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Miracle drug: Brazil approves never-tested cancer medicine.
Kuchenbecker, Ricardo S; Mota, Daniel M.
Afiliación
  • Kuchenbecker RS; Graduate Studies in Epidemiology, Instituto de Avaliação de Tecnologia em Saúde (IATS), Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
  • Mota DM; Graduate Studies in Epidemiology, Instituto de Avaliação de Tecnologia em Saúde (IATS), Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
J Oncol Pharm Pract ; 23(5): 399-400, 2017 Jul.
Article en En | MEDLINE | ID: mdl-27566738
Background Brazil recently approved synthetic phosphoetanolamine, a popularly dubbed 'cancer pill', a substance that has been shown to kill cancer cells in lab animal models but was not yet formally accessed in humans, and thus despite the existence of any evidence of its efficacy and safety. Methods The authors describe the recent decision of Brazil to aprove phosphoetanolamine in the context of growing 'judicialization' to promote access to medicines and thus reinforcing a growing sense of legal uncertainty. Results The approval of phosphoetanolamine despite the existence of any evidence of its efficacy and safety represents to the authors one of the saddest and surrealistic episodes in Brazil's recent public health history. Brazil's current economic crisis is fueling the 'judicialization' to promote access to medicines and thus reinforcing a growing sense of legal uncertainty in the context of rising economic constrains and a progressive failing state. The authors state that the Phosphoetanolamine's approval bill violates current legal prohibition of commercialisation of drugs without the Brazilian national drug regulatory agency's approval and thus may represent a potential menace to Brazil's pharmacogovernance and the country's governance to health technology assessment at the Brazilian national health systems. Conclusion Phosphoetanolamine's approval illustrates that the combination of flawed decision making, economic crisis and political interference may threaten weak governance mechanisms for drug regulation and health technology assessment and thus representing an extra burden in the sustainability of universal access-based national health systems.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aprobación de Drogas / Etanolaminas / Antineoplásicos Tipo de estudio: Health_technology_assessment / Prognostic_studies Límite: Humans País/Región como asunto: America do sul / Brasil Idioma: En Revista: J Oncol Pharm Pract Asunto de la revista: FARMACIA Año: 2017 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aprobación de Drogas / Etanolaminas / Antineoplásicos Tipo de estudio: Health_technology_assessment / Prognostic_studies Límite: Humans País/Región como asunto: America do sul / Brasil Idioma: En Revista: J Oncol Pharm Pract Asunto de la revista: FARMACIA Año: 2017 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Reino Unido