Clopidogrel/Acetylsalicylic acid Teva

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

clopidogrel, Acetylsalicylic acid

Available from:

Teva Pharma B.V.

ATC code:

B01AC30

INN (International Name):

clopidogrel, acetylsalicylic acid

Therapeutic group:

combinations

Therapeutic area:

Acute Coronary Syndrome; Myocardial Infarction

Therapeutic indications:

Clopidogrel/Acetylsalicylic acid Teva is indicated for the prevention of atherothrombotic events in adult patients already taking both clopidogrel and acetylsalicylic acid (ASA). Clopidogrel/Acetylsalicylic acid Teva is a fixed‑dose combination medicinal product for continuation of therapy in:Non‑ST segment elevation acute coronary syndrome (unstable angina or non‑Q‑wave myocardial infarction) including patients undergoing a stent placement following percutaneous coronary interventionST segment elevation acute myocardial infarction in medically treated patients eligible for thrombolytic therapy

Product summary:

Revision: 1

Authorization status:

Withdrawn

Authorization date:

2014-09-01

Patient Information leaflet

                                59
B. PACKAGE LEAFLET
Medicinal product no longer authorised
60
PACKAGE LEAFLET: INFORMATION FOR THE USER
CLOPIDOGREL/ACETYLSALICYLIC ACID TEVA 75 MG/75 MG FILM-COATED TABLETS
clopidogrel/acetylsalicylic acid
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 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/Acetylsalicylic acid Teva is and what it is used for
2.
What you need to know before you take Clopidogrel/Acetylsalicylic acid
Teva
3.
How to take Clopidogrel/Acetylsalicylic acid Teva
4.
Possible side effects
5.
How to store Clopidogrel/Acetylsalicylic acid Teva
6.
Contents of the pack and other information
1.
WHAT CLOPIDOGREL/ACETYLSALICYLIC ACID TEVA IS AND WHAT IT IS USED FOR
Clopidogrel/Acetylsalicylic acid Teva contains clopidogrel and
acetylsalicylic acid (ASA) 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 in some types of blood
vessels (called arteries), antiplatelet medicinal products reduce the
chances of blood clots forming (a
process called atherothrombosis).
Clopidogrel/Acetylsalicylic acid Teva is taken by adults to prevent
blood clots forming in hardened
arteries which can lead to atherothrombotic events (such as stroke,
heart attack, or death).
You have been prescribed Clopidogrel/Acetylsalicylic acid Teva in
place of the two separate
medicines, clopidogrel and ASA, to help prevent blood clots because
you have experienced a severe
type of chest pain known as ‘unst
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
Medicinal product no longer authorised
2
1.
NAME OF THE MEDICINAL PRODUCT
Clopidogrel/Acetylsalicylic acid Teva 75 mg/75 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film-coated tablet contains 75 mg of clopidogrel (as hydrogen
sulphate) and 75 mg of
acetylsalicylic acid (ASA).
Excipient with known effect:
Each film-coated tablet contains 102.6 mg of lactose (as lactose
monohydrate).
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet (tablet)
Yellow, film-coated capsule shaped tablets. The tablets have a length
of 14.0 mm and a width of
6.8 mm.
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Clopidogrel/Acetylsalicylic acid Teva is indicated for the prevention
of atherothrombotic events in
adult patients already taking both clopidogrel and acetylsalicylic
acid (ASA).
Clopidogrel/Acetylsalicylic acid Teva is a fixed-dose combination
medicinal product for continuation
of therapy in:

