Fevaxyn Pentofel

Riik: Euroopa Liit

keel: inglise

Allikas: EMA (European Medicines Agency)

Osta kohe

Infovoldik Infovoldik (PIL)
01-03-2022
Toote omadused Toote omadused (SPC)
01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande (PAR)
07-06-2013

Toimeaine:

inactivated feline rhinotracheitis virus, inactivated feline calicivirus, inactivated feline Chlamydophila felis, inactivated feline leukaemia virus, inactivated feline panleukopenia virus

Saadav alates:

Zoetis Belgium SA 

ATC kood:

QI06AL01

INN (Rahvusvaheline Nimetus):

inactivated feline panleukopenia virus, calicivirus, rhinotracheitis virus, leukaemia virus and Chlamydophila felis

Terapeutiline rühm:

Cats

Terapeutiline ala:

Immunologicals

Näidustused:

For the active immunisation of healthy cats nine weeks or older against feline panleukopenia and feline leukaemia viruses and against respiratory diseases caused by feline rhinotracheitis virus, feline calicivirus and Chlamydophila felis.

Toote kokkuvõte:

Revision: 20

Volitamisolek:

Authorised

Loa andmise kuupäev:

1997-02-05

Infovoldik

                                14
B. PACKAGE LEAFLET
15
PACKAGE LEAFLET:
FEVAXYN PENTOFEL, SUSPENSION FOR INJECTION FOR CATS
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:
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
BELGIUM
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Fevaxyn Pentofel, suspension for injection for cats
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Per dose of 1 ml (single dose syringe):
ACTIVE COMPONENTS
RELATIVE POTENCY (R.P.)
Inactivated feline panleucopenia virus, strain CU4
Inactivated feline calicivirus, strain 255
Inactivated feline rhinotracheitis virus, strain 605
Inactivated
_Chlamydophila felis_
,
_ _
strain Cello
Inactivated feline leukaemia virus, strain 61E
≥ 8.50
≥ 1.26
≥ 1.39
≥ 1.69
≥ 1.45
ADJUVANTS
Ethylene/maleic anhydride (EMA-31)
Neocryl
Emulsigen SA
1% (v/v)
3% (v/v)
5% (v/v)
4.
INDICATION(S)
For the active immunisation of healthy cats 9 weeks or older against
feline panleucopenia and feline leukaemia
viruses and against respiratory diseases caused by feline
rhinotracheitis virus, feline calicivirus and
_Chlamydophila felis._
5.
CONTRAINDICATIONS
None.
6.
ADVERSE REACTIONS
Vaccinated cats may develop post-vaccinal reactions including
transient fever, vomiting, anorexia and/or
depression which usually disappear within 24 hours.
16
A local reaction with swelling, pain, pruritus or hair loss at the
injection site may be observed.
Anaphylactic reactions with oedema, pruritus, respiratory and cardiac
distress, severe gastrointestinal signs
(including haematemesis and haemorrhagic diarrhoea) or shock have been
seen during the first hours after
vaccination in very rare cases.
The frequency of adverse reactions is defined using the following
convention:
- very common (more than 1 in 10 animals treated displaying adverse
reaction(s))
- common (more than 1 but less than 10 animals in 100 animals tre
                                
                                Lugege kogu dokumenti
                                
                            

Toote omadused

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Fevaxyn Pentofel, suspension for injection for cats
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Per dose of 1 ml (single dose syringe):
ACTIVE COMPONENTS
RELATIVE POTENCY (R.P.)
Inactivated feline panleucopenia virus, strain CU4
Inactivated feline calicivirus, strain 255
Inactivated feline rhinotracheitis virus, strain 605
Inactivated
_Chlamydophila felis_
,
_ _
strain
_ _
Cello
Inactivated feline leukaemia virus, strain 61E
≥ 8.50
≥ 1.26
≥ 1.39
≥ 1.69
≥ 1.45
ADJUVANTS
Ethylene/maleic anhydride (EMA-31)
Neocryl
Emulsigen SA
1% (v/v)
3% (v/v)
5% (v/v)
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Suspension for injection.
Vaccine appearance is a pale milky pink liquid which should be free
from solid particles.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Cats.
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the active immunisation of healthy cats 9 weeks or older against
feline panleucopenia and feline leukaemia
viruses and against respiratory diseases caused by feline
rhinotracheitis virus, feline calicivirus and
_Chlamydophila felis._
4.3
CONTRAINDICATIONS
None.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Vaccination does not affect the course of feline leukaemia virus
(FeLV) infection in cats already infected with
FeLV at the time of vaccination, implying that such cats will excrete
FeLV irrespective of vaccination;
consequently, these animals will constitute a hazard to susceptible
cats in their environment. It is therefore
recommended that cats with a significant risk of having been exposed
to FeLV be tested for FeLV antigen prior
to vaccination. Test negative animals can be vaccinated, while
test-positive cats should be isolated from other
3
cats and retested within 1–2 months. Cats positive at the second
testing should be considered as being
permanently infected with FeLV and should be handled accordingly. Cats
negative at second testing can be
vaccinated since, in all 
                                
