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dc.contributor.authorOtero Losada, Matildees
dc.contributor.authorPetrovsky, Nikolaies
dc.contributor.authorAlami, Abdallahes
dc.contributor.authorCrispo, James A. G.es
dc.contributor.authorMattison, Donaldes
dc.contributor.authorCapani, Franciscoes
dc.contributor.authorGoetz, Christopheres
dc.contributor.authorKrewski, Danieles
dc.contributor.authorPérez Lloret, Santiagoes
dc.date.accessioned2022-10-31T12:33:45Z-
dc.date.available2022-10-31T12:33:45Z-
dc.date.issued2022-
dc.identifier.citationOtero Losada, M. et al. Disproportionality analysis of adverse neurological and psychiatric reactions with the ChAdOx1(Oxford-AstraZeneca) and BNT162b2 (Pfizer- BioNTech) COVID-19 vaccines in the United Kingdom [en línea]. Expert Opinion on Drug Safety. 2022. doi: 10.1080/14740338.2022.2120607. Disponible en: https://repositorio.uca.edu.ar/handle/123456789/15361es
dc.identifier.issn1474-0338 (impreso)-
dc.identifier.issn1744-764X (en línea)-
dc.identifier.urihttps://repositorio.uca.edu.ar/handle/123456789/15361-
dc.description.abstractAbstract: Background: Information on neurological and psychiatric adverse events following immunization (AEFIs) with COVID-19 vaccines is limited. Research design & methods: We examined and compared neurological and psychiatric AEFIS reports related to BNT162b2 (Pfizer-BioNTech) and ChAdOx1 (Oxford-AstraZeneca) COVID-19 vaccines and recorded in the United Kingdom Medicines and Healthcare products Regulatory Agency between 9 December 2020 and 30 June 2021. Results: As of 30 June 2021, 46.1 million doses of ChAdOx1 and 30.3 million doses of BNT162b2 had been administered. The most frequently reported AEFI was headache with 1,686 and 575 cases per million doses of ChAdOx1 and BNT162b2, respectively. AEFIs more frequently reported after CHAdOx1 compared with BNT162b2 vaccination were Guillain-Barré syndrome (OR, 95% CI = 2.53, 1.82–3.51), freezing (6.66, 3.12–14.22), cluster headache (1.53, 1.28–1.84), migraine (1.23,1.17–1.30), postural dizziness (1.24,1.13–1.37), tremor (2.86, 2.68–3.05), headache (1.40, 1.38–1.43), paresthesia (1.11, 1.06–1.16), delirium (1.85, 1.45–2.36), hallucination (2.20, 1.82–2.66), poor quality sleep (1.53, 1.26–1.85), and nervousness (1.54, 1.26–1.89) Reactions less frequently reported with ChAdOx1 than with BNT162b2 were Bell’s palsy (0.47, 0.41–0.55), anosmia (0.58, 0.47–0.71), facial paralysis (0.35, 0.29– 0.41), dysgeusia (0.68, 0.62–0.73), presyncope (0.48, 0.42–0.55), syncope (0.63, 0.58–0.67), and anxiety (0.75 (0.67–0.85). Conclusion: Neurological and psychiatric AEFIs were relatively infrequent, but each vaccine was associated with a distinctive toxic profile. Plain Language Summary We examined reports on adverse neurological and psychiatric effects following immunization with BNT162b2 (Pfizer-BioNTech) and ChAdOx1 (Oxford-AstraZeneca) for COVID-19 to the United Kingdom Medicines and Healthcare products Regulatory Agency between 9 December 2020 and 30 June 2021. Adverse effects following immunization (AEFIs) were relatively infrequent. Compared to BNT162b2, Guillain-Barré syndrome, freezing phenomenon, cluster headache, migraine, postural dizziness, tremor, headache, paresthesia, delirium, hallucination, poor quality sleep, and nervousness were more frequently reported for ChAdOx1. Reactions less frequently reported for ChAdOx1 than for BNT162b2 were Bell’s palsy, anosmia, facial paralysis, dysgeusia, presyncope, syncope, and anxiety.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherTaylor & Francises
dc.rightsAcceso restringido*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.sourceExpert Opinion on Drug Safety. 2022es
dc.subjectCOVID-19es
dc.subjectBNT162b2es
dc.subjectVACUNASes
