Suvaxyn PCV

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

porcine circovirus recombinant virus (CPCV) 1-2, inactivated

Available from:

Zoetis Belgium SA

ATC code:

QI09AA07

INN (International Name):

adjuvanted inactivated vaccine against porcine circovirus type 2 in piglets

Therapeutic group:

Pigs (piglets)

Therapeutic area:

Immunologicals

Therapeutic indications:

Active immunisation of pigs over the age of three weeks against porcine circovirus type 2 (PCV2) to reduce viral load in blood and lymphoid tissues, and the lesions in lymphoid tissues associated with PCV2 infection, as well as to reduce clinical signs - including loss of daily weight gain, and mortality associated with post-weaning multisystemic wasting syndrome.

Product summary:

Revision: 13

Authorization status:

Withdrawn

Authorization date:

2009-07-24

Patient Information leaflet

                                Medicinal product no longer authorised
16
B. PACKAGE LEAFLET
Medicinal product no longer authorised
17
PACKAGE LEAFLET:
SUVAXYN
PCV SUSPENSION 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:
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
BELGIUM
Manufacturer responsible for batch release:
Zoetis Manufacturing & Research Spain, S.L.
Ctra. Camprodón s/n "la Riba"
17813 Vall de Bianya
Girona
SPAIN
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Suvaxyn PCV suspension for injection for pigs
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
One dose of 2 ml contains:
ACTIVE SUBSTANCE:
Inactivated recombinant Porcine Circovirus type 1 expressing the
Porcine Circovirus type 2 ORF2 protein
1.6
≤
RP*
≤
5.3
ADJUVANTS:
Sulfolipo-cyclodextrin (SLCD)
4 mg
Squalane
64 mg
EXCIPIENTS:
Thiomersal
0.1 mg
*
Relative Potency unit determined by ELISA antigen quantification (
_in vitro_
potency test) compared
to a reference vaccine.
A milky white to pink opaque liquid, free from visible particles
4.
INDICATION(S)
Active immunisation of pigs over the age of 3 weeks against Porcine
Circovirus Type 2 (PCV2) to
reduce viral load in blood and lymphoid tissues, and the lesions in
lymphoid tissues associated with
PCV2 infection, as well as to reduce clinical signs - including loss
of daily weight gain, and mortality
associated with Post-Weaning Multisystemic Wasting Syndrome (PMWS).
Onset of immunity: from 3 weeks post-vaccination.
Duration of immunity: 19 weeks post-vaccination
Medicinal product no longer authorised
18
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
A transient increase in body temperature (up to 1.7 °C) is very
common during the first 24 hours after
vaccination. This resolves spontaneously within 48 hours without
treatment.
Local tissue reactions in the form of swelling at the injection site
are very common and may last for up
to 26 days. The 
                                
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Summary of Product characteristics

