Intuniv

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

gvanfacinijev klorid

Available from:

Takeda Pharmaceuticals International AG Ireland Branch

ATC code:

C02AC02

INN (International Name):

guanfacine

Therapeutic group:

Antiadrenergic agents, centrally acting, Antihypertensives,

Therapeutic area:

Motnja deficita pri hiperaktivnosti

Therapeutic indications:

Intuniv is indicated for the treatment of attention deficit hyperactivity disorder (ADHD) in children and adolescents 6 17 years old for whom stimulants are not suitable, not tolerated or have been shown to be ineffective. Intuniv mora biti uporabljena kot del celovite ADHD zdravljenje programa, običajno vključujejo tudi psihološke, izobraževalnih in socialnih ukrepov.

Product summary:

Revision: 12

Authorization status:

Pooblaščeni

Authorization date:

2015-09-17

Patient Information leaflet

                                26
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
Takeda Pharmaceuticals International AG Ireland Branch
Block 2 Miesian Plaza
50-58 Baggot Street Lower
Dublin 2
D02 HW68
Irska
12.
ŠTEVILKA(E) DOVOLJENJA (DOVOLJENJ) ZA PROMET
EU/1/15/1040/001 7 tablet s podaljšanim sproščanjem
EU/1/15/1040/002 28 tablet s podaljšanim sproščanjem
13.
ŠTEVILKA SERIJE
Lot
14.
NAČIN IZDAJANJA ZDRAVILA
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
Intuniv 1 mg
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA
Vsebuje dvodimenzionalno črtno kodo z edinstveno oznako.
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI
PC
SN
NN
27
PODATKI, KI MORAJO BITI NAJMANJ NAVEDENI NA PRETISNEM OMOTU ALI
DVOJNEM TRAKU
PRETISNI OMOTI
1.
IME ZDRAVILA
Intuniv 1 mg tablete s podaljšanim sproščanjem
gvanfacin
2.
IME IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
Takeda Pharmaceuticals International AG Ireland Branch (kot logotip
imetnika dovoljenja)
3.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
EXP
4.
ŠTEVILKA SERIJE
Lot
5.
DRUGI PODATKI
28
PODATKI NA ZUNANJI OVOJNINI
ŠKATLA
1.
IME ZDRAVILA
Intuniv 2 mg tablete s podaljšanim sproščanjem
gvanfacin
2.
NAVEDBA ENE ALI VEČ UČINKOVIN
Ena tableta vsebuje 2 mg gvanfacina v obliki gvanfacinijevega klorida.
3.
SEZNAM POMOŽNIH SNOVI
Vsebuje tudi laktozo. Za nadaljnje informacije glejte navodilo za
uporabo.
4.
FARMACEVTSKA OBLIKA IN VSEBINA
7 tablet s podaljšanim sproščanjem
28 tablet s podaljšanim sproščanjem
84 tablet s podaljšanim sproščanjem
5.
POSTOPEK IN POT(I) UPORABE ZDRAVILA
Pred uporabo preberite priloženo navodilo!
peroralna uporaba
Tableto pogoltnite célo. Tablete ne smete žvečiti, razdeliti ali
zdrobiti.
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
9.
POSEBNA NAVODILA ZA SHRAN
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
Za to zdravilo se izvaja dodatno spremljanje varnosti. Tako bodo
hitreje na voljo nove informacije
o njegovi varnosti. Zdravstvene delavce naprošamo, da poročajo o
katerem koli domnevnem
neželenem učinku zdravila. Glejte poglavje 4.8, kako poročati o
neželenih učinkih.
1.
IME ZDRAVILA
Intuniv 1 mg tablete s podaljšanim sproščanjem
Intuniv 2 mg tablete s podaljšanim sproščanjem
Intuniv 3 mg tablete s podaljšanim sproščanjem
Intuniv 4 mg tablete s podaljšanim sproščanjem
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Intuniv 1 mg tableta s podaljšanim sproščanjem
Ena tableta vsebuje 1 mg gvanfacina v obliki gvanfacinijevega klorida.
_Pomožna(e) snov(i) z znanim učinkom:_
Ena tableta vsebuje 22,41 mg laktoze (v obliki monohidrata).
Intuniv 2 mg tableta s podaljšanim sproščanjem
Ena tableta vsebuje 2 mg gvanfacina v obliki gvanfacinijevega klorida
_Pomožna(e) snov(i) z znanim učinkom:_
Ena tableta vsebuje 44,82 mg laktoze (v obliki monohidrata).
Intuniv 3 mg tableta s podaljšanim sproščanjem
Ena tableta vsebuje 3 mg gvanfacina v obliki gvanfacinijevega klorida
_Pomožna(e) snov(i) z znanim učinkom:_
Ena tableta vsebuje 37,81 mg laktoze (v obliki monohidrata).
Intuniv 4 mg tableta s podaljšanim sproščanjem
Ena tableta vsebuje 4 mg gvanfacina v obliki gvanfacinijevega klorida.
_Pomožna(e) snov(i) z znanim učinkom:_
Ena 4 mg tableta vsebuje 50,42 mg laktoze (v obliki monohidrata).
Za celoten seznam pomožnih snovi glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
