{"id":83603,"date":"2020-04-17T22:51:01","date_gmt":"2020-04-18T01:51:01","guid":{"rendered":"https:\/\/megalabs.global\/eng\/?p=83603"},"modified":"2020-04-23T18:41:05","modified_gmt":"2020-04-23T21:41:05","slug":"sarilumab","status":"publish","type":"post","link":"https:\/\/megalabs.global\/eng\/sarilumab\/","title":{"rendered":"Sarilumab"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><p>[vc_row row_height_percent=&#8221;0&#8243; override_padding=&#8221;yes&#8221; h_padding=&#8221;2&#8243; top_padding=&#8221;3&#8243; bottom_padding=&#8221;3&#8243; overlay_alpha=&#8221;100&#8243; gutter_size=&#8221;3&#8243; shift_y=&#8221;0&#8243; row_height_use_pixel=&#8221;&#8221;][vc_column column_width_use_pixel=&#8221;yes&#8221; gutter_size=&#8221;3&#8243; overlay_alpha=&#8221;50&#8243; shift_x=&#8221;0&#8243; shift_y=&#8221;0&#8243; medium_width=&#8221;0&#8243; zoom_width=&#8221;0&#8243; zoom_height=&#8221;0&#8243; column_width_pixel=&#8221;800&#8243;][vc_column_text]El Sarilumab es un antagonista del receptor de interleucina-6 (IL-6) indicado para tratamiento de pacientes adultos con reumatoide moderadamente a severamente activo artritis que ha tenido una respuesta inadecuada o intolerancia a uno o m\u00e1s f\u00e1rmacos antirreum\u00e1ticos modificadores de la enfermedad (FARME).<br \/>\nFue aprobado en Estados Unidos en el 2017.(9)<\/p>\n<p><strong>Dosis y administraci\u00f3n propuestas para COVID-19 (1)<\/strong><\/p>\n<p><em><strong>Adultos<\/strong><\/em><br \/>\n200 o 400 mg IV en una \u00fanica infusi\u00f3n.<br \/>\n<em><strong>Pedi\u00e1tricas.<\/strong><\/em><br \/>\nNo hay dosis establecidas en ni\u00f1os. De acuerdo a FT, no se ha establecido la seguridad y eficacia de Sa-rilumab IV en menores de 2 a\u00f1os.<\/p>\n<p><strong>Precauciones y advertencias (2)<\/strong><br \/>\n\u2022 Infecciones graves: se recomienda evitar su uso durante una infecci\u00f3n activa.<br \/>\n\u2022 Neutropenia, trombocitopenia, enzimas hep\u00e1ticas elevadas, anormalidades lip\u00eddicas: se reco-mienda controlar par\u00e1metros de laboratorio.<br \/>\n\u2022 Perforaci\u00f3n gastrointestinal: el riesgo puede aumentar con la diverticulitis concurrente o el uso concomitante de AINE o corticosteroides. Se recomienda evaluar r\u00e1pidamente los signos o s\u00ednto-mas abdominales agudos.<br \/>\n\u2022 Reacciones de hipersensibilidad.<br \/>\n\u2022 Vacunas vivas: se recomienda evitar su uso debido al riesgo de infecci\u00f3n.<\/p>\n<p><strong>Eventos adversos (2)<\/strong><br \/>\nLas infecciones graves m\u00e1s frecuentemente observadas con Sarilumab incluyen la neumon\u00eda y la celulitis. Se han notificado casos de infecci\u00f3n oportunista. En los estudios cl\u00ednicos realizados con el producto registrado en FDA como referente (Kevzara), dentro de los eventos adversos m\u00e1s reportados estuvieron la neutropenia, trombocitopenia e infecciones respiratorias altas.<br \/>\nLas reacciones adversas m\u00e1s frecuentes observadas con Sarilumab en estudios cl\u00ednicos fueron neutropenia, ALT elevada, eritema en el lugar de la inyecci\u00f3n, infecciones del tracto respiratorio superior e infecciones del tracto urinario.<\/p>\n<p><strong>Estudios cl\u00ednicos con COVID-19<\/strong><br \/>\n\u2022 Evaluation of the Efficacy and Safety of Sarilumab in Hospitalized Patients With COVID-19. (3)[\/vc_column_text][vc_single_image media=&#8221;83604&#8243; media_width_use_pixel=&#8221;yes&#8221; alignment=&#8221;center&#8221; media_width_pixel=&#8221;716&#8243;][vc_column_text]Link a informaci\u00f3n del producto de FDA:<\/p>\n<p><a href=\"http:\/\/www.accessdata.fda.gov\/drugsatfda_docs\/label\/2018\/761037s001lbl.