Evidence map›Paper›PMID 42307213›Full record

ArticleCNS neuroscience & therapeutics2026

Ocular Adverse Events Associated With Antidepressants: A Large-Scale Data Analysis From the FAERS Database.

Yiming Peng, Yichen Cao, Hanhan Liu, Junlong Ma, Guoping Yang

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yiming PengCenter of Clinical Pharmacology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yichen CaoCenter of Clinical Pharmacology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hanhan LiuDepartment of Ophthalmology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID 0000-0003-1985-6776
Junlong MaDepartment of Pharmacy, National Clinical Research Center for Geriatric Diseases, Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID 0000-0003-1949-1201
Guoping YangCenter of Clinical Pharmacology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID 0000-0001-5930-586X

Funding

National Natural Science Foundation of China 82474009
6 · The paper itself

Abstract

objectiveGlobal antidepressant use has risen substantially, raising concerns about their potential ocular adverse effects. Nevertheless, large-scale comprehensive assessments of ocular side effects associated with various classes of antidepressants remain limited.

methodsA retrospective pharmacovigilance analysis was performed using the FDA Adverse Event Reporting System (FAERS) from Q1 2015 to Q4 2024. Reports associated with antidepressants were systematically extracted, and disproportionality analyses were performed to identify potential associations with ocular adverse events (AEs).

results62,020 ocular AE reports were identified for 13,348 patients (median age, 44 years), with higher susceptibility observed in females. Norepinephrine-dopamine disinhibitors (NDDIs) showed the strongest association with eye disorders (IC 3.84, 95% CI 3.75-3.90), while selective serotonin reuptake inhibitors (SSRIs) showed the greatest number of positive associations across key ocular AEs. Analysis of the 36 antidepressants with sufficient case reports for ocular neuromuscular disorders revealed that 33 were associated with such disorders, most notably mydriasis, miosis, and anisocoria.

conclusionThis study delineates the ocular risks of antidepressants, highlighting higher toxicity for NDDIs and SSRIs and widespread associations with ocular neuromuscular disorders. Vigilant monitoring and early intervention are warranted to ensure safe clinical use.

Indexed as

Antidepressive AgentsEye DiseasesAdolescentAdultAdverse Drug Reaction Reporting SystemsAgedFemaleHumansMaleMiddle AgedPharmacovigilanceRetrospective StudiesSex FactorsUnited StatesUnited States Food and Drug AdministrationYoung AdultAntidepressive AgentsantidepressantsFAERSNDDIsocular adverse eventspharmacovigilanceSSRIs

Identifiers

PMID42307213
PMCPMC13274231

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.