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For Immediate Release Contact: James W. Heins/Purdue Pharma /203-588-8069 Purdue Pharma Restates Physician Prescribing Information for OxyContin® Tablets
Stamford, CT - July 25, 2001 - Purdue Pharma L.P. has made changes to the physician prescribing information for OxyContin® (oxycodone HCI controlled-release) Tablets as part of the companys efforts to help reduce the serious problem of abuse and diversion of the prescription pain medication. These voluntary changes were developed in cooperation with the U.S. Food and Drug Administration. The FDA is requesting that all manufacturers of opioid analgesics review their labeling and voluntarily make similar changes to their package inserts. We believe these changes to our package insert will further enhance our efforts to minimize abuse and diversion of OxyContin® Tablets, while continuing to ensure that legitimate patients continue to have access to this medication, stated Michael Friedman, Chief Operating Officer of Purdue Pharma. While we believe that the prior package insert provided accurate and proper information about the drug, given the recent serious problem of abuse and diversion of the product in some areas of the country, the company believes it is appropriate to make these changes at this time. We urged the FDA to join with us in calling for all manufacturers of opioid analgesics to make similar package insert changes in recognition of the growing problem of prescription drug abuse. I am pleased that Purdue is the first analgesic manufacturer to voluntarily make these changes. We are calling upon other makers of opioid analgesics to follow Purdues lead. Purdue sent a letter last week to more than 800,000 healthcare professionals outlining the revisions of the prescribing information for OxyContin® (see attachment). The revised package insert is also available on the companys website at www.purduepharma.com. The package insert is the standing reference for healthcare professionals for information on prescription medications. It includes the FDA-approved indication for use, data from clinical trials, adverse effects and warnings. Highlights of the changes to the OxyContin® package insert include:
The INDICATIONS AND USAGE section now reads:
Purdue Pharma has implemented a
comprehensive
program to combat drug diversion and
help ensure that legitimate patients continue to have appropriate
access to the medications they need. The company is introducing an
educational program alerting teenagers and pre-teens about the
dangers of prescription drug abuse. Purdue offers free
tamper-resistant prescription pads and educational materials that
help physicians and pharmacists reduce diversion of prescription
drugs, and conducts medical education programs to educate healthcare
professionals about proper pain management. The company is also
working with law enforcement to curb diversion of prescription drugs
through theft and fraud. Finally, Purdue is investing more than $50
million a year on research to develop new forms of pain relievers
that would be resistant to abuse. |
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Copyright © 2001 Purdue Pharma L. P. Reprinted with permission. |


