Porcilis ColiClos

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

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

Available from:

Intervet International BV

ATC code:

QI09AB08

INN (International Name):

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

Therapeutic group:

Pigs

Therapeutic area:

Immunologicals

Therapeutic indications:

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.,

Product summary:

Revision: 5

Authorization status:

Authorised

Authorization date:

2012-06-14

Patient Information leaflet

                                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 
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                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
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 26-06-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 26-06-2020
Public Assessment Report Public Assessment Report Bulgarian 13-06-2013
Patient Information leaflet Patient Information leaflet Spanish 26-06-2020
Public Assessment Report Public Assessment Report Spanish 13-06-2013
Patient Information leaflet Patient Information leaflet Czech 26-06-2020
Public Assessment Report Public Assessment Report Czech 13-06-2013
Patient Information leaflet Patient Information leaflet Danish 26-06-2020
Public Assessment Report Public Assessment Report Danish 13-06-2013
Patient Information leaflet Patient Information leaflet German 26-06-2020
Public Assessment Report Public Assessment Report German 13-06-2013
Patient Information leaflet Patient Information leaflet Estonian 26-06-2020
Public Assessment Report Public Assessment Report Estonian 13-06-2013
Patient Information leaflet Patient Information leaflet Greek 26-06-2020
Public Assessment Report Public Assessment Report Greek 13-06-2013
Patient Information leaflet Patient Information leaflet French 26-06-2020
Public Assessment Report Public Assessment Report French 13-06-2013
Patient Information leaflet Patient Information leaflet Italian 26-06-2020
Public Assessment Report Public Assessment Report Italian 13-06-2013
Patient Information leaflet Patient Information leaflet Latvian 26-06-2020
Public Assessment Report Public Assessment Report Latvian 13-06-2013
Patient Information leaflet Patient Information leaflet Lithuanian 26-06-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 26-06-2020
Public Assessment Report Public Assessment Report Lithuanian 13-06-2013
Patient Information leaflet Patient Information leaflet Hungarian 26-06-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 26-06-2020
Public Assessment Report Public Assessment Report Hungarian 13-06-2013
Patient Information leaflet Patient Information leaflet Maltese 26-06-2020
Public Assessment Report Public Assessment Report Maltese 13-06-2013
Patient Information leaflet Patient Information leaflet Dutch 26-06-2020
Public Assessment Report Public Assessment Report Dutch 13-06-2013
Patient Information leaflet Patient Information leaflet Polish 26-06-2020
Public Assessment Report Public Assessment Report Polish 13-06-2013
Patient Information leaflet Patient Information leaflet Portuguese 26-06-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 26-06-2020
Public Assessment Report Public Assessment Report Portuguese 13-06-2013
Patient Information leaflet Patient Information leaflet Romanian 26-06-2020
Public Assessment Report Public Assessment Report Romanian 13-06-2013
Patient Information leaflet Patient Information leaflet Slovak 26-06-2020
Public Assessment Report Public Assessment Report Slovak 13-06-2013
Patient Information leaflet Patient Information leaflet Slovenian 26-06-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 26-06-2020
Public Assessment Report Public Assessment Report Slovenian 13-06-2013
Patient Information leaflet Patient Information leaflet Finnish 26-06-2020
Public Assessment Report Public Assessment Report Finnish 13-06-2013
Patient Information leaflet Patient Information leaflet Swedish 26-06-2020
Public Assessment Report Public Assessment Report Swedish 13-06-2013
Patient Information leaflet Patient Information leaflet Norwegian 26-06-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 26-06-2020
Patient Information leaflet Patient Information leaflet Icelandic 26-06-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 26-06-2020
Patient Information leaflet Patient Information leaflet Croatian 26-06-2020