a chemical in the packaging or contents of many products, may cause long-term health effects, including cancers of the breast, brain and testicles; lowered sperm counts, early puberty and other reproductive system defects; diabetes; attention deficit disorder, asthma, and autism. […]
Last week, AAHF contacted the Senate Finance Committee, which is working on proposals to improve patient care and reduce healthcare costs. We asked committee members to look at two sections in particular: Health Information Technology (HealthIT), and Comparative Effectiveness Research (CER).
The US Food and Drug Administration (FDA) issued a warning letter to cereal manufacturer General Mills for claiming on its cereal box that Cheerios can help lower cholesterol, and saying on their website that “diets rich in whole grain foods can reduce the risk of heart disease.” The letter, dated May 5, called the above […]
In New Ulm, Minnesota, the parents of a thirteen-year-old cancer patient are undergoing child protection assessment hearings because they chose doctor-prescribed dietary therapy instead of chemotherapy.
On May 1, consumers were urged by the FDA to immediately stop using fourteen Hydroxycut weight loss products. The manufacturer recalled Hydroxicut after the FDA received 23 reports of liver damage under the Adverse Event Reporting system that now includes dietary supplements—several reports of jaundice, one incident that required a liver transplant, and one death.
A study by the Environmental Working Group (EWG) has completed a two-year study sampling the blood and urine of activists from Rachel’s Network, which funded the study, using four independent labs to analyze for toxic chemicals.
Thanks to AAHF legislative director Tami Wahl, the Michigan state legislature is hearing the concerns of AAHF on the creation of rules to implement the bill on licensure of dietitians and nutritionists in Michigan. Read Tami’s analysis: