Package Leaflet: Information for the User
Rivaroxaban Teva 20 mg film-coated tablets EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
This medicine contains the active substance rivaroxaban and is used in adults to:
This medicine is used in children and adolescents under 18 years of age and with a body weight of 30 kg or more to:
This medicine belongs to a group of medicines called antithrombotic agents. It works by blocking a factor in the blood that is involved in blood clotting (factor Xa) and thus reduces the tendency of the blood to form clots.
Do not take Rivaroxaban Teva
Do not take this medicine and inform your doctor if any of these apply to you.
Warnings and precautions
Consult your doctor or pharmacist before taking this medicine.
Be careful with Rivaroxaban Teva
Tell your doctor if you have any of these conditionsbefore taking this medicine. Your doctor will decide if you should be treated with this medicine and if you should be kept under closer observation.
If you need surgery:
Children and adolescents
Rivaroxaban 20 mg tablets are not recommended in children with a body weight below 30 kg.There is not enough information about the use of rivaroxaban in children and adolescents for the indications in adults.
Other medicines and Rivaroxaban Teva
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including those obtained without a prescription.
If any of the above applies to you,tell your doctorbefore taking this medicine, as the effect of rivaroxaban may be increased. Your doctor will decide if you should be treated with this medicine and if you should be kept under closer observation.
If your doctor considers that you have a higher risk of developing a stomach or intestinal ulcer, they may recommend that you also take a preventive treatment.
If any of the above applies to you,tell your doctorbefore taking this medicine, as the effect of rivaroxaban may be reduced. Your doctor will decide if you should be treated with this medicine and if you should be kept under closer observation.
Pregnancy and breastfeeding
Do not takerivaroxaban if you are pregnant or breastfeeding. If there is a possibility that you may become pregnant, use a reliable contraceptive while taking rivaroxaban. If you become pregnant while taking rivaroxaban, inform your doctor immediately, who will decide how you should be treated.
Driving and using machines
Rivaroxaban may cause dizziness (a common side effect) or fainting (an uncommon side effect) (see section 4, "Possible side effects"). You should not drive, ride a bicycle, or use tools or machines if you are affected by these symptoms.
This medicine contains lactose
If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
This medicine contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per tablet; this is essentially "sodium-free".
Follow exactly the instructions of administration of this medicine indicated by your doctor. If you are in doubt, consult your doctor or pharmacist again.
You must take this medicine with food.
Swallow the tablets, preferably with water.
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 puree, immediately before taking it. Then take food.
If necessary, your doctor may also administer the crushed rivaroxaban tablet through a gastric tube.
What dose to take
Adults
The recommended dose is one rivaroxaban 20 mg tablet once a day.
If you have kidney problems, the dose may be reduced to one rivaroxaban 15 mg 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 rivaroxaban 15 mg tablet once a day (or to one rivaroxaban 10 mg tablet once a day if your kidneys do not work properly) in addition to an antiplatelet medicine such as clopidogrel.
The recommended dose is one rivaroxaban 15 mg tablet twice a day for the first 3 weeks. For treatment after 3 weeks, the recommended dose is one rivaroxaban 20 mg tablet once a day.
After at least 6 months of treatment for blood clots, your doctor may decide to continue treatment with one rivaroxaban 10 mg tablet once a day or one rivaroxaban 20 mg tablet once a day.
If you have kidney problems and are taking one rivaroxaban 20 mg tablet once a day, your doctor may decide to reduce the dose of treatment to one rivaroxaban 15 mg tablet once a day after 3 weeks if the risk of bleeding is higher than the risk of having another blood clot.
Children and adolescents
The dose of rivaroxaban depends on body weight and will be calculated by the doctor.
Take each dose of rivaroxaban with a drink (e.g. water or juice) during a meal. Take the tablets every day at approximately the same time. Consider setting an alarm to remind you.
For parents or caregivers: observe the child to ensure they take the entire dose.
Since the dose of rivaroxaban is based on body weight, it is important to attend scheduled visits with the doctor, as it may be necessary to adjust the dose as the weight changes. Never adjust the dose of rivaroxaban on your own. Your doctor will adjust the dose if necessary.
Do not divide the tablet to try to obtain a fraction of the tablet dose. If a smaller dose is required, please use an alternative presentation of rivaroxaban available.
