Side effects reported by European consumers for medications for erectile dysfunction

Objective: To characterise consumer adverse drug reaction (ADR) reports for phosphodiesterase type 5 (PDE5) inhibitors. Methods: We included ADR reports submitted by adults to the European ADR database (EudraVigialnce) from 2007 to 2011. ADRs were classified according to type, seriousness and age a...

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Main Authors: Lise Aagaard, Ebba Holme Hansen
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Journal of Research in Pharmacy Practice
Subjects:
Online Access:http://www.jrpp.net/article.asp?issn=2319-9644;year=2013;volume=2;issue=2;spage=93;epage=95;aulast=Aagaard
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author Lise Aagaard
Ebba Holme Hansen
author_facet Lise Aagaard
Ebba Holme Hansen
author_sort Lise Aagaard
collection DOAJ
description Objective: To characterise consumer adverse drug reaction (ADR) reports for phosphodiesterase type 5 (PDE5) inhibitors. Methods: We included ADR reports submitted by adults to the European ADR database (EudraVigialnce) from 2007 to 2011. ADRs were classified according to type, seriousness and age and sex of consumers. The unit of analysis was one ADR. Findings: Totally, 328 ADRs were reported for sildenafil and vardenafil, and only 5% of these were serious. The largest number of reported ADRs was found for sildenafil, i.e., "lack of efficacy" and/or "drug efficacy decreased" ( n = 134) and "headache" ( n = 21). Conclusion: ADRs reported by consumers for PDE5 inhibitors were relatively low, and only few ADRs were serious.
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spelling doaj.art-7e30d486e44a48c7b2046cba5caee8ea2022-12-21T19:46:55ZengWolters Kluwer Medknow PublicationsJournal of Research in Pharmacy Practice2319-96442279-042X2013-01-0122939510.4103/2279-042X.117390Side effects reported by European consumers for medications for erectile dysfunctionLise AagaardEbba Holme HansenObjective: To characterise consumer adverse drug reaction (ADR) reports for phosphodiesterase type 5 (PDE5) inhibitors. Methods: We included ADR reports submitted by adults to the European ADR database (EudraVigialnce) from 2007 to 2011. ADRs were classified according to type, seriousness and age and sex of consumers. The unit of analysis was one ADR. Findings: Totally, 328 ADRs were reported for sildenafil and vardenafil, and only 5% of these were serious. The largest number of reported ADRs was found for sildenafil, i.e., "lack of efficacy" and/or "drug efficacy decreased" ( n = 134) and "headache" ( n = 21). Conclusion: ADRs reported by consumers for PDE5 inhibitors were relatively low, and only few ADRs were serious.http://www.jrpp.net/article.asp?issn=2319-9644;year=2013;volume=2;issue=2;spage=93;epage=95;aulast=AagaardAdverse drug reactions; consumers; erectile dysfunction; EudraVigilance; pharmacovigilance
spellingShingle Lise Aagaard
Ebba Holme Hansen
Side effects reported by European consumers for medications for erectile dysfunction
Journal of Research in Pharmacy Practice
Adverse drug reactions; consumers; erectile dysfunction; EudraVigilance; pharmacovigilance
title Side effects reported by European consumers for medications for erectile dysfunction
title_full Side effects reported by European consumers for medications for erectile dysfunction
title_fullStr Side effects reported by European consumers for medications for erectile dysfunction
title_full_unstemmed Side effects reported by European consumers for medications for erectile dysfunction
title_short Side effects reported by European consumers for medications for erectile dysfunction
title_sort side effects reported by european consumers for medications for erectile dysfunction
topic Adverse drug reactions; consumers; erectile dysfunction; EudraVigilance; pharmacovigilance
url http://www.jrpp.net/article.asp?issn=2319-9644;year=2013;volume=2;issue=2;spage=93;epage=95;aulast=Aagaard
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