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The information drug dispensing was modeled with PRE2DUP method as time\u2010varying measure updated at every dispensing and then divided into three dose categories which were low dose (&lt;\u20091.0 Defined Daily Doses [DDDs] per day), medium to high dose (1.0\u2013&lt;\u20093.0 DDDs\/day) and very high\u2010dose (\u2265\u20093.0 DDDs\/day). Risk of mortality was studied with Cox regression models.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The study included 48,124 incident\n                      <jats:styled-content style=\"fixed-case\">BZDR<\/jats:styled-content>\n                      users aged 18\u201365\u2009years (44.4% male). During the 5\u2010year follow\u2010up, 2294 (4.9%) individuals died. Compared to non\u2010use periods,\n                      <jats:styled-content style=\"fixed-case\">BZDRs<\/jats:styled-content>\n                      use was associated with increased mortality risk (adjusted Hazard Ratio\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      1.28, 95% Confidence Interval\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      1.16\u20131.41). Compared to the time periods when\n                      <jats:styled-content style=\"fixed-case\">BZDRs<\/jats:styled-content>\n                      were not used, both medium to high\u2010dose use (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      1.58, 1.36\u20131.74) and very\u2010high\u2010dose use (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      2.68, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      2.20\u20133.26) were associated with an increased risk of all\u2010cause mortality, whereas low dose use was not. The highest risk estimates were observed during very high\u2010dose use and for potentially preventable deaths such as overdoses (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      6.18, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      3.77\u201310.12), suicides (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      4.46, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      2.79\u20137.13), and accidents (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      3.77, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      2.66\u20135.35).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Persons using\n                      <jats:styled-content style=\"fixed-case\">BZDRs<\/jats:styled-content>\n                      in very high doses are at a six\u2010fold increased risk of overdose deaths compared to non\u2010use, and those using\n                      <jats:styled-content style=\"fixed-case\">BZDRs<\/jats:styled-content>\n                      in medium to high doses are at a three\u2010fold increased risk. In low doses, however, the risk of all\u2010cause mortality was not elevated. The mortality risk strongly associates with higher doses and is often characterized by concomitant use of more than one\n                      <jats:styled-content style=\"fixed-case\">BZDRs<\/jats:styled-content>\n                      at the same time.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/acps.70121","type":"journal-article","created":{"date-parts":[[2026,6,22]],"date-time":"2026-06-22T04:35:33Z","timestamp":1782102933000},"page":"342-351","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Benzodiazepine Use and Mortality Risk: A Nationwide Cohort Study on New Benzodiazepine Users With a 5\u2010Year Follow\u2010Up"],"prefix":"10.1111","volume":"154","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5819-0586","authenticated-orcid":false,"given":"Hanna","family":"S\u00e4rkil\u00e4","sequence":"first","affiliation":[{"name":"Department of Psychiatry, Clinical Institute 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