{"id":14183,"date":"2021-10-05T06:19:32","date_gmt":"2021-10-05T13:19:32","guid":{"rendered":"https:\/\/fuentesfidedignas.com.mx\/?p=14183"},"modified":"2021-10-05T06:19:35","modified_gmt":"2021-10-05T13:19:35","slug":"jj-pide-autorizacion-para-vacuna-de-refuerzo-contra-el-covid-19","status":"publish","type":"post","link":"https:\/\/fuentesfidedignas.com.mx\/index.php\/2021\/10\/05\/jj-pide-autorizacion-para-vacuna-de-refuerzo-contra-el-covid-19\/","title":{"rendered":"J&#038;J pide autorizaci\u00f3n para vacuna de refuerzo contra el Covid-19"},"content":{"rendered":"\n<p><br><strong><em><br>La firma dijo que su presentaci\u00f3n incluye datos de un estudio en etapa tard\u00eda que hall\u00f3 resultados significativos<\/em><\/strong><\/p>\n\n\n\n<p>Estados Unidos. &#8211; Johnson &amp; Johnson (J&amp;J) dijo el martes que envi\u00f3 datos a la Administraci\u00f3n de Medicamentos y Alimentos de Estados Unidos (FDA, por sus siglas en ingl\u00e9s) para su autorizaci\u00f3n de uso de emergencia de una inyecci\u00f3n de refuerzo de su vacuna contra el Covid-19 en personas de 18 a\u00f1os o m\u00e1s.<\/p>\n\n\n\n<p>La presentaci\u00f3n se produce despu\u00e9s de que la FDA program\u00f3 la semana pasada la reuni\u00f3n de su comit\u00e9 asesor de expertos para el 15 de octubre para discutir si se debe autorizar una segunda inyecci\u00f3n de la vacuna de dosis \u00fanica de J&amp;J.<\/p>\n\n\n\n<p>La firma dijo que su presentaci\u00f3n incluye datos de un estudio en etapa tard\u00eda que hall\u00f3 que un refuerzo de su vacuna administrado 56 d\u00edas despu\u00e9s de la dosis primaria proporcion\u00f3 un 94% de protecci\u00f3n contra el Covid-19 sintom\u00e1tico en los Estados Unidos y un 100% de protecci\u00f3n contra la enfermedad grave, al menos 14 d\u00edas despu\u00e9s de la inoculaci\u00f3n del refuerzo.<\/p>\n\n\n\n<p>La FDA ya autoriz\u00f3 una dosis de refuerzo de la vacuna desarrollada por Pfizer Inc y su socio BioNTech para personas de 65 a\u00f1os o m\u00e1s, gente con alto riesgo de enfermedad grave y otras expuestas regularmente al virus.<\/p>\n\n\n\n<p>Moderna tambi\u00e9n present\u00f3 su solicitud de autorizaci\u00f3n para una inyecci\u00f3n de refuerzo de su vacuna de dos dosis el mes pasado.<\/p>\n\n\n\n<p>J&amp;J dijo que planea enviar los datos a otros reguladores, a la Organizaci\u00f3n Mundial de la Salud y a los Grupos Asesores T\u00e9cnicos de Inmunizaci\u00f3n Nacional para informar sobre la toma de decisiones sobre las estrategias locales de administraci\u00f3n de vacunas, seg\u00fan sea necesario.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La firma dijo que su presentaci\u00f3n incluye datos de un estudio en etapa tard\u00eda que hall\u00f3 resultados significativos Estados Unidos. &#8211; Johnson &amp; Johnson (J&amp;J) dijo el martes que envi\u00f3 datos a la Administraci\u00f3n de Medicamentos y Alimentos de Estados Unidos (FDA, por sus siglas en ingl\u00e9s) para su autorizaci\u00f3n de uso de 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