Patient info Open main menu

Mesalazine Tillotts 800 mg modified-release tablets – patient leaflet, side effects, dosage

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

Medicine status: Prescription only (POM) Details

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

Patient leaflet - Mesalazine Tillotts 800 mg modified-release tablets

1. What Mesalazine Tillotts 800 mg MR tablets are and what they are used for

Mesalazine Tillotts 800 mg MR tablets contain the active substance mesalazine. This is an anti-inflammatory medicine used to treat ulcerative colitis and Crohn’s ileo-colitis.

Mesalazine Tillotts 800 mg MR tablets are used: • to treat and prevent further episodes of ulcerative colitis

  • to prevent further episodes of Crohn’s ileo-colitis once the disease has been brought under control. Ulcerative colitis is a disease of the large bowel (colon) or back passage (rectum), in which the lining of the bowel becomes inflamed (red and swollen). Crohn’s ileo-colitis is a disease that affects the small bowel (terminal ileum) and the large bowel (colon) in which the lining of the bowel becomes inflamed. This can lead to ulcers, abscesses and narrowing (strictures) in the bowel.

Mesalazine Tillotts 800 mg MR tablets acts locally at the site of inflammation (colon, rectum and terminal ileum) to reduce this inflammation.

2. What you need to know before you take Mesalazine Tillotts 800 mg MR tablets

Do not take Mesalazine Tillotts 800 mg MR tablets

  • If you are allergic to mesalazine or any of the other ingredients of this medication (listed in section 6) • If you are allergic to salicylates (e. g. aspirin) • If you have severe kidney problems
  • If you have severe liver problems

Warnings and precautions

Talk to your doctor before taking Mesalazine Tillotts 800 mg MR tablets if you have any medical conditions or illnesses, particularly if you have: • ever had any problems with your kidneys. This is especially important if you are elderly. • any lung problems, e. g. asthma.

  • suffered an allergy to sulfasalazine in the past. • ever had allergic reactions of your heart such as inflammation of the heart muscle or heart sac. If you have had previous suspected mesalazine-induced allergic reactions of your heart, then Mesalazine Tillotts 800 mg MR tablets must not be taken. Mesalazine Tillotts 800 mg MR tablets can be taken with care if you have had a previous allergic reaction of the heart not caused by mesalazine.
  • ever developed a severe skin rash or skin peeling, blistering and/or mouth sores after using mesalazine.

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

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 mesalazine and seek medical attention immediately if you notice any of the symptoms related to these serious skin reactions described in section 4. If you have an ulcer of the stomach or intestine, you may take Mesalazine Tillotts 800 mg MR tablets with care. Kidney stones may develop with use of Mesalazine Tillotts 800 mg MR tablets. Symptoms may include

pain in sides of abdomen and blood in urine. Take care to drink sufficient amount of liquid during treatment with Mesalazine Tillotts 800 mg MR tablets. 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.

Test for your liver, kidney and blood

Before and while you are taking Mesalazine Tillotts 800 mg MR tablets, your doctor may want to monitor you from time to time, to check that your liver, kidneys, blood and lungs are all right.

There have been a few reports of intact tablets in the stool. What appear to be intact tablets may sometimes be the remains of the tablet coating. If you often observe tablets or tablet shells in the stool, you should consult your doctor.

Children and adolescents

Mesalazine Tillotts 800 mg MR tablets is only recommended for use in children 6 years and older. Other medicines and Mesalazine Tillotts 800 mg MR tablets

Tell your doctor or pharmacist if you are taking or have recently taken or might take any other medicines such as:

  • drugs affecting the immune system (e.g. azathioprine, or 6-mercaptopurine or thioguanine) • drugs that prevent the formation of blood clots (anticoagulants, e.g., warfarin)

Mesalazine Tillotts 800 mg MR tablets with food, drink and alcohol

You may eat and drink normally (including alcohol), when taking Mesalazine Tillotts 800 mg MR tablets. Pregnancy and breast-feeding and fertility

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.

Driving and using machines

Mesalazine Tillotts 800 mg MR tablets are not expected to affect your ability to drive or operate machinery. However, if you are affected in anyway do not drive or operate machinery.

