Antidepressants and the risk of hyponatremia: A multi‐institutional cohort study using observational medical outcomes partnership—Common Data Model

Read full text
Authors: Kyungyeon Jung, Ju Hwan Kim, Da Eun Hyeon, Junqing Ji, Min Young Lee, Hayun Choi, Dong Yun Lee, Min Woo Kim, Yoonmin Jang, S. H. Hwang, Jaehyeong Cho, Seok Young Song
+10 more Sang Youl Rhee, Jae Myung Cha, Won‐Woo Seo, Chang‐Won Jeong, Seung-Jin Kwag, Woo Jin Kim, Jaeuk Hwang, Min Ho Kim, R W Park, Ju‐Young Shin
Cited by: 2
References: 25

Abstract

AIM: Hyponatremia is a common yet potentially serious adverse event associated with antidepressants. Identifying the antidepressant class with the least risk of hyponatremia would improve patient safety. METHODS: Using electronic medical records from 15 hospitals standardized into Observational Medical Outcomes Partnership Common Data Model (2003-2023), we identified patients diagnosed with depression who initiated antidepressants, including selective serotonin reuptake inhibitor (SSRI), serotonin-norepinephrine reuptake inhibitor (SNRI), tricyclic antidepressants (TCA) or others (agomelatine, bupropion, mirtazapine, moclobemide and trazodone) for at least 30 days. The index date was defined as the first antidepressant prescription, and four mutually exclusive cohorts were constructed based on the antidepressant class prescribed on index date. Each cohort was compared with all other antidepressants. The primary outcome was incident hyponatremia (serum sodium

Fields of Study & Subjects

Electrolyte and hormonal disorders Treatment of Major Depression Electroconvulsive Therapy Studies

Publication details

Journal / source
British Journal of Clinical Pharmacology
Publisher
Wiley
Volume
92
Issue
6
Pages
1706–1715
Publication date
13 January 2026
Language
EN