Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.
The electronic medicines compendium (emc) no longer publishes a Summary of Product Characteristics for this product, which usually means it is no longer marketed in the UK. The patient leaflet below is kept for reference, but the product may not be available.
If you were prescribed this medicine, other products containing Tranexamic acid may still be available. Do not stop your treatment — ask your pharmacist or GP what to use instead.
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Tranexamic acid belongs to a group of medicines called anti-fibrinolytic drugs. These are used to stop or reduce unwanted bleeding. When you bleed your body forms clots to stop the bleeding. In some people these break down causing too much bleeding. Tranexamic acid stops these clots dissolving and so reduces unwanted bleeding. Tranexamic acid Tillomed tablets are used to prevent or reduce bleeding for a short period of time in many different conditions. You may have been prescribed it for one of the following:
e Tranexamic acid Tillomed tablets
Do not take Tranexamic acid Tillomed tablets if
Warnings and precautions Talk to your doctor or pharmacist before taking Tranexamic acid Tillomed tablets if:
Tranexamic acid Tillomed tablets
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure. Important: Your doctor will choose the dose that is right for you. Your dose will be shown clearly on the label that your pharmacist puts on your medicine. If it does not, or you are not sure, ask your doctor or pharmacist. Remember: Your medicine should always be taken with a glass of water. The tablets should be swallowed whole. Do not crush or chew them. Use in adults and the elderly:
Use in patients with kidney problems: Your doctor will tell you how much to take. The dose you take may be lower than the usual adult dose. If you take more Tranexamic acid Tillomed tablets than you should If you accidentally take too much of your medicine, immediately tell your doctor or go to the nearest hospital casualty department. Taking too many Tranexamic acid Tillomed tablets may cause diarrhoea or may make you feel sick, be sick or be dizzy or light-headed upon standing. If you forget to take Tranexamic acid Tillomed tablets Do not take a double dose to make up for a missed dose. Simply take the next dose as planned. If you have any further questions on the use of this medicine, ask your doctor or pharmacist. 4.
Like all medicines, this medicine can cause side effects, although not everybody gets them. Stop taking Tranexamic acid Tillomed tablets and go to hospital immediately if you experience any of the following symptoms: • • • •
an allergic reaction: swelling of your throat and/or tongue, difficulty swallowing, difficulty breathing or shortness of breath, dizziness itchy, red or swollen skin rash pain, swelling or redness in your leg chest pain
Stop taking Tranexamic acid Tillomed tablets and tell your doctor immediately if you experience any of the following symptoms: Rare (may affect up to 1 in 1,000 people)
5.
Tranexamic acid Tillomed tablets
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 after "EXP". The expiry date refers to the last day of that month. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help to protect the environment. 6.
What Tranexamic acid Tillomed tablets contain The active substance is Tranexamic acid. Each tablet contains 500 mg Tranexamic acid. The other ingredients are: maize starch, sodium starch glycolate, povidone,silica colloidal anhydrous, talc, magnesium stearate, hypromellose, titanium dioxide, macrogol. What Tranexamic acid Tillomed tablets looks like and contents of the pack Tranexamic acid Tillomed tablets are. white coloured, circular, biconvex film coated tablets. Tranexamic acid Tllomed tablets are supplied in: Blister packs (Alu/PVC/ PVDC clear) containing 10, 20, 30, 50, 60 and 100 tablets. Not all pack sizes are marketed. Marketing Authorisation Holder and Manufacturer Marketing Authorisation Holder Tillomed Laboratories Ltd, 220 Butterfield Great Marlings Luton, LU2 8DL United Kingdom Manufacturer Tillomed Laboratories Ltd 220 Butterfield Great Marlings Luton, LU2 8DL United Kingdom This leaflet was last revised in 04/2026
Tranexamic acid Tillomed 500 mg film-coated Tablets comes as tablet containing 500mg. Always follow the dose your doctor or pharmacist has given you, and read the leaflet that comes with the medicine.
