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FDA News Digest for November 5, 2007



FDA News Digest

November 5, 2007

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NOTE TO SUBSCRIBERS

 

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IN THIS WEEK'S ISSUE

 

»  News

    --  FDA Probe Shows That Consumers Continue to Buy Risky Drugs Online

    --  Manufacturer Agrees to Suspend Marketing of Bleeding-Control Drug Trasylol

    --  More Than $300,000 in Drugs, Supplements Seized From St. Louis Company

    --  FDA Requests Recall of Illegal 'True Man' and 'Energy Max' Drug Products

»  Congressional Testimony

»  Safety Alerts/Recalls

»  Upcoming Public Meetings

»  Consumer Health Information

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NEWS
 
FDA Probe Shows That Consumers Continue to Buy Risky Drugs Online
A yearlong FDA investigation suggests that consumers may be buying drugs online to avoid the need to get a prescription from their doctor. An agency sampling of imported drugs also indicates that consumers continue to spend money unnecessarily on potentially risky drugs bought online.
 
Manufacturer Agrees to Suspend Marketing of Bleeding-Control Drug Trasylol
Bayer Pharmaceuticals Corp. has agreed to suspend marketing of Trasylol, a drug used to control bleeding during heart surgery, pending a detailed review of preliminary results from a study that suggests an increased risk of death.
 
More Than $300,000 in Drugs, Supplements Seized From St. Louis Company
At FDA's request, U.S. marshals have seized more than $300,000 in human and animal drugs, dietary supplements, and ingredients to make these products from St. Louis-based General Therapeutics Corp. FDA says the products were maintained under unsanitary conditions, and some of the products lacked FDA approval.
 
FDA Requests Recall of Illegal 'True Man' and 'Energy Max' Drug Products
FDA has asked America True Man Health Inc. to recall its True Man Sexual Energy Nutrient Capsules and Energy Max Energy Supplement Men's Formula Capsules because the agency considers the products to be illegal drugs that contain potentially harmful ingredients. The products are often advertised as "all-natural" alternatives to approved erectile dysfunction (ED) drugs, but they contain substances similar in structure to approved ED drugs.
 
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CONGRESSIONAL TESTIMONY

 

Nov. 1 -- FDA Commissioner Andrew C. von Eschenbach, M.D., appeared before the House Subcommittee on Oversight and Investigations.

    Subject: FDA's foreign drug inspection program

http://www.fda.gov/ola/2007/foreigndrugs110107.html

 

To view an archive of past testimony by FDA officials, go to

http://www.fda.gov/ola/listing.html

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SAFETY ALERTS/RECALLS

Animal Product Recall: