Buprenorphine transdermal system utilization
Author:
Affiliation:
1. Medical Affairs Strategic Research, Purdue Pharma L.P, Stamford, CT, USA
Funder
Purdue Pharma L.P.
Publisher
Informa UK Limited
Subject
General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/00325481.2017.1267537
Reference8 articles.
1. FDA announces safety labeling changes and postmarket study requirements for extended-release and long-acting opioid analgesics. Silver Spring (MD): US Food and Drug Administration; 2013 [cited 2016 Oct 28]. Available from: http://www.fda.gov/NewsEvents/Newsroom/PressAnnoucements/ucm367726.htm
2. CDC Guideline for Prescribing Opioids for Chronic Pain — United States, 2016
3. FDA announces enhanced warnings for immediate-release opioids pain medications related to risks of misuse, abuse, addiction, overdose, and death. Silver Spring (MD: US Food and Drug Administration; 2016 [cited 2016 Oct 28]. Available from: http://www.fda.gov/NewsEvents/Newsroom/PressAnnoucements/ucm491739.htm
4. On deriving the dose–effect relation of an unknown second component: An example using buprenorphine preclinical data
5. Buprenorphine maintenance and mu-opioid receptor availability in the treatment of opioid use disorder: Implications for clinical use and policy
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