Regranex

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

becaplermin

Available from:

Janssen-Cilag International NV

ATC code:

D03AX06

INN (International Name):

becaplermin

Therapeutic group:

Preparazzjonijiet għat-trattament ta 'feriti u ulċeri

Therapeutic area:

Wound Healing; Skin Ulcer

Therapeutic indications:

Regranex huwa indikat, b ' assoċjazzjoni ma ' oħra miżuri ta ' kura tajba ferita, biex jippromwovu granulazzjoni u b'hekk il-fejqan ta ' sħiħa tal-ħxuna, neuropathic, kroniċi, diabetic ulċeri inqas minn jew ugwali għal 5 cm2.

Product summary:

Revision: 18

Authorization status:

Irtirat

Authorization date:

1999-03-29

Patient Information leaflet

                                B. FULJETT TA’ TAGĦRIF
13
Prodott mediċinali li m’għadux awtorizzat
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦAL MIN QED JAGĦMEL UŻU
MINNU
REGRANEX
® 0.01% ĠELL
Becaplermin
AQRA SEW DAN IL-FULJETT KOLLU QABEL TIBDA TUŻA DIN IL-MEDIĊINA.
•
Żomm dan il-fuljett. Jista’ jkollok bżonn terġa’ taqrah.
•
Jekk ikollok aktar mistoqsijiet, staqsi lit-tabib jew lill-ispiżjar
tiegħek.
•
Din il-mediċina ġiet mogħtija lilek. M’għandekx tgħaddiha lil
persuni oħra. Tista’
tagħmlilhom il-ħsara, anki jekk ikollhom l-istess sintomi bħal
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 jew lill-ispiżjar tiegħek.
F’DAN IL-FULJETT:
1.
X’inhu REGRANEX u għalxiex jintuża
2.
Qabel ma tuża REGRANEX
3.
Kif għandek tuża REGRANEX
4.
Effetti sekondarji li jista’ jkollu
5.
Kif taħżen REGRANEX
6.
Aktar tagħrif
1.
X’INHU REGRANEX U GĦALXIEX JINTUŻA
L-isem tal-mediċina tiegħek hija REGRANEX. Huwa fih sustanza msejħa
becaplermin. Becaplermin
huwa Fattur tat-Tkabbir Derivat mill-Platelet uman rikombinanti
(rhPDGF-BB).
REGRANEX jintuża biex jgħin it-tkabbir ta’ tessut normali biex
jitfejqu ulċeri fil-ġilda. Huwa jintuża
flimkien ma’ miżuri tajbin oħra għall-kura tal-feriti biex jgħin
fil-fejqan tal-ulċeri.
Miżuri tajbin oħra għall-kura tal-feriti jinkludu:
•
It-tabib jew professjonista fil-kura tas-saħħa tiegħek ineħħi
l-ġilda mejta/debris minn ġol-
ferita kull meta hemm il-bżonn
•
Tneħħi l-piż minn fuq saqajk, forsi billi tilbes żarbun ortopediku
speċjali jew b’metodi oħra
•
It-tabib jew professjonista fil-kura tas-saħħa tiegħek jittratta
kull infezzjoni fil-ferita –
trattament b’REGRANEX għandu jitwaqqaf jekk il-ferita tinfetta
ruħha
•
Tkompli tara t-tabib jew professjonista fil-kura tas-saħħa tiegħek
u ssegwi il-pjan ta’
trattament tiegħek
REGRANEX jintuża għall-ulċeri fil-ġilda li:
•
Mhumiex akb
                                
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Summary of Product characteristics

