ArticleNeuropsychopharmacology reports2026
Self-Reported Adverse Events in Psychiatric Outpatients Taking Hypnotics: Higher Real-World Frequencies Than Those Listed in Package Inserts.
Article in Neuropsychopharmacology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionBenzodiazepines (BZDs) are associated with dependence, tolerance, withdrawal, and various adverse effects, and switching to other drug classes is often recommended. Although non-BZD hypnotics are reported in package inserts to have similar but less frequent adverse events, real-world patients often have complex psychiatric and medical backgrounds, and the actual frequency of subjective adverse events may differ substantially from that reported in package inserts. This study aimed to elucidate subjective symptoms potentially related to psychotropic medications using real-world patient data.
methodsThis prospective cohort study included patients at the Akebono Clinic who were taking a single hypnotic agent. A total of 314 patients were analyzed. Insomnia severity was assessed using the Athens Insomnia Scale, and 11 self-reported adverse events were evaluated.
resultsThe frequency of insomnia was 72% for non-BZDs, 52% for BZDs, and 70% for dual orexin receptor antagonists (DORAs) (significantly lower for BZDs; p = 0.0036). Among the 11 self-reported symptoms, two items (thirst and nightmares) were reported as "always" or "often" by more than 10% of patients; three items (constipation, head heaviness/headache, and abnormal behavior during sleep) by 5%-10%; and four items (lightheadedness, vertigo, abdominal pain, and tremor) by 3%-5%. There were no differences in adverse-event frequencies among non-BZDs, BZDs, and DORAs. Multivariate analyses showed that adverse events were associated with female sex, age < 60 years, and schizophrenia, depression, and anxiety disorders, but not with hypnotic drug classes.
conclusionsSubjective adverse events in patients taking hypnotics occurred more frequently than those reported in package inserts, indicating a clear discrepancy between controlled trial data and real-world clinical experience. Because adverse events were more strongly associated with patient characteristics-such as psychiatric comorbidities, physical conditions, and concomitant medications-than with hypnotic drug class, routine assessment of subjective symptoms through interviews or questionnaires is essential in clinical practice.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.