{"id":12601,"date":"2021-08-11T15:41:27","date_gmt":"2021-08-11T18:41:27","guid":{"rendered":"https:\/\/redenoticiaz.com.br\/litoralsp\/2021\/08\/11\/anvisa-libera-uso-emergencial-de-anticorpo-para-tratamento-contra-covid-19"},"modified":"2021-08-11T15:44:27","modified_gmt":"2021-08-11T18:44:27","slug":"anvisa-libera-uso-emergencial-de-anticorpo-para-tratamento-contra-covid-19","status":"publish","type":"post","link":"https:\/\/redenoticiaz.com.br\/litoralsp\/2021\/08\/11\/anvisa-libera-uso-emergencial-de-anticorpo-para-tratamento-contra-covid-19","title":{"rendered":"Anvisa libera uso emergencial de anticorpo para tratamento contra Covid-19"},"content":{"rendered":"<p>Nesta quarta-feira (11) a Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (<a href=\"https:\/\/www.gov.br\/anvisa\/pt-br\">Anvisa<\/a>) autorizou o uso emergencial de um medicamento contra a Covid-19. \u00c9 o\u00a0<strong>Regkirona<\/strong><strong>\u00a0(regdanvimabe),\u00a0<\/strong>um anticorpo monoclonal. Antes dele, o \u00f3rg\u00e3o j\u00e1 tinha liberado o uso dos medicamentos Regn-CoV2, desenvolvido pela farmac\u00eautica Roche, e da associa\u00e7\u00e3o dos anticorpos banlanivimabe e etesevimabe, produzido pela farmac\u00eautica pela Eli Lilly. Al\u00e9m disso, autorizou o registro do antiviral experimental remdesivir.<\/p>\n<p>Sobre o Regkirona, \u00e9 um mecanismo que auxilia na reprodu\u00e7\u00e3o de anticorpos que ajudam no combate a alguma doen\u00e7a espec\u00edfica. Contudo,\u00a0<span class=\"highlight highlighted\">o uso do medicamento n\u00e3o previne a doen\u00e7a. A diretora da Anvisa, Meiruze Freitas, tamb\u00e9m relatora falou da libera\u00e7\u00e3o do rem\u00e9dio, mas volta a pedir que a popula\u00e7\u00e3o se vacine contra a Covid-19.<\/span><\/p>\n<div class=\"mc-column content-text active-extra-styles\" data-block-type=\"raw\" data-block-weight=\"34\" data-block-id=\"5\">\n<blockquote class=\"content-blockquote theme-border-color-primary-before\"><p><span class=\"highlight highlighted\">&#8221;O ato de se vacinar \u00e9 uma prote\u00e7\u00e3o individual e coletiva<\/span>. Com a vacina\u00e7\u00e3o \u00e9 que vamos combater a pandemia e reduzir os riscos de cepas que possam driblar as vacinas&#8221;, afirmou a relatora.<\/p><\/blockquote>\n<\/div>\n<div class=\"mc-column content-text active-extra-styles \" data-block-type=\"unstyled\" data-block-weight=\"34\" data-block-id=\"6\">\n<p class=\"content-text__container \" data-track-category=\"Link no Texto\" data-track-links=\"\">Em seu parecer, Freitas explicou que\u00a0<span class=\"highlight highlighted\">o medicamento n\u00e3o previne a doen\u00e7a<\/span>, apenas ajuda no tratamento de pessoas j\u00e1 contaminadas que apresentam casos leves e moderados e que n\u00e3o necessitam de suplementa\u00e7\u00e3o de oxig\u00eanio.<\/p>\n<h3 data-track-category=\"Link no Texto\">Conhe\u00e7a mais sobre o medicamento<\/h3>\n<div class=\"mc-column content-text active-extra-styles\" data-block-type=\"raw\" data-block-weight=\"103\" data-block-id=\"11\">\n<ul class=\"content-unordered-list\">\n<li>Anticorpo monoclonal \u00fanico que t\u00eam como alvo a prote\u00edna espicular S do SARS-CoV-2;<\/li>\n<li>O tratamento \u00e9 indicado para adultos que n\u00e3o necessitam de suplementa\u00e7\u00e3o de oxig\u00eanio;<\/li>\n<li>Ele n\u00e3o \u00e9 recomendado para pacientes graves;<\/li>\n<li>O tratamento deve ser iniciado assim que poss\u00edvel ap\u00f3s o teste viral positivo para SARS-CoV-2 e dentro de 7 dias do in\u00edcio dos sintomas;<\/li>\n<li>Uso restrito a hospitais, sob prescri\u00e7\u00e3o m\u00e9dica e sua venda \u00e9 proibida ao com\u00e9rcio;<\/li>\n<li>N\u00e3o h\u00e1 efic\u00e1cia cl\u00ednica do produto contra a variante brasileira P1;<\/li>\n<li>Ainda n\u00e3o existem dados sobre o uso do medicamento em gestantes e lactantes;<\/li>\n<li>Ele n\u00e3o substitui as vacinas contra a Covid-19.<\/li>\n<\/ul>\n<\/div>\n<div class=\"mc-column content-text active-extra-styles \" data-block-type=\"unstyled\" data-block-weight=\"63\" data-block-id=\"12\">\n<p class=\"content-text__container \" data-track-category=\"Link no Texto\" data-track-links=\"\">A aplica\u00e7\u00e3o \u00e9 intravenosa, com dose \u00fanica restrita a 40mg\/kg, e o tratamento deve ser iniciado ap\u00f3s o teste viral positivo para a Covid-19 e\u00a0<span class=\"highlight highlighted\">dentro de 7 dias do in\u00edcio dos sintomas<\/span>. O uso\u00a0<span class=\"highlight highlighted\">\u00e9 restrito a hospitais e a venda \u00e9 proibida ao com\u00e9rcio.