論文・技術情報追加のお知らせ

①GLP-1 receptor agonist-associated tumor adverse events: A real-world study from 2004 to 2021 based on FAERS.

GLP-1受容体作動薬に関連する腫瘍の有害事象探索研究

対象DB：FAERS

②A real-world pharmacovigilance study of FDA Adverse Event Reporting System (FAERS) events for osimertinib.

オシメルチニブのファーマコビジランス研究

対象DB：FAERS

③Doxycycline use and adverse pregnancy or neonatal outcomes: A descriptive study using the United States Food and Drug Administration Adverse Event Reporting System database.

ドキシサイクリンによる母体および新生児への有害転帰調査

対象DB：FAERS

④Benzonatate Exposure Trends and Adverse Events.

小児患者におけるベンゾナテート曝露による薬剤関連有害事象調査

対象DB：FAERS

⑤A real-world pharmacovigilance study of severe cutaneous adverse reactions associated with antiepileptic drug combination therapy: data mining of FDA adverse event reporting system.

抗てんかん薬併用療法に伴う重篤な皮膚副作用のファーマコビジランス研究

対象DB：FAERS

⑥Direct-acting antiviral agent use and gastrointestinal safety in patients with chronic hepatitis C: a pharmacovigilance study based on FDA Adverse Event Reporting System.

C型慢性肝炎患者における直接作用型抗ウイルス剤による消化管有害事象調査

対象DB：FAERS

⑦Central nervous system adverse events of ceftazidime/avibactam: A retrospective study using Food and Drug Administration Adverse Event Reporting System.

セフタジジム／アビバクタムの中枢神経系有害事象調査研究

対象DB：FAERS

⑧Inhibitory Effect of alpha1 Receptor Antagonists on Paclitaxel-Induced Peripheral Neuropathy in a Rodent Model and Clinical Database.

パクリタキセル誘発性末梢神経障害に対するα1受容体拮抗薬の抑制効果研究

対象DB：FAERS