| Literature DB >> 31060597 |
Kosuke Ebina1, Motomu Hashimoto2, Wataru Yamamoto2,3, Toru Hirano4, Ryota Hara5, Masaki Katayama6, Akira Onishi7, Koji Nagai8, Yonsu Son9, Hideki Amuro9, Keiichi Yamamoto10, Yuichi Maeda4, Koichi Murata2, Sadao Jinno7, Tohru Takeuchi8, Makoto Hirao11, Atsushi Kumanogoh4, Hideki Yoshikawa11.
Abstract
Following publication of the original article [1], the authors noticed that two corrections were not implemented during the production process.Entities:
Year: 2019 PMID: 31060597 PMCID: PMC6503435 DOI: 10.1186/s13075-019-1897-8
Source DB: PubMed Journal: Arthritis Res Ther ISSN: 1478-6354 Impact factor: 5.156
Fig. 1Drug survival rates due to lack of effectiveness in a non-adjusted cases and b adjusted cases. Adjusted confounders were baseline sex, age, disease duration, concomitant prednisolone and methotrexate, and number of previously used bDMARDs. ABT = abatacept, ADA = adalimumab, CZP = certolizumab pegol, ETN = etanercept, GLM = golimumab, IFX = infliximab, TCZ = tocilizumab, bDMARDs = biological disease-modifying antirheumatic drugs
Fig. 2Drug survival rates due to toxic adverse events in a non-adjusted cases and b adjusted cases. Adjusted confounders were baseline sex, age, disease duration, concomitant prednisolone and methotrexate, and number of previously used bDMARDs. ABT = abatacept, ADA = adalimumab, CZP = certolizumab pegol, ETN = etanercept, GLM = golimumab, IFX = infliximab, TCZ = tocilizumab, bDMARDs = biological disease-modifying antirheumatic drugs