Loading…
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...
Saved in:
Published in: | Drug safety 2021-03, Vol.44 (3), p.351-359 |
---|---|
Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c474t-a02a3ce66d131d79777a6e4451ccd2a00cd1b1b74190e21c9b83f1cfed3f484f3 |
---|---|
cites | cdi_FETCH-LOGICAL-c474t-a02a3ce66d131d79777a6e4451ccd2a00cd1b1b74190e21c9b83f1cfed3f484f3 |
container_end_page | 359 |
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 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7892734</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2493542128</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-a02a3ce66d131d79777a6e4451ccd2a00cd1b1b74190e21c9b83f1cfed3f484f3</originalsourceid><addsrcrecordid>eNp9kUFvEzEQhS0EoqHwBzhZ4rwwYztrLwckVAJFqkhVlbPlrGfTLRs72E4oN356HVKBuHCZGcnvfTPWY-wlwmsE0G-yAtGqBgQ0gIeqHrEZou4a7JR4zGaAqJp5h-0Je5bzLQAY0Zqn7ERKMTfQmhn7tdi7aefKGAOPA19uxzh6vtxT8jETv6JtTCXzMfDLKqJQ5-tErpDnP8Zywxd3hYIn31zRRK46vripJLqLgd7yy5jLxqVvVMaw5h9ccXxIccMFQMtLrB3Nc_ZkcFOmFw_9lH39uLg-O28ulp8-n72_aHqlVWkcCCd7aluPEr3utNauJaXm2PdeOIDe4wpXWmEHJLDvVkYO2A_k5aCMGuQpe3fkbnerDfm-fiW5yW7TWC_8aaMb7b8vYbyx67i32nRCS1UBrx4AKX7fUS72Nu5SqDdboTo5VwKFqSpxVPUp5pxo-LMBwR5Ss8fUbM3L_k7NHtDyaMpVHNaU_qL_47oHsn-Z6w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2493542128</pqid></control><display><type>article</type><title>Evaluation of Opioid Overdose Reports in Patients Treated with Extended-Release Naltrexone: Postmarketing Data from 2006 to 2018</title><source>Nexis UK</source><source>Springer Nature</source><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</creator><creatorcontrib>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</creatorcontrib><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 <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 & 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 >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 <10/10,000 patients exposed. Our findings are limited by the nature of spontaneously reported safety data.</description><subject>Adverse events</subject><subject>Dosage</subject><subject>Drug dosages</subject><subject>Drug overdose</subject><subject>Drug Safety and Pharmacovigilance</subject><subject>Drug tolerance</subject><subject>Latency</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mortality</subject><subject>Naltrexone</subject><subject>Narcotics</subject><subject>Opioid receptors</subject><subject>Original</subject><subject>Original Research Article</subject><subject>Overdose</subject><subject>Patients</subject><subject>Pharmacology/Toxicology</subject><subject>Pretreatment</subject><subject>Safety</subject><subject>Sensitivity analysis</subject><issn>0114-5916</issn><issn>1179-1942</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kUFvEzEQhS0EoqHwBzhZ4rwwYztrLwckVAJFqkhVlbPlrGfTLRs72E4oN356HVKBuHCZGcnvfTPWY-wlwmsE0G-yAtGqBgQ0gIeqHrEZou4a7JR4zGaAqJp5h-0Je5bzLQAY0Zqn7ERKMTfQmhn7tdi7aefKGAOPA19uxzh6vtxT8jETv6JtTCXzMfDLKqJQ5-tErpDnP8Zywxd3hYIn31zRRK46vripJLqLgd7yy5jLxqVvVMaw5h9ccXxIccMFQMtLrB3Nc_ZkcFOmFw_9lH39uLg-O28ulp8-n72_aHqlVWkcCCd7aluPEr3utNauJaXm2PdeOIDe4wpXWmEHJLDvVkYO2A_k5aCMGuQpe3fkbnerDfm-fiW5yW7TWC_8aaMb7b8vYbyx67i32nRCS1UBrx4AKX7fUS72Nu5SqDdboTo5VwKFqSpxVPUp5pxo-LMBwR5Ss8fUbM3L_k7NHtDyaMpVHNaU_qL_47oHsn-Z6w</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Jain, Priya</creator><creator>McKinnell, Kimberley</creator><creator>Marino, Rose</creator><creator>Vunnava, Prashanthi</creator><creator>Liles-Burden, Marie A.</creator><creator>Desai, Avani</creator><creator>Wenten, Madé</creator><creator>Fratantonio, James</creator><creator>Akerman, Sarah C.</creator><creator>Sullivan, Maria A.</creator><creator>Bloomgren, Gary</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7T2</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5519-7256</orcidid></search><sort><creationdate>20210301</creationdate><title>Evaluation of Opioid Overdose Reports in Patients Treated with Extended-Release Naltrexone: Postmarketing Data from 2006 to 2018</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-a02a3ce66d131d79777a6e4451ccd2a00cd1b1b74190e21c9b83f1cfed3f484f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adverse events</topic><topic>Dosage</topic><topic>Drug dosages</topic><topic>Drug overdose</topic><topic>Drug Safety and Pharmacovigilance</topic><topic>Drug tolerance</topic><topic>Latency</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mortality</topic><topic>Naltrexone</topic><topic>Narcotics</topic><topic>Opioid receptors</topic><topic>Original</topic><topic>Original Research Article</topic><topic>Overdose</topic><topic>Patients</topic><topic>Pharmacology/Toxicology</topic><topic>Pretreatment</topic><topic>Safety</topic><topic>Sensitivity analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>SpringerOpen(OpenAccess)</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Nursing & Allied Health Database</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & 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 >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 <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> |
fulltext | fulltext |
identifier | ISSN: 0114-5916 |
ispartof | Drug safety, 2021-03, Vol.44 (3), p.351-359 |
issn | 0114-5916 1179-1942 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7892734 |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T09%3A24%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Evaluation%20of%20Opioid%20Overdose%20Reports%20in%20Patients%20Treated%20with%20Extended-Release%20Naltrexone:%20Postmarketing%20Data%20from%202006%20to%202018&rft.jtitle=Drug%20safety&rft.au=Jain,%20Priya&rft.date=2021-03-01&rft.volume=44&rft.issue=3&rft.spage=351&rft.epage=359&rft.pages=351-359&rft.issn=0114-5916&rft.eissn=1179-1942&rft_id=info:doi/10.1007/s40264-020-01020-4&rft_dat=%3Cproquest_pubme%3E2493542128%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c474t-a02a3ce66d131d79777a6e4451ccd2a00cd1b1b74190e21c9b83f1cfed3f484f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2493542128&rft_id=info:pmid/33258068&rfr_iscdi=true |