dc.subjectChAdOx1es
dc.subjectFARMACOLOGIAes
dc.subjectNEUROLOGIAes
dc.subjectPSIQUIATRIAes
dc.subjectVIGILANCIAes
dc.subjectEFECTOS ADVERSOSes
dc.titleDisproportionality analysis of adverse neurological and psychiatric reactions with the ChAdOx1(Oxford-AstraZeneca) and BNT162b2 (Pfizer- BioNTech) COVID-19 vaccines in the United Kingdomes
dc.typeArtículoes
dc.identifier.doi10.1080/14740338.2022.2120607-
uca.disciplinaMEDICINAes
uca.issnrd1es
uca.affiliationFil: Otero Losada, Matilde. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes
uca.affiliationFil: Otero Losada, Matilde. Universidad Abierta Interamericana. Centro de Altos Estudios en Ciencias Humanas y de La Salud; Argentinaes
uca.affiliationFil: Petrovsky, Nikolai. Universidad de Flinders; Australiaes
uca.affiliationFil: Petrovsky, Nikolai. Vaxine; Australiaes
uca.affiliationFil: Alami, Abdallah. Universidad de Ottawa. Facultad de Medicina. Centro McLaughlin para la Evaluación de Riesgos para la Salud de la Población; Canadáes
uca.affiliationFil: Alami, Abdallah. Risk Sciences International; Canadáes
uca.affiliationFil: Crispo, James A. G. Universidad de Carleton. Escuela de Matemáticas y Estadística; Canadáes
uca.affiliationFil: Crispo, James A. G. Escuela de Medicina del Norte de Ontario. División de Ciencias Humanas; Canadáes
uca.affiliationFil: Crispo, James A. Universidad de British Columbia. Facultad de Ciencias Farmacéuticas; Canadáes
uca.affiliationFil: Mattison, Donald. Vaxine; Australiaes
uca.affiliationFil: Mattison, Donald. Risk Sciences International; Canadáes
uca.affiliationFil: Mattison, Donald. Universidad de Carolina del Sur. Arnold School of Public Health; Estdos Unidoses
uca.affiliationFil: Mattison, Donald. Universidad de Ottawa. Escuela de Epidemiología y Salud Pública; Canadáes
uca.affiliationFil: Capani, Francisco. Universidad Abierta Interamericana. Centro de Altos Estudios en Ciencias Humanas y de La Salud; Argentinaes
uca.affiliationFil: Capani, Francisco. Universidad Autónoma de Chile. Facultad de Ciencias de la Salud; Chilees
uca.affiliationFil: Capani, Francisco. Universidad John F. Kennedy. Departamento de Biología; Argentinaes
uca.affiliationFil: Goetz, Christopher. Universidad Rush. Centro Médico. Departamento de Ciencias Neurológicas; Estados Unidoses
uca.affiliationFil: Krewski, Daniel. Universidad de Ottawa. Facultad de Medicina. Centro McLaughlin para la Evaluación de Riesgos para la Salud de la Población; Canadáes
uca.affiliationFil: Krewski, Daniel. Risk Sciences International; Canadáes
uca.affiliationFil: Pérez Lloret, Santiago. Pontificia Universidad Católica Argentina. Laboratorio de Investigación en Ciencia de Datos; Argentinaes
uca.affiliationFil: Pérez Lloret, Santiago. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Fisiología; Argentinaes
uca.versionpublishedVersiones
item.languageiso639-1en-
item.grantfulltextreserved-
item.fulltextWith Fulltext-
crisitem.author.deptFacultad de Psicología y Psicopedagogía-
crisitem.author.deptCentro de Investigaciones en Psicología y Psicopedagogía (CIPP)-
crisitem.author.deptConsejo Nacional de Investigaciones Científicas y Técnicas-
crisitem.author.deptInstituto de Investigaciones Cardiológicas-
crisitem.author.deptLaboratorio de Neurobiología Molecular-
crisitem.author.deptConsejo Nacional de Investigaciones Científicas y Técnicas-
crisitem.author.orcid0000-0003-0342-0628-
crisitem.author.orcid0000-0001-9069-6512-
crisitem.author.parentorgPontificia Universidad Católica Argentina-
crisitem.author.parentorgFacultad de Psicología y Psicopedagogía-
crisitem.author.parentorgConsejo Nacional de Investigaciones Científicas y Técnicas-
crisitem.author.parentorgInstituto de Investigaciones Biomédicas - BIOMED-
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