Clopidogrel 1A Pharma

Nazione: Unione Europea

Lingua: inglese

Fonte: EMA (European Medicines Agency)

Compra

Foglio illustrativo Foglio illustrativo (PIL)
28-02-2011
Scheda tecnica Scheda tecnica (SPC)
28-02-2011

Principio attivo:

clopidogrel

Commercializzato da:

Acino Pharma GmbH 

Codice ATC:

B01AC04

INN (Nome Internazionale):

clopidogrel

Gruppo terapeutico:

Antithrombotic agents

Area terapeutica:

Peripheral Vascular Diseases

Indicazioni terapeutiche:

Clopidogrel is indicated in adults for the prevention of atherothrombotic events in: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.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.For further information please refer to section 5.1.

Dettagli prodotto:

Revision: 1

Stato dell'autorizzazione:

Withdrawn

Data dell'autorizzazione:

2009-07-28

Foglio illustrativo

                                22
B. PACKAGE LEAFLET
Medicinal product no longer authorised
23
PACKAGE LEAFLET: INFORMATION FOR THE USER
CLOPIDOGREL 1A PHARMA 75 MG FILM-COATED TABLETS
Clopidogrel
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE.
-
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. Do not pass it on to
others. It may harm them,
even if their symptoms are the same as yours.
-
If any of the side effects gets serious, or if you notice any side
effects not listed in this leaflet,
please tell your doctor or pharmacist,
IN THIS LEAFLET
:
1.
What Clopidogrel 1A Pharma is and what it is used for
2.
Before you take Clopidogrel 1A Pharma
3.
How to take Clopidogrel 1A Pharma
4.
Possible side effects
5.
How to store Clopidogrel 1A Pharma
6.
Further information
1.
WHAT CLOPIDOGREL 1A PHARMA IS AND WHAT IT IS USED FOR
Clopidogrel 1A Pharma contains the active ingredient Clopidogrel which
belongs to a group of
medicines called antiplatelet medicinal products. Platelets (so-called
thrombocytes) are very small
structures, 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 1A Pharma is taken 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 1A Pharma 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 (disturbed blood flow in arms or legs
caused by vascular
occlusions) or
-
You have experienced a severe type of chest pain known as ‘unstable
angina’ or ‘myocardial
                                
                                Leggi il documento completo
                                
                            

Scheda tecnica

                                _ _
_ _
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
1.
NAME OF THE MEDICINAL PRODUCT
Clopidogrel 1A Pharma 75 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 75 mg of Clopidogrel (as besilate).
Excipients: each tablet contains 3.80 mg hydrogenated castor oil.
For a full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
White to off-white, marbled, round and biconvex film-coated tablets.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Clopidogrel is indicated in adults for the prevention of
atherothrombotic events in:

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.

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.
For further information please refer to section 5.1.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION

Adults and elderly
Clopidogrel should be given as a single daily dose of 75 mg with or
without food.
In patients suffering from acute coronary syndrome:
-
Non-ST segment elevation acute coronary syndrome (unstable angina or
non-Q-wave
myocardial infarction): Clopidogrel treatment should be initiated with
a single 300 mg loading
dose and then continued at 75 mg once a day (with acetylsalicylic acid
(ASA) 75 mg-325 mg
daily). Since higher doses of ASA were associated with higher bleeding
risk it is recommended
that the dose of ASA should not be higher than 100 mg. The optimal
duration of treatment has
not been formally established. Clinical trial data support u
                                
                                Leggi il documento completo
                                
                            

Documenti in altre lingue

Foglio illustrativo Foglio illustrativo bulgaro 28-02-2011
Scheda tecnica Scheda tecnica bulgaro 28-02-2011
Foglio illustrativo Foglio illustrativo spagnolo 28-02-2011
Scheda tecnica Scheda tecnica spagnolo 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione spagnolo 28-02-2011
Foglio illustrativo Foglio illustrativo ceco 28-02-2011
Scheda tecnica Scheda tecnica ceco 28-02-2011
Foglio illustrativo Foglio illustrativo danese 28-02-2011
Scheda tecnica Scheda tecnica danese 28-02-2011
Foglio illustrativo Foglio illustrativo tedesco 28-02-2011
Scheda tecnica Scheda tecnica tedesco 28-02-2011
Foglio illustrativo Foglio illustrativo estone 28-02-2011
Scheda tecnica Scheda tecnica estone 28-02-2011
Foglio illustrativo Foglio illustrativo greco 28-02-2011
Scheda tecnica Scheda tecnica greco 28-02-2011
Foglio illustrativo Foglio illustrativo francese 28-02-2011
Scheda tecnica Scheda tecnica francese 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione francese 28-02-2011
Foglio illustrativo Foglio illustrativo italiano 28-02-2011
Scheda tecnica Scheda tecnica italiano 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione italiano 28-02-2011
Foglio illustrativo Foglio illustrativo lettone 28-02-2011
Scheda tecnica Scheda tecnica lettone 28-02-2011
Foglio illustrativo Foglio illustrativo lituano 28-02-2011
Scheda tecnica Scheda tecnica lituano 28-02-2011
Foglio illustrativo Foglio illustrativo ungherese 28-02-2011
Scheda tecnica Scheda tecnica ungherese 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione ungherese 28-02-2011
Foglio illustrativo Foglio illustrativo maltese 28-02-2011
Scheda tecnica Scheda tecnica maltese 28-02-2011
Foglio illustrativo Foglio illustrativo olandese 28-02-2011
Scheda tecnica Scheda tecnica olandese 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione olandese 28-02-2011
Foglio illustrativo Foglio illustrativo polacco 28-02-2011
Scheda tecnica Scheda tecnica polacco 28-02-2011
Foglio illustrativo Foglio illustrativo portoghese 28-02-2011
Scheda tecnica Scheda tecnica portoghese 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione portoghese 28-02-2011
Foglio illustrativo Foglio illustrativo rumeno 28-02-2011
Scheda tecnica Scheda tecnica rumeno 28-02-2011
Foglio illustrativo Foglio illustrativo slovacco 28-02-2011
Scheda tecnica Scheda tecnica slovacco 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione slovacco 28-02-2011
Foglio illustrativo Foglio illustrativo sloveno 28-02-2011
Scheda tecnica Scheda tecnica sloveno 28-02-2011
Foglio illustrativo Foglio illustrativo finlandese 28-02-2011
Scheda tecnica Scheda tecnica finlandese 28-02-2011
Relazione pubblica di valutazione Relazione pubblica di valutazione finlandese 28-02-2011
Foglio illustrativo Foglio illustrativo svedese 28-02-2011
Scheda tecnica Scheda tecnica svedese 28-02-2011

Cerca alert relativi a questo prodotto

Visualizza cronologia documenti