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Ledraxen 6,000 IU (60 mg)/0.6 mL, solution for injection in pre-filled syringe – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) ▼ Additional monitoring Details

Medicine strength:
6 000 IU
Contains active substance:
ATC code:

Patient leaflet - Ledraxen 6 000 IU (60 mg)/0.6 ml solution for injection in Pre-filled syringe

1. What Ledraxen is and what it is used for

Ledraxen contains the active substance called enoxaparin sodium that is a low molecular weight heparin (LMWH).

Ledraxen works in two ways.

  1. 1) Stopping existing blood clots from getting any bigger. This helps your body to break them down and stops them from causing you harm
  2. 2) Stopping new blood clots from forming in your blood.

Ledraxen can be used to:

  • Treat blood clots that are in your blood
  • Stop blood clots from forming in your blood in the following situations: – Before and after an operation

    • When you have short‐term illness and will not be able to move around for some time
    • If you have experienced a blood clot due to cancer to prevent further clots from forming
  • Stop blood clots from forming when you have unstable angina (a condition when not enough blood gets to your heart) or after a heart attack
  • Stop blood clots forming in the tubes of your dialysis machine (used for people with severe kidney problems).

2. What you need to know before you use Ledraxen

Do not use Ledraxen if:

  • you are allergic to:

    • enoxaparin sodium or any of the other ingredients of this medicine (listed in section 6).
    • heparin or other low molecular weight heparins such as nadroparin, tinzaparin or dalteparin.

Signs of an allergic reaction include: rash, swallowing or breathing problems, swelling of your lips, face, throat or tongue.

  • you have had a reaction to heparin that caused a severe drop in the number of your clotting cells (platelets) within the last 100 days
  • you have antibodies against enoxaparin in your blood.
  • you are bleeding heavily or have a condition with a high risk of bleeding such as:

    • stomach ulcer, recent surgery of the brain or eyes or recent bleeding stroke. • If you are using Ledraxen to treat blood clots in your body and going to have within 24 hours:
    • A spinal or lumbar puncture.
    • An operation with epidural or spinal anaesthesia.

Do not use Ledraxen if any of the above apply to you.

If you are not sure, talk to your doctor or pharmacist before using Ledraxen. Warnings and precautions

Ledraxen should not be used interchangeably with other medicines belonging to the group of low molecular weight heparins. This is because they are not exactly the same and do not have the same activity and instructions for use. Talk to your doctor or pharmacist before using Ledraxen if:

  • you have ever had a reaction to heparin that caused a severe drop in the number of your clotting cells (platelets)
  • you have had a heart valve fitted
  • you have endocarditis (an infection of the inner lining of the heart) • you have history of gastric ulcer
  • you have had a recent stroke
  • you have high blood pressure
  • you have diabetes or problems with blood vessels in the eye caused by diabetes (called diabetic retinopathy)
  • you have had an operation recently on your eyes or brain • you are elderly (over 65 years old) and especially if you are over 75 years old • you have kidney problems
  • you have liver problems
  • you are underweight or overweight
  • you have high level of potassium in your blood (this may be checked with a blood test)
  • you are currently using medicines which affect bleeding (see section below –Other medicines).

    • you have any problem with your spine or you have had spinal surgery. If any of the above apply to you (or you are not sure), talk to your doctor or pharmacist before using Ledraxen.

This medicine contains less than 1 mmol (23 mg) of sodium per dose, i.e. it is essentially “sodium-free”.

Tests and checks

You may have a blood test before you start using this medicine and at intervals while you are using it; this is to check the level of the clotting cells (platelets) and potassium in your blood.

Other medicines and Ledraxen

Tell your doctor or pharmacist if you are using any other medicines, have recently used or might use any other medicines.

