Package Leaflet: Information for the User
ClopidogrelFarmalider75 mg film-coated tablets EFG
Clopidogrel, besylate
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 Farmalider belongs to a group of medications called antiplatelet agents. Platelets are very small cells found in the blood, smaller than red or white blood cells, and they aggregate when blood clots. Antiplatelet agents, by preventing this aggregation, reduce the likelihood of blood clots (a process called thrombosis) forming.
Clopidogrel Farmalider is administered 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 cerebral infarction, myocardial infarction, or death). You have been prescribed Clopidogrel Farmalider to help prevent the formation of blood clots and reduce the risk of these serious events, as:
Do not take Clopidogrel Farmalider:
If you think any of these may apply to you, or if you have any doubts, consult your doctor before taking Clopidogrel.
Warnings and Precautions
Consult your doctor or pharmacist before starting to take Clopidogrel Farmalider.
Before starting treatment with Clopidogrel Farmalider, inform your doctor if you are in any of the following situations:
During treatment with Clopidogrel Farmalider
Children and Adolescents
Clopidogrel Farmalider should not be administered to children or adolescents.
Taking Clopidogrel Farmalider with other medications
Tell your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication.
Some medications may affect the use of Clopidogrel or vice versa.
Concomitant administration of Clopidogrel with oral anticoagulants (medications used to decrease blood clotting) is not recommended.
You must explicitly inform your doctor if you are taking ticlopidine, another antiplatelet agent, non-steroidal anti-inflammatory drugs, medications commonly used to treat pain and/or inflammation of muscles or joints, or if you are taking heparin, or any other medication used to decrease blood clotting, if you are taking a proton pump inhibitor (e.g., omeprazol) for stomach discomfort or if you are taking antiretrovirals (medications to treat HIV infection).
A dose of acetylsalicylic acid administered occasionally (not exceeding 1,000 mg in 24 hours) should not cause any problems, but prolonged use in other circumstances should be discussed with your doctor.
Taking Clopidogrel Farmalider with food and drinks
Clopidogrel Farmalider can be taken with or without food.
Pregnancy and Breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
It is preferable not to use this medication during pregnancy and breastfeeding.
Driving and Using Machines
It is unlikely that Clopidogrel will affect your ability to drive or operate machinery.
This medication contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow the administration instructions of this medication exactly as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended dose is one 75 mg tablet of Clopidogrel Farmalider per day, administered orally, with or without food, and at the same time each day.
You should take Clopidogrel Farmalider for as long as your doctor continues to prescribe it.
If you take more Clopidogrel Farmalider than you should
Contact your doctor or go to the nearest hospital emergency department, as there is a higher risk of bleeding. In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20 (indicating the medication and the amount ingested).
If you forget to take Clopidogrel Farmalider
If you forget to take a dose of Clopidogrel Farmalider, 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 the forgotten doses.
In the 7, 14, 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 interrupt treatment with Clopidogrel Farmalider
Do not interrupt your treatment. Contact your doctor or pharmacist before stopping this medication.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medications, Clopidogrel Farmalider can have side effects, although not everyone will experience them.
Contact your doctor immediately if you experience
These may be signs of an allergic reaction.
The most common side effect reported with Clopidogrel(affecting 1 to 10 patients out of 100) 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 bleeding, or joint bleeding have also been reported.
If you experience prolonged bleeding while taking Clopidogrel Farmalider
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 "Take special care with Clopidogrel").
Other side effects reported with Clopidogrel are
Common side effects (affecting 1 to 10 people out of 100): Diarrhea, abdominal pain, indigestion, or heartburn.
Uncommon side effects (affecting 1 to 10 people out of 1,000): headache, stomach ulcer, vomiting, nausea, constipation, excess gas in the stomach or intestine, rash, itching, dizziness, tingling sensation, and numbness.
Rare side effects (affecting 1 to 10 people out of 10,000): vertigo.
Very rare side effects (affecting less than 1 person out of 10,000): jaundice, severe abdominal pain with or without back pain; fever, difficulty breathing, sometimes associated with cough; generalized allergic reactions; 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, eosinophilic pneumonia, acquired hemophilia A.
Side effects of unknown frequency: hypersensitivity reactions.
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 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 contribute to providing 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 packaging after CAD. The expiration date is the last day of the month indicated.
No special storage conditions are required.
Do not use this medication if you observe any visible signs of deterioration.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE collection point in the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Composition of Clopidogrel Farmalider
Appearance of the Product and Package Contents
Clopidogrel Farmalider tablets are round, biconvex, pink, and film-coated.
They are available in packages of 28 and 100 tablets in PVC/PE/PVDC-Aluminum or Aluminum/Aluminum blisters.
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Farmalider, S.A.
c/ Aragoneses 15
28108 Alcobendas - Madrid
Spain
Manufacturer
FARMALIDER, S.A.
c/ Aragoneses 15
28108 Alcobendas - Madrid
Spain
Or
PHARMATHEN S.A.
6, Dervenakion Str (Pallini Attikis)
Date of the last revision of this package leaflet: October 2020
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/