ACT-HIB VACUNA CONJUGADA HAEMOPHILUS TIPO B

Información principal

  • Denominación comercial:
  • ACT-HIB VACUNA CONJUGADA HAEMOPHILUS TIPO B
  • formulario farmacéutico:
  • POLVO LIOFILIZADO PARA SOLUCION INYECTABLE
  • Composición:
  • POR VIAL ; VACUNA CONTRA EL HAEMOPHILUS INFLUENZAE TIPO B 10 MCG
  • Vía de administración:
  • INTRAMUSCULAR SUBCUTANEA
  • Unidades en paquete:
  • Caja de cartón con 10 viales de vidrio incoloro x 5 mL; Caja de cartón con 20 frascos de vidrio tipo I incoloro + caja con 20 fr
  • tipo de receta:
  • CON RECETA MEDICA
  • Usar para:
  • Humanos
  • Tipo de medicina:
  • medicina biológica

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.


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Localización

  • Disponible en:
  • ACT-HIB VACUNA CONJUGADA HAEMOPHILUS TIPO B
    Perú
  • Idioma:
  • español

Información terapéutica

  • Grupo terapéutico:
  • Haemophilus influenzae B, antígeno purificado conjugado

Otros datos

Estado

  • Fuente:
  • DIGEMID - Dirección General de Medicamentos, Insumos y Drogas - Peru
  • Estado de Autorización:
  • VENCIDO
  • Número de autorización:
  • BE00145
  • Fecha de autorización:
  • 18-03-2008
  • última actualización:
  • 20-07-2018
  • 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.

17-10-2018

Pest categorisation of Stagonosporopsis andigena

Pest categorisation of Stagonosporopsis andigena

Published on: Tue, 16 Oct 2018 00:00:00 +0200 The Panel on Plant Health performed a pest categorisation of Stagonosporopsis andigena, the causal agent of black blight of potato, for the EU. The pest is a well‐defined fungal species and reliable methods exist for its detection and identification. S. andigena is present in Bolivia and Peru. The pest is not known to occur in the EU and is listed in Annex IAI of Directive 2000/29/EC as Phoma andina, meaning its introduction into the EU is prohibited. The ma...

Europe - EFSA - European Food Safety Authority Publications

17-10-2018

Pest categorisation of Thecaphora solani

Pest categorisation of Thecaphora solani

Published on: Tue, 16 Oct 2018 00:00:00 +0200 The Panel on Plant Health performed a pest categorisation of the fungus Thecaphora solani, the causal agent of smut of potato, for the EU. The identity of the pest is well established and reliable methods exist for its detection and identification. T. solaniis present in Bolivia, Chile, Colombia, Ecuador, Mexico, Panama, Peru and Venezuela. The pathogen is not known to occur in the EU and is listed in Annex IAI of Directive 2000/29/EC, meaning its introducti...

Europe - EFSA - European Food Safety Authority Publications

7-9-2018

Jacent recalls Crave Party Candles

Jacent recalls Crave Party Candles

Candles which can spontaneously re-ignite are prohibited in Canada by the Candles Regulations under the Canada Consumer Product Safety Act as they can re-ignite after disposal, potentially causing fires.

Health Canada

14-8-2018

Inhibidores de SGLT-2 y riesgo de amputación

En un estudio que compara el riesgo de amputación en pacientes con diabetes tipo 2 que inician tratamiento con diferentes fármacos, se halló un aumento asociado a las gliflozinas en comparación con metformina, sulfonilureas y tiazolidindionas. JAMA Internal Medicine, 13 de agosto de 2018

REDCIMLAC - Red de Centros de Información de Medicamentos de Latinoamérica y el Caribe

17-4-2018

Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and Tadalafil

Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and Tadalafil

Overland Park, KS, Epic Products, LLC is voluntarily recalling all lots of Euphoric capsules, packaged in 1 count blister cards, 3 count bottles, and 12 count bottles to the consumer level. FDA analysis found samples of Euphoric to be tainted with undeclared sildenafil and tadalafil, active ingredients in two FDA-approved prescription drug products, also known as phosphodiesterase 5-inhibitors (PDE-5 inhibitors), used to treat male erectile dysfunction (ED). The presence of sildenafil and tadalafil in E...

FDA - U.S. Food and Drug Administration

24-3-2011

Danish Pharmacovigilance Update, 17 March 2011

Danish Pharmacovigilance Update, 17 March 2011

This month’s issue of Danish Pharmacovigilance Update includes articles about reports of serious side effects in Japan from the childhood vaccines Prevenar (PCV7)® and Act-Hib® and reports of serious side effects in France from the childhood vaccine Prevenar13®.

Danish Medicines Agency

21-9-2018

Scientific guideline:  Reflection paper on the use of aminopenicillins and their beta-lactamase inhibitor combinations in animals in the European Union: development of resistance and impact on human and animal health, draft: consultation open

Scientific guideline: Reflection paper on the use of aminopenicillins and their beta-lactamase inhibitor combinations in animals in the European Union: development of resistance and impact on human and animal health, draft: consultation open

The objective of this document is to review available information on the use of aminopenicillins and their beta-lactamase inhibitor combinations in veterinary medicines in the EU, their effect on the emergence of antimicrobial resistance (AMR) and the potential impact of resistance on human and animal health. The document provides information for the risk profiling, as recommended by the Antimicrobial Advice ad hoc Expert Group (AMEG) of the EMA.

Europe - EMA - European Medicines Agency

29-8-2018

Cinryze (Shire Services BVBA)

Cinryze (Shire Services BVBA)

Cinryze (Active substance: C1 inhibitor, human) - Centralised - Yearly update - Commission Decision (2018)5767 of Wed, 29 Aug 2018

Europe -DG Health and Food Safety

23-8-2018

EU/3/18/1979 (Bayer AG)

EU/3/18/1979 (Bayer AG)

EU/3/18/1979 (Active substance: Human monoclonal IgG2 antibody against tissue factor pathway inhibitor) - Corrigendum - Commission Decision (2018)1246 of Thu, 23 Aug 2018

Europe -DG Health and Food Safety