Revista de Direito Sanitário (Mar 2016)

Editorial

  • DALLARI, Sueli Gandolfi

DOI
https://doi.org/10.11606/issn.2316-9044.v17i1p7-13
Journal volume & issue
Vol. 17, no. 1
pp. 7 – 13

Abstract

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One more time, I have to start our conversation by drawing attention to serious risks that are being imposed on the health and the health law in Brazil today. Unfortunately we live in a time of distrust on institutions, a scenario where profiteers of all kinds flourish. This is what is happening now with the health legislation in the Brazilian Congress. On April 13, 2016, Brazilian Federal Law n. 13269 was enacted, without vetoes, authorizing patients with cancer to be cared with the synthetic substance phosphoethanolamine. And on April 20, 2016, the Brazilian Federal Senate approved the production and sale of weight-loss drugs containing sibutramine, amfepramone, fenproporex and mazindol. In both cases, the Brazilian National Health Surveillance Agency (Anvisa) ‒ responsible for the registration of medicines, ensuring their quality, safety and efficacy ‒ had spoken unfavorably.

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