Important information about some of the ingredients of Mesalazine Tillotts 800 mg MR tablets

People who are intolerant to lactose should note that Mesalazine Tillotts 800 mg MR tablets contain a small amount of lactose. If you doctor has told you that you have intolerance to some sugars, contact your doctor before taking this medicine. This medicine contains less than 1 mmol sodium (23 mg) per dosage unit, i.e. is essentially “sodium-free”.

3. How to take Mesalazine Tillotts 800 mg MR tablets

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

Mesalazine Tillotts 800 mg MR tablets should be taken before meals. This medication must be swallowed whole preferably with some liquid. Do not chew, crush or break the tablets before swallowing them. Whilst taking this medication ensure you drink adequate fluids to remain well hydrated, especially after severe or prolonged episodes of vomiting and/ or diarrhoea, high fever or heavy sweating. This is to avoid problems with your kidney.

The recommended dose is:

Adults (including the elderly)

To treat acute phases of ulcerative colitis your daily dose is 3 to 6 tablets.

3 tablets may be taken once daily or in divided doses (as advised by your doctor).

Above 3 tablets a day should be taken in divided doses.

To prevent ulcerative colitis or Crohn’s ileo-colitis your daily dose is 2 to 3 tablets once daily or in divided doses. Do not take more than 6 tablets per day, and do not take more than 3 tablets together at the same time.

Use in children and adolescents

Mesalazine Tillotts 800 mg MR tablets are only recommended for use in children 6 years and older. The daily dose depends on the child’s weight. • To treat acute phases of ulcerative colitis: 20-30 kg weight: one tablet per day.

30-40 kg weight: one to two tablets per day in divided doses.

Mesalazine Tillotts 800 mg Modified-Release Tablets

mesalazine

Above 40 kg weight: two to three tablets per day in divided doses.

The total dose should not exceed 4 g/day.

  • To prevent ulcerative colitis or Crohn’s ileo-colitis: 30-40 kg weight: one tablet per day.

Above 40 kg weight: one to two tablets per day in divided doses.

The total dose should not exceed 2 g/day. It is generally recommended that half the adult dose may be given to children up to 40 kg weight; and the normal adult dose to those above 40 kg. If you take more Mesalazine Tillotts 800 mg MR tablets than you should

You should not take a higher dose than your doctor has prescribed for you. Contact your nearest hospital casualty department or a doctor for advice if you or anyone else has swallowed too many tablets or if you think a child has swallowed any. Take this leaflet, and any tablets that you still have to show the doctor. If you forget to take Mesalazine Tillotts 800 mg MR tablets

If you forget to take a dose at the right time, take one as soon as you remember, unless it is nearly time to take the next one. Do not take a double dose to make up for a forgotten dose.

If you stop taking Mesalazine Tillotts 800 mg MR tablets

Do not stop taking Mesalazine Tillotts 800 mg MR tablets without talking to your doctor first even if you feel better.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. Possible side-effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. Organ specific side effects affecting the heart, lungs, liver, kidneys, pancreas, skin and subcutaneous tissue have been reported. Stop taking the medicine and seek urgent medical advice immediately if you experience any of the following:

  • 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
  • Unexplained bruising (without injury), bleeding under your skin, purple spots or patches under your skin, 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).
  • Lung disease (scarring of lung tissue, allergic reaction) resulting in difficulty in breathing, cough, wheezing and collection of fluid in the lungs, pneumonia
  • Abnormal liver function tests, hepatitis (inflammation of the liver giving rise to flu-like symptoms and jaundice)
  • Inflammation of the heart with signs like chest pains or palpitations
  • Disorder of the immune system (lupus-like syndrome) which can cause inflammation of the heart sac or membranes around the lungs and heart, rash and /or joint pain
  • Kidney problems (associated with blood in urine and/or swelling in feet and ankles), kidney failure, which may be reversible if treatment is stopped early Tell your doctor immediately 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) (frequency not known [cannot be estimated from the available data]). The following side effects have been reported at the approximate frequencies shown:

Common (may affect up to 1 in 10 people)

  • rash
  • indigestion

Uncommon (may affect up to 1 in 100 people)

  • fever
  • high number of white blood cells called eosinophil granulocytes
  • sensation of tingling, pricking and numbness
  • hives, itching skin
  • chest pain

Rare (may affect up to 1 in 1000 people)

  • headache
  • dizziness
  • diarrhoea, stomach pain, wind (flatulence), feeling of unease and discomfort in the stomach with an urge to vomit and vomiting
  • increased sensitivity of your skin to sun and ultraviolet light (photosensitivity).

