論文・技術情報追加のお知らせ

①Medication overdose data analysis: a review of medication error reports in the FDA adverse event reporting system (FAERS).

サブグループ解析による、過剰摂取リスクが高い薬剤調査研究

対象DB：FAERS

②Otolaryngologic Side Effects After COVID-19 Vaccination.

COVID-19ワクチン接種後における、耳鼻咽喉関連有害事象の発生頻度評価研究

対象DB：VAERS

③Fluid retention-associated adverse events in patients treated with BCR::ABL1 inhibitors based on FDA Adverse Event Reporting System (FAERS): a retrospective pharmacovigilance study.

BCR-ABL1阻害剤投与患者における、体液貯留関連有害事象の調査研究

対象DB：FAERS

④Bioinformatics-guided Disproportionality Analysis of Sevoflurane-Induced Nephrogenic Diabetes Insipidus using the FDA Adverse Event Reporting System (FAERS) Database.

セボフルランによる腎性糖尿病性不感症発生の調査研究

対象DB：FAERS

⑤Dental Disorders Reported to the FDA Adverse Event Reporting System in Association with Buprenorphine: An Analysis by Ingredient Composition and Route of Administration.

ブプレノルフィン投与による歯科疾患リスク評価研究

対象DB：FAERS

⑥Identifying Medications Underlying Communication Atypicalities in Psychotic and Affective Disorders: A Pharmacovigilance Study Within the FDA Adverse Event Reporting System.

精神病性障害および感情障害患者における、コミュニケーション特異性と関連する薬剤の探索研究

対象DB：FAERS

⑦Analysis of Corticosteroid-Induced Glaucoma Using the Japanese Adverse Drug Event Reporting Database.

副腎皮質ステロイドによる緑内障のリスク調査研究

対象DB：JADER