  • Warfarin – used for thinning the blood
  • Aspirin (also known as acetylsalicylic acid or ASA), clopidogrel or other medicines used to stop blood clots from forming (see also in section 3, “Changing of anticoagulant medicine”)
  • Dextran injection – used as a blood replacer
  • Ibuprofen, diclofenac, ketorolac or other medicines known as non-steroidal anti-inflammatory agents which are used to treat pain and swelling in arthritis and other conditions
  • Prednisolone, dexamethasone or other medicines used to treat asthma, rheumatoid arthritis and other conditions
  • Medicines which increase potassium level in your blood such as potassium salts, water pills, some medicines for heart problems.

Operations and Anaesthetics

If you are going to have a spinal or lumbar puncture, or an operation where an epidural or spinal anaesthetic is used, tell your doctor that you are using Ledraxen. Pregnancy and breast-feeding

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. If you are pregnant and have a mechanical heart valve, you may be at an increased risk of developing blood clots. Your doctor should discuss this with you. If you are breast-feeding or plan to breast-feed, you should ask your doctor for advice before taking this medicine.

Children and adolescents

The safety and efficacy of Ledraxen has not been evaluated in children or adolescents.

Driving and using machines

Ledraxen does not affect the ability to drive and operate machinery. It is advised that the trade name and batch number of the product you are using are recorded by your healthcare professional.

3. How to use Ledraxen

Always use this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

Having this medicine

  • Your doctor or nurse will normally give you Ledraxen. This is because it needs to be given as an injection.
  • Ledraxen is usually given by injection underneath the skin (subcutaneous). • Ledraxen can be given by injection into your vein (intravenous) after certain types of heart attack or operation.
  • Ledraxen can be added to the tube leaving the body (arterial line) at the start of the dialysis session.
  • Do not inject Ledraxen into a muscle.

How much will be given to you

  • Your doctor will decide how much Ledraxen to give you. The amount will depend on the reason it is being used.
  • If you have problems with your kidneys you may be given a smaller amount of Ledraxen.
  • Treating blood clots that are in your blood

    • The usual dose is 150 IU (1.5 mg) for every kilogram of your weight each day or 100 IU (1 mg) for every kilogram of your weight twice a day. • Your doctor will decide how long you should receive Ledraxen. 2. Stopping blood clots forming in your blood in the following situations operation or periods of limited mobility due to an illness
    • The dose will depend on how likely you are to develop a clot. You will be given 2,000 IU (20 mg) or 4,000 IU (40 mg) of Ledraxen each day. • If you are going to have an operation your first injection will be usually given 2 hours or 12 hours before your operation.
    • If you have restricted mobility due to illness, you will normally be given 4,000 IU (40 mg) of Ledraxen each day.
    • Your doctor will decide how long you should receive Ledraxen. 3. Stopping blood clots when you have unstable angina or after you have had a heart attack

Ledraxen can be used for two different types of heart attack. The amount of Ledraxen given to you will depend on your age and the kind of heart attack you have had.

NSTEMI (Non‐ST segment elevation myocardial infarction) type of heart attack: • The usual dose is 100 IU (1 mg) for every kilogram of weight every 12 hours. • Your doctor will normally ask you to take aspirin (acetylsalicylic acid) as well. • Your doctor will decide how long you should receive Ledraxen. STEMI (ST segment elevation myocardial infarction) type of heart attack if you are under 75 years old:

  • An initial dose of 3,000 IU (30 mg) of Ledraxen will be given as injection into your vein.
  • At the same time you will also be given Ledraxen as an injection underneath your skin (subcutaneous injection). The usual dose is 100 IU (1 mg) for every kilogram of your weight, every 12 hours.
  • Your doctor will normally ask you to take aspirin (acetylsalicylic acid) as well. • Your doctor will decide how long you should receive Ledraxen.

    STEMI type of heart attack if you are 75 years old or older:

    • The usual dose is 75 IU (0.75 mg) for every kilogram of your weight, every 12 hours.
    • The maximum amount of Ledraxen given for the first two injections is 7,500 IU (75 mg).
    • Your doctor will decide how long you should receive Ledraxen. For patients that have an operation called percutaneous coronary intervention (PCI): Depending on when you were last given Ledraxen, your doctor may decide to give an additional dose of Ledraxen before a PCI operation. This is by injection into your vein.
    1. 4.

