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Creosote - FDA Information

FDA Announces New Advisory Committee to Address Risk Communication
The U.S. Food and Drug Administration (FDA) today announced a new advisory committee designed to counsel the agency on how to strengthen the communication of risks and benefits of FDA-regulated products to the public.
FDA Approves Continuous 7-Day Glucose Monitoring System
The U.S. Food and Drug Administration today approved a device that measures glucose levels continuously for up to seven days in people with diabetes.
FDA Approves the First Drug to Treat Irritability Associated with Autism, Risperdal
The approval is the first for the use of a drug to treat behaviors associated with autism in children. These behaviors are included under the general heading of irritability, and include aggression, deliberate self-injury, and temper tantrums.
FDA Approves New Drug for Skin Cancer, Zolinza
The U.S. Food and Drug Administration (FDA) today approved Zolinza (vorinostat) capsules for the treatment of cutaneous T-cell lymphoma (CTCL), a type of skin cancer, to be used when the disease persists, gets worse, or comes back during or after treatment with other medicines.
FDA Statement on Foodborne E. coli O157:H7 Outbreak in Spinach--Update: Friday, October 6, 2006
To date, 199 cases of illness due to E. coli O157:H7 infection have been reported to CDC, including 31 cases of Hemolytic Uremic Syndrome (HUS), 102 hospitalizations and three deaths.
FDA Seeks Injunction Against Orthopedic Implant Device Manufacturer
The FDA is seeking a permanent injunction against Endotec Incorporated of Orlando, Florida, and Michael J. Pappas, Ph.D., President; Frederick F. Buechel, M.D., Medical Director; and Jared Pappas, Director of Regulatory Affairs, to stop the illegal distribution of unapproved, total joint replacement devices.
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