Impact of EMA regulatory label changes on hydroxyzine initiation, discontinuation and switching to other medicines in Denmark, Scotland, England and the Netherlands: An interrupted time series regression analysis

BACKGROUND: Hydroxyzine is indicated for the management of anxiety, skin and sleep disorders. In 2015, the European Medicines Agency (EMA) concluded that hydroxyzine was pro-arrhythmogenic and changes to the product information were implemented in Europe. This study aimed to evaluate their impact in Denmark, Scotland, England and the Netherlands. METHOD: Quarterly time series analyses measuring hydroxyzine initiation, discontinuation, and switching to other antihistamines, benzodiazepines and antidepressants in Denmark, England, Scotland and the Netherlands from 2009 to 2018. Data were analyse... Mehr ...

Verfasser: Morales, DR
Macfarlane, T
MacDonald, TM
Hallas, J
Ernst, MT
Herings, RMC
Smits, E
Overbeek, JA
Mitchell, L
Morant, S
Mackenzie, I
Doney, ASF
Robertson, C
Bennie, M
Wei, L
Nicholson, L
Morris, C
Flynn, RWF
Dokumenttyp: Artikel
Erscheinungsdatum: 2021
Schlagwörter: hydroxyzine / pharmacoepidemiology / pharmacovigilance / prescribing / regulation / time-series
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29186115
Datenquelle: BASE; Originalkatalog
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Link(s) : https://discovery.ucl.ac.uk/id/eprint/10119605/1/Wei_LW_pds.5191.pdf