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">www.accessdata.fda.gov\/drugsatfda_docs\/label\/2018\/761037s001lbl.pdf<\/a>.<\/p>\n<p>(1) Tratamientos disponibles para el manejo de la infecci\u00f3n respiratoria por SARS-CoV-2. AEMPS2020.<\/p>\n<p>Available from:<br \/>\n<a href=\"https:\/\/www.aemps.gob.es\/la-aemps\/ultima-informacion-de-la-aemps-acerca-del-covid%e2%80%9119\/tratamientos-disponibles-para-el-manejo-de-la-infeccion-respiratoria-por-sars-cov-2\/\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.aemps.gob.es\/la-aemps\/ultima-informacion-de-la-aemps-acerca-del-covid%e2%80%9119\/tratamientos-disponibles-para-el-manejo-de-la-infeccion-respiratoria-por-sars-cov-2\/<\/a>.<\/p>\n<p>(2) Inserto de Kevzara Food and Drug Administration2018.<\/p>\n<p>Available from:<br \/>\n<a href=\"https:\/\/www.accessdata.fda.gov\/drugsatfda_docs\/label\/2018\/761037s001lbl.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/www.accessdata.fda.gov\/drugsatfda_docs\/label\/2018\/761037s001lbl.pdf<\/a>.<\/p>\n<p>(3) Evaluation of the Efficacy and Safety of Sarilumab in Hospitalized Patients With COVID-19 2020.<\/p>\n<p>Available from: <a href=\"https:\/\/clinicaltrials.gov\/ct2\/show\/NCT04315298\" target=\"_blank\" rel=\"noopener noreferrer\">https:\/\/clinicaltrials.gov\/ct2\/show\/NCT04315298<\/a>.[\/vc_column_text][vc_empty_space empty_h=&#8221;3&#8243;][vc_row_inner row_inner_height_percent=&#8221;0&#8243; overlay_alpha=&#8221;50&#8243; gutter_size=&#8221;3&#8243; border_color=&#8221;color-877404&#8243; border_style=&#8221;solid&#8221; shift_y=&#8221;0&#8243; z_index=&#8221;0&#8243; css=&#8221;.vc_custom_1572995729128{border-top-width: 1px !important;border-bottom-width: 1px !important;padding-top: 18px !important;padding-bottom: 18px !important;}&#8221; el_class=&#8221;descarga-pdf&#8221; limit_content=&#8221;&#8221;][vc_column_inner width=&#8221;1\/1&#8243;][vc_icon position=&#8221;left&#8221; icon_image=&#8221;82110&#8243; icon_color=&#8221;color-877404&#8243; media_size=&#8221;42&#8243; text_font=&#8221;font-195522&#8243; text_weight=&#8221;700&#8243; linked_title=&#8221;yes&#8221; title=&#8221;Descargar Documento&#8221; link=&#8221;url:%2Fwp-content%2Fuploads%2F2020%2F04%2FConexion-Sarilumab.pdf|title:Conexion%20Sarilumab|target:%20_blank|&#8221;]Conexion Sarilumab[\/vc_icon][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row]<\/p>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>Inyectable<\/p>\n","protected":false},"author":1,"featured_media":80575,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[94],"tags":[],"class_list":["post-83603","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-farmacos"],"_links":{"self":[{"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/posts\/83603","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/comments?post=83603"}],"version-history":[{"count":0,"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/posts\/83603\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/media\/80575"}],"wp:attachment":[{"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/media?parent=83603"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/categories?post=83603"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/megalabs.global\/eng\/wp-json\/wp\/v2\/tags?post=83603"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}