                                ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
1
Prodott mediċinali li m’għadux awtorizzat
1.
ISEM IL-PRODOTT MEDIĊINALI
REGRANEX 0.01% ġell
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
_ _
Kull gramma ta’ ġell fih 100 μg ta’ becaplermin*.
*Fattur tat-Tkabbir Derivat mill-Platelet uman rikombinanti – BB
(rhPDGF-BB) prodott ġo
_Saccharomyces cerevisiae_
bit-teknoloġija tad-DNA rikombinanti.
Sustanzi mhux attivi:
Kull gramma fiha E218 (methyl parahydroxybenzoate) 1.56 mg u E216
(propyl parahydroxybenzoate)
0.17 mg, ara sezzjoni 4.4.
Għall-lista kompleta ta’ sustanzi mhux attivi, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Ġell
REGRANEX huwa ġell ċar minn mingħajr kulur sa kulur it-tiben.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
REGRANEX huwa indikat flimkien ma’ miżuri tajbin għall-kura
tal-feriti, sabiex jippromwovu l-
granulazzjoni u l-konsegwenti fejqan ta’ ulċeri dijabetiċi
ta’ħxuna sħiħa newropatiċi, kroniċi ta’ inqas
minn jew daqs 5cm
2
.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Trattament b’REGRANEX għandu jinbeda u jiġi segwit mit-tobba
(speċjalisti jew mhux speċjalisti) li
għandhom esperjenza fil-maneġġjar ta’ feriti dijabetiċi.
REGRANEX għandu dejjem jintuża flimkien ma’ kura tajba ta’
feriti konsistenti f’debridement
inizjali (sabiex jitneħħa t-tessut nekrotiku u/jew infettat kollu),
debridement addizzjonali kif ikun
neċessarju u reġimen li fih ma jkunx hemm piż sabiex tiġi
allevjata l-pressjoni minn fuq l-ulċera.
REGRANEX għandu jiġi applikat bħala saff irqiq kontinwu fuq
iż-żoni intieri li fihom l-ulċeri darba
kuljum bl-użu ta’ strument għall-applikazzjoni nadif. Is-sit(i)
tal-applikazzjoni għandhom jiġu
mgħottija b’garża niedja bl-ilma bil-melħ (saline) li żżomm
ambjent niedi għall-fejqan tal-feriti.
REGRANEX m’għandux jintuża b’garża okklużiva.
-
Tubu ta’ REGRANEX għandu jintuża fuq pazjent wieħed biss.
-
Għandu jkun hemm attenzjoni waqt l-użu biex tiġi evitata
kontaminazzjoni
                                
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Patient Information leaflet Patient Information leaflet Bulgarian 15-08-2012
Summary of Product characteristics Summary of Product characteristics Bulgarian 15-08-2012
Public Assessment Report Public Assessment Report Bulgarian 15-08-2012
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Public Assessment Report Public Assessment Report Spanish 15-08-2012
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Public Assessment Report Public Assessment Report Greek 15-08-2012
Patient Information leaflet Patient Information leaflet English 15-08-2012
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Patient Information leaflet Patient Information leaflet Latvian 15-08-2012
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Patient Information leaflet Patient Information leaflet Lithuanian 15-08-2012
Summary of Product characteristics Summary of Product characteristics Lithuanian 15-08-2012
Public Assessment Report Public Assessment Report Lithuanian 15-08-2012
Patient Information leaflet Patient Information leaflet Hungarian 15-08-2012
Summary of Product characteristics Summary of Product characteristics Hungarian 15-08-2012
Public Assessment Report Public Assessment Report Hungarian 15-08-2012
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Patient Information leaflet Patient Information leaflet Romanian 15-08-2012
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Patient Information leaflet Patient Information leaflet Slovak 15-08-2012
Public Assessment Report Public Assessment Report Slovak 15-08-2012
Patient Information leaflet Patient Information leaflet Slovenian 15-08-2012
Summary of Product characteristics Summary of Product characteristics Slovenian 15-08-2012
Public Assessment Report Public Assessment Report Slovenian 15-08-2012
Patient Information leaflet Patient Information leaflet Finnish 15-08-2012
Public Assessment Report Public Assessment Report Finnish 15-08-2012
Patient Information leaflet Patient Information leaflet Swedish 15-08-2012
Public Assessment Report Public Assessment Report Swedish 15-08-2012
Patient Information leaflet Patient Information leaflet Norwegian 15-08-2012
Summary of Product characteristics Summary of Product characteristics Norwegian 15-08-2012
Patient Information leaflet Patient Information leaflet Icelandic 15-08-2012
Summary of Product characteristics Summary of Product characteristics Icelandic 15-08-2012

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