Suvaxyn Circo+MH RTU

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

Inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2 ORF2 protein, Inactivated Mycoplasma hyopneumoniae, strain P-5722-3

Available from:

Zoetis Belgium SA

ATC code:

QI09AL

INN (International Name):

Porcine circovirus and porcine enzootic pneumonia vaccine (inactivated)

Therapeutic group:

Pigs

Therapeutic area:

Inactivated viral and inactivated bacterial vaccines

Therapeutic indications:

For active immunisation of pigs from 3 weeks of age against porcine circovirus type 2 (PCV2) to reduce viral load in blood and lymphoid tissues and fecal shedding caused by infection with PCV2.For active immunisation of pigs over the age of 3 weeks against Mycoplasma hyopneumoniae to reduce lung lesions caused by infection with M. hyopneumoniae.

Product summary:

Revision: 7

Authorization status:

Authorised

Authorization date:

2015-11-06

Patient Information leaflet

                                15
B. PACKAGE LEAFLET
16
PACKAGE LEAFLET:
SUVAXYN CIRCO+MH RTU 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 authorization holder and manufacturer responsible for batch
release:
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
BELGIUM
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Suvaxyn Circo+MH RTU emulsion for injection for pigs
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Each dose (2 ml) contains:
ACTIVE SUBSTANCES:
Inactivated recombinant chimeric porcine circovirus type 1 containing
the
porcine circovirus type 2 ORF2 protein
Inactivated
_Mycoplasma hyopneumoniae, _
strain P-5722-3
_ _
2.3 – 12.4 RP*
1.5 – 3.8 RP*
ADJUVANT:
Squalane
Poloxamer 401
Polysorbate 80
0.4% (v/v)
0.2% (v/v)
0.032% (v/v)
EXCIPIENTS:
Thiomersal
0.2 mg
*
Relative potency unit determined by ELISA antigen quantification (
_in vitro _
potency test) compared
to a reference vaccine.
White homogenous emulsion.
4.
INDICATION(S)
For active immunisation of pigs from 3 weeks of age against Porcine
Circovirus type 2 (PCV2) to
reduce viral load in blood and lymphoid tissues and fecal shedding
caused by infection with
PCV2.
For active immunization of pigs from 3 weeks of age against
_Mycoplasma hyopneumoniae _
to reduce
lung lesions caused by infection with
_M. hyopneumoniae_
.
Onset of immunity: 3 weeks after vaccination.
Duration of immunity: 23 weeks after vaccination.
17
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
A transient increase in body temperature (on average 1 °C) was very
commonly observed during the first
24 hours after vaccination in laboratory and field trials. In
individual pigs the temperature increase
compared to pre-treatment may commonly exceed 2 °C. This resolves
spontaneously within 48 hours
without treatment.
Local tissue reactions in the form of swelling at the injection site,
which may be associated with local
heat, redness and pain at palpatio
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Suvaxyn Circo+MH RTU emulsion for injection for pigs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each dose (2 ml) contains:
ACTIVE SUBSTANCES:
Inactivated recombinant chimeric porcine circovirus type 1 containing
the
porcine circovirus type 2 ORF2 protein
Inactivated
_Mycoplasma hyopneumoniae, _
strain P-5722-3
_ _
2.3 – 12.4 RP*
1.5 – 3.8 RP*
ADJUVANT:
Squalane
Poloxamer 401
Polysorbate 80
EXCIPIENTS:
0.4% (v/v)
0.2% (v/v)
0.032% (v/v)
Thiomersal
0.2 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
Emulsion for injection.
White homogenous emulsion.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Pigs (for fattening).
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For active immunisation of pigs from 3 weeks of age against Porcine
Circovirus type 2 (PCV2) to
reduce viral load in blood and lymphoid tissues and fecal shedding
caused by infection with PCV2.
For active immunization of pigs from the age of 3 weeks against
_Mycoplasma hyopneumoniae _
to
reduce lung lesions caused by infection with
_M. hyopneumoniae_
.
Onset of immunity: 3 weeks after vaccination.
Duration of immunity: 23 weeks after vaccination.
4.3
CONTRAINDICATIONS
None.
3
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Vaccinate only healthy animals.
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
