Pharmacy Guide

Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.

Pharmacy Guide

Patient leaflets and SmPCs, drug interaction checker, official dosages and NHS pharmacy opening hours — all in one place.

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Tranexamic acid Tillomed 500 mg film-coated Tablets

⚠ This medicine appears to have been discontinued

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.

Active substance: Tranexamic acid

Equivalent medicines (same active substance, strength and form)

Source: electronic medicines compendium (emc)
Official leaflet: Read the PIL on emc

What it is and what it is used for

for

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:

  • Following prostate surgery (post-prostatectomy)
  • Following bladder surgery
  • Heavy periods (menorrhagia)
  • Nose bleeds (epistaxis)
  • Cervical surgery (conisation of the cervix)
  • Bleeding inside the eye (prevention of recurrent haemorrhage in traumatic hyphaema)
  • Tooth removal (dental extraction) in haemophiliacs (people who bleed more easily than normal). You will know if this refers to you
  • A hereditary disease called angioneurotic oedema (HANO). A doctor will have told you if you have this. The name of your medicine is Tranexamic acid Tillomed 500 mg film-coated tablets, but will be referred to as Tranexamic acid Tillomed tablets throughout this leaflet. 2.

What you need to know before you take it

e Tranexamic acid Tillomed tablets

Do not take Tranexamic acid Tillomed tablets if

  • You are allergic to tranexamic acid or any of the other ingredients of this medicine (listed in section 6)
  • You have serious problems with your kidneys (kidney failure)
  • You have or have ever had a blood clot in your blood vessels (called a `thrombosis').
  • You have a history of convulsions
  • You are at risk of excessive bleeding as a result of a bleeding disorder called consumption coagulopathy If any of the above applies to you talk to your doctor or pharmacist.

Warnings and precautions Talk to your doctor or pharmacist before taking Tranexamic acid Tillomed tablets if:

  • You have blood in your urine. This may increase the risk of blockage of the urinary tract
  • You have ever had any uncontrollable bleeding
  • You take oral contraceptives. These may increase the risk of blood clots forming
  • You have disseminated intravascular coagulation (DIC), a disease where your blood starts to clot throughout your body
  • You have been taking medicine to treat a hereditary disease called angioneurotic oedema (HANO) every day for a long time. If so, you may need to have regular eye tests and blood tests to check your liver is working properly
  • You are a woman with irregular periods
  • You or your family have a history of blood clots in your blood vessels (called a `thrombosis')
  • Anyone in your family has suffered from blood clots in their blood vessels
  • You have kidney disease. Other medicines and Tranexamic acid Tillomed tablets Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines (including medicines obtained without a prescription), in particular the following:
  • Fibrinolytic drugs (used to help dissolve blood clots), such as streptokinase. This is because Tranexamic acid Tillomed tablets will stop these drugs working Pregnancy, breast-feeding 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 taking this medicine. Driving and using machines Tranexamic acid Tillomed tablets has no or little effect on the ability to drive and use machines. Visual disturbances may occur after taking tranexamic acid. Tranexamic acid Tillomed tablets contain, sodium This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially 'sodiumfree'. 3.

How to take it

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:

  • The usual dose is 2 or 3 tablets taken two to three times daily
  • The exact dose you take will depend on why you have been prescribed these tablets
  • Follow your doctor's instructions about how many tablets to take, when to take them and for how long. Use in children and adolescents: Your doctor will tell you exactly how much medicine you should give your child. They will work out the dose according to how much your child weighs.

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.

Possible side effects

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)

  • itchy, red or swollen skin
  • problems with your eyesight, especially your colour vision
  • a blood clot in your eye. This may cause bleeding in the eye, or a loss of vision. Very rare (may affect up to 1 in 10,000 people)
  • a blood clot in your blood vessels (called a `thrombosis')
  • feeling sick (nausea) or being sick (vomiting), diarrhoea. These are usually mild and pass very quickly, but if they continue, tell your doctor or pharmacist
  • diarrhoea. This is usually mild and passes very quickly, but if it continues, tell your doctor or pharmacist. Frequency not known (cannot be estimated from the available data)
  • seizures, particularly in cases of misuse
  • sudden onset kidney problems due to death of the tissue in the outer part of the kidney (acute renal cortical necrosis)
  • an allergic reaction that usually recurs at the same site(s) on re-exposure to the medication and may include round or oval patches of redness and swelling of the skin, blistering, and itching (fixed drug eruption). Darkening of the skin in affected areas, which might persist after healing, may also occur. Reporting of side effects If you get 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 Yellow Card Scheme at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

5.

How to store it

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.

Contents of the pack and other information

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

Frequently asked questions about Tranexamic acid Tillomed 500 mg film-coated Tablets

How do I take Tranexamic acid Tillomed 500 mg film-coated Tablets?

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.

What is the active substance in Tranexamic acid Tillomed 500 mg film-coated Tablets?

The active substance in Tranexamic acid Tillomed 500 mg film-coated Tablets is tranexamic acid.

Are there equivalent medicines to Tranexamic acid Tillomed 500 mg film-coated Tablets?

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.

Where does this information come from?

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.

Can I get Tranexamic acid Tillomed 500 mg film-coated Tablets without a prescription?

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.

About this leaflet

The text above reproduces the patient information leaflet approved for this medicine, restructured for easier reading.

Medical disclaimer: This page is for information only and does not replace advice from your doctor or pharmacist. Always read the leaflet supplied with your medicine. If you are unwell, call NHS 111; in an emergency, call 999.

Medicines with the same active substance: Tranexamic acid (8 medicines)
See every medicine containing this substance, or browse the full A–Z of active substances.
⚕For healthcare professionals — Summary of Product Characteristics (SmPC)Full SmPC: dosage, interactions, contraindications, warnings+
Technical information intended for healthcare professionals (doctors and pharmacists). The Summary of Product Characteristics (SmPC) is the official document approved by the MHRA/EMA. It does not replace the patient leaflet or a doctor’s advice.

4.1. Therapeutic indications

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

4.2. Posology and method of administration

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.

4.3. Contraindications

• 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

4.4. Special warnings and precautions for use

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'.

4.5. Interaction with other medicinal products and other forms of interaction

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.

4.6. Fertility, pregnancy and lactation

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.

4.7. Effects on ability to drive and use machines

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.

4.8. Undesirable effects

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.

4.9. Overdose

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 about this leaflet

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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