The active substance in Tranexamic acid Tillomed 500 mg film-coated Tablets is tranexamic acid.
Medicines with the same active substance, strength and form include: Evana Heavy Period Relief 500 mg tablets, Tranexamic Acid 500 mg Tablets. They are interchangeable only if your prescriber or pharmacist says so.
This leaflet reproduces the patient information leaflet approved for Tranexamic acid Tillomed 500 mg film-coated Tablets, as published on the electronic medicines compendium (emc). The version printed inside your medicine’s packaging is the one that applies to you.
Whether a medicine is available over the counter or on prescription only depends on its licence. Check the leaflet, or ask your pharmacist — they can tell you straight away.
The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.
Short-term use for haemorrhage or risk of haemorrhage in increased fibrinolysis or fibrinogenolysis. Local fibrinolysis as occurs in the following conditions:
• Prostatectomy and bladder surgery
• Menorrhagia
• Severe epistaxis
• Conisation of the cervix
• Prevention of recurrent haemorrhage in traumatic hyphaema
• Hereditary angioneurotic oedema
• Management of dental extraction in haemophiliacs
Posology
1. Local fibrinolysis: The recommended standard dosage is 15-25 mg/kg bodyweight (i.e. 2-3 tablets) two to three times daily. For the indications listed below the following doses may be used:
1a. Prostatectomy: Prophylaxis and treatment of haemorrhage in high risk patients should commence pre- or post-operatively with Tranexamic Acid Injection; thereafter 2 tablets three to four times daily until macroscopic haematuria is no longer present.
1b. Menorrhagia: Recommended dosage is 2 tablets 3 times daily as long as needed for up to 4 days. If very heavy menstrual bleeding, dosage may be increased. A total dose of 4g daily (8 tablets) should not be exceeded. Treatment with Tranexamic acid should not be initiated until menstrual bleeding has started.
1c. Severe epistaxis: Where recurrent bleeding is anticipated oral therapy (2 tablets three times daily) should be administered for 7 days.
1d. Conisation of the cervix: 3 tablets three times daily for 12-14 days.
1e. Prevention of recurrent haemorrhage in traumatic hyphaema: 2-3 tablets three times daily for 7 days. The dose is based on 25 mg/kg three times a day.
2. Hereditary angioneurotic oedema: Some patients are aware of the onset of the illness; suitable treatment for these patients is intermittently 2-3 tablets two to three times daily for some days. Other patients are treated continuously at this dosage.
3. Haemophilia: In the management of dental extractions 2-3 tablets every eight hours for 6-8 days. The dose is based on 25 mg/kg.
Renal insufficiency: By extrapolation from clearance data relating to the intravenous dosage form, the following reduction in the oral dosage is recommended for patients with mild to moderate renal insufficiency.
Serum Creatinine (μmol/l)
Dose tranexamic acid
120-249
15 mg/kg body weight twice daily
250-500
15 mg/kg body weight/day
Children's dosage: This should be calculated according to body weight at 25 mg/kg per dose. However, data on efficacy, posology and safety for these indications are limited.
Elderly patients: No reduction in dosage is necessary unless there is evidence of renal failure (see guidelines below).
Method of administration
Route of administration: Oral.
• Hypersensitivity to tranexamic acid or any of the excipients listed in section 6.
• Severe renal impairment (Serum Creatinine > 500 μmol/l) because of risk of accumulation
• Active thromboembolic disease
• History of venous or arterial thrombosis
• Fibrinolytic conditions following consumption coagulopathy
• History of convulsions
In case of haematuria of renal origin (especially in haemophilia), there is a riskfor urinary obstruction at the lower levels of the tract.
If left untreated, urinary obstruction may lead to serious consequences such as renal insufficiency, urinary tract infection, hydronephrosis, and anuria. Therefore, close monitoring is recommended for those patients with haematuria or risk of haematuria from the upper urinary tract.
In the long-term treatment of patients with hereditary angioneurotic oedema, regular eye examinations (e.g. visual acuity, slit lamp, intraocular pressure, visual fields) and liver function tests should be performed.
