Jesse_Goodman - HOUSE HEARING ON FLU VACCINE

HOUSE HEARING ON FLU VACCINE

Centers for Disease Control and Prevention director Dr. Julie Gerberding and and Food and Drug Administration Center for Biologics Evaluation and Research Director Dr. Jesse Goodman give testimony during a House Committee on Government Reform hearing on Thursday, Feb. 10, 2005, in Washington. Gerberding gave an update about the status of flu vaccines. (UPI Photo/Kamenko Pajic)


UPI Related News
WASHINGTON, Sept. 15 (UPI) -- The U.S. Food and Drug Administration announced approval Tuesday of four vaccines to be used against the H1N1 influenza virus, also called swine flu.
WASHINGTON, Jan. 20 (UPI) -- The U.S. Food and Drug Administration has approved RiaSTAP for the treatment of bleeding in patients with a rare genetic defect.
WASHINGTON, Oct. 13 (UPI) -- The U.S. Food and Drug Administration has approved for marketing the first product in the United States that protects people with hereditary angioedema.
WASHINGTON, Oct. 13 (UPI) -- The U.S. Food and Drug Administration has approved a new use for the blood product Kogenate FS in children with the most severe form of hemophilia.
WASHINGTON, Oct. 7 (UPI) -- The U.S. Food and Drug Administration said it is entering into a collaboration to create better safety and efficacy tests for experimental malaria vaccines.
WASHINGTON, March 20 (UPI) -- The U.S. Food and Drug Administration approved a medical adhesive -- a fibrin sealant called Artiss -- for use in attaching skin grafts to burn patients.
WASHINGTON, Feb. 21 (UPI) -- The U.S. Food and Drug Administration approved a new treatment for hemophilia A -- a rare, hereditary blood-clotting disorder.
WASHINGTON, Jan. 17 (UPI) -- The U.S. Food and Drug Administration announced approval Thursday of the first clotting solution made using recombinant DNA techniques.
WASHINGTON, Jan. 16 (UPI) -- The U.S. Food and Drug Administration has expanded use of a liquid protein sealant to help control bleeding during general surgery.
WASHINGTON, Jan. 14 (UPI) -- The U.S. Food and Drug Administration has licensed 14 new tests for determining a person's blood type.
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