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Adverse Drug Reaction Reports Received Through the Mobile App, VigiBIP®: A Comparison with Classical Methods of Reporting

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Abstract

Introduction

The use of mobile apps is increasing in medicine. In pharmacovigilance, mobile apps may help to increase adverse drug reaction reporting and improve the communication of safety issues. The Toulouse University Pharmacovigilance Center has developed VigiBIP®, a free smartphone app available on Android and Apple stores, for reporting adverse drug reactions and requesting drug safety information.

Objective

The present study was performed to compare the main characteristics of spontaneous adverse drug reaction reports received through VigiBIP® with classical methods of reporting (phone, e-mail, fax, letter, website) during 25 months (2015–17).

Methods

Using the Chi squared test, we compared the type of reporter, adverse drug reaction seriousness, drugs involved and reported ADRs using VigiBIP® and classical methods of reporting

Results

A total of 4102 reports were received by the Toulouse University Pharmacovigilance Center, including 4.7% through VigiBip®. Patients’ reports were significantly more frequent with VigiBip® (6.7%) than with classical methods (3.4%) [p = 0.01]. Reported adverse drug reactions and involved drugs differed according to the method of reporting used.

Conclusion

Our study shows that a mobile app is an additional tool used in pharmacovigilance. Types of reporters and adverse drug reactions in VigiBIP were different to those seen in classical methods of reporting.

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References

  1. Pouyanne P, Haramburu F, Imbs JL, Begaud B. Admissions to hospital caused by adverse drug reactions: cross sectional incidence study. French Pharmacovigilance Centres. BMJ. 2000;320(7241):1036.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Pirmohamed M, James S, Meakin S, Green C, Scott AK, Walley TJ, et al. Adverse drug reactions as a cause of admission to hospital: prospective analysis to 18,820 patients. BMJ. 2004;329(7456):15–9.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Benard-Laribière A, Miremont-Salamé G, Pérault-Pochat MC, Noize P, Haramburu F, EMIR Study Group on behalf of the French Network of Pharmacovigilance Centres. Incidence of hospital admissions due to adverse drug reactions in France: the EMIR study. Fundam Clin Pharmacol. 2015;29(1):106–11.

    Article  PubMed  Google Scholar 

  4. Figueiras A, Herdeiro MT, Polónia J, Gestal-Otero JJ. An educational intervention to improve physician reporting of adverse drug reactions: a cluster-randomized controlled trial. JAMA. 2006;296(9):1086–93.

    Article  CAS  PubMed  Google Scholar 

  5. Herdeiro MT, Polónia J, Gestal-Otero JJ, Figueiras A. Improving the reporting of adverse drug reactions: a cluster-randomized trial among pharmacists in Portugal. Drug Saf. 2008;31(4):335–44.

    Article  PubMed  Google Scholar 

  6. Bäckström M, Mjörndal T. A small economic inducement to stimulate increased reporting of adverse drug reactions: a way of dealing with an old problem? Eur J Clin Pharmacol. 2006;62(5):381–5.

    Article  PubMed  Google Scholar 

  7. Anderson C, Krska J, Murphy E, Avery A, Yellow Card Study Collaboration. The importance of direct patient reporting of suspected adverse drug reactions: a patient perspective. Br J Clin Pharmacol. 2011;72(5):806–22.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Gony M, Badie K, Sommet A, Jacquot J, Baudrin D, Gauthier P, et al. Improving adverse drug reaction reporting in hospitals: results of the French Pharmacovigilance in Midi-Pyrénées region (PharmacoMIP) network 2-year pilot study. Drug Saf. 2010;33(5):409–16.

    Article  PubMed  Google Scholar 

  9. Jacquot J, Gony M, Baudrin D, Chastel X, Montastruc JL, Bagheri H. Could we improve notification of adverse drugs reactions in hospital? Assessment of 5 years of network PharmacoMIP’s activities. Therapie. 2012;67(3):231–6.

    Article  PubMed  Google Scholar 

  10. Abadie D, Chebane L, Bert M, Durrieu G, Montastruc JL. Online reporting of adverse drug reactions: a study from a regional pharmacovigilance center. Therapie. 2014;69(5):395–400.

    Article  PubMed  Google Scholar 

  11. Knezevic MZ, Bivolarevic IC, Peric TS, Jankovic SM. Using Facebook to increase spontaneous reporting of adverse drug reactions. Drug Saf. 2011;34(4):351–2.

    Article  PubMed  Google Scholar 

  12. Istepanian RS. Mobile applications for diabetes management: efficacy issues and regulatory challenges. Lancet Diabetes Endocrinol. 2015;3(12):921–3.

    Article  PubMed  Google Scholar 

  13. De Vries ST, Wong L, Sutcliffe A, Houÿez F, Ruiz CL. Mol PG; IMI Web-RADR Work Package 3b Consortium. Factors influencing the use of a mobile app for reporting adverse drug reactions and receiving safety information: a qualitative study. Drug Saf. 2017;40(5):443–55.

    Article  PubMed  Google Scholar 

  14. Edwards IR, Aronson JK. Adverse drug reactions: definitions, diagnosis, and management. Lancet. 2000;356(9237):1255–9.

    Article  CAS  PubMed  Google Scholar 

  15. Miremont-Salamé G, Théophile H, Haramburu F, Bégaud B. Causality assessment in pharmacovigilance: the French method and its successive updates. Therapie. 2016;71(2):179–86.

    Article  PubMed  Google Scholar 

  16. Durrieu G, Jacquot J, Baudrin D, Mège M, Rousseau V, Bagheri H, et al. Improving adverse drug reaction reporting by general practitioners through clinical research assistants visits. Therapie. 2017;72(3):351–5.

    Article  PubMed  Google Scholar 

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Correspondence to Jean-Louis Montastruc.

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Funding

No sources of funding were received for the preparation of this article.

Conflict of interest

François Montastruc, Haleh Bagheri, Isabelle Lacroix, Christine Damase-Michel, Leila Chebane, Vanessa Rousseau, Emilie Jouanjus, Maryse Lapeyre-Mestre, Geneviève Durrieu and Jean-Louis Montastruc have no conflicts of interest directly relevant to the content of this study. The content of this article only involved its authors and the opinions and conclusions are not necessarily those of Agence Nationale de Sécurité du Médicament. The authors of this article are solely responsible for the conclusions.

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Montastruc, F., Bagheri, H., Lacroix, I. et al. Adverse Drug Reaction Reports Received Through the Mobile App, VigiBIP®: A Comparison with Classical Methods of Reporting. Drug Saf 41, 511–514 (2018). https://doi.org/10.1007/s40264-017-0630-2

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