Literature DB >> 19154708

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

Daphney Nasrallah-Irles1, Anne Castot, Laure Thomas, Samy Babai, Bernard Delorme, Hervé Le-Louët.   

Abstract

BACKGROUND: The expected evolution of monitoring systems for health products, aims at increasing the involvement of patients into health products safety system. As a result, it seems necessary to consider the ability for patients to directly report their own adverse events.
METHODS: A pilot study has been undertaken by Afssaps (Health Agency) for 23 patient associations using a reporting form specially created for patients.
RESULTS: According to the analysis of the first 200 reports, received from June 2006 to August 2007, the reported adverse events are mostly serious in terms of consequences on patients' quality of life and expected. The quality of information shows that the proposed tools are adequate and could be used in case of a future change in legislation allowing patient reporting of adverse events.
CONCLUSION: The patient, eventually helped by his association, may provide contributory safety information, especially regarding side effects affecting daily life.

Entities:  

Mesh:

Year:  2009        PMID: 19154708     DOI: 10.2515/therapie:2008060

Source DB:  PubMed          Journal:  Therapie        ISSN: 0040-5957            Impact factor:   2.070


  4 in total

1.  Comment on "Patient Reporting in the EU: Analysis of EudraVigilance Data".

Authors:  Farid Kheloufi; Anne Default; Frank Rouby; Olivier Blin; Joelle Micallef
Journal:  Drug Saf       Date:  2017-10       Impact factor: 5.606

2.  Informativeness of patient initial reports of adverse drug reactions. Can it be improved by a pharmacovigilance centre?

Authors:  F Kheloufi; A Default; F Rouby; D Laugier-Castellan; M Boyer; B Rodrigues; J Ponte-Astoul; M J Jean-Pastor; O Blin; J Micallef
Journal:  Eur J Clin Pharmacol       Date:  2017-04-08       Impact factor: 2.953

3.  The Role of European Patient Organizations in Pharmacovigilance.

Authors:  Cristiano Matos; Gerda Weits; Florence van Hunsel
Journal:  Drug Saf       Date:  2019-04       Impact factor: 5.606

4.  First French experience of ADR reporting by patients after a mass immunization campaign with Influenza A (H1N1) pandemic vaccines: a comparison of reports submitted by patients and healthcare professionals.

Authors:  Geneviève Durrieu; Aurore Palmaro; Laure Pourcel; Céline Caillet; Angeline Faucher; Alexis Jacquet; Shéhérazade Ouaret; Marie Christine Perault-Pochat; Carmen Kreft-Jais; Anne Castot; Maryse Lapeyre-Mestre; Jean-Louis Montastruc
Journal:  Drug Saf       Date:  2012-10-01       Impact factor: 5.606

  4 in total

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