Circovac

Maa: Euroopan unioni

Kieli: englanti

Lähde: EMA (European Medicines Agency)

Osta se nyt

Pakkausseloste Pakkausseloste (PIL)
08-12-2021
Valmisteyhteenveto Valmisteyhteenveto (SPC)
08-12-2021

Aktiivinen ainesosa:

inactivated porcine circovirus type 2 (PCV2)

Saatavilla:

CEVA-Phylaxia Oltóanyagtermelõ Zrt.

ATC-koodi:

QI09AA07

INN (Kansainvälinen yleisnimi):

adjuvanted inactivated vaccine against porcine circovirus type 2

Terapeuttinen ryhmä:

Pigs (gilts and sows)

Terapeuttinen alue:

Immunologicals for suidae

Käyttöaiheet:

Sows and giltsPassive immunisation of piglets via the colostrum, after active immunisation of sows and gilts, to reduce lesions in lymphoid tissues associated with PCV2 infection and as an aid to reduce PCV2-linked mortality.PigletsActive immunisation of piglets to reduce faecal excretion of PCV2 and virus load in blood, and as an aid to reduce PCV2-linked clinical signs, including wasting, weight loss and mortality, as well as to reduce virus load and lesions in lymphoid tissues associated with PCV2 infection.

Tuoteyhteenveto:

Revision: 12

Valtuutuksen tilan:

Authorised

Valtuutus päivämäärä:

2007-06-21

Pakkausseloste

                                17
B. PACKAGE LEAFLET
18
PACKAGE LEAFLET FOR:
CIRCOVAC EMULSION AND SUSPENSION FOR EMULSION FOR INJECTION FOR PIGS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
CEVA-Phylaxia Veterinary Biologicals Co. Ltd., Szállás u. 5.,
Budapest, 1107, Hungary
Manufacturer for batch release:
MERIAL, Laboratoire Porte des Alpes, Rue de l'Aviation, F-69800 Saint
Priest, France
CEVA-Phylaxia Veterinary Biologicals Co. Ltd., Szállás u. 5.,
Budapest, 1107, Hungary
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Circovac
Emulsion and suspension for emulsion for injection for pigs
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Pale opalescent liquid prior to reconstitution
Each ml of reconstituted vaccine contains:
ACTIVE SUBSTANCE:
Inactivated porcine circovirus type 2 (PCV2)
.................................................

1.8 log10 ELISA Units
EXCIPIENT:
Thiomersal
...................................................................................................................................
0.10 mg
ADJUVANT:
Light paraffin oil
............................................................................................................
247 to 250.5 mg
4.
INDICATION(S)
PIGLETS
: Active immunisation of piglets to reduce faecal excretion of PCV2
and virus load in blood,
and as an aid to reduce PCV2 linked clinical signs, including wasting,
weight loss and mortality as
well as to reduce virus load and lesions in lymphoid tissues
associated with PCV2 infection.
Onset of immunity: 2 weeks.
Duration of immunity: at least 14 weeks after vaccination.
SOWS AND GILTS:
Passive immunisation of piglets via the colostrum, after active
immunisation of sows
and gilts, to reduce lesions in lymphoid tissues associated with PCV2
infection and as an aid to reduce
PCV2-linked mortality.
Duration of immunity: up to 5 weeks after transfer of passive
antibodies through colostrum intake.
5.
CONTRAINDI
                                
                                Lue koko asiakirja
                                
                            

Valmisteyhteenveto

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Circovac emulsion and suspension for emulsion for injection for pigs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each ml of reconstituted vaccine contains:
ACTIVE SUBSTANCE:
Inactivated porcine circovirus type 2 (PCV2)
.................................................

1.8 log10 ELISA Units
EXCIPIENT:
Thiomersal
...................................................................................................................................
0.10 mg
ADJUVANT:
Light paraffin oil
............................................................................................................
247 to 250.5 mg
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Emulsion and suspension for emulsion for injection.
Pale opalescent liquid prior to reconstitution.
The reconstituted vaccine is a homogeneous white emulsion.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Pigs (gilts, sows and piglets from 3 weeks of age).
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
PIGLETS
: Active immunisation of piglets to reduce faecal excretion of PCV2
and virus load in blood,
and as an aid to reduce PCV2-linked clinical signs, including wasting,
weight loss and mortality as
well as to reduce virus load and lesions in lymphoid tissues
associated with PCV2 infection.
Onset of immunity: 2 weeks
Duration of immunity: at least 14 weeks after vaccination.
SOWS AND GILTS
: Passive immunisation of piglets via the colostrum, after active
immunisation of sows
and gilts, to reduce lesions in lymphoid tissues associated with PCV2
infection and as an aid to reduce
PCV2-linked mortality.
Duration of immunity: up to 5 weeks after transfer of passive
antibodies through colostrum intake.
4.3
CONTRAINDICATIONS
None.
3
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Sows: None.
Piglets: The efficacy of the vaccine in the face of intermediate to
high levels of maternally derived
antibodies has been demonstrated.
4.5
SPECIAL PRECAUTIONS FOR USE
SPE
                                
                                Lue koko asiakirja
                                
                            

Asiakirjat muilla kielillä

Pakkausseloste Pakkausseloste bulgaria 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto bulgaria 08-12-2021
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta bulgaria 19-09-2017
Pakkausseloste Pakkausseloste espanja 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto espanja 08-12-2021
Pakkausseloste Pakkausseloste tšekki 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto tšekki 08-12-2021
Pakkausseloste Pakkausseloste tanska 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto tanska 08-12-2021
Pakkausseloste Pakkausseloste saksa 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto saksa 08-12-2021
Pakkausseloste Pakkausseloste viro 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto viro 08-12-2021
Pakkausseloste Pakkausseloste kreikka 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto kreikka 08-12-2021
Pakkausseloste Pakkausseloste ranska 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto ranska 08-12-2021
Pakkausseloste Pakkausseloste italia 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto italia 08-12-2021
Pakkausseloste Pakkausseloste latvia 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto latvia 08-12-2021
Pakkausseloste Pakkausseloste liettua 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto liettua 08-12-2021
Pakkausseloste Pakkausseloste unkari 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto unkari 08-12-2021
Pakkausseloste Pakkausseloste malta 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto malta 08-12-2021
Pakkausseloste Pakkausseloste hollanti 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto hollanti 08-12-2021
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta hollanti 19-09-2017
Pakkausseloste Pakkausseloste puola 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto puola 08-12-2021
Pakkausseloste Pakkausseloste portugali 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto portugali 08-12-2021
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta portugali 19-09-2017
Pakkausseloste Pakkausseloste romania 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto romania 08-12-2021
Pakkausseloste Pakkausseloste slovakki 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto slovakki 08-12-2021
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta slovakki 19-09-2017
Pakkausseloste Pakkausseloste sloveeni 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto sloveeni 08-12-2021
Julkisesta arviointikertomuksesta Julkisesta arviointikertomuksesta sloveeni 19-09-2017
Pakkausseloste Pakkausseloste suomi 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto suomi 08-12-2021
Pakkausseloste Pakkausseloste ruotsi 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto ruotsi 08-12-2021
Pakkausseloste Pakkausseloste norja 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto norja 08-12-2021
Pakkausseloste Pakkausseloste islanti 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto islanti 08-12-2021
Pakkausseloste Pakkausseloste kroatia 08-12-2021
Valmisteyhteenveto Valmisteyhteenveto kroatia 08-12-2021

Näytä asiakirjojen historia