Biologicals and biosimilars: safety issues in Europe

• Autor(a) principal: Portela, Maria da Conceição
• Data de Publicação: 2017
• Outros Autores: Sinogas, Carlos, Almeida, Fernando, Baptista-Leite, Ricardo, Castro-Caldas, Alexandre
• Tipo de documento: Artigo
• Idioma: por
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10174/27226; https://doi.org/http://dx.doi.org/10.1080/14712598.2017.1330409

ABSTRACT Introduction: Medicinal products of a biological origin are approved by the EMA at a centralized level. However, there is no harmonization about their use in Europe. The current regulation referring to the safety of biological medicinal products and biosimilars in Europe has been identified. The safety associated with medicinal products of a biological origin is assured by the pharmacovigilance system, which has evolved, but doesn’t yet incorporate all of the specific information from this market segment, namely that related to the identification of drugs, and its use – including the prescription and dispensing, given the possibility of interchangeability and substitution. The terminology, information systems and traceability systems aren’t entirely appropriate to ensure the safety requirements for therapy with medicinal products of a biological origin. Areas covered: This article aims to identify the prescription and dispensing profiles of reference biological medicines and biosimilars in the EU, and the determinants that support their safe use. Expert opinion: The European pharmacovigilance system must evolve to ensure the safety along all of the biologicals’ therapeutic cycle. It must consider the safety for each of the medicines in addition to their safety pattern related to the eventual switching procedure.