Arepanrix

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

qasma-virus tal-influwenza, inattivat, li fih antiġen*:/California/7/2009 (H1N1)v like strain (X-179A)*propagati fil-bajd.

Available from:

GlaxoSmithKline Biologicals S.A.

ATC code:

J07BB02

INN (International Name):

pandemic influenza vaccine (H1N1)v (split virion, inactivated, adjuvanted)

Therapeutic group:

Vaċċini ta 'l-influwenza

Therapeutic area:

Influenza, Human; Immunization; Disease Outbreaks

Therapeutic indications:

Profilassi tal-influwenza f'sitwazzjoni pandemika ddikjarata uffiċjalment. Il-vaċċin kontra l-influwenza pandemika għandu jintuża skond il-gwida uffiċjali.

Product summary:

Revision: 1

Authorization status:

Irtirat

Authorization date:

2010-03-23

Patient Information leaflet

                                Prodott mediċinali li m’għadux awtorizzat
34
B. FULJETT TA’ TAGĦRIF
Prodott mediċinali li m’għadux awtorizzat
35
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦAL MIN QED JAGĦMEL UŻU
MINNU
AREPANRIX SUSPENSJONI U EMULSJONI GĦAL EMULSJONI GĦALL-INJEZZJONI
Vaċċin ta’ l-influwanza pandemika (H1N1) (virion maqsum,
inattivat, stimulat)
GĦAL L-AKTAR INFORMAZZJONI RIĊENTI JEKK JOGĦĠBOK IKKONSULTA
MAS-SIT TA’ L-AĠENZIJA EWROPEA
DWAR IL-MEDIĊINI (EMEA): HTTP://WWW.EMEA.EUROPA.EU/.
AQRA DAN IL-FULJETT KOLLU QABEL MA’ TIEĦU DAN IL-VAĊĊIN.
-
Żomm dan il-fuljett. Jista jkollok bżonn terġa’ taqrah.
-
Jekk ikollok aktar mistoqsijiet, staqsi lit-tabib jew l-infermier
tiegħek.
-
Jekk xi wieħed mill-effetti sekondarji jiggrava jew jekk tinnota xi
effetti sekondarji li m’humiex
imsemmijin f’dan il-fuljett, jekk jogħġbok, għid lit-tabib
tiegħek.
F’DAN IL-FULJETT:
1.
X’inhu Arepanrix u għalxiex jintuża
2.
Qabel ma tieħu Arepanrix
3.
Kif għandek tieħu Arepanrix
4.
Effetti sekondarji li jista’ jkollu
5.
Kif taħżen Arepanrix
6.
Aktar tagħrif
1.
X'INHU AREPANRIX U GĦALXIEX JINTUŻA
Arepanrix huwa vaċċin kontra l-influwenza pandemika (influwenza).
Influwenza pandemika hija tip ta’ influwenza li tfaqqa’
f’intervalli ta’ għaxar snin u li tinfirex malajr
madwar id-dinja. Is-sintomi ta’ l-influwenza pandemika huma simili
għal dawk ta’ l-influwenza
normali imma jistgħu ikunu aktar severi.
Meta persuna tingħata l-vaċċin, is-sistema immuni (is-sistema ta’
difiża naturali tal-ġisem) tipproduċi
protezzjoni għaliha nnifisha (antikorpi) kontra l-marda. L-ebda
wieħed mill-ingredjenti ma jista’
jikkawża l-influwenza.
Bħal ma’ bil-vaċċini kollha, Arepanrix jista’ ma jipproteġġix
għal kollox il-persuni mlaqqma kollha.
2.
QABEL MA’ TIEĦU AREPANRIX
M’GĦANDEKX TIEĦU AREPANRIX:
•
jekk xi darba kellek reazzjoni allerġika f’daqqa waħda li tkun
ta’ periklu għal-ħajja għal
kwalunkwe ingredjent ta’ Arepanrix (dawn huma mniżżla fl-aħħar
tal-fulj
                                
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Summary of Product characteristics

