How to use AMCHAFIBRIN 500 mg FILM-COATED TABLETS
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This page provides general information and does not replace a doctor’s consultation. Always consult a doctor before taking any medication. Seek urgent medical care if symptoms are severe.
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Introduction
Package Leaflet: Information for the User
Amchafibrin 500 mg Film-Coated Tablets
tranexamic acid
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
- Keep this package leaflet, as you may need to read it again. If you have any questions, consult your doctor or pharmacist.
- This medication has been prescribed to you only, and you should not give it to others, even if they have the same symptoms as you, as it may harm them.
- If you experience side effects, consult your doctor or pharmacist, even if they are side effects not listed in this package leaflet. See section 4.
Contents of the Package Leaflet
- What Amchafibrin is and what it is used for
- What you need to know before taking Amchafibrin
- How to take Amchafibrin
- Possible side effects
5 Conservation of Amchafibrin
- Contents of the pack and further information
1. What Amchafibrin is and what it is used for
Amchafibrin contains the active ingredient tranexamic acid, which belongs to a group of medications called antifibrinolytics.
This medication is indicated for the treatment and prevention of excessive bleeding associated with abnormal bleeding, such as:
- any type of prostate or bladder surgery,
- abnormally heavy and prolonged menstrual bleeding,
- patients with a tendency to bleed abnormally (hemophiliacs) who undergo dental surgery (extractions),
- localized swelling that affects the mouth and upper respiratory tract (hereditary angioedema).
2. What you need to know before taking Amchafibrin
Do not take Amchafibrin:
- If you are allergic to the active ingredient or any of the other components of this medication (listed in section 6).
- If you have a tendency to form blood clots (thrombi).
- If you are at risk of excessive bleeding due to a coagulation disorder called consumption coagulopathy.
- If you have severe kidney problems (severe renal insufficiency).
- If you have a history of seizures.
In case of doubt, consult your doctor or pharmacist.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Amchafibrin:
- If you have impaired renal function.
- If you have hematuria (blood in the urine) of renal origin, as a clot may form in the urethra that prevents urine from coming out.
- If you are taking oral contraceptives, due to the increased risk of thrombosis.
Other medications and Amchafibrin
Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication.
It is important to inform your doctor if you are taking any of the following medications:
- Fibrinolytic medications (used to help break down blood clots). This is because tranexamic acid would cancel the effect of these medications.
- Oral contraceptives.
In case of doubt, consult your doctor or pharmacist.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Tranexamic acid is excreted in breast milk, although in minimal amounts. If you are breastfeeding, consult your doctor or pharmacist before taking this medication.
Children
The primary use of tranexamic acid in children is for dental extraction. Use with caution. The dose of this medication in children and adolescents should be calculated based on body weight.
Driving and using machines
No studies have been conducted on the effects on the ability to drive and use machines. In case of dizziness or drowsiness, it is not recommended to drive vehicles or operate machinery.
3. How to take Amchafibrin
Follow the administration instructions for this medication exactly as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Adults:
Usual dose
Take 2 to 3 tablets, 2-3 times a day.
The exact dose for you depends on the reason why this medication has been prescribed to you. Follow your doctor's instructions regarding how many tablets to take, when to take them, and the duration of treatment.
Dose in certain specific cases:
- Total or partial prostate removal (prostatectomy): during the first 3 days after surgery, take 2 tablets, 3 to 4 times a day, until there is no blood in the urine.
- Abnormally heavy and prolonged menstrual bleeding (metrorrhagia): take 2 tablets, 3 times a day, for 3 or 4 days. Do not exceed a total dose of 4 g per day (8 tablets). Treatment with Amchafibrin should not be started until menstrual bleeding has begun.
Use in advanced age
No dose reduction is necessary unless there is renal insufficiency.
Renal insufficiency
This medication may accumulate in patients with renal insufficiency, so the dose should be reduced in these cases.
Use in children and adolescents
Your doctor will indicate the exact dose to be given to the child. Your doctor will calculate the dose based on the child's weight.
In case of doubt, ask your doctor or pharmacist.
If you take more Amchafibrin than you should
If you take more Amchafibrin than you should, you may experience nausea, vomiting, orthostatic symptoms, and/or hypotension. In this case, vomiting should be induced, gastric lavage should be performed, and treatment with activated charcoal should be started. Maintain high fluid intake to favor renal elimination.
In case of overdose, consult your doctor or pharmacist immediately, or call the Toxicology Information Service. Tel. 91 562 04 20. Bring this package leaflet with you.
If you forget to take Amchafibrin
Do not take a double dose to make up for forgotten doses, but continue taking this medication as usual.
If you interrupt treatment with Amchafibrin
Do not interrupt treatment with this medication without consulting your doctor.
If you have any further questions about the use of this medication, ask your doctor or pharmacist.
4. Possible side effects
Like all medications, this medication can cause side effects, although not everyone experiences them.
Immediately inform your doctor of any of the following situations:
- If you experience a rash or allergic reaction such as itching, swelling of the lips/tongue, or wheezing/difficulty breathing. In such cases, stop taking the tablets immediately and inform your doctor as soon as possible.
