Nobilis IB Primo QX

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

live avian infectious bronchitis virus, strain D388

Available from:

Intervet International B.V.

ATC code:

QI01AD07

INN (International Name):

avian infectious bronchitis virus strain D388

Therapeutic group:

Chicken

Therapeutic area:

Live viral vaccines, Domestic fowl

Therapeutic indications:

For active immunisation of chickens in order to reduce respiratory signs of avian infectious bronchitis caused by QX-like variants of infectious bronchitis virus.

Product summary:

Revision: 5

Authorization status:

Authorised

Authorization date:

2014-09-04

Patient Information leaflet

                                16
MINIMUM PARTICULARS TO APPEAR ON SMALL IMMEDIATE PACKAGING UNITS
LABEL - LYOPHILISATE CUPS
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Nobilis IB Primo QX
2.
QUANTITY OF THE ACTIVE SUBSTANCE(S)
Live IBV, D388
3.
CONTENTS BY WEIGHT, BY VOLUME OR BY NUMBER OF DOSES
1,000 doses (3-100 spheres)
2,500 doses (3-100 spheres)
5,000 doses (3-100 spheres)
10,000 doses (3-400 spheres)
4.
ROUTE(S) OF ADMINISTRATION
See package leaflet.
5.
WITHDRAWAL PERIOD(S)
6.
BATCH NUMBER
Lot
7.
EXPIRY DATE
EXP
8.
THE WORDS “FOR ANIMAL TREATMENT ONLY”
For animal treatment only.
17
PARTICULARS TO APPEAR ON IMMEDIATE PACKAGING
LABEL - SOLVENT VIALS
1.
NAME OF THE VETERINARY PRODUCT
Solvent Oculo/Nasal
2.
CONTENTS BY WEIGHT, BY VOLUME OR BY NUMBER OF DOSES
35 ml
3.
ROUTE OF ADMINISTRATION
Read the vaccine package before use.
4.
STORAGE CONDITIONS
Store below 25 °C.
Do not freeze.
5.
BATCH NUMBER
Lot
6.
EXPIRY DATE
EXP
7.
THE WORDS “FOR ANIMAL TREATMENT ONLY”
For animal treatment only.
18
B. PACKAGE LEAFLET
19
PACKAGE LEAFLET:
NOBILIS IB PRIMO QX LYOPHILISATE AND SOLVENT FOR OCULONASAL SUSPENSION
FOR CHICKENS
NOBILIS IB PRIMO QX LYOPHILISATE FOR OCULONASAL SUSPENSION FOR
CHICKENS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder and manufacturer responsible for batch
release:
Intervet International B.V.
Wim de Körverstraat 35
5831 AN Boxmeer
The Netherlands
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Nobilis IB Primo QX lyophilisate and solvent for oculonasal suspension
for chickens
Nobilis IB Primo QX lyophilisate for oculonasal suspension for
chickens
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Each dose of reconstituted vaccine contains:
Live attenuated avian infectious bronchitis virus, strain D388: 10
4.0
– 10
5.5
EID
50
1
1
50% egg infective dose.
Lyophilisate: Off white, predominantly sphere shaped.
Solvent (Solvent Oculo/Nasal): blue-coloured solution.
4.
INDICATION(S)
For 
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Nobilis IB Primo QX lyophilisate and solvent for oculonasal suspension
for chickens
Nobilis IB Primo QX lyophilisate for oculonasal suspension for
chickens
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each dose of reconstituted vaccine contains:
ACTIVE SUBSTANCE:
Live attenuated avian infectious bronchitis virus, strain D388: 10
4.0
– 10
5.5
EID
50
1
1
50% egg infective dose
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Lyophilisate and solvent for oculonasal suspension
Lyophilisate for oculonasal suspension.
Lyophilisate: Off white, predominantly sphere shaped.
Solvent (Solvent Oculo/Nasal): blue-coloured solution.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Chickens.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For active immunisation of chickens in order to reduce respiratory
signs of avian infectious bronchitis
caused by QX-like variants of infectious bronchitis virus (IBV).
Onset of immunity: 3 weeks.
Duration of immunity: 8 weeks.
4.3
CONTRAINDICATIONS
None.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Vaccinate healthy animals only.
The vaccine virus is capable of spreading to in contact birds for a
minimum of 20 days after
vaccination and appropriate care should be taken to separate
vaccinated from non-vaccinated chickens.
Precautionary measures should be taken to prevent spreading to
wildlife. The premises must be
cleaned and disinfected after each production round.
This vaccine should only be used after it has been established that
the QX-like IBV variant strain is
epidemiologically relevant. It is important to avoid introduction of
the IB D388 vaccine virus into
premises in which the wild type strain is not present. The IB D388
vaccine should only be applied in
3
hatcheries to chickens from 1 day of age or older if adequate controls
are in place to avoid the spread
of the vaccine virus to birds that will be transported to non-IB QX
exposed flocks.
The vaccine has been demonstr
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 26-04-2021
Summary of Product characteristics Summary of Product characteristics Bulgarian 26-04-2021
Public Assessment Report Public Assessment Report Bulgarian 28-01-2021
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Public Assessment Report Public Assessment Report Latvian 28-01-2021
Patient Information leaflet Patient Information leaflet Lithuanian 26-04-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 26-04-2021
Public Assessment Report Public Assessment Report Lithuanian 28-01-2021
Patient Information leaflet Patient Information leaflet Hungarian 26-04-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 26-04-2021
Public Assessment Report Public Assessment Report Hungarian 28-01-2021
Patient Information leaflet Patient Information leaflet Maltese 26-04-2021
Public Assessment Report Public Assessment Report Maltese 28-01-2021
Patient Information leaflet Patient Information leaflet Dutch 26-04-2021
Public Assessment Report Public Assessment Report Dutch 28-01-2021
Patient Information leaflet Patient Information leaflet Polish 26-04-2021
Public Assessment Report Public Assessment Report Polish 28-01-2021
Patient Information leaflet Patient Information leaflet Portuguese 26-04-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 26-04-2021
Public Assessment Report Public Assessment Report Portuguese 28-01-2021
Patient Information leaflet Patient Information leaflet Romanian 26-04-2021
Public Assessment Report Public Assessment Report Romanian 28-01-2021
Patient Information leaflet Patient Information leaflet Slovak 26-04-2021
Public Assessment Report Public Assessment Report Slovak 28-01-2021
Patient Information leaflet Patient Information leaflet Slovenian 26-04-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 26-04-2021
Public Assessment Report Public Assessment Report Slovenian 28-01-2021
Patient Information leaflet Patient Information leaflet Finnish 26-04-2021
Public Assessment Report Public Assessment Report Finnish 28-01-2021
Patient Information leaflet Patient Information leaflet Swedish 26-04-2021
Public Assessment Report Public Assessment Report Swedish 28-01-2021
Patient Information leaflet Patient Information leaflet Norwegian 26-04-2021
Summary of Product characteristics Summary of Product characteristics Norwegian 26-04-2021
Patient Information leaflet Patient Information leaflet Icelandic 26-04-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 26-04-2021
Patient Information leaflet Patient Information leaflet Croatian 26-04-2021
Public Assessment Report Public Assessment Report Croatian 28-01-2021