Ticagrelor Alter 90 mg film-coated tablets EFG
What is ticagrelor
Ticagrelor contains the active substance ticagrelor. It belongs to a group of medicines called antiplatelet agents.
What is ticagrelor 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 illness.
How ticagrelor works
Ticagrelor works on cells called platelets (also known as thrombocytes). These tiny blood cells help stop bleeding by clumping together to block small 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 block blood flow.
Do not take ticagrelor if:
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 taking ticagrelor if:
Your doctor may want to stop treatment with this medicine 5 days before surgery.
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
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines. This is because ticagrelor may affect how some medicines work and some medicines may affect ticagrelor.
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:
Also, inform your doctor that because you are taking ticagrelor, you may have a higher risk of bleeding if your doctor administers fibrinolytics, often referred to as ‘clot dissolvers’, such as streptokinase or alteplase.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Ticagrelor should not be used if you are pregnant or may become pregnant. Women should use appropriate contraceptive methods to prevent pregnancy while taking this medicine.
Consult your doctor before taking this medicine if you are breastfeeding. Your doctor will explain the benefits and risks of taking ticagrelor during this period.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Driving and using machines
Ticagrelor 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.
Always take this medicine exactly as your doctor has told you. If you are unsure, consult your doctor or pharmacist.
How much to take
Taking ticagrelor with other blood clotting medicines
Your doctor will also usually prescribe acetylsalicylic acid. 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
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 than you should
If you take more ticagrelor than you should, talk to a doctor or go to the hospital immediately. Take 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 Toxicological Information Service, telephone 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to take ticagrelor
If you stop taking ticagrelor
Do not stop taking ticagrelor without consulting your doctor. Take this medicine regularly and for as long as your doctor tells you. If you stop taking ticagrelor, you may increase the risk of having another heart attack or stroke, or dying from a heart or blood vessel-related illness.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them. With this medicine, the following side effects may occur:
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:
Signs of a blood clotting problem called Thrombotic Thrombocytopenic Purpura (TTP) such as:
Tell your doctor if you notice any of the following:
Other possible side effects
Very common(may affect more than 1 in 10 people)
Common(may affect up to 1 in 10 people)
Uncommon(may affect up to 1 in 100 people)
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 outer packaging and on the blister after “EXP”. The expiry date is the last day of the month shown.
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 a pharmacy for disposal. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Ticagrelor Alter Composition
The active ingredient is ticagrelor.
Each film-coated tablet contains 90 mg of ticagrelor.
The other components are:
Tablet core: mannitol (E-421), calcium hydrogen phosphate dihydrate, crospovidone (Type A), hypromellose, and magnesium stearate.
Coating: hypromellose, titanium dioxide, macrogol 400, yellow iron oxide (E-172), and talc.
Product Appearance and Packaging Content
Round, biconvex tablets, yellow in color, with an approximate diameter of 9.1 mm.
Available in PVC/PVDC-Al or OPA/Al/PVC-Al blister packs. Packs containing 56 tablets.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Laboratorios Alter, S.A.
C/ Mateo Inurria 30
28036 Madrid
Spain
Manufacturer
ELPEN Pharmaceutical Co., Inc.
Marathonos Ave. 95,
Pikermi Attiki,
19009
Greece
Date of Last Revision of this Leaflet: April 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/