Adverse drug reaction related to drug shortage: A retrospective study on the French National Pharmacovigilance Database.


Journal

British journal of clinical pharmacology
ISSN: 1365-2125
Titre abrégé: Br J Clin Pharmacol
Pays: England
ID NLM: 7503323

Informations de publication

Date de publication:
03 2023
Historique:
revised: 08 09 2022
received: 12 07 2022
accepted: 16 09 2022
pubmed: 1 10 2022
medline: 17 2 2023
entrez: 30 9 2022
Statut: ppublish

Résumé

Drug shortages are a growing global health issue. The aim of the study was to evaluate the consequences of drug shortages on patient safety based on data recorded in the French National Pharmacovigilance Database. All cases involving drug shortages reported from 1985 to the end of 2019 were extracted from the database. Following the selection process, 462 cases were included. The number of cases increased significantly from 2004 to 2019. Cases mainly involved drugs from the nervous system (22.1%, 95% confidence interval [CI] 17.5-27.0%), the cardiovascular system (16.4%, 95% CI 11.9-21.4%) and anti-infectives for systemic use (14.3%, 95% CI 9.7-19.2%) ATC classes. Most of the cases reported an adverse drug reaction (ADR) belonging to the SOC nervous system (21%, 95% CI 18-24%), skin and subcutaneous (14%, 95% CI 11-17%), general (13%, 95% CI 10-17%) and gastrointestinal (8%, 95% CI 5-11%) disorders. Disease worsening was observed in 15.9% of the cases, mostly related to a lack of efficacy of the replacement drug. Half of the cases were considered as serious. Evolution was favourable in 79.4% of the cases. Death and/or life-threatening situations were reported in 5.8% of the cases. Medication errors (MEs) were identified in 51 cases (11%), mostly occurring at the administration step and involving a human factor. This study emphasizes the clinical impact of drug shortage in terms of ADRs, ME and inefficiency. These observations underline the importance of a global health policy programme to limit the occurrence of drug shortages and to reinforce the information provided to patients and health care professionals in this context to limit risk.

Identifiants

pubmed: 36177609
doi: 10.1111/bcp.15550
doi:

Substances chimiques

Pharmaceutical Preparations 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1080-1088

Informations de copyright

© 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

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Auteurs

Delphine Bourneau-Martin (D)

Department of Pharmacology-Toxicology and Pharmacovigilance, University Hospital of Angers, Angers, France.

Marina Babin (M)

Department of Pharmacology-Toxicology and Pharmacovigilance, University Hospital of Angers, Angers, France.

Aurélie Grandvuillemin (A)

Centre Régional de Pharmacovigilance de Dijon, CHU Dijon Bourgogne, Dijon, France.

Charlotte Mullet (C)

Department of Pharmacology-Toxicology and Pharmacovigilance, University Hospital of Angers, Angers, France.

Francesco Salvo (F)

Univ. Bordeaux, INSERM, BPH, U1219, Bordeaux, France.
Service de Pharmacologie, CHU de Bordeaux, Bordeaux, France.

Allison Singier (A)

Univ. Bordeaux, INSERM, BPH, U1219, Bordeaux, France.

Morgane Cellier (M)

Department of Pharmacology-Toxicology and Pharmacovigilance, University Hospital of Angers, Angers, France.

Audrey Fresse (A)

CHRU de Nancy - Hôpitaux de Brabois, Centre Régional de Pharmacovigilance, Vandœuvre-lès-Nancy, France.

Claire de Canecaude (C)

Service de Pharmacologie Médicale et Clinique, Centre de Pharmacovigilance, de Pharmacoépidémiologie et d'Informations sur Le Médicament, Faculté de Médecine, Centre Hospitalier Universitaire, Faculté de Médecine, Toulouse, France.

Tessa Pietri (T)

Aix-Marseille Université, Inserm, UMR 1106, Assistance publique - Hôpitaux de Marseille, Service de pharmacologie clinique, Centre régional de pharmacovigilance, Marseille, France.

Guillaume Drablier (G)

Department of Pharmacology-Toxicology and Pharmacovigilance, University Hospital of Angers, Angers, France.

Hélène Geniaux (H)

Regional Pharmacovigilance Centre of Limoges, Department of Pharmacology-Toxicology and Pharmacovigilance, CHU Limoges, Limoges, France.

Laurence Lagarce (L)

Department of Pharmacology-Toxicology and Pharmacovigilance, University Hospital of Angers, Angers, France.

Marie-Laure Laroche (ML)

Regional Pharmacovigilance Centre of Limoges, Department of Pharmacology-Toxicology and Pharmacovigilance, CHU Limoges, Limoges, France.
UR 24134 (Vie Santé: Vieillissement, Fragilité, Prévention, e-Santé), IFR OMEGA HEALTH, Université de Limoges, Limoges, France.

Marie Briet (M)

Department of Pharmacology-Toxicology and Pharmacovigilance, University Hospital of Angers, Angers, France.
Université d'Angers, Angers, France.
MitoVasc Research Institute, UMR CNRS 6214 INSERM 1083, Angers, France.

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