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CLOPIDOGREL HEC PHARM 75 mg FILM-COATED TABLETS

CLOPIDOGREL HEC PHARM 75 mg FILM-COATED TABLETS

This page is for general information. Consult a doctor for personal advice. Call emergency services if symptoms are severe.
About the medicine

How to use CLOPIDOGREL HEC PHARM 75 mg FILM-COATED TABLETS

Introduction

Package Leaflet: Information for the User

Clopidogrel HEC Pharm 75 mg film-coated tabletsEFG

clopidogrel

Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.

  • Keep this package leaflet, as you may need to read it again.
  • If you have any questions, consult your doctor or pharmacist.
  • This medication has been prescribed to you only, and you should not give it to others, even if they have the same symptoms as you, as it may harm them.
  • If you experience side effects, consult your doctor or pharmacist, even if they are side effects not listed in this package leaflet. See section 4.

Contents of the package leaflet

  1. What is Clopidogrel HEC Pharm and what is it used for
  2. What you need to know before taking Clopidogrel HEC Pharm
  3. How to take Clopidogrel HEC Pharm
  4. Possible side effects
  5. Storage of Clopidogrel HEC Pharm
  6. Package contents and additional information

1. What is Clopidogrel HEC Pharm and what is it used for

This medication 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.

This medication 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 to help prevent the formation of blood clots and reduce the risk of these serious events, as you:

  • suffer from a process that causes the hardening of the arteries (also called atherosclerosis), and
  • have previously suffered a myocardial infarction, a stroke, or suffer from a disease called peripheral arterial disease, or
  • have suffered a severe type of chest pain, known as "unstable angina" or "myocardial infarction". For the treatment of this disease, your doctor may need to place a stent in the obstructed or narrowed artery to restore adequate blood flow. Your doctor may also have prescribed acetylsalicylic acid (a substance present in many medications used to relieve pain and reduce fever, as well as to prevent blood clots).
  • have experienced symptoms of a stroke that disappear within a short period (also known as a transient ischemic attack) or a mild ischemic stroke. Your doctor may also administer acetylsalicylic acid to you during the first 24 hours.
  • 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 and acetylsalicylic acid for this disease. Your doctor will have prescribed clopidogrel plus acetylsalicylic acid if you cannot take "oral anticoagulants" and do not have a risk of severe bleeding.

2. What you need to know before taking Clopidogrel HEC Pharm

Do not take Clopidogrel HEC Pharm

  • If you are allergic (hypersensitive) to clopidogrel or any of the other components of this medication (listed in section 6).
  • If you have an active bleeding disorder, such as a stomach ulcer or bleeding in the brain.
  • If you have a severe liver disease.

If you think any of these may apply to you, or if you are unsure, consult your doctor before taking clopidogrel.

Warnings and precautions

Before starting treatment with clopidogrel, inform your doctor if you are in any of the following situations:

  • If you have a risk of bleeding (bleeding) because:
  • you have a disease that involves a risk of internal bleeding (such as a stomach ulcer).
  • you have a blood disorder that predisposes you to internal bleeding (bleeding in tissues, organs, or joints of the body).
  • you have recently had a serious injury.
  • you have recently undergone surgery (including dental surgery).
  • you are scheduled to undergo surgery (including dental surgery) within the next seven days.
  • If you have had a blood clot in an artery of the brain (ischemic stroke) in the last 7 days.
  • If you have liver or kidney disease.
  • If you have had an allergy or reaction to any medication used to treat your disease.
  • If you have had a history of non-traumatic cerebral hemorrhage.

During treatment with clopidogrel:

  • Inform your doctor if you are scheduled to undergo surgery (including dental surgery).
  • Inform your doctor immediately if you develop a disorder (also known as Thrombotic Thrombocytopenic Purpura or TTP) that includes fever and bruising (bruises) under the skin that can appear as localized red spots, with or without unexplained extreme fatigue, confusion, yellowing of the skin or eyes (jaundice) (see section 4 "Possible side effects").
  • If you cut or injure yourself, bleeding may take longer than usual to stop. This is related to the way the medication works, 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").
  • Your doctor may ask you to have blood tests.

Children and adolescents

This medication should not be given to children as it is not effective.

Taking Clopidogrel HEC Pharm with other medications

Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication, including those obtained without a prescription. Some medications may affect the use of clopidogrel or vice versa.

You must explicitly inform your doctor if you are taking:

  • medications that may increase the risk of bleeding, such as:
  • oral anticoagulants, medications used to decrease blood clotting,
  • non-steroidal anti-inflammatory drugs, medications used to treat pain and/or muscle or joint inflammation,
  • heparin, or any other injectable medication used to decrease blood clotting,
  • ticlopidine, or other antiplatelet agents,
  • a serotonin reuptake inhibitor (such as fluoxetine or fluvoxamine and other medications of the same type), medications used to treat depression,
  • rifampicin (used for severe infections)
  • omeprazole or esomeprazole, medications used to treat stomach discomfort,
  • fluconazole or voriconazole, medications used to treat fungal infections,
  • efavirenz, or other antiretroviral medications (used to treat HIV infections),
  • carbamazepine, a medication used to treat some forms of epilepsy,
  • moclobemide, a medication used to treat depression,
  • repaglinide, a medication used to treat diabetes,
  • paclitaxel, a medication used to treat cancer,
  • opioids: if you are being treated with clopidogrel, you should inform your doctor before being prescribed any opioid (used to treat severe pain),
  • rosuvastatin (used to reduce cholesterol levels).

