論文・技術情報追加のお知らせ

①Assessment of the real-world safety profile of vedolizumab using the United States Food and Drug Administration adverse event reporting system.

ベドリズマブの安全性プロファイリング

対象DB：FAERS

②Tumor lysis syndrome associated with bortezomib: A post-hoc analysis after signal detection using the US Food and Drug Administration Adverse Event Reporting System.

ボルテゾミブに関連する腫瘍溶解症候群についてのシグナル検出解析

対象DB：FAERS

③Reports of atypical shoulder pain and dysfunction following inactivated influenza vaccine, Vaccine Adverse Event Reporting System (VAERS), 2010-2017.

不活化インフルエンザワクチンによる非定型的な肩の痛みと機能障害に関する症例解析

対象DB：VAERS

④Subtype-Dependent Reporting of Stroke With SGLT2 Inhibitors: Implications From a Japanese Pharmacovigilance Study.

SGLT2阻害剤による脳卒中関連リスク調査研究

対象DB：JADER

⑤Structure and process of dementia care and patient outcomes after hip surgery in elderly people with dementia: A retrospective observational study in Japan.

股関節手術後の認知症高齢者ケアと転帰の関連性についての調査研究

対象DB：DPC