
Ask a doctor about a prescription for APIXABAN KERN PHARMA 5 mg FILM-COATED TABLETS
Package Leaflet: Information for the Patient
Apixaban Kern Pharma 5 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
This medication contains the active substance apixaban and belongs to a group of medications called anticoagulants. This medication helps prevent the formation of blood clots by blocking Factor Xa, an important element in blood coagulation.
Apixaban is used in adults:
Do not take Apixaban Kern Pharma if:
Warnings and precautions
Tell your doctor, pharmacist, or nurse before taking this medication if you have any of the following conditions:
Be careful with apixaban
If you need to undergo surgery or a procedure that may cause bleeding, your doctor will tell you to temporarily stop taking this medication for a while. If you are unsure whether a procedure may cause bleeding, consult your doctor.
Children and adolescents
This medication is not recommended for use in children and adolescents under 18 years of age.
Other medications and Apixaban Kern Pharma
Tell your doctor, pharmacist, or nurse if you are taking, have recently taken, or may need to take other medications.
Some medications may increase the effects of apixaban, and other medications may decrease its effects. Your doctor will decide if you should be treated with apixaban if you are taking these medications and if you should be monitored more closely.
The following medications may increase the effects of apixaban and increase the risk of unwanted bleeding:
The following medications may reduce the ability of apixaban to prevent blood clots.
Pregnancy and breastfeeding
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 medication.
Pregnancy
The effects of apixaban on pregnancy and the fetus are unknown. You should not take this medication if you are pregnant. Inform your doctor, pharmacist, or nurse immediatelyif you become pregnant while taking this medication.
Breastfeeding
It is unknown whether apixaban is excreted in human milk. Ask your doctor or pharmacist before taking this medication during breastfeeding. They will tell you whether to interrupt breastfeeding or whether to stop or not start taking this medication.
Driving and using machines
This medication has no influence on the ability to drive or use machines.
Apixaban Kern Pharma contains lactose and sodium
This medication contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
This medication contains less than 1 mmol of sodium (23 mg) per tablet, which is essentially "sodium-free".
Follow the instructions for administration of this medication exactly as indicated by your doctor or pharmacist. If you are unsure, consult your doctor, pharmacist, or nurse again.
Dosage
Take the tablet with water. This medication can be taken with or without food.
Try to take the tablets at the same time each day to achieve a better treatment effect.
If you have difficulty swallowing the tablet whole, talk to your doctor about other possible ways to take this medication. The tablet can be crushed and mixed with water, 5% glucose in water, apple juice, or apple puree, immediately before taking it.
Instructions for crushing:
If necessary, your doctor may also administer the crushed apixaban tablet mixed in 60 ml of water or 5% glucose in water through a nasogastric tube.
Take Apixaban Kern Pharma according to the following recommendations:
To prevent the formation of a blood clot in the heart in patients with an irregular heartbeat and at least one additional risk factor.
The recommended dose is one apixaban 5mgtablet twice a day.
The recommended dose is one apixaban 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 you should 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 twoapixaban 5mgtablets twice 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 oneapixaban 5mgtablet twice a day, for example, one tablet in the morning and one in the evening.
To prevent blood clots from recurring after 6 months of treatment
The recommended dose is one apixaban 2.5mgtablet twice a day, for example, one tablet in the morning and one in the evening.
Your doctor will tell you how long you should continue the treatment.
Your doctor may change your anticoagulant treatment as follows:
Stop taking this medication. Start treatment with other anticoagulant medications (e.g., heparin) at the time you would take the next apixaban tablet.
Stop taking other anticoagulant medications. Start treatment with apixaban at the time you would take the next dose of the other anticoagulant medication, and then continue as usual.
Stop taking the medication containing a vitamin K antagonist. Your doctor will need to perform blood tests and tell you when to start taking apixaban.
If your doctor tells you to start taking a medication containing a vitamin K antagonist, continue taking apixaban for at least 2 days after your first dose of the medication containing a vitamin K antagonist. Your doctor will need to perform blood tests and tell you when to stop taking apixaban.
Patients undergoing cardioversion
If your heartbeat needs to be restored through a process called cardioversion, take this medication 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 take more apixaban than you should
Tell your doctor immediatelyif you have taken a dose larger than the prescribed dose of this medication. Bring the medication package to your doctor, even if there are no tablets left.
If you take more apixaban than the recommended dose, you may increase the risk of bleeding. If bleeding occurs, surgery, blood transfusions, or other treatments may be necessary to reverse the anti-factor Xa activity.
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 medication and the amount taken.
If you forget to take Apixaban Kern Pharma
If you are unsure what to do or if you forget to take more than one dose,ask your doctor, pharmacist, or nurse.
If you interrupt treatment with Apixaban Kern Pharma
Do not interrupt treatment with this medication without first talking to your doctor, as the risk of developing a blood clot may be higher if treatment is interrupted too soon.
If you have any other questions about the use of this medication, ask your doctor, pharmacist, or nurse.
Like all medications, apixaban can produce adverse effects, although not all people suffer from them. The most frequent adverse effect of this medication is bleeding, which can put the patient's life at risk and requires immediate medical attention.
The following adverse effects have been reported when taking apixaban to prevent the formation of blood clots in the heart in patients with irregular heartbeats and at least one additional risk factor.
Frequent Adverse Effects (may affect up to 1 in 10people)
Infrequent Adverse Effects (may affect up to 1 in 100people)
Rare Adverse Effects (may affect up to 1 in 1,000people)
Very Rare Adverse Effects (may affect up to 1 in 10,000people)
Unknown Frequency (cannot be estimated from available data)
The following adverse effects have been reported when taking apixaban to treat or prevent blood clots from recurring in the veins of the legs and blood vessels of the lungs.
Frequent Adverse Effects (may affect up to 1 in 10people)
Infrequent Adverse Effects (may affect up to 1 in 100people)
Rare Adverse Effects (may affect up to 1 in 1,000people)
Unknown Frequency (cannot be estimated from available data)
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect that is not listed in this leaflet. You can also report them 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 shown on the blister pack and carton after CAD. The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE collection point in your pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Composition ofApixaban Kern Pharma
The active ingredientis apixaban.
Apixaban Kern Pharma 5 mg: each tablet contains 5 mg of apixaban.
The other ingredientsare:
Appearance of the Product and Package Contents
The film-coated tablets are oval (10 mm x 5 mm approximately), pink, and contain 5 mg of the active ingredient apixaban.
Patient Information Card: Information Management
Inside the packaging of this medication, along with the leaflet, 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 apixaban. You should keep this card with you at all times.
Marketing Authorization Holder
Kern Pharma, S.L.
Venus, 72 - Pol. Ind. Colón II
08228 Terrassa - Barcelona
Spain
Manufacturer
Pharmadox Healthcare Ltd.
KW20A Kordin Industrial Park,
Paola PLA 3000,
Malta
or
Adalvo Limited
Malta Life Sciences Park,
Building 1, Level 4, Sir Temi Zammit Buildings,
San Gwann, SGN 3000
Malta
Date of the Last Revision of this Leaflet: April 2025
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.
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