Leaflet: information for the user
Efient 10 mg film-coated tablets
Efient 5 mg film-coated tablets
prasugrel
Read this leaflet carefully before you start taking the medicine, because it contains important information for you.
Efient contains the active ingredient prasugrel, which belongs to a group of medications known as antiplatelet agents. Platelets are very small cells that circulate in the blood. When a blood vessel is damaged, for example when it is cut, platelets aggregate to help form a blood clot (thrombus). Therefore, platelets are essential in helping to stop bleeding. The formation of clots in hardened blood vessels, such as arteries, can be very dangerous as it prevents blood flow, causing a heart attack (myocardial infarction), stroke (cerebrovascular accident) or death. Clots in arteries that supply blood to the heart can also reduce blood flow, causing unstable angina (severe chest pain).
Efient inhibits platelet aggregation, thereby reducing the possibility of blood clots forming.
You have been prescribed Efient because you have suffered a myocardial infarction or unstable angina and have undergone a procedure to open blocked heart arteries. You may have had one or more stents placed in the blocked or narrowed artery to restore blood flow to the heart. Efient reduces the possibility of future myocardial infarctions, stroke (cerebrovascular accident) or death due to one of these atherothrombotic events. Your doctor will also prescribe acetylsalicylic acid (e.g. aspirin), another antiplatelet agent.
Consult your doctor before starting to take Efient.
Consult your doctor or pharmacist before starting to take Efient if you are in any of the following situations:
You must contact your doctor immediately if you develop a disease called Thrombotic Thrombocytopenic Purpura (or TTP). TTP is associated with fever and bruises (hematomas) under the skin that appear as localized red spots, with or without extreme fatigue, confusion, yellowing of the skin or eyes (jaundice) (see section 4 “Possible side effects”)
Children and adolescents
Efient should not be used in children or adolescents under 18 years of age.
Other medications and Efient
Inform your doctor if you are taking, have taken recently, or may have to take any other medication, including those acquired without a prescription, dietary supplements, and herbal products.
It is especially important to inform your doctor if you are being treated with:
If administered together with Efient, these medications may increase the risk of bleeding.
Inform your doctor if you are taking morphine or other opioids (used to treat acute pain).
Use other medications while taking Efient only if your doctor indicates that you can do so.
Inform your doctor if you become pregnant or are trying to become pregnant while taking Efient. You should take Efient only after discussing the potential benefits and any potential risk to the fetus with your doctor.
If you are pregnant or breastfeeding, or if you think you may be pregnant or are planning to become pregnant, consult your doctor or pharmacist before using this medication.
Driving and operating machines
Efient is unlikely to affect your ability to drive and operate machines.
Efient contains lactose and sodium
If your doctor has indicated that you have an intolerance to certain sugars, consult with him before taking this medication.
This medication contains less than 1 mmol of sodium (23 mg) per tablet; it is essentially “sodium-free”.
Follow exactly the administration instructions for this medication as indicated by your doctor. If in doubt, consult your doctor or pharmacist again.
The usual dose of Efient is 10 mg per day. Your treatment will begin with a single dose of 60 mg. If your weight is less than 60 kg or you are over 75 years old, the dose is 5 mg of Efient per day. Your doctor will also instruct you to take acetylsalicylic acid and the exact dose you should take (usually between 75 mg and 325 mg per day).
You can take Efient with or without food. Take your dose every day at approximately the same time.
Do not break or split the tablet.
It is essential that you inform your doctor, dentist, and pharmacist that you are taking Efient.
If you take more Efient than you should
Contact your doctor or hospital directly as you may be at risk of excessive bleeding. You should show your doctor the Efient packaging.
If you forget to take Efient
If you forget to take your daily scheduled dose, take Efient when you remember. If you forget to take your dose for an entire day, take your usual dose of Efient the next day. Do not take a double dose to compensate for the missed doses. In the 14, 28, 56, 84, and 98 tablet packs, you can check the last day you took an Efient tablet by looking at the calendar printed on the blister pack.
If you interrupt treatment with Efient
Do not stop your treatment without consulting your doctor. If you stop taking Efient too soon, the risk of having a myocardial infarction may increase.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
Contact your doctorimmediatelyif you experience any of the following symptoms:
They may be signs of a stroke. A stroke is a rare side effect of Efient in patients who have never had a stroke or a transient ischemic attack.
