Versican Plus Pi

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

canine parainfluenza type-2 virus, strain CPiV-2 Bio 15 (live attenuated)

Available from:

Zoetis Belgium SA

ATC code:

QI07AD08

INN (International Name):

canine parainfluenza virus

Therapeutic group:

Dogs

Therapeutic area:

Immunologicals for canidae, Live viral vaccines

Therapeutic indications:

Active immunisation of dogs from six weeks of age to prevent clinical signs (nasal and ocular discharge) and reduce viral excretion caused by canine parainfluenza virus.

Product summary:

Revision: 5

Authorization status:

Authorised

Authorization date:

2014-07-03

Patient Information leaflet

                                15
B. PACKAGE LEAFLET
16
PACKAGE LEAFLET:
VERSICAN PLUS PI LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION
FOR DOGS
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
BELGIUM
Manufacturer responsible for batch release:
Bioveta, a.s.,
Komenského 212,
683 23 Ivanovice na Hané,
CZECH REPUBLIC
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Versican Plus Pi lyophilisate and solvent for suspension for injection
for dogs
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Each dose of 1 ml contains:
ACTIVE SUBSTANCES:
LYOPHILISATE (LIVE ATTENUATED):
MINIMUM
MAXIMUM_ _
Canine parainfluenza Type 2 virus, strain CPiV-2 Bio 15
10
3.1
TCID
50
*
10
5.1
TCID
50
*
SOLVENT:
Water for injections (
_Aqua ad iniectabilia_
)
1ml
*
Tissue culture infectious dose 50%
Lyophilisate: spongy matter of white colour.
Solvent: clear colourless liquid.
4.
INDICATION(S)
Active immunisation of dogs from 6 weeks of age:
−
to prevent clinical signs (nasal and ocular discharge) and reduce
viral excretion caused by
canine parainfluenza virus.
Onset of immunity:
3 weeks after completion of the primary course.
17
Duration of immunity:
At least one year following the primary vaccination course.
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
A transient swelling (up to 5 cm) may commonly be observed at the
injection site following
subcutaneous administration in dogs. This can be painful, warm or
reddened. Any such swelling will
either have spontaneously resolved or be greatly diminished by 14 days
after vaccination.
Anorexia and decreased activity are rarely observed.
Hypersensitivity reactions (e.g. gastrointestinal signs such as
diarrhoea and vomiting, anaphylaxis,
angioedema, dyspnoea, circulatory shock, collapse) may occur rarely.
If such a reaction occurs,
appropriate treatment should be administered without delay. Such
reactions may evolve to
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Versican Plus Pi lyophilisate and solvent for suspension for injection
for dogs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each dose of 1 ml contains:
ACTIVE SUBSTANCES:
LYOPHILISATE (LIVE ATTENUATED):
MINIMUM
MAXIMUM_ _
Canine parainfluenza Type 2 virus, strain CPiV-2 Bio 15
10
3.1
TCID
50
*
10
5.1
TCID
50
*
SOLVENT:
Water for injections (
_Aqua ad iniectabilia_
)
1 ml
*
Tissue culture infectious dose 50%
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Lyophilisate and solvent for suspension for injection.
The visual appearance is as follows:
Lyophilisate: spongy matter of white colour.
Solvent: clear colourless liquid.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Active immunisation of dogs from 6 weeks of age:
−
to prevent clinical signs (nasal and ocular discharge) and reduce
viral excretion caused by
canine parainfluenza virus.
Onset of immunity:
3 weeks after completion of the primary course.
Duration of immunity:
At least one year following the primary vaccination course.
4.3
CONTRAINDICATIONS
None.
3
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
A good immune response is reliant on a fully competent immune system.
Immunocompetence of the
animal may be compromised by a variety of factors including poor
health, nutritional status, genetic
factors, concurrent drug therapy and stress.
Vaccinate healthy animals only.
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
The live attenuated virus vaccine strain CPiV may be shed by
vaccinated animals following
vaccination. However, due to the low pathogenicity of this strain, it
is not necessary to keep
