Nobilis OR Inac

Nazione: Unione Europea

Lingua: inglese

Fonte: EMA (European Medicines Agency)

Compra

Foglio illustrativo Foglio illustrativo (PIL)
01-10-2022
Scheda tecnica Scheda tecnica (SPC)
01-10-2022

Principio attivo:

inactivated whole cell suspension of Ornithobacterium rhinotracheale serotype A, strain B3263/91

Commercializzato da:

Intervet International BV

Codice ATC:

QI01AB07

INN (Nome Internazionale):

adjuvanted inactivated vaccine against Ornithobacterium rhinotracheale serotype A

Gruppo terapeutico:

Chicken

Area terapeutica:

Immunologicals for aves

Indicazioni terapeutiche:

For passive immunisation of broilers induced by active immunisation of female broiler breeders to reduce infection with Ornithobacterium rhinotracheale serotype A when this agent is involved. Under field conditions passive immunity is transferred during lay for 43 weeks after the last vaccination of broiler breeders, resulting in a duration of passive immunity in broilers of at least 14 days after hatching.,

Dettagli prodotto:

Revision: 7

Stato dell'autorizzazione:

Withdrawn

Data dell'autorizzazione:

2003-01-24

Foglio illustrativo

                                Medicinal product no longer authorised
15
B. PACKAGE LEAFLET
Medicinal product no longer authorised
16
PACKAGE LEAFLET
Nobilis OR inac emulsion for injection for chickens
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE IN THE EEA
Marketing authorisation holder and manufacturer:
Intervet International
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Nobilis OR inac emulsion for injection for chickens
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Per dose of 0.25 ml:
Inactivated whole cell suspension of _Ornithobacterium rhinotracheale_
serotype A strain B3263/91 1 x
10
7
cells *
* inducing a mean titre in the chickens of the potency test of at
least 11.2 (log
2
).
Light liquid paraffin: 107.21 mg
Traces of formaldehyde
4.
INDICATION(S)
For passive immunisation of broilers induced by active immunisation of
female broiler breeders to
reduce infection with _Ornithobacterium rhinotracheale_ serotype A
when this agent is involved.
Under field conditions passive immunity is transferred during lay for
43 weeks after the last
vaccination of broiler breeders, resulting in a duration of passive
immunity in broilers of at least 14
days after hatching.
5.
CONTRAINDICATIONS
Do not use for birds in lay
6.
ADVERSE REACTIONS
In laboratory studies, a local transient swelling was found at post
mortem examination in up to 40% of
the birds for at least 14 days after subcutaneous vaccination. Under
field conditions, sporadic local and
systemic clinical reactions have been reported.
If you notice any serious effects or other effects not mentioned in
this leaflet, please inform your
veterinary surgeon.
Medicinal product no longer authorised
17
7.
TARGET SPECIES
Chickens
8.
DOSAGE FOR EACH SPECIES, ROUTE(S) AND METHOD OF ADMINISTRATION
Single dose of 0.25 ml.
Subcutaneous injection in the neck or intramuscular injection in the
breast of the chicken.
9.
ADVICE ON CORRECT ADMINISTRATION

                                
                                Leggi il documento completo
                                
                            

Scheda tecnica

                                Medicinal product no longer authorised
1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Nobilis OR inac emulsion for injection for chickens
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Per dose of 0.25 ml:
ACTIVE SUBSTANCE
Inactivated whole cell suspension of _Ornithobacterium rhinotracheale_
serotype A, strain B3263/91 1 x
10
7
cells *
* inducing a mean titre in the chickens of the potency test of at
least 11.2 (log
2
).
ADJUVANT
Light liquid paraffin:
107.21 mg
EXCIPIENTS
Traces of formaldehyde
For a list of excipients, see section 6.1
3.
PHARMACEUTICAL FORM
Emulsion for injection
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Chickens
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For passive immunisation of broilers induced by active immunisation of
female broiler breeders to
reduce infection with _Ornithobacterium rhinotracheale_ serotype A
when this agent is involved.
Under field conditions passive immunity is transferred during lay for
43 weeks after the last
vaccination of broiler breeders, resulting in a duration of passive
immunity in broilers of at least 14
days after hatching.
4.3
CONTRAINDICATIONS
Do not use in birds in lay.
4.4
SPECIAL WARNINGS
None
Medicinal product no longer authorised
3
4.5
SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
Allow vaccine to reach room temperature (15-25°C) before using the
vaccine.
Shake well before use.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE
VETERINARY MEDICINAL PRODUCT TO
ANIMALS
To the user:
This product contains mineral oil. Accidental injection/self injection
may result in severe pain and
swelling, particularly if injected into a joint or finger, and in rare
cases could result in the loss of the
affected finger if prompt medical attention is not given.
If you are accidentally injected with this product, seek prompt
medical advice even if only a very
small amount is injected and take the package insert with you.
If pain persists for mo
                                
