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Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee
This study measured the exposure to different categories of medicinal products discussed by the European Union (EU) Pharmacovigilance Risk Assessment Committee from September to November 2018 in four electronic primary care health databases: IQVIA Medical Research Data‐UK, IQVIA Medical Research Dat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158204/ https://www.ncbi.nlm.nih.gov/pubmed/31955404 http://dx.doi.org/10.1002/cpt.1775 |
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author | Flynn, Robert Hedenmalm, Karin Murray‐Thomas, Tarita Pacurariu, Alexandra Arlett, Peter Shepherd, Hilary Myles, Puja Kurz, Xavier |
author_facet | Flynn, Robert Hedenmalm, Karin Murray‐Thomas, Tarita Pacurariu, Alexandra Arlett, Peter Shepherd, Hilary Myles, Puja Kurz, Xavier |
author_sort | Flynn, Robert |
collection | PubMed |
description | This study measured the exposure to different categories of medicinal products discussed by the European Union (EU) Pharmacovigilance Risk Assessment Committee from September to November 2018 in four electronic primary care health databases: IQVIA Medical Research Data‐UK, IQVIA Medical Research Data‐France, IQVIA Medical Research Data‐Germany, and Clinical Practice Research Datalink Aurum, in the entire lifespan of each database until August 31, 2018. The assessment of 83 centrally authorized products and 45 nationally authorized products showed that coverage was better for products marketed for longer duration and worse for orphan drugs. The ability to detect associations against hypothetical comparators was better for more common events and for larger effect sizes. Coverage of advanced therapies was worse for those typically administered in a specialized rather than primary care setting. This study shows that to enable better informed regulatory decisions there is a need to access complementary data sources, particularly capturing secondary care prescribing. |
format | Online Article Text |
id | pubmed-7158204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71582042020-04-20 Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee Flynn, Robert Hedenmalm, Karin Murray‐Thomas, Tarita Pacurariu, Alexandra Arlett, Peter Shepherd, Hilary Myles, Puja Kurz, Xavier Clin Pharmacol Ther Research This study measured the exposure to different categories of medicinal products discussed by the European Union (EU) Pharmacovigilance Risk Assessment Committee from September to November 2018 in four electronic primary care health databases: IQVIA Medical Research Data‐UK, IQVIA Medical Research Data‐France, IQVIA Medical Research Data‐Germany, and Clinical Practice Research Datalink Aurum, in the entire lifespan of each database until August 31, 2018. The assessment of 83 centrally authorized products and 45 nationally authorized products showed that coverage was better for products marketed for longer duration and worse for orphan drugs. The ability to detect associations against hypothetical comparators was better for more common events and for larger effect sizes. Coverage of advanced therapies was worse for those typically administered in a specialized rather than primary care setting. This study shows that to enable better informed regulatory decisions there is a need to access complementary data sources, particularly capturing secondary care prescribing. John Wiley and Sons Inc. 2020-02-12 2020-04 /pmc/articles/PMC7158204/ /pubmed/31955404 http://dx.doi.org/10.1002/cpt.1775 Text en © 2020 European Medicines Agency. Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Flynn, Robert Hedenmalm, Karin Murray‐Thomas, Tarita Pacurariu, Alexandra Arlett, Peter Shepherd, Hilary Myles, Puja Kurz, Xavier Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee |
title | Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee |
title_full | Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee |
title_fullStr | Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee |
title_full_unstemmed | Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee |
title_short | Ability of Primary Care Health Databases to Assess Medicinal Products Discussed by the European Union Pharmacovigilance Risk Assessment Committee |
title_sort | ability of primary care health databases to assess medicinal products discussed by the european union pharmacovigilance risk assessment committee |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158204/ https://www.ncbi.nlm.nih.gov/pubmed/31955404 http://dx.doi.org/10.1002/cpt.1775 |
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