Respiporc Flu3

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

inactivated influenza-A virus / swine

Available from:

CEVA Santé Animale

ATC code:

QI09AA03

INN (International Name):

inactivated influenza-A virus, swine

Therapeutic group:

Pigs

Therapeutic area:

Immunologicals

Therapeutic indications:

Active immunisation of pigs from the age of 56 days onwards, including pregnant sows, against swine influenza caused by subtypes H1N1, H3N2 and H1N2 to reduce clinical signs and viral lung load after infection.Onset of immunity: 7 days after primary vaccinationDuration of immunity: 4 months in pigs vaccinated between the age of 56 and 96 days and 6 months in pigs vaccinated for the first time at 96 days and above.Active immunisation of pregnant sows after finished primary immunisation by administration of a single dose 14 days prior to farrowing to develop high colostral immunity, which provides clinical protection of piglets for at least 33 days after birth.

Product summary:

Revision: 5

Authorization status:

Authorised

Authorization date:

2010-01-14

Patient Information leaflet

                                18
B. PACKAGE LEAFLET
19
PACKAGE LEAFLET:
RESPIPORC FLU3
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
Ceva Santé Animale
10 av. de La Ballastière
33500 Libourne
France
Manufacturer responsible for batch release:
IDT Biologika GmbH
Am Pharmapark
06861 Dessau-Rosslau
Germany
Ceva-Phylaxia Veterinary Biologicals Co. Ltd.
Szállás u. 5.
1107 Budapest
Hungary
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Respiporc FLU3 suspension for injection for pigs
3.
STATEMENT OF THE ACTIVE SUBSTANCES AND OTHER INGREDIENTS
Each dose of 2 ml contains:
ACTIVE SUBSTANCES:
Strains of inactivated Influenza A virus/swine/
Bakum/IDT1769/2003 (H3N2)
≥ 10.53 log
2
GMNU
1
Haselünne/IDT2617/2003 (H1N1)
≥ 10.22 log
2
GMNU
1
Bakum/1832/2000 (H1N2)
≥ 12.34 log
2
GMNU
1
1
GMNU = Geometric mean of neutralizing units induced in Guinea pigs
after twice immunisation with 0.5
ml of this vaccine
ADJUVANT:
Carbomer 971 P NF
2.0 mg
20
EXCIPIENT:
Thiomersal
0.21 mg
Clear, yellowish orange to pink coloured suspension for injection.
4.
INDICATION(S)
Active immunisation of pigs from the age of 56 days onwards including
pregnant sows against swine
influenza caused by subtypes H1N1, H3N2 and H1N2 to reduce clinical
signs and viral lung load after
infection.
Onset of immunity:
7 days after primary vaccination
Duration of immunity:
4 months in pigs vaccinated between the age of 56 and 96 days and
6 months in pigs vaccinated for the first time at 96 days and above.
Active immunisation of pregnant sows after finished primary
immunisation by administration of a single
dose 14 days prior to farrowing to develop high colostral immunity
which provides clinical protection of
piglets for at least 33 days after birth.
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
A transient slight swelling may occur on very rare occasions after
vaccination at the site of injection,
regressing within 2 days. On
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Respiporc FLU3 suspension for injection for pigs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each dose of 2 ml contains:
ACTIVE SUBSTANCES:
Strains of inactivated Influenza A virus/swine/
Bakum/IDT1769/2003 (H3N2)
≥ 10.53 log
2
GMNU
1
Haselünne/IDT2617/2003 (H1N1)
≥ 10.22 log
2
GMNU
1
Bakum/1832/2000 (H1N2)
≥ 12.34 log
2
GMNU
1
1
GMNU = Geometric mean of neutralizing units induced in Guinea pigs
after twice immunisation with
0.5 ml of this vaccine
ADJUVANT:
Carbomer 971 P NF
2.0 mg
EXCIPIENT:
Thiomersal
0.21 mg
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Clear, yellowish orange to pink coloured suspension for injection.
4.
CLINICAL PARTICULARS
4.1.
TARGET SPECIES
Pigs
4.2.
INDICATION FOR USE, SPECIFYING THE TARGET SPECIES
Active immunisation of pigs from the age of 56 days onwards including
pregnant sows against swine
influenza caused by subtypes H1N1, H3N2 and H1N2 to reduce clinical
signs and viral lung load after
infection.
Onset of immunity:
7 days after primary vaccination
Duration of immunity:
4 months in pigs vaccinated between the age of 56 and 96 days and
6 months in pigs vaccinated for the first time at 96 days and above.
3
Active immunisation of pregnant sows after finished primary
immunisation by administration of a single
dose 14 days prior to farrowing to develop high colostral immunity