Very rare (may affect up to 1 in 10000 people)

  • severe reduction in blood cells which can cause weakness, bruising or make infections more likely,

    low blood cell counts; reduction in blood platelets which increases the risk of bleeding

    • allergic reactions such as rash or skin eruption
    • fever that occurs while taking the medicine and which disappears when the medicine is stopped (drug fever)
    • immune system disease that can involve organs and joints
    • ulcerative colitis involving the entire large intestine
    • abnormal or damaged nerves giving a sensation of numbness or tingling
    • inflamed pancreas (associated with pain in upper abdomen and back and feeling sick)
    • abnormal liver function tests, hepatitis (inflammation of the liver giving rise to flu-like symptoms and jaundice)
    • muscle or joint pain
    • hair loss
    • reversible decrease in sperm production Not known (frequency cannot be estimated from available data)
    • inflammation of the membranes of the pleural cavity surrounding the lungs (pleurisy)
    • intolerance to mesalazine sometimes with worsening symptoms of underlying disease
    • kidney stones and associated kidney pain (see also section 2)
    • weight loss
    • laboratory test results out of normal range 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 any 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 Mesalazine Tillotts 800 mg MR tablets

Keep out of the sight and reach of children. Do not store above 25 °C.

Keep the tablets in the original package to protect them from moisture.

Do not use this medicine after the expiry date which is stated on the outer packaging.

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

6. Contents of the pack and other information

Is this leaflet hard to see or read? Telephone 0800 1985000 for help.

What Mesalazine Tillotts 800 mg MR tablets contain

The active substance is mesalazine. Each tablet contains 800 mg mesalazine

The other ingredients are lactose monohydrate, sodium starch glycolate (Type A), triethyl citrate, talc E553b, methacrylic acide – methylmethacrylate copolymer (1:2), povidone E1201, magnesium stearate (vegetable origin), iron oxides E172, macrogol 6000 What Mesalazine Tillotts 800 mg MR tablets look like and contents of the pack

Mesalazine Tillotts 800 mg Modified-release tablets are red-brown, oblong, tablets.

They are available in pack sizes of 90 or 180 tablets. Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer The marketing authorisation holder is:

Tillotts Pharma UK Ltd,

Wellingore Hall, Wellingore

Lincolnshire, LN5 0HX, UK

Tel: + 44 (0) 1522 813500

e-mail: ukinfo@tillotts.com

The manufacturers are:

Haupt Pharma Wülfing GmbH,31028 Gronau, Germany

Rottendorf Pharma GmbH, 59320 Ennigerloh, Germany

Tillotts Pharma GmbH, 79618 Rheinfelden, Germany To listen to or request a copy of this leaflet in Braille, large print or audio please call, free of charge: 0800 198 5000 (UK only)

Please be ready to give the following information: Product name

Mesalazine Tillotts 800 mg Modified -release tablets

Reference number PL 36633/0017

This is a service provided by the Royal National Institute of Blind People.

This leaflet was last revised in September 2025.

15601-1

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 36633/0017

Last revision stated in the text: September 2025 · 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 Mesalazine Tillotts 800 mg modified-release tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Mesalazine
Strength 800 mg
Pharmaceutical form Gastro-resistant tablet
Red-brown, oblong, modified-release tablet.
How is it taken Oral
Excipients Lactose monohydrate, Sodium starch glycolate (Type A), Magnesium stearate (vegetable origin), Talc E553b, Povidone E1201, Methacrylic acid – methyl methacrylate copolymer (1:2), Triethyl citrate, Iron oxides E172, Macrogol 6000.
Pack sizes 90 tablet, 180 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years.
Storage Do not store above 25 °C. Store in the original package to protect from moisture.
Drug group (ATC) Intestinal anti-inflammatory 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 PL 36633/0017 (first authorised 26 November 2025)
Marketing authorisation holder Tillotts Pharma UK Limited
Codes GTIN 7640129620197, 7640129620203, 7640129622887, 7640129622894 · 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.