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The post-marketing safety of Esketamine among older adults(≥ 65): an real-world pharmacovigilance study.

Bin Deng, Zhiwen Fu, Linjie Li, Yusen Xu, Zihe Yang, Xuejia Zhai, Yongning Lv

BMC pharmacology & toxicology August 29, 2025 DOI: 10.1186/s40360-025-00992-2 via PubMed

Summary

Older adults (65 years or older) treated with esketamine experience a higher risk of severe psychiatric and general adverse events compared to younger adults. Analysis of FDA Adverse Event Reporting System data from 2019 to 2024, covering 536 reports from older adults and 3,566 from younger adults, found that older adults had a higher incidence of dissociation, suicidal ideation, depression, and anxiety. They also reported more general and administration site conditions, indicating greater susceptibility to systemic and local reactions. Gastrointestinal and respiratory disorders were less frequent in older adults, but their potential impact remains critical. These findings highlight the need for careful patient selection, monitoring, and tailored treatment protocols for older adults receiving esketamine.

Study at a glance

Characteristics Retrospective pharmacovigilance analysis Peer reviewed
Sample size 4,102
Population Adults (under 65 years) and older adults (65 years and older) with esketamine-related adverse event reports in the FDA Adverse Event Reporting System
Topics Ketamine
Keywords Adverse events Faers Older adults Real-world data analysis
Citations 3
Key finding Older adults treated with esketamine have a higher risk of severe psychiatric adverse events (dissociation, suicidal ideation, depression, anxiety) and general adverse events compared to younger adults.

Abstract

AIMS: This study aims to investigate the safety profile of Esketamine, with a particular focus on comparing adverse events (AEs) between adults (< 65 years) and older adults (≥ 65 years) using data from the FDA Adverse Event Reporting System (FAERS). METHODS: We conducted a comprehensive analysis of FAERS data from 2019 to 2024, identifying 6,452 Esketamine-related AE reports. After removing data without age information, these reports were categorized into two age groups: 536 from older adults and 3,566 from younger adults. Reporting odds ratios (RORs) were calculated to determine the relative risk of specific AEs in each age group. RESULTS: At system Organ Class (SOC)level, the Esketamine-related AEs of both adults group and older adults group were seen in 17 organ systems. The analysis revealed significant differences in AE profiles of psychiatric disorders between the two age groups. Older adults had a higher incidence of dissociation, suicidal ideation, depression, and anxiety, compared to younger adults. Additionally, older adults reported more general and administration site conditions, suggesting a greater susceptibility to systemic and local reactions. Gastrointestinal and respiratory disorders were less frequent in older adults, but their potential impact remains critical. CONCLUSIONS: The findings highlight a higher risk of severe psychiatric and general AEs in older adults treated with Esketamine, necessitating careful patient selection, monitoring, and tailored treatment protocols.

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