which provides clinical protection of
piglets for at least 33 days after birth.
4.3.
CONTRAINDICATIONS
None.
4.4.
SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
4.5.
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
Not applicable.
Special precautions to be taken by the person administering the
veterinary medicinal product to animals
In case of accidental self-injection only a minor injection site
reaction is expected.
4.6.
ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
A transient slight swelling may occur on very rare occasions after
vaccination at the site of injection,
reg
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 18-09-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 18-09-2020
Public Assessment Report Public Assessment Report Bulgarian 16-02-2021
Patient Information leaflet Patient Information leaflet Spanish 18-09-2020
Public Assessment Report Public Assessment Report Spanish 16-02-2021
Patient Information leaflet Patient Information leaflet Czech 18-09-2020
Public Assessment Report Public Assessment Report Czech 16-02-2021
Patient Information leaflet Patient Information leaflet Danish 18-09-2020
Public Assessment Report Public Assessment Report Danish 16-02-2021
Patient Information leaflet Patient Information leaflet German 18-09-2020
Public Assessment Report Public Assessment Report German 16-02-2021
Patient Information leaflet Patient Information leaflet Estonian 18-09-2020
Public Assessment Report Public Assessment Report Estonian 16-02-2021
Patient Information leaflet Patient Information leaflet Greek 18-09-2020
Public Assessment Report Public Assessment Report Greek 16-02-2021
Patient Information leaflet Patient Information leaflet French 18-09-2020
Public Assessment Report Public Assessment Report French 16-02-2021
Patient Information leaflet Patient Information leaflet Italian 18-09-2020
Public Assessment Report Public Assessment Report Italian 16-02-2021
Patient Information leaflet Patient Information leaflet Latvian 18-09-2020
Public Assessment Report Public Assessment Report Latvian 16-02-2021
Patient Information leaflet Patient Information leaflet Lithuanian 18-09-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 18-09-2020
Public Assessment Report Public Assessment Report Lithuanian 16-02-2021
Patient Information leaflet Patient Information leaflet Hungarian 18-09-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 18-09-2020
Public Assessment Report Public Assessment Report Hungarian 16-02-2021
Patient Information leaflet Patient Information leaflet Maltese 18-09-2020
Public Assessment Report Public Assessment Report Maltese 16-02-2021
Patient Information leaflet Patient Information leaflet Dutch 18-09-2020
Public Assessment Report Public Assessment Report Dutch 16-02-2021
Patient Information leaflet Patient Information leaflet Polish 18-09-2020
Public Assessment Report Public Assessment Report Polish 16-02-2021
Patient Information leaflet Patient Information leaflet Portuguese 18-09-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 18-09-2020
Public Assessment Report Public Assessment Report Portuguese 16-02-2021
Patient Information leaflet Patient Information leaflet Romanian 18-09-2020
Public Assessment Report Public Assessment Report Romanian 16-02-2021
Patient Information leaflet Patient Information leaflet Slovak 18-09-2020
Public Assessment Report Public Assessment Report Slovak 16-02-2021
Patient Information leaflet Patient Information leaflet Slovenian 18-09-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 18-09-2020
Public Assessment Report Public Assessment Report Slovenian 16-02-2021
Patient Information leaflet Patient Information leaflet Finnish 18-09-2020
Public Assessment Report Public Assessment Report Finnish 16-02-2021
Patient Information leaflet Patient Information leaflet Swedish 18-09-2020
Public Assessment Report Public Assessment Report Swedish 16-02-2021
Patient Information leaflet Patient Information leaflet Norwegian 18-09-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 18-09-2020
Patient Information leaflet Patient Information leaflet Icelandic 18-09-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 18-09-2020
Patient Information leaflet Patient Information leaflet Croatian 18-09-2020
Public Assessment Report Public Assessment Report Croatian 16-02-2021

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