Impact of EMA regulatory label changes on systemic diclofenac initiation, discontinuation, and switching to other pain medicines in Scotland, England, Denmark, and The Netherlands.
Analgesics
/ therapeutic use
Analgesics, Non-Narcotic
/ therapeutic use
Analgesics, Opioid
/ therapeutic use
Anti-Inflammatory Agents, Non-Steroidal
/ therapeutic use
Chronic Pain
/ drug therapy
Denmark
Diclofenac
/ therapeutic use
Drug Labeling
England
Humans
Netherlands
Practice Patterns, Physicians'
/ statistics & numerical data
Scotland
/ epidemiology
diclofenac
impact
pharmacoepidemiology
pharmacovigilance
prescribing
regulation
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
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
296-305Informations de copyright
© 2020 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd.
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