Purevax RC

Land: Europeiska unionen

Språk: engelska

Källa: EMA (European Medicines Agency)

Köp det nu

Bipacksedel Bipacksedel (PIL)
29-03-2022
Produktens egenskaper Produktens egenskaper (SPC)
29-03-2022

Aktiva substanser:

attenuated feline rhinotracheitis herpesvirus (FHV F2 strain), inactivated feline calicivirosis antigens (FCV 431 and G1 strains)

Tillgänglig från:

Boehringer Ingelheim Vetmedica GmbH

ATC-kod:

QI06AH08

INN (International namn):

vaccine against feline viral rhinotracheitis and feline calicivirosis

Terapeutisk grupp:

Cats

Terapiområde:

Immunologicals for felidae,

Terapeutiska indikationer:

Active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs.Onsets of immunity isone week after primary vaccination course.The duration of immunity is one year after primary vaccination course and three years after the last re-vaccination.

Produktsammanfattning:

Revision: 16

Bemyndigande status:

Authorised

Tillstånd datum:

2005-02-23

Bipacksedel

                                14
B. PACKAGE LEAFLET
15
PACKAGE LEAFLET
PUREVAX RC LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
GERMANY
Manufacturing authorisation holder responsible for batch release:
Boehringer Ingelheim Animal Health France SCS
Laboratoire Porte des Alpes
Rue de l'Aviation
69800 Saint Priest
FRANCE
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Purevax RC lyophilisate and solvent for suspension for injection.
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Per dose of 1 ml or 0.5 ml:
ACTIVE SUBSTANCES:
LYOPHILISATE:
Attenuated feline rhinotracheitis herpesvirus (FHV F2 strain)
.......................................
≥
10
4.9
CCID
50
1
Inactivated feline calicivirus (FCV 431 and FCV G1 strains) antigens
..........................
≥
2.0 ELISA U.
EXCIPIENT:
Gentamicin, at most
.......................................................................................................................
16.5 µg
SOLVENT:
Water for
injection.......................................................................................................
q.s. 1 ml or 0.5 ml.
1
cell culture infective dose 50%.
Lyophilisate: homogeneous beige pellet.
Solvent: clear colourless liquid.
4.
INDICATION(S)
Active immunisation of cats aged 8 weeks and older:
-
against feline viral rhinotracheitis to reduce clinical signs,
-
against calicivirus infection to reduce clinical signs.
Onsets of immunity: 1 week after primary vaccination course.
Duration of immunity: 1 year after primary vaccination course and 3
years after the last re-vaccination.
16
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
Transient apathy and anorexia as well as hyperthermia (lasting usually
for 1or 2 days) were commonly
observed during safety and field studies. A local reaction (slight
pain at palpation, itching or limited
oede
                                
                                Läs hela dokumentet
                                
                            

Produktens egenskaper

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Purevax RC lyophilisate and solvent for suspension for injection
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Per dose of 1 ml or 0.5 ml:
Lyophilisate:
ACTIVE SUBSTANCES:
Attenuated feline rhinotracheitis herpesvirus (FHV F2 strain)
.......................................
≥
10
4.9
CCID
50
1
Inactivated feline calicivirus (FCV 431 and G1 strains) antigens
..................................
≥
2.0 ELISA U.
EXCIPIENT:
Gentamicin, at most
.......................................................................................................................
16.5 µg
Solvent:
Water for injections
.....................................................................................................
q.s. 1 ml or 0.5 ml.
1
cell culture infective dose 50%
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Lyophilisate and solvent for suspension for injection.
Lyophilisate: homogeneous beige pellet.
Solvent: clear colourless liquid.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Cats.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Active immunisation of cats aged 8 weeks and older:
-
against feline viral rhinotracheitis to reduce clinical signs,
-
against calicivirus infection to reduce clinical signs.
Onsets of immunity: 1week after primary vaccination course.
Duration of immunity: 1 year after primary vaccination course and 3
years after the last re-vaccination.
4.3
CONTRAINDICATIONS
None.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Vaccinate healthy animals only.
3
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
None.
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 physician.
4.6
ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
Transient apathy and anorexia as well as hyperthermia (lasting usually
for 1 or 2 days
                                
