Literature DB >> 30357648

The Role of European Patient Organizations in Pharmacovigilance.

Cristiano Matos1,2, Gerda Weits3, Florence van Hunsel3.   

Abstract

INTRODUCTION: Patient organizations have a privileged position to be active agents for promoting pharmacovigilance and patient engagement, encouraging direct patient reporting and improving the awareness of pharmacovigilance. AIM: The objective of this study was to understand the role of European patient organizations as stakeholders to optimize patient involvement in pharmacovigilance.
METHODS: A descriptive correlational study was conducted to investigate the opinions and attitudes of patient organizations regarding general patient involvement in pharmacovigilance, and their initiatives to support drug safety through a web-based questionnaire during the months of March and April 2018.
RESULTS: A total of 1898 patient organizations were invited to participate in the survey, including 89 pan-European organizations. In total, 337 questionnaires (17.76%) were collected from 31 countries, including 297 complete answers (88.31%). A large number of organizations stated that they would like to increase the awareness of patients regarding specific adverse drug reactions (ADRs) related to their medicines (43.19%, n  = 130); however, 38.54% (n  = 116) declared they do not have any pharmacovigilance goals. Barriers to supporting pharmacovigilance activities include low budget to promote pharmacovigilance among members (45.45%, n  = 135), lack of resources to participate in pharmacovigilance activities (43.77%, n  = 130), or lack of support from the National Competent Authorities (33.33%, n  = 99). Organizations inform patients to report ADRs (40.40%; n  = 120), information regarding new ADRs related to their medicines (40.07%; n  = 119), or when a new drug is marketed (30.98%; n  = 92); however, more than one-third indicated that they never had any involvement in pharmacovigilance (34.68%; n  = 103).
CONCLUSION: Bringing pharmacovigilance stakeholders and patient organizations together could create a more optimal reporting culture. Patient organizations appear to have an important role in encouraging patients to talk with their doctors/pharmacists about ADRs experienced, or to help him/her report the ADRs to the pharmacovigilance systems. Lack of resources, budget, and support from NCAs are seen as the main barriers to being involved in pharmacovigilance awareness.

Entities:  

Mesh:

Year:  2019        PMID: 30357648     DOI: 10.1007/s40264-018-0748-x

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  27 in total

Review 1.  Experiences with adverse drug reaction reporting by patients: an 11-country survey.

Authors:  Florence van Hunsel; Linda Härmark; Shanthi Pal; Sten Olsson; Kees van Grootheest
Journal:  Drug Saf       Date:  2012-01-01       Impact factor: 5.606

2.  Principles and methods of validity and reliability testing of questionnaires used in social and health science researches.

Authors:  Oladimeji Akeem Bolarinwa
Journal:  Niger Postgrad Med J       Date:  2015 Oct-Dec

Review 3.  Patient reporting of suspected adverse drug reactions: a review of published literature and international experience.

Authors:  A Blenkinsopp; P Wilkie; M Wang; P A Routledge
Journal:  Br J Clin Pharmacol       Date:  2007-02       Impact factor: 4.335

4.  Pharmacovigilance implemented by patients: A necessity in the 21st century.

Authors:  Jean Lafond
Journal:  Therapie       Date:  2016-03-15       Impact factor: 2.070

5.  The contribution of direct patient reported ADRs to drug safety signals in the Netherlands from 2010 to 2015.

Authors:  Florence van Hunsel; Susan de Waal; Linda Härmark
Journal:  Pharmacoepidemiol Drug Saf       Date:  2017-05-19       Impact factor: 2.890

6.  [Adverse drug reactions: a pilot study on patient reporting through patient associations].

Authors:  Daphney Nasrallah-Irles; Anne Castot; Laure Thomas; Samy Babai; Bernard Delorme; Hervé Le-Louët
Journal:  Therapie       Date:  2009-01-21       Impact factor: 2.070

7.  Adverse drug reaction reports of patients and healthcare professionals-differences in reported information.

Authors:  Leàn Rolfes; Florence van Hunsel; Sarah Wilkes; Kees van Grootheest; Eugène van Puijenbroek
Journal:  Pharmacoepidemiol Drug Saf       Date:  2014-07-31       Impact factor: 2.890

8.  The role of patient advocacy organisations in neuromuscular disease R&D--The case of the Dutch neuromuscular disease association VSN.

Authors:  Wouter Boon; Ria Broekgaarden
Journal:  Neuromuscul Disord       Date:  2010-02       Impact factor: 4.296

9.  The Impact of Experiencing Adverse Drug Reactions on the Patient's Quality of Life: A Retrospective Cross-Sectional Study in the Netherlands.

Authors:  Leàn Rolfes; Florence van Hunsel; Katja Taxis; Eugène van Puijenbroek
Journal:  Drug Saf       Date:  2016-08       Impact factor: 5.606

10.  The Quality of Clinical Information in Adverse Drug Reaction Reports by Patients and Healthcare Professionals: A Retrospective Comparative Analysis.

Authors:  Leàn Rolfes; Florence van Hunsel; Laura van der Linden; Katja Taxis; Eugène van Puijenbroek
Journal:  Drug Saf       Date:  2017-07       Impact factor: 5.606

View more
  4 in total

1.  Inappropriate Prescriptions in Older People-Translation and Adaptation to Portuguese of the STOPP/START Screening Tool.

Authors:  Luís Monteiro; Matilde Monteiro-Soares; Cristiano Matos; Inês Ribeiro-Vaz; Andreia Teixeira; Carlos Martins
Journal:  Int J Environ Res Public Health       Date:  2022-06-04       Impact factor: 4.614

Review 2.  The Importance of Direct Patient Reporting of Adverse Drug Reactions in the Safety Monitoring Process.

Authors:  Kamila Sienkiewicz; Monika Burzyńska; Izabela Rydlewska-Liszkowska; Jacek Sienkiewicz; Ewelina Gaszyńska
Journal:  Int J Environ Res Public Health       Date:  2021-12-31       Impact factor: 3.390

3.  Diabetes patient's pharmacovigilance knowledge and risk perception: the influence of being part of a patient organisation.

Authors:  Cristiano Matos; Florence van Hunsel; Rogério Tavares Ribeiro; Dulce Nascimento do Ó; João Filipe Raposo
Journal:  Ther Adv Drug Saf       Date:  2020-09-04

4.  Communicating Adverse Drug Reaction Insights Through Patient Organizations: Experiences from a Pilot Study in the Netherlands.

Authors:  Linda Härmark; Gerda Weits; Rietje Meijer; Federica Santoro; G Niklas Norén; Florence van Hunsel
Journal:  Drug Saf       Date:  2020-08       Impact factor: 5.606

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.