ANESTOP

Información principal

  • Denominación comercial:
  • ANESTOP
  • Dosis:
  • 5 %
  • formulario farmacéutico:
  • Ungüento
  • Usar para:
  • Humanos
  • Tipo de medicina:
  • medicamento alopático

Documentos

  • para el público en general:
  • El prospecto de información de este producto no está disponible actualmente, puede enviar una petición a nuestro servicio al cliente y le notificaremos tan pronto como nos sea posible para conseguirlo.


    Solicitar el prospecto de información al público.

Localización

  • Disponible en:
  • ANESTOP
    Cuba
  • Idioma:
  • español

Otros datos

Estado

  • Fuente:
  • CECMED - Autoridad Reguladora de Medicamentos, Equipos y Dispositivos Médicos - Cuba
  • Número de autorización:
  • m17053a01
  • última actualización:
  • 10-05-2018

Ficha Técnica

RESUMEN DE LAS CARACTERÍSTICAS DEL PRODUCTO

Nombre del producto:

ANESTOP®

(clorhidrato de lidocaína)

Forma farmacéutica:

Ungüento

Fortaleza:

Presentación:

Estuche por un tubo de AL con 25 g.

Titular del Registro Sanitario, país:

EMPRESA LABORATORIO FARMACÉUTICO

"ROBERTO ESCUDERO", LA HABANA, CUBA.

Fabricante, país:

EMPRESA LABORATORIO FARMACÉUTICO

ROBERTO ESCUDERO, UNIDAD EMPRESARIAL DE BASE

(UEB) "PRODUCCIÓN ESTOMATOLÓGICOS Y

DISPENSARIALES", ARTEMISA, CUBA.

Número de Registro Sanitario:

M-17-053-A01

Fecha de Inscripción:

31 de marzo de 2017

Composición:

Cada 100 g contiene:

Clorhidrato de lidocaína

5,0 g

Plazo de validez:

36 meses

Condiciones de almacenamiento:

Almacenar por debajo de 30 ˚C.

Indicaciones terapéuticas:

Anestesia Tópica previa a la infiltración.

Extracción de dientes caducos y de dientes flojos.

Detartrajes.

Adaptación de coronas.

Eliminación de reflejos en la toma de impresiones.

Anestesia de la dentina y la pulpa expuesta.

Contraindicaciones:

Hipersensibilidad al Clorhidrato de Lidocaína

Precauciones:

No presenta.

Advertencias especiales y precauciones de uso:

Embarazo: cruza la barrera placentaria. Categoría de riesgo para el embarazo B

Efectos indeseables:

No presenta.

Posología y método de administración:

Según facultativo.

Modo de administración: Tópica

Interacción con otros productos medicinales y otras formas de interacción:

Con soluciones desinfectantes puede causar liberación de metales pesados de estas

soluciones y producir irritación cutánea.

Uso en Embarazo y lactancia:

Embarazo: cruza la barrera placentaria. Categoría de riesgo para el embarazo B

Efectos sobre la conducción de vehículos/maquinarias:

No procede.

Sobredosis:

No procede.

Propiedades farmacodinámicas:

No presenta.

Propiedades

farmacocinéticas

(Absorción,

distribución,

biotransformación,

eliminación):

No presenta.

Instrucciones de uso, manipulación y destrucción del remanente no utilizable del

producto:

Seque previamente la mucosa y aplique el Ungüento en cantidad suficiente para cubrir la

zona, frote sobre la misma con una torunda de algodón o con la yema del dedo. El efecto

anestésico se produce pasado 1 minuto, con una duración aproximada de 20 minutos.

Fecha de aprobación/ revisión del texto: 31 de Marzo de 2017.

  • El prospecto de información de este producto no está disponible actualmente, puede enviar una petición a nuestro servicio al cliente y le notificaremos tan pronto como nos sea posible para conseguirlo.

    Solicitar el prospecto de información al público.



  • Los documentos en otros idiomas están disponibles aquí

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