Clopidogrel HCS

Land: Europese Unie

Taal: Engels

Bron: EMA (European Medicines Agency)

Koop het nu

Bijsluiter Bijsluiter (PIL)
01-08-2018
Productkenmerken Productkenmerken (SPC)
01-08-2018

Werkstoffen:

clopidogrel (as hydrochloride)

Beschikbaar vanaf:

HCS bvba 

ATC-code:

B01AC04

INN (Algemene Internationale Benaming):

clopidogrel

Therapeutische categorie:

Antithrombotic agents

Therapeutisch gebied:

Peripheral Vascular Diseases; Acute Coronary Syndrome; Myocardial Infarction; Stroke

therapeutische indicaties:

Secondary prevention of atherothrombotic eventsClopidogrel is indicated in:Adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease.Adult patients suffering from acute coronary syndrome:Non-ST segment elevation acute coronary syndrome (unstable angina or non-Q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (ASA).ST segment elevation acute myocardial infarction, in combination with ASA in medically treated patients eligible for thrombolytic therapy.Prevention of atherothrombotic and thromboembolic events in atrial fibrillationIn adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with Vitamin K antagonists (VKA) and who have a low bleeding risk, clopidogrel is indicated in combination with ASA for the prevention of atherothrombotic and thromboembolic events, including stroke. For further information please refer to section 5.1.

Product samenvatting:

Revision: 8

Autorisatie-status:

Authorised

Autorisatie datum:

2010-10-28

Bijsluiter

                                28
B. PACKAGE LEAFLET
29
PACKAGE LEAFLET: INFORMATION FOR THE USER
CLOPIDOGREL HCS 75 MG FILM-COATED TABLETS
Clopidogrel
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 have any side effects, including any side effects not listed in
this leaflet, talk to your
doctor or pharmacist. See section 4.
WHAT IS IN THIS LEAFLET
:
1.
What Clopidogrel HCS is and what it is used for
2.
What you need to know before you take Clopidogrel HCS
3.
How to take Clopidogrel HCS
4.
Possible side effects
5.
How to store Clopidogrel HCS
6.
Contents of the pack and other information
1.
WHAT CLOPIDOGREL HCS IS AND WHAT IT IS USED FOR
Clopidogrel HCS contains clopidogrel and belongs to a group of
medicines called antiplatelet
medicinal products. Platelets are very small structures in the blood,
which clump together during blood
clotting. By preventing this clumping, antiplatelet medicinal products
reduce the chances of blood
clots forming (a process called thrombosis).
Clopidogrel HCS is taken by adults to prevent blood clots (thrombi)
forming in hardened blood
vessels (arteries), a process known as atherothrombosis, which can
lead to atherothrombotic events
(such as stroke, heart attack, or death).
You have been prescribed Clopidogrel HCS to help prevent blood clots
and reduce the risk of these
severe events because:
-
You have a condition of hardening of arteries (also known as
atherosclerosis), and
-
You have previously experienced a heart attack, stroke or have a
condition known as peripheral
arterial disease,
or
-
You have experienced a severe type of chest pain known as ‘unstable
angina’ or ‘myocardial
infarction’ (heart attack). For the treatment of this condition your
doctor
                                
                                Lees het volledige document
                                
                            

Productkenmerken

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Clopidogrel HCS 75 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 75 mg of clopidogrel (as
hydrochloride).
Excipients with known effect
:
Each film-coated tablet contains 13 mg of hydrogenated castor oil.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Pink, round and slightly convex film-coated tablets.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
_Secondary prevention of atherothrombotic events _
Clopidogrel is indicated in:
•
Adult patients suffering from myocardial infarction (from a few days
until less than 35 days),
ischaemic stroke (from 7 days until less than 6 months) or established
peripheral arterial
disease.
•
Adult patients suffering from acute coronary syndrome:
-
Non-ST segment elevation acute coronary syndrome (unstable angina or
non-Q-wave
myocardial infarction), including patients undergoing a stent
placement following
percutaneous coronary intervention, in combination with
acetylsalicylic acid (ASA).
-
ST segment elevation acute myocardial infarction, in combination with
ASA in medically
treated patients eligible for thrombolytic therapy.
_Prevention of atherothrombotic and thromboembolic events in atrial
fibrillation _
In adult patients with atrial fibrillation who have at least one risk
factor for vascular events, are not
suitable for treatment with Vitamin K antagonists (VKA) and who have a
low bleeding risk,
clopidogrel is indicated in combination with ASA for the prevention of
atherothrombotic and
thromboembolic events, including stroke.
For further information please refer to section 5.1.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
•
Adults and elderly (over 65 years)
Clopidogrel should be given as a single daily dose of 75 mg.
In patients suffering from acute coronary syndrome:
−
Non-ST segment elevation acute coronary syndrome (unstable angina or
non-Q-wave
myocardial infarction): clopidogr
                                
