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Pain Medicine Experts Recommend Monitoring, Education for All Opioid Medicines
Date:5/27/2009

American Academy of Pain Medicine Submits Comments on REMS; Leaders in Pain Research and Treatment Available to Media to Discuss Abuse, Diversion, and Pain Treatment

GLENVIEW, Ill., May 27 /PRNewswire/ -- As the U.S. Food and Drug Administration (FDA) conducts public hearings this week on Risk Evaluation and Mitigation Strategy (REMS), physician leaders from the American Academy of Pain Medicine (AAPM), the premiere medical association for physicians and teams who treat pain, are available to discuss comments it submitted to the FDA on behalf of their pain patients.

The most important aspect of the proposed FDA REMS is that it is developed with the best interests of patients in mind, according to the AAPM. Among the priorities its leaders gave the FDA:

  1. Prescription monitoring programs with accurate and real-time data
  2. Monitoring of all opioids, not only slow release opioids
  3. Education for physicians, pharmacists, and patients about medicines and monitoring

"We urge the FDA to balance safety and access when considering REMS for opioid pain medicines," said Scott Fishman, MD, University of California at Davis, and past president of the AAPM. "Under-treated pain and prescription drug abuse are both serious public health issues that deserve equal attention. The FDA has the opportunity to implement policy that will improve opioid safety, but it must use care to avoid unnecessary barriers that will reduce appropriate access for patients with serious and legitimate pain."

On May 27-28, 2009, the FDA will hold public hearings on its proposed REMS for extended release pain medications such as morphine, oxycodone and methadone. AAPM members ha
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SOURCE American Academy of Pain Medicine
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