                                Lugege kogu dokumenti
                                
                            

Dokumendid teistes keeltes

Infovoldik Infovoldik bulgaaria 01-03-2022
Toote omadused Toote omadused bulgaaria 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande bulgaaria 07-06-2013
Infovoldik Infovoldik hispaania 01-03-2022
Toote omadused Toote omadused hispaania 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande hispaania 07-06-2013
Infovoldik Infovoldik tšehhi 01-03-2022
Toote omadused Toote omadused tšehhi 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande tšehhi 07-06-2013
Infovoldik Infovoldik taani 01-03-2022
Toote omadused Toote omadused taani 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande taani 07-06-2013
Infovoldik Infovoldik saksa 01-03-2022
Toote omadused Toote omadused saksa 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande saksa 07-06-2013
Infovoldik Infovoldik eesti 01-03-2022
Toote omadused Toote omadused eesti 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande eesti 07-06-2013
Infovoldik Infovoldik kreeka 01-03-2022
Toote omadused Toote omadused kreeka 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande kreeka 07-06-2013
Infovoldik Infovoldik prantsuse 01-03-2022
Toote omadused Toote omadused prantsuse 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande prantsuse 07-06-2013
Infovoldik Infovoldik itaalia 01-03-2022
Toote omadused Toote omadused itaalia 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande itaalia 07-06-2013
Infovoldik Infovoldik läti 01-03-2022
Toote omadused Toote omadused läti 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande läti 07-06-2013
Infovoldik Infovoldik leedu 01-03-2022
Toote omadused Toote omadused leedu 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande leedu 07-06-2013
Infovoldik Infovoldik ungari 01-03-2022
Toote omadused Toote omadused ungari 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande ungari 07-06-2013
Infovoldik Infovoldik malta 01-03-2022
Toote omadused Toote omadused malta 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande malta 07-06-2013
Infovoldik Infovoldik hollandi 01-03-2022
Toote omadused Toote omadused hollandi 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande hollandi 07-06-2013
Infovoldik Infovoldik poola 01-03-2022
Toote omadused Toote omadused poola 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande poola 07-06-2013
Infovoldik Infovoldik portugali 01-03-2022
Toote omadused Toote omadused portugali 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande portugali 07-06-2013
Infovoldik Infovoldik rumeenia 01-03-2022
Toote omadused Toote omadused rumeenia 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande rumeenia 07-06-2013
Infovoldik Infovoldik slovaki 01-03-2022
Toote omadused Toote omadused slovaki 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande slovaki 07-06-2013
Infovoldik Infovoldik sloveeni 01-03-2022
Toote omadused Toote omadused sloveeni 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande sloveeni 07-06-2013
Infovoldik Infovoldik soome 01-03-2022
Toote omadused Toote omadused soome 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande soome 07-06-2013
Infovoldik Infovoldik rootsi 01-03-2022
Toote omadused Toote omadused rootsi 01-03-2022
Avaliku hindamisaruande Avaliku hindamisaruande rootsi 07-06-2013
Infovoldik Infovoldik norra 01-03-2022
Toote omadused Toote omadused norra 01-03-2022
Infovoldik Infovoldik islandi 01-03-2022
Toote omadused Toote omadused islandi 01-03-2022
Infovoldik Infovoldik horvaadi 01-03-2022
Toote omadused Toote omadused horvaadi 01-03-2022

Vaadake dokumentide ajalugu