Trumenba

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Neisseria meningitidis serogroup B fHbp (fHbp lipidat rikombinanti (proteina li jgħaqqad il-fattur H)) subfamilja A; Neisseria meningitidis serogroup B fHbp (fHbp lipidat rikombinanti (proteina li jgħaqqad il-fattur H)) subfamilja B

Available from:

Pfizer Europe MA EEIG

ATC code:

J07AH09

INN (International Name):

meningococcal group b vaccine (recombinant, adsorbed)

Therapeutic group:

Bacterial vaccines, Meningococcal vaccines

Therapeutic area:

Meninġite, Meningokokkali

Therapeutic indications:

Trumenba huwa indikat għall-immunizzazzjoni attiva ta 'individwi ta' 10 snin jew aktar biex jipprevjenu mard meningokokkali invażiv ikkawżat minn Neisseria meningitidis serogroup B. L-użu ta ' dan il-vaċċin għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.

Product summary:

Revision: 16

Authorization status:

Awtorizzat

Authorization date:

2017-05-24

Patient Information leaflet

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Trumenba suspensjoni għall-injezzjoni f’siringa mimlija għal-lest
Vaċċin meningokokkali tal-grupp B (rikombinanti, adsorbita)
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
doża waħda (0.5 mL) fiha:
_Neisseria meningitidis_ serogrupp B fHbp sottofamilja A
1,2,3
60 mikrogramma
_Neisseria meningitidis_ serogrupp B fHbp sottofamilja B
1,2,3
60 mikrogramma
1
fHbp (proteina tat-twaħħil tal-fattur H) lipidata rikombinanti
2
Prodotta f’ċelluli_ Escherichia coli _permezz ta’ teknoloġija
tad-DNA rikombinanti
3
Adsorbita fuq aluminium phosphate (0.25 milligramma ta’ aluminju
għal kull doża)
Għal-lista sħiħa ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Suspensjoni għall-injezzjoni.
Suspensjoni likwida bajda.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Trumenba jintuża għal immunizzazzjoni attiva ta’ individwi li
għandhom 10 snin jew aktar biex tiġi
evitata l-marda meningokokkali invażiva kkawżata minn _Neisseria
meningitidis_ serogrupp B.
Ara sezzjoni 5.1 għal informazzjoni dwar ir-rispons immuni kontra
razez speċifiċi ta’ serogrupp B.
L-użu ta’ dan il-vaċċin għandu jkun skont
ir-rakkomandazzjonijiet uffiċjali.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Pożoloġija
_Serje primarja_
2 dożi: (0.5 mL kull waħda) mogħtija f’intervall ta’ 6 xhur
(ara sezzjoni 5.1).
3 dożi: 2 dożi (0.5 mL kull waħda) mogħtija mill-inqas xahar ’il
bogħod minn xulxin, segwiti mit-
tielet doża mogħtija mill-inqas 4 xhur wara t-tieni doża (ara
sezzjoni 5.1).
_Doża booster_
Għandha tiġi kkunsidrata doża booster wara kwalunkwe kors
tad-dożaġġ għal individwi li jinsabu
f’riskju kontinwu ta’ marda meningokokkali invażiva (ara sezzjoni
5.1).
_Popolazzjonijiet pedjatriċi oħrajn_
3
Is-sigurtà u l-effikaċja ta’ Trumenba fi tfal ta’ età inqas
minn 10 snin ma ġewx determinati._ Data_
disponibbli attwalment għal tfal ta’ età ta’ sena sa 9 snin hija
deskritt
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Trumenba suspensjoni għall-injezzjoni f’siringa mimlija għal-lest
Vaċċin meningokokkali tal-grupp B (rikombinanti, adsorbita)
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
doża waħda (0.5 mL) fiha:
_Neisseria meningitidis_ serogrupp B fHbp sottofamilja A
1,2,3
60 mikrogramma
_Neisseria meningitidis_ serogrupp B fHbp sottofamilja B
1,2,3
60 mikrogramma
1
fHbp (proteina tat-twaħħil tal-fattur H) lipidata rikombinanti
2
Prodotta f’ċelluli_ Escherichia coli _permezz ta’ teknoloġija
tad-DNA rikombinanti
3
Adsorbita fuq aluminium phosphate (0.25 milligramma ta’ aluminju
għal kull doża)
Għal-lista sħiħa ta’ eċċipjenti, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Suspensjoni għall-injezzjoni.
Suspensjoni likwida bajda.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Trumenba jintuża għal immunizzazzjoni attiva ta’ individwi li
għandhom 10 snin jew aktar biex tiġi
evitata l-marda meningokokkali invażiva kkawżata minn _Neisseria
meningitidis_ serogrupp B.
Ara sezzjoni 5.1 għal informazzjoni dwar ir-rispons immuni kontra
razez speċifiċi ta’ serogrupp B.
L-użu ta’ dan il-vaċċin għandu jkun skont
ir-rakkomandazzjonijiet uffiċjali.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Pożoloġija
_Serje primarja_
2 dożi: (0.5 mL kull waħda) mogħtija f’intervall ta’ 6 xhur
(ara sezzjoni 5.1).
3 dożi: 2 dożi (0.5 mL kull waħda) mogħtija mill-inqas xahar ’il
