Impact of EMA regulatory label changes on systemic diclofenac initiation, discontinuation, and switching to other pain medicines in Scotland, England, Denmark, and The Netherlands.


Journal

Pharmacoepidemiology and drug safety
ISSN: 1099-1557
Titre abrégé: Pharmacoepidemiol Drug Saf
Pays: England
ID NLM: 9208369

Informations de publication

Date de publication:
03 2020
Historique:
received: 15 07 2019
revised: 25 11 2019
accepted: 13 12 2019
pubmed: 4 1 2020
medline: 19 3 2021
entrez: 4 1 2020
Statut: ppublish

Résumé

In June 2013 a European Medicines Agency referral procedure concluded that diclofenac was associated with an elevated risk of acute cardiovascular events and contraindications, warnings, and changes to the product information were implemented across the European Union. This study measured the impact of the regulatory action on the prescribing of systemic diclofenac in Denmark, The Netherlands, England, and Scotland. Quarterly time series analyses measuring diclofenac prescription initiation, discontinuation and switching to other systemic nonsteroidal anti-inflammatory (NSAIDs), topical NSAIDs, paracetamol, opioids, and other chronic pain medication in those who discontinued diclofenac. Absolute effects were estimated using interrupted time series regression. Overall, diclofenac prescription initiations fell during the observation periods of all countries. Compared with Denmark where there appeared to be a more limited effect, the regulatory action was associated with significant immediate reductions in diclofenac initiation in The Netherlands (-0.42%, 95% CI, -0.66% to -0.18%), England (-0.09%, 95% CI, -0.11% to -0.08%), and Scotland (-0.67%, 95% CI, -0.79% to -0.55%); and falling trends in diclofenac initiation in the Netherlands (-0.03%, 95% CI, -0.06% to -0.01% per quarter) and Scotland (-0.04%, 95% CI, -0.05% to -0.02% per quarter). There was no significant impact on diclofenac discontinuation in any country. The regulatory action was associated with modest differences in switching to other pain medicines following diclofenac discontinuation. The regulatory action was associated with significant reductions in overall diclofenac initiation which varied by country and type of exposure. There was no impact on discontinuation and variable impact on switching.

Identifiants

pubmed: 31899936
doi: 10.1002/pds.4955
pmc: PMC7079064
doi:

Substances chimiques

Analgesics 0
Analgesics, Non-Narcotic 0
Analgesics, Opioid 0
Anti-Inflammatory Agents, Non-Steroidal 0
Diclofenac 144O8QL0L1

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

296-305

Informations de copyright

© 2020 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd.

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Auteurs

Daniel R Morales (DR)

MEMO Research, University of Dundee, UK.

Steve V Morant (SV)

MEMO Research, University of Dundee, UK.

Thomas M MacDonald (TM)

MEMO Research, University of Dundee, UK.

Isla S Mackenzie (IS)

MEMO Research, University of Dundee, UK.

Alexander S F Doney (ASF)

MEMO Research, University of Dundee, UK.

Lyn Mitchell (L)

MEMO Research, University of Dundee, UK.

Marion Bennie (M)

Strathclyde Onstitute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK.

Chris Robertson (C)

Dept of Mathematics and Statistics, University of Strathclyde, Glasgow, UK.

Jesper Hallas (J)

Dept of Clinical Pharmacology and Pharmacy, University of Southern Denmark, Odense, Denmark.

Anton Pottegard (A)

Dept of Clinical Pharmacology and Pharmacy, University of Southern Denmark, Odense, Denmark.

Martin Thomsen Ernst (MT)

Dept of Clinical Pharmacology and Pharmacy, University of Southern Denmark, Odense, Denmark.

Li Wei (L)

School of Pharmacy, University College London, London, UK.

Lizzie Nicholson (L)

Electronic Data Research and Innovation Service, NHS National Services Scotland, Edinburgh, UK.

Carole Morris (C)

Electronic Data Research and Innovation Service, NHS National Services Scotland, Edinburgh, UK.

Ron M C Herings (RMC)

PHARMO Institute for Drug Outcomes Research, Utrecht, The Netherlands.

Jetty A Overbeek (JA)

PHARMO Institute for Drug Outcomes Research, Utrecht, The Netherlands.

Elisabeth Smits (E)

PHARMO Institute for Drug Outcomes Research, Utrecht, The Netherlands.

Robert W V Flynn (RWV)

MEMO Research, University of Dundee, UK.

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Classifications MeSH