Parvoduk

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

live attenuated Muscovy duck parvovirus

Available from:

Merial

ATC code:

QI01BD03

INN (International Name):

live attenuated Muscovy duck parvovirus

Therapeutic group:

Ducks

Therapeutic area:

Immunologicals for aves, duck parvovirus, Live viral vaccines

Therapeutic indications:

Active immunisation of ducks to prevent mortality1 and to reduce weight loss and lesions of duck parvovirosis and Derzsy's disease.1In absence of maternally derived antibodies.

Product summary:

Revision: 2

Authorization status:

Withdrawn

Authorization date:

2014-04-11

Patient Information leaflet

                                Medicinal product no longer authorised
17
_ _
B. PACKAGE LEAFLET
Medicinal product no longer authorised
18
PACKAGE LEAFLET:
PARVODUK CONCENTRATE AND SOLVENT FOR SUSPENSION FOR INJECTION FOR
MUSCOVY DUCKS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
MERIAL
29 avenue Tony Garnier
69007 Lyon,
FRANCE
Manufacturer responsible for batch release:
MERIAL
Laboratory of Lyon Porte des Alpes
Rue de l’Aviation,
69800 Saint Priest
FRANCE
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Parvoduk concentrate and solvent for suspension for injection for
Muscovy ducks
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENTS
Each reconstituted dose of 0.2 ml contains:
Active substance:
Live attenuated Muscovy duck parvovirus strain GM 199
...................... 2.6–4.8 log
10
CCID
50
*
* Cell culture infectious dose 50%.
Concentrate and solvent for suspension for injection.
The concentrate is opalescent and homogeneous.
The solvent is clear and colourless.
4.
INDICATION(S)
Active immunisation of Muscovy ducks to reduce weight loss and lesions
of Muscovy duck
parvovirosis and Derzsy’s disease and, in the absence of maternally
derived antibodies, to also
prevent mortality.
Onset of immunity: 11 days after the primary vaccination course
Duration of immunity: 26 days after the primary vaccination course
The demonstrated duration of immunity protects the birds during the
period when they are most
susceptible to Muscovy duck parvovirosis and Derzsy’s disease.
Medicinal product no longer authorised
19
5.
CONTRAINDICATIONS
Do not use in birds in lay.
6.
ADVERSE REACTIONS
None.
If you notice any side effects, even those not already listed in this
package leaflet or you think that the
medicine has not worked, please inform your veterinary surgeon.
7.
TARGET SPECIES
Muscovy ducks.
8.
DOSAGE FOR EACH SPECIES, ROUTE(S) AND METHOD OF ADMINISTRATION
For subcutaneous use.
Administer one dose of 0.2 ml by s
                                
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Summary of Product characteristics