tableta s podaljšanim sproščanjem
Intuniv 1 mg tableta s podaljšanim sproščanjem
Okrogle, bele do belkaste tablete, 7,14 mm v premeru, z vtisnjenim
napisom ‘1MG’ na eni strani in
‘503’ na drugi strani.
3
Intuniv 2 mg tableta s podaljšanim sproščanjem
Ovalne, bele do belkaste tablete, velike 12,34 mm x 6,10 mm, z
vtisnjenim napisom ‘2MG’ na eni
strani in ‘503’ na drugi strani.
Intuniv 3 mg tableta s podaljšanim sproščanjem
Okrogle, zelene tablete, 7,94 mm v pre
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 16-02-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 16-02-2023
Public Assessment Report Public Assessment Report Bulgarian 06-10-2015
Patient Information leaflet Patient Information leaflet Spanish 16-02-2023
Public Assessment Report Public Assessment Report Spanish 06-10-2015
Patient Information leaflet Patient Information leaflet Czech 16-02-2023
Public Assessment Report Public Assessment Report Czech 06-10-2015
Patient Information leaflet Patient Information leaflet Danish 16-02-2023
Public Assessment Report Public Assessment Report Danish 06-10-2015
Patient Information leaflet Patient Information leaflet German 16-02-2023
Public Assessment Report Public Assessment Report German 06-10-2015
Patient Information leaflet Patient Information leaflet Estonian 16-02-2023
Public Assessment Report Public Assessment Report Estonian 06-10-2015
Patient Information leaflet Patient Information leaflet Greek 16-02-2023
Public Assessment Report Public Assessment Report Greek 06-10-2015
Patient Information leaflet Patient Information leaflet English 16-02-2023
Public Assessment Report Public Assessment Report English 06-10-2015
Patient Information leaflet Patient Information leaflet French 16-02-2023
Public Assessment Report Public Assessment Report French 06-10-2015
Patient Information leaflet Patient Information leaflet Italian 16-02-2023
Public Assessment Report Public Assessment Report Italian 06-10-2015
Patient Information leaflet Patient Information leaflet Latvian 16-02-2023
Public Assessment Report Public Assessment Report Latvian 06-10-2015
Patient Information leaflet Patient Information leaflet Lithuanian 16-02-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 16-02-2023
Public Assessment Report Public Assessment Report Lithuanian 06-10-2015
Patient Information leaflet Patient Information leaflet Hungarian 16-02-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 16-02-2023
Public Assessment Report Public Assessment Report Hungarian 06-10-2015
Patient Information leaflet Patient Information leaflet Maltese 16-02-2023
Public Assessment Report Public Assessment Report Maltese 06-10-2015
Patient Information leaflet Patient Information leaflet Dutch 16-02-2023
Public Assessment Report Public Assessment Report Dutch 06-10-2015
Patient Information leaflet Patient Information leaflet Polish 16-02-2023
Public Assessment Report Public Assessment Report Polish 06-10-2015
Patient Information leaflet Patient Information leaflet Portuguese 16-02-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 16-02-2023
Public Assessment Report Public Assessment Report Portuguese 06-10-2015
Patient Information leaflet Patient Information leaflet Romanian 16-02-2023
Public Assessment Report Public Assessment Report Romanian 06-10-2015
Patient Information leaflet Patient Information leaflet Slovak 16-02-2023
Public Assessment Report Public Assessment Report Slovak 06-10-2015
Patient Information leaflet Patient Information leaflet Finnish 16-02-2023
Public Assessment Report Public Assessment Report Finnish 06-10-2015
Patient Information leaflet Patient Information leaflet Swedish 16-02-2023
Public Assessment Report Public Assessment Report Swedish 06-10-2015
Patient Information leaflet Patient Information leaflet Norwegian 16-02-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 16-02-2023
Patient Information leaflet Patient Information leaflet Icelandic 16-02-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 16-02-2023
Patient Information leaflet Patient Information leaflet Croatian 16-02-2023
Public Assessment Report Public Assessment Report Croatian 06-10-2015

Search alerts related to this product

View documents history