Efient

Țară: Uniunea Europeană

Limbă: engleză

Sursă: EMA (European Medicines Agency)

Cumpara asta acum

Prospect Prospect (PIL)
16-11-2022

Ingredient activ:

prasugrel

Disponibil de la:

Substipharm

Codul ATC:

B01AC22

INN (nume internaţional):

prasugrel

Grupul Terapeutică:

Antithrombotic agents

Zonă Terapeutică:

Acute Coronary Syndrome; Angina, Unstable; Myocardial Infarction

Indicații terapeutice:

Efient, co-administered with acetylsalicylic acid (ASA), is indicated for the prevention of atherothrombotic events in patients with acute coronary syndrome (i.e. unstable angina, non-ST-segment-elevation myocardial infarction [UA / NSTEMI] or ST-segment-elevation myocardial infarction [STEMI]) undergoing primary or delayed percutaneous coronary intervention (PCI).

Rezumat produs:

Revision: 25

Statutul autorizaţiei:

Authorised

Data de autorizare:

2009-02-24

Prospect

                                32
B. PACKAGE LEAFLET
33
PACKAGE LEAFLET: INFORMATION FOR THE USER
EFIENT 10 MG FILM-COATED TABLETS
EFIENT 5 MG FILM-COATED TABLETS
prasugrel
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 Efient is and what it is used for
2.
What you need to know before you take Efient
3.
How to take Efient
4.
Possible side effects
5.
How to store Efient
6.
Contents of the pack and other information
1.
WHAT EFIENT IS AND WHAT IT IS USED FOR
Efient, which contains the active substance prasugrel, belongs to a
group of medicines called anti-
platelet agents. Platelets are very small cell particles that
circulate in the blood. When a blood vessel is
damaged, for example if it is cut, platelets clump together to help
form a blood clot (thrombus).
Therefore, platelets are essential to help stop bleeding. If clots
form within a hardened blood vessel
such as an artery they can be very dangerous as they can cut off the
blood supply, causing a heart attack
(myocardial infarction), stroke or death. Clots in arteries supplying
blood to the heart may also reduce
the blood supply, causing unstable angina (a severe chest pain).
Efient inhibits the clumping of platelets and so reduces the chance of
a blood clot forming.
You have been prescribed Efient because you have already had a heart
attack or unstable angina and
you have been treated with a procedure to open blocked arteries in the
heart. You may also have had
one or more stents placed to keep open a blocked or narrowed artery
supplying blood to the heart.
Efient redu
                                
                                Citiți documentul complet
                                
                            

Caracteristicilor produsului

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Efient 10 mg film-coated tablets.
Efient 5 mg film-coated tablets.
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
_Efient 10 mg: _
Each tablet contains 10 mg prasugrel (as hydrochloride).
Excipient(s) with known effect
Each tablet contains 2.1 mg lactose monohydrate.
_ _
_Efient 5 mg: _
Each tablet contains 5 mg prasugrel (as hydrochloride).
Excipient(s) with known effect
Each tablet contains 2.7 mg lactose monohydrate.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet).
_Efient 10 mg: _
Beige and double-arrow shaped tablets, debossed with “10 MG” on
one side and “4759” on the other.
_ _
_ _
_Efient 5 mg: _
Yellow and double-arrow shaped tablets, debossed with “5 MG” on
one side and “4760” on the other.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS_ _
Efient, co-administered with acetylsalicylic acid (ASA), is indicated
for the prevention of
atherothrombotic events in adult patients with acute coronary syndrome
(i.e. unstable angina, non-ST
segment elevation myocardial infarction [UA/NSTEMI] or ST segment
elevation myocardial
infarction [STEMI]) undergoing primary or delayed percutaneous
coronary intervention (PCI).
For further information please refer to section 5.1.
4.2.
POSOLOGY AND METHOD OF ADMINISTRATION_ _
Posology
_Adults _
Efient should be initiated with a single 60 mg loading dose and then
continued at 10 mg once a day. In
UA/NSTEMI patients, where coronary angiography is performed within 48
hours after admission, the
loading dose should only be given at the time of PCI (see sections
4.4, 4.8 and 5.1). Patients taking
Efient should also take ASA daily (75 mg to 325 mg).
3
In patients with acute coronary syndrome (ACS) who are managed with
PCI, premature
discontinuation of any antiplatelet agent, including Efient, could
result in an increased risk of
thrombosis, myocardial infarction or death due to the patient’s
underlying disease. A treatment of up
to 12
                                