                                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
Parvoduk concentrate and solvent for suspension for injection for
Muscovy ducks
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each reconstituted dose of 0.2 ml contains:
ACTIVE SUBSTANCE:
Live attenuated Muscovy duck parvovirus strain GM 199
............................... 2.6–4.8 log
10
CCID
50
*
* Cell culture infectious dose 50%.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Concentrate and solvent for suspension for injection.
The concentrate is opalescent and homogeneous.
The solvent is clear and colourless.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Muscovy ducks.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Active immunisation of Muscovy ducks to reduce weight loss and lesions
of Muscovy duck
parvovirosis and Derzsy’s disease and, in the absence of maternally
derived antibodies, to also
prevent mortality.
Onset of immunity: 11 days after the primary vaccination course
Duration of immunity: 26 days after the primary vaccination course
The demonstrated duration of immunity protects the birds during the
period when they are most
susceptible to Muscovy duck parvovirosis and Derzsy’s disease.
4.3
CONTRAINDICATIONS
Do not use in birds in lay.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Vaccinate healthy animals only.
Medicinal product no longer authorised
3
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
The entire flock should be vaccinated to lower the risk of any
circulation of the vaccine strain and
virus recombination.
Special precautions to be taken by the person administering the
veterinary medicinal product to
animals
Not applicable.
4.6
ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
None.
4.7
USE DURING PREGNANCY, LACTATION OR LAY
Do not use in birds in lay (see section 4.3).
4.8
INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF
INTERACTION
No information is avail
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 15-04-2019
Summary of Product characteristics Summary of Product characteristics Bulgarian 15-04-2019
Public Assessment Report Public Assessment Report Bulgarian 15-04-2019
Patient Information leaflet Patient Information leaflet Spanish 15-04-2019
Public Assessment Report Public Assessment Report Spanish 15-04-2019
Patient Information leaflet Patient Information leaflet Czech 15-04-2019
Public Assessment Report Public Assessment Report Czech 15-04-2019
Patient Information leaflet Patient Information leaflet Danish 15-04-2019
Public Assessment Report Public Assessment Report Danish 15-04-2019
Patient Information leaflet Patient Information leaflet German 15-04-2019
Public Assessment Report Public Assessment Report German 15-04-2019
Patient Information leaflet Patient Information leaflet Estonian 15-04-2019
Public Assessment Report Public Assessment Report Estonian 15-04-2019
Patient Information leaflet Patient Information leaflet Greek 15-04-2019
Public Assessment Report Public Assessment Report Greek 15-04-2019
Patient Information leaflet Patient Information leaflet French 15-04-2019
Public Assessment Report Public Assessment Report French 15-04-2019
Patient Information leaflet Patient Information leaflet Italian 15-04-2019
Public Assessment Report Public Assessment Report Italian 15-04-2019
Patient Information leaflet Patient Information leaflet Latvian 15-04-2019
Public Assessment Report Public Assessment Report Latvian 15-04-2019
Patient Information leaflet Patient Information leaflet Lithuanian 15-04-2019
Summary of Product characteristics Summary of Product characteristics Lithuanian 15-04-2019
Public Assessment Report Public Assessment Report Lithuanian 15-04-2019
Patient Information leaflet Patient Information leaflet Hungarian 15-04-2019
Summary of Product characteristics Summary of Product characteristics Hungarian 15-04-2019
Public Assessment Report Public Assessment Report Hungarian 15-04-2019
Patient Information leaflet Patient Information leaflet Maltese 15-04-2019
Public Assessment Report Public Assessment Report Maltese 15-04-2019
Patient Information leaflet Patient Information leaflet Dutch 15-04-2019
Public Assessment Report Public Assessment Report Dutch 15-04-2019
Patient Information leaflet Patient Information leaflet Polish 15-04-2019
Public Assessment Report Public Assessment Report Polish 15-04-2019
Patient Information leaflet Patient Information leaflet Portuguese 15-04-2019
Summary of Product characteristics Summary of Product characteristics Portuguese 15-04-2019
Public Assessment Report Public Assessment Report Portuguese 15-04-2019
Patient Information leaflet Patient Information leaflet Romanian 15-04-2019
Public Assessment Report Public Assessment Report Romanian 15-04-2019
Patient Information leaflet Patient Information leaflet Slovak 15-04-2019
Public Assessment Report Public Assessment Report Slovak 15-04-2019
Patient Information leaflet Patient Information leaflet Slovenian 15-04-2019
Summary of Product characteristics Summary of Product characteristics Slovenian 15-04-2019
Public Assessment Report Public Assessment Report Slovenian 15-04-2019
Patient Information leaflet Patient Information leaflet Finnish 15-04-2019
Public Assessment Report Public Assessment Report Finnish 15-04-2019
Patient Information leaflet Patient Information leaflet Swedish 15-04-2019
Public Assessment Report Public Assessment Report Swedish 15-04-2019
Patient Information leaflet Patient Information leaflet Norwegian 15-04-2019
Summary of Product characteristics Summary of Product characteristics Norwegian 15-04-2019
Patient Information leaflet Patient Information leaflet Icelandic 15-04-2019
Summary of Product characteristics Summary of Product characteristics Icelandic 15-04-2019
Patient Information leaflet Patient Information leaflet Croatian 15-04-2019
Public Assessment Report Public Assessment Report Croatian 15-04-2019

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