bogħod minn xulxin, segwiti mit-
tielet doża mogħtija mill-inqas 4 xhur wara t-tieni doża (ara
sezzjoni 5.1).
_Doża booster_
Għandha tiġi kkunsidrata doża booster wara kwalunkwe kors
tad-dożaġġ għal individwi li jinsabu
f’riskju kontinwu ta’ marda meningokokkali invażiva (ara sezzjoni
5.1).
_Popolazzjonijiet pedjatriċi oħrajn_
3
Is-sigurtà u l-effikaċja ta’ Trumenba fi tfal ta’ età inqas
minn 10 snin ma ġewx determinati._ Data_
disponibbli attwalment għal tfal ta’ età ta’ sena sa 9 snin hija
deskritt
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 20-10-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 20-10-2023
Public Assessment Report Public Assessment Report Bulgarian 06-06-2017
Patient Information leaflet Patient Information leaflet Spanish 20-10-2023
Public Assessment Report Public Assessment Report Spanish 06-06-2017
Patient Information leaflet Patient Information leaflet Czech 20-10-2023
Public Assessment Report Public Assessment Report Czech 06-06-2017
Patient Information leaflet Patient Information leaflet Danish 20-10-2023
Public Assessment Report Public Assessment Report Danish 06-06-2017
Patient Information leaflet Patient Information leaflet German 20-10-2023
Public Assessment Report Public Assessment Report German 06-06-2017
Patient Information leaflet Patient Information leaflet Estonian 20-10-2023
Public Assessment Report Public Assessment Report Estonian 06-06-2017
Patient Information leaflet Patient Information leaflet Greek 20-10-2023
Public Assessment Report Public Assessment Report Greek 06-06-2017
Patient Information leaflet Patient Information leaflet English 20-10-2023
Public Assessment Report Public Assessment Report English 06-06-2017
Patient Information leaflet Patient Information leaflet French 20-10-2023
Public Assessment Report Public Assessment Report French 06-06-2017
Patient Information leaflet Patient Information leaflet Italian 20-10-2023
Public Assessment Report Public Assessment Report Italian 06-06-2017
Patient Information leaflet Patient Information leaflet Latvian 20-10-2023
Public Assessment Report Public Assessment Report Latvian 06-06-2017
Patient Information leaflet Patient Information leaflet Lithuanian 20-10-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 20-10-2023
Public Assessment Report Public Assessment Report Lithuanian 06-06-2017
Patient Information leaflet Patient Information leaflet Hungarian 20-10-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 20-10-2023
Public Assessment Report Public Assessment Report Hungarian 06-06-2017
Patient Information leaflet Patient Information leaflet Dutch 20-10-2023
Public Assessment Report Public Assessment Report Dutch 06-06-2017
Patient Information leaflet Patient Information leaflet Polish 20-10-2023
Public Assessment Report Public Assessment Report Polish 06-06-2017
Patient Information leaflet Patient Information leaflet Portuguese 20-10-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 20-10-2023
Public Assessment Report Public Assessment Report Portuguese 06-06-2017
Patient Information leaflet Patient Information leaflet Romanian 20-10-2023
Public Assessment Report Public Assessment Report Romanian 06-06-2017
Patient Information leaflet Patient Information leaflet Slovak 20-10-2023
Public Assessment Report Public Assessment Report Slovak 06-06-2017
Patient Information leaflet Patient Information leaflet Slovenian 20-10-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 20-10-2023
Public Assessment Report Public Assessment Report Slovenian 06-06-2017
Patient Information leaflet Patient Information leaflet Finnish 20-10-2023
Public Assessment Report Public Assessment Report Finnish 06-06-2017
Patient Information leaflet Patient Information leaflet Swedish 20-10-2023
Public Assessment Report Public Assessment Report Swedish 06-06-2017
Patient Information leaflet Patient Information leaflet Norwegian 20-10-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 20-10-2023
Patient Information leaflet Patient Information leaflet Icelandic 20-10-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 20-10-2023
Patient Information leaflet Patient Information leaflet Croatian 20-10-2023
Public Assessment Report Public Assessment Report Croatian 06-06-2017

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