Suvaxyn Circo+MH RTU

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
03-11-2021
Ciri produk Ciri produk (SPC)
03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
15-06-2017

Bahan aktif:

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

Boleh didapati daripada:

Zoetis Belgium SA

Kod ATC:

QI09AL

INN (Nama Antarabangsa):

Porcine circovirus and porcine enzootic pneumonia vaccine (inactivated)

Kumpulan terapeutik:

Pigs

Kawasan terapeutik:

Inactivated viral and inactivated bacterial vaccines

Tanda-tanda terapeutik:

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.

Ringkasan produk:

Revision: 7

Status kebenaran:

Authorised

Tarikh kebenaran:

2015-11-06

Risalah maklumat

                                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
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                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
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 03-11-2021
Ciri produk Ciri produk Bulgaria 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 15-06-2017
Risalah maklumat Risalah maklumat Sepanyol 03-11-2021
Ciri produk Ciri produk Sepanyol 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 15-06-2017
Risalah maklumat Risalah maklumat Czech 03-11-2021
Ciri produk Ciri produk Czech 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Czech 15-06-2017
Risalah maklumat Risalah maklumat Denmark 03-11-2021
Ciri produk Ciri produk Denmark 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 15-06-2017
Risalah maklumat Risalah maklumat Jerman 03-11-2021
Ciri produk Ciri produk Jerman 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 15-06-2017
Risalah maklumat Risalah maklumat Estonia 03-11-2021
Ciri produk Ciri produk Estonia 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 15-06-2017
Risalah maklumat Risalah maklumat Greek 03-11-2021
Ciri produk Ciri produk Greek 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Greek 15-06-2017
Risalah maklumat Risalah maklumat Perancis 03-11-2021
Ciri produk Ciri produk Perancis 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 15-06-2017
Risalah maklumat Risalah maklumat Itali 03-11-2021
Ciri produk Ciri produk Itali 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Itali 15-06-2017
Risalah maklumat Risalah maklumat Latvia 03-11-2021
Ciri produk Ciri produk Latvia 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 15-06-2017
Risalah maklumat Risalah maklumat Lithuania 03-11-2021
Ciri produk Ciri produk Lithuania 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 15-06-2017
Risalah maklumat Risalah maklumat Hungary 03-11-2021
Ciri produk Ciri produk Hungary 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 15-06-2017
Risalah maklumat Risalah maklumat Malta 03-11-2021
Ciri produk Ciri produk Malta 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Malta 15-06-2017
Risalah maklumat Risalah maklumat Belanda 03-11-2021
Ciri produk Ciri produk Belanda 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 15-06-2017
Risalah maklumat Risalah maklumat Poland 03-11-2021
Ciri produk Ciri produk Poland 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Poland 15-06-2017
Risalah maklumat Risalah maklumat Portugis 03-11-2021
Ciri produk Ciri produk Portugis 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 15-06-2017
Risalah maklumat Risalah maklumat Romania 03-11-2021
Ciri produk Ciri produk Romania 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Romania 15-06-2017
Risalah maklumat Risalah maklumat Slovak 03-11-2021
Ciri produk Ciri produk Slovak 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 15-06-2017
Risalah maklumat Risalah maklumat Slovenia 03-11-2021
Ciri produk Ciri produk Slovenia 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 15-06-2017
Risalah maklumat Risalah maklumat Finland 03-11-2021
Ciri produk Ciri produk Finland 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Finland 15-06-2017
Risalah maklumat Risalah maklumat Sweden 03-11-2021
Ciri produk Ciri produk Sweden 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 15-06-2017
Risalah maklumat Risalah maklumat Norway 03-11-2021
Ciri produk Ciri produk Norway 03-11-2021
Risalah maklumat Risalah maklumat Iceland 03-11-2021
Ciri produk Ciri produk Iceland 03-11-2021
Risalah maklumat Risalah maklumat Croat 03-11-2021
Ciri produk Ciri produk Croat 03-11-2021
Laporan Penilaian Awam Laporan Penilaian Awam Croat 15-06-2017