Safety and tolerability of empagliflozin in East Asian patients with type 2 diabetes: Pooled analysis of phase I–III clinical trials
Aims/Introduction We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes. Materials and Methods Data were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I–III trials. Adverse...
Saved in:
Published in | Journal of diabetes investigation Vol. 10; no. 2; pp. 418 - 428 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Japan
John Wiley & Sons, Inc
01.03.2019
John Wiley and Sons Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2040-1116 2040-1124 2040-1124 |
DOI | 10.1111/jdi.12910 |
Cover
Loading…
Abstract | Aims/Introduction
We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.
Materials and Methods
Data were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I–III trials. Adverse events (AEs) were analyzed in the subgroup of trial participants from East Asian countries/regions.
Results
In total, 709, 724 and 708 East Asian trial participants with type 2 diabetes received a placebo, EMPA 10 mg and EMPA 25 mg, respectively; total exposure was 953, 1,072, and 1,033 patient‐years in these groups, respectively. The EMPA and placebo groups had similar incidences of severe AEs, serious AEs and AEs leading to discontinuation. Incidences of hypoglycemia differed according to anti‐diabetes medication used at baseline. Higher rates of events consistent with genital infection were observed with EMPA (EMPA 1.5–1.7/100, placebo 0.2/100 patient‐years). Rates of AEs consistent with volume depletion were comparable among treatment groups (0.8–1.4/100 patient‐years), but in trial participants aged ≥65 years, the rate was greater with EMPA 25 mg (EMPA 25 mg 3.5/100, placebo 2.0/100 patient‐years). Incidences of events consistent with urinary tract infection, thromboembolic events, renal events, hepatic AEs, diabetic ketoacidosis, fractures and lower limb amputation were similar between EMPA and the placebo.
Conclusions
In the present pooled analysis, EMPA was well tolerated in East Asian type 2 diabetes patients based on >2,100 patient‐years’ exposure, consistent with results from the overall analysis population.
In this pooled analysis of safety data from 15 Phase I–III trials, empagliflozin 10 and 25 mg were well tolerated in East Asian patients with type 2 diabetes based on >3,000 patient‐years’ exposure, consistent with results from the overall analysis population. The incidence of hypoglycemia differed according to glucose‐lowering medication used at baseline. Genital infections, but not UTIs, were more frequent in patients treated with empagliflozin than placebo. |
---|---|
AbstractList | Aims/Introduction
We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.
Materials and Methods
Data were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I–III trials. Adverse events (AEs) were analyzed in the subgroup of trial participants from East Asian countries/regions.
Results
In total, 709, 724 and 708 East Asian trial participants with type 2 diabetes received a placebo, EMPA 10 mg and EMPA 25 mg, respectively; total exposure was 953, 1,072, and 1,033 patient‐years in these groups, respectively. The EMPA and placebo groups had similar incidences of severe AEs, serious AEs and AEs leading to discontinuation. Incidences of hypoglycemia differed according to anti‐diabetes medication used at baseline. Higher rates of events consistent with genital infection were observed with EMPA (EMPA 1.5–1.7/100, placebo 0.2/100 patient‐years). Rates of AEs consistent with volume depletion were comparable among treatment groups (0.8–1.4/100 patient‐years), but in trial participants aged ≥65 years, the rate was greater with EMPA 25 mg (EMPA 25 mg 3.5/100, placebo 2.0/100 patient‐years). Incidences of events consistent with urinary tract infection, thromboembolic events, renal events, hepatic AEs, diabetic ketoacidosis, fractures and lower limb amputation were similar between EMPA and the placebo.
Conclusions
In the present pooled analysis, EMPA was well tolerated in East Asian type 2 diabetes patients based on >2,100 patient‐years’ exposure, consistent with results from the overall analysis population.
In this pooled analysis of safety data from 15 Phase I–III trials, empagliflozin 10 and 25 mg were well tolerated in East Asian patients with type 2 diabetes based on >3,000 patient‐years’ exposure, consistent with results from the overall analysis population. The incidence of hypoglycemia differed according to glucose‐lowering medication used at baseline. Genital infections, but not UTIs, were more frequent in patients treated with empagliflozin than placebo. We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes. Data were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I-III trials. Adverse events (AEs) were analyzed in the subgroup of trial participants from East Asian countries/regions. In total, 709, 724 and 708 East Asian trial participants with type 2 diabetes received a placebo, EMPA 10 mg and EMPA 25 mg, respectively; total exposure was 953, 1,072, and 1,033 patient-years in these groups, respectively. The EMPA and placebo groups had similar incidences of severe AEs, serious AEs and AEs leading to discontinuation. Incidences of hypoglycemia differed according to anti-diabetes medication used at baseline. Higher rates of events consistent with genital infection were observed with EMPA (EMPA 1.5-1.7/100, placebo 0.2/100 patient-years). Rates of AEs consistent with volume depletion were comparable among treatment groups (0.8-1.4/100 patient-years), but in trial participants aged ≥65 years, the rate was greater with EMPA 25 mg (EMPA 25 mg 3.5/100, placebo 2.0/100 patient-years). Incidences of events consistent with urinary tract infection, thromboembolic events, renal events, hepatic AEs, diabetic ketoacidosis, fractures and lower limb amputation were similar between EMPA and the placebo. In the present pooled analysis, EMPA was well tolerated in East Asian type 2 diabetes patients based on >2,100 patient-years' exposure, consistent with results from the overall analysis population. Aims/IntroductionWe investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.Materials and MethodsData were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I–III trials. Adverse events (AEs) were analyzed in the subgroup of trial participants from East Asian countries/regions.ResultsIn total, 709, 724 and 708 East Asian trial participants with type 2 diabetes received a placebo, EMPA 10 mg and EMPA 25 mg, respectively; total exposure was 953, 1,072, and 1,033 patient‐years in