You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT JAMA
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 296 No. 12, September 27, 2006 TABLE OF CONTENTS
  JAMA
  •  Online Features
  Medical News & Perspectives
 This Article
 •Full text
 •PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citing articles on Web of Science (1)
 •Contact me when this article is cited
 Related Content
 •Similar articles in JAMA
 Topic Collections
 •Injury Prevention & Control
 •Drug Therapy
 •Adverse Effects
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

MIT, FDA Develop Safety Monitoring Tool

Bridget M. Kuehn

JAMA. 2006;296:1457.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Technology currently being used to monitor for early signs of bioterrorism and naturally occurring outbreaks may soon help improve the US Food and Drug Administration's (FDA) postmarketing surveillance system.

Scientists at the Massachusetts Institute of Technology (MIT) in Cambridge are developing a computer surveillance system that would mine databases from hospitals, health maintenance organizations, and federal agencies to help the FDA identify early signs of safety problems with prescription drugs and medical devices. The collaboration between the FDA and MIT’s Center for Biomedical Innovation was announced in August.


Figure 60114
Technology used to monitor disease outbreaks identified 3 and 4 year olds as key spreaders of influenza who should be vaccinated. The technology is now being modified to monitor for drug safety and device problems. (Photo credit: Alix/www.sciencesource.com)

The system will supplement the FDA's Adverse Events Reporting System, which relies on voluntary reports submitted by physicians or . . . [Full Text of this Article]

COLLABORATIVE EFFORT



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2006 American Medical Association. All Rights Reserved.