vaccinated dogs separated from non-vaccinated dogs.
Special precautions to be taken by the person administering the
veterinary medicinal product to
animals
In case of accidental self-injection, seek medical advice immediately
and show the package leaflet or
the label to the
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 16-05-2019
Summary of Product characteristics Summary of Product characteristics Bulgarian 16-05-2019
Public Assessment Report Public Assessment Report Bulgarian 20-10-2014
Patient Information leaflet Patient Information leaflet Spanish 16-05-2019
Public Assessment Report Public Assessment Report Spanish 20-10-2014
Patient Information leaflet Patient Information leaflet Czech 16-05-2019
Public Assessment Report Public Assessment Report Czech 20-10-2014
Patient Information leaflet Patient Information leaflet Danish 16-05-2019
Public Assessment Report Public Assessment Report Danish 20-10-2014
Patient Information leaflet Patient Information leaflet German 16-05-2019
Public Assessment Report Public Assessment Report German 20-10-2014
Patient Information leaflet Patient Information leaflet Estonian 16-05-2019
Public Assessment Report Public Assessment Report Estonian 20-10-2014
Patient Information leaflet Patient Information leaflet Greek 16-05-2019
Public Assessment Report Public Assessment Report Greek 20-10-2014
Patient Information leaflet Patient Information leaflet French 16-05-2019
Public Assessment Report Public Assessment Report French 20-10-2014
Patient Information leaflet Patient Information leaflet Italian 16-05-2019
Public Assessment Report Public Assessment Report Italian 20-10-2014
Patient Information leaflet Patient Information leaflet Latvian 16-05-2019
Public Assessment Report Public Assessment Report Latvian 20-10-2014
Patient Information leaflet Patient Information leaflet Lithuanian 16-05-2019
Summary of Product characteristics Summary of Product characteristics Lithuanian 16-05-2019
Public Assessment Report Public Assessment Report Lithuanian 20-10-2014
Patient Information leaflet Patient Information leaflet Hungarian 16-05-2019
Summary of Product characteristics Summary of Product characteristics Hungarian 16-05-2019
Public Assessment Report Public Assessment Report Hungarian 20-10-2014
Patient Information leaflet Patient Information leaflet Maltese 16-05-2019
Public Assessment Report Public Assessment Report Maltese 20-10-2014
Patient Information leaflet Patient Information leaflet Dutch 16-05-2019
Public Assessment Report Public Assessment Report Dutch 20-10-2014
Patient Information leaflet Patient Information leaflet Polish 16-05-2019
Public Assessment Report Public Assessment Report Polish 20-10-2014
Patient Information leaflet Patient Information leaflet Portuguese 16-05-2019
Summary of Product characteristics Summary of Product characteristics Portuguese 16-05-2019
Public Assessment Report Public Assessment Report Portuguese 20-10-2014
Patient Information leaflet Patient Information leaflet Romanian 16-05-2019
Public Assessment Report Public Assessment Report Romanian 20-10-2014
Patient Information leaflet Patient Information leaflet Slovak 16-05-2019
Public Assessment Report Public Assessment Report Slovak 20-10-2014
Patient Information leaflet Patient Information leaflet Slovenian 16-05-2019
Summary of Product characteristics Summary of Product characteristics Slovenian 16-05-2019
Public Assessment Report Public Assessment Report Slovenian 20-10-2014
Patient Information leaflet Patient Information leaflet Finnish 16-05-2019
Public Assessment Report Public Assessment Report Finnish 20-10-2014
Patient Information leaflet Patient Information leaflet Swedish 16-05-2019
Public Assessment Report Public Assessment Report Swedish 20-10-2014
Patient Information leaflet Patient Information leaflet Norwegian 16-05-2019
Summary of Product characteristics Summary of Product characteristics Norwegian 16-05-2019
Patient Information leaflet Patient Information leaflet Icelandic 16-05-2019
Summary of Product characteristics Summary of Product characteristics Icelandic 16-05-2019
Patient Information leaflet Patient Information leaflet Croatian 16-05-2019
Public Assessment Report Public Assessment Report Croatian 20-10-2014

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