論文・技術情報追加のお知らせ

①Finasteride Use Is Associated with Higher Odds of Obstructive Sleep Apnea: Results from the US Food and Drug Administration Adverse Events Reporting System.

フィナステリド投与後の閉塞性睡眠時無呼吸症候群の安全性シグナル研究

対象DB：FAERS

②Linezolid and the risk of lactic acidosis: Data mining and analysis of the FDA Adverse Event Reporting System.

リネゾリドによる乳酸アシドーシスのリスクに関するデータマイニングと分析研究

対象DB：FAERS

③Comparison of Data Mining Methods for the Signal Detection of Adverse Drug Events with a Hierarchical Structure in Postmarketing Surveillance.

ツリー構造に分類される有害事象のデータマイニング手法比較研究

対象DB：KAERS

④Safety concerns of sodium-glucose co-transporter-2 inhibitors in type 1 diabetes: A real-world study from the perspective of the Food and Drug Administration Adverse Event Reporting System.

1型糖尿病におけるSGLT2阻害薬の安全性調査研究

対象DB：FAERS

⑤Signals of adverse drug reactions communicated by pharmacovigilance stakeholders: protocol for a scoping review of the global literature.

ファーマコビジランス活動における因果関係推測にむけたエビデンス・文献、経過時間のレビュープロトコル研究

対象DB：VigiBase

⑥Evaluation of the safety profile of rotavirus vaccines: a pharmacovigilance analysis on American and European data.

ロタウイルスワクチンの安全性プロファイルの評価研究

対象DB：VAERS,VigiBase

⑦Assessment of adverse reactions to alpha-lipoic acid containing dietary supplements through spontaneous reporting systems.

α-リポ酸含有栄養補助食品の副作用評価研究

対象DB：IPS,VigiBase