- If you experience blood clots in the veins (a rare side effect that may affect up to 1 in 1,000 people), especially in the legs (symptoms are swelling, pain, and redness in the legs), which can move through the blood vessels to the lungs and cause chest pain and difficulty breathing. If you experience any of these symptoms, seek medical attention immediately.
Rare (affect 1 to 10 patients in every 1,000)
- Visual disturbances, especially in color vision.
- Formation of a blood clot in an eye. This can cause bleeding in the eye or vision loss.
- Itching, redness, or swelling of the skin.
Very rare (affect less than 1 patient in every 10,000)
- Formation of a blood clot in the blood vessels (i.e., thrombosis).
- Allergic reactions that can cause difficulty breathing or dizziness.
- Nausea.
- Vomiting.
- Diarrhea.
- Seizures or convulsions.
- General feeling of discomfort (malaise) and low blood pressure (hypotension), with or without loss of consciousness.
Nausea, vomiting, and diarrhea are usually mild and disappear quickly; however, if they persist, inform your doctor or pharmacist.
Reporting side effects
If you experience any side effects, consult your doctor or pharmacist, even if they are possible side effects not listed in this package leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
5. Conservation of Amchafibrin
Keep this medication out of the sight and reach of children.
Do not store above 30°C.
Do not use this medication after the expiration date shown on the packaging after "CAD" or "EXP". The expiration date is the last day of the month indicated.
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.
6. Contents of the pack and further information
Composition of Amchafibrin
- The active ingredient is tranexamic acid. Each film-coated tablet contains 500 mg of tranexamic acid.
- The other components are: microcrystalline cellulose, low-substituted hydroxypropylcellulose, talc, magnesium stearate, povidone, anhydrous colloidal silica, butyl methacrylate basic copolymer, titanium dioxide (E 171), macrogol, and vanillin.
Appearance of the product and contents of the pack
White, oval, film-coated tablets with a score on one side.
The tablets are presented in PVC/PVDC-Aluminum blisters, and the available pack size is 30 tablets.
Marketing authorization holder and manufacturer
Marketing authorization holder
Viatris Healthcare Limited
Damastown Industrial Park
Mulhuddart, Dublin 15
Dublin
Ireland
Manufacturer
Madaus GmbH
Lütticher Str. 5
53842 Troisdorf,
Germany
You can request more information about this medication from the local representative of the marketing authorization holder:
Viatris Pharmaceuticals, S.L.
C/General Aranaz, 86
28027 Madrid
Spain
Date of the last revision of this package leaflet:November 2022
Detailed and updated information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) https://www.aemps.gob.es/
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- Country of registration
- Dosage formTABLET, 500 mg
- ATC codeB02AA02
- Average pharmacy price4.62 EUR
- Active substance
- Prescription requiredYes
- Manufacturer
- This information is for reference only and does not constitute medical advice. Always consult a doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
- Alternatives to AMCHAFIBRIN 500 mg FILM-COATED TABLETSDosage form: TABLET, 500 mgActive substance: tranexamic acidManufacturer: Apc Instytut Sp. Z O.O.Prescription requiredDosage form: INJECTABLE, 100 mg/mlActive substance: tranexamic acidManufacturer: Baxter Holding B.V.Prescription requiredDosage form: TABLET, 500 mgActive substance: tranexamic acidManufacturer: Zentiva K.S.Prescription required
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Frequently Asked Questions
AMCHAFIBRIN 500 mg FILM-COATED TABLETS requires a prescription in Spain. You can check with a doctor online whether this medicine may be appropriate for your situation.
The active ingredient in AMCHAFIBRIN 500 mg FILM-COATED TABLETS is tranexamic acid. This information helps identify medicines with the same composition but different brand names.
The average pharmacy price for AMCHAFIBRIN 500 mg FILM-COATED TABLETS is around 4.62 EUR. Prices may vary depending on the manufacturer and dosage form.
AMCHAFIBRIN 500 mg FILM-COATED TABLETS is manufactured by Viatris Healthcare Limited. Pharmacy brands and packaging may differ depending on the distributor.
Doctors such as Family doctors, Psychiatrists, Dermatologists, Cardiologists, Endocrinologists, Gastroenterologists, Pulmonologists, Nephrologists, Rheumatologists, Hematologists, Infectious disease physicians, Allergists, Geriatricians, Paediatricians, Oncologists may assess whether AMCHAFIBRIN 500 mg FILM-COATED TABLETS is appropriate, depending on your situation and local regulations. You can book an online consultation to discuss your symptoms and possible next steps.
Spain has a well-developed healthcare infrastructure across major cities such as Madrid, Barcelona, Valencia, and Seville. Pharmacies are widely available and operate under strict regulations, ensuring access to prescribed medications.
You can buy AMCHAFIBRIN 500 mg FILM-COATED TABLETS in Madrid, Barcelona, Seville, or Valencia at any local pharmacy with a valid prescription.
To obtain a prescription, you can use Oladoctor:
Other medicines with the same active substance (tranexamic acid) include TRANEXAMIC ACID APC INSTYTUT 500 mg FILM-COATED TABLETS, TRANEXAMIC ACID BAXTER 100 mg/mL INJECTABLE SOLUTION, TRANEXAMIC ACID ZENTIVA 500 mg FILM-COATED TABLETS. These may have different brand names or formulations but contain the same therapeutic ingredient. Always consult a doctor before switching or starting a new medicine.
