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Zyduco XL 1200 mg gastro-resistant prolonged-release tablets – patient leaflet, side effects, dosage

Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
1200 mg
Contains active substance:
ATC code:

Patient leaflet - Zyduco XL 1200 mg gastro-resistant prolonged-release tablets

1. What Zyduco XL is and what it is used for

Pharmacotherapeutic group: Aminosalicylic acid and similar agents. Zyduco XL gastro-resistant, prolonged release tablets contain the active substance Mesalazine, which is an anti-inflammatory drug for the treatment of ulcerative colitis. Ulcerative colitis is a disease of the colon (large bowel) and rectum (back passage), where the lining of the gut becomes red and swollen (inflamed) resulting in symptoms of frequent and bloody stools together with stomach cramps.

When given for an acute episode of ulcerative colitis, Zyduco XL acts through the entire colon and rectum to treat the inflammation and reduce symptoms. The tablets can also be taken to help prevent recurrence of ulcerative colitis.

2. What you need to know before you take Zyduco XL

Do not take Zyduco XL

  • If you are allergic (hypersensitive) to a family of drugs known as salicylates (which

    include acetylsalicylic acid (Aspirin)

  • If you are allergic (hypersensitive) to Mesalazine or any of the other ingredients of

    this medicine (listed in section 6 of this leaflet)

  • If you have severe kidney or severe liver problems

Warnings and precautions

Mesalazine may produce red-brown urine discoloration after contact with sodium hypochlorite bleach in the toilet water. It concerns a chemical reaction between Mesalazine and bleach and is harmless.

Talk to your doctor before using Zyduco XL

  • If you have any kidney or liver problems
  • If you have previously had inflammation of the heart (which may be the result of an

    infection in the heart)

  • If you have ever developed a severe skin rash or skin peeling, blistering and/or

    mouth sores after using Zyduco XL

  • If you have had a previous allergic reaction to sulphasalazine (another medicine

    used to treat ulcerative colitis)

  • If you have narrowing or blockage of the stomach or the gut
  • If you have lung problems

Before and periodically during treatment with Zyduco XL, your doctor may take samples of your urine and blood to check that your kidneys and liver are working well and that your blood is healthy.

Kidney stones may develop with the use of Zyduco XL. Symptoms may include pain in the sides of the abdomen and blood in the urine. Take care to drink a sufficient amount of liquid during treatment with Zyduco XL.

Serious skin reactions including Drug reaction with eosinophilia and systemic symptoms (DRESS), Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) have been reported in association with Mesalazine treatment. Stop using Zyduco XL and seek medical attention immediately if you notice any of the symptoms related to these serious skin reactions described in section 4.

Talk to your doctor

If you experience strong or recurrent headache, disturbed vision, or ringing or buzzing in the ears contact your doctor immediately.

Children and adolescents

Zyduco XL is not recommended to be given to children and adolescents weighing 50 kg or less and not in children below the age of 10 years due to lack of data on safety and efficacy (see section 3).

Other medicines and Zyduco XL

Studies have shown that Zyduco XL does not interfere with the following antibiotics, used to treat infections: amoxicillin, metronidazole, or sulfamethoxazole. However, Zyduco XL may interact with some other medicines. Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

  • Mesalazine or sulphasalazine (taken for treatment of ulcerative colitis)
  • Non-steroidal anti-inflammatory drugs (for example medicines containing acetylsalicylic acid (Aspirin), ibuprofen or diclofenac)
  • Azathioprine or 6-mercaptopurine or other medicines known to affect how your bone marrow works (known as ‘immunosuppressant’ medicines which reduce the activity of your body’s immune system). Bone marrow is the material inside your bones that produces blood cells.
  • Coumarin-type anticoagulants (medicines which increase the time it takes for your blood to clot) e.g., warfarin.

Zyduco XL with food and drink

Zyduco XL should be taken with food at the same time each day. The tablets should be swallowed whole and must not be crushed or chewed.

Pregnancy and breast-feeding

Since Mesalazine crosses the placenta in pregnancy and is excreted in breast milk in small quantities, you should only use Zyduco XL during pregnancy or whilst breast-feeding if your doctor tells you to.

Adverse outcomes [including low blood cell counts (white blood cells, red blood cells, and platelets)] were reported in infants born to mothers who took Zyduco XL during pregnancy. Diarrhoea has been reported in breastfed infants of mothers who took Zyduco XL.

If you are pregnant or breast feeding, think you might be pregnant or are planning to have a baby, ask your doctor for advice about taking Zyduco XL.

Interference with laboratory tests

If you are undergoing urine tests, it is important to tell the doctor or nurse you are taking or have recently taken this medicine as it can affect some results.

