<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-14T02:15:07Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/12114" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/12114</identifier><datestamp>2025-10-24T10:25:58Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Enhanced Safety Surveillance of GSK’s Inactivated Quadrivalent Seasonal Influenza Vaccine in Belgium, Germany, and Spain During the 2022/2023 Influenza Season</dc:title>
   <dc:creator>Salamanca de la Cueva, Ignacio</dc:creator>
   <dc:creator>Gerber, Jennifer</dc:creator>
   <dc:creator>Hastie, Andrew</dc:creator>
   <dc:creator>Brotons, Carlos</dc:creator>
   <dc:creator>PANZER, Falko</dc:creator>
   <dc:creator>Pirçon, Jean-Yves</dc:creator>
   <dc:creator>Martínez-Gómez, Xavier</dc:creator>
   <dc:subject>Grip - Vacunació</dc:subject>
   <dc:subject>Vacunes antigripals</dc:subject>
   <dc:subject>Virus de la grip</dc:subject>
   <dc:subject>DISEASES::Virus Diseases::RNA Virus Infections::Orthomyxoviridae Infections::Influenza, Human</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/prevention &amp; control</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Biological Therapy::Immunomodulation::Immunotherapy::Immunization::Immunotherapy, Active::Vaccination</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/adverse effects</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Complex Mixtures::Biological Products::Vaccines::Vaccines, Inactivated</dc:subject>
   <dc:subject>ENFERMEDADES::virosis::infecciones por virus ARN::infecciones por Orthomyxoviridae::gripe humana</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/prevención &amp; control</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapia biológica::inmunomodulación::inmunoterapia::inmunización::inmunoterapia activa::vacunación</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/efectos adversos</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::mezclas complejas::productos biológicos::vacunas::vacunas inactivadas</dc:subject>
   <dcterms:abstract>Safety surveillance; Influenza Vaccine; Influenza season</dcterms:abstract>
   <dcterms:abstract>Vigilancia de seguridad; Vacuna antigripal; Gripe estacional</dcterms:abstract>
   <dcterms:abstract>Vigilància de seguretat; Vacuna antigripal; Grip estacional</dcterms:abstract>
   <dcterms:abstract>Background&#xd;
Seasonal influenza is prevented through annual vaccination, especially in children and older adults. These vaccines are annually updated based on World Health Organization recommendations and require continuous safety monitoring.&#xd;
Objective&#xd;
We assessed the frequency and severity of adverse events within 7 days of administering GSK’s inactivated quadrivalent seasonal influenza vaccine (IIV4) in Belgium, Germany, and Spain during the 2022/2023 influenza season.&#xd;
Methods&#xd;
In this enhanced safety surveillance study, adults who received GSK’s IIV4 and parents/guardians/legally acceptable representatives of vaccinated children (aged 6 months–17 years) were invited to complete adverse drug reaction cards reporting adverse events within 7 days post-vaccination.&#xd;
Results&#xd;
In total, 1332 participants (53.6% female) received at least one dose of GSK’s IIV4, including 43 children who received two doses. Overall, 97.8% of adverse drug reaction cards were completed and returned in the study. All participants in Belgium were adults, while 54.7% and 7.4% in Spain and Germany, respectively, were pediatric participants aged 6 months–17 years. After Dose 1, across all age groups, 49.8% of participants reported at least one adverse event. The most common adverse events (cumulative frequency >5%) following Dose 1 were injection-site pain (37.6%), fatigue (15.0%), headache (13.2%), injection-site swelling (9.3%), myalgia (7.6%), and injection-site erythema (7.4%). Across all countries, adverse events were most common in adults aged 18–65 years (59.7%), followed by those aged 3–17 years (47.0%), >65 years (35.7%), and 6–35 months (23.5%). After Dose 2, 18.6% of participants reported at least one adverse event, with general disorders and administration site conditions again being the most frequent.&#xd;
Conclusions&#xd;
Across all age and risk groups for serious disease, no serious adverse events related to GSK’s IIV4 were reported within 7 days post-vaccination. This study supports and confirms the acceptable safety profile of GSK’s IIV4 across all recommended age groups.</dcterms:abstract>
   <dcterms:abstract>GlaxoSmithKline Biologicals S.A funded this study (GlaxoSmithKline [GSK] study identifier: 213829) and was involved in all stages of the study, including analysis of the data. GlaxoSmithKline Biologicals S.A also funded all costs associated with the development and publishing of the manuscript.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-24T10:25:58Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-24T10:25:58Z</dcterms:available>
   <dcterms:created>2025-10-24T10:25:58Z</dcterms:created>
   <dcterms:issued>2024-10-23T12:29:49Z</dcterms:issued>
   <dcterms:issued>2024-10-23T12:29:49Z</dcterms:issued>
   <dcterms:issued>2024-11</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/12114</dc:identifier>
   <dc:relation>Drug Safety;47</dc:relation>
   <dc:relation>https://doi.org/10.1007/s40264-024-01456-y</dc:relation>
   <dc:rights>Attribution-NonCommercial 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>Adis</dc:publisher>
   <dc:source>Scientia</dc:source>
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