You must also contact your doctorimmediatelyif you notice any of the following symptoms:
Inform your doctorquicklyif you experience any of the following symptoms:
They may be signs of bleeding, the most common side effect of Efient. Although rare, severe bleeding can cause death.
Common side effects (may affect up to 1 in 10 people)
Rare side effects (may affect up to 1 in 100 people)
Very rare side effects (may affect up to 1 in 1,000 people)
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through thenational notification system included in theAppendix V.By reporting side effects, you can contribute to providing more information about the safety of this medicine.
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Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Store in the original packaging to protect it from air and moisture.
Medications should not be disposed of through drains or in the trash. Ask your pharmacist how to dispose of the packaging and medications that you no longer need. This will help protect the environment.
Composition of Efient
Efient 10 mg: Each tablet contains 10 mg of prasugrel (as hydrochloride).
Efient 5 mg: Each tablet contains 5 mg of prasugrel (as hydrochloride).
Microcrystalline cellulose, mannitol (E421), sodium croscarmellose, hypromellose (E464), magnesium stearate, lactose monohydrate, titanium dioxide (E171), triacetin (E1518), iron oxide red (only in 10 mg tablets) (E172), iron oxide yellow (E172), and talc.
Appearance of the product and contents of the package
Efient 10 mg: The tablets are beige in color and have a double arrow shape, with "10 MG" engraved on one side and "4759" on the other.
Efient 5 mg: The tablets are yellow in color and have a double arrow shape, with "5 MG" engraved on one side and "4760" on the other.
Efient is available in packages of 14, 28, 30, 30 (x1), 56, 84, 90 (x1), and 98 tablets.
Only some package sizes may be marketed.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization:
SUBSTIPHARM
24 rue Erlanger
75016 Paris
France
Responsible for manufacturing:
Daiichi Sankyo Europe GmbH
Luitpoldstrasse 1
85276 Pfaffenhofen
Germany
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
Belgium/België/Belgien SUBSTIPHARM Tel: 080077098 | Lithuania SUBSTIPHARM Tel: +33 1 43 18 13 00 |
... Zentiva, k.s ... +359 24417136 | Luxembourg/Luxemburg SUBSTIPHARM Tel: 80024806 |
Czech Republic Zentiva, k.s. Tel: +420 267 241 111 | Hungary Zentiva Pharma Kft. Tel: +36 1 299 1058 |
Denmark Kurantis ApS Tel: +45 33 60 89 88 | Malta SUBSTIPHARM Tel: +33 1 43 18 13 00 |
Germany SUBSTIPHARM Tel: 08001801783 | Netherlands SUBSTIPHARM Tel: 08000228089 |
Estonia SUBSTIPHARM Tel: +33 1 43 18 13 00 | Norway Kurantis ApS Tel: +45 33 60 89 88 |
Greece Pharmaserb Hellas Tel: +30 210 620 8372 | Austria SUBSTIPHARM Tel: 0800298153 |
Spain SUBSTIPHARM Tel: 900993317 | Poland Berlin-Chemie/Menarini Polska Sp. z o.o. Tel: +48 22 566 21 00 |
France SUBSTIPHARM Tel: +33 1 43 18 13 00 | Portugal SUBSTIPHARM Tel: 800833006 |
Croatia SUBSTIPHARM Tel: +33 1 43 18 13 00 | Romania SUBSTIPHARM Tel: +33 1 43 18 13 00 |
Ireland SUBSTIPHARM Tel: 1800300170 | Slovenia Zentiva, k.s. Tel: +386 360 00 408 |
Iceland Kurantis ApS Tel: +45 33 60 89 88 | Slovakia Zentiva, a.s. Tel: +421 2 3918 3010 |
Italy SUBSTIPHARM Tel: 8007800 88 | Finland Kurantis ApS Tel: +45 33 60 89 88 |
Cyprus SUBSTIPHARM Tel: +33 1 43 18 13 00 | Sweden Kurantis ApS Tel: +45 33 60 89 88 |
Lithuania SUBSTIPHARM Tel: +33 1 43 18 13 00 | United Kingdom SUBSTIPHARM Tel: 1800300170 |
Last review date of this leaflet: {MM/YYYY}.
Other sources of information
Detailed information about this medication is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.