Protaphane

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

Insulin human

Available from:

Novo Nordisk A/S

ATC code:

A10AC01

INN (International Name):

insulin human (rDNA)

Therapeutic group:

Zdravila, ki se uporabljajo pri diabetesu

Therapeutic area:

Sladkorna bolezen

Therapeutic indications:

Zdravljenje diabetes mellitus.

Product summary:

Revision: 18

Authorization status:

Pooblaščeni

Authorization date:

2002-10-07

Patient Information leaflet

                                18
9.
POSEBNA NAVODILA ZA SHRANJEVANJE
Pred odprtjem: shranjujte v hladilniku. Ne zamrzujte.
Med uporabo: shranjujte pri temperaturi do 25
°
C. Ne shranjujte v hladilniku in ne zamrzujte.
Vialo shranjujte v zunanji ovojnini za zagotovitev zaščite pred
svetlobo.
10.
POSEBNI VARNOSTNI UKREPI ZA ODSTRANJEVANJE NEUPORABLJENIH
ZDRAVIL ALI IZ NJIH NASTALIH ODPADNIH SNOVI, KADAR SO POTREBNI
Po vsakem injiciranju injekcijsko iglo in brizgo ustrezno zavrzite.
11.
IME IN NASLOV IMETNIKA DOVOLJENJA ZA PROMET Z ZDRAVILOM
Novo Nordisk A/S, Novo Allé, DK-2880 Bagsvaerd, Danska
12.
ŠTEVILKE DOVOLJENJ ZA PROMET
EU/1/02/233/001
1 viala z 10 ml
EU/1/02/233/002
5 vial z 10 ml
13.
ŠTEVILKA SERIJE
Lot:
14.
NAČIN IZDAJANJA ZDRAVILA
15.
NAVODILA ZA UPORABO
16.
PODATKI V BRAILLOVI PISAVI
Protaphane 40
17.
EDINSTVENA OZNAKA – DVODIMENZIONALNA ČRTNA KODA_ _
Vsebuje dvodimenzionalno črtno kodo z edinstveno oznako.
18.
EDINSTVENA OZNAKA – V BERLJIVI OBLIKI_ _
PC
SN
NN
19
PODATKI, KI MORAJO BITI NAJMANJ NAVEDENI NA MANJŠIH STIČNIH
OVOJNINAH
NALEPKA (VIALA)
1.
IME ZDRAVILA IN POT UPORABE
Protaphane 40 mednarodnih enot/ml
suspenzija za injiciranje
humani insulin
za s.c. uporabo
2.
POSTOPEK
UPORABE
3.
DATUM IZTEKA ROKA UPORABNOSTI ZDRAVILA
EXP/
4.
ŠTEVILKA SERIJE
Lot:
5.
VSEBINA, IZRAŽENA Z MASO, PROSTORNINO ALI ŠTEVILOM ENOT
10 ml
6.
DRUGI PODATKI
Novo Nordisk A/S
20
PODATKI NA ZUNANJI OVOJNINI
ŠKATLA (VIALA)
1.
IME ZDRAVILA
Protaphane 100 mednarodnih enot/ml
suspenzija za injiciranje
humani insulin
2.
NAVEDBA ENE ALI VEČ UČINKOVIN
Ena viala vsebuje 10 ml, kar ustreza 1.000 mednarodnim enotam. 1 ml
suspenzije vsebuje
100 mednarodnih enot humanega insulina (kar ustreza 3,5 mg),
3.
SEZNAM POMOŽNIH SNOVI
cinkov klorid, glicerol, metakrezol, fenol, natrijev hidrogenfosfat
dihidrat, natrijev
hidroksid/klorovodikovo kislino za uravnavanje pH, protaminijev sulfat
in vodo za injekcije.
4.
FARMACEVTSKA OBLIKA IN VSEBINA
suspenzija za injiciranje
1 viala z 10 ml
5 vial z 10 ml
5.
POSTOPEK IN POT UPORABE ZDRAVILA
za subkutano uporab
                                
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Summary of Product characteristics

