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Evaluation of Opioid Overdose Reports in Patients Treated with Extended-Release Naltrexone: Postmarketing Data from 2006 to 2018

Introduction After treatment with naltrexone extended-release injectable suspension (XR-NTX), a µ-opioid receptor antagonist, opioid tolerance is reduced from pretreatment baseline. Patients may be vulnerable to opioid overdose if they attempt to override the blockade during treatment, at the end of...

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Published in:Drug safety 2021-03, Vol.44 (3), p.351-359
Main Authors: Jain, Priya, McKinnell, Kimberley, Marino, Rose, Vunnava, Prashanthi, Liles-Burden, Marie A., Desai, Avani, Wenten, Madé, Fratantonio, James, Akerman, Sarah C., Sullivan, Maria A., Bloomgren, Gary
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container_issue 3
container_start_page 351
container_title Drug safety
container_volume 44
creator Jain, Priya
McKinnell, Kimberley
Marino, Rose
Vunnava, Prashanthi
Liles-Burden, Marie A.
Desai, Avani
Wenten, Madé
Fratantonio, James
Akerman, Sarah C.
Sullivan, Maria A.
Bloomgren, Gary
description Introduction After treatment with naltrexone extended-release injectable suspension (XR-NTX), a µ-opioid receptor antagonist, opioid tolerance is reduced from pretreatment baseline. Patients may be vulnerable to opioid overdose if they attempt to override the blockade during treatment, at the end of a dosing interval, after missing a dose, or after discontinuing treatment. Objective We analyzed postmarketing data to characterize reporting rates of opioid overdose during treatment with and after discontinuation of XR-NTX. Methods Postmarketing adverse event reports within the XR-NTX safety database, received 2006–2018, for patients treated with XR-NTX for any indication were reviewed for opioid overdose cases. Assessable cases were categorized by timing of the event from the last dose of XR-NTX (latency): ≤28 days (on treatment), 29–56 days, and >56 days from last dose of XR-NTX. Within each latency group, cases were further classified as serious and, of those, cases that had a fatal outcome. Results During the 12-year period, an estimated 495,602 patients received XR-NTX. Opioid overdose was reported in 161 cases; of these, 66 contained sufficient information to determine latency. Reporting rates of opioid overdose per 10,000 patients treated were similar among latency groups: 0.54 for ≤28 days (0.24 fatal), 0.34 for 29–56 days (0.16 fatal), and 0.44 for >56 days (0.40 fatal) from the last dose of XR-NTX. Conclusions Over the 12-year period, the reporting rates of opioid overdose were similar during treatment with or after discontinuation of XR-NTX and
doi_str_mv 10.1007/s40264-020-01020-4
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Patients may be vulnerable to opioid overdose if they attempt to override the blockade during treatment, at the end of a dosing interval, after missing a dose, or after discontinuing treatment. Objective We analyzed postmarketing data to characterize reporting rates of opioid overdose during treatment with and after discontinuation of XR-NTX. Methods Postmarketing adverse event reports within the XR-NTX safety database, received 2006–2018, for patients treated with XR-NTX for any indication were reviewed for opioid overdose cases. Assessable cases were categorized by timing of the event from the last dose of XR-NTX (latency): ≤28 days (on treatment), 29–56 days, and &gt;56 days from last dose of XR-NTX. Within each latency group, cases were further classified as serious and, of those, cases that had a fatal outcome. Results During the 12-year period, an estimated 495,602 patients received XR-NTX. Opioid overdose was reported in 161 cases; of these, 66 contained sufficient information to determine latency. Reporting rates of opioid overdose per 10,000 patients treated were similar among latency groups: 0.54 for ≤28 days (0.24 fatal), 0.34 for 29–56 days (0.16 fatal), and 0.44 for &gt;56 days (0.40 fatal) from the last dose of XR-NTX. Conclusions Over the 12-year period, the reporting rates of opioid overdose were similar during treatment with or after discontinuation of XR-NTX and &lt;10/10,000 patients exposed. Our findings are limited by the nature of spontaneously reported safety data.</description><identifier>ISSN: 0114-5916</identifier><identifier>EISSN: 1179-1942</identifier><identifier>DOI: 10.1007/s40264-020-01020-4</identifier><identifier>PMID: 33258068</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adverse events ; Dosage ; Drug dosages ; Drug overdose ; Drug Safety and Pharmacovigilance ; Drug tolerance ; Latency ; Medicine ; Medicine &amp; Public Health ; Mortality ; Naltrexone ; Narcotics ; Opioid receptors ; Original ; Original Research Article ; Overdose ; Patients ; Pharmacology/Toxicology ; Pretreatment ; Safety ; Sensitivity analysis</subject><ispartof>Drug safety, 2021-03, Vol.44 (3), p.351-359</ispartof><rights>The Author(s) 2020</rights><rights>Copyright Springer Nature B.V. Mar 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-a02a3ce66d131d79777a6e4451ccd2a00cd1b1b74190e21c9b83f1cfed3f484f3</citedby><cites>FETCH-LOGICAL-c474t-a02a3ce66d131d79777a6e4451ccd2a00cd1b1b74190e21c9b83f1cfed3f484f3</cites><orcidid>0000-0002-5519-7256</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,27911,27912</link.rule.ids></links><search><creatorcontrib>Jain, Priya</creatorcontrib><creatorcontrib>McKinnell, Kimberley</creatorcontrib><creatorcontrib>Marino, Rose</creatorcontrib><creatorcontrib>Vunnava, Prashanthi</creatorcontrib><creatorcontrib>Liles-Burden, Marie A.