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Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions

BACKGROUND: Bilastine, a non-sedating H(1)-antihistamine, is indicated to treat the symptoms of allergic disorders (e.g. rhinoconjunctivitis and urticaria) in adults and adolescents and, more recently, in children. Following its marketing approval, many questions regarding the ideal use of bilastine...

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Autores principales: Leceta, Amalia, García, Aintzane, Sologuren, Ander, Campo, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioExcel Publishing Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366504/
https://www.ncbi.nlm.nih.gov/pubmed/34457015
http://dx.doi.org/10.7573/dic.2021-5-1
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author Leceta, Amalia
García, Aintzane
Sologuren, Ander
Campo, Cristina
author_facet Leceta, Amalia
García, Aintzane
Sologuren, Ander
Campo, Cristina
author_sort Leceta, Amalia
collection PubMed
description BACKGROUND: Bilastine, a non-sedating H(1)-antihistamine, is indicated to treat the symptoms of allergic disorders (e.g. rhinoconjunctivitis and urticaria) in adults and adolescents and, more recently, in children. Following its marketing approval, many questions regarding the ideal use of bilastine in various clinical practice situations have been received by the Medical Information Department (MID) of Faes Farma Spain. This article is an update of a previous review, with a focus on recent clinical information on the use of bilastine in paediatric and other populations. METHODS: Results of recent clinical studies in paediatric and other populations as well as questions received and responses provided by the Faes Farma MID. RESULTS: The information regarding the use of bilastine in paediatric patients is the most relevant aspect of this updated review. The stepwise approval of the paediatric formulations in various countries started with the European Medicines Agency approval in 2017 in accordance with a 2009 Paediatric Investigation Plan, followed by approval in other countries. The queries that are most commonly received by the Faes Farma MID include the potential for drug interactions involving bilastine and other frequently used drugs, and the use of bilastine in special populations or to treat specific symptoms related to allergic conditions. As the concomitant use of many medications is not permitted during clinical trials, the advice provided regarding the concomitant use of other medications with bilastine considers the pharmacological properties of both the drug in question and bilastine, as well as expert opinion. Likewise, advice regarding the use of bilastine in special populations (e.g. patients with renal impairment, obesity, lactose intolerance, and elderly or pregnant individuals) or to treat specific symptoms (e.g. treatment-resistant urticaria, pruritus or BASCULE syndrome) considers the best evidence from a variety of sources, including clinical studies, real-world experience, guideline recommendations and expert opinion. CONCLUSION: This updated review provides current data regarding the best use of bilastine in specific situations and patients and identifies areas in which further knowledge is required. Although decisions regarding the use of bilastine may be aided by expert opinion that relies on knowledge of the underlying science, additional research and evidence are required to answer certain queries regarding the use of bilastine.
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spelling pubmed-83665042021-08-27 Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions Leceta, Amalia García, Aintzane Sologuren, Ander Campo, Cristina Drugs Context Review BACKGROUND: Bilastine, a non-sedating H(1)-antihistamine, is indicated to treat the symptoms of allergic disorders (e.g. rhinoconjunctivitis and urticaria) in adults and adolescents and, more recently, in children. Following its marketing approval, many questions regarding the ideal use of bilastine in various clinical practice situations have been received by the Medical Information Department (MID) of Faes Farma Spain. This article is an update of a previous review, with a focus on recent clinical information on the use of bilastine in paediatric and other populations. METHODS: Results of recent clinical studies in paediatric and other populations as well as questions received and responses provided by the Faes Farma MID. RESULTS: The information regarding the use of bilastine in paediatric patients is the most relevant aspect of this updated review. The stepwise approval of the paediatric formulations in various countries started with the European Medicines Agency approval in 2017 in accordance with a 2009 Paediatric Investigation Plan, followed by approval in other countries. The queries that are most commonly received by the Faes Farma MID include the potential for drug interactions involving bilastine and other frequently used drugs, and the use of bilastine in special populations or to treat specific symptoms related to allergic conditions. As the concomitant use of many medications is not permitted during clinical trials, the advice provided regarding the concomitant use of other medications with bilastine considers the pharmacological properties of both the drug in question and bilastine, as well as expert opinion. Likewise, advice regarding the use of bilastine in special populations (e.g. patients with renal impairment, obesity, lactose intolerance, and elderly or pregnant individuals) or to treat specific symptoms (e.g. treatment-resistant urticaria, pruritus or BASCULE syndrome) considers the best evidence from a variety of sources, including clinical studies, real-world experience, guideline recommendations and expert opinion. CONCLUSION: This updated review provides current data regarding the best use of bilastine in specific situations and patients and identifies areas in which further knowledge is required. Although decisions regarding the use of bilastine may be aided by expert opinion that relies on knowledge of the underlying science, additional research and evidence are required to answer certain queries regarding the use of bilastine. BioExcel Publishing Ltd 2021-08-10 /pmc/articles/PMC8366504/ /pubmed/34457015 http://dx.doi.org/10.7573/dic.2021-5-1 Text en Copyright © 2021 Leceta A, García A, Sologuren A, Campo C. https://creativecommons.org/licenses/by-nc-nd/4.0/Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0 which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified later. No commercial use without permission.
spellingShingle Review
Leceta, Amalia
García, Aintzane
Sologuren, Ander
Campo, Cristina
Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions
title Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions
title_full Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions
title_fullStr Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions
title_full_unstemmed Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions
title_short Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions
title_sort bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366504/
https://www.ncbi.nlm.nih.gov/pubmed/34457015
http://dx.doi.org/10.7573/dic.2021-5-1
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