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Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study

INTRODUCTION: Pharmacovigilance, the monitoring of drug safety after marketing approval, highly depends on the adequate reporting of adverse drug reactions (ADRs). To improve pharmacovigilance awareness and future ADR reporting among medical students, we developed and evaluated a student-run pharmac...

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Autores principales: Schutte, Tim, Tichelaar, Jelle, Reumerman, Michael O., van Eekeren, Rike, Rolfes, Leàn, van Puijenbroek, Eugène P., Richir, Milan C., van Agtmael, Michiel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384963/
https://www.ncbi.nlm.nih.gov/pubmed/28120270
http://dx.doi.org/10.1007/s40264-016-0502-1
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author Schutte, Tim
Tichelaar, Jelle
Reumerman, Michael O.
van Eekeren, Rike
Rolfes, Leàn
van Puijenbroek, Eugène P.
Richir, Milan C.
van Agtmael, Michiel A.
author_facet Schutte, Tim
Tichelaar, Jelle
Reumerman, Michael O.
van Eekeren, Rike
Rolfes, Leàn
van Puijenbroek, Eugène P.
Richir, Milan C.
van Agtmael, Michiel A.
author_sort Schutte, Tim
collection PubMed
description INTRODUCTION: Pharmacovigilance, the monitoring of drug safety after marketing approval, highly depends on the adequate reporting of adverse drug reactions (ADRs). To improve pharmacovigilance awareness and future ADR reporting among medical students, we developed and evaluated a student-run pharmacovigilance programme. METHODS: In this project, teams of medical students (first- to fifth-year) assessed real ADR reports, as submitted to the national pharmacovigilance centre. After assessment of causality, including identification of a potential pharmacological explanation for the ADR, the students wrote a personalized feedback letter to the reporter, as well as a summary for the European Medicines Agency (EMA) and World Health Organization (WHO) pharmacovigilance databases. This student assessment was then verified and evaluated by staff from The Netherlands Pharmacovigilance Centre Lareb (Lareb), using an e-questionnaire. Student attitudes, intentions, skills, and knowledge of ADR reporting were evaluated using the e-questionnaire, before and after participation in the programme. RESULTS: From May 2014 to January 2015, a total of 43 students assessed 100 different ADR reports selected by Lareb staff (n = 3). Student assessments were rated as useful (93%), scientifically substantiated (90%), accurate (92%), and complete (92%), and, on average, did not cost Lareb staff extra time. Medical students were positive about ADR reporting, and their awareness of ADR reporting increased significantly following participation in the programme (p < 0.05). After participation in the programme, the students intended to report serious ADRs in their future practice, and their knowledge of pharmacovigilance and ADR reporting showed they had a high overall level of pharmacological understanding. CONCLUSION: The student-run pharmacovigilance programme is a win–win venture. It offers students a valuable ‘pharmacovigilance experience’, creates awareness in future doctors, and has the potential to increase pharmacovigilance skills and knowledge. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40264-016-0502-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-53849632017-04-24 Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study Schutte, Tim Tichelaar, Jelle Reumerman, Michael O. van Eekeren, Rike Rolfes, Leàn van Puijenbroek, Eugène P. Richir, Milan C. van Agtmael, Michiel A. Drug Saf Original Research Article INTRODUCTION: Pharmacovigilance, the monitoring of drug safety after marketing approval, highly depends on the adequate reporting of adverse drug reactions (ADRs). To improve pharmacovigilance awareness and future ADR reporting among medical students, we developed and evaluated a student-run pharmacovigilance programme. METHODS: In this project, teams of medical students (first- to fifth-year) assessed real ADR reports, as submitted to the national pharmacovigilance centre. After assessment of causality, including identification of a potential pharmacological explanation for the ADR, the students wrote a personalized feedback letter to the reporter, as well as a summary for the European Medicines Agency (EMA) and World Health Organization (WHO) pharmacovigilance databases. This student assessment was then verified and evaluated by staff from The Netherlands Pharmacovigilance Centre Lareb (Lareb), using an e-questionnaire. Student attitudes, intentions, skills, and knowledge of ADR reporting were evaluated using the e-questionnaire, before and after participation in the programme. RESULTS: From May 2014 to January 2015, a total of 43 students assessed 100 different ADR reports selected by Lareb staff (n = 3). Student assessments were rated as useful (93%), scientifically substantiated (90%), accurate (92%), and complete (92%), and, on average, did not cost Lareb staff extra time. Medical students were positive about ADR reporting, and their awareness of ADR reporting increased significantly following participation in the programme (p < 0.05). After participation in the programme, the students intended to report serious ADRs in their future practice, and their knowledge of pharmacovigilance and ADR reporting showed they had a high overall level of pharmacological understanding. CONCLUSION: The student-run pharmacovigilance programme is a win–win venture. It offers students a valuable ‘pharmacovigilance experience’, creates awareness in future doctors, and has the potential to increase pharmacovigilance skills and knowledge. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40264-016-0502-1) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-01-25 2017 /pmc/articles/PMC5384963/ /pubmed/28120270 http://dx.doi.org/10.1007/s40264-016-0502-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research Article
Schutte, Tim
Tichelaar, Jelle
Reumerman, Michael O.
van Eekeren, Rike
Rolfes, Leàn
van Puijenbroek, Eugène P.
Richir, Milan C.
van Agtmael, Michiel A.
Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study
title Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study
title_full Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study
title_fullStr Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study
title_full_unstemmed Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study
title_short Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study
title_sort feasibility and educational value of a student-run pharmacovigilance programme: a prospective cohort study
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384963/
https://www.ncbi.nlm.nih.gov/pubmed/28120270
http://dx.doi.org/10.1007/s40264-016-0502-1
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