                                Citiți documentul complet
                                
                            

Documente în alte limbi

Prospect Prospect bulgară 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului bulgară 16-11-2022
Raport public de evaluare Raport public de evaluare bulgară 18-02-2016
Prospect Prospect spaniolă 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului spaniolă 16-11-2022
Raport public de evaluare Raport public de evaluare spaniolă 18-02-2016
Prospect Prospect cehă 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului cehă 16-11-2022
Raport public de evaluare Raport public de evaluare cehă 18-02-2016
Prospect Prospect daneză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului daneză 16-11-2022
Raport public de evaluare Raport public de evaluare daneză 18-02-2016
Prospect Prospect germană 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului germană 16-11-2022
Raport public de evaluare Raport public de evaluare germană 18-02-2016
Prospect Prospect estoniană 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului estoniană 16-11-2022
Raport public de evaluare Raport public de evaluare estoniană 18-02-2016
Prospect Prospect greacă 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului greacă 16-11-2022
Raport public de evaluare Raport public de evaluare greacă 18-02-2016
Prospect Prospect franceză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului franceză 16-11-2022
Raport public de evaluare Raport public de evaluare franceză 18-02-2016
Prospect Prospect italiană 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului italiană 16-11-2022
Raport public de evaluare Raport public de evaluare italiană 18-02-2016
Prospect Prospect letonă 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului letonă 16-11-2022
Raport public de evaluare Raport public de evaluare letonă 18-02-2016
Prospect Prospect lituaniană 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului lituaniană 16-11-2022
Raport public de evaluare Raport public de evaluare lituaniană 18-02-2016
Prospect Prospect maghiară 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului maghiară 16-11-2022
Raport public de evaluare Raport public de evaluare maghiară 18-02-2016
Prospect Prospect malteză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului malteză 16-11-2022
Raport public de evaluare Raport public de evaluare malteză 18-02-2016
Prospect Prospect olandeză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului olandeză 16-11-2022
Raport public de evaluare Raport public de evaluare olandeză 18-02-2016
Prospect Prospect poloneză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului poloneză 16-11-2022
Raport public de evaluare Raport public de evaluare poloneză 18-02-2016
Prospect Prospect portugheză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului portugheză 16-11-2022
Raport public de evaluare Raport public de evaluare portugheză 18-02-2016
Prospect Prospect română 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului română 16-11-2022
Raport public de evaluare Raport public de evaluare română 18-02-2016
Prospect Prospect slovacă 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului slovacă 16-11-2022
Raport public de evaluare Raport public de evaluare slovacă 18-02-2016
Prospect Prospect slovenă 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului slovenă 16-11-2022
Raport public de evaluare Raport public de evaluare slovenă 18-02-2016
Prospect Prospect finlandeză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului finlandeză 16-11-2022
Raport public de evaluare Raport public de evaluare finlandeză 18-02-2016
Prospect Prospect suedeză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului suedeză 16-11-2022
Raport public de evaluare Raport public de evaluare suedeză 18-02-2016
Prospect Prospect norvegiană 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului norvegiană 16-11-2022
Prospect Prospect islandeză 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului islandeză 16-11-2022
Prospect Prospect croată 16-11-2022
Caracteristicilor produsului Caracteristicilor produsului croată 16-11-2022
Raport public de evaluare Raport public de evaluare croată 18-02-2016

Căutați alerte legate de acest produs

Vizualizați istoricul documentelor