RESUMO
BACKGROUND: There are safety concerns with using unlicensed medicines across countries including Brazil. Consequently this needs to be evaluated and concerns address if pertinent. AIM: Investigate such purchases by the Brazilian Federal Government from 2004 to 2013. METHODS: Procurement data from a public-access databank that contains procurement information of the Brazilian Federal Government. Each procured item was cross-referenced to its active drug approval status in the Brazilian National Register (DOU). Exploratory analysis and trend measures were performed for the variables for mapping and characterizing the purchases of non-market approved drugs. RESULTS: 614 (0.14%) purchases in ten years corresponding to 64 unlicensed medicines - some of which had orphan drug status - and 48 different active substances; with a growing trend in recent years. Medicines in 51% of purchases were procured before obtaining marketing approval - with eventual refusals occurring in 17.8% and cancellation due to lack of efficacy and/or safety concerns in 1.1%. Health litigation accounted for 81.9% of purchases and growing in recent years. CONCLUSIONS: Overall a low rate of unlicensed medicine use. However there are concerns given the current regulations in Brazil and the recent increase in the use of unlicensed medicines with increased litigation.
Assuntos
Comércio/legislação & jurisprudência , Aprovação de Drogas , Governo Federal , Preparações Farmacêuticas/economia , Brasil , Comércio/estatística & dados numéricos , Bases de Dados Factuais , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/epidemiologia , Humanos , Produção de Droga sem Interesse Comercial/economia , Produção de Droga sem Interesse Comercial/legislação & jurisprudênciaRESUMO
The demographic transition in Brazil has led to substantial aging of the population and an increased prevalence of age-related diseases such as dementia and Alzheimer's Disease (AD). The Brazilian Ministry of Health finances AD medication and, since 2002, a Clinical Protocol and Therapeutic Guidelines (PCDT) for this condition have been made available. This study investigated the acquisition of medication for AD in the Integrated System of Administration of General Services (SIASG) database. A profile of purchases, expenditures and prices from 2008 to 2013 was prepared. All medication and forms of treatment of AD were investigated, including those not contained in the PCDT protocol. Unit prices were deflated to December 2013 by the IPCA (Brazilian Pricing Index). More than 47 million units of medication for AD were acquired and expenditures attained 90.1 million Brazilian reals. The purchase of the various administration routes of rivastigmine were in the forefront. Medication not listed in the protocol represented 3% of expenditures and purchases resulting from health litigation were negligible. Over the period, a reduction of corrected weighted average prices of PCDT and non-PCDT medication was observed.
Assuntos
Doença de Alzheimer/tratamento farmacológico , Gastos em Saúde , Idoso , Doença de Alzheimer/economia , Brasil , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fármacos Neuroprotetores/uso terapêutico , Dinâmica Populacional , Prevalência , Rivastigmina/uso terapêuticoRESUMO
Resumo O processo de transição demográfica brasileiro tem levado a substancial envelhecimento populacional e a aumento na prevalência de síndromes demenciais, entre as quais se destaca a Doença de Alzheimer (DA). Desde 2002, o tratamento farmacológico da doença possui Protocolo Clínico e Diretrizes Terapêuticas (PCDT) específico e os medicamentos recomendados são de financiamento pelo Ministério da Saúde. O estudo investigou a aquisição dos medicamentos utilizados no tratamento da DA a partir do Sistema Integrado de Administração de Serviços Gerais, traçando um perfil evolutivo das quantidades adquiridas, gastos e preços praticados no período de 2008 a 2013. Foram analisados os dados relativos a todas as apresentações adquiridas, inclusive as ausentes do PCDT. Os preços unitários foram deflacionados para dezembro/2013, pelo IPCA. Foram compradas mais de 47 milhões de unidades e gastos R$ 90,1 milhões com medicamentos para DA. Destaca-se nos gastos a participação da rivastigmina em suas diversas apresentações. Medicamentos não indicados pelo PCDT representaram 3% dos gastos, com percentuais de compra associados ao atendimento de ações judiciais pouco expressivos. No período, ocorreu redução dos preços médios ponderados corrigidos de todos os medicamentos, mesmo dos não presentes no PCDT.
Abstract The demographic transition in Brazil has led to substantial aging of the population and an increased prevalence of age-related diseases such as dementia and Alzheimer’s Disease (AD). The Brazilian Ministry of Health finances AD medication and, since 2002, a Clinical Protocol and Therapeutic Guidelines (PCDT) for this condition have been made available. This study investigated the acquisition of medication for AD in the Integrated System of Administration of General Services (SIASG) database. A profile of purchases, expenditures and prices from 2008 to 2013 was prepared. All medication and forms of treatment of AD were investigated, including those not contained in the PCDT protocol. Unit prices were deflated to December 2013 by the IPCA (Brazilian Pricing Index). More than 47 million units of medication for AD were acquired and expenditures attained 90.1 million Brazilian reals. The purchase of the various administration routes of rivastigmine were in the forefront. Medication not listed in the protocol represented 3% of expenditures and purchases resulting from health litigation were negligible. Over the period, a reduction of corrected weighted average prices of PCDT and non-PCDT medication was observed.
Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Idoso , Gastos em Saúde , Doença de Alzheimer/tratamento farmacológico , Brasil , Dinâmica Populacional , Prevalência , Fármacos Neuroprotetores/uso terapêutico , Doença de Alzheimer/economia , Rivastigmina/uso terapêuticoRESUMO
Esta nota tem por objetivo discutir alguns aspectos relacionados ao fornecimento de equipamentos de proteção individual (EPIs) e outros materiais necessários à minimização do risco de contágio pelo coronavírus por trabalhadores em estabelecimentos de saúde, especialmente o aumento de preços desses produtos em virtude do crescimento da demanda por causa da pandemia de Covid-19.