Lonsurf

Country: European Union

Language: Bulgarian

Source: EMA (European Medicines Agency)

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Active ingredient:

trifluridine, tipiracil хидрохлорид

Available from:

Les Laboratoires Servier

ATC code:

L01BC59

INN (International Name):

trifluridine, tipiracil

Therapeutic group:

Антинеопластични средства

Therapeutic area:

Колоректални неоплазми

Therapeutic indications:

Colorectal cancerLonsurf is indicated in combination with bevacizumab for the treatment of adult patients with metastatic colorectal cancer (CRC) who have received two prior anticancer treatment regimens including fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapies, anti-VEGF agents, and/or anti-EGFR agents. Lonsurf is indicated as monotherapy for the treatment of adult patients with metastatic colorectal cancer (CRC) who have been previously treated with, or are not considered candidates for, available therapies including fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapies, anti-VEGF agents, and anti EGFR agentsGastric cancerLonsurf is indicated as monotherapy for the treatment of adult patients with metastatic gastric cancer including adenocarcinoma of the gastroesophageal junction, who have been previously treated with at least two prior systemic treatment regimens for advanced disease.

Product summary:

Revision: 9

Authorization status:

упълномощен

Authorization date:

2016-04-25

Patient Information leaflet

                                41
Б. ЛИСТОВКА
42
ЛИСТОВКА: ИНФОРМАЦИЯ ЗА ПАЦИЕНТА
LONSURF 15 MG/6,14 MG ФИЛМИРАНИ ТАБЛЕТКИ
LONSURF 20 MG/8,19 MG ФИЛМИРАНИ ТАБЛЕТКИ
трифлуридин/типирацил
(trifluridine/tipiracil)
.
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 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
лекарствени 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 Lonsurf и за какво се
използва
2.
Какво трябва да знаете, преди да
приемете Lonsurf
3.
Как да приемате Lonsurf
4.
Възможни нежелани реакции
5.
Как да съхранявате Lonsurf
6.
Съдържание на опаковката и
допълнителна информация
1.
КАКВО ПРЕДСТАВЛЯВА LONSURF И ЗА КАКВО СЕ
ИЗПОЛЗВА
Lonsurf е вид противораково
химиотерап
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ПРИЛОЖЕНИЕ І
КРАТКА ХАРАКТЕРИСТИКА НА ПРОДУКТА
2
1.
ИМЕ НА ЛЕКАРСТВЕНИЯ ПРОДУКТ
Lonsurf 15 mg/6,14 mg филмирани таблетки
Lonsurf 20 mg/8,19 mg филмирани таблетки
2.
КАЧЕСТВЕН И КОЛИЧЕСТВЕН СЪСТАВ
Lonsurf 15 mg/6,14 mg филмирани таблетки
Всяка филмирана таблетка съдържа 15 mg
трифлуридин (trifluridine) и 6,14 mg типирацил
(tipiracil ) (под формата на хидрохлорид).
_Помощно вещество с известно действие
_
Всяка филмирана таблетка съдържа 90,735
mg лактоза монохидрат.
Lonsurf 20 mg/8,19 mg филмирани таблетки
Всяка филмирана таблетка съдържа 20 mg
трифлуридин (trifluridine) и 8,19 mg типирацил
(tipiracil) (под формата на хидрохлорид).
_Помощно вещество с известно действие
_
Всяка филмирана таблетка съдържа 120,980
mg лактоза монохидрат.
За пълния списък на помощните
вещества вижте точка 6.1.
3.
ЛЕКАРСТВЕНА ФОРМА
Филмирана таблетка (таблетка)
Lonsurf 15 mg/6,14 mg филмирани таблетки
Таблетката е филмирана, бяла,
двойноизпъкнала, с кръгла форма, с
диаметър 7,1 mm и
дебелина 2,7 mm. От едната страна със
сиво мастило на таблетката е
отпечатано „15“, а от
другата страна -„102“ и „15 mg“.
Lonsurf 20 mg/8,19 mg филмирани таблетки
Таблетката е филмирана, бледочервена,
двойноизпъкнала, с кръгла форма, с
диаметър 7,6 mm и
дебелина 3,2 
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Spanish 11-09-2023
Public Assessment Report Public Assessment Report Spanish 11-09-2023
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Patient Information leaflet Patient Information leaflet Greek 11-09-2023
Public Assessment Report Public Assessment Report Greek 11-09-2023
Patient Information leaflet Patient Information leaflet English 11-09-2023
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Patient Information leaflet Patient Information leaflet French 11-09-2023
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Patient Information leaflet Patient Information leaflet Latvian 11-09-2023
Public Assessment Report Public Assessment Report Latvian 11-09-2023
Patient Information leaflet Patient Information leaflet Lithuanian 11-09-2023
Summary of Product characteristics Summary of Product characteristics Lithuanian 11-09-2023
Public Assessment Report Public Assessment Report Lithuanian 11-09-2023
Patient Information leaflet Patient Information leaflet Hungarian 11-09-2023
Summary of Product characteristics Summary of Product characteristics Hungarian 11-09-2023
Public Assessment Report Public Assessment Report Hungarian 11-09-2023
Patient Information leaflet Patient Information leaflet Maltese 11-09-2023
Public Assessment Report Public Assessment Report Maltese 11-09-2023
Patient Information leaflet Patient Information leaflet Dutch 11-09-2023
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Patient Information leaflet Patient Information leaflet Polish 11-09-2023
Public Assessment Report Public Assessment Report Polish 11-09-2023
Patient Information leaflet Patient Information leaflet Portuguese 11-09-2023
Summary of Product characteristics Summary of Product characteristics Portuguese 11-09-2023
Public Assessment Report Public Assessment Report Portuguese 11-09-2023
Patient Information leaflet Patient Information leaflet Romanian 11-09-2023
Public Assessment Report Public Assessment Report Romanian 11-09-2023
Patient Information leaflet Patient Information leaflet Slovak 11-09-2023
Public Assessment Report Public Assessment Report Slovak 11-09-2023
Patient Information leaflet Patient Information leaflet Slovenian 11-09-2023
Summary of Product characteristics Summary of Product characteristics Slovenian 11-09-2023
Public Assessment Report Public Assessment Report Slovenian 11-09-2023
Patient Information leaflet Patient Information leaflet Finnish 11-09-2023
Public Assessment Report Public Assessment Report Finnish 11-09-2023
Patient Information leaflet Patient Information leaflet Swedish 11-09-2023
Public Assessment Report Public Assessment Report Swedish 11-09-2023
Patient Information leaflet Patient Information leaflet Norwegian 11-09-2023
Summary of Product characteristics Summary of Product characteristics Norwegian 11-09-2023
Patient Information leaflet Patient Information leaflet Icelandic 11-09-2023
Summary of Product characteristics Summary of Product characteristics Icelandic 11-09-2023
Patient Information leaflet Patient Information leaflet Croatian 11-09-2023
Public Assessment Report Public Assessment Report Croatian 11-09-2023

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