these groups, respectively. The EMPA and placebo groups had similar incidences of severe AEs, serious AEs and AEs leading to discontinuation. Incidences of hypoglycemia differed according to anti‐diabetes medication used at baseline. Higher rates of events consistent with genital infection were observed with EMPA (EMPA 1.5–1.7/100, placebo 0.2/100 patient‐years). Rates of AEs consistent with volume depletion were comparable among treatment groups (0.8–1.4/100 patient‐years), but in trial participants aged ≥65 years, the rate was greater with EMPA 25 mg (EMPA 25 mg 3.5/100, placebo 2.0/100 patient‐years). Incidences of events consistent with urinary tract infection, thromboembolic events, renal events, hepatic AEs, diabetic ketoacidosis, fractures and lower limb amputation were similar between EMPA and the placebo.ConclusionsIn the present pooled analysis, EMPA was well tolerated in East Asian type 2 diabetes patients based on >2,100 patient‐years’ exposure, consistent with results from the overall analysis population. Abstract Aims/Introduction We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes. Materials and Methods Data were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I–III trials. Adverse events (AEs) were analyzed in the subgroup of trial participants from East Asian countries/regions. Results In total, 709, 724 and 708 East Asian trial participants with type 2 diabetes received a placebo, EMPA 10 mg and EMPA 25 mg, respectively; total exposure was 953, 1,072, and 1,033 patient‐years in these groups, respectively. The EMPA and placebo groups had similar incidences of severe AEs, serious AEs and AEs leading to discontinuation. Incidences of hypoglycemia differed according to anti‐diabetes medication used at baseline. Higher rates of events consistent with genital infection were observed with EMPA (EMPA 1.5–1.7/100, placebo 0.2/100 patient‐years). Rates of AEs consistent with volume depletion were comparable among treatment groups (0.8–1.4/100 patient‐years), but in trial participants aged ≥65 years, the rate was greater with EMPA 25 mg (EMPA 25 mg 3.5/100, placebo 2.0/100 patient‐years). Incidences of events consistent with urinary tract infection, thromboembolic events, renal events, hepatic AEs, diabetic ketoacidosis, fractures and lower limb amputation were similar between EMPA and the placebo. Conclusions In the present pooled analysis, EMPA was well tolerated in East Asian type 2 diabetes patients based on >2,100 patient‐years’ exposure, consistent with results from the overall analysis population. We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.AIMS/INTRODUCTIONWe investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.Data were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I-III trials. Adverse events (AEs) were analyzed in the subgroup of trial participants from East Asian countries/regions.MATERIALS AND METHODSData were pooled from participants with type 2 diabetes evenly randomized to a placebo, EMPA 10 mg or EMPA 25 mg in 15 phase I-III trials. Adverse events (AEs) were analyzed in the subgroup of trial participants from East Asian countries/regions.In total, 709, 724 and 708 East Asian trial participants with type 2 diabetes received a placebo, EMPA 10 mg and EMPA 25 mg, respectively; total exposure was 953, 1,072, and 1,033 patient-years in these groups, respectively. The EMPA and placebo groups had similar incidences of severe AEs, serious AEs and AEs leading to discontinuation. Incidences of hypoglycemia differed according to anti-diabetes medication used at baseline. Higher rates of events consistent with genital infection were observed with EMPA (EMPA 1.5-1.7/100, placebo 0.2/100 patient-years). Rates of AEs consistent with volume depletion were comparable among treatment groups (0.8-1.4/100 patient-years), but in trial participants aged ≥65 years, the rate was greater with EMPA 25 mg (EMPA 25 mg 3.5/100, placebo 2.0/100 patient-years). Incidences of events consistent with urinary tract infection, thromboembolic events, renal events, hepatic AEs, diabetic ketoacidosis, fractures and lower limb amputation were similar between EMPA and the placebo.RESULTSIn total, 709, 724 and 708 East Asian trial participants with type 2 diabetes received a placebo, EMPA 10 mg and EMPA 25 mg, respectively; total exposure was 953, 1,072, and 1,033 patient-years in these groups, respectively. The EMPA and placebo groups had similar incidences of severe AEs, serious AEs and AEs leading to discontinuation. Incidences of hypoglycemia differed according to anti-diabetes medication used at baseline. Higher rates of events consistent with genital infection were observed with EMPA (EMPA 1.5-1.7/100, placebo 0.2/100 patient-years). Rates of AEs consistent with volume depletion were comparable among treatment groups (0.8-1.4/100 patient-years), but in trial participants aged ≥65 years, the rate was greater with EMPA 25 mg (EMPA 25 mg 3.5/100, placebo 2.0/100 patient-years). Incidences of events consistent with urinary tract infection, thromboembolic events, renal events, hepatic AEs, diabetic ketoacidosis, fractures and lower limb amputation were similar between EMPA and the placebo.In the present pooled analysis, EMPA was well tolerated in East Asian type 2 diabetes patients based on >2,100 patient-years' exposure, consistent with results from the overall analysis population.CONCLUSIONSIn the present pooled analysis, EMPA was well tolerated in East Asian type 2 diabetes patients based on >2,100 patient-years' exposure, consistent with results from the overall analysis population. |
Author | Yasui, Atsutaka Ma, Ronald Ching Wan Lee, Jisoo Seino, Yutaka Okamura, Tomoo Kohler, Sven Kaspers, Stefan Zeller, Cordula Lee, Moon‐Kyu Ji, Linong Chang, Tien‐Jyun Yabe, Daisuke |
AuthorAffiliation | 3 Nippon Boehringer Ingelheim Co., Ltd. Tokyo Japan 5 Sungkyunkwan University School of Medicine Seoul Korea 2 Kyoto University Kyoto Japan 8 Boehringer Ingelheim Pharma GmbH & Co. KG Biberach an der Riss Germany 10 Kansai Electric Power Hospital Osaka Japan 9 Boehringer Ingelheim International GmbH Ingelheim Germany 1 Kansai Electric Power Medical Research Institute Kobe Japan 6 The Chinese University of Hong Kong Shatin New Territories Hong Kong SAR China 4 Peking University People's Hospital Beijing China 7 National Taiwan University Hospital Taipei City Taiwan |