Driving and using machines

Zyduco XL is unlikely to have any effect on your ability to drive or use machines.

Zyduco XL contains sodium

This medicine contains less than 1 mmol sodium (23 mg) per the maximum recommended dose (4 tablets), that is to say essentially ‘sodium-free’.

3. How to take Zyduco XL

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

The recommended dose for adults is 2.4 g to 4.8 g (two to four tablets) taken once a day for an acute episode of ulcerative colitis. If you are taking the highest daily dose of 4.8 g/day, you should be evaluated after 8 weeks treatment. Once your symptoms have cleared and to help prevent recurrence of another episode, your doctor should direct you to take 2.4 g (two tablets) once a day.

For an acute episode of ulcerative colitis (first 8 weeks of treatment) in children and adolescents weighing more than 50 kg and age 10 years or older, the recommended dose is 2.4 g to 4.8 g (two to four tablets) taken once a day.

To prevent recurrence of another episode of ulcerative colitis in children and adolescents weighing more than 50 kg and age 10 years or older, the recommended dose is 2.4 g (two tablets) taken once a day.

Remember to take your tablets at the same time each day with food. The tablets should be swallowed whole and must not be crushed or chewed.

Whilst taking this medicine, ensure you drink fluids to remain well hydrated especially after severe or prolonged episodes of vomiting and/or diarrhoea, high fever or heavy sweating.

Zyduco XL is not recommended to be given to children and adolescents weighing 50 kg or less and not in children below the age of 10 years due to lack of data on safety and efficacy.

If you take too much Zyduco XL, you may have one or more of the following symptoms: tinnitus (ringing in ears), dizziness, headache, confusion, drowsiness, shortness of breath, excess loss of water (associated with sweating, diarrhoea and vomiting), low blood sugar (which can cause light-headedness), rapid breathing, changes in the blood chemistry and increased body temperature.

If you do take too many tablets, contact your doctor, pharmacist or hospital casualty department straight away. Take your tablet pack with you.

If you forget to take Zyduco XL

It is important to take your Zyduco XL tablets every day, even when you don’t have any symptoms of ulcerative colitis. Always finish the prescribed course. If you forget to take your tablets, then take them as usual the next day. Do not take a double dose to make up for a forgotten tablet.

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.

Tell your doctor immediately

  • If you experience symptoms such as cramping, severe stomach pain, bloody and

    excessive stools (diarrhoea), fever, headache or rash. These symptoms could be a sign of Acute Intolerance Syndrome which can happen during an acute episode of ulcerative colitis. This is a serious condition which occurs rarely, but means your treatment would have to be stopped immediately.

  • If you develop unexplained bruising (without injury), rash, anaemia (feeling tired,

    weak and looking pale, especially on lips, nails and inside of eyelids), fever (high temperature), sore throat or unusual bleeding (e.g. nose bleeds).

  • If you notice reddish non-elevated, target-like or circular patches on the trunk, often

    with central blisters, skin peeling, ulcers of mouth, throat, nose, genitals and eyes, widespread rash, fever and enlarged lymph nodes. These serious skin rashes can be preceded by fever and flu-like symptoms.

  • If you develop allergic swelling of tongue, lips and around eyes.
  • If you experience strong or recurrent headache, disturbed vision, or ringing or

    buzzing in the ears. These could be symptoms of increased pressure within your skull (idiopathic intracranial hypertension).

Common side effects, occurring in less than 1 in 10 patients are: headache; changes in blood pressure, flatulence (passing wind); nausea (feeling sick); bloated or painful stomach; inflammation which causes

abdominal pain or diarrhoea; diarrhoea; indigestion; vomiting (being sick); abnormal liver function test; itching; rash, joint pain; back pain; weakness, fatigue (feeling extremely tired); fever (high temperature).

Uncommon side effects, seen in less than 1 in 100 patients are: a reduction in blood platelets which increases the risk of bleeding and bruising; dizziness; feeling sleepy or tired; trembling or shaking; ear pain; racing heartbeat; throat pain; an inflamed pancreas (associated with pain in upper abdomen and back and feeling sick); rectal polyp (a non-cancerous growth in the back passage causing symptoms such as constipation and bleeding); acne; hair loss; muscle pain; hives; swollen face.

Rare side effects, seen in less than 1 in 1000 patients are: kidney failure; severe reduction in the number of white blood cells that makes infection more likely; increased sensitivity of your skin to sun and ultraviolet light (photosensitivity).

