Package Leaflet: Information for the User
Clopidogrel TAD 75 mg film-coated tablets EFG
clopidogrel
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Contents of the package leaflet:
Clopidogrel TAD contains clopidogrel and belongs to a group of medications called antiplatelet agents. Platelets are very small cells found in the blood, and they aggregate when the blood clots. Antiplatelet agents, by preventing this aggregation, reduce the likelihood of blood clots (a process called thrombosis) forming.
Clopidogrel TAD is administered to adults to prevent the formation of blood clots (thrombi) in blood vessels (arteries) that have become hardened, a process known as atherothrombosis, which can cause atherothrombotic events (such as stroke, myocardial infarction, or death).
You have been prescribed Clopidogrel TAD to help prevent the formation of blood clots and reduce the risk of these serious events, as:
you have an irregular heartbeat, a disease called "atrial fibrillation", and you cannot take medications known as "oral anticoagulants" (vitamin K antagonists) that prevent the formation of new clots and prevent the growth of existing clots. You will have been told that "oral anticoagulants" are more effective than acetylsalicylic acid or the combined use of Clopidogrel TAD and acetylsalicylic acid for this disease. Your doctor will have prescribed Clopidogrel TAD plus acetylsalicylic acid if you cannot take "oral anticoagulants" and do not have a risk of severe bleeding.
Do not take Clopidogrel TAD:
If you think any of these may affect you, or if you have any doubts, consult your doctor before taking Clopidogrel TAD.
Warnings and precautions
Before starting treatment with Clopidogrel TAD, inform your doctor if you are in any of the following situations:
During treatment with Clopidogrel TAD:
Children and adolescents
This medication should not be given to children as it is not effective.
Other medications and Clopidogrel TAD
Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication, including those purchased without a prescription.
Some medications may affect the use of Clopidogrel TAD or vice versa.
You must explicitly inform your doctor if you are taking:
If you have suffered severe chest pain (unstable angina or myocardial infarction), you may have been prescribed Clopidogrel TAD in combination with acetylsalicylic acid, a substance present in many medications used to relieve pain and reduce fever. A dose of acetylsalicylic acid administered occasionally (not exceeding 1,000 mg in 24 hours) is generally not a problem, but prolonged use in other circumstances should be discussed with your doctor.
Taking Clopidogrel TAD with food and drinks
Clopidogrel TAD can be taken with or without food.
Pregnancy and breastfeeding
It is preferable not to take this medication during pregnancy.
If you are pregnant or think you may be pregnant, you should inform your doctor or pharmacist before taking Clopidogrel TAD. If you become pregnant while taking Clopidogrel TAD, consult your doctor immediately, as it is not recommended to take clopidogrel during pregnancy.
You should not breastfeed while taking this medication.
If you are breastfeeding or plan to do so, inform your doctor before taking this medication.
Consult your doctor or pharmacist before using any medication.
Driving and using machines
It is unlikely that Clopidogrel TAD will affect your ability to drive or operate machinery.
Follow the instructions for administration of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended dose, even for patients with a disease called "atrial fibrillation" (an irregular heartbeat), is one 75 mg tablet of Clopidogrel TAD per day, administered orally, with or without food, and at the same time each day.
If you have suffered severe chest pain (unstable angina or myocardial infarction), your doctor may prescribe 300 mg of Clopidogrel TAD (4 tablets of 75 mg) to be taken once at the start of treatment. Afterward, the recommended dose is one 75 mg tablet of Clopidogrel TAD per day, as described above.
You should take Clopidogrel TAD for as long as your doctor continues to prescribe it.
If you take more Clopidogrel TAD than you should
Contact your doctor or go to the emergency department of the nearest hospital, as there is a greater risk of bleeding.
If you forget to take Clopidogrel TAD
If you forget to take a dose of Clopidogrel TAD, but remember before 12 hours have passed since the time you should have taken the medication, take the tablet immediately and the next one at the usual time.
If you forget for more than 12 hours, simply take the next dose at the usual time. Do not take a double dose to make up for a missed tablet.
If you stop treatment with Clopidogrel TAD
Do not stop your treatment unless your doctor tells you to. Contact your doctor or pharmacist before stopping this medication.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone will experience them.
Contact your doctor immediately if you experience:
The most common side effect reported with Clopidogrel TAD is bleeding.
Bleeding can occur in the stomach or intestine, bruising, hematoma (abnormal bleeding or bruising under the skin), nosebleeds, blood in urine. A reduced number of cases of bleeding in the blood vessels of the eyes, intracranial bleeding, pulmonary or joint bleeding have also been reported.
If you experience prolonged bleeding while taking Clopidogrel TAD
If you cut or injure yourself, bleeding may take a little longer than usual to stop. This is related to the mechanism of action of the medication, as it prevents the blood's ability to form clots. For minor cuts or injuries, such as cuts while shaving, this is usually not a problem. However, if you are concerned about your bleeding, consult your doctor immediately (see section 2 "Warnings and precautions").
Other side effects include:
Common side effects (may affect up to 1 in 10 people):
Diarrhea, abdominal pain, indigestion, or heartburn.
Uncommon side effects (may affect up to 1 in 100 people):
Headache, stomach ulcer, vomiting, nausea, constipation, excess gas in the stomach or intestine, rash, itching, dizziness, tingling, and numbness.
