Porcilis ColiClos

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Risalah maklumat Risalah maklumat (PIL)
26-06-2020
Ciri produk Ciri produk (SPC)
26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam (PAR)
13-06-2013

Bahan aktif:

Clostridium perfringens type C / Escherichia coli F4ab / E. coli F4ac / E. coli F5 / E. coli F6 / E. coli LT

Boleh didapati daripada:

Intervet International BV

Kod ATC:

QI09AB08

INN (Nama Antarabangsa):

vaccine to provide passive immunity to the progeny against Escherichia coli and Clostridium perfringens in pigs

Kumpulan terapeutik:

Pigs

Kawasan terapeutik:

Immunologicals

Tanda-tanda terapeutik:

For the passive immunisation of progeny by active immunisation of sows and gilts to reduce mortality and clinical signs during the first days of life, caused by those Escherichia coli strains which express the adhesins F4ab (K88ab), F4ac (K88ac), F5 (K99) or F6 (987P) and caused by Clostridium perfringens type C.,

Ringkasan produk:

Revision: 5

Status kebenaran:

Authorised

Tarikh kebenaran:

2012-06-14

Risalah maklumat

                                16
B. PACKAGE LEAFLET
17
PACKAGE LEAFLET:
PORCILIS COLICLOS 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:
Intervet International B.V.
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands
Manufacturer(s) responsible for batch release:
Intervet International B.V.
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands
MSD Animal Health UK Ltd
Walton Manor, Walton, Milton Keynes
Buckinghamshire, MK7 7AJ, UK
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Porcilis ColiClos suspension for injection for pigs
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENTS
Each dose of 2 ml contains:
ACTIVE SUBSTANCES:
_Escherichia coli _
components:
- F4ab fimbrial adhesin

9.7 log
2
Ab titre
1
- F4ac fimbrial adhesin

8.1 log
2
Ab titre
1
- F5 fimbrial adhesin

8.4 log
2
Ab titre
1
- F6 fimbrial adhesin

7.8 log
2
Ab titre
1
- LT toxoid

10.9 log
2
Ab titre
1
_Clostridium perfringens_
component:
- Type C (strain 578) beta toxoid
≥20 IU
2
1
Mean antibody titre (Ab) obtained after vaccination of mice with a
1/20 or 1/40 sow dose
2
International units of beta antitoxin according to Ph. Eur.
ADJUVANT:
dl-

-tocopheryl acetate
150 mg
Aqueous, white to nearly white suspension for injection.
4.
INDICATION(S)
18
For the passive immunisation of progeny by active immunisation of sows
and gilts to reduce mortality
and clinical signs during the first days of life, caused by those
_E. coli_
strains, which express the
adhesins F4ab (K88ab), F4ac (K88ac), F5 (K99) or F6 (987P) and caused
by
_C. perfringens_
type C.
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
_In laboratory studies and field trials: _
An increase in body temperature up to 2°C was very commonly observed
on the day of vaccination.
Reduced activity and lack of appetite on the day of vaccination
commonly occurred and/or a
sometimes painful and hard swelling up to 10 cm diameter for up 
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Porcilis ColiClos suspension for injection for pigs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each dose of 2 ml contains:
ACTIVE SUBSTANCES:
_Escherichia coli _
components:
- F4ab fimbrial adhesin

9.7 log
2
Ab titre
1
- F4ac fimbrial adhesin

8.1 log
2
Ab titre
1
- F5 fimbrial adhesin

8.4 log
2
Ab titre
1
- F6 fimbrial adhesin

7.8 log
2
Ab titre
1
- LT toxoid

10.9 log
2
Ab titre
1
_Clostridium perfringens_
component:
- Type C (strain 578) beta toxoid
≥20 IU
2
1
Mean antibody titre (Ab) obtained after vaccination of mice with a
1/20 or 1/40 sow dose
2
International units of beta antitoxin according to Ph. Eur.
ADJUVANT:
dl-

