RESUMO
Pharmacists now face the biggest challenges in the history of the profession: the use of digital technologies in pharmacy practice and education and the outbreak of coronavirus disease 2019. Worldwide, pharmaceutical care and pharmacy education via digital technologies have significantly increased and will be incorporated into patient care and the teaching-learning process, respectively. Thus, in this new era of pharmacy practice and education, curricula should promote the development of specific competencies for the cognitive, conscious, and effective use of digital tools. This requires the training of "disruptive" educators, who are capable of using teaching-learning methods adapted to the digital environment and educational processes suitable for stimulating the use of effective disruptive technologies. This commentary argues that the pharmacy profession can no longer wait for the slow integration of digital technologies into pharmacy practice and education.
Assuntos
COVID-19 , Educação em Farmácia , Assistência Farmacêutica , Farmácia , COVID-19/epidemiologia , Humanos , Farmacêuticos/psicologiaRESUMO
In Brazil, package inserts provide key information on pharmaceuticals. The current study analyzes the evolution of package inserts and the impact on this process by scientific research and development, globalization of information, and various health policies. The study began with a retrospective review of Brazilian health legislation until 1920, the year when the National Public Health Department was created. The analysis of documents on the evolution of health regulation in Brazil began with the Brazilian Pharmaceutical Collection-Health Rulings. The second stage of the study involved a search of standards and norms in VISALEGIS: Health Surveillance Legislation, Portal for Legislation from the National Congressional Information System and the Health Legislation System. Package inserts became an important vehicle for information in the country and underwent important regulatory changes in the latter half of the 20th century. From 1946 to 2006, the number of mandatory items increased, with more in-depth description. However, the standardization of information for medicines with the same active ingredient failed to materialize, despite its importance and the various legal initiatives in this direction.
Assuntos
Rotulagem de Medicamentos/história , Embalagem de Medicamentos/história , Legislação de Medicamentos/história , Brasil , Rotulagem de Medicamentos/legislação & jurisprudência , Embalagem de Medicamentos/legislação & jurisprudência , História do Século XX , História do Século XXI , Estudos RetrospectivosRESUMO
Desenvolve uma análise da evolução histórica da bula, procurando observar a influência do desenvolvimento científico, da globalização da informação e das diferentes políticas de saúde.(AU)
Assuntos
Bulas de Medicamentos , Legislação como Assunto , Vigilância Sanitária , Brasil , Política de Saúde , História da MedicinaRESUMO
No Brasil, a bula é usada como fonte de informação sobre medicamentos. O estudo desenvolveu uma análise de sua evolução histórica, procurando observar a influência do desenvolvimento científico, da globalização da informação e das diferentes políticas de saúde. Procedeu-se uma revisão retrospectiva da legislação sanitária brasileira até 1920, ano da instituição do Departamento Nacional de Saúde Pública. A análise documental sobre a evolução da regulamentação sanitária no Brasil se iniciou pela Coleção Farmácia Brasileira - Portarias Sanitárias. Na segunda etapa as normas foram pesquisadas nos portais: VISALEGIS - Legislação em Vigilância Sanitária, Portal de Legislação do Sistema de Informações do Congresso Nacional e Sistema de Legislação da Saúde - Saúde Legis. A bula tornou-se um importante veículo informativo no Brasil, passou por profundas transformações regulamentares na segunda metade do século XX. Entre 1946 e 2006 o número de itens obrigatórios aumentou e sua descrição aprofundou. Entretanto, a padronização da informação para os medicamentos com o mesmo princípio ativo não se efetivou, não obstante sua importância e apesar das diferentes iniciativas observadas nas normas legais.
In Brazil, package inserts provide key information on pharmaceuticals. The current study analyzes the evolution of package inserts and the impact on this process by scientific research and development, globalization of information, and various health policies. The study began with a retrospective review of Brazilian health legislation until 1920, the year when the National Public Health Department was created. The analysis of documents on the evolution of health regulation in Brazil began with the Brazilian Pharmaceutical Collection - Health Rulings. The second stage of the study involved a search of standards and norms in VISALEGIS: Health Surveillance Legislation, Portal for Legislation from the National Congressional Information System and the Health Legislation System. Package inserts became an important vehicle for information in the country and underwent important regulatory changes in the latter half of the 20th century. From 1946 to 2006, the number of mandatory items increased, with more in-depth description. However, the standardization of information for medicines with the same active ingredient failed to materialize, despite its importance and the various legal initiatives in this direction.