                                Lees het volledige document
                                
                            

Documenten in andere talen

Bijsluiter Bijsluiter Bulgaars 01-08-2018
Productkenmerken Productkenmerken Bulgaars 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Bulgaars 04-08-2015
Bijsluiter Bijsluiter Spaans 01-08-2018
Productkenmerken Productkenmerken Spaans 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Spaans 04-08-2015
Bijsluiter Bijsluiter Tsjechisch 01-08-2018
Productkenmerken Productkenmerken Tsjechisch 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Tsjechisch 04-08-2015
Bijsluiter Bijsluiter Deens 01-08-2018
Productkenmerken Productkenmerken Deens 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Deens 04-08-2015
Bijsluiter Bijsluiter Duits 01-08-2018
Productkenmerken Productkenmerken Duits 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Duits 04-08-2015
Bijsluiter Bijsluiter Estlands 01-08-2018
Productkenmerken Productkenmerken Estlands 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Estlands 04-08-2015
Bijsluiter Bijsluiter Grieks 01-08-2018
Productkenmerken Productkenmerken Grieks 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Grieks 04-08-2015
Bijsluiter Bijsluiter Frans 01-08-2018
Productkenmerken Productkenmerken Frans 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Frans 04-08-2015
Bijsluiter Bijsluiter Italiaans 01-08-2018
Productkenmerken Productkenmerken Italiaans 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Italiaans 04-08-2015
Bijsluiter Bijsluiter Letlands 01-08-2018
Productkenmerken Productkenmerken Letlands 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Letlands 04-08-2015
Bijsluiter Bijsluiter Litouws 01-08-2018
Productkenmerken Productkenmerken Litouws 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Litouws 04-08-2015
Bijsluiter Bijsluiter Hongaars 01-08-2018
Productkenmerken Productkenmerken Hongaars 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Hongaars 04-08-2015
Bijsluiter Bijsluiter Maltees 01-08-2018
Productkenmerken Productkenmerken Maltees 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Maltees 04-08-2015
Bijsluiter Bijsluiter Nederlands 01-08-2018
Productkenmerken Productkenmerken Nederlands 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Nederlands 04-08-2015
Bijsluiter Bijsluiter Pools 01-08-2018
Productkenmerken Productkenmerken Pools 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Pools 04-08-2015
Bijsluiter Bijsluiter Portugees 01-08-2018
Productkenmerken Productkenmerken Portugees 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Portugees 04-08-2015
Bijsluiter Bijsluiter Roemeens 01-08-2018
Productkenmerken Productkenmerken Roemeens 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Roemeens 04-08-2015
Bijsluiter Bijsluiter Slowaaks 01-08-2018
Productkenmerken Productkenmerken Slowaaks 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Slowaaks 04-08-2015
Bijsluiter Bijsluiter Sloveens 01-08-2018
Productkenmerken Productkenmerken Sloveens 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Sloveens 04-08-2015
Bijsluiter Bijsluiter Fins 01-08-2018
Productkenmerken Productkenmerken Fins 01-08-2018
Bijsluiter Bijsluiter Zweeds 01-08-2018
Productkenmerken Productkenmerken Zweeds 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Zweeds 04-08-2015
Bijsluiter Bijsluiter Noors 01-08-2018
Productkenmerken Productkenmerken Noors 01-08-2018
Bijsluiter Bijsluiter IJslands 01-08-2018
Productkenmerken Productkenmerken IJslands 01-08-2018
Bijsluiter Bijsluiter Kroatisch 01-08-2018
Productkenmerken Productkenmerken Kroatisch 01-08-2018
Openbaar beoordelingsrapport Openbaar beoordelingsrapport Kroatisch 04-08-2015

Zoekwaarschuwingen met betrekking tot dit product

Bekijk de geschiedenis van documenten