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Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine

PURPOSE: Flunarizine (fz) and cinnarizine (cz) have well-known extrapyramidal side effects (EPSEs). The aim of this study was to evaluate the incidence and occurrence time of cz- and fz-related EPSEs. METHOD: Patients who took fz or cz for more than 1 month were identified from the longitudinal heal...

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Autores principales: Jhang, Kai-Ming, Huang, Jing-Yang, Nfor, Oswald Ndi, Tung, Yu-Chun, Ku, Wen-Yuan, Lee, Chun-Te, Liaw, Yung-Po
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486934/
https://www.ncbi.nlm.nih.gov/pubmed/28386684
http://dx.doi.org/10.1007/s00228-017-2247-x
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author Jhang, Kai-Ming
Huang, Jing-Yang
Nfor, Oswald Ndi
Tung, Yu-Chun
Ku, Wen-Yuan
Lee, Chun-Te
Liaw, Yung-Po
author_facet Jhang, Kai-Ming
Huang, Jing-Yang
Nfor, Oswald Ndi
Tung, Yu-Chun
Ku, Wen-Yuan
Lee, Chun-Te
Liaw, Yung-Po
author_sort Jhang, Kai-Ming
collection PubMed
description PURPOSE: Flunarizine (fz) and cinnarizine (cz) have well-known extrapyramidal side effects (EPSEs). The aim of this study was to evaluate the incidence and occurrence time of cz- and fz-related EPSEs. METHOD: Patients who took fz or cz for more than 1 month were identified from the longitudinal health insurance database 2005 and 2010. Excluded were patients with any of the underlying diseases that may cause parkinsonism. Drug-induced EPSEs were defined as the new diagnosis of parkinsonism, dyskinesia, or secondary dystonia during drug use or within 3 months after discontinuing the medication. Age- and sex-matched controls were included in this study. RESULTS: Recruited for analysis were individuals who took fz (n = 26,133) and cz (n = 7186). The incidence rates of fz- and cz-induced EPSEs were 21.03 and 10.3 per 10,000 person-months, respectively. The hazard ratios (HRs) of EPSEs among fz and cz subjects were 8.03 (95% CI 6.55–9.84) and 3.41 (95% CI 2.50–4.63) when compared with the control individuals. Both fz and cz patients had a higher cumulative incidence of EPSEs than their control individuals (p < 0.001). Among subjects who took fz, the incidence of EPSEs was higher in the second than first year of drug exposure (45.59 vs 21.03 per 10,000 person-months). CONCLUSIONS: Fz and cz significantly increased the risk of parkinsonism, dyskinesia, and dystonia. Potential benefits and risks should be weighed when considering long-term use of these drugs especially fz. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00228-017-2247-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-54869342017-07-17 Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine Jhang, Kai-Ming Huang, Jing-Yang Nfor, Oswald Ndi Tung, Yu-Chun Ku, Wen-Yuan Lee, Chun-Te Liaw, Yung-Po Eur J Clin Pharmacol Pharmacoepidemiology and Prescription PURPOSE: Flunarizine (fz) and cinnarizine (cz) have well-known extrapyramidal side effects (EPSEs). The aim of this study was to evaluate the incidence and occurrence time of cz- and fz-related EPSEs. METHOD: Patients who took fz or cz for more than 1 month were identified from the longitudinal health insurance database 2005 and 2010. Excluded were patients with any of the underlying diseases that may cause parkinsonism. Drug-induced EPSEs were defined as the new diagnosis of parkinsonism, dyskinesia, or secondary dystonia during drug use or within 3 months after discontinuing the medication. Age- and sex-matched controls were included in this study. RESULTS: Recruited for analysis were individuals who took fz (n = 26,133) and cz (n = 7186). The incidence rates of fz- and cz-induced EPSEs were 21.03 and 10.3 per 10,000 person-months, respectively. The hazard ratios (HRs) of EPSEs among fz and cz subjects were 8.03 (95% CI 6.55–9.84) and 3.41 (95% CI 2.50–4.63) when compared with the control individuals. Both fz and cz patients had a higher cumulative incidence of EPSEs than their control individuals (p < 0.001). Among subjects who took fz, the incidence of EPSEs was higher in the second than first year of drug exposure (45.59 vs 21.03 per 10,000 person-months). CONCLUSIONS: Fz and cz significantly increased the risk of parkinsonism, dyskinesia, and dystonia. Potential benefits and risks should be weighed when considering long-term use of these drugs especially fz. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00228-017-2247-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-04-06 2017 /pmc/articles/PMC5486934/ /pubmed/28386684 http://dx.doi.org/10.1007/s00228-017-2247-x Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Pharmacoepidemiology and Prescription
Jhang, Kai-Ming
Huang, Jing-Yang
Nfor, Oswald Ndi
Tung, Yu-Chun
Ku, Wen-Yuan
Lee, Chun-Te
Liaw, Yung-Po
Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine
title Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine
title_full Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine
title_fullStr Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine
title_full_unstemmed Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine
title_short Extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine
title_sort extrapyramidal symptoms after exposure to calcium channel blocker-flunarizine or cinnarizine
topic Pharmacoepidemiology and Prescription
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486934/
https://www.ncbi.nlm.nih.gov/pubmed/28386684
http://dx.doi.org/10.1007/s00228-017-2247-x
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