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Adverse drug reactions in neonates: a brief analysis of the FDA adverse event reporting system

IntroductionDrug trials in neonates are scarce, and the neonates may consequently be at risk of adverse drug reactions (ADRs). Spontaneous ADR reporting is an important tool for expanding the knowledge on drug safety in neonates. This study explores the quality of current neonatal ADR reports and th...

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書誌詳細
主要な著者: Pernille Kähler Byskov, Christoffer Storm Baden, Jon Trærup Andersen, Espen Jimenez-Solem, Ramus Huan Olsen, Christina Gade, Ulrik Lausten-Thomsen
フォーマット: Artigo
言語:Inglês
出版事項: Frontiers Media S.A. 2024-06-01
シリーズ:Frontiers in Pharmacology
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オンライン・アクセス:https://www.frontiersin.org/articles/10.3389/fphar.2024.1395982/full
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