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FDA News Digest
December 18, 2007
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IN THIS WEEK'S ISSUE
» News
-- New Type of 'Beta Blocker' Drug Approved to Treat High Blood Pressure
-- FDA Rule Requires Warning on Nonoxynol 9 OTC Contraceptive Products
-- Genetic Test Recommended for Patients with Asian Ancestry Taking Carbamazepine
» Upcoming Public Meetings
» Consumer Health Information
FDA has approved Bystolic (nebivolol) for the treatment of high blood pressure. Bystolic is a "beta blocker," a well-established class of medications that reduces blood pressure by reducing the force with which the heart pumps. Nearly one in three adults in the United States has high blood pressure, also called hypertension, which can increase the risks for stroke, heart failure, heart attack, kidney failure, and death.
http://www.fda.gov/bbs/topics/NEWS/2007/NEW01757.html
FDA Rule Requires Warning on Nonoxynol 9 OTC Contraceptive Products
FDA has issued a final rule today requiring manufacturers of over-the-counter (OTC) stand-alone vaginal contraceptive and spermicidal products containing the chemical ingredient nonoxynol 9 (N9) to include a warning that the chemical N9 does not provide protection against infection from HIV (the virus that causes AIDS) or other sexually transmitted diseases. Stand-alone spermicides include gels, foams, films, or inserts containing N9 that are used by themselves for contraception.
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[What is an RSS feed? See http://www.fda.gov/bbs/topics/news/newsfeeds.html.]
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SAFETY ALERTS/RECALLS
Safety Alert:
› FDA is warning consumers not to use 3.5-oz. packages of Swad brand sindoor, an orange or red powder used in some traditional South Asian Pacific ceremonies that is applied to the face or scalp. The product contains high levels of lead. Although the product was not intended to be sold for food use, its labeling is confusing and implies that it may be used as food. Illinois health officials have confirmed two cases of lead poisoning in consumers who used the product as an ingredient in home-cooked meals.
Food Recalls:
› Back to Nature Sesame Ginger Rice Thins Crackers (with "Best When Used By" date of 22FEB2008)
Reason for recall: some product may contain a milk ingredient that is not declared on the label
http://www.fda.gov/oc/po/firmrecalls/backtonature12_07.html