                                Medicinal product no longer authorised
1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Suvaxyn PCV suspension for injection for pigs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
One dose of 2 ml contains:
ACTIVE SUBSTANCE:
Inactivated recombinant Porcine Circovirus type 1 expressing the
Porcine Circovirus type 2 ORF2 protein
1.6
≤
RP*
≤
5.3
ADJUVANTS:
Sulfolipo-cyclodextrin (SLCD)
4 mg
Squalane
64 mg
EXCIPIENTS:
Thiomersal
0.1 mg
*
Relative Potency unit determined by ELISA antigen quantification (
_in vitro_
potency test) compared
to a reference vaccine.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Suspension for injection
A milky white to pink opaque liquid, free from visible particles
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Pigs (piglets) from 3 weeks of age.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Active immunisation of pigs over the age of 3 weeks against Porcine
Circovirus type 2 (PCV2) to
reduce viral load in blood and lymphoid tissues, and the lesions in
lymphoid tissues associated with
PCV2 infection, as well as to reduce clinical signs - including loss
of daily weight gain, and mortality
associated with Post-Weaning Multisystemic Wasting Syndrome (PMWS).
Onset of immunity: from 3 weeks post-vaccination.
Duration of immunity: 19 weeks post-vaccination.
4.3
CONTRAINDICATIONS
None.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Vaccinate healthy animals only.
Do not use in breeding boars.
Medicinal product no longer authorised
3
The benefit of the vaccination of pigs with very high levels of
maternally-derived antibodies, e.g. due
to vaccination of their mothers, has not been demonstrated.
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
Avoid stress in the animals before and after the time of vaccination.
Special precautions to be taken by the person administering the
veterinary medicinal product to
animals
In case of accidental self-injection, seek medical 
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 15-04-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 15-04-2020
Public Assessment Report Public Assessment Report Bulgarian 15-04-2020
Patient Information leaflet Patient Information leaflet Spanish 15-04-2020
Public Assessment Report Public Assessment Report Spanish 15-04-2020
Patient Information leaflet Patient Information leaflet Czech 15-04-2020
Public Assessment Report Public Assessment Report Czech 15-04-2020
Patient Information leaflet Patient Information leaflet Danish 15-04-2020
Public Assessment Report Public Assessment Report Danish 15-04-2020
Patient Information leaflet Patient Information leaflet German 15-04-2020
Public Assessment Report Public Assessment Report German 15-04-2020
Patient Information leaflet Patient Information leaflet Estonian 15-04-2020
Public Assessment Report Public Assessment Report Estonian 15-04-2020
Patient Information leaflet Patient Information leaflet Greek 15-04-2020
Public Assessment Report Public Assessment Report Greek 15-04-2020
Patient Information leaflet Patient Information leaflet French 15-04-2020
Public Assessment Report Public Assessment Report French 15-04-2020
Patient Information leaflet Patient Information leaflet Italian 15-04-2020
Public Assessment Report Public Assessment Report Italian 15-04-2020
Patient Information leaflet Patient Information leaflet Latvian 15-04-2020
Public Assessment Report Public Assessment Report Latvian 15-04-2020
Patient Information leaflet Patient Information leaflet Lithuanian 15-04-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 15-04-2020
Public Assessment Report Public Assessment Report Lithuanian 15-04-2020
Patient Information leaflet Patient Information leaflet Hungarian 15-04-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 15-04-2020
Public Assessment Report Public Assessment Report Hungarian 15-04-2020
Patient Information leaflet Patient Information leaflet Maltese 15-04-2020
Public Assessment Report Public Assessment Report Maltese 15-04-2020
Patient Information leaflet Patient Information leaflet Dutch 15-04-2020
Public Assessment Report Public Assessment Report Dutch 15-04-2020
Patient Information leaflet Patient Information leaflet Polish 15-04-2020
Public Assessment Report Public Assessment Report Polish 15-04-2020
Patient Information leaflet Patient Information leaflet Portuguese 15-04-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 15-04-2020
Public Assessment Report Public Assessment Report Portuguese 15-04-2020
Patient Information leaflet Patient Information leaflet Romanian 15-04-2020
Public Assessment Report Public Assessment Report Romanian 15-04-2020
Patient Information leaflet Patient Information leaflet Slovak 15-04-2020
Public Assessment Report Public Assessment Report Slovak 15-04-2020
Patient Information leaflet Patient Information leaflet Slovenian 15-04-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 15-04-2020
Public Assessment Report Public Assessment Report Slovenian 15-04-2020
Patient Information leaflet Patient Information leaflet Finnish 15-04-2020
Public Assessment Report Public Assessment Report Finnish 15-04-2020
Patient Information leaflet Patient Information leaflet Swedish 15-04-2020
Public Assessment Report Public Assessment Report Swedish 15-04-2020
Patient Information leaflet Patient Information leaflet Norwegian 15-04-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 15-04-2020
Patient Information leaflet Patient Information leaflet Icelandic 15-04-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 15-04-2020
Patient Information leaflet Patient Information leaflet Croatian 15-04-2020
Public Assessment Report Public Assessment Report Croatian 15-04-2020

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