Orfadin - FDA Information

FDA Issues Safety Alert on Avandia
Patients who are taking Avandia, especially those who are known to have underlying heart disease or who are at high risk of heart attack should talk to their doctor about this new information as they evaluate the available treatment options for their type 2 diabetes.
Joint Update: FDA/USDA Trace Adulterated Animal Feed to Poultry
The U.S. Department of Agriculture (USDA) and the U.S. Food and Drug Administration (FDA) have learned that byproducts from pet food manufactured with contaminated wheat gluten imported from China have been used in chicken feed on some farms in the state of Indiana.
FDA Re-Emphasizes Warnings to Consumers on Risks of Pet Turtles
FDA is urgently reminding the public that contact with baby turtles can pose a serious health risk to infants, small children, and adults with impaired immune systems as they can be natural hosts to Salmonella, a group of bacteria that can cause severe illness and death.
FDA Provides Web Access to Information on Post-Approval Device Studies
FDA's new Web page includes information on all post-approval device studies ordered by FDA since Jan. 1, 2005.
FDA Licenses First Biologic Product to Prevent Hepatitis B Reinfection in Liver Transplant Patients
The U.S. Food and Drug Administration (FDA) today announced the approval of HepaGam B for the prevention of hepatitis B reinfection in certain liver transplant patients. HepaGam B is the first product of its kind (an immune globulin product) approved for this purpose.
FDA Announces that Companies Must Stop Marketing Suppository Products Containing Trimethobenzamide
These products have been marketed under various names, including Tigan, Tebamide, T-Gen, Trimazide, and Trimethobenz.
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