Qtern

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

Saxagliptin, dapagliflozin propanediol monohidrat

Available from:

Astra Zeneca AB

ATC code:

A10BD21

INN (International Name):

saxagliptin, dapagliflozin

Therapeutic group:

Zdravila, ki se uporabljajo pri diabetesu

Therapeutic area:

Diabetes Mellitus, Type 2; Diabetes Mellitus; Nutritional and Metabolic Diseases; Metabolic Diseases; Glucose Metabolism Disorders

Therapeutic indications:

Qtern, fiksni odmerek kombinacija saxagliptin in dapagliflozin, je navedeno pri odraslih, starih 18 let in več, z vrsto 2 sladkorna bolezen:za izboljšanje glycaemic nadzor, ko metforminom in/ali sulfonil sečnine (SU) in eden od monocomponents od Qtern ne zagotavljajo ustrezne glycaemic nadzor,ko se že zdravijo z brezplačno kombinacija dapagliflozin in saxagliptin. (Glej točki 4. 2, 4. 4, 4. 5 in 5. 1, če so na voljo podatki o kombinacije študiral.

Product summary:

Revision: 11

Authorization status:

Pooblaščeni

Authorization date:

2016-07-15

Patient Information leaflet

                                33
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
AstraZeneca AB
SE-151 85 Södertälje
Švedska
12.
ŠTEVILKA(E) DOVOLJENJA(DOVOLJENJ) ZA PROMET
EU/1/16/1108/001 14 filmsko obloženih tablet
EU/1/16/1108/002 28 filmsko obloženih tablet
EU/1/16/1108/003 98 filmsko obloženih tablet
EU/1/16/1108/004 30 filmsko obloženih tablet
13.
ŠTEVILKA SERIJE
Lot
14.
NAČIN IZDAJANJA ZDRAVILA
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
qtern 5 mg/10 mg
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA
Vsebuje dvodimenzionalno črtno kodo z edinstveno oznako.
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI
PC
SN
NN
34
PODATKI, KI MORAJO BITI NAJMANJ NAVEDENI NA PRETISNEM OMOTU ALI
DVOJNEM TRAKU
PRETISNI OMOTI
1.
IME ZDRAVILA
Qtern 5 mg/10 mg tablete
saksagliptin/dapagliflozin
2.
IME IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
AstraZeneca AB
3.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
EXP
4.
ŠTEVILKA SERIJE
Lot
5.
DRUGI PODATKI
35
PODATKI, KI MORAJO BITI NAJMANJ NAVEDENI NA PRETISNEM OMOTU ALI
DVOJNEM TRAKU
KOLEDARSKI PRETISNI OMOTI
1.
IME ZDRAVILA
Qtern 5 mg/10 mg tablete
saksagliptin/dapagliflozin
2.
IME IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
AstraZeneca AB
3.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
EXP
4.
ŠTEVILKA SERIJE
Lot
5.
DRUGI PODATKI
Pon Tor Sre Čet Pet Sob Ned
36
B. NAVODILO ZA UPORABO
37
NAVODILO ZA UPORABO
QTERN 5 MG/10 MG FILMSKO OBLOŽENE TABLETE
saksagliptin/dapagliflozin
PRED ZAČETKOM JEMANJA ZDRAVILA NATANČNO PREBERITE NAVODILO, KER
VSEBUJE ZA VAS POMEMBNE
PODATKE!
-
Navodilo shranite. Morda ga boste želeli ponovno prebrati.
-
Če imate dodatna vprašanja, se posvetujte z zdravnikom, farmacevtom
ali medicinsko sestro.
-
Zdravilo je bilo predpisano vam osebno in ga ne smete dajati drugim.
Njim bi lahko celo
škodovalo, čeprav imajo znake bolezni, podobne vašim.
-
Če opazite kateri koli neželeni učinek, se posvetujte z zdravnikom
ali farmacevtom. Posvet
                                