                                Leggi il documento completo
                                
                            

Documenti in altre lingue

Foglio illustrativo Foglio illustrativo bulgaro 01-10-2022
Scheda tecnica Scheda tecnica bulgaro 01-10-2022
Foglio illustrativo Foglio illustrativo spagnolo 01-10-2022
Scheda tecnica Scheda tecnica spagnolo 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione spagnolo 03-10-2022
Foglio illustrativo Foglio illustrativo ceco 01-10-2022
Scheda tecnica Scheda tecnica ceco 01-10-2022
Foglio illustrativo Foglio illustrativo danese 01-10-2022
Scheda tecnica Scheda tecnica danese 01-10-2022
Foglio illustrativo Foglio illustrativo tedesco 01-10-2022
Scheda tecnica Scheda tecnica tedesco 01-10-2022
Foglio illustrativo Foglio illustrativo estone 01-10-2022
Scheda tecnica Scheda tecnica estone 01-10-2022
Foglio illustrativo Foglio illustrativo greco 01-10-2022
Scheda tecnica Scheda tecnica greco 01-10-2022
Foglio illustrativo Foglio illustrativo francese 01-10-2022
Scheda tecnica Scheda tecnica francese 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione francese 03-10-2022
Foglio illustrativo Foglio illustrativo italiano 01-10-2022
Scheda tecnica Scheda tecnica italiano 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione italiano 03-10-2022
Foglio illustrativo Foglio illustrativo lettone 01-10-2022
Scheda tecnica Scheda tecnica lettone 01-10-2022
Foglio illustrativo Foglio illustrativo lituano 01-10-2022
Scheda tecnica Scheda tecnica lituano 01-10-2022
Foglio illustrativo Foglio illustrativo ungherese 01-10-2022
Scheda tecnica Scheda tecnica ungherese 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione ungherese 03-10-2022
Foglio illustrativo Foglio illustrativo maltese 01-10-2022
Scheda tecnica Scheda tecnica maltese 01-10-2022
Foglio illustrativo Foglio illustrativo olandese 01-10-2022
Scheda tecnica Scheda tecnica olandese 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione olandese 03-10-2022
Foglio illustrativo Foglio illustrativo polacco 01-10-2022
Scheda tecnica Scheda tecnica polacco 01-10-2022
Foglio illustrativo Foglio illustrativo portoghese 01-10-2022
Scheda tecnica Scheda tecnica portoghese 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione portoghese 03-10-2022
Foglio illustrativo Foglio illustrativo rumeno 01-10-2022
Scheda tecnica Scheda tecnica rumeno 01-10-2022
Foglio illustrativo Foglio illustrativo slovacco 01-10-2022
Scheda tecnica Scheda tecnica slovacco 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione slovacco 03-10-2022
Foglio illustrativo Foglio illustrativo sloveno 01-10-2022
Scheda tecnica Scheda tecnica sloveno 01-10-2022
Foglio illustrativo Foglio illustrativo finlandese 01-10-2022
Scheda tecnica Scheda tecnica finlandese 01-10-2022
Relazione pubblica di valutazione Relazione pubblica di valutazione finlandese 03-10-2022
Foglio illustrativo Foglio illustrativo svedese 01-10-2022
Scheda tecnica Scheda tecnica svedese 01-10-2022

Visualizza cronologia documenti