Package Leaflet:information for the patient
Ticagrelor Combix 90 mg film-coated tablets EFG
Read all of this leaflet carefullybefore you start taking thismedicine,because it contains important informationfor you.
Contents of the pack
5 Storage of Ticagrelor Combix
What is Ticagrelor Combix
This medicine contains the active substance ticagrelor. It belongs to a group of medicines called antiplatelet agents.
What Ticagrelor Combix is used for
Ticagrelor in combination with acetylsalicylic acid (another antiplatelet agent) should only be used in adults. You have been prescribed this medicine because you have had:
This medicine reduces the risk of you having another heart attack, a stroke, or dying from a heart or blood vessel-related disease.
How Ticagrelor Combix works
Ticagrelor works on cells called ‘platelets’ (also called thrombocytes). These very small blood cells help stop bleeding by clumping together to block tiny holes in blood vessels that are cut or damaged.
However, platelets can also form clots inside damaged blood vessels in the heart and brain. This can be very dangerous because:
Ticagrelor helps prevent platelets from clumping together. This reduces the chance of a blood clot forming that could reduce blood flow.
Do not take Ticagrelor Combix
Do not take ticagrelor if you are in any of the above situations. If you are unsure, consult your doctor or pharmacist before taking this medicine.
Warnings and precautions
Consult your doctor or pharmacist before starting this medicine:
If any of the above applies to you (or if you are unsure), consult your doctor or pharmacist before taking this medicine.
If you are taking ticagrelor and heparin:
Children and adolescents
Ticagrelor is not recommended for children and adolescents under 18 years of age.
Other medicines and Ticagrelor Combix
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines. This is because this medicine may affect the way some medicines work and some medicines may affect this medicine.
Tell your doctor or pharmacist if you are taking any of the following medicines:
In particular, tell your doctor or pharmacist if you are taking any of the following medicines that increase the risk of bleeding:
Tell your doctor if, because you are taking ticagrelor, you may have a higher risk of bleeding if your doctor gives you fibrinolytics, often referred to as ‘clot dissolvers’, such as streptokinase or alteplase.
Pregnancy andbreast-feeding
This medicine should not be used if you are pregnant or may become pregnant. Women must use appropriate contraceptive methods to prevent pregnancy while taking this medicine.
Consult your doctor before taking this medicine if you are breast-feeding. Your doctor will explain the benefits and risks of taking this medicine during this period.
If you are pregnant or breast-feeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before taking this medicine.
Driving and using machines
This medicine is unlikely to affect your ability to drive or use machines. If you feel dizzy or confused while taking this medicine, be careful while driving or using machines.
Ticagrelor Combix contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially “sodium-free”.
Follow the instructions for administration of this medicine exactly as told by your doctor. If you are unsure, consult your doctor or pharmacist again.
How much to take
Taking Ticagrelor Combix with other medicines for blood clotting
Your doctor will also usually prescribe acetylsalicylic acid for you. This is a substance found in many medicines used to prevent blood clotting. Your doctor will tell you how much to take (usually between 75-150 mg daily).
How to take Ticagrelor Combix
You can take this medicine with or without food.
If you have difficulty swallowing the tablet
If you have difficulty swallowing the tablet, you can crush it and mix it with water as follows:
If you are in the hospital, this tablet may be given to you mixed with a little water through a tube in your nose (nasogastric tube).
If you take more Ticagrelor Combix than you should
If you take more ticagrelor than you should, consult your doctor or go to the hospital immediately. Bring the medicine pack with you. You may have a higher risk of bleeding.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, telephone: 91 562 04 20, indicating the medicine and the amount taken.
If you forget to take Ticagrelor Combix
If you stop taking Ticagrelor Combix
Do not stop taking this medicine without consulting your doctor. Take this medicine regularly and for as long as your doctor tells you. If you stop taking this medicine, you may increase the risk of having another heart attack or stroke or dying from a heart or blood vessel-related disease.
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. The following side effects may occur with this medicine:
Ticagrelor affects blood clotting, so most side effects are related to bleeding. Bleeding can occur anywhere in the body. Some level of bleeding is common (such as bruising and nosebleeds). Severe bleeding is rare but can be life-threatening.
Tell your doctor immediately if you notice any of the following - you may need urgent medical treatment:
Tell your doctor if you notice any of the following:
Other possible side effects
Frequency not known (cannot be estimated from the available data)
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this 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 carton and blister after “EXP”. The expiry date refers to the last day of the month shown.
PVC/PVDC-Aluminum blisters: store below 30°C. Store in the original package to protect from light.
PVC/PE/PVDC-Aluminum blisters: this medicine does not require any special storage temperature. Store in the original package to protect from light.
Medicines should not be disposed of via wastewater or household waste. Return any unused medicine to a pharmacy for disposal. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Ticagrelor Combix Composition
Tablet core:hypromellose, mannitol (E421), microcrystalline cellulose, sodium carboxymethyl starch (type A), and magnesium stearate.
Tablet coating:hypromellose, titanium dioxide (E171), macrogol, talc, and yellow iron oxide (E172).
Product Appearance and Packaging Content
Round, biconvex, yellow tablets, with an approximate diameter of 9.1 mm, film-coated, marked with a "90" on one side and smooth on the other.
Ticagrelor Combix 90 mg is available in PVC/PVDC-Aluminum or PVC/PE/PVDC-Aluminum blisters in packs of 56 tablets.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Laboratorios Combix, S.L.U.
C/ Badajoz 2, Edificio 2
28223 Pozuelo de Alarcón (Madrid)
Spain
Manufacturer
Genepharm S.A.
18th km, Marathonos Avenue,
Pallini Attikis, 15351
Greece
Date of the Last Revision of thisProspectus: July 2024
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/