      Stopping blood clots from forming in the tubes of your dialysis machine

      • The usual dose is 100 IU (1 mg) for every kilogram of your weight. • Ledraxen is added to the tube leaving the body (arterial line) at the start of the dialysis session.

        This amount is usually enough for a 4-hour session.

        However, your doctor may give you a further dose of 50 IU to 100 IU (0.5 to 1 mg) for every kilogram of your weight, if necessary.

Giving yourself an injection of Ledraxen

If you are able to give Ledraxen to yourself, your doctor or nurse will show you how to do this. Do not try to inject yourself if you have not been trained how to do so. If you are not sure what to do, talk to your doctor or nurse immediately. Performing the injection properly under the skin (called “subcutaneous injection”) will help reduce pain and bruising at the injection site.

Before injecting yourself with Ledraxen

  • Collect together the items that you need: syringe, alcohol swab or soap and water, and sharps container

  • Check the expiry date on the medicine. Do not use if the date has passed • Check the syringe is not damaged and the medicine in it is a clear solution. If not, use another syringe
  • Make sure you know how much you are going to inject
  • Check your stomach to see if the last injection caused any redness, change in skin colour, swelling, oozing or is still painful. If so talk to your doctor or nurse Instruction for use of the syringe

Appropriate use of syringes is necessary to reduce the risk of pain and appearance of bruises at the injection site. Be careful to follow the instructions. Instructions for syringes without safety system

  • Preparation of the injection site:

Before performing the injection, wash your hands and dry them. Use a cotton ball to clean (without rubbing) the area chosen for the injection.

Choose a different area of the stomach for each injection.

  • Remove the protective cap from the needle.

The appearance of a drop at the end of the needle is possible. In this case, remove the drop before injection by tapping on the body of the syringe (with the needle pointing downwards).

  • Perform the injection:

The pre-filled syringe is ready for immediate use. Choose an area on the right or left side of your stomach. This should be at least 5 cm away from your belly button (navel) and out towards your sides. Hold the syringe so that the needle is pointing downwards (vertically at a 90 º angle), into the thickness of a skin fold pinched between the thumb and index finger of the operator. The fold should be held throughout the entire injection.

  • Immediately throw away the syringe in the appropriate container. Any unused medicinal product or waste material should be disposed of in accordance with local requirements.

Instructions for syringes with safety system

  • Preparation of the injection site:

Before performing the injection, wash your hands and dry them. Use a cotton ball to clean (without rubbing) the area chosen for the injection.

Choose a different area of the stomach for each injection.

  • First, bend the trap toward the side by approximately 90 degrees. Important: do not remove the cap before bending the trap.
  • Remove the protective cap from the needle.

The appearance of a drop at the end of the needle is possible. In this case, remove the drop before injection by tapping on the body of the syringe (with the needle pointing down).

315 mm

  • Perform the injection:

The pre-filled syringe is ready for immediate use. Choose an area on the right or left side of your stomach. This should be at least 5 cm away from your belly button (navel) and out towards your sides. Hold the syringe so that the needle is pointing downwards (vertically at a 90 º angle), into the thickness of a skin fold pinched between the thumb and index finger of the operator. The fold should be held throughout the entire injection.• Secure the needle-trap:

Place the trap against a hard, stable surface, using one hand. Important: Do not use your finger to secure the needle in the trap. Then press down the trap. Bend the trap until the needle audibly clicks into the plastic part.When you have finished

  1. 1) To avoid bruising, do not rub the injection site after you have injected yourself.
  2. 2) Drop the used syringe into a sharps container. Close the container lid tightly and place the container out of reach of children. When the container is full, dispose of it as your doctor or pharmacist has instructed.

Any unused medicinal product or waste material should be disposed of in accordance with local requirements.

Changing of anticoagulant treatment

  • Changing from Ledraxen to blood thinners called vitamin-K antagonists (e.g. warfarin)

    Your doctor will request you perform blood tests called INR and tell you when to stop Ledraxen accordingly.

