Package Leaflet: Information for the User
Tranexamic Acid Baxter 100 mg/ml Solution for Injection and Infusion EFG
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the Package Leaflet
Tranexamic Acid Baxter solution for injection and infusion contains tranexamic acid, which belongs to a group of medicines called antihemorrhagics, antifibrinolytics, amino acids.
This medicine is used in adults and children over one year of age to prevent and treat bleeding due to a process that inhibits blood coagulation called fibrinolysis.
The specific indications include the following:
Do not useTranexamic Acid Baxter:
Due to the risk of cerebral edema and seizures, intrathecal and intraventricular injection and intracerebral application are not recommended.
If you think any of these situations apply to you, or if you have any doubts, talk to your doctor before using this medicine.
Warnings and precautions
Talk to your doctor, pharmacist, or nurse if any of these circumstances apply to you. This will help them decide if this medicine is suitable for you.
UsingTranexamic Acid Baxterwith other medicines
Tell your doctor, nurse, or pharmacist if you are taking, have recently taken, or might take any other medicines.
Specifically, you should inform them if you use:
Pregnancy, breastfeeding, and fertility
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 using this medicine.
Tranexamic acid is excreted in breast milk, therefore, the use of this medicine is not recommended during breastfeeding.
Driving and using machines
No studies have been performed on the ability to drive and use machines.
Tranexamic Acid solution for injection and infusion will be administered to you by slow injection or infusion into a vein.
Your doctor will decide the correct dose for you and for how long you should receive it.
Use in children
If this medicine is given to a child over one year of age, the dose should be based on the child's weight.
Your doctor will decide the correct dose for the child and for how long they should receive it.
Use in elderly patients
No dose reduction is necessary unless there are signs of renal insufficiency.
Use in patients with kidney problems
If you have kidney problems, the dose of tranexamic acid will be reduced according to the results of a blood test (serum creatinine level).
Use in patients with liver failure
No dose reduction is necessary.
Method of administration
This medicine should only be administered slowly into a vein.
This medicine should not be injected into a muscle.
If you use moreTranexamic Acid Baxterthan the recommended dose
If you have received a higher dose of tranexamic acid than recommended, you may experience a temporary drop in blood pressure. Talk to your doctor or pharmacist immediately.
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 medicine and the amount ingested.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The side effects reported withtranexamic acidare as follows:
The following side effects have been reported with tranexamic acid
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, pharmacist, or nurse, even if they are not listed in this leaflet. You can also report side effects directly through the Spanish Medicines Agency's website: 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 vial after EXP. The expiry date is the last day of the month shown.
Do not freeze.
After first opening: the solution for injection and infusion is for single use only. The unused solution should be discarded.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Chemical and physical stability have been demonstrated for 24 hours at 25°C.
From a microbiological point of view, the product should be used immediately. If not used immediately, the in-use storage times and conditions are the responsibility of the user and would normally not be longer than 24 hours at 2-8°C, unless the dilution has been made in controlled and validated aseptic conditions.
Composition ofTranexamic Acid Baxter
The active substance is tranexamic acid.
Each ml contains 100 mg of tranexamic acid.
Each 5 ml vial contains 500 mg of tranexamic acid.
Each 10 ml vial contains 1000 mg of tranexamic acid.
The other ingredient is water for injections.
Appearance and packaging
Tranexamic Acid Baxter is a solution for injection and infusion.
Clear, colorless, and essentially free from visible particles.
6 ml glass type I vial filled with 5 ml, in blister and cardboard box.
10 ml glass type I vial filled with 10 ml, in blister and cardboard box.
Pack sizes
5 vials of 5 ml,
10 vials of 5 ml,
5 vials of 10 ml,
10 vials of 10 ml.
Not all pack sizes may be marketed.
Marketing authorization holder
Baxter Holding B.V.
Kobaltweg 49,
3542CE Utrecht, Netherlands
Manufacturer
Bieffe Medital S.p.A.,
Via Nuova Provinciale, 23034 Grossotto (SO) Italy.
You can obtain further information on this medicine from the local representative of the marketing authorization holder:
Baxter S.L.
Pouet de Camilo, 2. 46394 Ribarroja del Turia (Valencia)
Spain
This medicine is authorized in the Member States of the European Economic Area under the following names:
Austria Tranexamic acid Baxter 100 mg/ml Solution for injection/infusion
Belgium Tranexamic acid Baxter 100 mg/ml solution for injection/infusion
Denmark Tranexamic acid Baxter 100 mg/ml injection/infusion solution
Estonia Tranexamic acid Baxter
Finland Tranexamic acid Baxter 100 mg/ml solution for injection/infusion
Greece Tranexamic acid Baxter 100 mg/ml solution for injection/infusion
Germany Tranexamic acid Baxter 100 mg/ml Solution for injection/infusion
Hungary Tranexamic acid Baxter 100 mg/ml oldatos injekció
Ireland Tranexamic acid 100 mg/ml solution for injection/infusion
Italy Acido Tranexamico Baxter 100 mg/ml soluzione iniettabile/infusione
Latvia Tranexamic acid Baxter 100 mg/ml šķīstums injekcijām/infūzijām
Lithuania Tranexamic acid Baxter 100mg/ml injekcinis tirpalas
Netherlands Tranexaminezuur Baxter 100 mg/ml, oplossing voor injectie/infusie
Norway Tranexamic acid Baxter
Poland Tranexamic acid Baxter
Portugal Ácido Tranexâmico Baxter
Slovakia Tranexamic acid Baxter 100 mg/ml injekčný roztok
Spain Ácido tranexámico Baxter 100 mg/ml solución inyectable y para perfusión EFG
Sweden Tranexamic acid Baxter 100 mg/ml solution for injection/infusion
United Kingdom Tranexamic acid 100 mg/ml solution for injection/infusion
Date of last revision of this leaflet:April 2020
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/