                                Prodott mediċinali li m’għadux awtorizzat
1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
Prodott mediċinali li m’għadux awtorizzat
2
1.
ISEM TAL-PRODOTT MEDIĊINALI
Arepanrix suspensjoni u emulsjoni għal emulsjoni għall-injezzjoni.
Vaċċin għal influwenza pandemika (H1N1)v (virion maqsum, mhux
attivat, stimulat)
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
Wara li titħallat, doża 1 (0.5 ml) ikun fiha:
Virus maqsum, mhux attivat ta’ l-influwenza li jkun fih antiġen
*
ekwivalenti għal:
_ _
Razza (X-179A) tixbaħ lil A/California/2009 (H1N1)v
3.75 mikrogrammi
**
*
imnissla fil-bajd
**
emagglutinina
Dan il-vaċċin hu konformi mar-rakkomandazzjonijiet tal-WHO u
d-deċiżjoni ta’ l-UE dwar l-
influwenza pandemika.
AS03 stimulant magħmul minn squalene (10.69 milligrammi), DL-
α
-tocopherol (11.86 milligrammi)
u polysorbate 80 (4.86 milligrammi)
Is-suspensjoni u l-emulsjoni ladarba jitħalltu jipproduċu vaċċin
b’ħafna dożi ġo kunjett. Ara sezzjoni
6.5 għan-numru ta’ dożi li fih kull kunjett.
Sustanzi mhux attivi: Il-vaċċin fih 5 mikrogrammi thiomersal
Għal-lista kompleta ta’ sustanzi mhux attivi, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Suspensjoni u emulsjoni għal emulsjoni għall-injezzjoni.
Is-suspensjoni hija bla kulur sa abjad maħmuġ, tkanġi, u jista’
jkollha ftit sediment.
L-emulsjoni hija likwidu omoġenu bajdani.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Profilassi ta’ influwenza f’sitwazzjoni ta’ influwenza pandemika
ddikjarata uffiċjalment (ara
sezzjonijiet 4.2 u 5.1).
Il-vaċċin ta’ l-influwenza pandemika għandu jintuża skont Gwidi
Uffiċjali.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Poż
oloġija
Ir-rakkomandazzjonijiet tad-doża jieħdu f’kunsiderazzjoni dejta
disponibbli minn:
•
Studji kliniċi li għadhom għaddejjin f’individwi b’saħħithom
li rċevew doża waħda ta’
Arepanrix (H1N1)
Prodott mediċinali li m’għadux awtorizzat
3
•
Studji kliniċi f’individwi b’saħħithom (inkluż pazjenti
anzjani) li 
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 25-10-2011
Summary of Product characteristics Summary of Product characteristics Bulgarian 25-10-2011
Public Assessment Report Public Assessment Report Bulgarian 25-10-2011
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Public Assessment Report Public Assessment Report Spanish 25-10-2011
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Patient Information leaflet Patient Information leaflet Latvian 25-10-2011
Public Assessment Report Public Assessment Report Latvian 25-10-2011
Patient Information leaflet Patient Information leaflet Lithuanian 25-10-2011
Summary of Product characteristics Summary of Product characteristics Lithuanian 25-10-2011
Public Assessment Report Public Assessment Report Lithuanian 25-10-2011
Patient Information leaflet Patient Information leaflet Hungarian 25-10-2011
Summary of Product characteristics Summary of Product characteristics Hungarian 25-10-2011
Public Assessment Report Public Assessment Report Hungarian 25-10-2011
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Patient Information leaflet Patient Information leaflet Polish 25-10-2011
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Patient Information leaflet Patient Information leaflet Portuguese 25-10-2011
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Public Assessment Report Public Assessment Report Portuguese 25-10-2011
Patient Information leaflet Patient Information leaflet Romanian 25-10-2011
Public Assessment Report Public Assessment Report Romanian 25-10-2011
Patient Information leaflet Patient Information leaflet Slovak 25-10-2011
Public Assessment Report Public Assessment Report Slovak 25-10-2011
Patient Information leaflet Patient Information leaflet Slovenian 25-10-2011
Summary of Product characteristics Summary of Product characteristics Slovenian 25-10-2011
Public Assessment Report Public Assessment Report Slovenian 25-10-2011
Patient Information leaflet Patient Information leaflet Finnish 25-10-2011
Public Assessment Report Public Assessment Report Finnish 25-10-2011
Patient Information leaflet Patient Information leaflet Swedish 25-10-2011
Public Assessment Report Public Assessment Report Swedish 25-10-2011
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Summary of Product characteristics Summary of Product characteristics Norwegian 25-10-2011
Patient Information leaflet Patient Information leaflet Icelandic 25-10-2011
Summary of Product characteristics Summary of Product characteristics Icelandic 25-10-2011

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