Neocolipor

Country: European Union

Language: Estonian

Source: EMA (European Medicines Agency)

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Active ingredient:

E. coli adhesin F4 (F4ab, F4ac, F4ad), E. coli adhesin F5, E. coli adhesin F6, E. coli adhesin F41

Available from:

Boehringer Ingelheim Vetmedica GmbH

ATC code:

QI09AB02

INN (International Name):

Neonatal piglet colibacillosis vaccine (inactivated)

Therapeutic group:

Sows; Sows (nullipar)

Therapeutic area:

Immunologicals for suidae, Inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia)

Therapeutic indications:

E sünnitusjärgne põrsaste enterotoksikoosi vähendamine. coli tüved, mis ekspresseerivad adhesiine F4ab, F4ac, F4ad, F5, F6 ja F41 esimestel elupäevadel.

Product summary:

Revision: 14

Authorization status:

Volitatud

Authorization date:

1998-04-14

Patient Information leaflet

                                13
B. PAKENDI INFOLEHT
14
PAKENDI INFOLEHT:
NEOCOLIPOR
1.
MÜÜGILOA HOIDJA NING, KUI NEED EI KATTU, RAVIMIPARTII
VÄLJASTAMISE EEST VASTUTAVA TOOTMISLOA HOIDJA NIMI JA AADRESS
Müügiloa hoidja:
Boehringer Ingelheim Vetmedica GmbH
55216 Ingelheim/Rhein
SAKSAMAA
Partii väljastamise eest vastutav tootja:
Boehringer Ingelheim Animal Health France SCS
Laboratoire Porte des Alpes
Rue de l’Aviation
F-69800 SAINT PRIEST
Prantsusmaa
2.
VETERINAARRAVIMI NIMETUS
Neocolipor süstesuspensioon
3.
TOIMEAINE(D) JA MUUD ABIAINE(D)
_1 DOOSI 2 ML KOHTA: _
_ _
E. coli adhesiinid F4 (F4ab, F4ac, F4ad),
vähemalt..................................................................
2.1 SA.U*
E.coli adhesiin F5, vähemalt
.....................................................................................................
1.7 SA.U*
E.coli adhesiin F6, vähemalt
.....................................................................................................
1.4 SA.U*
E.coli adhesiin F41, vähemalt
..................................................................................................
1.7 SA.U*
*: 1 SA.U: kogus, mis on küllaldane omandamaks aglutineerivate
antikehade tiitri 1 log
10
merisigadel.
Adjuvant:
Alumiinium (hüdroksiidina)
......................................................................................................
1.4 mg
4.
NÄIDUSTUS(ED)
Adjuveeritud inaktiveeritud vaktsiin
_ E. coli_
tüvede, milles on ekspresseerunud adhesiinid F4ab, F4ac,
F4ad, F5, F6 and F41, põhjustatud põrsaste neonataalse
enterotoksikoosi vähendamiseks.
5.
VASTUNÄIDUSTUSED
Ei ole
6.
KÕRVALTOIMED
Vaktsineerimine võib põhjustada kerget kehatemperatuuri tõusu
(vähem kui 1,5°C maksimaalselt 24
tunni jooksul).
Kui täheldate tõsiseid kõrvaltoimeid või muid toimeid, mida pole
käesolevas pakendi infolehes
mainitud, palun teavitage sellest oma veterinaararsti.
15
7.
LOOMALIIGID
Siga (emised ja nooremised)
8.
ANNUSTAMINE LOOMALIIGITI, MANUSTAMISTEE(D) JA –MEETOD
Üks 2 ml doos vastavalt järgnevale skeemile:
Esmane vak
                                
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Summary of Product characteristics

