Package Leaflet: Information for the Patient
Rivaroxaban HEC Pharm 15 mg film-coated tablets EFG
Rivaroxaban HEC Pharm 20 mg film-coated tablets EFG
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Contents of the Package Leaflet
Rivaroxaban HEC contains the active substance rivaroxaban.
Rivaroxaban is used in adults to:
Rivaroxaban belongs to a group of medications called antithrombotic agents. It works by blocking a factor involved in blood clotting (factor Xa) and thus reducing the tendency of blood to form clots.
Do not take Rivaroxaban HEC
Do not take rivaroxaban and inform your doctorif any of these circumstances apply to you.
Warnings and precautions
Consult your doctor or pharmacist before starting to take rivaroxaban.
Be careful with Rivaroxaban HEC
Tell your doctor if you have any of these conditionsbefore taking rivaroxaban. Your doctor will decide if you should be treated with this medication and if you should be closely monitored.
If you need surgery
Children and adolescents
This medication is not recommended for persons under 18 years of age. There is not enough information about its use in children and adolescents.
Other medications and Rivaroxaban HEC
Tell your doctor or pharmacist if you are using, have recently used, or may need to use any other medication, including those purchased without a prescription.
If any of the above circumstances apply to you, tell your doctorbefore taking this medication, as the effect of rivaroxaban may be increased. Your doctor will decide if you should be treated with this medication and if you should be closely monitored.
If your doctor considers that you have a higher risk of developing stomach or intestinal ulcers, they will recommend that you use a preventive treatment for ulcers.
If any of the above circumstances apply to you, tell your doctorbefore taking this medication, as the effect of rivaroxaban may be decreased. Your doctor will decide if you should be treated with rivaroxaban and if you should be closely monitored.
Pregnancy and breastfeeding
Do not take rivaroxaban if you are pregnant or breastfeeding. If there is any possibility that you may become pregnant, use a reliable contraceptive while taking rivaroxaban. If you become pregnant while taking this medication, tell your doctor immediately, who will decide how you should be treated.
Driving and using machines
Rivaroxaban may cause dizziness (common side effect) or fainting (uncommon side effect) (see section 4, "Possible side effects"). You should not drive or use machines if you are affected by these symptoms.
Rivaroxaban HEC contains lactose and sodium
If your doctor has told you that you have an intolerance to certain sugars, consult them before taking this medication.
This medication contains less than 1 mmol of sodium (23 mg) per tablet; it is essentially "sodium-free".
Follow the instructions for administration of this medication exactly as indicated by your doctor. If you are unsure, consult your doctor or pharmacist again.
What dose to take
If you have kidney problems, the dose may be reduced to one 15 mg rivaroxaban tablet once a day.
If you need to undergo a procedure to treat blocked blood vessels in your heart (called percutaneous coronary intervention - PCI with stent placement), there is limited evidence to reduce the dose to one 15 mg rivaroxaban tablet once a day (or to one 10 mg rivaroxaban tablet once a day if your kidneys are not functioning properly) in addition to an antiplatelet medication such as clopidogrel.
The recommended dose is one 15 mg rivaroxaban tablet twice a day for the first 3 weeks. For treatment after 3 weeks, the recommended dose is one 20 mg rivaroxaban tablet once a day.
After at least 6 months of treatment for blood clots, your doctor may decide to continue treatment with one 10 mg rivaroxaban tablet once a day or one 20 mg rivaroxaban tablet once a day.
If you have kidney problems and are taking one 20 mg rivaroxaban tablet once a day, your doctor may decide to reduce the treatment dose to one 15 mg rivaroxaban tablet once a day after 3 weeks if the risk of bleeding is higher than the risk of having another blood clot.
Take each dose of rivaroxaban preferably with water during a meal.
If you have difficulty swallowing the tablet whole, consult your doctor about other ways to take rivaroxaban. The tablet can be crushed and mixed with water or apple sauce, immediately before taking it. Then, take food.
If necessary, your doctor can also administer the crushed rivaroxaban tablet through a gastric tube.
When to take Rivaroxaban HEC
Take the tablets every day, until your doctor tells you to stop.
Try to take the tablets at the same time each day to remember when to take them.
Your doctor will decide how long you should continue taking the treatment.
To prevent the formation of blood clots in the brain (stroke) or in other blood vessels:
If you need to undergo a procedure to normalize your heartbeat, called cardioversion, take rivaroxaban at the times indicated by your doctor.