  • Changing from blood thinners called vitamin-K antagonists (e.g. warfarin) to Ledraxen

    Stop taking the vitamin-K antagonist. Your doctor will request you perform blood tests called INR and tell you when to start Ledraxen accordingly. – Changing from Ledraxen to treatment with direct oral anticoagulant Stop taking Ledraxen. Start taking the direct oral anticoagulant 0-2 hours before the time you would have had the next injection, then continue as normal. – Changing from treatment with direct oral anticoagulant to Ledraxen Stop taking direct oral anticoagulant. Do not start treatment with Ledraxen until 12 hours after the final dose of direct oral anticoagulant.

If you use more Ledraxen than you should

If you think that you have used too much or too little Ledraxen, tell your doctor, nurse or pharmacist immediately, even if you have no signs of a problem. If a child accidentally injects or swallows Ledraxen, take them to a hospital causualty department straight away.

If you forget to use Ledraxen

If you forget to give yourself a dose, have it as soon as you remember. Do not give yourself a double dose on the same day to make up for a forgotten dose. Keeping a diary will help to make sure you do not miss a dose.

If you stop using Ledraxen

It is important for you to keep having Ledraxen injections until your doctor decides to stop them. If you stop, you could get a blood clot which can be very dangerous. If you have any further questions on the use of this medicine, ask your doctor or pharmacist or nurse.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Serious side effects Ledraxen

Stop using Ledraxen and talk to a doctor or nurse straight away if you get any signs of a severe allergic reaction (such as rash, difficulty breathing or swallowing, swelling of the face, lips, tongue, oral cavity, throat or eyes).

Stop using enoxaparin and seek medical attention immediately if you notice any of the following symptoms:

  • A red, scaly widespread rash with bumps under the skin and blisters accompanied by fever. The symptoms usually appear at the initiation of treatment (acute generalised exanthematous pustulosis).

Like other similar medicines to reduce blood clotting, Ledraxen may cause bleeding. This may be life‐threatening. In some cases the bleeding may not be obvious. Talk to your doctor straight away if: • you have any bleeding that does not stop by itself

  • you have signs of too much bleeding such as being very weak, tired, pale, or dizzy with headache or unexplained swelling.

Your doctor may decide to keep you under closer observation or change your medicine.

You should tell your doctor straight away:

  • If you have any sign of blockage of a blood vessel by a blood clot such as:

    • cramping pain, redness, warmth, or swelling in one of your legs – these are symptoms of deep vein thrombosis
    • breathlessness, chest pain, fainting or coughing up blood – these are symptoms of a pulmonary embolism.
  • If you have a painful rash of dark red spots under the skin which do not go away when you put pressure on them.

Your doctor may request you perform a blood test to check your platelet count. Overall list of possible side effects:

Very common (may affect more than 1 in 10 people)

  • Bleeding.
  • Increases in liver enzymes.

Common (may affect up to 1 in 10 people)

  • You bruise more easily than usual. This could be because of a blood problem with low platelet counts.
  • Pink patches on your skin. These are more likely to appear in the area you have been injected with Ledraxen.
  • Skin rash (hives, urticaria).
  • Itchy red skin.
  • Bruising or pain at the injection site.
  • Decreased red blood cell count.
  • High platelet counts in the blood.
  • Headache.

Uncommon (may affect up to 1 in 100 people)

  • Sudden severe headache. This could be a sign of bleeding in the brain.
  • A feeling of tenderness and swelling in your stomach. You may have bleeding in your stomach.
  • Large red irregularly shaped skin lesions with or without blisters.
  • Skin irritation (local irritation).
  • You notice yellowing of your skin or eyes and your urine becomes darker in colour. This could be a liver problem.