-tocopheryl acetate
150 mg
For the full list of excipients, see section 6.1
3.
PHARMACEUTICAL FORM
Suspension for injection.
Aqueous, white to nearly white.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Pigs (sows and gilts)
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the passive immunisation of progeny by active immunisation of sows
and gilts to reduce mortality
and clinical signs during the first days of life, caused by those
_E. coli_
strains, which express the
adhesins F4ab (K88ab), F4ac (K88ac), F5 (K99) or F6 (987P) and caused
by
_C. perfringens_
type C.
4.3
CONTRAINDICATIONS
None.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Vaccinate healthy animals only.
3
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
Protection of piglets is achieved by colostrum intake. Therefore, care
should be taken to ensure that
each piglet ingests a sufficient quantity of colostrum.
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)
_In laboratory studies and field trials: _
An increase in body temperature up to 2°C was very commo
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 26-06-2020
Ciri produk Ciri produk Bulgaria 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 13-06-2013
Risalah maklumat Risalah maklumat Sepanyol 26-06-2020
Ciri produk Ciri produk Sepanyol 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 13-06-2013
Risalah maklumat Risalah maklumat Czech 26-06-2020
Ciri produk Ciri produk Czech 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Czech 13-06-2013
Risalah maklumat Risalah maklumat Denmark 26-06-2020
Ciri produk Ciri produk Denmark 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 13-06-2013
Risalah maklumat Risalah maklumat Jerman 26-06-2020
Ciri produk Ciri produk Jerman 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 13-06-2013
Risalah maklumat Risalah maklumat Estonia 26-06-2020
Ciri produk Ciri produk Estonia 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 13-06-2013
Risalah maklumat Risalah maklumat Greek 26-06-2020
Ciri produk Ciri produk Greek 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Greek 13-06-2013
Risalah maklumat Risalah maklumat Perancis 26-06-2020
Ciri produk Ciri produk Perancis 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 13-06-2013
Risalah maklumat Risalah maklumat Itali 26-06-2020
Ciri produk Ciri produk Itali 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Itali 13-06-2013
Risalah maklumat Risalah maklumat Latvia 26-06-2020
Ciri produk Ciri produk Latvia 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 13-06-2013
Risalah maklumat Risalah maklumat Lithuania 26-06-2020
Ciri produk Ciri produk Lithuania 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 13-06-2013
Risalah maklumat Risalah maklumat Hungary 26-06-2020
Ciri produk Ciri produk Hungary 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 13-06-2013
Risalah maklumat Risalah maklumat Malta 26-06-2020
Ciri produk Ciri produk Malta 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Malta 13-06-2013
Risalah maklumat Risalah maklumat Belanda 26-06-2020
Ciri produk Ciri produk Belanda 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 13-06-2013
Risalah maklumat Risalah maklumat Poland 26-06-2020
Ciri produk Ciri produk Poland 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Poland 13-06-2013
Risalah maklumat Risalah maklumat Portugis 26-06-2020
Ciri produk Ciri produk Portugis 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 13-06-2013
Risalah maklumat Risalah maklumat Romania 26-06-2020
Ciri produk Ciri produk Romania 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Romania 13-06-2013
Risalah maklumat Risalah maklumat Slovak 26-06-2020
Ciri produk Ciri produk Slovak 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 13-06-2013
Risalah maklumat Risalah maklumat Slovenia 26-06-2020
Ciri produk Ciri produk Slovenia 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 13-06-2013
Risalah maklumat Risalah maklumat Finland 26-06-2020
Ciri produk Ciri produk Finland 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Finland 13-06-2013
Risalah maklumat Risalah maklumat Sweden 26-06-2020
Ciri produk Ciri produk Sweden 26-06-2020
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 13-06-2013
Risalah maklumat Risalah maklumat Norway 26-06-2020
Ciri produk Ciri produk Norway 26-06-2020
Risalah maklumat Risalah maklumat Iceland 26-06-2020
Ciri produk Ciri produk Iceland 26-06-2020
Risalah maklumat Risalah maklumat Croat 26-06-2020
Ciri produk Ciri produk Croat 26-06-2020