Orfadin

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

нитисинона

Available from:

Swedish Orphan Biovitrum International AB

ATC code:

A16AX04

INN (International Name):

nitisinone

Therapeutic group:

Други стомашно-чревния тракт и обмяната на веществата средства,

Therapeutic area:

Tyrosinemias

Therapeutic indications:

Hereditary tyrosinemia type 1 (HT 1)Orfadin is indicated for the treatment of adult and paediatric (in any age range) patients with confirmed diagnosis of hereditary tyrosinemia type 1 (HT 1) in combination with dietary restriction of tyrosine and phenylalanine. Alkaptonuria (AKU)Orfadin is indicated for the treatment of adult patients with alkaptonuria (AKU).

Product summary:

Revision: 21

Authorization status:

упълномощен

Authorization date:

2005-02-21

Patient Information leaflet

                                37
Б. ЛИСТОВКА
38
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПОТРЕБИТЕЛЯ
ORFADIN 2 MG ТВЪРДИ КАПСУЛИ
ORFADIN 5 MG ТВЪРДИ КАПСУЛИ
ORFADIN 10 MG ТВЪРДИ КАПСУЛИ
ORFADIN 20 MG ТВЪРДИ КАПСУЛИ
нитисинон (nitisinone)
ПРОЧЕТЕТЕ ВНИМАТЕЛНО ЦЯЛАТА ЛИСТОВКА,
ПРЕДИ ДА ЗАПОЧНЕТЕ ДА ПРИЕМАТЕ 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 Orfadin и за какво се
използва
2.
Какво трябва да знаете, преди да
приемете Orfadin
3.
Как да приемате Orfadin
4.
Възможни нежелани реакции
5.
Как да съхранявате Orfadin
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА ORFADIN И ЗА КАКВО СЕ
ИЗПОЛЗВА
Orfadi
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ I
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Orfadin 2 mg твърди капсули
Orfadin 5 mg твърди капсули
Orfadin 10 mg твърди капсули
Orfadin 20 mg твърди капсули
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Всяка капсула съдържа 2 mg нитисинон
(nitisinone).
Всяка капсула съдържа 5 mg нитисинон
(nitisinone).
Всяка капсула съдържа 10 mg нитисинон
(nitisinone).
Всяка капсула съдържа 20 mg нитисинон
(nitisinone).
_ _
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Твърда капсула
Бели, непрозрачни капсули, (6x16 mm), с
отпечатано в черно “NTBC 2mg” върху
тялото на
капсулата.
Бели, непрозрачни капсули, (6x16 mm), с
отпечатано в черно “NTBC 5mg” върху
тялото на
капсулата.
Бели, непрозрачни капсули, (6x16 mm), с
отпечатано в черно “NTBC 10mg” върху
тялото на
капсулата.
Бели, непрозрачни капсули, (6x16 mm), с
отпечатано в черно “NTBC 20mg” върху
тялото на
капсулата.
Капсулата съдържа бял до почти бял
прах.
4.
КЛИНИЧНИ ДАННИ
4.1
ТЕРАПЕВТИЧНИ ПОКАЗАНИЯ
Наследствена тирозинемия тип 1 (HT-1)
Orfadin е показан за лечение на възрастни
и педиатрични пациенти (във всички
възрастови
граници) с потвърдена диагноза
наследствена тирозинемия тип 1 (HT-1) в
комбинация с
ограничав
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 14-04-2023
Public Assessment Report Public Assessment Report Spanish 11-01-2021
Patient Information leaflet Patient Information leaflet Czech 14-04-2023
Public Assessment Report Public Assessment Report Czech 11-01-2021
Patient Information leaflet Patient Information leaflet Danish 14-04-2023
Public Assessment Report Public Assessment Report Danish 11-01-2021
Patient Information leaflet Patient Information leaflet German 14-04-2023
Public Assessment Report Public Assessment Report German 11-01-2021
Patient Information leaflet Patient Information leaflet Estonian 14-04-2023
Public Assessment Report Public Assessment Report Estonian 11-01-2021
Patient Information leaflet Patient Information leaflet Greek 14-04-2023
Public Assessment Report Public Assessment Report Greek 11-01-2021
Patient Information leaflet Patient Information leaflet English 14-04-2023
Public Assessment Report Public Assessment Report English 11-01-2021
Patient Information leaflet Patient Information leaflet French 14-04-2023
Public Assessment Report Public Assessment Report French 11-01-2021
Patient Information leaflet Patient Information leaflet Italian 14-04-2023
Public Assessment Report Public Assessment Report Italian 11-01-2021
Patient Information leaflet Patient Information leaflet Latvian 14-04-2023
Public Assessment Report Public Assessment Report Latvian 11-01-2021
Patient Information leaflet Patient Information leaflet Lithuanian 14-04-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 14-04-2023
Public Assessment Report Public Assessment Report Lithuanian 11-01-2021
Patient Information leaflet Patient Information leaflet Hungarian 14-04-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 14-04-2023
Public Assessment Report Public Assessment Report Hungarian 11-01-2021
Patient Information leaflet Patient Information leaflet Maltese 14-04-2023
Public Assessment Report Public Assessment Report Maltese 11-01-2021
Patient Information leaflet Patient Information leaflet Dutch 14-04-2023
Public Assessment Report Public Assessment Report Dutch 11-01-2021
Patient Information leaflet Patient Information leaflet Polish 14-04-2023
Public Assessment Report Public Assessment Report Polish 11-01-2021
Patient Information leaflet Patient Information leaflet Portuguese 14-04-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 14-04-2023
Public Assessment Report Public Assessment Report Portuguese 11-01-2021
Patient Information leaflet Patient Information leaflet Romanian 14-04-2023
Public Assessment Report Public Assessment Report Romanian 11-01-2021
Patient Information leaflet Patient Information leaflet Slovak 14-04-2023
Public Assessment Report Public Assessment Report Slovak 11-01-2021
Patient Information leaflet Patient Information leaflet Slovenian 14-04-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 14-04-2023
Public Assessment Report Public Assessment Report Slovenian 11-01-2021
Patient Information leaflet Patient Information leaflet Finnish 14-04-2023
Public Assessment Report Public Assessment Report Finnish 11-01-2021
Patient Information leaflet Patient Information leaflet Swedish 14-04-2023
Public Assessment Report Public Assessment Report Swedish 11-01-2021
Patient Information leaflet Patient Information leaflet Norwegian 14-04-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 14-04-2023
Patient Information leaflet Patient Information leaflet Icelandic 14-04-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 14-04-2023
Patient Information leaflet Patient Information leaflet Croatian 14-04-2023
Public Assessment Report Public Assessment Report Croatian 11-01-2021

Search alerts related to this product

View documents history