Porcilis Pesti


Adjuvanted vaccine against classical swine fever

This medicine is now withdrawn from use in the European Union.


The marketing authorisation for Porcilis Pesti has been withdrawn at the request of the marketing authorisation holder

This EPAR was last updated on 19/08/2021

Authorisation details

Product details
Porcilis Pesti
Agency product number
Active substance
Classical Swine Fever Virus (CSFV) -E2 subunit antigen
International non-proprietary name (INN) or common name
Adjuvanted vaccine against classical swine fever
Anatomical therapeutic chemical veterinary (ATCvet) codes
Publication details
Marketing-authorisation holder
Intervet International BV
Date of issue of marketing authorisation valid throughout the European Union
Contact address
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands

Product information

16/09/2011 Porcilis Pesti - EMEA/V/C/000046 - R/0011

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Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

You can find product information documents for centrally authorised human medicines on this website. For centrally authorised veterinary medicines authorised or updated from February 2022, see the Veterinary Medicines Information website.

Pharmacotherapeutic group

Immunologicals for suidae

Therapeutic indication

Active immunisation of pigs from the age of 5 weeks onwards to prevent mortality and to reduce clinical signs of Classical Swine Fever, as well as to reduce infection with and excretion of CSF field virus.
The onset of protection is 2 weeks.
The duration of protection is 6 months.

Assessment history

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