Oslif Breezhaler

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Patient Information leaflet Patient Information leaflet (PIL)
08-09-2021
Summary of Product characteristics Summary of Product characteristics (SPC)
08-09-2021
Public Assessment Report Public Assessment Report (PAR)
12-10-2017

Active ingredient:

индакатерол малеат

Available from:

Novartis Europharm Limited 

ATC code:

R03AC18

INN (International Name):

indacaterol

Therapeutic group:

Лекарства за обструктивна заболявания на дихателните пътища,

Therapeutic area:

Белодробна болест, хронична обструктивна болест

Therapeutic indications:

Oslif Breezhaler е показан за поддържащо бронходилататорно лечение на обструкция на въздушен поток при възрастни пациенти с хронична обструктивна белодробна болест.

Product summary:

Revision: 17

Authorization status:

упълномощен

Authorization date:

2009-11-29

Patient Information leaflet

                                57
Б. ЛИСТОВКА
58
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
OSLIF BREEZHALER 150 МИКРОГРАМА ПРАХ ЗА
ИНХАЛАЦИИ, ТВЪРДИ КАПСУЛИ
OSLIF BREEZHALER 300 МИКРОГРАМА ПРАХ ЗА
ИНХАЛАЦИИ, ТВЪРДИ КАПСУЛИ
индакатерол (indacaterol)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ЗАПОЧНЕТЕ ДА ИЗПОЛЗВАТЕ ТОВА
ЛЕКАРСТВО, ТЪЙ КАТО ТЯ СЪДЪРЖА ВАЖНА
ЗА ВАС ИНФОРМАЦИЯ.
-
Запазете тази листовка. Може да се
наложи да я прочетете отново.
-
Ако имате някакви допълнителни
въпроси, попитайте Вашия лекар или
фармацевт.
-
Това лекарство е предписано лично на
Вас. Не го преотстъпвайте на други
хора. То може
да им навреди, независимо че
признаците на тяхното заболяване са
същите като Вашите.
-
Ако получите някакви нежелани
реакции, уведомете Вашия лекар или
фармацевт. Това
включва и всички възможни нежелани
реакции, неописани в тази листовка.
Вижте
точка 4.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА
1.
Какво представлява Oslif Breezhaler и за
какво се използва
2.
Какво трябва да знаете, преди да
използвате Oslif Breezhaler
3.
Как да използвате Oslif Breezhaler
4.
Възможни нежелани реакции
5.
Как да съхранявате Oslif Breezhaler
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА OSLIF BREEZHALER И ЗА
КАКВО С
                                
                                Read the complete document

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Oslif Breezhaler 150 микрограма прах за
инхалация, твърди капсули
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Всяка капсула съдържа индакатерол
малеат, съответстващ на 150 микрограма
индакатерол
(indacaterol).
Освободената от накрайника на
инхалатора доза е индакатерол малеат,
съответстваща на
120 микрограма индакатерол.
Помощно вещество с известно действие
Всяка капсула съдържа 24,8 mg лактоза.
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Прах за инхалация, твърда капсула
Прозрачни (неоцветени) капсули,
съдържащи бял прах с надпис “IDL 150”,
отпечетан в черно
над черна черта, и логото на
компанията (
), отпечатано в черно под черната
черта.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Oslif Breezhaler е показан за продължително
бронходилататорно лечение на
обструкция на
въздухоносните пътища при възрастни
пациенти с хронична обструктивна
белодробна болест
(ХОББ).
4.2
ДОЗИРОВКА И НАЧИН НА ПРИЛОЖЕНИЕ
Дозировка
Препоръчваната доза е инхалиране на
съдържанието на една капсула от 150
микрограма
веднъж дневно, като се използва
инхалатора Oslif Bre
                                
                                Read the complete document

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Active ingredient индакатерол малеат

