2023年8月7日~2023年8月20日の間に収集した論文情報を追加しました。(2/5)
①A real-world disproportionality analysis of ospemifene: data mining of the public version of FDA adverse event reporting system.
オスペミフェンに関連する有害事象評価研究
対象DB:FAERS
②A real-world disproportionality analysis of Rucaparib: Post-marketing Pharmacovigilance Data.
ルカパリブに関連する有害事象評価研究
③Screening for clinically relevant drug-drug interactions between direct oral anticoagulants and antineoplastic agents: a pharmacovigilance approach.
直接経口抗凝固薬と抗悪性腫瘍薬間の薬物相互作用調査研究
④Drug-associated kidney injury in children: a disproportionality analysis of the FDA Adverse Event Reporting System.
小児における、腎障害リスクのある薬剤調査研究
⑤Angiotensin Receptor Blocker-Related Sprue-like Enteropathy: Review of Food and Drug Administration Adverse Event Reporting System.
オルメサルタンとスプルー様腸症との関連性調査研究
⑥Safety signals of albumin-bound paclitaxel: Data mining of the Food and Drug Administration adverse event reporting system.
アルブミン結合パクリタキセルの安全性評価研究
⑦Safety analysis of pemigatinib leveraging the US Food and Drug administration adverse event reporting system.
ペミガチニブの有害事象調査研究
Date
(PubMed追加日)