Skytrofa (previously Lonapegsomatropin Ascendis Pharma)

Country: European Union

Language: Slovenian

Source: EMA (European Medicines Agency)

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Active ingredient:

Lonapegsomatropin

Available from:

Ascendis Pharma Endocrinology Division A/S

ATC code:

H01AC09

INN (International Name):

lonapegsomatropin

Therapeutic group:

Hipofize in hipotalamični hormoni in analogi

Therapeutic area:

Growth and Development

Therapeutic indications:

Growth failure in children and adolescents aged from 3 years up to 18 years due to insufficient endogenous growth hormone secretion (growth hormone deficiency [GHD]),.

Product summary:

Revision: 4

Authorization status:

Pooblaščeni

Authorization date:

2022-01-11

Patient Information leaflet

                                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
Skytrofa 3 mg prašek in vehikel za raztopino za injiciranje v vložku
Skytrofa 3,6 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 4,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 5,2 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 6,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 7,6 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 9,1 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 11 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 13,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Zdravilo Skytrofa je sestavljeno iz somatropina, prehodno
konjugiranega na nosilec
metoksipolietilenglikol (mPEG) prek lastniškega povezovalca TransCon.
Jakost zdravila Skytrofa
vedno označuje količino komponente somatropina.
Skytrofa 3 mg prašek in vehikel za raztopino za injiciranje v vložku
En dvoprekatni vložek vsebuje 3 mg somatropina,* kar je enakovredno
8,6 mg lonapegsomatropina, in
0,279 ml vehikla. Po rekonstituciji je koncentracija na osnovi
beljakovine somatropina** 11 mg/ml.
Skytrofa 3,6 mg prašek in vehikel za raztopino za injiciranje v
vložku
En dvoprekatni vložek vsebuje 3,6 mg somatropina,* kar je enakovredno
10,3 mg
lonapegsomatropina, in 0,329 ml vehikla. Po rekonstituciji je
koncentracija na osnovi beljakovine
somatropina** 11 mg/ml.
Skytrofa 4,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
En dvoprekatni vložek vsebuje 4,3 mg somatropina,* kar je enakovredno
12,3 mg
lonapegsomatropina, in 0,388 ml vehikla. Po rekonstituciji je
koncentracija na osnovi 
                                
                                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
Skytrofa 3 mg prašek in vehikel za raztopino za injiciranje v vložku
Skytrofa 3,6 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 4,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 5,2 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 6,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 7,6 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 9,1 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 11 mg prašek in vehikel za raztopino za injiciranje v
vložku
Skytrofa 13,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
2.
KAKOVOSTNA IN KOLIČINSKA SESTAVA
Zdravilo Skytrofa je sestavljeno iz somatropina, prehodno
konjugiranega na nosilec
metoksipolietilenglikol (mPEG) prek lastniškega povezovalca TransCon.
Jakost zdravila Skytrofa
vedno označuje količino komponente somatropina.
Skytrofa 3 mg prašek in vehikel za raztopino za injiciranje v vložku
En dvoprekatni vložek vsebuje 3 mg somatropina,* kar je enakovredno
8,6 mg lonapegsomatropina, in
0,279 ml vehikla. Po rekonstituciji je koncentracija na osnovi
beljakovine somatropina** 11 mg/ml.
Skytrofa 3,6 mg prašek in vehikel za raztopino za injiciranje v
vložku
En dvoprekatni vložek vsebuje 3,6 mg somatropina,* kar je enakovredno
10,3 mg
lonapegsomatropina, in 0,329 ml vehikla. Po rekonstituciji je
koncentracija na osnovi beljakovine
somatropina** 11 mg/ml.
Skytrofa 4,3 mg prašek in vehikel za raztopino za injiciranje v
vložku
En dvoprekatni vložek vsebuje 4,3 mg somatropina,* kar je enakovredno
12,3 mg
lonapegsomatropina, in 0,388 ml vehikla. Po rekonstituciji je
koncentracija na osnovi 
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 06-11-2023
Public Assessment Report Public Assessment Report Bulgarian 04-02-2022
Patient Information leaflet Patient Information leaflet Spanish 06-11-2023
Public Assessment Report Public Assessment Report Spanish 04-02-2022
Patient Information leaflet Patient Information leaflet Czech 06-11-2023
Public Assessment Report Public Assessment Report Czech 04-02-2022
Patient Information leaflet Patient Information leaflet Danish 06-11-2023
Public Assessment Report Public Assessment Report Danish 04-02-2022
Patient Information leaflet Patient Information leaflet German 06-11-2023
Public Assessment Report Public Assessment Report German 04-02-2022
Patient Information leaflet Patient Information leaflet Estonian 06-11-2023
Public Assessment Report Public Assessment Report Estonian 04-02-2022
Patient Information leaflet Patient Information leaflet Greek 06-11-2023
Public Assessment Report Public Assessment Report Greek 04-02-2022
Patient Information leaflet Patient Information leaflet English 06-11-2023
Public Assessment Report Public Assessment Report English 04-02-2022
Patient Information leaflet Patient Information leaflet French 06-11-2023
Public Assessment Report Public Assessment Report French 04-02-2022
Patient Information leaflet Patient Information leaflet Italian 06-11-2023
Public Assessment Report Public Assessment Report Italian 04-02-2022
Patient Information leaflet Patient Information leaflet Latvian 06-11-2023
Public Assessment Report Public Assessment Report Latvian 04-02-2022
Patient Information leaflet Patient Information leaflet Lithuanian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 06-11-2023
Public Assessment Report Public Assessment Report Lithuanian 04-02-2022
Patient Information leaflet Patient Information leaflet Hungarian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 06-11-2023
Public Assessment Report Public Assessment Report Hungarian 04-02-2022
Patient Information leaflet Patient Information leaflet Maltese 06-11-2023
Public Assessment Report Public Assessment Report Maltese 04-02-2022
Patient Information leaflet Patient Information leaflet Dutch 06-11-2023
Public Assessment Report Public Assessment Report Dutch 04-02-2022
Patient Information leaflet Patient Information leaflet Polish 06-11-2023
Public Assessment Report Public Assessment Report Polish 04-02-2022
Patient Information leaflet Patient Information leaflet Portuguese 06-11-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 06-11-2023
Public Assessment Report Public Assessment Report Portuguese 04-02-2022
Patient Information leaflet Patient Information leaflet Romanian 06-11-2023
Public Assessment Report Public Assessment Report Romanian 04-02-2022
Patient Information leaflet Patient Information leaflet Slovak 06-11-2023
Public Assessment Report Public Assessment Report Slovak 04-02-2022
Patient Information leaflet Patient Information leaflet Finnish 06-11-2023
Public Assessment Report Public Assessment Report Finnish 04-02-2022
Patient Information leaflet Patient Information leaflet Swedish 06-11-2023
Public Assessment Report Public Assessment Report Swedish 04-02-2022
Patient Information leaflet Patient Information leaflet Norwegian 06-11-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 06-11-2023
Patient Information leaflet Patient Information leaflet Icelandic 06-11-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 06-11-2023
Patient Information leaflet Patient Information leaflet Croatian 06-11-2023
Public Assessment Report Public Assessment Report Croatian 04-02-2022

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