Edoxaban Teva 15 mg film-coated tablets EFG
Edoxaban Teva 30 mg film-coated tablets EFG
Edoxaban Teva 60 mg film-coated tablets EFG
Read the entire package leaflet carefully before you start taking this medicine, as it contains important information for you.
Edoxaban Teva contains the active substance edoxaban and belongs to a group of medicines called anticoagulants. This medicine helps to prevent the formation of blood clots. It works by blocking the activity of Factor Xa, an important component of blood clotting.
Edoxaban Teva is used in adults:
Do not take Edoxaban Teva
Talk to your doctor or pharmacist before starting to take edoxaban,
Edoxaban 15 mg is only indicated when switching from edoxaban 30 mg to a vitamin K antagonist (e.g. warfarin) (see section 3. How to take Edoxaban Teva).
Be careful with edoxaban,
If you need to have surgery,
In emergency situations, your doctor will help determine the necessary actions regarding edoxaban.
Edoxaban Teva is not recommended in children and adolescents under 18 years of age.
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
If you are taking any of the following:
If any of the above applies to you, tell your doctorbefore taking edoxaban, as these medicines may increase the effects of edoxaban and the risk of unwanted bleeding. Your doctor will decide whether you should be treated with this medicine and whether you should be kept under observation.
If you are taking any of the following:
If any of the above applies to you, tell your doctorbefore taking edoxaban, as the effect of this medicine may be reduced. Your doctor will decide whether you should be treated with edoxaban and whether you should be kept under observation.
Do not take edoxaban if you are pregnant or breastfeeding. If there is a possibility that you may become pregnant, use an effective contraceptive while taking edoxaban. If you become pregnant while taking this medicine, inform your doctor immediately, who will decide how you should be treated.
Edoxaban has no or negligible influence on the ability to drive and use machines.
If your doctor has told you that you have an intolerance to some sugars, consult with them before taking this medicine.
This medicine contains less than 1 mmol of sodium (23 mg) per dose, i.e. it is essentially "sodium-free".
Follow the instructions for administration of this medicine exactly as told by your doctor or pharmacist. If you are unsure, consult your doctor or pharmacist again.
The recommended dose is one 60 mgtablet once a day.
Swallow the tablet, preferably with water.
Edoxaban Teva can be taken with or without food.
If you have difficulty swallowing the tablet whole, talk to your doctor about other ways to take edoxaban. The tablet can be crushed and mixed with water or apple sauce immediately before taking it. If necessary, your doctor may also administer the crushed edoxaban tablet through a tube in the nose (nasogastric tube) or through the stomach (gastric feeding tube).
Switching from vitamin K antagonists (e.g. warfarin) to edoxaban
Stop taking the vitamin K antagonist (e.g. warfarin). Your doctor will have to do a blood test and will tell you when to start taking edoxaban.
Switching from non-vitamin K antagonist oral anticoagulants (dabigatran, rivaroxaban or apixaban) to edoxaban
Stop taking the previous medicines (e.g. dabigatran, rivaroxaban or apixaban) and start taking edoxaban at the time of the next scheduled dose of the anticoagulant.
Switching from parenteral anticoagulants (e.g. heparin) to edoxaban
Stop taking the anticoagulant (e.g. heparin) and start taking edoxaban at the time of the next scheduled dose of the anticoagulant.
Switching from edoxaban to vitamin K antagonists (e.g. warfarin)
If you are currently taking 60 mg of edoxaban:
Your doctor will tell you to reduce the dose of edoxaban to one 30 mg tablet once a day and take it together with a vitamin K antagonist (e.g. warfarin). Your doctor will have to do a blood test and will tell you when to stop taking edoxaban.
If you are currently taking 30 mg (reduced dose) of edoxaban:
Your doctor will tell you to reduce the dose of edoxaban to one 15 mg tablet once a day and take it together with a vitamin K antagonist (e.g. warfarin). Your doctor will have to do a blood test and will tell you when to stop taking edoxaban.
Switching from edoxaban to non-vitamin K antagonist oral anticoagulants (dabigatran, rivaroxaban or apixaban)
Stop taking edoxaban and start the non-vitamin K antagonist anticoagulant (e.g. dabigatran, rivaroxaban or apixaban) at the time of the next scheduled dose of edoxaban.
Switching from edoxaban to parenteral anticoagulants (e.g. heparin)
Stop taking edoxaban and start the parenteral anticoagulant (e.g. heparin) at the time of the next scheduled dose of edoxaban.
If you need to have your irregular heartbeat restored to normal through a procedure called cardioversion, take edoxaban at the times indicated by your doctor to prevent the formation of blood clots in the brain and in other blood vessels of your body.
Tell your doctor immediately if you have taken too many edoxaban tablets. If you take more edoxaban than recommended, you may increase the risk of bleeding.
In case of overdose or accidental ingestion, consult your doctor or call the Toxicology Information Service, telephone 91 562 04 20, indicating the medicine and the amount taken.