In children and adolescents who cannot swallow whole tablets, please use an alternative presentation of rivaroxaban available.
If an alternative presentation of rivaroxaban is not available, you can crush the rivaroxaban tablet and mix it with water or apple puree immediately before taking it. Take some food after taking this mixture. If necessary, your doctor may also administer the crushed rivaroxaban tablet through a gastric tube.
If you spit out the dose or vomit
Call your doctor if you spit out the dose or vomit repeatedly after taking rivaroxaban.
When to start treatment with Rivaroxaban Teva
Take the tablets every day, until your doctor tells you to stop.
Try to take the tablets at the same time every 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 it is necessary to normalize your heartbeat through a procedure called cardioversion, take rivaroxaban at the times indicated by your doctor.
If you forget to take Rivaroxaban Teva
Adults, children, and adolescents:
Adults:
If you take more Rivaroxaban Teva than you should
Call your doctor immediately if you have taken too many rivaroxaban tablets. Taking too much rivaroxaban increases the 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 medicine and the amount taken.
If you stop taking Rivaroxaban Teva
Do not stoptreatment with rivaroxaban without talking to your doctor first, as rivaroxaban treats and prevents serious conditions.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
Like other similar medicines to reduce blood clot formation, rivaroxaban can cause bleeding that can endanger the patient's life. Excessive bleeding can cause a sudden drop in blood pressure (shock). In some cases, the bleeding may not be evident.
Tell your doctor immediately if you experience any of the following symptoms:
Your doctor will decide whether to keep you under closer observation or change your treatment.
The frequency of these adverse effects is very rare (up to 1 in 10,000).
The frequencies of severe allergic reactions are very rare (anaphylactic reactions, including anaphylactic shock; may affect up to 1 in 10,000 people) and uncommon (angioedema and allergic edema; may affect up to 1 in 100 people).
General list of possible adverse effects found in adults, children, and adolescents:
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):
Very Rare(may affect up to 1 in 10,000 people)
Frequency not known(frequency cannot be estimated from available data):
Adverse effects in children and adolescents
In general, the adverse effects observed in children and adolescents treated with rivaroxaban were similar to those observed in adults and their severity was mainly mild to moderate.
Adverse effects that were more frequently observed in children and adolescents:
Very frequent(may affect more than 1 in 10 people)
Frequent(may affect up to 1 in 10 people)
Uncommon(may affect up to 1 in 100 people)
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 to the Spanish Pharmacovigilance System for Human Use Medicines: https://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 the 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.
Crushed tablets
Crushed tablets are stable in water or apple puree for up to 4 hours.
Medicines should not be thrown away through wastewater or household waste. Deposit the packaging and medicines that you no longer need in the SIGRE Point of the pharmacy. Ask your pharmacist how to dispose of the packaging and medicines that you no longer need. This way, you will help protect the environment.
Composition of Rivaroxaban Teva
Core of the tablet:sodium lauryl sulfate, lactose monohydrate, hypromellose, sodium croscarmellose, and magnesium stearate.
Coating of the tablet:partially hydrolyzed polyvinyl alcohol (E1203), macrogol 3350, talc (E553b), and red iron oxide (E 172).
Appearance of the product and package contents
Rivaroxaban Teva 20 mg film-coated tablets are red, round, approximately 8 mm in diameter, engraved with "T" on one side, and with "7R" on the other.
They are available in:
Only some package sizes may be marketed.
Marketing authorization holder and manufacturer
Marketing authorization holder
Teva GmbH
Graf-Arco-Str. 3
Ulm, 89079
Germany
Manufacturer
Balkanpharma - Dupnitsa AD
3, Samokovsko Shosse Str.
BG-2600 DUPNITSA
Bulgaria
or
Actavis Group PTC ehf,
Dalshraun 1, Hafnarfjoerdur,
220, Iceland
Local representative
Teva Pharma, S.L.U.
C/Anabel Segura, 11 Edificio Albatros B, 1ª Planta
Alcobendas, 28108 Madrid (Spain)
Date of the last revision of this prospectus:November 2023
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/
You can access detailed and updated information about this medicine by scanning the QR code included in the packaging with your mobile phone (smartphone). You can also access this information at the following internet address: https://cima.aemps.es/cima/dochtml/p/85820/P_85820.html