Cufence

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

trientine dihydrochloride

Available from:

Univar Solutions BV

ATC code:

A16A

INN (International Name):

trientine dihydrochloride

Therapeutic group:

Drugi zdravljene bolezni prebavil in presnove izdelki,

Therapeutic area:

Hepatolentikularna degeneracija

Therapeutic indications:

Cufence je primerna za zdravljenje wilsonova bolezen pri bolnikih nestrpni do D-Penicillamine terapija, pri odraslih in otrok, starih 5 let ali starejši.

Product summary:

Revision: 5

Authorization status:

Pooblaščeni

Authorization date:

2019-07-25

Patient Information leaflet

                                18
10.
POSEBNI VARNOSTNI UKREPI ZA ODSTRANJEVANJE NEUPORABLJENIH
ZDRAVIL ALI IZ NJIH NASTALIH ODPADNIH SNOVI, KADAR SO POTREBNI
11.
IME IN NASLOV IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
Univar Solutions BV
Schouwburgplein 30
3012 CL Rotterdam
Nizozemska
12.
ŠTEVILKA (E) DOVOLJENJA (DOVOLJENJ) ZA PROMET
EU/1/19/1365/002
13.
ŠTEVILKA SERIJE
Lot
14.
NAČIN IZDAJANJA ZDRAVILA
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
Cufence 100mg
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA_ _
Vsebuje dvodimenzionalno črtno kodo z edinstveno oznako.
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI
PC
SN
NN
19
PODATKI NA PRIMARNI OVOJNINI
STEKLENICA
1.
IME ZDRAVILA
Cufence 100 mg trde kapsule
trientin
2.
NAVEDBA ENE ALI VEČ UČINKOVIN
Ena kapsula vsebuje 150 mg trientinijevega diklorida, kar ustreza 100
mg trientina.
3.
SEZNAM POMOŽNIH SNOVI
4.
FARMACEVTSKA OBLIKA IN VSEBINA
Trda kapsula
200 kapsul
5.
POSTOPEK IN POT(I) UPORABE ZDRAVILA
Pred uporabo preberite priloženo navodilo!
peroralna uporaba
6.
POSEBNO OPOZORILO O SHRANJEVANJU ZDRAVILA ZUNAJ DOSEGA IN
POGLEDA OTROK
Zdravilo shranjujte nedosegljivo otrokom!
7.
DRUGA POSEBNA OPOZORILA, ČE SO POTREBNA
8.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
EXP
Po prvem odprtju lahko steklenico shranjujete 3 mesece.
9.
POSEBNA NAVODILA ZA SHRANJEVANJE
Steklenica mora biti tesno zaprta za zagotovitev zaščite pred vlago.
20
10.
POSEBNI VARNOSTNI UKREPI ZA ODSTRANJEVANJE NEUPORABLJENIH
ZDRAVIL ALI IZ NJIH NASTALIH ODPADNIH SNOVI, KADAR SO POTREBNI
11.
IME IN NASLOV IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
Univar Solutions BV
Schouwburgplein 30
3012 CL Rotterdam
Nizozemska
12.
ŠTEVILKA (E) DOVOLJENJA (DOVOLJENJ) ZA PROMET
EU/1/19/1365/002
13.
ŠTEVILKA SERIJE
Lot
14.
NAČIN IZDAJANJA ZDRAVILA
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA_ _
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI
21
PODATKI NA ZUNANJI OVOJNINI
KARTON
1.
IME ZDRAVILA
Cufence 200 mg trde kapsule
trientin
2.
NAVEDBA ENE ALI VEČ UČINKOVIN
                                