AuthorAffiliation_xml | – name: 7 National Taiwan University Hospital Taipei City Taiwan – name: 8 Boehringer Ingelheim Pharma GmbH & Co. KG Biberach an der Riss Germany – name: 10 Kansai Electric Power Hospital Osaka Japan – name: 5 Sungkyunkwan University School of Medicine Seoul Korea – name: 9 Boehringer Ingelheim International GmbH Ingelheim Germany – name: 1 Kansai Electric Power Medical Research Institute Kobe Japan – name: 4 Peking University People's Hospital Beijing China – name: 2 Kyoto University Kyoto Japan – name: 6 The Chinese University of Hong Kong Shatin New Territories Hong Kong SAR China – name: 3 Nippon Boehringer Ingelheim Co., Ltd. Tokyo Japan |
Author_xml | – sequence: 1 givenname: Daisuke orcidid: 0000-0002-5334-7687 surname: Yabe fullname: Yabe, Daisuke organization: Kyoto University – sequence: 2 givenname: Atsutaka surname: Yasui fullname: Yasui, Atsutaka organization: Nippon Boehringer Ingelheim Co., Ltd – sequence: 3 givenname: Linong surname: Ji fullname: Ji, Linong organization: Peking University People's Hospital – sequence: 4 givenname: Moon‐Kyu orcidid: 0000-0002-8728-7184 surname: Lee fullname: Lee, Moon‐Kyu organization: Sungkyunkwan University School of Medicine – sequence: 5 givenname: Ronald Ching Wan orcidid: 0000-0002-1227-803X surname: Ma fullname: Ma, Ronald Ching Wan organization: Shatin New Territories – sequence: 6 givenname: Tien‐Jyun orcidid: 0000-0001-9437-5847 surname: Chang fullname: Chang, Tien‐Jyun organization: National Taiwan University Hospital – sequence: 7 givenname: Tomoo surname: Okamura fullname: Okamura, Tomoo organization: Nippon Boehringer Ingelheim Co., Ltd – sequence: 8 givenname: Cordula surname: Zeller fullname: Zeller, Cordula organization: Boehringer Ingelheim Pharma GmbH & Co. KG – sequence: 9 givenname: Stefan surname: Kaspers fullname: Kaspers, Stefan organization: Boehringer Ingelheim International GmbH – sequence: 10 givenname: Jisoo surname: Lee fullname: Lee, Jisoo organization: Boehringer Ingelheim International GmbH – sequence: 11 givenname: Sven surname: Kohler fullname: Kohler, Sven organization: Boehringer Ingelheim International GmbH – sequence: 12 givenname: Yutaka orcidid: 0000-0002-1099-7989 surname: Seino fullname: Seino, Yutaka email: yutaka.seino@kepmri.org organization: Kansai Electric Power Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30099847$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kt1qFDEUgAep2Fp74QtIwBu92DZ_k8l4IZRadaSgoF6HTH52s2Qn0yRrGa-88gV8Q5_EbHdbbNFD4ITkOx-H5Dyu9oYwmKp6iuAxKnGy1O4Y4RbBB9UBhhTOEMJ073aP2H51lNISliCcM9Y8qvYJhG3LaXNQ_fwsrckTkIMGOXgTZe-8KwfBArMa5dw768N3N4CyzmXK4DQ5OYBRZmeGnMCVywuQp9EADLSTvckmvQKfQnHpYpV-Si5tbONCJgO63z9-dV0HlHeDU9KDHJ306Un10JZkjnb5sPr69vzL2fvZxcd33dnpxUwxWMMZN8xaxjBRrbGsJZBoS3rMKKFMc9wYqnGrGVWGWMY5koTWWGlVW6ukxIocVt3Wq4NcijG6lYyTCNKJ64MQ50LG7JQ3oic1Y23LatzUlCLOsUG071mtampJ0xfX661rXPcro1V5jij9Hendm8EtxDx8E4xCiCkughc7QQyXa5OyWLmkjPdyMGGdBIa8aVtKOSzo83voMqxjed1CoULVvDRaqGd_d3Tbys13F-BkC6gYUorGCuVy-cmwadB5gaDYzJQoMyWuZ6pUvLxXcSP9F7uzXzlvpv-D4sObblvxB9hs23Y |
CitedBy_id | crossref_primary_10_1093_ndt_gfae158 crossref_primary_10_4140_TCP_n_2023_276 crossref_primary_10_1080_14740338_2020_1694659 crossref_primary_10_1371_journal_pone_0234065 crossref_primary_10_1002_cpdd_970 crossref_primary_10_1111_dom_15901 crossref_primary_10_1111_jdi_13915 crossref_primary_10_1016_j_hfc_2022_03_001 crossref_primary_10_7759_cureus_17573 crossref_primary_10_1080_14740338_2022_2054987 crossref_primary_10_1111_jcpt_13521 crossref_primary_10_2147_DMSO_S193528 crossref_primary_10_1002_edm2_183 crossref_primary_10_1111_jdi_14097 crossref_primary_10_1007_s13300_019_0604_8 crossref_primary_10_1016_j_pcd_2022_11_005 crossref_primary_10_3390_metabo11110794 crossref_primary_10_1080_14740338_2020_1782884 crossref_primary_10_1111_dom_14626 crossref_primary_10_1111_dom_13931 crossref_primary_10_1097_FJC_0000000000001498 crossref_primary_10_1111_jdi_13728 crossref_primary_10_1080_14740338_2023_2213477 crossref_primary_10_1080_14740338_2022_2107200 crossref_primary_10_1002_pds_5313 crossref_primary_10_1111_jdi_14226 crossref_primary_10_1111_dom_16282 crossref_primary_10_1016_j_jacasi_2022_03_009 crossref_primary_10_1111_jdi_13150 crossref_primary_10_1136_bmjdrc_2020_001856 |
Cites_doi | 10.1177/1479164114561992 10.1056/NEJMoa1504720 10.1253/circj.CJ-16-1148 10.1080/14656566.2016.1219341 10.1016/S2213-8587(15)00389-7 10.2337/dc17-1551 10.2337/dc12-2673 10.1111/dom.12699 10.1016/S2213-8587(13)70208-0 10.1038/nrgastro.2013.34 10.2337/dc13-2105 10.1111/dom.12081 10.1111/dme.12814 10.1016/S2213-8587(14)70227-X 10.1016/S2213-8587(13)70084-6 10.2337/dc14-1096 10.1007/s12325-017-0573-0 10.1517/14740338.2015.1034105 10.1016/j.clinthera.2015.05.511 10.1111/jdi.12626 10.1016/S0140-6736(15)61412-X 10.1056/NEJMoa1611925 10.1111/jdi.12110 10.1507/endocrj.EJ16-0295 10.2147/DDDT.S92060 10.1007/s00228-014-1730-x 10.1111/dom.12185 10.1186/s12933-015-0314-0 10.1016/j.jdiacomp.2016.10.008 10.1007/s40264-014-0213-4 10.2337/dc18-0165 10.1530/ERC-12-0290 10.2337/dc17-1525 10.1016/S2213-8587(17)30182-1 10.1111/dom.12073 10.1111/nyas.12098 10.1007/s13300-018-0385-5 10.1056/NEJMoa1515920 10.1002/hep.27259 10.1111/dom.13061 10.1007/s12325-014-0126-8 10.2215/CJN.09750913 10.7150/ijms.22224 10.1016/j.clinthera.2016.09.001 10.1111/dom.12188 10.1186/s12933-014-0169-9 10.1016/j.diabres.2015.05.044 10.2337/dc13-3055 10.1007/s11892-015-0602-9 10.2337/dc12-0413 10.1111/dom.12503 |
ContentType | Journal Article |
Copyright | 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd. 2019. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
Copyright_xml | – notice: 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd – notice: 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd. – notice: 2019. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
DBID | 24P AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7T5 7TM 7X7 7XB 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH H94 K9. M0S PHGZM PHGZT PIMPY PKEHL PQEST PQQKQ PQUKI 7X8 5PM DOA |
DOI | 10.1111/jdi.12910 |
DatabaseName | Wiley Online Library Open Access CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Immunology Abstracts Nucleic Acids Abstracts ProQuest Health & Medical Collection ProQuest Central (purchase pre-March 2016) Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials ProQuest Central ProQuest One Community College ProQuest Central Health Research Premium Collection Health Research Premium Collection (Alumni) AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) Health & Medical Collection (Alumni) ProQuest Central Premium ProQuest One Academic Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest One Academic Eastern Edition Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Hospital Collection (Alumni) ProQuest Central ProQuest Health & Medical Complete Health Research Premium Collection ProQuest One Academic UKI Edition Health and Medicine Complete (Alumni Edition) ProQuest Central Korea AIDS and Cancer Research Abstracts Immunology Abstracts ProQuest Central (New) ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE Publicly Available Content Database MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: 24P name: Wiley Online Library Open Access url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html sourceTypes: Publisher – sequence: 3 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 4 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 5 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
