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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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Principais autores: Pernille Kähler Byskov, Christoffer Storm Baden, Jon Trærup Andersen, Espen Jimenez-Solem, Ramus Huan Olsen, Christina Gade, Ulrik Lausten-Thomsen
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2024-06-01
coleção:Frontiers in Pharmacology
Assuntos:
pharmacology
adverse drug events
neonatal pharmacology
public health
pharmacovigilance
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fphar.2024.1395982/full
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