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

ST segment elevation acute myocardial infarction 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 population
Clopidogrel/Acetylsalicylic acid Teva should be given as a single
daily 75 mg/75 mg dose.
Clopidogrel/Acetylsalicylic acid Teva is used following initiation of
therapy with clopidogrel and
ASA given separately.
-
_In patients with non-ST segment elevation acute coronary syndrome_
(unstable angina or
non-Q-wave myocardial infarction): The optimal duration of treatment
has not been formally
established. Clinical trial data support use up to 12 months, and the
maximum benefit was seen
at 3 months (see section 5.1). If the use of the combination of
clopidogrel/acetylsalic
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 28-04-2017
Summary of Product characteristics Summary of Product characteristics Bulgarian 28-04-2017
Public Assessment Report Public Assessment Report Bulgarian 28-04-2017
Patient Information leaflet Patient Information leaflet Spanish 28-04-2017
Public Assessment Report Public Assessment Report Spanish 28-04-2017
Patient Information leaflet Patient Information leaflet Czech 28-04-2017
Public Assessment Report Public Assessment Report Czech 28-04-2017
Patient Information leaflet Patient Information leaflet Danish 28-04-2017
Public Assessment Report Public Assessment Report Danish 28-04-2017
Patient Information leaflet Patient Information leaflet German 28-04-2017
Public Assessment Report Public Assessment Report German 28-04-2017
Patient Information leaflet Patient Information leaflet Estonian 28-04-2017
Patient Information leaflet Patient Information leaflet Greek 28-04-2017
Public Assessment Report Public Assessment Report Greek 28-04-2017
Patient Information leaflet Patient Information leaflet French 28-04-2017
Public Assessment Report Public Assessment Report French 28-04-2017
Patient Information leaflet Patient Information leaflet Italian 28-04-2017
Public Assessment Report Public Assessment Report Italian 28-04-2017
Patient Information leaflet Patient Information leaflet Latvian 28-04-2017
Public Assessment Report Public Assessment Report Latvian 28-04-2017
Patient Information leaflet Patient Information leaflet Lithuanian 28-04-2017
Summary of Product characteristics Summary of Product characteristics Lithuanian 28-04-2017
Public Assessment Report Public Assessment Report Lithuanian 28-04-2017
Patient Information leaflet Patient Information leaflet Hungarian 28-04-2017
Summary of Product characteristics Summary of Product characteristics Hungarian 28-04-2017
Public Assessment Report Public Assessment Report Hungarian 28-04-2017
Patient Information leaflet Patient Information leaflet Maltese 28-04-2017
Public Assessment Report Public Assessment Report Maltese 28-04-2017
Patient Information leaflet Patient Information leaflet Dutch 28-04-2017
Public Assessment Report Public Assessment Report Dutch 28-04-2017
Patient Information leaflet Patient Information leaflet Polish 28-04-2017
Public Assessment Report Public Assessment Report Polish 28-04-2017
Patient Information leaflet Patient Information leaflet Portuguese 28-04-2017
Summary of Product characteristics Summary of Product characteristics Portuguese 28-04-2017
Public Assessment Report Public Assessment Report Portuguese 28-04-2017
Patient Information leaflet Patient Information leaflet Romanian 28-04-2017
Public Assessment Report Public Assessment Report Romanian 28-04-2017
Patient Information leaflet Patient Information leaflet Slovak 28-04-2017
Public Assessment Report Public Assessment Report Slovak 28-04-2017
Patient Information leaflet Patient Information leaflet Slovenian 28-04-2017
Summary of Product characteristics Summary of Product characteristics Slovenian 28-04-2017
Public Assessment Report Public Assessment Report Slovenian 28-04-2017
Patient Information leaflet Patient Information leaflet Finnish 28-04-2017
Public Assessment Report Public Assessment Report Finnish 28-04-2017
Patient Information leaflet Patient Information leaflet Swedish 28-04-2017
Public Assessment Report Public Assessment Report Swedish 28-04-2017
Patient Information leaflet Patient Information leaflet Norwegian 28-04-2017
Summary of Product characteristics Summary of Product characteristics Norwegian 28-04-2017
Patient Information leaflet Patient Information leaflet Icelandic 28-04-2017
Summary of Product characteristics Summary of Product characteristics Icelandic 28-04-2017
Patient Information leaflet Patient Information leaflet Croatian 28-04-2017
Public Assessment Report Public Assessment Report Croatian 28-04-2017