The following side effects have been reported but it is not known exactly how often they occur:

Severe reduction in blood cells which can cause weakness or bruising; low blood cell counts; allergic reaction (hypersensitivity); serious allergic reaction which causes difficulty in breathing or dizziness; serious illness with blistering of the skin (possibly leading to peeling of the skin and resulting in painful, raw areas), mouth, eyes and genitals; allergic reaction which causes skin rash, fever and inflammation of internal organs; neuropathy (abnormal or damaged nerves giving a sensation of numbness and tingling); inflammation of the heart and lining around the heart; inflammation of the lung; difficulty in breathing or wheezing; gall stones; hepatitis (inflammation of the liver giving rise to flu-like symptoms and jaundice); hepatotoxicity (liver damage that may present as abnormal liver tests); allergic swelling of tongue, lips and around eyes; skin redness; skin rash typically on face, skin sensitivity to sunlight along with joint pain, arthritis, fatigue and overall feeling sickness; kidney problems (such as inflammation

and scarring of the kidney); kidney stones and associated pain (see also section 2); reversible decrease in sperm production.

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-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 Zyduco XL

  • Keep this medicine out of the sight and reach of children.
  • Store below 25°C.
  • Store in the original package in order to protect from moisture.
  • Do not use this medicine after the expiry date which is stated on the box after EXP.

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

  • Do not throw away any medicines via waste water or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. Contents of the pack and other information

What Zyduco XL contains

  • The active substance is Mesalazine 1200 mg.
  • The other ingredients are: Carmellose sodium, Sodium Starch Glycolate Type A,

    Hypromellose 15 CPS, Microcrystalline Cellulose, Silica Colloidal Anhydrous, Magnesium Stearate, Methacrylic Acid-Methyl Methacrylate Copolymer (1:2), Methacrylic Acid-Methyl Methacrylate Copolymer (1:1), Triethyl Citrate, Talc, Hypromellose, Talc, Macrogol, Titanium dioxide (E171), Iron oxide Red (E172) and Iron oxide yellow (E172).

What Zyduco XL looks like and contents of the pack

Pale red-brown, oval shaped, biconvex, bevel film coated tablets debossed with the ‘711’ on one side and plain on other side. The tablet should be free of all physical defects. The tablet length is approximately 20.8 mm and width is approximately 10.4 mm.

Zyduco XL is supplied in foil blister strips which are contained in a cardboard box. The pack contains 60 tablets and 120 tablets. Zyduco XL also supplied in 120’s HDPE Bottle Pack. All packs may not be marketed.

Marketing Authorisation Holder and Manufacturer

Zydus Pharmaceuticals UK Ltd

Sandretto Building

Cavalry Hill Industrial Park

Weedon Northampton

England NN74PP

United Kingdom

This leaflet was last revised in Dec-25.

To request a copy of this leaflet in Braille, large print or audio format, contact the licence holder at the above address or telephone: 0800 9956034 / email: DrugSafety@ZydusUK.com

XXXXXXX

240 mm

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PLGB 58839/0018

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 Zyduco XL 1200 mg gastro-resistant prolonged-release tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Mesalazine
Strength 1200 mg
Pharmaceutical form Modified-release tablet
Pale red-brown, oval shaped, biconvex, bevel film coated tablets debossed with the ‘711’ on one side and plain on other side. The tablet should be free of all physical defects.
The tablet length is approximately 20.8 mm and width is approximately 10.4 mm.
How is it taken Oral
Excipients Carmellose Sodium, Sodium Starch Glycolate Type A, Hypromellose 15 CPS, Microcrystalline Cellulose, Silica Colloidal Anhydrous, Magnesium Stearate, Functional Coating, Methacrylic Acid-Methyl Methacrylate Copolymer (1:2), Methacrylic Acid-Methyl Methacrylate Copolymer (1:1), Triethyl Citrate, Talc, Hypromellose, Macrogol, Titanium dioxide (E171), Iron oxide Red (E172), Iron oxide yellow (E172)
Pack sizes 60 tablet, 120 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 2 years
Storage Store below 25°C.
Store in the original package in order to protect from moisture.
Drug group (ATC) Aminosalicylic acid and similar agents
  1. A Alimentary tract and metabolism drugs
    1. A07 Antidiarrheals, intestinal antiinflammatory/antiinfective agents
      1. A07E Intestinal antiinflammatory agents
        1. A07EC Aminosalicylic acid and similar agents
          1. A07EC02 mesalazine
Marketing authorisation PLGB 58839/0018 (first authorised 13 August 2024)
Marketing authorisation holder Zydus Pharmaceuticals UK Ltd
Codes GTIN 5070003280179, 5070003280186 · BNF 01050100

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.