Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maria Das Dores Graciano Silva"'
Autor:
Renata Rezende de Menezes, Maria das Dores Graciano Silva, Antônio Luiz Pinho Ribeiro, Marcelo Martins Pinto Filho, Gláucia Helena Martinho, Luna Elisabeth Carvalho Ferreira, Maria Auxiliadora Parreiras Martins
Publikováno v:
Exploratory Research in Clinical and Social Pharmacy, Vol 3, Iss , Pp 100064- (2021)
Background: Causality assessment of adverse drug reactions (ADRs) is an essential approach in pharmacovigilance. The World Health Organization-Uppsala Monitoring Center (WHO-UMC) system has been considered one of the most adequate method for establis
Externí odkaz:
https://doaj.org/article/e2295487b0b64651915fd894765f3c8d
Publikováno v:
Infarma: Pharmaceutical Sciences, Vol 29, Iss 3, Pp 235-240 (2017)
O objetivo do presente trabalho foi avaliar a implantação de estratégias de busca ativa de reações adversas a medicamentos (RAM) com o auxílio de ferramentas informatizadas em um programa de farmacovigilância de um hospital privado de grande p
Externí odkaz:
https://doaj.org/article/987b30b4abec4c0ba16dbdbff9b9a697
Autor:
ERICA RIBEIRO COTRIM, JOSIANE MOREIRA DA COSTA, MARIA DAS DORES GRACIANO SILVA, ALINE DE OLIVEIRA MAGALHÃES MOURÃO
Publikováno v:
Revista Brasileira de Farmácia Hospitalar e Serviços de Saúde, Vol 4, Iss 2 (2019)
Objetivo: O presente estudo tem como objetivo identificar ajustes de doses de antimicrobianos em prescrições de pacientes internados em um hospital de ensino que apresentaram alterações em exames de mensuração do clearance de creatinina. Métod
Externí odkaz:
https://doaj.org/article/0efa5f2f56d4456f8cab154d3058c82e
Autor:
Maria das Dores Graciano Silva, Mário Borges Rosa, Bryony Dean Franklin, Adriano Max Moreira Reis, Leni Márcia Anchieta, Joaquim Antônio César Mota
Publikováno v:
Clinics, Vol 66, Iss 10, Pp 1691-1697 (2011)
OBJECTIVE: To analyze the prevalence and types of prescribing and dispensing errors occurring with high-alert medications and to propose preventive measures to avoid errors with these medications. INTRODUCTION: The prevalence of adverse events in hea
Externí odkaz:
https://doaj.org/article/e6255a24c8d84b88b65d6d7c0348a405
Publikováno v:
Biblioteca Digital de Teses e Dissertações da UFMGUniversidade Federal de Minas GeraisUFMG.
Medication is essential in healthcare. The errors that occur in the medication use process contribute to increase the potential risk of adverse events. The pediatric population is more susceptible to the drug-related adverse effects than adults. Beca
Externí odkaz:
http://hdl.handle.net/1843/ECJS-7W8MRJ
Autor:
Aline L. Andrade, Gisele C. Goulart, Maria das Dores Graciano Silva, Mariana Martins Gonzaga do Nascimento, Adriano Max Moreira Reis, Cristiane de Paula Rezende, Cássia L. Ferreira, Renata Rezende de Menezes, Letícia L. Maciel
Publikováno v:
Revista Brasileira de Farmácia Hospitalar e Serviços de Saúde, Vol 12, Iss 2 (2021)
Objective: To describe the identification of drugs with similar primary packaging available in a large teaching hospital. Methods: This is a descriptive study carried out using a multi-step approach. First, the small volume parenteral drugs and oral
Autor:
Antonio Luiz Pinho Ribeiro, Luna Elisabeth Carvalho Ferreira, Marcelo Martins Pinto Filho, Maria das Dores Graciano Silva, Maria Auxiliadora Parreiras Martins, Gláucia Helena Martinho, Renata Rezende de Menezes
Publikováno v:
Exploratory Research in Clinical and Social Pharmacy, Vol 3, Iss, Pp 100064-(2021)
Background Causality assessment of adverse drug reactions (ADRs) is an essential approach in pharmacovigilance. The World Health Organization-Uppsala Monitoring Center (WHO-UMC) system has been considered one of the most adequate method for establish
Autor:
Maria Auxiliadora Parreiras Martins, Luciana de Gouvêa Viana, João Antonio de Queiroz Oliveira, Renata Rezende de Menezes, Maria das Dores Graciano Silva, Luiz Guilherme Passaglia, Antonio Luiz Pinho Ribeiro, José Luiz Padilha da Silva
Publikováno v:
British Journal of Clinical Pharmacology. 84:2252-2259
Aims Adverse drug events (ADEs) can seriously compromise the safety and quality of care provided to hospitalized patients, requiring the adoption of accurate methods to monitor them. We sought to prospectively evaluate the accuracy of the triggers pr
Autor:
Maria das Dores Graciano Silva, Janaína Martins Bretas, Mariana Martins Gonzaga do Nascimento
Publikováno v:
Infarma: Pharmaceutical Sciences, Vol 29, Iss 3, Pp 235-240 (2017)
O objetivo do presente trabalho foi avaliar a implantação de estratégias de busca ativa de reações adversas a medicamentos (RAM) com o auxílio de ferramentas informatizadas em um programa de farmacovigilância de um hospital privado de grande p
Autor:
Maria Das Dores Graciano Silva, Maria Auxiliadora Parreiras Martins, Luciana de Gouvêa Viana, Luiz Guilherme Passaglia, Renata Rezende de Menezes, João Antonio de Queiroz Oliveira, Jose Luiz Padilha da Silva, Antonio Luiz Pinho Ribeiro
Publikováno v:
Repositório Institucional da UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Aims: Adverse drug events (ADEs) can seriously compromise the safety and quality of care provided to hospitalized patients, requiring the adoption of accurate methods to monitor them. We sought to prospectively evaluate the accuracy of the triggers p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e405f5cdc1b4c73543f25cd43e99cc82
https://europepmc.org/articles/PMC6138496/
https://europepmc.org/articles/PMC6138496/