Evidence map›Paper›PMID 42748074›Full record

ArticlePediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology2026

Pediatric spontaneous-reporting patterns for biologics approved or used for asthma: Analysis of the FDA adverse event reporting system.

Yue Zhang, Yile Liu, Lingli Chen, Yating Chen, Xiangrong Zheng

Abstract read
In one paragraph

Article in Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Pediatric spontaneous-reporting patterns for biologics approved or used for asthma: Analysis of the FDA adverse event reporting system.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Article
4 · The record

Corrections and comments

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

5 authors.

Yue ZhangDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID https://orcid.org/0009-0001-9976-7732
Yile LiuDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID https://orcid.org/0009-0008-6568-389X
Lingli ChenDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yating ChenDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID https://orcid.org/0000-0001-7035-9543
Xiangrong ZhengDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, Hunan, China.

Funding

the Degree and Postgraduate Education Reform Project of Central South University 2023JGB116the Natural Science Foundation of Hunan Province, China 2025JJ90181
6 · The paper itself

Abstract

backgroundPediatric post-marketing evidence for biologics used for asthma remains limited and uneven across agents. We characterized pediatric spontaneous-reporting patterns for biologics approved or used for asthma in the FDA Adverse Event Reporting System.

methodsWe analyzed pediatric reports involving omalizumab, mepolizumab, benralizumab, dupilumab, and tezepelumab from 2015 through 2025. Reports were summarized by age, sex, reporting year, outcomes, and preferred terms. Serious-outcome and indication-linked classifications were performed. Disproportionality was assessed using reporting odds ratios, proportional reporting ratios, chi-square statistics, and information components. Pediatric signals were compared with adult findings and interpreted according to method agreement, report volume, and sparse-data restrictions.

resultsWe identified 5155 pediatric reports. Dupilumab accounted for 3787 reports (73.5%) and omalizumab for 1152 (22.3%). Serious outcomes were reported in 1273 reports (24.7%), with substantial variation across biologics. Dupilumab showed prominent injection-site, dermatologic, and ocular reporting, whereas omalizumab showed respiratory, asthma-related, hypersensitivity-related, and vital-sign reporting. Of 43 pediatric signals supported by at least two disproportionality criteria, 31 were also identified in adults. After restricting to terms with at least five reports, 33 signals remained for the main analysis. Narrow anaphylaxis-related domains occurred in 17 dupilumab, 113 omalizumab, 3 mepolizumab, 3 benralizumab, and no tezepelumab reports. Among dupilumab reports, 83.4% were classified as asthma-related and 15.2% as mixed indications.

conclusionsPediatric FAERS reports showed biologic-specific reporting patterns. These patterns may reflect potential drug-related events, underlying disease activity, treatment failure, indication mix, monitoring, and reporting practices. The findings are hypothesis-generating and do not establish incidence, causality, or asthma-specific safety profiles.

Indexed as

Adverse Drug Reaction Reporting SystemsAnti-Asthmatic AgentsAsthmaBiological ProductsAdolescentAntibodies, Monoclonal, HumanizedChildChild, PreschoolFemaleHumansInfantMaleOmalizumabUnited StatesUnited States Food and Drug AdministrationAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedBiological ProductsdupilumabOmalizumabadverse event reportingbiologicsdisproportionality analysisdupilumabFAERSomalizumabpediatric asthmapharmacovigilance

Identifiers

PMID42748074
PMCPMC13580972

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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 OpenQuestion graph.