Package Leaflet:information for the user
Tikata90 mg film-coated tablets EFG
ticagrelor
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
5 Storage of Tikata
What isTikata
Tikata contains the active substance ticagrelor. It belongs to a group of medicines called antiplatelet agents.
What Tikata is used for
This medicine, in combination with acetylsalicylic acid (another antiplatelet agent), is to be used only 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 Tikata works
This medicine works on cells called 'platelets' (also called thrombocytes). These very small 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:
Tikata helps prevent platelets from clumping together. This reduces the chance of a blood clot forming that could block blood flow.
Do not take Tikataif:
Do not take this medicine 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 Tikata if:
Your doctor may want to stop your 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 Tikata and heparin:
Children and adolescents
This medicine is not recommended for children and adolescents under 18 years of age.
Other medicines and Tikata
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines. This is because Tikata may affect how some medicines work and some medicines may affect Tikata.
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:
clarithromycin (used to treat bacterial infections), nefazodone (an antidepressant), ritonavir and atazanavir (used to treat HIV and AIDS), cisapride (used to treat stomach acidity), and ergot alkaloids (used to treat migraines and headaches).
Tell your doctor that, because you are taking Tikata, 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 should 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 Tikata 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.
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 Tikata with other medicines for blood clotting
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 Tikata
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 Tikata than you should
If you take more of this medicine than you should, consult your 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 Tikata
If you stop taking Tikata
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:
Tikata 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
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, even if they are not listed in this leaflet. You can also report side effects directly via the Spanish Medicines Monitoring System for Human Use: 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 blister and carton 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. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Tikata Composition
The active ingredient is ticagrelor. Each film-coated tablet contains 90 mg of ticagrelor.
The other components are:
Tablet core:mannitol (E421), calcium hydrogen phosphate dihydrate, crospovidone (type A), hypromellose, magnesium stearate (E470b)
Tablet film coating:hypromellose (E464), titanium dioxide (E171), talc, macrogol 400, yellow iron oxide (E172).
Appearance ofTikataand Package Contents
Film-coated tablet (tablet): The tablets are round, biconvex, yellow, film-coated with a diameter of approximately 9.1 mm.
This medication is available in:
Not all pack sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Adamed Laboratorios, S.L.U.
c/ de las Rosas de Aravaca, 31 - 2ª planta
28023 Madrid
Spain
Manufacturer
ELPEN Pharmaceutical Co., Inc,
Marathonos Ave. 95, Pikermi Attiki,
19009, Greece
This medication is authorized in the Member States of the European Economic Areaand in the United Kingdom (Northern Ireland)with the following names:
Spain Tikata 60 mg film-coated tablets EFG
Tikata 90 mg film-coated tablets EFG
Italy Tikata
Date of the last revision of thisleaflet: January 2024
Detailed information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/)