Respiporc Flu3

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Bipacksedel Bipacksedel (PIL)
18-09-2020
Produktens egenskaper Produktens egenskaper (SPC)
18-09-2020

Aktiva substanser:

inactivated influenza-A virus / swine

Tillgänglig från:

CEVA Santé Animale

ATC-kod:

QI09AA03

INN (International namn):

inactivated influenza-A virus, swine

Terapeutisk grupp:

Pigs

Terapiområde:

Immunologicals

Terapeutiska indikationer:

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.

Produktsammanfattning:

Revision: 5

Bemyndigande status:

Authorised

Tillstånd datum:

2010-01-14

Bipacksedel

                                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
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                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
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 18-09-2020
Produktens egenskaper Produktens egenskaper bulgariska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 16-02-2021
Bipacksedel Bipacksedel spanska 18-09-2020
Produktens egenskaper Produktens egenskaper spanska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 16-02-2021
Bipacksedel Bipacksedel tjeckiska 18-09-2020
Produktens egenskaper Produktens egenskaper tjeckiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 16-02-2021
Bipacksedel Bipacksedel danska 18-09-2020
Produktens egenskaper Produktens egenskaper danska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 16-02-2021
Bipacksedel Bipacksedel tyska 18-09-2020
Produktens egenskaper Produktens egenskaper tyska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 16-02-2021
Bipacksedel Bipacksedel estniska 18-09-2020
Produktens egenskaper Produktens egenskaper estniska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 16-02-2021
Bipacksedel Bipacksedel grekiska 18-09-2020
Produktens egenskaper Produktens egenskaper grekiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 16-02-2021
Bipacksedel Bipacksedel franska 18-09-2020
Produktens egenskaper Produktens egenskaper franska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 16-02-2021
Bipacksedel Bipacksedel italienska 18-09-2020
Produktens egenskaper Produktens egenskaper italienska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 16-02-2021
Bipacksedel Bipacksedel lettiska 18-09-2020
Produktens egenskaper Produktens egenskaper lettiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 16-02-2021
Bipacksedel Bipacksedel litauiska 18-09-2020
Produktens egenskaper Produktens egenskaper litauiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 16-02-2021
Bipacksedel Bipacksedel ungerska 18-09-2020
Produktens egenskaper Produktens egenskaper ungerska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 16-02-2021
Bipacksedel Bipacksedel maltesiska 18-09-2020
Produktens egenskaper Produktens egenskaper maltesiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 16-02-2021
Bipacksedel Bipacksedel nederländska 18-09-2020
Produktens egenskaper Produktens egenskaper nederländska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 16-02-2021
Bipacksedel Bipacksedel polska 18-09-2020
Produktens egenskaper Produktens egenskaper polska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 16-02-2021
Bipacksedel Bipacksedel portugisiska 18-09-2020
Produktens egenskaper Produktens egenskaper portugisiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 16-02-2021
Bipacksedel Bipacksedel rumänska 18-09-2020
Produktens egenskaper Produktens egenskaper rumänska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 16-02-2021
Bipacksedel Bipacksedel slovakiska 18-09-2020
Produktens egenskaper Produktens egenskaper slovakiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 16-02-2021
Bipacksedel Bipacksedel slovenska 18-09-2020
Produktens egenskaper Produktens egenskaper slovenska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 16-02-2021
Bipacksedel Bipacksedel finska 18-09-2020
Produktens egenskaper Produktens egenskaper finska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 16-02-2021
Bipacksedel Bipacksedel svenska 18-09-2020
Produktens egenskaper Produktens egenskaper svenska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 16-02-2021
Bipacksedel Bipacksedel norska 18-09-2020
Produktens egenskaper Produktens egenskaper norska 18-09-2020
Bipacksedel Bipacksedel isländska 18-09-2020
Produktens egenskaper Produktens egenskaper isländska 18-09-2020
Bipacksedel Bipacksedel kroatiska 18-09-2020
Produktens egenskaper Produktens egenskaper kroatiska 18-09-2020
Offentlig bedömningsrapport Offentlig bedömningsrapport kroatiska 16-02-2021

Visa dokumenthistorik