индакатерол малеат

ATC code R03AC18

R03AC18

Marketed by Novartis Europharm Limited 

Novartis Europharm Limited 

INN (International Name) indacaterol

indacaterol

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 08-09-2021
Summary of Product characteristics Summary of Product characteristics Spanish 08-09-2021
Public Assessment Report Public Assessment Report Spanish 12-10-2017
Patient Information leaflet Patient Information leaflet Czech 08-09-2021
Summary of Product characteristics Summary of Product characteristics Czech 08-09-2021
Public Assessment Report Public Assessment Report Czech 12-10-2017
Patient Information leaflet Patient Information leaflet Danish 08-09-2021
Summary of Product characteristics Summary of Product characteristics Danish 08-09-2021
Public Assessment Report Public Assessment Report Danish 12-10-2017
Patient Information leaflet Patient Information leaflet German 08-09-2021
Summary of Product characteristics Summary of Product characteristics German 08-09-2021
Public Assessment Report Public Assessment Report German 12-10-2017
Patient Information leaflet Patient Information leaflet Estonian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Estonian 08-09-2021
Public Assessment Report Public Assessment Report Estonian 12-10-2017
Patient Information leaflet Patient Information leaflet Greek 08-09-2021
Summary of Product characteristics Summary of Product characteristics Greek 08-09-2021
Public Assessment Report Public Assessment Report Greek 12-10-2017
Patient Information leaflet Patient Information leaflet English 08-09-2021
Summary of Product characteristics Summary of Product characteristics English 08-09-2021
Public Assessment Report Public Assessment Report English 12-10-2017
Patient Information leaflet Patient Information leaflet French 08-09-2021
Summary of Product characteristics Summary of Product characteristics French 08-09-2021
Public Assessment Report Public Assessment Report French 12-10-2017
Patient Information leaflet Patient Information leaflet Italian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Italian 08-09-2021
Public Assessment Report Public Assessment Report Italian 12-10-2017
Patient Information leaflet Patient Information leaflet Latvian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Latvian 08-09-2021
Public Assessment Report Public Assessment Report Latvian 12-10-2017
Patient Information leaflet Patient Information leaflet Lithuanian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 08-09-2021
Public Assessment Report Public Assessment Report Lithuanian 12-10-2017
Patient Information leaflet Patient Information leaflet Hungarian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 08-09-2021
Public Assessment Report Public Assessment Report Hungarian 12-10-2017
Patient Information leaflet Patient Information leaflet Maltese 08-09-2021
Summary of Product characteristics Summary of Product characteristics Maltese 08-09-2021
Public Assessment Report Public Assessment Report Maltese 12-10-2017
Patient Information leaflet Patient Information leaflet Dutch 08-09-2021
Summary of Product characteristics Summary of Product characteristics Dutch 08-09-2021
Public Assessment Report Public Assessment Report Dutch 12-10-2017
Patient Information leaflet Patient Information leaflet Polish 08-09-2021
Summary of Product characteristics Summary of Product characteristics Polish 08-09-2021
Public Assessment Report Public Assessment Report Polish 12-10-2017
Patient Information leaflet Patient Information leaflet Portuguese 08-09-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 08-09-2021
Public Assessment Report Public Assessment Report Portuguese 12-10-2017
Patient Information leaflet Patient Information leaflet Romanian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Romanian 08-09-2021
Public Assessment Report Public Assessment Report Romanian 12-10-2017
Patient Information leaflet Patient Information leaflet Slovak 08-09-2021
Summary of Product characteristics Summary of Product characteristics Slovak 08-09-2021
Public Assessment Report Public Assessment Report Slovak 12-10-2017
Patient Information leaflet Patient Information leaflet Slovenian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 08-09-2021
Public Assessment Report Public Assessment Report Slovenian 12-10-2017
Patient Information leaflet Patient Information leaflet Finnish 08-09-2021
Summary of Product characteristics Summary of Product characteristics Finnish 08-09-2021
Public Assessment Report Public Assessment Report Finnish 12-10-2017
Patient Information leaflet Patient Information leaflet Swedish 08-09-2021
Summary of Product characteristics Summary of Product characteristics Swedish 08-09-2021
Public Assessment Report Public Assessment Report Swedish 12-10-2017
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Summary of Product characteristics Summary of Product characteristics Norwegian 08-09-2021
Patient Information leaflet Patient Information leaflet Icelandic 08-09-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 08-09-2021
Patient Information leaflet Patient Information leaflet Croatian 08-09-2021
Summary of Product characteristics Summary of Product characteristics Croatian 08-09-2021
Public Assessment Report Public Assessment Report Croatian 12-10-2017

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