<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Okada N</submitter><funding>JSPS KAKENHI</funding><pagination>174-181</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6346261</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>Breakpoint cluster region-Abelson murine leukemia (BCR-ABL) inhibitors markedly improve the prognosis of chronic myeloid leukemia. However, high treatment adherence is necessary for successful treatment with BCR-ABL inhibitors. Therefore, an adequate understanding of the adverse event profiles of BCR-ABL inhibitors is essential. Although many adverse events are observed in trials, an accurate identification of adverse events based only on clinical trial results is difficult because of strict entry criteria or limited follow-up durations. In particular, BCR-ABL inhibitor-induced impaired glucose metabolism remains controversial. Pharmacovigilance evaluations using spontaneous reporting systems are useful for analyzing drug-related adverse events in clinical settings. Therefore, we conducted</pubmed_abstract><journal>Cancer medicine</journal><pubmed_title>Pharmacovigilance evaluation of the relationship between impaired glucose metabolism and BCR-ABL inhibitor use by using an adverse drug event reporting database.</pubmed_title><pmcid>PMC6346261</pmcid><funding_grant_id>17K15506</funding_grant_id><pubmed_authors>Niimura T</pubmed_authors><pubmed_authors>Zamami Y</pubmed_authors><pubmed_authors>Goda M</pubmed_authors><pubmed_authors>Ishizawa K</pubmed_authors><pubmed_authors>Takechi K</pubmed_authors><pubmed_authors>Okada N</pubmed_authors><pubmed_authors>Ishida S</pubmed_authors><pubmed_authors>Chuma M</pubmed_authors><pubmed_authors>Hamano H</pubmed_authors><pubmed_authors>Imanishi M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pharmacovigilance evaluation of the relationship between impaired glucose metabolism and BCR-ABL inhibitor use by using an adverse drug event reporting database.</name><description>Breakpoint cluster region-Abelson murine leukemia (BCR-ABL) inhibitors markedly improve the prognosis of chronic myeloid leukemia. However, high treatment adherence is necessary for successful treatment with BCR-ABL inhibitors. Therefore, an adequate understanding of the adverse event profiles of BCR-ABL inhibitors is essential. Although many adverse events are observed in trials, an accurate identification of adverse events based only on clinical trial results is difficult because of strict entry criteria or limited follow-up durations. In particular, BCR-ABL inhibitor-induced impaired glucose metabolism remains controversial. Pharmacovigilance evaluations using spontaneous reporting systems are useful for analyzing drug-related adverse events in clinical settings. Therefore, we conducted</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-04-04T18:57:26.321Z</modification><creation>2019-03-26T22:41:56Z</creation></dates><accession>S-EPMC6346261</accession><cross_references><pubmed>30561126</pubmed><doi>10.1002/cam4.1920</doi></cross_references></HashMap>