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2009-09-16 00:07:18
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Vikram Kothandaraman
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H1N1 Pandemic May Have Peaked in October in U.S., According to Quest Diagnostics (Popularity:  ): Rates of infection by the 2009 H1N1 influenza virus may have peaked in late October, but the pandemic flu virus continues to be a potential source of illness in all age groups, including the elderly, according to a new report by Quest Diagnostics Incorporated (NYSE: DGX), the world's leading provider of diagnostic testing, information and services.
In its most recent Quest Diagnostics Health Trends(TM) Report "Testing for H1N1 in America," Quest ...
FDA Commissioner Addresses Nation's Doctors on H1N1 Vaccine (Popularity: ): Dr. Margaret Hamburg, Commissioner of Food and Drugs, today sent a letter to America's doctors, thanking them for their efforts during the 2009 H1N1 influenza outbreak and providing information on the safety of the 2009 H1N1 vaccines.
"Some of your patients may be asking how the FDA, the manufacturers and the scientific community can have confidence in vaccines that were available just six months after the 2009 H1N1 virus emerged," Dr. ...
AMA Has Chance to Rescind Support of HR 3962; AMA Shout-Out from Public Urges Doctors to Answer to PATIENTS Not AMA Leadership (Popularity: ): Members of the AMA are trying a last-minute tactic to introduce an emergency resolution rescinding the AMA's support of HR 3962.
"We want to remind physicians that they are responsible to their PATIENTS, not the leadership of the AMA," said Kathryn Serkes, Director of Policy for the Association of American Physicians and Surgeons, and Take Back Medicine, a coalition of other medical groups.
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FDA Publishes Guidance on Diagnostic Tests for 2009 H1N1 Influenza Virus (Popularity: ): The U.S. Food and Drug Administration today published a guidance document that should help manufacturers develop diagnostic tests for the 2009 H1N1 influenza virus. Although there are not any FDA-approved or cleared tests that diagnose this specific infection, during this pandemic manufacturers can submit a request to the FDA for an Emergency Use Authorization (EUA). If granted, the EUA will allow the test to be used during the national public ...
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