{"id":19798,"date":"2022-05-10T20:28:11","date_gmt":"2022-05-10T23:28:11","guid":{"rendered":"https:\/\/portaldasaudenews.com\/?p=19798"},"modified":"2022-05-10T20:28:11","modified_gmt":"2022-05-10T23:28:11","slug":"anvisa-aprova-uso-de-remedio-derivado-de-cannabis-medicinal","status":"publish","type":"post","link":"https:\/\/portaldasaudenews.com\/?p=19798","title":{"rendered":"Anvisa aprova uso de rem\u00e9dio derivado de cannabis medicinal"},"content":{"rendered":"<p>&nbsp;<\/p>\n<p><span style=\"font-weight: 400;\">Pela primeira vez na hist\u00f3ria, a Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (Anvisa) aprovou o uso e comercializa\u00e7\u00e3o no Brasil de um produto derivado de cannabis medicinal com concentra\u00e7\u00e3o de THC acima de 0,2%. O Extrato de\u202fCannabis sativa\u202fGreenCare (160,32 mg\/ml) \u00e9 um fitoter\u00e1pico e teve autoriza\u00e7\u00e3o publicada no Di\u00e1rio Oficial da Uni\u00e3o (DOU) de segunda-feira, 9.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Este \u00e9 o 16\u00ba produto \u00e0 base de cannabis aprovado pela Anvisa, mas o primeiro acima de 0,2% de concentra\u00e7\u00e3o de THC. Os outros produtos tem THC residual, ou seja, n\u00e3o ultrapassa esse limite. A nova regulamenta\u00e7\u00e3o autoriza um marcador ativo, com sua fun\u00e7\u00e3o prevista.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u201cA diferen\u00e7a nas concentra\u00e7\u00f5es \u00e9 importante, pois possibilita alternativas terap\u00eauticas diferenciadas para o atendimento, considerando a diversidade de indica\u00e7\u00f5es e perfis de pacientes\u201d, explica o CEO da GreenCare, Martim Prado Mattos.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">O fitoter\u00e1pico ser\u00e1 oferecido em forma de solu\u00e7\u00e3o, com 20 mg\/ml de canabidiol (CBD) e cerca de 0,2% de tetrahidrocanabinol (THC).A expectativa da GreenCare \u00e9 que o produto fabricado na Col\u00f4mbia chegue ao Brasil dentro de seis meses.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">A Anvisa pondera que o uso deve ser indicado pelo m\u00e9dico que atende o paciente, com avalia\u00e7\u00e3o individual de cada caso.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><span style=\"font-weight: 400;\">*Via A Tarde<\/span><\/p>\n<p><span style=\"font-weight: 400;\">*Foto: iStock\/Getty Images<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&nbsp; Pela primeira vez na hist\u00f3ria, a Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (Anvisa) aprovou o<\/p>\n","protected":false},"author":1,"featured_media":7570,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false,"_monsterinsights_skip_tracking":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[48,28],"tags":[],"class_list":["post-19798","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-brasil","category-saude-brasil"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - 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