Evidence map›Paper›PMID 41883496›Full record

ArticleFrontiers in pharmacology2026

Comparative pharmacovigilance of non-benzodiazepine receptor agonists versus dual orexin receptor antagonists for insomnia in older adults.

Shuqing Gao, Xiaotang Feng, Qi Li, Jingyi Fan

Abstract read
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Article in Frontiers in pharmacology, 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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Shuqing GaoDepartment of Psychiatry, Nanjing Youan Hospital, Nanjing, China.
Xiaotang FengDepartment of Psychiatry, Nanjing Youan Hospital, Nanjing, China.
Qi LiDepartment of Psychiatry, Nanjing Youan Hospital, Nanjing, China.
Jingyi FanDepartment of Psychiatry, Nanjing Youan Hospital, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The accelerating global aging trend has positioned insomnia in the elderly as a major public health challenge. Although cognitive behavioral therapy is the first-line intervention, pharmacological treatment remains widely used. However, significant safety concerns exist regarding the use of traditional non-benzodiazepine sedative-hypnotics (nBZRAs) in older adults, while long-term real-world safety evidence for newer dual orexin receptor antagonists (DORAs) remains scarce. Addressing this evidence gap is critical for guiding safe medication use in the aging population. Methods: We conducted a pharmacovigilance study utilizing the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database, covering reports from the first quarter of 2004 to the second quarter of 2025. We included reports for patients aged ≥65 years where a target nBZRA or DORA was listed as the primary suspect drug. A comprehensive disproportionality analysis was performed using the Reporting Odds Ratio (ROR), Proportional Reporting Ratio (PRR), Information Component (IC), and Empirical Bayesian Geometric Mean (EBGM), with stringent thresholds to minimize false positives. Results: A total of 5,447 reports for elderly patients were analyzed. The study revealed distinct adverse event profiles between the two drug classes. nBZRAs, particularly eszopiclone, showed the strongest signals related to therapeutic failure (e.g., "Drug ineffective," "Insomnia") alongside a unique signal for "Dysgeusia". In contrast, DORAs exhibited strong and consistent signals for "Dream-abnormality" events concordant with their sleep-wake modulation mechanism, including "Nightmare," "Abnormal dreams," and "Hallucination". Notably, none of the studied drugs generated a statistically significant signal for "Fall" within this dataset. System Organ Class analysis showed that psychiatric and nervous system disorders had the highest incidence. Conclusion: These findings highlight distinct safety profiles: nBZRAs are linked to therapeutic failure and dysgeusia, while DORAs are associated with neuropsychiatric events such as nightmares and hallucinations.

Indexed as

DORAsFAERSinsomnianBZRAsolder adults

Identifiers

PMID41883496
PMCPMC13008954

What Socratic holds

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Registered trials

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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 Socratic graph.