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Analysis of extemporaneous oral liquid from commercially available drugs in hospital

dc.contributor.authorBenzi, Jhohann Richard de Lima
dc.contributor.authorMastroianni, Patrícia De Carvalho [UNESP]
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:30:30Z
dc.date.available2018-12-11T17:30:30Z
dc.date.issued2016-07-01
dc.description.abstractThe objective of this study was to identify drugs that received dose adjustments (DA) and pharmaceutical alternatives (PA) that avoid DA, and calculate the economic percentage of this replacement. A descriptive, observational and cross-sectional study was performed in a second level hospital. The pharmacy and nursing services was accompanied to identify the drugs that received DA and the compounding techniques. After identifying all the drugs that received DA, was identified in the Brazilian market the corresponding pharmaceutical alternative, with the Drugs Price List of Brazilian Health Regulatory Agency. For those drugs that was not available any PA, was performed a research of studies that describe compounding techniques in international scientific databases. Was identify 88 drugs that received DA, and these, 50 do not have any PA. Were identified compounding techniques to 40 drugs. Although any drug has your own particularity of compounding, the compounding techniques can be grouped in five categories. The standardization of 29 drugs can reduce in 28% the DA procedure and cost saving of 34,85%/month. We can conclude that every three drugs prescribed, one received DA and every three DA, one can be avoided by the selection of 29 PA, saving cost as well. The use and standardization of five techniques would attend the pharmaceutics recommendations for better dissolution, bioavailability and patient safety.en
dc.description.affiliationFaculdade de Ciências Farmacêuticas de Ribeirão Preto USP Universidade de São Paulo
dc.description.affiliationFaculdade de Ciências Farmacêuticas UNESP Universidade Estadual Paulista
dc.description.affiliationUnespFaculdade de Ciências Farmacêuticas UNESP Universidade Estadual Paulista
dc.format.extent517-525
dc.identifierhttp://dx.doi.org/10.1590/s1984-82502016000300017
dc.identifier.citationBrazilian Journal of Pharmaceutical Sciences, v. 52, n. 3, p. 517-525, 2016.
dc.identifier.doi10.1590/s1984-82502016000300017
dc.identifier.fileS1984-82502016000300517.pdf
dc.identifier.issn2175-9790
dc.identifier.issn1984-8250
dc.identifier.lattes4160558780902988
dc.identifier.orcid0000-0001-8467-7278
dc.identifier.scieloS1984-82502016000300517
dc.identifier.scopus2-s2.0-85006014896
dc.identifier.urihttp://hdl.handle.net/11449/178474
dc.language.isoeng
dc.relation.ispartofBrazilian Journal of Pharmaceutical Sciences
dc.relation.ispartofsjr0,214
dc.relation.ispartofsjr0,214
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectDrugs/descritive study/off-label use
dc.subjectPatient safety
dc.subjectPharmaceutical preparations/hospitals
dc.subjectPharmacoeconomics
dc.titleAnalysis of extemporaneous oral liquid from commercially available drugs in hospitalen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.author.lattes4160558780902988[2]
unesp.author.orcid0000-0001-8467-7278[2]
unesp.departmentFármacos e Medicamentos - FCFpt

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