If you take more Rivaroxaban HEC than you should
Call your doctor immediately if you have taken too many rivaroxaban tablets. Taking too much rivaroxaban increases the risk of bleeding.
If you forget to take Rivaroxaban HEC
If you stop taking Rivaroxaban HEC
Do not stop taking rivaroxaban without consulting your doctor first, as rivaroxaban treats and prevents serious conditions.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, rivaroxaban can cause adverse effects, although not all people suffer from them.
Like other similar medicines (antithrombotic agents), rivaroxaban can cause bleeding, which can put the patient's life at risk. Excessive bleeding can cause a sudden drop in blood pressure (shock). In some cases, the bleeding may not be evident. Possible secondary effects that may be a sign of hemorrhage.
Possible Adverse Effects that May be Signs of Bleeding:
Inform your doctor immediatelyif you experience skin reactions such as:
Your doctor will decide whether to keep you under closer observation or modify your treatment.
Possible Adverse Effects that May be Signs of Severe Skin Reaction:
Inform your doctor immediatelyif you experience any of the following side effects:
Possible Adverse Effects that May be Signs of Severe Skin Reaction:
Inform your doctor immediatelyif you suffer from any of the following adverse effects:
General List of Possible Adverse Effects:
Frequent(may affect up to 1 in 10 patients)
Uncommon(may affect up to 1 in 100 patients)
Rare(may affect up to 1 in 1,000 patients)
Frequency Not Known(frequency cannot be estimated from available data)
Reporting of Adverse Effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that is not listed in this prospectus. You can also report them directly through the Spanish Medicines Monitoring System for Human Use: www.notificaRAM.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medicine.
Keep this medicine out of sight and reach of children.
Do not use this medicine after the expiration date that appears on the packaging and on each blister after "CAD" or "EXP". The expiration date is the last day of the month indicated.
This medicine does not require special storage conditions.
Medicines should not be thrown away through drains or into the trash. Deposit the packaging and medicines you no longer need at the SIGRE point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medicines you no longer need. This way, you will help protect the environment.
Composition ofRivaroxaban HEC
Core of the tablet:microcrystalline cellulose, lactose monohydrate, sodium croscarmellose, hypromellose, sodium lauryl sulfate, and magnesium stearate. See section 2 "Rivaroxaban HEC contains lactose and sodium"
Coating of the tablet:
Rivaroxaban 15 mg film-coated tablets EFG: poly(vinyl alcohol), macrogol, titanium dioxide (E171), talc, and yellow iron oxide (E172).
Rivaroxaban 20 mg film-coated tablets EFG: poly(vinyl alcohol), macrogol, titanium dioxide (E171), and talc.
Appearance of Rivaroxaban HEC and Package Contents
Rivaroxaban HEC Pharm 15 mg film-coated tablets (5 mm in diameter) are round, yellow or light yellow, film-coated tablets with the inscription "L31" on one side and blank on the other.
Rivaroxaban HEC Pharm 20 mg film-coated tablets (6 mm in diameter) are round, white or off-white, film-coated tablets with the inscription "L85" on one side and blank on the other.
15 mg: They are packaged in blisters, in blister packs of 14, 28, 42, or 98 film-coated tablets.
20 mg: They are packaged in blisters, in blister packs of 28 or 98 film-coated tablets.
Only some package sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
HEC Pharm GmbH
Gabriele-Tergit-Promenade 17,
10963 Berlin,
Germany
Manufacturer
Formula Pharmazeutische And Chemische Entnicklungs GmbH
Goerzalle 305 b
Lichterfelde, D-14167 Berlin
Germany
This medicine is authorized in the Member States of the European Economic Area under the following names:
Germany | Rivaroxaban HEC Pharm 15 mg Filmtabletten Rivaroxaban HEC Pharm 20 mg Filmtabletten |
France | Rivaroxaban HEC Pharm 15 mg, comprimé pelliculé Rivaroxaban HEC Pharm 20 mg, comprimé pelliculé |
Italy | Rivaroxaban HEC Pharm |
Spain | Rivaroxabán HEC Pharm 15 mg film-coated tablets EFG Rivaroxabán HEC Pharm 20 mg film-coated tablets EFG |
Date of the Last Revision of this Prospectus:February 2022.
Other Sources of Information
Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/