Εμφάνιση απλής εγγραφής

dc.creatorMichel M.C., Gravas S.en
dc.date.accessioned2023-01-31T08:59:53Z
dc.date.available2023-01-31T08:59:53Z
dc.date.issued2016
dc.identifier10.1517/14740338.2016.1160055
dc.identifier.issn14740338
dc.identifier.urihttp://hdl.handle.net/11615/76619
dc.description.abstractIntroduction: We have reviewed the safety and tolerability of β3-adrenoceptor agonists, specifically mirabegron and solabegron, a newly emerging drug class for the treatment of the overactive bladder syndrome. We discuss them mechanistically in the context of expression and other preclinical data.Areas covered: Based on a systematic PubMed search, incidence of overall adverse events, hypertension, dry mouth, and constipation are comparable between mirabegron or solabegron and placebo. Hypertension is the most frequently observed adverse event, but has a similar incidence with mirabegron and placebo. Nevertheless, severe uncontrolled hypertension has become a contraindication for use of mirabegron based on observation of severe hypertension in association with mirabegron exposure. The overall incidence of adverse events is also similar between mirabegron and the muscarinic receptor antagonist tolterodine, but the incidence of dry mouth is much lower with mirabegron.Expert opinion: The high β3-adrenoceptor mRNA expression in the human ovaries is not associated with reproductive side effects. Generally, β3-adrenoceptors exhibit a rather restricted expression in human tissues, which may explain the overall good tolerability of agonists acting on this receptor. We propose that expression profiles and functional preclinical studies can be important tools in the prediction of adverse event profiles in first-in-class drugs. © 2016 Informa UK Limited, trading as Taylor & Francis Group.en
dc.language.isoenen
dc.sourceExpert Opinion on Drug Safetyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84961390353&doi=10.1517%2f14740338.2016.1160055&partnerID=40&md5=efe3f08bc981a8d726d456094282eba0
dc.subjectbeta 3 adrenergic receptor stimulating agenten
dc.subjectbeta adrenergic receptoren
dc.subjectmirabegronen
dc.subjectmuscarinic receptor blocking agenten
dc.subjectplaceboen
dc.subjectsolabegronen
dc.subjectsolifenacinen
dc.subjecttolterodineen
dc.subjecttranscriptomeen
dc.subjectacetanilide derivativeen
dc.subjectaniline derivativeen
dc.subjectbenzoic acid derivativeen
dc.subjectbeta 3 adrenergic receptoren
dc.subjectbeta 3 adrenergic receptor stimulating agenten
dc.subjectbiphenyl derivativeen
dc.subjectmirabegronen
dc.subjectsolabegronen
dc.subjectthiazole derivativeen
dc.subjectageden
dc.subjectconstipationen
dc.subjectdrug safetyen
dc.subjectdrug tolerabilityen
dc.subjectdrug withdrawalen
dc.subjectexperimental studyen
dc.subjectheadacheen
dc.subjecthumanen
dc.subjecthypertensionen
dc.subjectincidenceen
dc.subjectmeta analysis (topic)en
dc.subjectmulticenter study (topic)en
dc.subjectoveractive bladderen
dc.subjectphase 2 clinical trial (topic)en
dc.subjectphase 3 clinical trial (topic)en
dc.subjectprotein expressionen
dc.subjectprotein functionen
dc.subjectrandomized controlled trial (topic)en
dc.subjectReviewen
dc.subjectrhinopharyngitisen
dc.subjectsystematic review (topic)en
dc.subjecturinary tract infectionen
dc.subjecturine retentionen
dc.subjectxerostomiaen
dc.subjectanimalen
dc.subjectdrug effectsen
dc.subjectgene expression profilingen
dc.subjectgeneticsen
dc.subjectpathophysiologyen
dc.subjectUrinary Bladder, Overactiveen
dc.subjectAcetanilidesen
dc.subjectAdrenergic beta-3 Receptor Agonistsen
dc.subjectAniline Compoundsen
dc.subjectAnimalsen
dc.subjectBenzoatesen
dc.subjectBiphenyl Compoundsen
dc.subjectGene Expression Profilingen
dc.subjectHumansen
dc.subjectReceptors, Adrenergic, beta-3en
dc.subjectThiazolesen
dc.subjectUrinary Bladder, Overactiveen
dc.subjectTaylor and Francis Ltden
dc.titleSafety and tolerability of β 3-adrenoceptor agonists in the treatment of overactive bladder syndrome - Insight from transcriptosome and experimental studiesen
dc.typeotheren


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