Dafiro HCT

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

valsartan, hydrochlorothiazide, Amlodipine besilate

Available from:

Novartis Europharm Limited

ATC code:

C09DX01

INN (International Name):

amlodipine besilate, valsartan, hydrochlorothiazide

Therapeutic group:

Sredstva, ki delujejo na sistem renin-angiotenzin

Therapeutic area:

Hipertenzija

Therapeutic indications:

Zdravljenje esencialne hipertenzije kot nadomestno zdravljenje pri odraslih bolnikih, katerih krvni tlak, ustrezno nadzoruje na kombinacijo Amlodipin in valsartan hidroklorotiazid (skupino), bodisi kot tri formulacije eno komponento ali kot a dvojina-komponente in eno komponento oblikovanja.

Product summary:

Revision: 26

Authorization status:

Pooblaščeni

Authorization date:

2009-11-03

Patient Information leaflet

                                35
9.
POSEBNA NAVODILA ZA SHRANJEVANJE
Shranjujte pri temperaturi do 30 °C.
Shranjujte v originalni ovojnini za zagotovitev zaščite pred vlago.
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
Novartis Europharm Limited
Vista Building
Elm Park, Merrion Road
Dublin 4
Irska
12.
ŠTEVILKA(E) DOVOLJENJA(DOVOLJENJ) ZA PROMET
EU/1/09/574/001
14 filmsko obloženih tablet
EU/1/09/574/002
28 filmsko obloženih tablet
EU/1/09/574/003
30 filmsko obloženih tablet
EU/1/09/574/004
56 filmsko obloženih tablet
EU/1/09/574/005
90 filmsko obloženih tablet
EU/1/09/574/006
98 filmsko obloženih tablet
EU/1/09/574/007
280 filmsko obloženih tablet
EU/1/09/574/008
56 x 1 filmsko obložena tableta (za enkratni odmerek)
EU/1/09/574/009
98 x 1 filmsko obložena tableta (za enkratni odmerek)
EU/1/09/574/010
280 x 1 filmsko obložena tableta (za enkratni odmerek)
13.
ŠTEVILKA SERIJE
Lot
14.
NAČIN IZDAJANJA ZDRAVILA
Predpisovanje in izdaja zdravila je le na recept.
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
Dafiro HCT 5 mg/160 mg/12,5 mg
36
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA_ _
Vsebuje dvodimenzionalno črtno kodo z edinstveno oznako.
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI_ _
PC
SN
NN
37
PODATKI NA ZUNANJI OVOJNINI
VMESNA ŠKATLA SKUPNEGA PAKIRANJA (BREZ “BLUE BOX” PODATKOV)
1.
IME ZDRAVILA
Dafiro HCT 5 mg/160 mg/12,5 mg filmsko obložene tablete
amlodipin/valsartan/hidroklorotiazid
2.
NAVEDBA ENE ALI VEČ UČINKOVIN
Ena tableta vsebuje 5 mg amlodipina (v obliki amlodipinijevega
besilata), 160 mg valsartana in
12,5 mg hidroklorotiazida.
3.
SEZNAM POMOŽNIH SNOVI
4.
FARMACEVTSKA OBLIKA IN VSEBINA
filmsko obložena tableta
14 filmsko obloženih tablet. Del skupnega pakiranja. Ni namenjen
ločeni prodaji.
70x1 filmsko obložena tableta. Del skupnega pakiranja. Ni namenjen
ločeni prodaji.
5.
POSTOPEK IN POT(I) UPORABE ZDRAVILA
Pred uporabo preberite priloženo n
                                