DocumentTitleAlternate | Yabe et al |
EISSN | 2040-1124 |
EndPage | 428 |
ExternalDocumentID | oai_doaj_org_article_b35669965275441882e14bb65c54f37b PMC6400242 30099847 10_1111_jdi_12910 JDI12910 |
Genre | article Journal Article |
GeographicLocations | Japan Hong Kong China East Asia China Taiwan |
GeographicLocations_xml | – name: Japan – name: China – name: East Asia – name: Taiwan – name: Hong Kong China |
GrantInformation_xml | – fundername: Eli Lilly and Company Diabetes Alliance – fundername: Boehringer Ingelheim |
GroupedDBID | --- 05W 0R~ 1OC 24P 31~ 4.4 50Y 5DZ 5VS 7X7 8-0 8-1 8FI 8FJ AAHHS AANHP AAZKR ABDBF ABJNI ABUWG ACBWZ ACCFJ ACCMX ACGFO ACPRK ACRPL ACUHS ACXQS ACYXJ ADBBV ADKYN ADNMO ADPDF ADRAZ ADZMN AEEZP AEGXH AENEX AEQDE AFKRA AHMBA AIAGR AIWBW AJBDE ALIPV ALMA_UNASSIGNED_HOLDINGS ALUQN AOIJS ASPBG AVUZU AVWKF AZFZN BAWUL BCNDV BDRZF BENPR BPHCQ BVXVI CAG CCPQU COF DIK EBD EBS EJD FYUFA GODZA GROUPED_DOAJ GX1 HMCUK HYE HZ~ KQ8 LH4 LW6 M48 MY. O9- OK1 OVD PIMPY PQQKQ PROAC RPM RX1 SUPJJ TEORI UKHRP WIN AAYXX AGQPQ CITATION PHGZM PHGZT CGR CUY CVF ECM EIF NPM 3V. 7T5 7TM 7XB 8FK AAMMB AEFGJ AGXDD AIDQK AIDYY AZQEC DWQXO H94 K9. PKEHL PQEST PQUKI 7X8 5PM PUEGO |
ID | FETCH-LOGICAL-c6050-8e6ff6623c9ef69303df3b264346d827e4d29d64ce3f6881a3452cdc5ffcaa2c3 |
IEDL.DBID | M48 |
ISSN | 2040-1116 2040-1124 |
IngestDate | Wed Aug 27 01:30:18 EDT 2025 Thu Aug 21 17:32:38 EDT 2025 Thu Jul 10 23:58:02 EDT 2025 Wed Aug 13 11:26:39 EDT 2025 Wed Feb 19 02:27:21 EST 2025 Tue Jul 01 02:48:42 EDT 2025 Thu Apr 24 22:53:53 EDT 2025 Wed Jan 22 16:21:43 EST 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | Genital infection Adverse drug event Sodium-glucose cotransporter 2 inhibitor |
Language | English |
License | Attribution-NonCommercial 2018 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c6050-8e6ff6623c9ef69303df3b264346d827e4d29d64ce3f6881a3452cdc5ffcaa2c3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These authors contributed equally. |
ORCID | 0000-0002-1227-803X 0000-0002-5334-7687 0000-0001-9437-5847 0000-0002-1099-7989 0000-0002-8728-7184 |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.1111/jdi.12910 |
PMID | 30099847 |
PQID | 2187958965 |
PQPubID | 1006415 |
PageCount | 11 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_b35669965275441882e14bb65c54f37b pubmedcentral_primary_oai_pubmedcentral_nih_gov_6400242 proquest_miscellaneous_2087994480 proquest_journals_2187958965 pubmed_primary_30099847 crossref_citationtrail_10_1111_jdi_12910 crossref_primary_10_1111_jdi_12910 wiley_primary_10_1111_jdi_12910_JDI12910 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | March 2019 |
PublicationDateYYYYMMDD | 2019-03-01 |
PublicationDate_xml | – month: 03 year: 2019 text: March 2019 |
PublicationDecade | 2010 |
PublicationPlace | Japan |
PublicationPlace_xml | – name: Japan – name: Richmond – name: Hoboken |
PublicationTitle | Journal of diabetes investigation |
PublicationTitleAlternate | J Diabetes Investig |
PublicationYear | 2019 |
Publisher | John Wiley & Sons, Inc John Wiley and Sons Inc Wiley |
Publisher_xml | – name: John Wiley & Sons, Inc – name: John Wiley and Sons Inc – name: Wiley |
References | 2017; 5 2015; 12 2015; 15 2015; 37 2017; 64 2015; 14 2017; 8 2015; 17 2014; 70 2015; 38 2013; 4 2013; 1 2017; 81 2015; 3 2015; 386 2013; 20 2015; 32 2015; 10 2013; 1281 2018; 41 2016; 18 2012; 35 2016; 17 2015; 9 2016; 38 2017; 377 2018; 20 2016; 4 2017; 31 2018; 9 2013; 15 2013; 36 2014; 2 2018; 4 2013; 10 2015; 61 2015; 373 2017; 34 2015; 110 2015b; 14 2014; 16 2014; 37 2016; 375 2017 2015 2018; 15 2014; 31 e_1_2_7_5_1 e_1_2_7_3_1 e_1_2_7_9_1 e_1_2_7_7_1 e_1_2_7_19_1 e_1_2_7_17_1 e_1_2_7_15_1 e_1_2_7_41_1 e_1_2_7_13_1 e_1_2_7_43_1 e_1_2_7_11_1 e_1_2_7_45_1 e_1_2_7_47_1 e_1_2_7_26_1 e_1_2_7_49_1 e_1_2_7_28_1 e_1_2_7_50_1 e_1_2_7_25_1 e_1_2_7_31_1 e_1_2_7_52_1 e_1_2_7_23_1 e_1_2_7_33_1 e_1_2_7_54_1 e_1_2_7_21_1 e_1_2_7_35_1 e_1_2_7_56_1 e_1_2_7_37_1 e_1_2_7_39_1 e_1_2_7_6_1 e_1_2_7_4_1 e_1_2_7_8_1 e_1_2_7_18_1 e_1_2_7_16_1 e_1_2_7_40_1 e_1_2_7_2_1 e_1_2_7_14_1 e_1_2_7_42_1 e_1_2_7_12_1 e_1_2_7_44_1 e_1_2_7_10_1 e_1_2_7_46_1 e_1_2_7_48_1 e_1_2_7_27_1 e_1_2_7_29_1 e_1_2_7_51_1 e_1_2_7_30_1 e_1_2_7_53_1 e_1_2_7_24_1 e_1_2_7_32_1 e_1_2_7_55_1 e_1_2_7_22_1 e_1_2_7_34_1 e_1_2_7_57_1 e_1_2_7_20_1 e_1_2_7_36_1 e_1_2_7_38_1 |
References_xml | – volume: 2 start-page: 369 year: 2014 end-page: 384 article-title: Efficacy and safety of empagliflozin added to existing antidiabetes treatment in patients with type 2 diabetes and chronic kidney disease: a randomised, double‐blind, placebo‐controlled trial publication-title: Lancet Diabetes Endocrinol – volume: 36 start-page: 3396 year: 2013 end-page: 3404 article-title: Empagliflozin as add‐on to metformin plus sulfonylurea in patients with type 2 diabetes: a 24‐week, randomized, double‐blind, placebo‐controlled trial publication-title: Diabetes Care – volume: 14 start-page: 154 year: 2015 article-title: Safety, tolerability and effects on cardiometabolic risk factors of empagliflozin monotherapy in drug‐naïve patients with type 2 diabetes: a double‐blind extension of a Phase III randomized controlled trial publication-title: Cardiovasc Diabetol – volume: 37 start-page: 1650 year: 2014 end-page: 1659 article-title: Empagliflozin as add‐on to metformin in patients with type 2 diabetes: a 24‐week, randomized, double‐blind, placebo‐controlled trial publication-title: Diabetes Care – volume: 10 start-page: 1257 year: 2015 end-page: 1272 article-title: Renal control of calcium, phosphate, and magnesium homeostasis publication-title: Clin J Am Soc Nephrol – volume: 41 start-page: e4 year: 2018 end-page: e5 article-title: Empagliflozin and assessment of lower limb amputations in the EMPA‐REG OUTCOME trial publication-title: Diabetes Care – volume: 37 start-page: 815 year: 2014 end-page: 829 article-title: Safety profile of dapagliflozin for type 2 diabetes: pooled analysis of clinical studies for overall safety and rare events publication-title: Drug Saf – volume: 20 start-page: 161 year: 2013 end-page: 171 article-title: Enhancers and attenuators of risk associations of chronic hepatitis B virus infection with hepatocellular carcinoma in type 2 diabetes publication-title: Endocr Relat Cancer – volume: 37 start-page: 1815 year: 2014 end-page: 1823 article-title: Improved glucose control with weight loss, lower insulin doses, and no increased hypoglycemia with empagliflozin added to titrated multiple daily injections of insulin in obese inadequately controlled type 2 diabetes publication-title: Diabetes Care – volume: 37 start-page: 1773 year: 2015 end-page: 1788 article-title: Empagliflozin as add‐on to pioglitazone with or without metformin in patients with type 2 diabetes publication-title: Clin Ther – volume: 10 start-page: 307 year: 2013 end-page: 318 article-title: NAFLD in Asia – as common and important as in the West publication-title: Nat Rev Gastroenterol Hepatol – volume: 81 start-page: 227 year: 2017 end-page: 234 article-title: Empagliflozin and cardiovascular outcomes in Asian patients with type 2 diabetes and established cardiovascular disease – results from EMPA‐REG OUTCOME publication-title: Circ J – volume: 34 start-page: 1707 year: 2017 end-page: 1726 article-title: Safety and tolerability of empagliflozin in patients with type 2 diabetes: pooled analysis of Phase I‐III clinical trials publication-title: Adv Ther – volume: 16 start-page: 147 year: 2014 end-page: 158 article-title: Empagliflozin improves glycaemic and weight control as add‐on therapy to pioglitazone or pioglitazone plus metformin in patients with type 2 diabetes: a 24‐week, randomized, placebo‐controlled trial publication-title: Diabetes Obes Metab – volume: 41 start-page: 1809 year: 2018 end-page: 1816 article-title: Analysis of fractures in patients with type 2 diabetes treated with empagliflozin in pooled data from placebo‐controlled trials and a head‐to‐head study versus glimepiride publication-title: Diabetes Care – volume: 1 start-page: 208 year: 2013 end-page: 219 article-title: Empagliflozin monotherapy with sitagliptin as an active comparator in patients with type 2 diabetes: a randomised, double‐blind, placebo‐controlled, phase 3 trial publication-title: Lancet Diabetes Endocrinol – volume: 4 start-page: 1801 year: 2018 end-page: 1808 article-title: Effect of empagliflozin on liver fat in patients with type 2 diabetes and nonalcoholic fatty liver disease: a randomized controlled trial (E‐LIFT Trial) publication-title: Diabetes Care – volume: 20 start-page: 438 year: 2018 end-page: 442 article-title: Luseogliflozin improves liver fat deposition compared to metformin in type 2 diabetes patients with non‐alcoholic fatty liver disease: a prospective randomized controlled pilot study publication-title: Diabetes Obes Metab – volume: 35 start-page: 1364 year: 2012 end-page: 1379 article-title: Management of hyperglycemia in type 2 diabetes: a patient‐centered approach: position statement of the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD) publication-title: Diabetes Care – volume: 377 start-page: 644 year: 2017 end-page: 657 article-title: Canagliflozin and cardiovascular and renal events in type 2 diabetes publication-title: N Engl J Med – volume: 15 start-page: 1154 year: 2013 end-page: 1160 article-title: Efficacy and safety of empagliflozin, a sodium glucose cotransporter 2 (SGLT2) inhibitor, as add‐on to metformin in type 2 diabetes with mild hyperglycaemia publication-title: Diabetes Obes Metab – volume: 17 start-page: 1995 year: 2016 end-page: 2003 article-title: Real‐world evidence for the safety of ipragliflozin in elderly Japanese patients with type 2 diabetes mellitus (STELLA‐ELDER): final results of a post‐marketing surveillance study publication-title: Expert Opin Pharmacother – volume: 31 start-page: 621 year: 2014 end-page: 638 article-title: Empagliflozin monotherapy in Japanese patients with type 2 diabetes mellitus: a randomized, 12‐week, double‐blind, placebo‐controlled, phase II trial publication-title: Adv Ther – volume: 9 start-page: 6009 year: 2015 end-page: 6017 article-title: Glucose abnormalities in Asian patients with chronic hepatitis C publication-title: Drug Des Devel Ther – volume: 1281 start-page: 64 year: 2013 end-page: 91 article-title: Type 2 diabetes in East Asians: similarities and differences with populations in Europe and the United States publication-title: Ann N Y Acad Sci – volume: 17 start-page: 936 year: 2015 end-page: 948 article-title: Impact of empagliflozin added‐on to basal insulin in type 2 diabetes inadequately controlled on basal insulin: a 78‐week randomized, double‐blind, placebo‐controlled trial publication-title: Diabetes Obes Metab – volume: 12 start-page: 78 year: 2015 end-page: 89 article-title: Probing SGLT2 as a therapeutic target for diabetes: basic physiology and consequences publication-title: Diab Vasc Dis Res – year: 2015 – volume: 14 start-page: 795 year: 2015b end-page: 800 article-title: Short‐term impacts of sodium/glucose co‐transporter 2 inhibitors in Japanese clinical practice: considerations for their appropriate use to avoid serious adverse events publication-title: Expert Opin Drug Saf – volume: 15 start-page: 613 year: 2013 end-page: 621 article-title: Safety, tolerability, pharmacokinetics and pharmacodynamics following 4 weeks’ treatment with empagliflozin once daily in patients with type 2 diabetes publication-title: Diabetes Obes Metab – volume: 64 start-page: 363 year: 2017 end-page: 367 article-title: Amelioration of fatty liver index in patients with type 2 diabetes on ipragliflozin: an association with glucose‐lowering effects publication-title: Endocr J – volume: 18 start-page: 1045 year: 2016 end-page: 1049 article-title: Efficacy and safety of empagliflozin in patients with type 2 diabetes from Asian countries: pooled data from four phase III trials publication-title: Diabetes Obes Metab – volume: 375 start-page: 323 year: 2016 end-page: 334 article-title: Empagliflozin and progression of kidney disease in type 2 diabetes publication-title: N Engl J Med – volume: 8 start-page: 766 year: 2017 end-page: 775 article-title: Safety and effectiveness of tofogliflozin in elderly Japanese patients with type 2 diabetes mellitus: a post‐marketing study (J‐STEP/EL Study) publication-title: J Diabetes Investig – volume: 32 start-page: 1555 year: 2015 end-page: 1567 article-title: Empagliflozin as add‐on to metformin in people with type 2 diabetes publication-title: Diabet Med – volume: 15 start-page: 602 year: 2015 article-title: β cell dysfunction versus insulin resistance in the pathogenesis of type 2 diabetes in East Asians publication-title: Curr Diab Rep – volume: 15 start-page: 937 year: 2018 end-page: 943 article-title: Susceptibility to serious skin and subcutaneous tissue disorders and skin tissue distribution of sodium‐dependent glucose co‐transporter type 2 (SGLT2) inhibitors publication-title: Int J Med Sci – volume: 4 start-page: 2 year: 2016 end-page: 3 article-title: Type 2 diabetes via β‐cell dysfunction in East Asian people publication-title: Lancet Diabetes Endocrinol – volume: 31 start-page: 494 year: 2017 end-page: 503 article-title: Place of sodium‐glucose cotransporter‐2 inhibitors in East Asian subjects with type 2 diabetes mellitus: insights into the management of Asian phenotype publication-title: J Diabetes Complications – volume: 3 start-page: 8 year: 2015 end-page: 10 article-title: Possible adverse effects of SGLT2 inhibitors on bone publication-title: Lancet Diabetes Endocrinol – volume: 15 start-page: 721 year: 2013 end-page: 728 article-title: A Phase IIb, randomized, placebo‐controlled study of the SGLT2 inhibitor empagliflozin in patients with type 2 diabetes publication-title: Diabetes Obes Metab – volume: 4 start-page: 613 year: 2013 end-page: 617 article-title: Pharmacokinetics, pharmacodynamics, safety and tolerability of 4 weeks’ treatment with empagliflozin in Japanese patients with type 2 diabetes mellitus publication-title: J Diabetes Investig – volume: 70 start-page: 1149 year: 2014 end-page: 1158 article-title: Efficacy and safety of canagliflozin in subjects with type 2 diabetes: systematic review and meta‐analysis publication-title: Eur J Clin Pharmacol – volume: 61 start-page: 77 year: 2015 end-page: 87 article-title: Global distribution and prevalence of hepatitis C virus genotypes publication-title: Hepatology – volume: 373 start-page: 2117 year: 2015 end-page: 2128 article-title: Empagliflozin, cardiovascular outcomes, and mortality in type 2 diabetes publication-title: N Engl J Med – volume: 14 start-page: 11 year: 2015 article-title: Effect of empagliflozin monotherapy on postprandial glucose and 24‐hour glucose variability in Japanese patients with type 2 diabetes mellitus: a randomized, double‐blind, placebo‐controlled, 4‐week study publication-title: Cardiovasc Diabetol – volume: 9 start-page: 863 year: 2018 end-page: 871 article-title: Empagliflozin induces transient diuresis without changing long‐term overall fluid balance in Japanese patients with type 2 diabetes publication-title: Diabetes Ther – volume: 386 start-page: 1546 year: 2015 end-page: 1555 article-title: Estimations of worldwide prevalence of chronic hepatitis B virus infection: a systematic review of data published between 1965 and 2013 publication-title: Lancet – year: 2017 – volume: 110 start-page: 82 year: 2015 end-page: 90 article-title: Empagliflozin as add‐on to metformin plus sulfonylurea in patients with type 2 diabetes publication-title: Diabetes Res Clin Pract – volume: 38 start-page: 420 year: 2015 end-page: 428 article-title: Empagliflozin reduces blood pressure in patients with type 2 diabetes and hypertension publication-title: Diabetes Care – volume: 38 start-page: 2265 year: 2016 end-page: 2276 article-title: Pharmacodynamic effects of single and multiple doses of empagliflozin in patients with type 2 diabetes publication-title: Clin Ther – volume: 5 start-page: 610 year: 2017 end-page: 621 article-title: Effects of empagliflozin on the urinary albumin‐to‐creatinine ratio in patients with type 2 diabetes and established cardiovascular disease: an exploratory analysis from the EMPA‐REG OUTCOME randomised, placebo‐controlled trial publication-title: Lancet Diabetes Endocrinol – ident: e_1_2_7_35_1 doi: 10.1177/1479164114561992 – ident: e_1_2_7_8_1 doi: 10.1056/NEJMoa1504720 – ident: e_1_2_7_11_1 doi: 10.1253/circj.CJ-16-1148 – ident: e_1_2_7_42_1 doi: 10.1080/14656566.2016.1219341 – ident: e_1_2_7_4_1 doi: 10.1016/S2213-8587(15)00389-7 – ident: e_1_2_7_56_1 doi: 10.2337/dc17-1551 – ident: e_1_2_7_15_1 doi: 10.2337/dc12-2673 – ident: e_1_2_7_39_1 – ident: e_1_2_7_7_1 doi: 10.1111/dom.12699 – ident: e_1_2_7_14_1 doi: 10.1016/S2213-8587(13)70208-0 – ident: e_1_2_7_44_1 doi: 10.1038/nrgastro.2013.34 – ident: e_1_2_7_2_1 – ident: e_1_2_7_16_1 doi: 10.2337/dc13-2105 – ident: e_1_2_7_26_1 doi: 10.1111/dom.12081 – ident: e_1_2_7_30_1 doi: 10.1111/dme.12814 – ident: e_1_2_7_38_1 – ident: e_1_2_7_53_1 doi: 10.1016/S2213-8587(14)70227-X – ident: e_1_2_7_20_1 doi: 10.1016/S2213-8587(13)70084-6 – ident: e_1_2_7_25_1 doi: 10.2337/dc14-1096 – ident: e_1_2_7_12_1 doi: 10.1007/s12325-017-0573-0 – ident: e_1_2_7_13_1 doi: 10.1517/14740338.2015.1034105 – ident: e_1_2_7_19_1 doi: 10.1016/j.clinthera.2015.05.511 – ident: e_1_2_7_43_1 doi: 10.1111/jdi.12626 – ident: e_1_2_7_46_1 doi: 10.1016/S0140-6736(15)61412-X – ident: e_1_2_7_55_1 doi: 10.1056/NEJMoa1611925 – ident: e_1_2_7_29_1 doi: 10.1111/jdi.12110 – ident: e_1_2_7_37_1 – ident: e_1_2_7_49_1 doi: 10.1507/endocrj.EJ16-0295 – ident: e_1_2_7_50_1 doi: 10.2147/DDDT.S92060 – ident: e_1_2_7_34_1 doi: 10.1007/s00228-014-1730-x – ident: e_1_2_7_22_1 doi: 10.1111/dom.12185 – ident: e_1_2_7_21_1 doi: 10.1186/s12933-015-0314-0 – ident: e_1_2_7_5_1 doi: 10.1016/j.jdiacomp.2016.10.008 – ident: e_1_2_7_33_1 doi: 10.1007/s40264-014-0213-4 – ident: e_1_2_7_47_1 doi: 10.2337/dc18-0165 – ident: e_1_2_7_51_1 doi: 10.1530/ERC-12-0290 – ident: e_1_2_7_54_1 doi: 10.2337/dc17-1525 – ident: e_1_2_7_10_1 doi: 10.1016/S2213-8587(17)30182-1 – ident: e_1_2_7_27_1 doi: 10.1111/dom.12073 – ident: e_1_2_7_6_1 doi: 10.1111/nyas.12098 – ident: e_1_2_7_41_1 doi: 10.1007/s13300-018-0385-5 – ident: e_1_2_7_9_1 doi: 10.1056/NEJMoa1515920 – ident: e_1_2_7_36_1 – ident: e_1_2_7_45_1 doi: 10.1002/hep.27259 – ident: e_1_2_7_48_1 doi: 10.1111/dom.13061 – ident: e_1_2_7_28_1 doi: 10.1007/s12325-014-0126-8 – ident: e_1_2_7_52_1 doi: 10.2215/CJN.09750913 – ident: e_1_2_7_57_1 doi: 10.7150/ijms.22224 – ident: e_1_2_7_40_1 doi: 10.1016/j.clinthera.2016.09.001 – ident: e_1_2_7_18_1 doi: 10.1111/dom.12188 – ident: e_1_2_7_31_1 doi: 10.1186/s12933-014-0169-9 – ident: e_1_2_7_17_1 doi: 10.1016/j.diabres.2015.05.044 – ident: e_1_2_7_23_1 doi: 10.2337/dc13-3055 – ident: e_1_2_7_3_1 doi: 10.1007/s11892-015-0602-9 – ident: e_1_2_7_32_1 doi: 10.2337/dc12-0413 – ident: e_1_2_7_24_1 doi: 10.1111/dom.12503 |
SSID | ssj0000388667 |
Score | 2.2921946 |
Snippet | Aims/Introduction
We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.
