Clopidogrel ratiopharm GmbH

Country: Evrópusambandið

Tungumál: enska

Heimild: EMA (European Medicines Agency)

Kauptu það núna

Vara einkenni Vara einkenni (SPC)
02-10-2019
Opinber matsskýrsla Opinber matsskýrsla (PAR)
28-02-2013

Virkt innihaldsefni:

clopidogrel

Fáanlegur frá:

Archie Samiel s.r.o.

ATC númer:

B01AC04

INN (Alþjóðlegt nafn):

clopidogrel

Meðferðarhópur:

Antithrombotic agents

Lækningarsvæði:

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

Ábendingar:

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.

Vörulýsing:

Revision: 12

Leyfisstaða:

Withdrawn

Leyfisdagur:

2009-07-28

Upplýsingar fylgiseðill

                                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
                                
                                Lestu allt skjalið
                                
                            

Vara einkenni

                                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
                                
                                Lestu allt skjalið
                                
                            

Skjöl á öðrum tungumálum

Upplýsingar fylgiseðill Upplýsingar fylgiseðill búlgarska 02-10-2019
Vara einkenni Vara einkenni búlgarska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla búlgarska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill spænska 02-10-2019
Vara einkenni Vara einkenni spænska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla spænska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill tékkneska 02-10-2019
Vara einkenni Vara einkenni tékkneska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla tékkneska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill danska 02-10-2019
Vara einkenni Vara einkenni danska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla danska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill þýska 02-10-2019
Vara einkenni Vara einkenni þýska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla þýska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill eistneska 02-10-2019
Vara einkenni Vara einkenni eistneska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla eistneska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill gríska 02-10-2019
Vara einkenni Vara einkenni gríska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla gríska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill franska 02-10-2019
Vara einkenni Vara einkenni franska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla franska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ítalska 02-10-2019
Vara einkenni Vara einkenni ítalska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla ítalska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill lettneska 02-10-2019
Vara einkenni Vara einkenni lettneska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla lettneska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill litháíska 02-10-2019
Vara einkenni Vara einkenni litháíska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla litháíska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill ungverska 02-10-2019
Vara einkenni Vara einkenni ungverska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla ungverska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill maltneska 02-10-2019
Vara einkenni Vara einkenni maltneska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla maltneska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill hollenska 02-10-2019
Vara einkenni Vara einkenni hollenska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla hollenska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill pólska 02-10-2019
Vara einkenni Vara einkenni pólska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla pólska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill portúgalska 02-10-2019
Vara einkenni Vara einkenni portúgalska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla portúgalska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill rúmenska 02-10-2019
Vara einkenni Vara einkenni rúmenska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla rúmenska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvakíska 02-10-2019
Vara einkenni Vara einkenni slóvakíska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla slóvakíska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill slóvenska 02-10-2019
Vara einkenni Vara einkenni slóvenska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla slóvenska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill finnska 02-10-2019
Vara einkenni Vara einkenni finnska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla finnska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill sænska 02-10-2019
Vara einkenni Vara einkenni sænska 02-10-2019
Opinber matsskýrsla Opinber matsskýrsla sænska 28-02-2013
Upplýsingar fylgiseðill Upplýsingar fylgiseðill norska 02-10-2019
Vara einkenni Vara einkenni norska 02-10-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill íslenska 02-10-2019
Vara einkenni Vara einkenni íslenska 02-10-2019
Upplýsingar fylgiseðill Upplýsingar fylgiseðill króatíska 02-10-2019
Vara einkenni Vara einkenni króatíska 02-10-2019

Leitaðu viðvaranir sem tengjast þessari vöru