Rare (may affect up to 1 in 1,000 people)

  • Severe allergic reaction. The signs may include: a rash, swallowing or breathing problems, swelling of your lips, face, throat or tongue.
  • Increased potassium in your blood. This is more likely to happen in people with kidney problems or diabetes. Your doctor will be able to check this by carrying out a blood test.
  • An increase in the number of eosinophils in your blood. Your doctor will be able to check this by carrying out a blood test.
  • Hair loss.
  • Osteoporosis (a condition where your bones are more likely to break) after long term use.
  • Tingling, numbness and muscular weakness (particularly in the lower part of your body) when you have had a spinal puncture or a spinal anaesthetic.
  • Lost of control over your bladder or bowel (so you cannot control when you go to the toilet).
  • Hard mass or lump at the injection site.

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme, Website: 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 Ledraxen

Do not store above 25°C.

Do not freeze.

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 label. The expiry date refers to the last day of that month.

Do not use this medicine if you notice any visible change in the appearance of the solution.

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.

6. Contents of the pack and other information

What Ledraxen contains

2,000 IU (20 mg)/0.2 mL solution for injection

  • The active substance is enoxaparin sodium
  • Each mL contains 100 mg of enoxaparin sodium

Each pre-filled syringe of 0.2 mL contains 2,000 IU anti-Xa activity (equivalent to 20 mg) of enoxaparin sodium

  • The other ingredient is water for injections.

4,000 IU (40 mg)/0.4 mL solution for injection

  • The active substance is enoxaparin sodium
  • Each mL contains 100 mg of enoxaparin sodium

Each pre-filled syringe of 0.4 mL contains 4,000 IU anti-Xa activity (equivalent to 40 mg) of enoxaparin sodium

  • The other ingredient is water for injections.

6,000 IU (60 mg)/0.6 mL solution for injection

  • The active substance is enoxaparin sodium
  • Each mL contains 100 mg of enoxaparin sodium

Each pre-filled syringe of 0.6 mL contains 6,000 IU anti-Xa activity (equivalent to 60 mg) of enoxaparin sodium

  • The other ingredient is water for injections.

8,000 IU (80 mg)/0.8 mL solution for injection

  • The active substance is enoxaparin sodium
  • Each mL contains 100 mg of enoxaparin sodium

Each pre-filled syringe of 0.8 mL contains 8,000 IU anti-Xa activity (equivalent to 80 mg) of enoxaparin sodium

  • The other ingredient is water for injections.

    10,000 IU (100 mg)/1 mL solution for injection

    • The active substance is enoxaparin sodium
    • Each mL contains 100 mg of enoxaparin sodium

Each pre-filled syringe of 1.0 mL contains 10,000 IU anti-Xa activity (equivalent to 100 mg) of enoxaparin sodium

  • The other ingredient is water for injections.

What Ledraxen looks like and contents of the pack

2,000 IU (20 mg)/0.2 mL solution for injection

Colourless or light yellow transparent liquid

0.2 mL of solution in a colourless type I glass syringe barrel with fixed needle and needle cap closed by chlorobutyl rubber stopper and a purple polypropylene plunger rod (with or without safety system). Supplied in packs of 1, 2, 6, 10, 20 and 50 pre-filled syringes.

4,000 IU (40 mg)/0.4 mL solution for injection

Colourless or light yellow transparent liquid

0.4 mL of solution in a colourless type I glass syringe barrel with fixed needle and needle cap closed by chlorobutyl rubber stopper and a yellow polypropylene plunger rod (with or without safety system). Supplied in packs of 1, 2, 6, 10, 20, 30 and 50 pre-filled syringes.

6,000 IU (60 mg)/0.6 mL solution for injection

Colourless or light yellow transparent liquid

0.6 mL of solution in a colourless type I glass graduated syringe barrel with fixed needle and needle cap closed by chlorobutyl rubber stopper and an orange polypropylene plunger rod (with or without safety system).

Supplied in packs of 1, 2, 6, 10, 12, 20, 24, 30 or 50 pre-filled syringes. 8,000 IU (80 mg)/0.8 mL solution for injection

Colourless or light yellow transparent liquid

0.8 mL of solution in a colourless type I glass graduated syringe barrel with fixed needle and needle cap closed by chlorobutyl rubber stopper and a brown polypropylene plunger rod (with or without safety system). Supplied in packs of 1, 2, 6, 10, 12, 20, 24, 30 and 50 pre-filled syringes.