Materials and Methods
Data... We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes. Data were pooled from participants with type 2... Aims/IntroductionWe investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.Materials and MethodsData were... We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes.AIMS/INTRODUCTIONWe investigated the safety and... Abstract Aims/Introduction We investigated the safety and tolerability of empagliflozin (EMPA) in East Asian patients with type 2 diabetes. Materials and... |
SourceID | doaj pubmedcentral proquest pubmed crossref wiley |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 418 |
SubjectTerms | Adverse drug event Aged Amputation Antidiabetics Benzhydryl Compounds - therapeutic use Biomarkers - analysis Blood Glucose - analysis Clinical trials Clinical Trials, Phase I as Topic Clinical Trials, Phase II as Topic Clinical Trials, Phase III as Topic Diabetes Diabetes mellitus Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 - drug therapy Diabetic ketoacidosis Drug-Related Side Effects and Adverse Reactions - epidemiology Female Follow-Up Studies Fractures Genital infection Glucosides - therapeutic use Glycated Hemoglobin A - analysis Humans Hypoglycemia Incidence Japan - epidemiology Ketoacidosis Male Maximum Tolerated Dose Middle Aged Original Patients Prognosis Randomized Controlled Trials as Topic Safety Sodium-Glucose Transporter 2 Inhibitors - therapeutic use Sodium–glucose cotransporter 2 inhibitor Thromboembolism Urinary tract Urinary tract infections |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQD4gL4k1KqQziwCWw8Wsdbi20aioVIUGl3iI_xjTSKqm66aGcOPEH-If8EsZONtoVRVyQcoiSieXYM5lvnPE3hLxCp-hg7nVuvcIARRRFbrSXuZw5VCEjHedx7_DJR3V0Ko7P5Nlaqa-YEzbQAw8D99ZyBBwIyiWLVG0FAkIohLVKOikCn9v49UWftxZMpW8w11ql8rEspsyhQauRViil8fjmDfq5uGt2zRklzv6bgOaf-ZLrODY5osN75O6IIOne0PP75Ba0D8jtk_Ef-UPy47MJ0F9T03radwu4HJi4r2kXKKDxf100YdF9a1qKx4FZ9nQvbqSkI8PqksalWRqXZimjq6XZd_RTh215bHUgMYmtXZyjC6TVr-8_q6qiqz2WNBUCWT4ip4cHX94f5WO1hdxhSDPLNagQFKIhV0KIBRK5D9wiXuJCec3mIDwrvRIOeFBaF4YLyZx3MgRnDHP8MdlquxaeEuq8RNhjXWmMiPyDugAAjkDDgA5M2Iy8Xg177UYq8lgRY1FPIYlv6jRDGXk5iV4M_Bs3Ce3HuZsEImV2uoCKVI-KVP9LkTKys5r5erTjZc1SMXaNT2XkxXQbLTD-VjEtdFcoM0OZEsNc7MeTQVGmnvCIwBEAZGS-oUIbXd280zbnieVbiYSfcKySsv397evjD1U62f4fw_CM3EFMWA5pdjtkq7-8gueIu3q7m0zsN-n4KGI priority: 102 providerName: Directory of Open Access Journals – databaseName: ProQuest Health & Medical Collection dbid: 7X7 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELagSIgL4s3SggziwCWwiR9JuKACrZpKRUhQaW-R40cbaZUsm_TQnrjxA_iH_BJmHCd0RUHKIUpGlhPP2N-Mx98Q8hIWRW1Tk0WVkeCg8DiOVGZEJOYaVEgJzRieHT76JA-O-eFCLELArQtpleOc6Cdq02qMkb9JfFnsLJfi3epbhFWjcHc1lNC4Tm4gdRmmdKWLdIqxINOJ9EVkE0ycA7OWgVzIJ_OY-jWsdnh29tKS5Jn7r4Kbf2dNXkazfjnav0NuBxxJd4eBv0uu2eYeuXkUdsrvkx9flLP9OVWNoX27tOuBj_ucto5amAJOlrVbthd1Q-HaU11Pd_E4JQ08qx3FAC3FAC1N6BigfUs_t9CWgVYHKhNsbXUKCyEtfn3_SYuioONRS-rrgXQPyPH-3tcPB1EouhBp8GzmUWalcxJAkc6twzqJzDhWAWxiXJosSS03SW4k15Y5mWWxYlwk2mjhnFYq0ewh2Wraxj4mVBsB6KfSuVIcaQiz2FrLAG8om7mEVzPyavzvpQ6M5FgYY1lOnompSz9EM_JiEl0NNBxXCb3HwZsEkDnbP2jXJ2UwxLJiAGDByRMJUv_F4GDYmFeVFFpwx1Lo1M449GUw5678o3wz8nx6DYaIuyuqse0ZyMxBJgdvF_rxaNCUqScMgTjggBlJN3Roo6ubb5r61JN9S-5hFPwrr23__vry8GPhb578_wu2yS0AffmQR7dDtvr1mX0KwKqvnnnr-Q3NzyHQ priority: 102 providerName: ProQuest – databaseName: Wiley Online Library Open Access dbid: 24P link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1La9VAFB5KC-JGrM-rVUZx4SZyM6-b6KpqS1OoFLTQXZhnG7gk5SZd1JUr_4D_sL-k50we9GIFIYuQnBkmmTk53zmZ8x1C3oFRtH7hssQ4BQ6KSNNEZ04mcm5hCWlpOcfc4aNv6uBEHJ7K0w3yacyF6fkhpoAbakb8XqOCa9PeVnJXfQBjhelVW5hai8T5TBxPARakOVGxgizDXXPQSA3MQnEnz9h6zR5F2v67sObfWyZvQ9loi_YfkgcDiKS7_axvkw1fPyL3jobf5I_J7-86-O6K6trRrln6VU_GfUWbQD3o_9myCsvmZ1VTOPZ029FdzKWkA8lqSzE6SzE6Sxkdo7Mf6XEDfTnotecxwd4uzsEK0uL615-iKOiYZkljLZD2CTnZ3_vx5SAZCi4kFryaeZJ5FYICQGRzH7BGIneBG4BMXCiXsYUXjuVOCet5UFmWai4ks87KEKzWzPKnZLNuav-cUOskIB9jc60FUhBmqfeeA9bQPgtMmBl5P7720g5s5FgUY1lOXomryjhDM_J2Er3oKTjuEvqMczcJIGt2vNCszspBCUvDAbyCgycZ0v6l4Fz4VBijpJUi8AUMamec-XJQ5bZksR57Bq1m5M10G5QQ_6zo2jeXIDMHmRw8XRjHs36hTCPhCMIBA8zIYm0JrQ11_U5dnUeibyUihIJ3FRfbv5--PPxaxJMX_y_6ktwH8Jf3--l2yGa3uvSvAGB15nVUpBs6biFt priority: 102 providerName: Wiley-Blackwell |