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Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
1.
IME ZDRAVILA
Qtern 5 mg/10 mg filmsko obložene tablete
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Ena tableta vsebuje 5 mg saksagliptina v obliki saksagliptinijevega
klorida in 10 mg dapagliflozina v
obliki dapagliflozin propandiol monohidrata.
Pomožna snov z znanim učinkom:
Ena tableta vsebuje 40 mg laktoze.
Za celoten seznam pomožnih snovi glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
filmsko obložena tableta (tableta)
Svetlorjave do rjave bikonveksne 0,8 cm velike okrogle filmsko
obložene tablete, ki imajo z modrim
črnilom na eni strani natisnjeno oznako "5/10" in na drugi strani
oznako "1122".
4.
KLINIČNI PODATKI
4.1
TERAPEVTSKE INDIKACIJE
Zdravilo Qtern (fiksna kombinacija saksagliptina in dapagliflozina) je
indicirano pri odraslih, starih
18 let ali več, s sladkorno boleznijo tipa 2:
-
za izboljšanje urejenosti glikemije, če metformin in/ali
sulfonilsečnina (SS) ter ena od
posameznih učinkovin v zdravilu Qtern ne zagotovijo ustrezne
urejenosti glikemije,
-
v primeru, da se bolnik že zdravi s prosto kombinacijo dapagliflozina
in saksagliptina.
(Glejte poglavja 4.2, 4.4, 4.5 in 5.1 za podatke, ki so na voljo o
raziskanih kombinacijah.)
4.2
ODMERJANJE IN NAČIN UPORABE
Odmerjanje
Priporočeni odmerek je ena tableta s 5 mg saksagliptina in 10 mg
dapagliflozina enkrat na dan (glejte
poglavji 4.5 in 4.8).
_Izpuščeni odmerek_
Če bolnik odmerek izpusti in je do naslednjega odmerka ≥ 12 ur, naj
odmerek vzame. Če odmerek
izpusti in je do naslednjega odmerka < 12 ur, mora izpuščeni odmerek
preskočiti; nato naj vzame
naslednji odmerek ob običajnem času.
_Posebne skupine bolnikov_
_Okvara ledvic_
Zdravila Qtern se ne sme uvesti pri bolnikih, ki imajo hitrost
glomerularne filtracije
[GFR -_ glomerular filtration rate_] < 60 ml/min. Zdravljenje je treba
prekiniti pri GFR trajno pod
45 ml/min. Prav tako se ga ne sme uporabljati pri bolnikih s končno
odpovedjo ledvic (glejte
poglavja 4.4, 4.8, 5.1, in 5.2).
Prilagoditev odmerka glede na delovanje ledv
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 07-02-2024
Public Assessment Report Public Assessment Report Bulgarian 27-07-2016
Patient Information leaflet Patient Information leaflet Spanish 07-02-2024
Public Assessment Report Public Assessment Report Spanish 27-07-2016
Patient Information leaflet Patient Information leaflet Czech 07-02-2024
Public Assessment Report Public Assessment Report Czech 27-07-2016
Patient Information leaflet Patient Information leaflet Danish 07-02-2024
Public Assessment Report Public Assessment Report Danish 27-07-2016
Patient Information leaflet Patient Information leaflet German 07-02-2024
Public Assessment Report Public Assessment Report German 27-07-2016
Patient Information leaflet Patient Information leaflet Estonian 07-02-2024
Public Assessment Report Public Assessment Report Estonian 27-07-2016
Patient Information leaflet Patient Information leaflet Greek 07-02-2024
Public Assessment Report Public Assessment Report Greek 27-07-2016
Patient Information leaflet Patient Information leaflet English 07-02-2024
Public Assessment Report Public Assessment Report English 27-07-2016
Patient Information leaflet Patient Information leaflet French 07-02-2024
Public Assessment Report Public Assessment Report French 27-07-2016
Patient Information leaflet Patient Information leaflet Italian 07-02-2024
Public Assessment Report Public Assessment Report Italian 27-07-2016
Patient Information leaflet Patient Information leaflet Latvian 07-02-2024
Public Assessment Report Public Assessment Report Latvian 27-07-2016
Patient Information leaflet Patient Information leaflet Lithuanian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 07-02-2024
Public Assessment Report Public Assessment Report Lithuanian 27-07-2016
Patient Information leaflet Patient Information leaflet Hungarian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 07-02-2024
Public Assessment Report Public Assessment Report Hungarian 27-07-2016
Patient Information leaflet Patient Information leaflet Maltese 07-02-2024
Public Assessment Report Public Assessment Report Maltese 27-07-2016
Patient Information leaflet Patient Information leaflet Dutch 07-02-2024
Public Assessment Report Public Assessment Report Dutch 27-07-2016
Patient Information leaflet Patient Information leaflet Polish 07-02-2024
Public Assessment Report Public Assessment Report Polish 27-07-2016
Patient Information leaflet Patient Information leaflet Portuguese 07-02-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 07-02-2024
Public Assessment Report Public Assessment Report Portuguese 27-07-2016
Patient Information leaflet Patient Information leaflet Romanian 07-02-2024
Public Assessment Report Public Assessment Report Romanian 27-07-2016
Patient Information leaflet Patient Information leaflet Slovak 07-02-2024
Public Assessment Report Public Assessment Report Slovak 27-07-2016
Patient Information leaflet Patient Information leaflet Finnish 07-02-2024
Public Assessment Report Public Assessment Report Finnish 27-07-2016
Patient Information leaflet Patient Information leaflet Swedish 07-02-2024
Public Assessment Report Public Assessment Report Swedish 27-07-2016
Patient Information leaflet Patient Information leaflet Norwegian 07-02-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 07-02-2024
Patient Information leaflet Patient Information leaflet Icelandic 07-02-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 07-02-2024
Patient Information leaflet Patient Information leaflet Croatian 07-02-2024
Public Assessment Report Public Assessment Report Croatian 27-07-2016

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