This is a discussion on FDA OKs emergency drug use to combat flu outbreak within the Biotechnology News forum, part of the Industry News and Updates category; The FDA has authorized the emergency use of antivirals and diagnostic tests to help fight the spread of swine flu ...
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The FDA has authorized the emergency use of antivirals and diagnostic tests to help fight the spread of swine flu in the United States.
The order, signed on Monday, gives the CDC the authority to use a clinical test not yet approved for swine flu, but is only available in a few government labs that will be testing samples. The FDA is also authorizing the use of Roche's Tamiflu in infants under the age of one. And Glaxo's Relenza is authorized for use against the flu. The FDA's actions are designed to guard physicians and other health workers from litigation. The Project BioShield Act of 2004 outlined the emergency authorization process, requiring the CDC and FDA to work as a team as it responds to a pandemic or bioterror attack. - read the report in the Wall Street Journal ALSO: 3M says that the N95 face mask, which is used to help protect people from the flu, is now on back order. "We've significantly increased production and we are working hard to meet the demand," said a spokesperson. Report Related Articles: Borders tightened as WHO raises pandemic threat level Biotech companies scramble as swine flu spreads Roche, Glaxo ramping up on flu meds U.S. declares swine flu health emergency Swine flu outbreak triggers pandemic alarm More... |
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