{"id":11046,"date":"2024-02-08T15:22:59","date_gmt":"2024-02-08T20:22:59","guid":{"rendered":"https:\/\/www.vecol.com.co\/?post_type=product&p=11046"},"modified":"2024-12-13T12:19:32","modified_gmt":"2024-12-13T17:19:32","slug":"cefiro-duo","status":"publish","type":"product","link":"https:\/\/www.vecol.com.co\/en\/product\/cefiro-duo\/","title":{"rendered":"CEFIRO DUO\u00ae"},"content":{"rendered":"\n\n\n\n\n\n\n
INDICACIONES<\/strong><\/td>\n\n
    \n
  • En bovinos y porcinos para el tratamiento de procesos infecciosos causados por microorganismos sensibles al principio Ceftiofur principalmente neumon\u00edas, fiebre de embarque, necrosis interdigital y endometritis en bovinos, neumon\u00edas en porcinos. En bovinos: Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, Fusobacterium necrophorum y Porphyromonas asaccharolytica (Bacteroides melaninogenicus<\/em>). En porcinos: Streptococcus suis, Actinobacillus pleuropneumoniae,Glaesserella parasuis, Salmonella choleraesuis, Pasteurella multocida.<\/em><\/li>\n<\/ul>\n

    \u2022 La terapia antimicrobiana se complementa en este producto con un antiinflamatorio no esteroide, el ketoprofeno, el cual ejerce actividad antiinflamatoria, analg\u00e9sica y antipir\u00e9tica.<\/p>\n<\/td>\n<\/tr>\n

ESPECIES DE DESTINO<\/strong><\/td>\nBovinos y porcinos<\/strong><\/td>\n<\/tr>\n
COMPOSICI\u00d3N<\/strong><\/p>\n

 <\/p>\n

 <\/p>\n

 <\/p>\n

 <\/p>\n

DOSIS Y VIA DE ADMINISTRACI\u00d3N<\/strong><\/td>\n

Cada 100ml de suspensi\u00f3n inyectable contiene:<\/p>\n

Ceftiofur clorhidrato 7,5 g<\/p>\n

Ketoprofeno 10,0 g<\/p>\n

Excipientes c.s.p. 100 ml<\/p>\n

 <\/p>\n

V\u00eda de administraci\u00f3n: Intramuscular profunda.<\/p>\n

Dosis:<\/p>\n

    \n
  • Bovinos: 1 ml\/ 33 kg de peso vivo, equivalente a 2,2 mg \/ kg de Ceftiofur y 3 mg \/ kg de Ketoprofeno. Repetir cada 24 horas.<\/li>\n
  • Porcinos: 1 ml \/ 25 kg de peso vivo, equivalente a 3 mg\/ kg de Ceftiofur 4 mg\/ kg de Ketoprofeno. Repetir cada 24 horas.<\/li>\n<\/ul>\n

    El uso de dosis m\u00e1s altas, durante un tiempo mayor o el suministro del medicamento por una v\u00eda diferente a la intramuscular profunda puede generar residuos perjudiciales en tejidos y\/o leche.<\/p>\n

    La mayor\u00eda de los animales responde al tratamiento dentro de 3 \u2013 5 d\u00edas. Si no se observa mejor\u00eda, ser\u00e1 necesario reevaluar el diagn\u00f3stico y la terapia.<\/td>\n<\/tr>\n

PRECAUCIONES Y ALMACENAMIENTO<\/strong><\/p>\n

 <\/td>\n

\n
    \n
  • El operador deber\u00e1 evitar el contacto directo del producto con la piel o las mucosas, con el fin de prevenir el riesgo de reacciones al\u00e9rgicas.<\/li>\n
  • Se recomienda utilizar guantes de l\u00e1tex para su administraci\u00f3n.<\/li>\n
  • Verificar que el sistema de inviolabilidad del producto y sus condiciones de almacenamiento previo a su uso sean las adecuadas, as\u00ed como que el mismo no haya caducado en referencia a la fecha de vencimiento expresada en el rotulo.<\/li>\n
  • El uso del producto puede generar resultados positivos a residuos de Ceftiofur cuando se utilizan pruebas cuya sensibilidad permite detectar en la leche de los animales tratados niveles inferiores a los establecidos por el ministerio de Salud y Protecci\u00f3n Social mediante la Resoluci\u00f3n No. 1382 de 2013 (100 p g \/ L, 0,1 p. p. m).<\/li>\n
  • Agitar bien antes de usar.<\/li>\n
  • Almacenar a una temperatura inferior 30\u00b0C y protegido de la luz solar.<\/li>\n
  • Descartar el producto una vez abierto el envase.<\/li>\n
  • Venta bajo f\u00f3rmula del M\u00e9dico Veterinario.<\/li>\n
  • Mant\u00e9ngase fuera del alcance de los ni\u00f1os y de los animales dom\u00e9sticos.<\/li>\n
  • La disposici\u00f3n de los envases o contenido residual debe hacerse seg\u00fan la normativa ambiental nacional vigente.<\/li>\n
  • USO VETERINARIO<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n
 <\/p>\n

CONTRAINDICACIONES E INTERACCIONES<\/strong><\/p>\n

 <\/p>\n

 <\/p>\n

 <\/p>\n

TIEMPO DE RETIRO<\/strong><\/p>\n

 <\/p>\n

 <\/p>\n

 <\/p>\n

PRESENTACION<\/strong><\/p>\n

 <\/p>\n

REGISTRO ICA<\/strong><\/td>\n

 <\/p>\n
    \n
  • No administrar en animales hipersensibles a alguno de los componentes del producto.<\/li>\n
  • No administrar junto a antiinflamatorios no esteroides (AINEs).<\/li>\n
  • Contraindicado en animales con ulcera y\/o sangrado gastrointestinal.<\/li>\n
  • Evitar su uso en animales deshidratados, hipovol\u00e9micos o hipotensos.<\/li>\n
  • No usar en animales con enfermedades cardiacas, hep\u00e1ticas o renales.<\/li>\n<\/ul>\n

     <\/p>\n

    Los bovinos y porcinos tratados no deben ser sacrificados para consumo humano hasta 4 d\u00edas despu\u00e9s de finalizado el tratamiento, no requiere tiempo de retiro en leche, el uso de dosis m\u00e1s altas que las aprobadas o la administraci\u00f3n por v\u00edas diferentes puede generar residuos perjudiciales en tejidos y\/o leche.<\/p>\n

     <\/p>\n

     <\/p>\n

    Caja con frascos 100 o 250 mL.<\/p>\n

     <\/p>\n

    11040-MV<\/strong><\/td>\n<\/tr>\n<\/tbody>\n<\/table>","protected":false},"excerpt":{"rendered":"

    En bovinos y porcinos para el tratamiento de procesos infecciosos causados por microorganismos sensibles al principio Ceftiofur principalmente neumon\u00edas, fiebre de embarque, necrosis interdigital y endometritis en bovinos, neumon\u00edas en porcinos. En bovinos: Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, Fusobacterium necrophorum y Porphyromonas asaccharolytica (Bacteroides melaninogenicus<\/em>). En porcinos: Streptococcus suis, Actinobacillus pleuropneumoniae,Glaesserella parasuis, Salmonella choleraesuis, Pasteurella multocida.<\/em><\/p>\n

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