Equilis West Nile

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

strain ta 'flavivirus chimaeric mhux attivat YF-WN

Available from:

Intervet International BV

ATC code:

QI05AA10

INN (International Name):

inactivated chimaeric flavivirus strain YF-WN

Therapeutic group:

Żwiemel

Therapeutic area:

Immunoloġiċi

Therapeutic indications:

Immunizzazzjoni attiva ta 'żwiemel kontra l-virus tal-West Nile (WNV) biex tnaqqas sinjali kliniċi ta' mard u leżjonijiet fil-moħħ u biex tnaqqas il-viremija. Il-bidu tal-immunità: 2 ġimgħat wara l-kors ta 'tilqim primarju ta' żewġ injezzjonijiet. Tul ta 'żmien tal-immunità: 12-il xahar.

Product summary:

Revision: 2

Authorization status:

Awtorizzat

Authorization date:

2013-06-06

Patient Information leaflet

                                B. FULJETT TA' TAGĦRIF FIL-PAKKETT
13
FULJETT TA’ TAGĦRIF FIL-PAKKETT
EQUILIS WEST NILE
Suspensjoni għall-injezzjoni għaż-żwiemel
1.
L-ISEM U L-INDIRIZZ TAS-SID TAL-AWTORIZZAZZJONI TAL-KUMMERĊ, U L-
ISEM U L-INDIRIZZ TAS-SID TAL-AWTORIZZAZZJONI TAL-MANIFATTURA
RESPONSABBLI LI JĦALLI L-KONSENJA TMUR FIS-SUQ , JEKK DIFFERENTI
Sid l-Awtorizzazzjoni tal-Kummerċ u l-manifattur li jħalli
l-konsenja tmur fis-suq :
Intervet International B.V.
Wim de Körverstraat 35
5831 AN Boxmeer
Olanda
2.
ISEM TAL-PRODOTT MEDIĊINALI VETERINARJU
Equilis West Nile Suspensjoni għall-injezzjoni għaż-żwiemel
3.
DIKJARAZZJONI TAS-SUSTANZA(I) ATTIVA(I) U INGREDJENT(I) OĦRA
Doża kull 1 ml
Strejn inattivat tal- virus kimeriċi Flavivirus YF-WN
≥ 492 AU
1
Iscom-Matrix
fih:
Saponin ippurifikat
250 mikrogrammi
Kolesterol
83 mikrogrammi
Fosfatidilkolajn
42 mikrogrammi
1
Partijiet antiġeniċi
iddeterminati bl' ELISA
Suspensjoni opalaxxenti.
4.
INDIKAZZJONI (JIET)
Immunizzazzjoni attiva ġħal żwiemel kontra l-virus West Nile (WNV),
biex tnaqqas is-sinjali kliniċi
tal-marda u l-leżjonijiet fil-moħħ, u sabiex tnaqqas il-viraemia.
Bidu ta’ immunita: Ġimgħatejn wara l-ewwel kors ta’ tilqim ta'
żewġ injezzjonijiet.
Kemm iddum l-immunita: 12 il-xahar
5
KONTRAINDIKAZZJONIJIET
Xejn
6.
EFFETTI MHUX MIXTIEQA
Fi studji tal-laboratorju u fil-prattika
Wara l-vaċċinazzjoni nefħa ħafifa li ma ddumx (diametru mass. 3
cm) tista’ komuni ħafna tfeġġ fejn
tingħata l-injezzjoni. Din n-nefħa tinżel fi żmien 1 sa 5 tijiem.
Temperatura tal-ġisem tista’ komuni
ħafna togħla ftit (mass. 1.5
°
C) għall-1 jew 2 ġranet.
Il-frekwenza ta’ effetti mhux mixtieqa hija definita skont din
il-konvenzjoni:
14
- komuni ħafna (aktar minn wieħed f’10 annimali li juru effetti
mhux mixtieqa matul il-perjodu ta’
kura waħda)
- komuni (aktar minn wieħed iżda inqas minn 10 annimali f’100
annimal)
- mhux komuni (aktar minn wieħed iżda inqas minn10 annimali
f’1,000 annimal)
- rari (aktar minn wieħed iżda inqas minn10 annima
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                ANNESS I
KARATTERISTIĊI TAL-PRODOTT FIL-QOSOR
1
1.
ISEM TAL-PRODOTT MEDIĊINALI VETERINARJU
Equilis West Nile suspensjoni għall-injezzjoni, għaż-żwiemel
2.
KOMPOŻIZZJONI KWALITATTIVA U KWANTITATTIVA
Kull Doża ta’ ml fiha:
SUSTANZA ATTIVA :
Strejn inattivat tal- virus kimeriċi flavivirus YF-WN
≥ 492 AU
1
SUSTANZI MHUX ATTIVI:
Iscom-Matrix
li fih:
Saponin ippurifikat
250 mikrogrammi
Kolesterol
83 mikrogrammi
Fosfatidilkolajn
42 mikrogrammi
1
Partijiet antiġeniċi
iddeterminati bl' ELISA
Għal-lista sħiħa ta’ l-ingredjenti (mhux attivi), ara s-sezzjoni
6.1.
3.
GĦAMLA FARMAĊEWTIKA
Suspensjoni għall-injezzjoni
Suspensjoni opalaxxenti.
4
TAGĦRIF KLINIKU
4.1
SPEĊI LI FUQHOM SER JINTUŻA L-PRODOTT
Żwiemel
4.2
INDIKAZZJONIJIET GĦAL UŻU TAL-PRODOTT LI JISPEĊIFIKAW L-ISPEĊI LI
FUQHOM SE JINTUŻA L-PRODOTT.
Immunizzazzjoni attiva ġħal żwiemel kontra l-virus West Nile (WNV),
biex tnaqqas is-sinjali kliniċi
tal-marda u l-leżjonijiet fil-moħħ, u sabiex tnaqqas il-viraemia.
Bidu ta’ immunita: Ġimgħatejn wara l-ewwel kors ta’ tilqim ta'
żewġ injezzjonijiet.
Kemm iddum l-immunita: 12 il-xahar
4.3
KONTRA INDIKAZZJONIJIET
Xejn
4.4
TWISSIJIET SPEĊJALI GĦAL KULL SPEĊI LI GĦALIHA HU INDIKAT
IL-PRODOTT
Laqqam annimali b’saħħithom biss.
4.5
PREKAWZJONIJIET SPEĊJALI GĦALL-UŻU
Prekawzjonijiet speċjali għall-użu fl-annimali
Mhux applikabbli.
2
Prekawzjonijiet speċjali li għandhom jittieħdu mill-persuna li
tamministra l-prodott mediċinali
veterinarju lill-annimali
F'każ li tinjetta lilek innifsek, fittex parir mediku immedjatament u
