FDA News Digest
November 24, 2003
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FDA OKs Cialis, Third Drug Approved for Treating Impotence

The third oral drug for treating erectile dysfunction (impotence) has
received FDA approval. Cialis (tadalafil) differs from other approved
impotence treatments in that it stays in the body longer. Cialis works by
relaxing muscles in the penis and blood vessels, allowing increased blood
flow into the penis, producing an erection. Erectile dysfunction affects
millions of men in the United States.
http://www.fda.gov/bbs/topics/ANSWERS/2003/ANS01265.html
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FDA Orders Green Onions from Eight Mexican Firms Held at Border

Following recent outbreaks of hepatitis A infections in Tennessee, Georgia
and Pennsylvania that were linked to raw green onions (scallions), FDA has
ordered raw green onions from eight Mexican companies to be detained at the
U.S.-Mexico border. The agency continues to investigate hepatitis A
outbreaks in North Carolina. FDA is working with federal, state and Mexican
authorities on the case.
http://www.fda.gov/bbs/topics/NEWS/2003/NEW00981.html
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FDA Offers Tips to Avoid Foodborne Illness This Holiday Season

FDA is encouraging consumers to pay special attention to how they handle and
prepare foods during the upcoming holiday season. Though foodborne illness
is not common during the holidays, many people -- including children, the
elderly, and those with weakened immune systems -- should be aware of the
risks.
http://www.fda.gov/bbs/topics/ANSWERS/2003/ANS01263.html
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Agency Seeks Public Comments on Managing Qualified Health Claims

FDA is requesting comments from the public on several topics involving
qualified health claims and other potential initiatives to help consumers
choose a healthy diet. Qualified health claims are ones not supported by
significant scientific agreement. Among other issues, FDA is seeking
comments on alternatives for regulating qualified health claims and on the
appropriateness and nature of dietary guidance statements on food labels.
http://www.fda.gov/bbs/topics/ANSWERS/2003/ANS01266.html
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New Law Lets FDA Charge Fees to Help Speed Animal Drug Review

The Animal Drug User Fee Act, signed Nov. 18, establishes a funding system
for FDA's review of new animal drugs. Under the law, the agency can charge
fees that will provide resources to help speed reviews and shorten the time
for introducing new therapies for treating pets and food-producing animals.
FDA is authorized to collect $5 million in user fees in fiscal year 2004.
http://www.fda.gov/bbs/topics/NEWS/2003/NEW00978.html
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Officials Praise Congressional Passage of Pediatric Research Act

Health and Human Services Secretary Tommy G. Thompson and FDA Commissioner
Mark B. McClellan, M.D., have issued a statement praising Congress for
passing the Pediatric Research Equity Act. When signed into law, the act
will enable FDA to require that drugs intended for pediatric use be tested
in children.
http://www.fda.gov/bbs/topics/NEWS/2003/NEW00979.html
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RECALL

The following product is being recalled for the reason shown. Go to the
linked page for more information.

Dean Milk Co. 2% Reduced Fat Milk (possible contamination with eggs)
http://www.fda.gov/oc/po/firmrecalls/dean11_03.html
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RECENT SPEECHES

FDA Commissioner Mark B. McClellan, M.D.; to the Drug Information
Association, Ottawa, Canada (Nov. 18)
http://www.fda.gov/oc/speeches/2003/canada1118.html
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RECENT TESTIMONY

FDA Acting Director of Vaccine Research and Review William Egan, Ph.D.,
before the House Subcommittee on Wellness and Human Rights (Nov. 13)
http://www.fda.gov/ola/2003/simianvirus1113.html
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Latest FDA Consumer Magazine Available Online

The latest issue of FDA Consumer, available online at
http://www.fda.gov/fdac/603_toc.html, has articles on the following topics:

*       Heart health -- Prevention is the best weapon against heart disease,
the nation's number one killer.
*       Menopausal hormone therapy -- FDA offers advice to women on using
hormones to treat menopause symptoms.
*       Tanning risks -- The facts on "sunless" and "natural" tans.
*       Genetically engineered foods -- FDA is working to meet the
challenges of regulating these future food products.
*       Climbing wheelchair -- A new device allows people with impaired
mobility to climb stairs, curbs, and more.
*       Orphan products -- How FDA is helping people with rare diseases.
*       Cochlear implants -- Children with these hearing implants have an
increased risk of developing bacterial meningitis.
*       FDA's bionic skeleton -- After three decades on the road as a
teaching device, "Yorick" comes to rest in the Smithsonian Institution.
*
*       The issue also has:
*
*       a commentary on diagnosing heart disease
*       a report on a California company that agreed to pay $92.4 million to
settle charges after pleading guilty to covering up medical device
malfunctions
*       the "fda.gov" column, which reviews and previews health-related
websites.
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