Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1080/14740338.2021.1897566 |
Texto Completo: | http://dx.doi.org/10.1080/14740338.2021.1897566 http://hdl.handle.net/11449/207452 |
Resumo: | Introduction: Considering the need for effective postmarketing surveillance of disease-modifying therapies (DMTs) in multiple sclerosis (MS), we analyzed the potential of the spontaneous reports for safety signal detection, verifying the completeness of the reports in the FDA Adverse Event Reporting System (FAERS). Methods: All reports with DMTs for MS considered the primary suspect cause of ADRs and registered between January 2004 and June 2019 were selected. The vigiGrade completeness score was applied and reports with a score greater than 0.80 were considered well documented. Descriptive statistical analysis and comparisons of well-documented reports by DMTs were performed. Results: A total of 297,926 reports were analyzed. The lowest completeness rates were observed for type of report (13.5%), dose (62.7%), and time from treatment start to the ADR (79.0%). Overall, 80.8% of reports were classified as well documented and those related to natalizumab had the highest proportion (92.4%, p < 0.001), while the lowest was observed for reports sent in 2017 (53.1%, p < 0.001) and for teriflunomide (48.5%, p < 0.001). Conclusions: The high proportion of well-documented reports for DMTs indicates that they can be a valuable source for safety signal detection. A more careful analysis should be performed for data from the groups identified with low completeness to avoid the disclosure of spurious results. |
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Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosisAdverse drug reactiondata accuracypharmacovigilancepostmarketingproduct surveillancespontaneous reportingIntroduction: Considering the need for effective postmarketing surveillance of disease-modifying therapies (DMTs) in multiple sclerosis (MS), we analyzed the potential of the spontaneous reports for safety signal detection, verifying the completeness of the reports in the FDA Adverse Event Reporting System (FAERS). Methods: All reports with DMTs for MS considered the primary suspect cause of ADRs and registered between January 2004 and June 2019 were selected. The vigiGrade completeness score was applied and reports with a score greater than 0.80 were considered well documented. Descriptive statistical analysis and comparisons of well-documented reports by DMTs were performed. Results: A total of 297,926 reports were analyzed. The lowest completeness rates were observed for type of report (13.5%), dose (62.7%), and time from treatment start to the ADR (79.0%). Overall, 80.8% of reports were classified as well documented and those related to natalizumab had the highest proportion (92.4%, p < 0.001), while the lowest was observed for reports sent in 2017 (53.1%, p < 0.001) and for teriflunomide (48.5%, p < 0.001). Conclusions: The high proportion of well-documented reports for DMTs indicates that they can be a valuable source for safety signal detection. A more careful analysis should be performed for data from the groups identified with low completeness to avoid the disclosure of spurious results.Pharmaceutical Sciences Postgraduate Research Program Health Sciences Sector Federal University of ParanáDepartment of Drugs and Medicines Faculty of Pharmaceutical Sciences São Paulo State University (UNESP)Department of Pharmacy Federal University of ParanáDepartment of Drugs and Medicines Faculty of Pharmaceutical Sciences São Paulo State University (UNESP)Federal University of ParanáUniversidade Estadual Paulista (Unesp)Araujo, Ariane G. S.Lucchetta, Rosa C. [UNESP]Tonin, Fernanda S.Pontarolo, RobertoBorba, Helena H. L.Wiens, Astrid2021-06-25T10:55:23Z2021-06-25T10:55:23Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1080/14740338.2021.1897566Expert Opinion on Drug Safety.1744-764X1474-0338http://hdl.handle.net/11449/20745210.1080/14740338.2021.18975662-s2.0-85102517680Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengExpert Opinion on Drug Safetyinfo:eu-repo/semantics/openAccess2024-06-24T13:45:38Zoai:repositorio.unesp.br:11449/207452Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:17:08.613655Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis |
title |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis |
spellingShingle |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis Araujo, Ariane G. S. Adverse drug reaction data accuracy pharmacovigilance postmarketing product surveillance spontaneous reporting Araujo, Ariane G. S. Adverse drug reaction data accuracy pharmacovigilance postmarketing product surveillance spontaneous reporting |
title_short |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis |
title_full |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis |
title_fullStr |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis |
title_full_unstemmed |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis |
title_sort |
Analysis of completeness for spontaneous reporting of disease-modifying therapies in multiple sclerosis |
author |
Araujo, Ariane G. S. |
author_facet |
Araujo, Ariane G. S. Araujo, Ariane G. S. Lucchetta, Rosa C. [UNESP] Tonin, Fernanda S. Pontarolo, Roberto Borba, Helena H. L. Wiens, Astrid Lucchetta, Rosa C. [UNESP] Tonin, Fernanda S. Pontarolo, Roberto Borba, Helena H. L. Wiens, Astrid |
author_role |
author |
author2 |
Lucchetta, Rosa C. [UNESP] Tonin, Fernanda S. Pontarolo, Roberto Borba, Helena H. L. Wiens, Astrid |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Federal University of Paraná Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Araujo, Ariane G. S. Lucchetta, Rosa C. [UNESP] Tonin, Fernanda S. Pontarolo, Roberto Borba, Helena H. L. Wiens, Astrid |
dc.subject.por.fl_str_mv |
Adverse drug reaction data accuracy pharmacovigilance postmarketing product surveillance spontaneous reporting |
topic |
Adverse drug reaction data accuracy pharmacovigilance postmarketing product surveillance spontaneous reporting |
description |
Introduction: Considering the need for effective postmarketing surveillance of disease-modifying therapies (DMTs) in multiple sclerosis (MS), we analyzed the potential of the spontaneous reports for safety signal detection, verifying the completeness of the reports in the FDA Adverse Event Reporting System (FAERS). Methods: All reports with DMTs for MS considered the primary suspect cause of ADRs and registered between January 2004 and June 2019 were selected. The vigiGrade completeness score was applied and reports with a score greater than 0.80 were considered well documented. Descriptive statistical analysis and comparisons of well-documented reports by DMTs were performed. Results: A total of 297,926 reports were analyzed. The lowest completeness rates were observed for type of report (13.5%), dose (62.7%), and time from treatment start to the ADR (79.0%). Overall, 80.8% of reports were classified as well documented and those related to natalizumab had the highest proportion (92.4%, p < 0.001), while the lowest was observed for reports sent in 2017 (53.1%, p < 0.001) and for teriflunomide (48.5%, p < 0.001). Conclusions: The high proportion of well-documented reports for DMTs indicates that they can be a valuable source for safety signal detection. A more careful analysis should be performed for data from the groups identified with low completeness to avoid the disclosure of spurious results. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-06-25T10:55:23Z 2021-06-25T10:55:23Z 2021-01-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1080/14740338.2021.1897566 Expert Opinion on Drug Safety. 1744-764X 1474-0338 http://hdl.handle.net/11449/207452 10.1080/14740338.2021.1897566 2-s2.0-85102517680 |
url |
http://dx.doi.org/10.1080/14740338.2021.1897566 http://hdl.handle.net/11449/207452 |
identifier_str_mv |
Expert Opinion on Drug Safety. 1744-764X 1474-0338 10.1080/14740338.2021.1897566 2-s2.0-85102517680 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Expert Opinion on Drug Safety |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1822218500996857856 |
dc.identifier.doi.none.fl_str_mv |
10.1080/14740338.2021.1897566 |