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Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
1.
IME ZDRAVILA
Dafiro HCT 5 mg/160 mg/12,5 mg filmsko obložene tablete
Dafiro HCT 10 mg/160 mg/12,5 mg filmsko obložene tablete
Dafiro HCT 5 mg/160 mg/25 mg filmsko obložene tablete
Dafiro HCT 10 mg/160 mg/25 mg filmsko obložene tablete
Dafiro HCT 10 mg/320 mg/25 mg filmsko obložene tablete
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Dafiro HCT 5 mg/160 mg/12,5 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 5 mg amlodipina (v obliki
amlodipinijevega besilata), 160 mg
valsartana in 12,5 mg hidroklorotiazida.
Dafiro HCT 10 mg/160 mg/12,5 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 10 mg amlodipina (v obliki
amlodipinijevega besilata), 160 mg
valsartana in 12,5 mg hidroklorotiazida.
Dafiro HCT 5 mg/160 mg/25 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 5 mg amlodipina (v obliki
amlodipinijevega besilata), 160 mg
valsartana in 25 mg hidroklorotiazida.
Dafiro HCT 10 mg/160 mg/25 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 10 mg amlodipina (v obliki
amlodipinijevega besilata), 160 mg
valsartana in 25 mg hidroklorotiazida.
Dafiro HCT 10 mg/320 mg/25 mg filmsko obložene tablete
Ena filmsko obložena tableta vsebuje 10 mg amlodipina (v obliki
amlodipinijevega besilata), 320 mg
valsartana in 25 mg hidroklorotiazida.
Za celoten seznam pomožnih snovi glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
filmsko obložena tableta (tableta)
Dafiro HCT 5 mg/160 mg/12,5 mg filmsko obložene tablete
Bele ovalne bikonveksne tablete z zaobljenim robom in oznako “NVR”
na eni strani in “VCL” na
drugi. Približna velikost: 15 mm (dolžina) x 5,9 mm (širina).
Dafiro HCT 10 mg/160 mg/12,5 mg filmsko obložene tablete
Bledo rumene ovalne bikonveksne tablete z zaobljenim robom in oznako
“NVR” na eni strani in
“VDL” na drugi. Približna velikost: 15 mm (dolžina) x 5,9 mm
(širina).
Dafiro HCT 5 mg/160 mg/25 mg filmsko obložene tablete
Rumene ovalne bikonveksne tablete z zaobljenim robom in o
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 27-09-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 27-09-2023
Public Assessment Report Public Assessment Report Bulgarian 12-12-2013
Patient Information leaflet Patient Information leaflet Spanish 27-09-2023
Public Assessment Report Public Assessment Report Spanish 12-12-2013
Patient Information leaflet Patient Information leaflet Czech 27-09-2023
Public Assessment Report Public Assessment Report Czech 12-12-2013
Patient Information leaflet Patient Information leaflet Danish 27-09-2023
Public Assessment Report Public Assessment Report Danish 12-12-2013
Patient Information leaflet Patient Information leaflet German 27-09-2023
Public Assessment Report Public Assessment Report German 12-12-2013
Patient Information leaflet Patient Information leaflet Estonian 27-09-2023
Public Assessment Report Public Assessment Report Estonian 12-12-2013
Patient Information leaflet Patient Information leaflet Greek 27-09-2023
Public Assessment Report Public Assessment Report Greek 12-12-2013
Patient Information leaflet Patient Information leaflet English 27-09-2023
Public Assessment Report Public Assessment Report English 12-12-2013
Patient Information leaflet Patient Information leaflet French 27-09-2023
Public Assessment Report Public Assessment Report French 12-12-2013
Patient Information leaflet Patient Information leaflet Italian 27-09-2023
Public Assessment Report Public Assessment Report Italian 12-12-2013
Patient Information leaflet Patient Information leaflet Latvian 27-09-2023
Public Assessment Report Public Assessment Report Latvian 12-12-2013
Patient Information leaflet Patient Information leaflet Lithuanian 27-09-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 27-09-2023
Public Assessment Report Public Assessment Report Lithuanian 12-12-2013
Patient Information leaflet Patient Information leaflet Hungarian 27-09-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 27-09-2023
Public Assessment Report Public Assessment Report Hungarian 12-12-2013
Patient Information leaflet Patient Information leaflet Maltese 27-09-2023
Public Assessment Report Public Assessment Report Maltese 12-12-2013
Patient Information leaflet Patient Information leaflet Dutch 27-09-2023
Public Assessment Report Public Assessment Report Dutch 12-12-2013
Patient Information leaflet Patient Information leaflet Polish 27-09-2023
Public Assessment Report Public Assessment Report Polish 12-12-2013
Patient Information leaflet Patient Information leaflet Portuguese 27-09-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 27-09-2023
Public Assessment Report Public Assessment Report Portuguese 12-12-2013
Patient Information leaflet Patient Information leaflet Romanian 27-09-2023
Public Assessment Report Public Assessment Report Romanian 12-12-2013
Patient Information leaflet Patient Information leaflet Slovak 27-09-2023
Public Assessment Report Public Assessment Report Slovak 12-12-2013
Patient Information leaflet Patient Information leaflet Finnish 27-09-2023
Public Assessment Report Public Assessment Report Finnish 12-12-2013
Patient Information leaflet Patient Information leaflet Swedish 27-09-2023
Public Assessment Report Public Assessment Report Swedish 12-12-2013
Patient Information leaflet Patient Information leaflet Norwegian 27-09-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 27-09-2023
Patient Information leaflet Patient Information leaflet Icelandic 27-09-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 27-09-2023
Patient Information leaflet Patient Information leaflet Croatian 27-09-2023
Public Assessment Report Public Assessment Report Croatian 12-12-2013

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