Are Your Collagen Supplement Doing The Job?
We are also requiring manufacturers of authorized testosterone products to conduct a well-designed clinical trial to address the question of whether an increased risk of heart attack or stroke exists among users of the products. We advocate patients and health care professionals to report side effects involving testosterone products to the FDA MedWatch program, using the information in the Contact FDA" carton at the bottom of the page.
Men and women in America have used testosterone therapy since the late 1930s, in many instances for more than 40 years - with just rare adverse effects. The amount of women in the United States now on testosterone treatment is estimated to be in the tens of thousands - miniscule compared with the millions prescribed oral estrogen-progestin regimens, like Premarin and Provera. It might still be a little while before the therapy reaches the mainstream, although with http://tinyurl.com/jkhvqy9 a growing recognition of the gains of testosterone for women, those numbers may rise.
Before this year, the U.S. Food and Drug Administration required manufacturers of all authorized testosterone products to add advice on the labels to clarify the approved uses of the drugs and contain advice about potential increased risks of heart attacks and strokes in patients taking testosterone. But patients and doctors must weigh dangers and the benefits of supplying testosterone supplementation to patients based on the advice provided by the FDA and other research.