</creatorcontrib><creatorcontrib>Desai, Avani</creatorcontrib><creatorcontrib>Wenten, Madé</creatorcontrib><creatorcontrib>Fratantonio, James</creatorcontrib><creatorcontrib>Akerman, Sarah C.</creatorcontrib><creatorcontrib>Sullivan, Maria A.</creatorcontrib><creatorcontrib>Bloomgren, Gary</creatorcontrib><title>Evaluation of Opioid Overdose Reports in Patients Treated with Extended-Release Naltrexone: Postmarketing Data from 2006 to 2018</title><title>Drug safety</title><addtitle>Drug Saf</addtitle><description>Introduction After treatment with naltrexone extended-release injectable suspension (XR-NTX), a µ-opioid receptor antagonist, opioid tolerance is reduced from pretreatment baseline. Patients may be vulnerable to opioid overdose if they attempt to override the blockade during treatment, at the end of a dosing interval, after missing a dose, or after discontinuing treatment. Objective We analyzed postmarketing data to characterize reporting rates of opioid overdose during treatment with and after discontinuation of XR-NTX. Methods Postmarketing adverse event reports within the XR-NTX safety database, received 2006–2018, for patients treated with XR-NTX for any indication were reviewed for opioid overdose cases. Assessable cases were categorized by timing of the event from the last dose of XR-NTX (latency): ≤28 days (on treatment), 29–56 days, and &gt;56 days from last dose of XR-NTX. Within each latency group, cases were further classified as serious and, of those, cases that had a fatal outcome. Results During the 12-year period, an estimated 495,602 patients received XR-NTX. Opioid overdose was reported in 161 cases; of these, 66 contained sufficient information to determine latency. Reporting rates of opioid overdose per 10,000 patients treated were similar among latency groups: 0.54 for ≤28 days (0.24 fatal), 0.34 for 29–56 days (0.16 fatal), and 0.44 for &gt;56 days (0.40 fatal) from the last dose of XR-NTX. Conclusions Over the 12-year period, the reporting rates of opioid overdose were similar during treatment with or after discontinuation of XR-NTX and &lt;10/10,000 patients exposed. 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Drug safety</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jain, Priya</au><au>McKinnell, Kimberley</au><au>Marino, Rose</au><au>Vunnava, Prashanthi</au><au>Liles-Burden, Marie A.</au><au>Desai, Avani</au><au>Wenten, Madé</au><au>Fratantonio, James</au><au>Akerman, Sarah C.</au><au>Sullivan, Maria A.</au><au>Bloomgren, Gary</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of Opioid Overdose Reports in Patients Treated with Extended-Release Naltrexone: Postmarketing Data from 2006 to 2018</atitle><jtitle>Drug safety</jtitle><stitle>Drug Saf</stitle><date>2021-03-01</date><risdate>2021</risdate><volume>44</volume><issue>3</issue><spage>351</spage><epage>359</epage><pages>351-359</pages><issn>0114-5916</issn><eissn>1179-1942</eissn><abstract>Introduction After treatment with naltrexone extended-release injectable suspension (XR-NTX), a µ-opioid receptor antagonist, opioid tolerance is reduced from pretreatment baseline. Patients may be vulnerable to opioid overdose if they attempt to override the blockade during treatment, at the end of a dosing interval, after missing a dose, or after discontinuing treatment. Objective We analyzed postmarketing data to characterize reporting rates of opioid overdose during treatment with and after discontinuation of XR-NTX. Methods Postmarketing adverse event reports within the XR-NTX safety database, received 2006–2018, for patients treated with XR-NTX for any indication were reviewed for opioid overdose cases. Assessable cases were categorized by timing of the event from the last dose of XR-NTX (latency): ≤28 days (on treatment), 29–56 days, and &gt;56 days from last dose of XR-NTX. Within each latency group, cases were further classified as serious and, of those, cases that had a fatal outcome. Results During the 12-year period, an estimated 495,602 patients received XR-NTX. Opioid overdose was reported in 161 cases; of these, 66 contained sufficient information to determine latency. Reporting rates of opioid overdose per 10,000 patients treated were similar among latency groups: 0.54 for ≤28 days (0.24 fatal), 0.34 for 29–56 days (0.16 fatal), and 0.44 for &gt;56 days (0.40 fatal) from the last dose of XR-NTX. Conclusions Over the 12-year period, the reporting rates of opioid overdose were similar during treatment with or after discontinuation of XR-NTX and &lt;10/10,000 patients exposed. Our findings are limited by the nature of spontaneously reported safety data.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>33258068</pmid><doi>10.1007/s40264-020-01020-4</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5519-7256</orcidid><oa>free_for_read</oa></addata></record>
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source Nexis UK; Springer Nature
subjects Adverse events
Dosage
Drug dosages
Drug overdose
Drug Safety and Pharmacovigilance
Drug tolerance
Latency
Medicine
Medicine & Public Health
Mortality
Naltrexone
Narcotics
Opioid receptors
Original
Original Research Article
Overdose
Patients
Pharmacology/Toxicology
Pretreatment
Safety
Sensitivity analysis
title Evaluation of Opioid Overdose Reports in Patients Treated with Extended-Release Naltrexone: Postmarketing Data from 2006 to 2018
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