Corlentor

Country: Unjoni Ewropea

Lingwa: Ingliż

Sors: EMA (European Medicines Agency)

Ixtrih issa

Ingredjent attiv:

ivabradine hydrochloride

Disponibbli minn:

Les Laboratoires Servier

Kodiċi ATC:

C01EB17

INN (Isem Internazzjonali):

ivabradine

Grupp terapewtiku:

CARDIAC THERAPY

Żona terapewtika:

Angina Pectoris; Heart Failure

Indikazzjonijiet terapewtiċi:

Symptomatic treatment of chronic stable angina pectorisIvabradine is indicated for the symptomatic treatment of chronic stable angina pectoris in coronary artery disease adults with normal sinus rhythm and heart rate ≥ 70 bpm. Ivabradine is indicated:in adults unable to tolerate or with a contraindication to the use of beta-blockersor in combination with beta-blockers in patients inadequately controlled with an optimal beta-blocker dose.Treatment of chronic heart failureIvabradine is indicated in chronic heart failure NYHA II to IV class with systolic dysfunction, in patients in sinus rhythm and whose heart rate is ≥ 75 bpm, in combination with standard therapy including beta-blocker therapy or when beta-blocker therapy is contraindicated or not tolerated.

Sommarju tal-prodott:

Revision: 26

L-istatus ta 'awtorizzazzjoni:

Authorised

Data ta 'l-awtorizzazzjoni:

2005-10-25

Fuljett ta 'informazzjoni

                                28
B. PACKAGE LEAFLET
29
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
CORLENTOR 5 MG FILM-COATED TABLETS
CORLENTOR 7.5 MG FILM-COATED TABLETS
ivabradine
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
-
Keep this leaflet. You may need to read it again.
-
If you have any further questions, ask your doctor or pharmacist.
-
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
-
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
:
1.
What Corlentor is and what it is used for
2.
What you need to know before you take Corlentor
3.
How to take Corlentor
4.
Possible side effects
5
How to store Corlentor
6.
Contents of the pack and other information
1.
WHAT CORLENTOR IS AND WHAT IT IS USED FOR
Corlentor (ivabradine) is a heart medicine used to treat:
-
Symptomatic stable angina pectoris (which causes chest pain) in adult
patients whose heart rate is
over or equal to 70 beats per minute.
It is used in adult patients who do not tolerate or cannot take
heart medicines called beta-blockers. It is also used in combination
with beta-blockers in adult
patients whose condition is not fully controlled with a beta-blocker.
-
Chronic heart failure in adult patients whose heart rate is over or
equal to 75 beats per minute. It
is used in combination with standard therapy, including beta-blocker
therapy or when beta-
blockers are contraindicated or not tolerated.
About stable angina pectoris (usually referred to as “angina”):
Stable angina is a heart disease which happens when the heart does not
receive enough oxygen. The
most common symptom of angina is chest pain or discomfort.
About chronic heart failure :
Chronic heart failure is a heart disease which happens when your heart
cannot pump enough blood to
the rest of your body. The most common s
                                
                                Aqra d-dokument sħiħ
                                
                            

Karatteristiċi tal-prodott

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Corlentor 5 mg film-coated tablets
Corlentor 7.5 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Corlentor 5 mg film-coated tablets
Each film-coated tablet contains 5 mg ivabradine (as hydrochloride).
_Excipient with known effect:_
Each film-coated tablet contains 63.91 mg lactose monohydrate.
Corlentor 7.5 mg film-coated tablets
Each film-coated tablet contains 7.5 mg ivabradine (as hydrochloride).
_Excipient with known effect:_
Each film-coated tablet contains 61.215 mg lactose monohydrate.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Corlentor 5 mg film-coated tablets
Salmon-coloured, oblong, film-coated tablet scored on both sides,
engraved with “5” on one face
and
on the other face.
The tablet can be divided into equal doses.
Corlentor 7.5 mg film-coated tablets
Salmon-coloured, triangular, film-coated tablet engraved with
“7.5” on one face and
on the other
face.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Symptomatic treatment of chronic stable angina pectoris
Ivabradine is indicated for the symptomatic treatment of chronic
stable angina pectoris in coronary
artery disease adults with normal sinus rhythm and heart rate ≥ 70
bpm. Ivabradine is indicated :
-
in adults unable to tolerate or with a contraindication to the use of
beta-blockers
-
or in combination with beta-blockers in patients inadequately
controlled with an optimal beta-
blocker dose.
Treatment of chronic heart failure
3
Ivabradine is indicated in chronic heart failure NYHA II to IV class
with systolic dysfunction, in adult
patients in sinus rhythm and whose heart rate is ≥ 75 bpm, in
combination with standard therapy
including beta-blocker therapy or when beta-blocker therapy is
contraindicated or not tolerated (see
section 5.1).
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
_Symptomatic treatment of chronic stable angina pectoris _
It is recommended that the decision to ini
                                
                                Aqra d-dokument sħiħ
                                
                            

Dokumenti f'lingwi oħra

Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Bulgaru 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Bulgaru 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Spanjol 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Spanjol 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ċek 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ċek 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Daniż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Daniż 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ġermaniż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ġermaniż 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ġermaniż 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Estonjan 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Estonjan 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Estonjan 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Grieg 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Grieg 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Franċiż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Franċiż 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Franċiż 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Taljan 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Taljan 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Latvjan 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Latvjan 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Litwanjan 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Litwanjan 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Litwanjan 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Ungeriż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Ungeriż 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Ungeriż 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Malti 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Malti 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Olandiż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Olandiż 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Olandiż 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Pollakk 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Pollakk 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Portugiż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Portugiż 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Portugiż 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Rumen 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Rumen 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Slovakk 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Slovakk 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Sloven 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Sloven 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Finlandiż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Finlandiż 12-10-2021
Rapport ta 'Valutazzjoni Pubblika Rapport ta 'Valutazzjoni Pubblika Finlandiż 25-02-2019
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Svediż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Svediż 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Norveġiż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Norveġiż 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Iżlandiż 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Iżlandiż 12-10-2021
Fuljett ta 'informazzjoni Fuljett ta 'informazzjoni Kroat 12-10-2021
Karatteristiċi tal-prodott Karatteristiċi tal-prodott Kroat 12-10-2021

Fittex twissijiet relatati ma 'dan il-prodott

Ara l-istorja tad-dokumenti