Grepid

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

clopidogrel (as besilate)

Available from:

Pharmathen S.A.

ATC code:

B01AC04

INN (International Name):

clopidogrel

Therapeutic group:

Antithrombotic agents

Therapeutic area:

Peripheral Vascular Diseases; Stroke; Myocardial Infarction

Therapeutic indications:

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 seven days until less than six 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 and who have a low bleeding risk, clopidogrel is indicated in combination with ASA for the prevention of atherothrombotic and thromboembolic events, including stroke.

Product summary:

Revision: 26

Authorization status:

Authorised

Authorization date:

2009-07-27

Patient Information leaflet

                                31
B. PACKAGE LEAFLET
32
PACKAGE LEAFLET: INFORMATION FOR THE USER
GREPID 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 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 Grepid is and what it is used for
2.
What you need to know before you take Grepid
3.
How to take Grepid
4.
Possible side effects
5.
How to store Grepid
6.
Contents of the pack and other information
1.
WHAT GREPID IS AND WHAT IT IS USED FOR
Grepid 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).
Grepid 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 Grepid 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 may have placed a
stent in the blocked or narrowed artery to restore effective 
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Grepid 75 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 75 mg of clopidogrel (as besilate).
Excipient(s)
with known effect:
Each film-coated tablet contains 2.47 mg of lactose (as monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet.
Pink, round, biconvex, 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),
ischemic 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 patients
undergoing percutaneous coronary intervention (including patients
undergoing a stent
placement) or medically treated patients eligible for
thrombolytic/fibrinolytic therapy.
_In patients with moderate to high-risk_
_Transient Ischemic Attack (TIA) or minor Ischemic Stroke (IS) _
Clopidogrel in combination with ASA is indicated in:
-
Adult patients with moderate to high-risk TIA (ABCD2
1
score ≥ 4) or minor IS (NIHSS
2
≤ 3)
within 24 hours of either the TIA or IS event.
_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
thromboem
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 15-01-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 15-01-2024
Public Assessment Report Public Assessment Report Bulgarian 05-08-2009
Patient Information leaflet Patient Information leaflet Spanish 15-01-2024
Public Assessment Report Public Assessment Report Spanish 05-08-2009
Patient Information leaflet Patient Information leaflet Czech 15-01-2024
Public Assessment Report Public Assessment Report Czech 05-08-2009
Patient Information leaflet Patient Information leaflet Danish 15-01-2024
Public Assessment Report Public Assessment Report Danish 05-08-2009
Patient Information leaflet Patient Information leaflet German 15-01-2024
Public Assessment Report Public Assessment Report German 05-08-2009
Patient Information leaflet Patient Information leaflet Estonian 15-01-2024
Public Assessment Report Public Assessment Report Estonian 05-08-2009
Patient Information leaflet Patient Information leaflet Greek 15-01-2024
Public Assessment Report Public Assessment Report Greek 05-08-2009
Patient Information leaflet Patient Information leaflet French 15-01-2024
Public Assessment Report Public Assessment Report French 05-08-2009
Patient Information leaflet Patient Information leaflet Italian 15-01-2024
Public Assessment Report Public Assessment Report Italian 05-08-2009
Patient Information leaflet Patient Information leaflet Latvian 15-01-2024
Public Assessment Report Public Assessment Report Latvian 05-08-2009
Patient Information leaflet Patient Information leaflet Lithuanian 15-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 15-01-2024
Public Assessment Report Public Assessment Report Lithuanian 05-08-2009
Patient Information leaflet Patient Information leaflet Hungarian 15-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 15-01-2024
Public Assessment Report Public Assessment Report Hungarian 05-08-2009
Patient Information leaflet Patient Information leaflet Maltese 15-01-2024
Public Assessment Report Public Assessment Report Maltese 05-08-2009
Patient Information leaflet Patient Information leaflet Dutch 15-01-2024
Public Assessment Report Public Assessment Report Dutch 05-08-2009
Patient Information leaflet Patient Information leaflet Polish 15-01-2024
Public Assessment Report Public Assessment Report Polish 05-08-2009
Patient Information leaflet Patient Information leaflet Portuguese 15-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 15-01-2024
Public Assessment Report Public Assessment Report Portuguese 05-08-2009
Patient Information leaflet Patient Information leaflet Romanian 15-01-2024
Public Assessment Report Public Assessment Report Romanian 05-08-2009
Patient Information leaflet Patient Information leaflet Slovak 15-01-2024
Public Assessment Report Public Assessment Report Slovak 05-08-2009
Patient Information leaflet Patient Information leaflet Slovenian 15-01-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 15-01-2024
Public Assessment Report Public Assessment Report Slovenian 05-08-2009
Patient Information leaflet Patient Information leaflet Finnish 15-01-2024
Public Assessment Report Public Assessment Report Finnish 05-08-2009
Patient Information leaflet Patient Information leaflet Swedish 15-01-2024
Public Assessment Report Public Assessment Report Swedish 05-08-2009
Patient Information leaflet Patient Information leaflet Norwegian 15-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 15-01-2024
Patient Information leaflet Patient Information leaflet Icelandic 15-01-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 15-01-2024
Patient Information leaflet Patient Information leaflet Croatian 15-01-2024

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