Enerzair Breezhaler

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

indacaterol, Glycopyrronium bromide, mometasone

Available from:

Novartis Europharm Limited

ATC code:

R03AL

INN (International Name):

indacaterol, glycopyrronium bromide, mometasone

Therapeutic group:

Лекарства за обструктивна заболявания на дихателните пътища,

Therapeutic area:

астма

Therapeutic indications:

Enerzair Breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Product summary:

Revision: 6

Authorization status:

упълномощен

Authorization date:

2020-07-03

Patient Information leaflet

                                47
Б. ЛИСТОВКА
48
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
ENERZAIR BREEZHALER 114 МИКРОГРАМА/46
МИКРОГРАМА/136 МИКРОГРАМА ПРАХ ЗА
ИНХАЛАЦИЯ,
ТВЪРДИ КАПСУЛИ
индакатерол/гликопирониум/мометазонов
фуроат (indacaterol/glycopyrronium/mometasone
furoate)
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,
фармацевт или
медицинска сестра.
-
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,
фармацевт или
медицинска сестра. Това включва и
всички възможни нежелани реакции,
неописани в
тази листовка. Вижте точка 4.
КАКВО СЪДЪРЖА ТАЗИ ЛИСТОВКА:
1.
Какво представлява Enerzair Breezhaler и за
какво се използва
2.
Какво трябва да знаете, преди да
използвате Enerzair Breezhaler
3.
Как да използвате Enerzair Breezhaler
4.
Възможни нежелани реакции
5.
Как да съхранявате Enerzair Breezhaler
6.
Съдържание на опаковката
                                
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Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Enerzair Breezhaler 114 микрограма/46
микрограма/136 микрограма прах за
инхалация, твърди
капсули
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Всяка капсула съдържа 150 µg
индакатерол (indacaterol) (като ацетат), 63 µg
гликопирониев
бромид (glycopyrronium bromide), което
съответства на 50 µg гликопирониум, и 160
µg
мометазонов фуроат (mometasone furoate).
Всяка доставена доза (дозата, която се
отделя от накрайника на инхалатора)
съдържа 114 µg
индакатерол (като ацетат), 58 µg
гликопирониев бромид, което
съответства на 46 µg
гликопирониум, и 136 µg мометазонов
фуроат.
Помощно(и) вещество(а) с известно
действие
Всяка капсула съдържа 25 mg лактоза
монохидрат.
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Прах за инхалация, твърда капсула
(прах за инхалация)
Капсули със зелено, прозрачно капаче и
безцветно, прозрачно тяло, съдържащи
бял прах, с код
на продукта “IGM150-50-160”, отпечатан в
черно над две черни линии върху
тялото, и логото
на продукта, отпечатано в черно и
оградено с черна линия върху капачето.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Enerzair Breezhaler е показан като поддъ
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 16-10-2023
Public Assessment Report Public Assessment Report Spanish 21-07-2020
Patient Information leaflet Patient Information leaflet Czech 16-10-2023
Public Assessment Report Public Assessment Report Czech 21-07-2020
Patient Information leaflet Patient Information leaflet Danish 16-10-2023
Public Assessment Report Public Assessment Report Danish 21-07-2020
Patient Information leaflet Patient Information leaflet German 16-10-2023
Public Assessment Report Public Assessment Report German 21-07-2020
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Public Assessment Report Public Assessment Report Greek 21-07-2020
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Patient Information leaflet Patient Information leaflet French 16-10-2023
Public Assessment Report Public Assessment Report French 21-07-2020
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Public Assessment Report Public Assessment Report Italian 21-07-2020
Patient Information leaflet Patient Information leaflet Latvian 16-10-2023
Public Assessment Report Public Assessment Report Latvian 21-07-2020
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 21-07-2020
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 21-07-2020
Patient Information leaflet Patient Information leaflet Maltese 16-10-2023
Public Assessment Report Public Assessment Report Maltese 21-07-2020
Patient Information leaflet Patient Information leaflet Dutch 16-10-2023
Public Assessment Report Public Assessment Report Dutch 21-07-2020
Patient Information leaflet Patient Information leaflet Polish 16-10-2023
Public Assessment Report Public Assessment Report Polish 21-07-2020
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 21-07-2020
Patient Information leaflet Patient Information leaflet Romanian 16-10-2023
Public Assessment Report Public Assessment Report Romanian 21-07-2020
Patient Information leaflet Patient Information leaflet Slovak 16-10-2023
Public Assessment Report Public Assessment Report Slovak 21-07-2020
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 21-07-2020
Patient Information leaflet Patient Information leaflet Finnish 16-10-2023
Public Assessment Report Public Assessment Report Finnish 21-07-2020
Patient Information leaflet Patient Information leaflet Swedish 16-10-2023
Public Assessment Report Public Assessment Report Swedish 21-07-2020
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 21-07-2020