Atectura Breezhaler

Country: European Union

Language: Estonian

Source: EMA (European Medicines Agency)

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Active ingredient:

indacaterol acetate, Mometasone furoate

Available from:

Novartis Europharm Limited 

ATC code:

R03AK

INN (International Name):

indacaterol, mometasone

Therapeutic group:

Ravimid hingamisteede obstruktiivsete haiguste,

Therapeutic area:

Astma

Therapeutic indications:

Atectura Breezhaler is indicated as a maintenance treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Product summary:

Revision: 9

Authorization status:

Volitatud

Authorization date:

2020-05-30

Patient Information leaflet

                                1
I LISA
RAVIMI OMADUSTE KOKKUVÕTE
2
1.
RAVIMPREPARAADI NIMETUS
Atectura Breezhaler 125 mikrogrammi/62,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Atectura Breezhaler 125 mikrogrammi/127,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Atectura Breezhaler 125 mikrogrammi/260 mikrogrammi
inhalatsioonipulber kõvakapslites
2.
KVALITATIIVNE JA KVANTITATIIVNE KOOSTIS
Atectura Breezhaler 125 mikrogrammi/62,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Üks kapsel sisaldab 150 µg indakaterooli (
_indacaterolum_
) (atsetaadina) ja 80 µg mometasoonfuroaati
(
_mometasoni furoas_
).
Üks inhaleeritav annus (annus, mis väljutatakse inhalaatori
huulikust) sisaldab 125 µg indakaterooli
(atsetaadina) ja 62,5 µg mometasoonfuroaati.
Atectura Breezhaler 125 mikrogrammi/127,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Üks kapsel sisaldab 150 µg indakaterooli (
_indacaterolum_
) (atsetaadina) ja 160 µg mometasoonfuroaati
(
_mometasoni furoas_
).
Üks inhaleeritav annus (annus, mis väljutatakse inhalaatori
huulikust) sisaldab 125 µg indakaterooli
(atsetaadina) ja 127,5 µg mometasoonfuroaati.
Atectura Breezhaler 125 mikrogrammi/260 mikrogrammi
inhalatsioonipulber kõvakapslites
Üks kapsel sisaldab 150 µg indakaterooli (
_indacaterolum_
) (atsetaadina) ja 320 µg mometasoonfuroaati
(
_mometasoni furoas_
).
Üks inhaleeritav annus (annus, mis väljutatakse inhalaatori
huulikust) sisaldab 125 µg indakaterooli
(atsetaadina) ja 260 µg mometasoonfuroaati.
Teadaolevat toimet omav(ad) abiaine(d)
Üks kapsel sisaldab ligikaudu 25 mg laktoosmonohüdraati.
Abiainete täielik loetelu vt lõik 6.1.
3.
RAVIMVORM
Inhalatsioonipulber kõvakapslis (inhalatsioonipulber).
Atectura Breezhaler 125 mikrogrammi/62,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Läbipaistvad (värvitud) kapslid, mis sisaldavad valget pulbrit.
Kapslikorpusele on ühe sinise joone
kohale sinise tindiga trükitud toote kood „IM150-80” ning
kapslikaanele on sinise tindiga trükitud
toote logo, mida ümbritseb kaks sinist joont.
Atectura Breezha
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
I LISA
RAVIMI OMADUSTE KOKKUVÕTE
2
1.
RAVIMPREPARAADI NIMETUS
Atectura Breezhaler 125 mikrogrammi/62,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Atectura Breezhaler 125 mikrogrammi/127,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Atectura Breezhaler 125 mikrogrammi/260 mikrogrammi
inhalatsioonipulber kõvakapslites
2.
KVALITATIIVNE JA KVANTITATIIVNE KOOSTIS
Atectura Breezhaler 125 mikrogrammi/62,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Üks kapsel sisaldab 150 µg indakaterooli (
_indacaterolum_
) (atsetaadina) ja 80 µg mometasoonfuroaati
(
_mometasoni furoas_
).
Üks inhaleeritav annus (annus, mis väljutatakse inhalaatori
huulikust) sisaldab 125 µg indakaterooli
(atsetaadina) ja 62,5 µg mometasoonfuroaati.
Atectura Breezhaler 125 mikrogrammi/127,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Üks kapsel sisaldab 150 µg indakaterooli (
_indacaterolum_
) (atsetaadina) ja 160 µg mometasoonfuroaati
(
_mometasoni furoas_
).
Üks inhaleeritav annus (annus, mis väljutatakse inhalaatori
huulikust) sisaldab 125 µg indakaterooli
(atsetaadina) ja 127,5 µg mometasoonfuroaati.
Atectura Breezhaler 125 mikrogrammi/260 mikrogrammi
inhalatsioonipulber kõvakapslites
Üks kapsel sisaldab 150 µg indakaterooli (
_indacaterolum_
) (atsetaadina) ja 320 µg mometasoonfuroaati
(
_mometasoni furoas_
).
Üks inhaleeritav annus (annus, mis väljutatakse inhalaatori
huulikust) sisaldab 125 µg indakaterooli
(atsetaadina) ja 260 µg mometasoonfuroaati.
Teadaolevat toimet omav(ad) abiaine(d)