10,000 IU (100 mg)/1 mL solution for injection

Colourless or light yellow transparent liquid

1.0 mL of solution in a colourless type I glass graduated syringe barrel with fixed needle and needle cap closed by chlorobutyl rubber stopper and a grey polypropylene plunger rod (with or without safety system). Supplied in packs of 1, 2, 6, 10, 12, 20, 24 and 30 pre-filled syringes.

For 0.2 mL and 0.4mL syringes, the syringes are not graduated. For 0.6 mL, 0.8 mL and 1 mL syringes, the syringes are graduated. Not all pack sizes may be marketed.

Marketing Authorisation Holder

Venipharm

4, Bureaux de la Colline

92210 Saint-Cloud

FRANCE

+33 1 47 11 04 47

venipharm@venipharm.com

Manufacturer

Centre Spécialités Pharmaceutiques

ZAC des Suzots

35 rue de la Chapelle

F-63450 Saint-Amant Tallende

FRANCE

Distributor

Venipharm LTD

Room 130,

Building 1,

Chalfont Park,

Gerrards Cross,

SL9 0BG,

United Kingdom

This leaflet was last revised in 11/2024

This medicinal product is authorised in the Member States of the EEA under the following names:

Germany: Enoxaparin Ledraxen

Sweden: Enoxaparin Ledraxen

Spain: Enoxaparina Ledraxen

France: Enoxaparine Arrow

Latvia: Enoxaparin sodium Ledraxen

Lettonia Enoxaparin sodium Ledraxen

Austria: Enoxaparin Ledraxen

Cyprus: Ledraxen

Czech Republic: Enoxaparin sodium Ledraxen

Estonia: Enoxaparin sodium Ledraxen

Finland: Enoxaparin Ledraxen

Croatia: Enoksaparinnatrij Ledraxen

Ireland: Enoxaparin sodium Ledraxen

Norway Enoxaparin Ledraxen

Poland: Enoxaparin sodium Ledraxen

Portugal: Enoxaparin Ledraxen

Slovakia: Ledraxen

Slovenia: Enoksaparin Ledraxen

Other sources of information

Detailed information on this medicine is available on the website of the Medicines & Healthcare products Regulatory Agency (MHRA).

8A1AAK9-03

8A1AAK9

Client:南京健友生化制药股份有限公司产品名称 :欧洲依诺英国版说明书Date:Brief:Date:Brief:
展开尺寸 : 315X297 (±1) mm 成品尺寸 : 105X38 (±1) mmItem No:8A1AAK9-03ArialMT; ArialNarrow; ArialNova; ArialNova-Bold; ArialNova-Italic;7.5 pt2024-10-15改版2024-11-08修改
CSH2024K0090DTP:Roy2024-11-01修改

315 mm

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 43843/0003

Last revision stated in the text: November 2024 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Ledraxen 6 000 IU (60 mg)/0.6 ml solution for injection in Pre-filled syringe

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Enoxaparin
Strength 6 000 IU
Pharmaceutical form Colourless or light yellow transparent liquid, the pH of the solution is between 5.5 and 7.5.
Excipients Water for injections.
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years.
Reconstituted product should be used immediately.
Storage Do not store above 25°C.
Do not freeze.
This medicinal product is for single use only. Discard any unused product.
Drug group (ATC) Antithrombotic agent, heparin group
  1. B Blood and blood forming organ drugs
    1. B01 Antithrombotic agents
      1. B01A Antithrombotic agents
        1. B01AB Heparin group antithrombotic drugs
          1. B01AB05 enoxaparin
Additional monitoring Yes ▼ – new safety information is collected quickly. Report any side effect to the Yellow Card scheme.
Marketing authorisation PL 43843/0003 (first authorised 3 November 2023)
Marketing authorisation holder Venipharm

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.1.0 of 12 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.