Clopidogrel HCS

Nazione: Unione Europea

Lingua: inglese

Fonte: EMA (European Medicines Agency)

Compra

Foglio illustrativo Foglio illustrativo (PIL)
01-08-2018
Scheda tecnica Scheda tecnica (SPC)
01-08-2018

Principio attivo:

clopidogrel (as hydrochloride)

Commercializzato da:

HCS bvba 

Codice ATC:

B01AC04

INN (Nome Internazionale):

clopidogrel

Gruppo terapeutico:

Antithrombotic agents

Area terapeutica:

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

Indicazioni terapeutiche:

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.

Dettagli prodotto:

Revision: 8

Stato dell'autorizzazione:

Authorised

Data dell'autorizzazione:

2010-10-28

Foglio illustrativo

                                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
                                
                                Leggi il documento completo
                                
                            

Scheda tecnica

                                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
                                
                                Leggi il documento completo
                                
                            

Documenti in altre lingue

Foglio illustrativo Foglio illustrativo bulgaro 01-08-2018
Scheda tecnica Scheda tecnica bulgaro 01-08-2018
Foglio illustrativo Foglio illustrativo spagnolo 01-08-2018
Scheda tecnica Scheda tecnica spagnolo 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione spagnolo 04-08-2015
Foglio illustrativo Foglio illustrativo ceco 01-08-2018
Scheda tecnica Scheda tecnica ceco 01-08-2018
Foglio illustrativo Foglio illustrativo danese 01-08-2018
Scheda tecnica Scheda tecnica danese 01-08-2018
Foglio illustrativo Foglio illustrativo tedesco 01-08-2018
Scheda tecnica Scheda tecnica tedesco 01-08-2018
Foglio illustrativo Foglio illustrativo estone 01-08-2018
Scheda tecnica Scheda tecnica estone 01-08-2018
Foglio illustrativo Foglio illustrativo greco 01-08-2018
Scheda tecnica Scheda tecnica greco 01-08-2018
Foglio illustrativo Foglio illustrativo francese 01-08-2018
Scheda tecnica Scheda tecnica francese 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione francese 04-08-2015
Foglio illustrativo Foglio illustrativo italiano 01-08-2018
Scheda tecnica Scheda tecnica italiano 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione italiano 04-08-2015
Foglio illustrativo Foglio illustrativo lettone 01-08-2018
Scheda tecnica Scheda tecnica lettone 01-08-2018
Foglio illustrativo Foglio illustrativo lituano 01-08-2018
Scheda tecnica Scheda tecnica lituano 01-08-2018
Foglio illustrativo Foglio illustrativo ungherese 01-08-2018
Scheda tecnica Scheda tecnica ungherese 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione ungherese 04-08-2015
Foglio illustrativo Foglio illustrativo maltese 01-08-2018
Scheda tecnica Scheda tecnica maltese 01-08-2018
Foglio illustrativo Foglio illustrativo olandese 01-08-2018
Scheda tecnica Scheda tecnica olandese 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione olandese 04-08-2015
Foglio illustrativo Foglio illustrativo polacco 01-08-2018
Scheda tecnica Scheda tecnica polacco 01-08-2018
Foglio illustrativo Foglio illustrativo portoghese 01-08-2018
Scheda tecnica Scheda tecnica portoghese 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione portoghese 04-08-2015
Foglio illustrativo Foglio illustrativo rumeno 01-08-2018
Scheda tecnica Scheda tecnica rumeno 01-08-2018
Foglio illustrativo Foglio illustrativo slovacco 01-08-2018
Scheda tecnica Scheda tecnica slovacco 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione slovacco 04-08-2015
Foglio illustrativo Foglio illustrativo sloveno 01-08-2018
Scheda tecnica Scheda tecnica sloveno 01-08-2018
Foglio illustrativo Foglio illustrativo finlandese 01-08-2018
Scheda tecnica Scheda tecnica finlandese 01-08-2018
Relazione pubblica di valutazione Relazione pubblica di valutazione finlandese 04-08-2015
Foglio illustrativo Foglio illustrativo svedese 01-08-2018
Scheda tecnica Scheda tecnica svedese 01-08-2018
Foglio illustrativo Foglio illustrativo norvegese 01-08-2018
Scheda tecnica Scheda tecnica norvegese 01-08-2018
Foglio illustrativo Foglio illustrativo islandese 01-08-2018
Scheda tecnica Scheda tecnica islandese 01-08-2018
Foglio illustrativo Foglio illustrativo croato 01-08-2018
Scheda tecnica Scheda tecnica croato 01-08-2018

Cerca alert relativi a questo prodotto

Visualizza cronologia documenti