                                Läs hela dokumentet
                                
                            

Dokument på andra språk

Bipacksedel Bipacksedel bulgariska 29-03-2022
Produktens egenskaper Produktens egenskaper bulgariska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport bulgariska 10-03-2021
Bipacksedel Bipacksedel spanska 29-03-2022
Produktens egenskaper Produktens egenskaper spanska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport spanska 10-03-2021
Bipacksedel Bipacksedel tjeckiska 29-03-2022
Produktens egenskaper Produktens egenskaper tjeckiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport tjeckiska 10-03-2021
Bipacksedel Bipacksedel danska 29-03-2022
Produktens egenskaper Produktens egenskaper danska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport danska 10-03-2021
Bipacksedel Bipacksedel tyska 29-03-2022
Produktens egenskaper Produktens egenskaper tyska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport tyska 10-03-2021
Bipacksedel Bipacksedel estniska 29-03-2022
Produktens egenskaper Produktens egenskaper estniska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport estniska 10-03-2021
Bipacksedel Bipacksedel grekiska 29-03-2022
Produktens egenskaper Produktens egenskaper grekiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport grekiska 10-03-2021
Bipacksedel Bipacksedel franska 29-03-2022
Produktens egenskaper Produktens egenskaper franska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport franska 10-03-2021
Bipacksedel Bipacksedel italienska 29-03-2022
Produktens egenskaper Produktens egenskaper italienska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport italienska 10-03-2021
Bipacksedel Bipacksedel lettiska 29-03-2022
Produktens egenskaper Produktens egenskaper lettiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport lettiska 10-03-2021
Bipacksedel Bipacksedel litauiska 29-03-2022
Produktens egenskaper Produktens egenskaper litauiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport litauiska 10-03-2021
Bipacksedel Bipacksedel ungerska 29-03-2022
Produktens egenskaper Produktens egenskaper ungerska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport ungerska 10-03-2021
Bipacksedel Bipacksedel maltesiska 29-03-2022
Produktens egenskaper Produktens egenskaper maltesiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport maltesiska 10-03-2021
Bipacksedel Bipacksedel nederländska 29-03-2022
Produktens egenskaper Produktens egenskaper nederländska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport nederländska 10-03-2021
Bipacksedel Bipacksedel polska 29-03-2022
Produktens egenskaper Produktens egenskaper polska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport polska 10-03-2021
Bipacksedel Bipacksedel portugisiska 29-03-2022
Produktens egenskaper Produktens egenskaper portugisiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport portugisiska 10-03-2021
Bipacksedel Bipacksedel rumänska 29-03-2022
Produktens egenskaper Produktens egenskaper rumänska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport rumänska 10-03-2021
Bipacksedel Bipacksedel slovakiska 29-03-2022
Produktens egenskaper Produktens egenskaper slovakiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport slovakiska 10-03-2021
Bipacksedel Bipacksedel slovenska 29-03-2022
Produktens egenskaper Produktens egenskaper slovenska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport slovenska 10-03-2021
Bipacksedel Bipacksedel finska 29-03-2022
Produktens egenskaper Produktens egenskaper finska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport finska 10-03-2021
Bipacksedel Bipacksedel svenska 29-03-2022
Produktens egenskaper Produktens egenskaper svenska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport svenska 10-03-2021
Bipacksedel Bipacksedel norska 29-03-2022
Produktens egenskaper Produktens egenskaper norska 29-03-2022
Bipacksedel Bipacksedel isländska 29-03-2022
Produktens egenskaper Produktens egenskaper isländska 29-03-2022
Bipacksedel Bipacksedel kroatiska 29-03-2022
Produktens egenskaper Produktens egenskaper kroatiska 29-03-2022
Offentlig bedömningsrapport Offentlig bedömningsrapport kroatiska 10-03-2021

Visa dokumenthistorik