Clopidogrel ratiopharm GmbH

Country: Kesatuan Eropah

Bahasa: Inggeris

Sumber: EMA (European Medicines Agency)

Beli sekarang

Download Risalah maklumat (PIL)
02-10-2019
Download Ciri produk (SPC)
02-10-2019
Download Laporan Penilaian Awam (PAR)
28-02-2013

Bahan aktif:

clopidogrel

Boleh didapati daripada:

Archie Samiel s.r.o.

Kod ATC:

B01AC04

INN (Nama Antarabangsa):

clopidogrel

Kumpulan terapeutik:

Antithrombotic agents

Kawasan terapeutik:

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

Tanda-tanda terapeutik:

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.

Ringkasan produk:

Revision: 12

Status kebenaran:

Withdrawn

Tarikh kebenaran:

2009-07-28

Risalah maklumat

                                B. PACKAGE LEAFLET
27
PACKAGE LEAFLET: INFORMATION FOR THE USER
CLOPIDOGREL RATIOPHARM GMBH 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 your 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 Clopidogrel ratiopharm GmbH is and what it is used for
2.
What you need to know before you take Clopidogrel ratiopharm GmbH
3.
How to take Clopidogrel ratiopharm GmbH
4.
Possible side effects
5.
How to store Clopidogrel ratiopharm GmbH
6.
Contents of the pack and other information
1.
WHAT CLOPIDOGREL RATIOPHARM GMBH IS AND WHAT IT IS USED FOR
Clopidogrel ratiopharm GmbH 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 ratiopharm GmbH 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 ratiopharm GmbH 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
                                
                                Baca dokumen lengkap
                                
                            

Ciri produk

                                ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
1
1.
NAME OF THE MEDICINAL PRODUCT
Clopidogrel ratiopharm GmbH 75 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 75 mg of clopidogrel (as besilate).
Excipients with known effect:
Each film-coated tablet contains 3.80 mg of hydrogenated castor oil.
For the 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 secondary prevention of
atherothrombotic events 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.
For further information please refer to section 5.1.
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
Posology
•
Adults and elderly
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): 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 sup
                                
                                Baca dokumen lengkap
                                
                            

Dokumen dalam bahasa lain

Risalah maklumat Risalah maklumat Bulgaria 02-10-2019
Ciri produk Ciri produk Bulgaria 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Bulgaria 28-02-2013
Risalah maklumat Risalah maklumat Sepanyol 02-10-2019
Ciri produk Ciri produk Sepanyol 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Sepanyol 28-02-2013
Risalah maklumat Risalah maklumat Czech 02-10-2019
Ciri produk Ciri produk Czech 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Czech 28-02-2013
Risalah maklumat Risalah maklumat Denmark 02-10-2019
Ciri produk Ciri produk Denmark 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Denmark 28-02-2013
Risalah maklumat Risalah maklumat Jerman 02-10-2019
Ciri produk Ciri produk Jerman 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Jerman 28-02-2013
Risalah maklumat Risalah maklumat Estonia 02-10-2019
Ciri produk Ciri produk Estonia 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Estonia 28-02-2013
Risalah maklumat Risalah maklumat Greek 02-10-2019
Ciri produk Ciri produk Greek 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Greek 28-02-2013
Risalah maklumat Risalah maklumat Perancis 02-10-2019
Ciri produk Ciri produk Perancis 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Perancis 28-02-2013
Risalah maklumat Risalah maklumat Itali 02-10-2019
Ciri produk Ciri produk Itali 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Itali 28-02-2013
Risalah maklumat Risalah maklumat Latvia 02-10-2019
Ciri produk Ciri produk Latvia 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Latvia 28-02-2013
Risalah maklumat Risalah maklumat Lithuania 02-10-2019
Ciri produk Ciri produk Lithuania 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Lithuania 28-02-2013
Risalah maklumat Risalah maklumat Hungary 02-10-2019
Ciri produk Ciri produk Hungary 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Hungary 28-02-2013
Risalah maklumat Risalah maklumat Malta 02-10-2019
Ciri produk Ciri produk Malta 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Malta 28-02-2013
Risalah maklumat Risalah maklumat Belanda 02-10-2019
Ciri produk Ciri produk Belanda 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Belanda 28-02-2013
Risalah maklumat Risalah maklumat Poland 02-10-2019
Ciri produk Ciri produk Poland 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Poland 28-02-2013
Risalah maklumat Risalah maklumat Portugis 02-10-2019
Ciri produk Ciri produk Portugis 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Portugis 28-02-2013
Risalah maklumat Risalah maklumat Romania 02-10-2019
Ciri produk Ciri produk Romania 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Romania 28-02-2013
Risalah maklumat Risalah maklumat Slovak 02-10-2019
Ciri produk Ciri produk Slovak 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Slovak 28-02-2013
Risalah maklumat Risalah maklumat Slovenia 02-10-2019
Ciri produk Ciri produk Slovenia 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Slovenia 28-02-2013
Risalah maklumat Risalah maklumat Finland 02-10-2019
Ciri produk Ciri produk Finland 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Finland 28-02-2013
Risalah maklumat Risalah maklumat Sweden 02-10-2019
Ciri produk Ciri produk Sweden 02-10-2019
Laporan Penilaian Awam Laporan Penilaian Awam Sweden 28-02-2013
Risalah maklumat Risalah maklumat Norway 02-10-2019
Ciri produk Ciri produk Norway 02-10-2019
Risalah maklumat Risalah maklumat Iceland 02-10-2019
Ciri produk Ciri produk Iceland 02-10-2019
Risalah maklumat Risalah maklumat Croat 02-10-2019
Ciri produk Ciri produk Croat 02-10-2019

Cari amaran yang berkaitan dengan produk ini