2015년 3월 17일 화요일

NGC Update Service: March 16, 2015

National Guideline Clearinghouse (NGC)

March 16, 2015


New This Week

Guideline Summaries

CancerControl Alberta
Clinical Pharmacogenetics Implementation Consortium
College of American Pathologists
Department of Veterans Affairs
National Institute for Health and Care Excellence (NICE)

Announcements

NGC Spotlight

Visit the Technical Assistant Videos page to learn more about NGC's Browse and Search features, and the My NGC Personalization feature.

Health Awareness Topics - March 2015

Conference News

  • The Guidelines International Network North America (G-I-N NA)continues to sponsor a monthly webinar series on topics of interest to the North American guideline community. Information on upcoming webinars, as well as audio files and slides from past webinars, is available on the G-I-N Web site.

U.S. Food and Drug Administration (FDA) Advisories

  • March 10, 2015Treanda (bendamustine hydrochloride) Solution by Teva: FDA is warning health care professionals not to use Treanda Injection (45 mg/0.5 mL or 180 mg/2 mL solution) with closed system transfer devices (CSTD), adapters, and syringes containing polycarbonate or acrylonitrile-butadiene-styrene (ABS). Most marketed CSTDs contain either polycarbonate or ABS and are not compatible with Treanda Injection (45 mg/0.5 mL or 180 mg/2 mL solution). FDA is requiring label changes for both the solution and the powder formulations of Treanda to reflect safe preparation information.
  • March 9, 2015Chantix (varenicline): FDA is warning that the prescription smoking cessation medicine Chantix (varenicline) can change the way people react to alcohol. Interactions between alcohol and Chantix have resulted in some patients experiencing increased intoxicating effects of alcohol, sometimes associated with aggressive behavior and/or amnesia. In addition, rare accounts of seizures in patients treated with Chantix have been reported. FDA has approved changes to the Chantix label to warn about these risks.
  • March 3, 2015Testosterone Products: FDA is requiring that the manufacturers of all approved prescription testosterone products change their labeling to clarify the approved uses of these medications. FDA is also requiring these manufacturers to add information to the labeling about a possible increased risk of heart attacks and strokes in patients taking testosterone.

NGC's Sister Resource



Look for Quality Measures in AHRQ's National Quality Measures Clearinghouse (NQMC).

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