Rare side effects (may affect up to 1 in 1,000 people):
Dizziness, breast enlargement in men.
Very rare side effects (may affect up to 1 in 10,000 people):
Jaundice; severe abdominal pain with or without back pain; fever, difficulty breathing, sometimes associated with cough; generalized allergic reactions (e.g., general feeling of heat with sudden general discomfort leading to fainting); swelling of the mouth; blisters on the skin; skin allergy; inflammation of the mouth mucosa (stomatitis); decreased blood pressure; confusion; hallucinations; joint pain; muscle pain; changes in taste or loss of taste of food.
Side effects with unknown frequency (cannot be estimated from available data): Hypersensitivity reactions with chest or abdominal pain, persistent symptoms of low blood sugar.
In addition, your doctor may observe changes in the results of your blood or urine tests.
Reporting side effects
If you experience any side effects, consult your doctor or pharmacist, even if they are side effects not listed in this package leaflet. You can also report them directly through the national reporting system included in Appendix V. By reporting side effects, you can help provide more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date shown on the carton and blister pack after EXP. The expiration date is the last day of the month indicated.
Store in the original packaging to protect from light and moisture.
Medications should not be disposed of through wastewater or household waste. Ask your pharmacist how to dispose of the packaging and any unused medication. This will help protect the environment.
Clopidogrel TAD Composition
Appearance of Clopidogrel TAD and Package Contents
Film-coated tablets are pink, round, and slightly convex.
Boxes of 7, 14, 28, 30, 50, 56, 84, 90, and 100 film-coated tablets in blisters.
Marketing Authorization Holder
TAD Pharma GmbH, Heinz-Lohmann-Straße 5, 27472 Cuxhaven, Germany
Manufacturers
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia; TAD Pharma GmbH, Heinz-Lohmann-Strasse 5, 27472 Cuxhaven, Germany
You can request more information about this medicinal product by contacting the local representative of the marketing authorization holder:
Belgium | Lithuania |
KRKA Belgium, SA. | UAB KRKA Lietuva |
Tel: + 32 (0) 487 50 73 62 | Tel: + 370 5 236 27 40 |
Bulgaria | Luxembourg |
KRKA Bulgaria EOOD | KRKA Belgium, SA. |
Tel: + 359 (02) 962 34 50 | Tel: + 32 (0) 487 50 73 62 (BE) |
Czech Republic | Hungary |
KRKA CR, s.r.o. | KRKA Magyarország Kereskedelmi Kft. |
Tel: + 420 (0) 221 115 150 | Tel: + 36 (1) 355 8490 |
Denmark | Malta |
KRKA Sverige AB | EJ Busuttil Ltd |
Tel: + 46 (0)8 643 67 66 (SE) | Tel: + 356 21445885 |
Germany | Netherlands |
TAD Pharma GmbH | KRKA Belgium, SA. |
Tel: + 49 (0) 4721 606-0 | Tel: + 32 (0) 487 50 73 62 (BE) |
Estonia | Norway |
KRKA, d.d., Novo mesto, Estonian branch | KRKA Sverige AB |
Tel: + 372 (0)6 671 658 | Tel: + 46 (0)8 643 67 66 (SE) |
Greece | Austria |
QUALIA PHARMA S.A. | KRKA Pharma GmbH, Vienna |
Tel: + 30 210 6256177 | Tel: + 43 (0)1 66 24 300 |
Spain | Poland |
KRKA Farmacéutica, S.L. | KRKA-POLSKA Sp. z o.o. |
Tel: + 34 911 61 03 81 | Tel: + 48 (0)22 573 7500 |
36 | |
France | Portugal |
KRKA France Eurl | KRKA Farmacêutica, Sociedade Unipessoal Lda. |
Tel: + 33 1 57 408 225 | Tel: + 351 (0)21 46 43 650 |
Croatia | Romania |
KRKA – FARMA d.o.o. | KRKA Romania S.R.L., Bucharest |
Tel: + 385 1 6312 100 | Tel: + 4 021 310 66 05 |
Ireland | Slovenia |
Clonmel Healthcare Ltd. | KRKA, d.d., Novo mesto |
Tel: + 353 52 6177778 | Tel: + 386 (0) 1 47 51 100 |
Iceland | Slovakia |
KRKA Sverige AB | KRKA Slovensko, s.r.o. |
Tel: + 46 (0)8 643 67 66 (SE) | Tel: + 421 (0) 2 571 04 501 |
Italy | Finland |
KRKA Farmaceutici Milano, S.r.l. | KRKA Finland Oy |
Tel: + 39 02 3300 8841 | Tel: + 358 20 754 5330 |
Cyprus | Sweden |
KI.PA. (PHARMACAL) LIMITED | KRKA Sverige AB |
Tel: + 357 (0)24 651 882 (CY) | Tel: + 46 (0)8 643 67 66 (SE) |
Latvia | United Kingdom |
KRKA Latvija SIA | KRKA UK Ltd. |
Tel: + 371 6733 86 10 | Tel: + 44 (0) 207 400 3352 |
Date of Last Revision of this Leaflet:
Detailed information on this medicinal product is available on the European Medicines Agency website http://www.ema.europa.eu