Literature DB >> 33386650

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.

Daniel R Morales1,2, Tatiana Macfarlane1, Thomas M MacDonald1, Jesper Hallas2, Martin Thomsen Ernst2, Ron M C Herings3, Elisabeth Smits3, Jetty A Overbeek3, Lyn Mitchell1, Steven Morant1, Isla Mackenzie1, Alexander S F Doney1, Chris Robertson4, Marion Bennie5, Li Wei6, Lizzie Nicholson7, Carole Morris7, Robert W F Flynn1.   

Abstract

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 analysed using interrupted time series regression.
RESULTS: Hydroxyzine initiation in quarter one 2010 in Denmark, Scotland, England and the Netherlands per 100 000 was: 23.5, 91.5, 35.9 and 34.4 respectively. Regulatory action was associated with a significant: immediate fall in hydroxyzine initiation per 100 000 in England (-12.05, 95%CI -18.47 to -5.63) and Scotland (-19.01, 95%CI -26.99 to -11.02); change to a negative trend in hydroxyzine initiation per 100 000/quarter in England (-1.72, 95%CI -2.69 to -0.75) and Scotland (-2.38, 95%CI -3.32 to -1.44). Regulatory action was associated with a significant: immediate rise in hydroxyzine discontinuation per 100 000 in England (3850, 95%CI 440-7240). No consistent changes were observed in the Netherlands or Denmark. Regulatory action was associated with no switching to other antihistamines, benzodiazepines or antidepressants following hydroxyzine discontinuation in any country.
CONCLUSION: The 2015 EMA regulatory action was associated with heterogeneous impact with reductions in hydroxyzine initiation varying by country. There was limited impact on discontinuation with no strong evidence suggesting unintended consequences of major switching to other antihistamines, benzodiazepines or antidepressants.
© 2021 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd.

Entities:  

Keywords:  hydroxyzine; pharmacoepidemiology; pharmacovigilance; prescribing; regulation; time-series

Year:  2021        PMID: 33386650     DOI: 10.1002/pds.5191

Source DB:  PubMed          Journal:  Pharmacoepidemiol Drug Saf        ISSN: 1053-8569            Impact factor:   2.890


  2 in total

Review 1.  Efficacy and Safety of Non-brain Penetrating H1-Antihistamines for the Treatment of Allergic Diseases.

Authors:  Kazuhiko Yanai; Takeo Yoshikawa; Martin K Church
Journal:  Curr Top Behav Neurosci       Date:  2022

2.  Hydroxyzine Initiation Following Drug Safety Advisories on Cardiac Arrhythmias in the UK and Canada: A Longitudinal Cohort Study.

Authors:  Richard L Morrow; Barbara Mintzes; Patrick C Souverein; Christine E Hallgreen; Bilal Ahmed; Elizabeth E Roughead; Marie L De Bruin; Sarah Brøgger Kristiansen; Joel Lexchin; Anna Kemp-Casey; Ingrid Sketris; Dee Mangin; Sallie-Anne Pearson; Lorri Puil; Ruth Lopert; Lisa Bero; Danijela Gnjidic; Ameet Sarpatwari; Colin R Dormuth
Journal:  Drug Saf       Date:  2022-04-19       Impact factor: 5.228

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.