You should take the tablet immediately and continue the next day with the usual once-daily tablet intake. Do not take a double dose on the same day to make up for the missed dose.
Do not stop taking Edoxaban Teva without first talking to your doctor, as edoxaban treats and prevents serious diseases.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Like other similar medicines (medicines to reduce blood clotting), edoxaban can cause bleeding, which can be life-threatening. In some cases, the bleeding may not be obvious.
If you experience a bleeding episode that does not stop by itself or if you experience signs of excessive bleeding (exceptional weakness, tiredness, paleness, dizziness, headache or unexplained swelling), consult your doctor immediately.
Your doctor will decide whether to keep you under closer observation or change your treatment.
Common(may affect up to 1 in 10 people)
Uncommon(may affect up to 1 in 100 people)
Rare(may affect up to 1 in 1,000 people)
Frequency Not Known(cannot be estimated from the available data)
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this package leaflet. You can also report side effects directly via the Spanish Medicines Monitoring System for Human Use: https://www.notificaram.es. By reporting side effects, you can help provide 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 expiry date which is stated on the packaging, blister or bottle after "EXP". The expiry date is the last day of the month stated.
This medicine does not require any special storage conditions.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to your pharmacist. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Edoxaban Teva 15 mg film-coated tablets EFG
Each tablet contains edoxaban tosilate monohydrate equivalent to 15 mg of edoxaban.
Edoxaban Teva 30 mg film-coated tablets EFG
Each tablet contains edoxaban tosilate monohydrate equivalent to 30 mg of edoxaban.
Edoxaban Teva 60 mg film-coated tablets EFG
Each tablet contains edoxaban tosilate monohydrate equivalent to 60 mg of edoxaban.
Edoxaban Teva 15 mg film-coated tablets EFG
Tablet core: Lactose monohydrate, croscarmellose sodium, hydroxypropylcellulose, purified water, magnesium stearate.
Coating: Hypromellose (E464), calcium carbonate (E170), macrogol (E1521), talc (E553b), yellow iron oxide (E172) and red iron oxide (E172).
Edoxaban Teva 30 mg film-coated tablets EFG
Tablet core: Lactose monohydrate, croscarmellose sodium, hydroxypropylcellulose, purified water, magnesium stearate.
Coating: Hypromellose (E464), calcium carbonate (E170), macrogol (E1521), talc (E553b) and red iron oxide (E172).
Edoxaban Teva 60 mg film-coated tablets EFG
Tablet core: Lactose monohydrate, croscarmellose sodium, hydroxypropylcellulose, purified water, magnesium stearate.
Coating: Hypromellose (E464), calcium carbonate (E170), macrogol (E1521), talc (E553b) and yellow iron oxide (E172).
Edoxaban Teva 15 mg film-coated tablets EFG are light orange in color, round in shape (approximately 6.4 mm in diameter) and bear the letters "TV" on one side and "15" on the other.
Edoxaban Teva 30 mg film-coated tablets EFG are pink in color, round in shape (approximately 8.5 mm in diameter) and bear the letters "TV" in relief on one side and "30" on the other.
Edoxaban Teva 60 mg film-coated tablets EFG are yellow in color, round in shape (approximately 10.5 mm in diameter) and bear the letters “TV” on one side and “60” on the other.
Edoxaban Teva is available in the following pack sizes:
Edoxaban Teva 15 mg film-coated tablets EFG are available in blisters of 10 film-coated tablets, in precut unit-dose blisters of 10 x 1 film-coated tablets or in bottles of 100 film-coated tablets.
Edoxaban Teva 30 mg film-coated tablets EFG are available in blisters of 10, 28, 30, 100 and 105 film-coated tablets, in precut unit-dose blisters of 10 x 1, 28 x 1, 30 x 1, 98 x 1 film-coated tablets or in bottles of 100 and 120 film-coated tablets.
Edoxaban Teva 60 mg film-coated tablets EFG are available in blisters of 10, 28, 30, 100 and 105 film-coated tablets, in precut unit-dose blisters of 10 x 1, 28 x 1, 30 x 1, 98 x 1 film-coated tablets or in bottles of 100 and 120 film-coated tablets.
Only some pack sizes may be marketed.
Marketing Authorization Holder
TEVA GmbH
Graf-Arco-Str.
389079 Ulm,
Germany
Manufacturer
Actavis Ltd.,
BLB015-016,
Bulebel Industrial estate,
Zejtun ZTN3000
Malta
or
TEVA Pharmaceuticals Ltd.
Pallagi út 13, Debrecen
4042 Hungary
For further information about this medicinal product, please contact the local representative of the marketing authorization holder:
Teva Pharma, S.L.U.
C/ Anabel Segura, 11, Edificio Albatros B, 1ª planta
28108, Alcobendas, Madrid (Spain)
Date of last revision of this leaflet: January 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/
You can access detailed and up-to-date information about this medicinal product 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/XXXXX.html
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