<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Nakajima A</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>An interim analysis of postmarketing surveillance reported the safety and efficacy of elobixibat, a laxative medication that inhibits the ileal bile acid transporter, at 4 weeks in approximately 1000 patients with chronic constipation in Japan. However, its long-term safety and efficacy in elderly patients remain unclear. This study aimed to conclude and report the final analysis of postmarketing surveillance, including 52-week safety and efficacy profiles in a clinical practice setting, using approximately 3000 patients.&lt;h4>Methods&lt;/h4>The overall survey period spanned from June 2018 to May 2022. Observation periods were set at 4 weeks (4-week treatment period) and 52 weeks (52-week treatment period). Adverse drug reactions and efficacy outcomes, including defecation fre</pubmed_abstract><journal>SAGE open medicine</journal><pagination>20503121251321659</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11863239</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A multicenter, postmarketing surveillance of elobixibat in patients with chronic constipation in Japan: A final analysis report.</pubmed_title><pmcid>PMC11863239</pmcid><pubmed_authors>Shimada Y</pubmed_authors><pubmed_authors>Umeyama M</pubmed_authors><pubmed_authors>Nakajima A</pubmed_authors><pubmed_authors>Arai Y</pubmed_authors><pubmed_authors>Higashikawa M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A multicenter, postmarketing surveillance of elobixibat in patients with chronic constipation in Japan: A final analysis report.</name><description>&lt;h4>Objective&lt;/h4>An interim analysis of postmarketing surveillance reported the safety and efficacy of elobixibat, a laxative medication that inhibits the ileal bile acid transporter, at 4 weeks in approximately 1000 patients with chronic constipation in Japan. However, its long-term safety and efficacy in elderly patients remain unclear. This study aimed to conclude and report the final analysis of postmarketing surveillance, including 52-week safety and efficacy profiles in a clinical practice setting, using approximately 3000 patients.&lt;h4>Methods&lt;/h4>The overall survey period spanned from June 2018 to May 2022. Observation periods were set at 4 weeks (4-week treatment period) and 52 weeks (52-week treatment period). Adverse drug reactions and efficacy outcomes, including defecation fre</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-04-03T23:44:13.29Z</modification><creation>2025-04-03T23:44:13.29Z</creation></dates><accession>S-EPMC11863239</accession><cross_references><pubmed>40012762</pubmed><doi>10.1177/20503121251321659</doi></cross_references></HashMap>