If you have suffered severe chest pain (unstable angina or myocardial infarction), a transient ischemic attack, or a mild ischemic stroke, you may have been prescribed clopidogrel 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 HEC Pharm with food and drinks

Clopidogrel 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. If you become pregnant while taking clopidogrel, 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 breastfeed, 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 will affect your ability to drive or operate machinery.

Clopidogrel HEC Pharm contains lactose

If your doctor has told you that you have an intolerance to certain sugars (e.g., lactose), consult with them before taking this medication.

Clopidogrel HEC Pharm contains hydrogenated castor oil

This may cause stomach upset and diarrhea.

3. How to take Clopidogrel HEC Pharm

Follow the administration instructions for this medication exactly as indicated by your doctor or pharmacist. If in 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 clopidogrel tablet per day, administered orally with or without food and at the same time every day.

If you have suffered severe chest pain (unstable angina or myocardial infarction), your doctor may prescribe 300 mg or 600 mg of clopidogrel (4 or 8 tablets of 75 mg) for you to take once at the start of treatment. Afterward, the recommended dose is one 75 mg clopidogrel tablet per day, as described above.

If you have experienced symptoms of a stroke that disappear within a short period (also known as a transient ischemic attack) or a mild ischemic stroke, your doctor may prescribe 300 mg of Clopidogrel HEC Pharm (4 tablets of 75 mg) once at the start of treatment. Afterward, the recommended dose is one 75 mg Clopidogrel HEC Pharm tablet per day, as described above, with acetylsalicylic acid for 3 weeks. Afterward, your doctor will prescribe either Clopidogrel HEC Pharm alone or acetylsalicylic acid alone.

You should take clopidogrel for as long as your doctor continues to prescribe it.

If you take more Clopidogrel HEC Pharm than you should

Contact your doctor or go to the emergency department of the nearest hospital, as there is a greater risk of bleeding.

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.

If you forget to take Clopidogrel HEC Pharm

If you forget to take a dose of clopidogrel, 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.

In the 28 and 84 tablet formats, you can check the last day you took a clopidogrel tablet by looking at the calendar printed on the blister pack.

If you stop taking Clopidogrel HEC Pharm

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.

4. Possible side effects

Like all medications, clopidogrel can have side effects, although not everyone will experience them.

Contact your doctor immediately if you experience:

  • Fever, signs of infection, or extreme fatigue. These symptoms may be due to a rare decrease in some blood cells.
  • Signs of liver problems, such as yellowing of the skin and/or eyes (jaundice), associated or not with bleeding that appears under the skin as red spots and/or confusion (see section 2 "Warnings and precautions").
  • Swelling of the mouth or skin disorders such as rashes and itching, blisters on the skin. These can be signs of an allergic reaction.

The most common side effect reported with clopidogrel is bleeding. Bleeding can occur in the stomach or intestine, bruising, hematoma (abnormal bleeding or bruising under the skin), nosebleeds, blood in the urine. A small number of cases of bleeding from the blood vessels in the eyes, intracranial bleeding, pulmonary bleeding, or joint bleeding have also been reported.

If you experience prolonged bleeding while taking clopidogrel

If you cut or injure yourself, it is possible that 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 sensation, 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., 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); decrease in 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.

Your doctor may also 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 Spanish Medication Surveillance System for Human Use: www.notificaRAM.es. By reporting side effects, you can help provide more information on the safety of this medication.

5. Storage of Clopidogrel HEC Pharm

Keep this medication out of the sight and reach of children.

Do not use this medication after the expiration date stated on the packaging and blister pack, after EXP. The expiration date is the last day of the month indicated.

This medication does not require special storage conditions.

Do not use this medication if you notice any visible signs of deterioration.

Medications should not be disposed of through wastewater or household waste. Place the packaging and any unused medication in the SIGRE collection point at your pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medication. This will help protect the environment.

6. Package Contents and Additional Information

Composition of Clopidogrel HEC Pharm

The active ingredient is clopidogrel. Each film-coated tablet contains 75 mg of clopidogrel (as hydrogen sulfate).

The other components are (see section 2 "Clopidogrel HEC Pharm contains lactose" and "Clopidogrel HEC Pharm contains hydrogenated castor oil"):

  • Tablet core: mannitol, microcrystalline cellulose, low-substituted hydroxypropylcellulose, crospovidone, colloidal silicon dioxide, hydrogenated castor oil.
  • Tablet coating: hypromellose, lactose monohydrate, titanium dioxide (E171), polyethylene glycol, red iron oxide (E172).

Appearance of the Product and Package Contents

Clopidogrel HEC Pharm 75 mg film-coated tablets are round, pink in color, and bear the engraving "C17" on one side and are smooth on the other. Clopidogrel HEC Pharm is available in cardboard boxes of 28, 30, 50, 84, and 100 tablets in OPA/Aluminum/PVC blisters.

Only some package sizes may be marketed.

Marketing Authorization Holder

HEC Pharm GmbH

Gabriele-Tergit-Promenade 17

D-10963 Berlin

Manufacturer

Formula Pharmazeutische und chemische Entwicklungs GmbH

Goerzallee 305b

D-14167 Berlin

This Medicinal Product is Authorized in the Member States of the European Economic Area under the Following Names:

Germany

Clopidogrel HEC Pharm 75 mg Film-Coated Tablets

France

CLOPIDOGREL HEC PHARM 75 mg, Film-Coated Tablet

Spain

Clopidogrel HEC Pharm 75 mg Film-Coated Tablets EFG

Date of the Last Revision of this Leaflet:June 2025

Detailed information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/

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