Title | Safety and tolerability of empagliflozin in East Asian patients with type 2 diabetes: Pooled analysis of phase I–III clinical trials |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjdi.12910 https://www.ncbi.nlm.nih.gov/pubmed/30099847 https://www.proquest.com/docview/2187958965 https://www.proquest.com/docview/2087994480 https://pubmed.ncbi.nlm.nih.gov/PMC6400242 https://doaj.org/article/b35669965275441882e14bb65c54f37b |
Volume | 10 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1La9wwEBZpAqWX0ne2TRa19NCLw9qSZblQStJuiAMblrYLezOyHonB2OmuA92eeuof6D_sL8lIflDTLRSMMfZIyNKM5xtZ-gah1-AUpY4U9zLFIEChvu8JrkIvnEhQIRFKQuze4dkFO1vQ82W43EFdjs22A9dbQzubT2qxKo6-fd28B4N_16_KUfkRuC270WoPHFJk7XPWonz3QSacM5dLNrDr56AIazmGBqUHnskR-G9DnX8vnvwT1DqvdPoA3W_hJD5uxv8h2tHlI3R31v4wf4x-fhZG1xssSoXrqtCrhpZ7gyuDNXwJLovcFNX3vMRwTMW6xsd2VyVu6VbX2M7TYjtPiwPczdO-xfMK6lJQa8NoYmu7vgJ_iJPfP34lSYK7DZfYZQVZP0GL0-mXD2dem3rBkxDfTDyumTEMoJGMtbHZEokyJAPwRChTPIg0VUGsGJWaGMa5LwgNA6lkaIwUIpDkKdotq1LvIyxVCBgok7EQ1JIRcl9rTQB1CM1NQLMRetN1eypbXnKbHqNI-_hE5akboRF61YteN2Qc24RO7Nj1ApY_292oVpdpa45pRgDGQqgXBpYA0IcwQ_s0y1goQ2pIBI066EY-7XQyDVxmdg6lRuhl_xjM0f5jEaWubkBmAjIxxLzQjmeNovQtIRaOAxoYoWigQoOmDp-U-ZWj_GbUgSnoK6ds_3779Pxj4i6e_7_oC3QPYGDcrKw7QLv16kYfAtSqszG6E9A5nKNlNEZ7J9OL-aexm7YYOxO7BYTpKm0 |
linkProvider | Scholars Portal |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEF6VVAIuiDeBAgsCiYtLvK_YSAi1NFXcNlEFrdSbWe-jjRTZIUmFwokbP4D_0R_VX8Ls-kEjCrdKPlj2aLX2zO58M7v7DUKvwCkq09VRkGkBAQoLw0BGmge8o8CEJFeUurPDg6HoH7KdI360gs7qszBuW2U9J_qJWhfK5cjfEl8WO4oF_zD5GriqUW51tS6hUZrFrll8g5Bt9j7ZAv2-JmS7d_CxH1RVBQIF0L0TREZYK8Drq9hYVwiQakszwAWUCR2RrmGaxFowZagVURRKyjhRWnFrlZREUWj3GlplFEKZFlrd7A33PzVZHcetInzZWuK26sFEIio6I799SI_Wwb-607oXnKCvFXAZwP17n-ZF_Owd4PZtdKtCrnijNLU7aMXkd9H1QbU2fw_9_CytmS-wzDWeF2MzLRnAF7iw2MCkczwe2XHxfZRjuHpyNscb7gAnrphdZ9ilhLFLCWOC65TwO7xfQFsaWi3JU1xrkxNwvTg5__ELJ0mC68Od2Fcgmd1Hh1eikAeolRe5eYSw0hzwVqZiKZkjPoxCYwwFhCNNZAnL2uhN_d9TVXGgu1Ic47SJhfQo9Spqo5eN6KQk_rhMaNMprxFwXN3-QTE9Tquhn2YUIDOElZw4ssEQQhoTsiwTXHFmaRc6tVarPq0mkFn6x9zb6EXzGoa-W8-RuSlOQaYDMjHE19CPh6WlND2hDvoD8mij7pINLXV1-U0-OvH04oJ54Ab_ylvbv78-3dlK_M3j_3_Bc3SjfzDYS_eS4e4TdBMgZ1zu4ltDrfn01DwFWDfPnlVjCaMvVz18fwP-u2A3 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELZKkSouqLyXFjAIJC6hG7-SICFU2K6allaVoNLeUsePNtIqWXa3QsuJGz-Af8PP4Zcwdh50ReFWKYcoGVlOZjz-xh5_g9BzmBSViXQc5FpAgMLCMJCx5gHvKzAhyRWl7uzwwaHYPWZ7Iz5aQT_bszAurbL1id5R60q5NfIt4stix4ngW7ZJizgaDN9OPgeugpTbaW3LadQmsm8WXyB8m71JB6DrF4QMdz693w2aCgOBAhjfD2IjrBWAAFRirCsKSLWlOWAEyoSOSWSYJokWTBlqRRyHkjJOlFbcWiUlURTavYauR5SHboxFo6hb33EsK8IXsCUuaQ9cimiIjXwikS5ewUzrzu1emA591YDLoO7fGZsXkbSfCofr6GaDYfF2bXS30Iopb6O1g2aX_g76_lFaM19gWWo8r8ZmWnOBL3BlsQH3czou7Lj6WpQYrh05m-Ntd5QTNxyvM-wWh7FbHMYEt4vDr_FRBW1paLWmUXGtTc5gEsbpr28_cJqmuD3miX0tktlddHwl6riHVsuqNA8QVpoD8spVIiVzFIhxaIyhgHWkiS1heQ-9bP97pho2dFeUY5x1UZEuMq-iHnrWiU5qCpDLhN455XUCjrXbP6imp1njBLKcAniGAJMTRzsYQnBjQpbngivOLI2gU5ut6rPGlcyyP4bfQ0-71-AE3M6OLE11DjJ9kEkg0oZ-3K8tpesJdUEAYJAeipZsaKmry2_K4swTjQvmIRz8K29t__76bG-Q-puH__-CJ2gNBm32IT3c30A3AHsmdTrfJlqdT8_NI8B38_yxH0gYnVz1yP0Na6ljBw |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Safety+and+tolerability+of+empagliflozin+in+East+Asian+patients+with+type+2+diabetes%3A+Pooled+analysis+of+phase+I%E2%80%93III+clinical+trials&rft.jtitle=Journal+of+diabetes+investigation&rft.au=Yabe%2C+Daisuke&rft.au=Yasui%2C+Atsutaka&rft.au=Ji%2C+Linong&rft.au=Lee%2C+Moon%E2%80%90Kyu&rft.date=2019-03-01&rft.issn=2040-1116&rft.eissn=2040-1124&rft.volume=10&rft.issue=2&rft.spage=418&rft.epage=428&rft_id=info:doi/10.1111%2Fjdi.12910&rft.externalDBID=10.1111%252Fjdi.12910&rft.externalDocID=JDI12910 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2040-1116&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2040-1116&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2040-1116&client=summon |