qis li turi l-pakkett jew il-fuljett ta’
informazzjoni li jkun gewwa il-pakkett lit-tabib.
4.6
EFFETTI MHUX MIXTIEQA (FREKWENZA U GRAVITÀ)
Fi studji tal-laboratorju u fil-prattika
Wara l-vaċċinazzjoni nefħa hafifa li ma ddumx (dijametru mass. 3
cm) tista’ komuni ħafna tfeġġ fejn
tingħata l-injezzjoni. Din n-nefħa normalment tinżel fi żmien 1 sa
5 tijiem. Temperatura tal-ġisem
tista’ togħla ftit (mass. 1.5
°
C) tista sseħħ komuni ħ
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 15-10-2018
Summary of Product characteristics Summary of Product characteristics Bulgarian 15-10-2018
Public Assessment Report Public Assessment Report Bulgarian 21-07-2013
Patient Information leaflet Patient Information leaflet Spanish 15-10-2018
Public Assessment Report Public Assessment Report Spanish 21-07-2013
Patient Information leaflet Patient Information leaflet Czech 15-10-2018
Public Assessment Report Public Assessment Report Czech 21-07-2013
Patient Information leaflet Patient Information leaflet Danish 15-10-2018
Public Assessment Report Public Assessment Report Danish 21-07-2013
Patient Information leaflet Patient Information leaflet German 15-10-2018
Public Assessment Report Public Assessment Report German 21-07-2013
Patient Information leaflet Patient Information leaflet Estonian 15-10-2018
Public Assessment Report Public Assessment Report Estonian 21-07-2013
Patient Information leaflet Patient Information leaflet Greek 15-10-2018
Public Assessment Report Public Assessment Report Greek 21-07-2013
Patient Information leaflet Patient Information leaflet English 15-10-2018
Public Assessment Report Public Assessment Report English 21-07-2013
Patient Information leaflet Patient Information leaflet French 15-10-2018
Public Assessment Report Public Assessment Report French 21-07-2013
Patient Information leaflet Patient Information leaflet Italian 15-10-2018
Public Assessment Report Public Assessment Report Italian 21-07-2013
Patient Information leaflet Patient Information leaflet Latvian 15-10-2018
Public Assessment Report Public Assessment Report Latvian 21-07-2013
Patient Information leaflet Patient Information leaflet Lithuanian 15-10-2018
Summary of Product characteristics Summary of Product characteristics Lithuanian 15-10-2018
Public Assessment Report Public Assessment Report Lithuanian 21-07-2013
Patient Information leaflet Patient Information leaflet Hungarian 15-10-2018
Summary of Product characteristics Summary of Product characteristics Hungarian 15-10-2018
Public Assessment Report Public Assessment Report Hungarian 21-07-2013
Patient Information leaflet Patient Information leaflet Dutch 15-10-2018
Public Assessment Report Public Assessment Report Dutch 21-07-2013
Patient Information leaflet Patient Information leaflet Polish 15-10-2018
Public Assessment Report Public Assessment Report Polish 21-07-2013
Patient Information leaflet Patient Information leaflet Portuguese 15-10-2018
Summary of Product characteristics Summary of Product characteristics Portuguese 15-10-2018
Public Assessment Report Public Assessment Report Portuguese 21-07-2013
Patient Information leaflet Patient Information leaflet Romanian 15-10-2018
Public Assessment Report Public Assessment Report Romanian 21-07-2013
Patient Information leaflet Patient Information leaflet Slovak 15-10-2018
Public Assessment Report Public Assessment Report Slovak 21-07-2013
Patient Information leaflet Patient Information leaflet Slovenian 15-10-2018
Summary of Product characteristics Summary of Product characteristics Slovenian 15-10-2018
Public Assessment Report Public Assessment Report Slovenian 21-07-2013
Patient Information leaflet Patient Information leaflet Finnish 15-10-2018
Public Assessment Report Public Assessment Report Finnish 21-07-2013
Patient Information leaflet Patient Information leaflet Swedish 15-10-2018
Public Assessment Report Public Assessment Report Swedish 21-07-2013
Patient Information leaflet Patient Information leaflet Norwegian 15-10-2018
Summary of Product characteristics Summary of Product characteristics Norwegian 15-10-2018
Patient Information leaflet Patient Information leaflet Icelandic 15-10-2018
Summary of Product characteristics Summary of Product characteristics Icelandic 15-10-2018
Patient Information leaflet Patient Information leaflet Croatian 15-10-2018