Respiporc Flu3

Pays: Union européenne

Langue: anglais

Source: EMA (European Medicines Agency)

Achète-le

Ingrédients actifs:

inactivated influenza-A virus / swine

Disponible depuis:

CEVA Santé Animale

Code ATC:

QI09AA03

DCI (Dénomination commune internationale):

inactivated influenza-A virus, swine

Groupe thérapeutique:

Pigs

Domaine thérapeutique:

Immunologicals

indications thérapeutiques:

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.

Descriptif du produit:

Revision: 5

Statut de autorisation:

Authorised

Date de l'autorisation:

2010-01-14

Notice patient

                                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
                                
                                Lire le document complet
                                
                            

Résumé des caractéristiques du produit

                                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
                                
                                Lire le document complet
                                
                            

Documents dans d'autres langues

Notice patient Notice patient bulgare 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation bulgare 16-02-2021
Notice patient Notice patient espagnol 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation espagnol 16-02-2021
Notice patient Notice patient tchèque 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation tchèque 16-02-2021
Notice patient Notice patient danois 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation danois 16-02-2021
Notice patient Notice patient allemand 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation allemand 16-02-2021
Notice patient Notice patient estonien 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation estonien 16-02-2021
Notice patient Notice patient grec 18-09-2020
Notice patient Notice patient français 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation français 16-02-2021
Notice patient Notice patient italien 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation italien 16-02-2021
Notice patient Notice patient letton 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation letton 16-02-2021
Notice patient Notice patient lituanien 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation lituanien 16-02-2021
Notice patient Notice patient hongrois 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation hongrois 16-02-2021
Notice patient Notice patient maltais 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation maltais 16-02-2021
Notice patient Notice patient néerlandais 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation néerlandais 16-02-2021
Notice patient Notice patient polonais 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation polonais 16-02-2021
Notice patient Notice patient portugais 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation portugais 16-02-2021
Notice patient Notice patient roumain 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation roumain 16-02-2021
Notice patient Notice patient slovaque 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation slovaque 16-02-2021
Notice patient Notice patient slovène 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation slovène 16-02-2021
Notice patient Notice patient finnois 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation finnois 16-02-2021
Notice patient Notice patient suédois 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation suédois 16-02-2021
Notice patient Notice patient norvégien 18-09-2020
Notice patient Notice patient islandais 18-09-2020
Notice patient Notice patient croate 18-09-2020
Rapport public d'évaluation Rapport public d'évaluation croate 16-02-2021

Rechercher des alertes liées à ce produit

Afficher l'historique des documents