                                1
PRILOGA I
POVZETEK GLAVNIH ZNAČILNOSTI ZDRAVILA
2
1.
IME ZDRAVILA
Protaphane 40 mednarodnih enot/ml suspenzija za injiciranje v viali
Protaphane 100 mednarodnih enot/ml suspenzija za injiciranje v viali
Protaphane Penfill 100 mednarodnih enot/ml suspenzija za injiciranje v
vložku
Protaphane InnoLet 100 mednarodnih enot/ml suspenzija za injiciranje v
napolnjenem injekcijskem
peresniku
Protaphane FlexPen 100 mednarodnih enot/ml suspenzija za injiciranje v
napolnjenem injekcijskem
peresniku
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Protaphane viala (40 mednarodnih enot/ml)
Ena viala vsebuje 10 ml, kar ustreza 400 mednarodnim enotam. 1 ml
suspenzije vsebuje
40 mednarodnih enot humanega insulina izofan (NPH)* (kar ustreza 1,4
mg).
Protaphane viala (100 mednarodnih enot/ml)
Ena viala vsebuje 10 ml, kar ustreza 1.000 mednarodnim enotam. 1 ml
suspenzije vsebuje
100 mednarodnih enot humanega insulina izofan (NPH)* (kar ustreza 3,5
mg).
Protaphane Penfill
En vložek vsebuje 3 ml, kar ustreza 300 mednarodnim enotam. 1 ml
suspenzije vsebuje
100 mednarodnih enot humanega insulina izofan (NPH)* (kar ustreza 3,5
mg).
Protaphane InnoLet/Protaphane FlexPen
En napolnjen injekcijski peresnik vsebuje 3 ml, kar ustreza 300
mednarodnim enotam. 1 ml suspenzije
vsebuje 100 mednarodnih enot humanega insulina izofan (NPH)* (kar
ustreza 3,5 mg).
*Humani insulin je pridobljen iz
_Saccharomyces cerevisiae_
s tehnologijo rekombinantne DNA.
Pomožna snov z znanim učinkom:
Zdravilo Protaphane vsebuje manj kot 1 mmol (23 mg) natrija na
odmerek, kar v bistvu pomeni "brez
natrija".
Za celoten seznam pomožnih snovi glejte poglavje 6.1.
3.
FARMACEVTSKA OBLIKA
suspenzija za injiciranje
Suspenzija je motna, bela in vodna.
4.
KLINIČNI PODATKI
4.1
TERAPEVTSKE INDIKACIJE
Zdravilo Protaphane je namenjeno zdravljenju sladkorne bolezni.
4.2
ODMERJANJE IN NAČIN UPORABE
ODMERJANJE
Moč humanega insulina izražamo v mednarodnih enotah.
3
Odmerjanje zdravila Protaphane je individualno in določeno skladno z
bolnikovimi potrebami.
Zdravnik se odloči, ali je 
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 27-10-2020
Public Assessment Report Public Assessment Report Bulgarian 23-09-2014
Patient Information leaflet Patient Information leaflet Spanish 27-10-2020
Public Assessment Report Public Assessment Report Spanish 23-09-2014
Patient Information leaflet Patient Information leaflet Czech 27-10-2020
Public Assessment Report Public Assessment Report Czech 23-09-2014
Patient Information leaflet Patient Information leaflet Danish 27-10-2020
Public Assessment Report Public Assessment Report Danish 23-09-2014
Patient Information leaflet Patient Information leaflet German 27-10-2020
Public Assessment Report Public Assessment Report German 23-09-2014
Patient Information leaflet Patient Information leaflet Estonian 27-10-2020
Public Assessment Report Public Assessment Report Estonian 23-09-2014
Patient Information leaflet Patient Information leaflet Greek 27-10-2020
Public Assessment Report Public Assessment Report Greek 23-09-2014
Patient Information leaflet Patient Information leaflet English 27-10-2020
Public Assessment Report Public Assessment Report English 23-09-2014
Patient Information leaflet Patient Information leaflet French 27-10-2020
Public Assessment Report Public Assessment Report French 23-09-2014
Patient Information leaflet Patient Information leaflet Italian 27-10-2020
Public Assessment Report Public Assessment Report Italian 23-09-2014
Patient Information leaflet Patient Information leaflet Latvian 27-10-2020
Public Assessment Report Public Assessment Report Latvian 23-09-2014
Patient Information leaflet Patient Information leaflet Lithuanian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 27-10-2020
Public Assessment Report Public Assessment Report Lithuanian 23-09-2014
Patient Information leaflet Patient Information leaflet Hungarian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 27-10-2020
Public Assessment Report Public Assessment Report Hungarian 23-09-2014
Patient Information leaflet Patient Information leaflet Maltese 27-10-2020
Public Assessment Report Public Assessment Report Maltese 23-09-2014
Patient Information leaflet Patient Information leaflet Dutch 27-10-2020
Public Assessment Report Public Assessment Report Dutch 23-09-2014
Patient Information leaflet Patient Information leaflet Polish 27-10-2020
Public Assessment Report Public Assessment Report Polish 23-09-2014
Patient Information leaflet Patient Information leaflet Portuguese 27-10-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 27-10-2020
Public Assessment Report Public Assessment Report Portuguese 23-09-2014
Patient Information leaflet Patient Information leaflet Romanian 27-10-2020
Public Assessment Report Public Assessment Report Romanian 23-09-2014
Patient Information leaflet Patient Information leaflet Slovak 27-10-2020
Public Assessment Report Public Assessment Report Slovak 23-09-2014
Patient Information leaflet Patient Information leaflet Finnish 27-10-2020
Public Assessment Report Public Assessment Report Finnish 23-09-2014
Patient Information leaflet Patient Information leaflet Swedish 27-10-2020
Public Assessment Report Public Assessment Report Swedish 23-09-2014
Patient Information leaflet Patient Information leaflet Norwegian 27-10-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 27-10-2020
Patient Information leaflet Patient Information leaflet Icelandic 27-10-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 27-10-2020
Patient Information leaflet Patient Information leaflet Croatian 27-10-2020

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