Üks kapsel sisaldab ligikaudu 25 mg laktoosmonohüdraati.
Abiainete täielik loetelu vt lõik 6.1.
3.
RAVIMVORM
Inhalatsioonipulber kõvakapslis (inhalatsioonipulber).
Atectura Breezhaler 125 mikrogrammi/62,5 mikrogrammi
inhalatsioonipulber kõvakapslites
Läbipaistvad (värvitud) kapslid, mis sisaldavad valget pulbrit.
Kapslikorpusele on ühe sinise joone
kohale sinise tindiga trükitud toote kood „IM150-80” ning
kapslikaanele on sinise tindiga trükitud
toote logo, mida ümbritseb kaks sinist joont.
Atectura Breezha
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 16-10-2023
Summary of Product characteristics Summary of Product characteristics Bulgarian 16-10-2023
Public Assessment Report Public Assessment Report Bulgarian 23-06-2020
Patient Information leaflet Patient Information leaflet Spanish 16-10-2023
Public Assessment Report Public Assessment Report Spanish 23-06-2020
Patient Information leaflet Patient Information leaflet Czech 16-10-2023
Public Assessment Report Public Assessment Report Czech 23-06-2020
Patient Information leaflet Patient Information leaflet Danish 16-10-2023
Public Assessment Report Public Assessment Report Danish 23-06-2020
Patient Information leaflet Patient Information leaflet German 16-10-2023
Public Assessment Report Public Assessment Report German 23-06-2020
Patient Information leaflet Patient Information leaflet Greek 16-10-2023
Public Assessment Report Public Assessment Report Greek 23-06-2020
Patient Information leaflet Patient Information leaflet English 16-10-2023
Public Assessment Report Public Assessment Report English 23-06-2020
Patient Information leaflet Patient Information leaflet French 16-10-2023
Public Assessment Report Public Assessment Report French 23-06-2020
Patient Information leaflet Patient Information leaflet Italian 16-10-2023
Public Assessment Report Public Assessment Report Italian 23-06-2020
Patient Information leaflet Patient Information leaflet Latvian 16-10-2023
Public Assessment Report Public Assessment Report Latvian 23-06-2020
Patient Information leaflet Patient Information leaflet Lithuanian 16-10-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 16-10-2023
Public Assessment Report Public Assessment Report Lithuanian 23-06-2020
Patient Information leaflet Patient Information leaflet Hungarian 16-10-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 16-10-2023
Public Assessment Report Public Assessment Report Hungarian 23-06-2020
Patient Information leaflet Patient Information leaflet Maltese 16-10-2023
Public Assessment Report Public Assessment Report Maltese 23-06-2020
Patient Information leaflet Patient Information leaflet Dutch 16-10-2023
Public Assessment Report Public Assessment Report Dutch 23-06-2020
Patient Information leaflet Patient Information leaflet Polish 16-10-2023
Public Assessment Report Public Assessment Report Polish 23-06-2020
Patient Information leaflet Patient Information leaflet Portuguese 16-10-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 16-10-2023
Public Assessment Report Public Assessment Report Portuguese 23-06-2020
Patient Information leaflet Patient Information leaflet Romanian 16-10-2023
Public Assessment Report Public Assessment Report Romanian 23-06-2020
Patient Information leaflet Patient Information leaflet Slovak 16-10-2023
Public Assessment Report Public Assessment Report Slovak 23-06-2020
Patient Information leaflet Patient Information leaflet Slovenian 16-10-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 16-10-2023
Public Assessment Report Public Assessment Report Slovenian 23-06-2020
Patient Information leaflet Patient Information leaflet Finnish 16-10-2023
Public Assessment Report Public Assessment Report Finnish 23-06-2020
Patient Information leaflet Patient Information leaflet Swedish 16-10-2023
Public Assessment Report Public Assessment Report Swedish 23-06-2020
Patient Information leaflet Patient Information leaflet Norwegian 16-10-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 16-10-2023
Patient Information leaflet Patient Information leaflet Icelandic 16-10-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 16-10-2023
Patient Information leaflet Patient Information leaflet Croatian 16-10-2023
Public Assessment Report Public Assessment Report Croatian 23-06-2020