                                1
LISA I
RAVIMI OMADUSTE KOKKUVÕTE
2
1.
VETERINAARRAVIMI NIMETUS
Neocolipor süstesuspensioon
2.
KVALITATIIVNE JA KVANTITATIIVNE KOOSTIS
_ _
TOIMEAINED:
1doos 2 ml sisaldab:
E.coli adhesiin F4 (F4ab, F4ac, F4ad), vähemalt
......................................................... 2.1 SA.U*
E.coli adhesiin F5, vähemalt
........................................................................................
1.7 SA.U*
E.coli adhesiin F6, vähemalt
........................................................................................
1.4 SA.U*
E.coli adhesiin F41, vähemalt
.....................................................................................
1.7 SA.U*
*: 1 SA.U: kogus, mis on küllaldane omandamaks aglutineerivate
antikehade tiitri 1 log
10
merisigadel.
ADJUVANT(ADJUVANDID):
Alumiinium (hüdroksiidina)
..........................................................................................
1.4 mg
ABIAINED:
Abiainete terviklik loetelu on esitatud lõigus 6.1.
3.
RAVIMVORM
Süstesupensioon
4.
KLIINILISED ANDMED
4.1
LOOMALIIGID
Siga (emised ja nooremised).
4.2
NÄIDUSTUSED, MÄÄRATES KINDLAKS VASTAVAD LOOMALIIGID
_ _
_E. coli_
tüvede, milles on ekspresseerunud adhesiinid F4ab, F4ac, F4ad, F5, F6
and F41, põhjustatud
põrsaste neonataalse enterotoksikoosi vähendamine esimestel
elupäevadel.
4.3
VASTUNÄIDUSTUSED
Ei ole
4.4
ERIHOIATUSED IGA LOOMALIIGI KOHTA
Ei ole.
4.5
ERIHOIATUSED
ERIHOIATUSED KASUTAMISEL LOOMADEL
-
Kuna põrsastel saavutatakse immuunsus ternespiima kaudu, peab iga
põrsas esimese 6 elutunni
jooksul saama piisavas koguses ternespiima.
-
Vaktsineerida ainult terveid loomi.
-
Mitte manustada koos teiste ravimitega.
3
ANTUD VETERINAARRAVIMIT LOOMADELE MANUSTAVA ISIKU POOLT RAKENDATAVAD
SPETSIAALSED
ETTEVAATUSABINÕUD
Juhuslikul ravimi süstimisel iseendale pöörduda viivitamatul arsti
poole ja näidata pakendi infolehte
või pakendi etiketti.
Pärast kasutamist pesta ja desinfitseerida käed.
4.6
KÕRVALTOIMED (SAGEDUS JA TÕSIDUS)
Vaktsineerimine võib põhjustada kerget kehatem
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 16-06-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 16-06-2020
Public Assessment Report Public Assessment Report Bulgarian 17-02-2021
Patient Information leaflet Patient Information leaflet Spanish 16-06-2020
Public Assessment Report Public Assessment Report Spanish 17-02-2021
Patient Information leaflet Patient Information leaflet Czech 16-06-2020
Public Assessment Report Public Assessment Report Czech 17-02-2021
Patient Information leaflet Patient Information leaflet Danish 16-06-2020
Public Assessment Report Public Assessment Report Danish 17-02-2021
Patient Information leaflet Patient Information leaflet German 16-06-2020
Public Assessment Report Public Assessment Report German 17-02-2021
Patient Information leaflet Patient Information leaflet Greek 16-06-2020
Public Assessment Report Public Assessment Report Greek 17-02-2021
Patient Information leaflet Patient Information leaflet English 16-06-2020
Public Assessment Report Public Assessment Report English 17-02-2021
Patient Information leaflet Patient Information leaflet French 16-06-2020
Public Assessment Report Public Assessment Report French 17-02-2021
Patient Information leaflet Patient Information leaflet Italian 16-06-2020
Public Assessment Report Public Assessment Report Italian 17-02-2021
Patient Information leaflet Patient Information leaflet Latvian 16-06-2020
Public Assessment Report Public Assessment Report Latvian 17-02-2021
Patient Information leaflet Patient Information leaflet Lithuanian 16-06-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 16-06-2020
Public Assessment Report Public Assessment Report Lithuanian 17-02-2021
Patient Information leaflet Patient Information leaflet Hungarian 16-06-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 16-06-2020
Public Assessment Report Public Assessment Report Hungarian 17-02-2021
Patient Information leaflet Patient Information leaflet Maltese 16-06-2020
Public Assessment Report Public Assessment Report Maltese 17-02-2021
Patient Information leaflet Patient Information leaflet Dutch 16-06-2020
Public Assessment Report Public Assessment Report Dutch 17-02-2021
Patient Information leaflet Patient Information leaflet Polish 16-06-2020
Public Assessment Report Public Assessment Report Polish 17-02-2021
Patient Information leaflet Patient Information leaflet Portuguese 16-06-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 16-06-2020
Public Assessment Report Public Assessment Report Portuguese 17-02-2021
Patient Information leaflet Patient Information leaflet Romanian 16-06-2020
Public Assessment Report Public Assessment Report Romanian 17-02-2021
Patient Information leaflet Patient Information leaflet Slovak 16-06-2020
Public Assessment Report Public Assessment Report Slovak 17-02-2021
Patient Information leaflet Patient Information leaflet Slovenian 16-06-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 16-06-2020
Public Assessment Report Public Assessment Report Slovenian 17-02-2021
Patient Information leaflet Patient Information leaflet Finnish 16-06-2020
Public Assessment Report Public Assessment Report Finnish 17-02-2021
Patient Information leaflet Patient Information leaflet Swedish 16-06-2020
Public Assessment Report Public Assessment Report Swedish 17-02-2021
Patient Information leaflet Patient Information leaflet Norwegian 16-06-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 16-06-2020
Patient Information leaflet Patient Information leaflet Icelandic 16-06-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 16-06-2020
Patient Information leaflet Patient Information leaflet Croatian 16-06-2020
Public Assessment Report Public Assessment Report Croatian 17-02-2021

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