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Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
1.
IME ZDRAVILA
Cufence 100 mg trde kapsule
Cufence 200 mg trde kapsule
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Cufence 100 mg trde kapsule
Ena trda kapsula vsebuje 150 mg trientinijevega diklorida, kar ustreza
100 mg trientina.
Cufence 200 mg trde kapsule
Ena trda kapsula vsebuje 300 mg trientinijevega diklorida, kar ustreza
200 mg trientina.
Za celoten seznam pomožnih snovi glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
Trda kapsula.
Cufence 100 mg trde kapsule
Bela ovalna kapsula velikosti 3 z napisom »Cufence 100« v sivi
barvi.
Cufence 200 mg trde kapsule
Bela ovalna kapsula velikosti 0 z napisom »Cufence« v sivi barvi.
4.
KLINIČNI PODATKI
4.1
TERAPEVTSKE INDIKACIJE
Zdravilo Cufence je indicirano za zdravljenje Wilsonove bolezni pri
odraslih, mladostnikih in otrocih,
starih 5 let ali več, ki ne prenašajo zdravljenja z D-penicilaminom.
4.2
ODMERJANJE IN NAČIN UPORABE
Zdravljenje z zdravilom Cufence sme uvesti le zdravnik specialist z
izkušnjami z zdravljenjem
Wilsonove bolezni.
Odmerjanje
Začetni odmerek običajno ustreza najmanjšemu priporočljivemu
odmerku in ga je treba naknadno
prilagoditi glede na bolnikov klinični odziv (glejte poglavje 4.4).
Priporočeni odmerek je med 800 in 1600 mg na dan, razdeljen v 2 do 4
odmerke.
Priporočeni odmerki zdravila Cufence so izraženi v mg baze trientina
(ne pa v mg soli trientinijevega
diklorida) (glejte poglavje 4.4).
Posebne skupine bolnikov
_ _
_Starejši _
3
Za zdravilo Cufuence ni na voljo dovolj podatkov za ugotovitev razlik
v odzivu med starejšimi in
mlajšimi bolniki. Na splošno velja, da je pri izboru odmerka
potrebna previdnost, zato običajno
začnemo z najmanjšim priporočljivim odmerkom za odrasle, zaradi
bolj pogoste zmanjšane jetrne,
ledvične ali srčne funkcije ter sočasnih bolezni ali zdravljenja z
drugimi zdravili.
_Okvara ledvic _
Podatkov o uporabi zdravila pri bolnikih z okvaro ledvic je malo. Zato
je priporočen odmerek pri
bolnikih z okvaro ledvic enak priporočenemu odmerku za od
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 12-12-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 12-12-2023
Public Assessment Report Public Assessment Report Bulgarian 28-10-2022
Patient Information leaflet Patient Information leaflet Spanish 12-12-2023
Public Assessment Report Public Assessment Report Spanish 28-10-2022
Patient Information leaflet Patient Information leaflet Czech 12-12-2023
Public Assessment Report Public Assessment Report Czech 28-10-2022
Patient Information leaflet Patient Information leaflet Danish 12-12-2023
Public Assessment Report Public Assessment Report Danish 28-10-2022
Patient Information leaflet Patient Information leaflet German 12-12-2023
Public Assessment Report Public Assessment Report German 28-10-2022
Patient Information leaflet Patient Information leaflet Estonian 12-12-2023
Public Assessment Report Public Assessment Report Estonian 28-10-2022
Patient Information leaflet Patient Information leaflet Greek 12-12-2023
Public Assessment Report Public Assessment Report Greek 28-10-2022
Patient Information leaflet Patient Information leaflet English 12-12-2023
Public Assessment Report Public Assessment Report English 28-10-2022
Patient Information leaflet Patient Information leaflet French 12-12-2023
Public Assessment Report Public Assessment Report French 28-10-2022
Patient Information leaflet Patient Information leaflet Italian 12-12-2023
Public Assessment Report Public Assessment Report Italian 28-10-2022
Patient Information leaflet Patient Information leaflet Latvian 12-12-2023
Public Assessment Report Public Assessment Report Latvian 28-10-2022
Patient Information leaflet Patient Information leaflet Lithuanian 12-12-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 12-12-2023
Public Assessment Report Public Assessment Report Lithuanian 28-10-2022
Patient Information leaflet Patient Information leaflet Hungarian 12-12-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 12-12-2023
Public Assessment Report Public Assessment Report Hungarian 28-10-2022
Patient Information leaflet Patient Information leaflet Maltese 12-12-2023
Public Assessment Report Public Assessment Report Maltese 28-10-2022
Patient Information leaflet Patient Information leaflet Dutch 12-12-2023
Public Assessment Report Public Assessment Report Dutch 28-10-2022
Patient Information leaflet Patient Information leaflet Polish 12-12-2023
Public Assessment Report Public Assessment Report Polish 28-10-2022
Patient Information leaflet Patient Information leaflet Portuguese 12-12-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 12-12-2023
Public Assessment Report Public Assessment Report Portuguese 28-10-2022
Patient Information leaflet Patient Information leaflet Romanian 12-12-2023
Public Assessment Report Public Assessment Report Romanian 28-10-2022
Patient Information leaflet Patient Information leaflet Slovak 12-12-2023
Public Assessment Report Public Assessment Report Slovak 28-10-2022
Patient Information leaflet Patient Information leaflet Finnish 12-12-2023
Public Assessment Report Public Assessment Report Finnish 28-10-2022
Patient Information leaflet Patient Information leaflet Swedish 08-11-2022
Public Assessment Report Public Assessment Report Swedish 28-10-2022
Patient Information leaflet Patient Information leaflet Norwegian 12-12-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 12-12-2023
Patient Information leaflet Patient Information leaflet Icelandic 12-12-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 12-12-2023
Patient Information leaflet Patient Information leaflet Croatian 12-12-2023
Public Assessment Report Public Assessment Report Croatian 28-10-2022

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