Patients with irregular menstrual bleeding should not use Tranexamic acid until the cause of irregular bleeding has been established. If menstrual bleeding is not adequately reduced by Tranexamic acid, an alternative treatment should be considered.
Tranexamic acid should be administered with care in patients receiving oral contraceptives because of the increased risk of thrombosis.
Patients with a previous thromboembolic event and a family history of thromboembolic disease (patients with thrombophilia) should use Tranexamic acid only if there is a strong medical indication and under strict medical supervision.
The blood levels are increased in patients with renal insufficiency. Therefore, a dose reduction is recommended (see section 4.2).
The use of tranexamic acid in cases of increased fibrinolysis due to disseminated intravascular coagulation is not recommended.
Patients who experience visual disturbance should be withdrawn from treatment.
Clinical experience with Tranexamic acid in menorrhagic children under 15 years of age is not available.
Cases of convulsions have been reported in association with tranexamic acid treatment. In cardiac surgery, most of the cases were reported following intravenous (i.v.) injection of tranexamic acid in high doses.
Tranexamic acid Tillomed 500 mg film-coated tablets contain sodium
This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially 'sodium-free'.
Tranexamic acid will counteract the thrombolytic effect of fibrinolytic preparations.
Drugs that exert effects on haemostasis should be given with caution to patients taking tranexamic acid. There is a theoretical risk of increased formation potential thrombi, for example with oestrogen.
Pregnancy
Although there is no evidence from animal studies of a teratogenic effect, the usual caution with use of drugs in pregnancy should be observed.
Tranexamic acid crosses the placenta.
Breastfeeding
Tranexamic acid passes into breast milk to a concentration of approximately one hundredth of the concentration in the maternal blood. An antifibrinolytic effect in the infant is unlikely.
Fertility
There are no clinical data on the effects of tranexamic acid on fertility.
Tranexamic acid 500 mg tablets has no or negligible influence on the ability to drive and use machines.
Visual disturbances may occur following administration of tranexamic acid.
Adverse events are listed below by system organ class and frequency. Frequencies are defined as: very common (≥1/l0), common (≥1/100 and <1/10), uncommon (≥1/1000 and <1/100), rare (≥ 1/10,000 and <1/1000) and very rare (<1/10,000) including isolated reports, not known (cannot be estimated from the available data).
Immune system disorders
Very rare: Hypersensitivity reactions including anaphylaxis
Eye disorders
Rare: Colour vision disturbances, retinal/artery occlusion
Cardiac disorders
Very rare: malaise with hypotension, with or without loss of consciousness (usually followed by an intravenous too fast, exceptionally after oral administration)
Vascular disorders
Rare: Thromboembolic events
Very rare: Arterial or venous thrombosis at any sites
Gastro-intestinal disorders
Very rare: Digestive effects such as nausea, vomiting and diarrhoea, may occur but disappear when the dosage is reduced.
Skin and subcutaneous tissue disorders
Rare: Allergic skin reactions
Frequency not known: Fixed drug eruption
Nervous system disorders
Frequency not known: convulsions, particularly in cases of misuse (refer to sections 4.3 and 4.4)
Renal and urinary disorders
Frequency not known: Acute renal cortical necrosis
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Signs and symptoms may include nausea, diarrhoea, vomiting, orthostatic symptoms and/or hypotension, dizziness, headache and convulsions. Initiate vomiting, then stomach lavage, and charcoal therapy. Maintain a high fluid intake to promote renal excretion. There is a risk of thrombosis in predisposed individuals. Anticoagulant treatment should be considered.
Ask anything about Tranexamic acid Tillomed 500 mg film-coated Tablets. The assistant answers only from this leaflet — if the leaflet does not cover it, it will say so. It does not give medical advice.
Answers come from the patient leaflet published on the electronic medicines compendium (emc). They are not medical advice. Ask a pharmacist or your GP if you are unsure. For urgent help call NHS 111, or 999 in an emergency.
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