\u00a0<\/span>J\u00e1 a incorpora\u00e7\u00e3o no Sistema \u00danico de Sa\u00fade (SUS)\u00a0<span class=\"highlight highlighted\">depende da avalia\u00e7\u00e3o do Minist\u00e9rio da Sa\u00fade.<\/span><\/p>\n<div class=\"mc-column content-text active-extra-styles \" data-block-type=\"unstyled\" data-block-weight=\"28\" data-block-id=\"13\">\n<p class=\"content-text__container \" data-track-category=\"Link no Texto\" data-track-links=\"\">A relatora explicou que a decis\u00e3o da Anvisa se orienta pela pondera\u00e7\u00e3o dos potenciais benef\u00edcios para a sa\u00fade p\u00fablica em compara\u00e7\u00e3o aos eventuais riscos decorrentes da atua\u00e7\u00e3o sanit\u00e1ria.<\/p>\n<\/div>\n<div class=\"mc-column content-text active-extra-styles \" data-block-type=\"unstyled\" data-block-weight=\"62\" data-block-id=\"14\">\n<p class=\"content-text__container \" data-track-category=\"Link no Texto\" data-track-links=\"\">&#8220;<span class=\"highlight highlighted\">Espero que essa autoriza\u00e7\u00e3o possa ajudar a aliviar a carga em nosso sistema de sa\u00fade<\/span>. A Ag\u00eancia deve usar de todas as vias poss\u00edveis para fazer com que novos tratamentos estejam dispon\u00edveis para os pacientes o mais r\u00e1pido poss\u00edvel. Que essa autoriza\u00e7\u00e3o de uso emergencial desse anticorpo monoclonal ofere\u00e7a ao profissional de sa\u00fade mais uma ferramenta no combate \u00e0 pandemia&#8221;, afirmou Freitas.<\/p>\n<h3 data-track-category=\"Link no Texto\">Riscos<\/h3>\n<\/div>\n<div class=\"mc-column content-text active-extra-styles \" data-block-type=\"unstyled\" data-block-weight=\"16\" data-block-id=\"15\">\n<p class=\"content-text__container \" data-track-category=\"Link no Texto\" data-track-links=\"\">Segundo a Anvisa, h\u00e1 riscos quanto ao uso do medicamento em idosos e pessoas obesas.<\/p>\n<\/div>\n<div class=\"mc-column content-text active-extra-styles \" data-block-type=\"unstyled\" data-block-weight=\"51\" data-block-id=\"17\">\n<p class=\"content-text__container \" data-track-category=\"Link no Texto\" data-track-links=\"\">Os fatores de risco tamb\u00e9m existem diante do uso do medicamento em indiv\u00edduos acima de 55 anos de idade que tenham doen\u00e7a cardiovascular ou doen\u00e7a pulmonar cr\u00f4nica, diabetes mellitus tipo 1 ou tipo 2, doen\u00e7a renal cr\u00f4nica, doen\u00e7a hep\u00e1tica cr\u00f4nica ou pessoas que estejam recebendo tratamento imunossupressor no momento.<\/p>\n<p data-track-category=\"Link no Texto\" data-track-links=\"\"><strong>LEIA TAMB\u00c9M<\/strong><\/p>\n<p data-track-category=\"Link no Texto\" data-track-links=\"\"><a href=\"https:\/\/redenoticiaz.com.br\/blog\/2021\/03\/12\/anvisa-libera-medicamento-e-aprova-em-definitivo-a-vacina-de-oxford\">Anvisa libera medicamento e aprova em definitivo a vacina de Oxford<\/a><\/p>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Nesta quarta-feira (11) a Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (Anvisa) autorizou o uso emergencial de um medicamento contra a Covid-19. \u00c9 o\u00a0Regkirona\u00a0(regdanvimabe),\u00a0um anticorpo monoclonal. Antes dele, o \u00f3rg\u00e3o j\u00e1 tinha liberado o uso dos medicamentos Regn-CoV2, desenvolvido pela farmac\u00eautica Roche, e da associa\u00e7\u00e3o dos anticorpos banlanivimabe e etesevimabe, produzido pela farmac\u00eautica pela Eli Lilly. Al\u00e9m &hellip;<\/p>\n","protected":false},"author":6,"featured_media":12602,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[23],"tags":[24,22194,29945,29946,2651],"class_list":["post-12601","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-saude","tag-anvisa","tag-combate-a-covid","tag-medicamento-liberado","tag-regkirona","tag-uso-emergencial"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Anvisa libera uso emergencial de anticorpo para tratamento contra Covid-19 - Litoral SP<\/title>\n<meta name=\"description\" content=\"a Ag\u00eancia Nacional de Vigil\u00e2ncia Sanit\u00e1ria (Anvisa) autorizou o uso emergencial de um medicamento contra a Covid-19. \u00c9 o\u00a0Regkirona\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/redenoticiaz.com.br\/litoralsp\/2021\/08\/11\/anvisa-libera-uso-emergencial-de-anticorpo-para-tratamento-contra-covid-19\" \/>\n<meta property=\"og:locale\" content=\"pt_BR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Anvisa libera uso emergencial de anticorpo para tratamento contra Covid-19 - 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