No information is available on the safety of this vaccine in breeding
boars. Do not use in breeding
boars.
Special precautions to be taken by the person administering the
veterinary medicinal product to animals
In case of accidental self-injection, seek medical advice immediately
and show the package leaflet or the
label to the physician.
4.6
ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
A transient increase in body temperature (on average 1 °C) was very
commonly observed during the
firs
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 03-11-2021
Summary of Product characteristics Summary of Product characteristics Bulgarian 03-11-2021
Public Assessment Report Public Assessment Report Bulgarian 15-06-2017
Patient Information leaflet Patient Information leaflet Spanish 03-11-2021
Public Assessment Report Public Assessment Report Spanish 15-06-2017
Patient Information leaflet Patient Information leaflet Czech 03-11-2021
Public Assessment Report Public Assessment Report Czech 15-06-2017
Patient Information leaflet Patient Information leaflet Danish 03-11-2021
Public Assessment Report Public Assessment Report Danish 15-06-2017
Patient Information leaflet Patient Information leaflet German 03-11-2021
Public Assessment Report Public Assessment Report German 15-06-2017
Patient Information leaflet Patient Information leaflet Estonian 03-11-2021
Public Assessment Report Public Assessment Report Estonian 15-06-2017
Patient Information leaflet Patient Information leaflet Greek 03-11-2021
Public Assessment Report Public Assessment Report Greek 15-06-2017
Patient Information leaflet Patient Information leaflet French 03-11-2021
Public Assessment Report Public Assessment Report French 15-06-2017
Patient Information leaflet Patient Information leaflet Italian 03-11-2021
Public Assessment Report Public Assessment Report Italian 15-06-2017
Patient Information leaflet Patient Information leaflet Latvian 03-11-2021
Public Assessment Report Public Assessment Report Latvian 15-06-2017
Patient Information leaflet Patient Information leaflet Lithuanian 03-11-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 03-11-2021
Public Assessment Report Public Assessment Report Lithuanian 15-06-2017
Patient Information leaflet Patient Information leaflet Hungarian 03-11-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 03-11-2021
Public Assessment Report Public Assessment Report Hungarian 15-06-2017
Patient Information leaflet Patient Information leaflet Maltese 03-11-2021
Public Assessment Report Public Assessment Report Maltese 15-06-2017
Patient Information leaflet Patient Information leaflet Dutch 03-11-2021
Public Assessment Report Public Assessment Report Dutch 15-06-2017
Patient Information leaflet Patient Information leaflet Polish 03-11-2021
Public Assessment Report Public Assessment Report Polish 15-06-2017
Patient Information leaflet Patient Information leaflet Portuguese 03-11-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 03-11-2021
Public Assessment Report Public Assessment Report Portuguese 15-06-2017
Patient Information leaflet Patient Information leaflet Romanian 03-11-2021
Public Assessment Report Public Assessment Report Romanian 15-06-2017
Patient Information leaflet Patient Information leaflet Slovak 03-11-2021
Public Assessment Report Public Assessment Report Slovak 15-06-2017
Patient Information leaflet Patient Information leaflet Slovenian 03-11-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 03-11-2021
Public Assessment Report Public Assessment Report Slovenian 15-06-2017
Patient Information leaflet Patient Information leaflet Finnish 03-11-2021
Public Assessment Report Public Assessment Report Finnish 15-06-2017
Patient Information leaflet Patient Information leaflet Swedish 03-11-2021
Public Assessment Report Public Assessment Report Swedish 15-06-2017
Patient Information leaflet Patient Information leaflet Norwegian 03-11-2021
Summary of Product characteristics Summary of Product characteristics Norwegian 03-11-2021
Patient Information leaflet Patient Information leaflet Icelandic 03-11-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 03-11-2021
Patient Information leaflet Patient Information leaflet Croatian 03-11-2021
Public Assessment Report Public Assessment Report Croatian 15-06-2017