Apobilen 5 mg film-coated tablets EFG
apixaban
Apobilen contains the active substance apixaban and belongs to a group of medicines called anticoagulants. This medicine helps prevent the formation of blood clots by blocking Factor Xa, an important element in blood coagulation.
Apobilen is used in adults:
an active or recent stomach or intestinal ulcer, or recent brain hemorrhage);
Tell your doctor, pharmacist, or nurse before starting to take Apobilen if you have any of these conditions:
Be careful with Apobilen
If you need to have surgery or a procedure that may cause bleeding, your doctor will tell you to temporarily stop taking this medicine for a while. If you are not sure if a procedure may cause bleeding, consult your doctor.
This medicine is not recommended for use in children and adolescents under 18 years of age.
Tell your doctor or pharmacist if you are using, have recently used, or might use other medicines.
Some medicines may increase the effects of Apobilen, and some medicines may decrease its effects. Your doctor will decide if you should be treated with Apobilen if you are taking these medicines and if you should be kept under closer observation.
The following medicines may increase the effects of Apobilen and increase the possibility of unwanted bleeding:
The following medicines may reduce Apobilen's ability to prevent blood clots:
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor, pharmacist, or nurse before using this medicine.
The effects of Apobilen on pregnancy and the fetus are unknown. You should not take this medicine if you are pregnant. Tell your doctor immediatelyif you become pregnant while taking this medicine.
It is unknown whether Apobilen is excreted in human milk. Ask your doctor, pharmacist, or nurse before taking this medicine during breastfeeding. They will tell you whether to interrupt breastfeeding or whether to stop or not start taking this medicine.
Apobilen has no influence on the ability to drive or use machines.
If your doctor has told you that you have an intolerance to some sugars, talk to them before taking this medicine.
This medicine contains less than 23 mg of sodium (1 mmol) per tablet, which is essentially "sodium-free".
Follow exactly the instructions for administration of this medicine given by your doctor or pharmacist. In case of doubt, consult your doctor, pharmacist, or nurse.
Take the tablet with water. Apobilen can be taken with or without food.
Try to take the tablets at the same time each day to achieve a better effect of the treatment.
If you have difficulty swallowing the tablet whole, talk to your doctor about other possible ways to take Apobilen. The tablet can be crushed and mixed with water, 5% glucose in water, apple juice, or apple puree, immediately before taking it.
If necessary, your doctor may also administer the crushed Apobilen tablet mixed in 60 ml of water or 5% glucose in water through a nasogastric tube. The tube should be flushed with 10 ml of water immediately after administering the dose of Apobilen.
To prevent the formation of a blood clot in the heart of patients with an irregular heartbeat and at least one additional risk factor.
The recommended dose of Apobilen is one Apobilen 5 mgtablet twice a day.
The recommended dose is one Apobilen 2.5 mgtablet twice a day if:
The recommended dose is one tablet twice a day, for example, take one tablet in the morning and one in the evening.
Your doctor will tell you how long to continue the treatment.
To treat blood clots in the veins of the legs and in the blood vessels of the lungs
The recommended dose is two tabletsof Apobilen 5 mgtwice a day for the first 7 days, for example, two tablets in the morning and two tablets in the evening.
After 7 days, the recommended dose is one tabletof Apobilen 5 mgtwice a day, for example, one tablet in the morning and one tablet in the evening.
To prevent blood clots from recurring after 6 months of treatment
The recommended dose is one Apobilen 2.5 mgtablet twice a day, for example, one tablet in the morning and one tablet in the evening.
Your doctor will tell you how long to continue the treatment.
Your doctor may change your anticoagulant treatment as follows:
Stop taking Apobilen. Start treatment with other anticoagulant medicines (e.g., heparin) at the time you would take the next Apobilen tablet.
Stop taking other anticoagulant medicines. Start treatment with Apobilen at the time you would take the next dose of an anticoagulant medicine, and then continue as usual.
Stop taking the medicine that contains a vitamin K antagonist. Your doctor will need to perform blood tests and tell you when to start taking Apobilen.
If your doctor tells you to start taking a medicine that contains a vitamin K antagonist, continue taking Apobilen for at least 2 days after your first dose of the medicine that contains a vitamin K antagonist. Your doctor will need to perform blood tests and tell you when to stop taking Apobilen.
If your heartbeat needs to be restored through a process called cardioversion, take this medicine at the times your doctor indicates to prevent blood clots in the blood vessels of the brain and other blood vessels in the body.
If you accidentally take more than the prescribed dose, contact your doctor, go to the nearest hospital immediately, or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medicine and the amount received.
Tell your doctor immediatelyif you have taken a dose greater than the prescribed dose of Apobilen. Take the medicine package to your doctor, even if there are no tablets left.
If you take more Apobilen than the recommended dose, you may increase the risk of bleeding. If bleeding occurs, surgery, blood transfusions, or other treatments that can reverse the anti-factor Xa activity may be necessary.
If you have doubts about what to do or if you have forgotten to take more than one dose,ask your doctor, pharmacist, or nurse.
Do not take a double dose to make up for forgotten doses.
Do not stop treatment with this medicine without talking to your doctor first, as the risk of developing a blood clot may be greater if treatment is stopped too soon.
If you have any other questions about the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them. The most common side effect of this medicine is bleeding, which can be life-threatening and requires immediate medical attention.
The following side effects have been reported when taking Apobilen to prevent the formation of blood clots in the heart in patients with an irregular heartbeat and at least one additional risk factor.
The following side effects have been reported when taking Apobilen to treat or prevent blood clots from recurring in the veins of the legs and in the blood vessels of the lungs.
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect that does not appear in this prospectus. You can also report it directly through the Spanish Pharmacovigilance System for Human Use Medicines: www.notificaRAM.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging and on each blister, after CAD. The expiration date is the last day of the indicated month.
This medication does not require special storage conditions.
Medications should not be thrown away through drains or into the trash. Deposit the packaging and medications 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 medications you no longer need. This way, you will help protect the environment.
Composition of Apobilen
See section 2 "Apobilen contains lactose (a type of sugar) and sodium".
Apobilen 5 mg film-coated tablets are pink, oval, film-coated tablets with dimensions of approximately 10.0 mm x 5.2 mm.
Only some package sizes may be marketed.
Inside the Apobilen packaging, along with the prospectus, you will find a Patient Information Card or your doctor may give you a similar card.
This Patient Information Card includes useful information for you and will alert other doctors that you are being treated with Apobilen. You must keep this card with you at all times.
Novalie Pharma S.L.
C/ Bélgica 64,
05004 – Ávila
Spain
Manufacturer:
PharmaPath S.A.
28is Oktovriou 1,
Agia Varvara, 123 51,
Greece
This medication is authorized in the member states of theEconomic European Areawith the following names:
Denmark Apobilen
Spain Apobilen 5 mg film-coated tablets EFG
Portugal Apobilen
Detailed information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/)