Eli Lilly and Company (NYSE: LLY) announced that the Oncologic Drugs Advisory Committee of the U.S. Food and Drug Administration (FDA) voted to recommend approval of its osteoporosis drug EVISTA(R) (raloxifene HCl) for a new use to reduce invasive breast cancer risk in two populations: postmenopausal women with osteoporosis and postmenopausal women at high risk for breast cancer.
The International AIDS Society (IAS) convened and facilitated a meeting between Act Up-Paris and Abbott in Sydney, Australia.
Castleberry’s Food Company announced that it is taking extra steps to ensure public safety by voluntarily expanding its recall originally announced on July18 due to the risk of botulinum toxin, a bacterium which can cause botulism.
Castleberry’s Food Company, a Georgia establishment owned by Bumble Bee Foods, LLC, is voluntarily expanding its July_19 recall of canned meat products that may contain Clostridium botulinum, Department of Consumer Protection Commissioner Jerry Farrell, Jr. announced.
The U.S. Food and Drug Administration is expanding its July_18 warning to consumers. This expansion is for consumers and pet owners regarding canned food products and dog food produced by Castleberry Food Company of Augusta, Ga., due to the risk of botulinum toxin.
What people have come to expect in cell phones and personal communicators may soon become common in health-care devices and products at home and in medical offices, thanks to new technology announced today by the University of Florida and IBM.
Dent Fresh U.S.A., Inc, Miami, Florida, is initiating a nationwide recall in accordance with the U.S. Food and Drug Administration (FDA) of the toothpaste made in China involving all:DentFresh Fluoride Mint Toothpaste 9 Oz (255g).
The U.S. Food and Drug Administration (FDA) is warning consumers not to eat 10 ounce cans of Castleberry?s Hot Dog Chili Sauce (UPC 3030000101), Austex Hot Dog Chili Sauce (UPC 3030099533), and Kroger Hot Dog Chili Sauce (UPC 1111083942) with ?best by? dates from April 30, 2009 through May 22, 2009 due to possible botulism contamination.
Restless legs syndrome (RLS) remains a common, yet often undiagnosed, neurological sensorimotor disorder, despite many years of research and increased disease recognition.
The U.S. Food and Drug Administration (FDA) approved for marketing the Prestige Cervical Disc, made by Medtronic Sofamor Danek of Memphis?the first artificial cervical (neck) disc for the treatment of cervical degenerative disc disease, one of the most common causes of neck and arm pain.