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Flagyl 500 mg suppositories – patient leaflet, side effects, dosage

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

Medicine status: Prescription only (POM) Details

Medicine strength:
500 mg
Contains active substance:

Patient leaflet - Flagyl 500 mg suppositories

1. WHAT FLAGYL® IS AND WHAT IT IS USED FOR

The name of this medicine is Flagyl® 500mg or 1g Suppositories (called Flagyl® in this leaflet). Flagyl® contains a medicine called metronidazole. This be-longs to a group of medicines called antibiotics. It works by killing the bacteria that cause infections in your body.

It can be used to:

  • Treat infections of the blood, brain, lung, bones, ge-nital tract, pelvic area and stomach
  • Prevent infections after surgery

If you need any further information on your illness, speak to your doctor.

2. WHAT YOU NEED TO KNOW BEFORE YOU USE FLAGYL®

Do not use Flagyl® if:

x You are allergic (hypersensitive) to metronidazole, nitroimi-dazoles (e.g. tinidazole) or any of the other ingredients of this medicine (see section 6). Signs of an allergic reaction include: a rash, swallowing or breathing problems, swelling of your lips, face, throat or tongue.

Do not use Flagyl® if any of the above apply to you. If you are not sure, talk to your doctor or pharmacist before using Flagyl®.

Warnings and precautions

Talk to your doctor or pharmacist before using Flagyl® if: • You have or have ever had a liver problem

  • You are having kidney dialysis (see section 3: ‘People ha-ving kidney dialysis’)
  • You have a disease of the nervous system

If you are not sure if any of the above apply to you, talk to your doctor or pharmacist before using Flagyl®.

Do this even if they have applied in the past.

Tell your doctor immediately and stop taking Flagyl® if you develop: stomach pain, anorexia (loss of appetite), nau-sea (feeling sick), vomiting (being sick), fever, malaise, fati-gue, vertigo (spinning sensation), jaundice, dark urine, putty or mastic-coloured stools or itching.

Cases of severe liver toxicity/acute liver failure, including cases with a fatal outcome, in patients with Cockayne syndro-me have been reported with Flagyl®.

If you are affected by Cockayne syndrome, your doctor should also monitor your liver function frequently while you are being treated with Flagyl® and afterwards.

Serious skin reactions including Stevens-Johnson syndro-me (SJS), toxic epidermal necrolysis (TEN), acute generalised exanthematous pustulosis (AGEP) have been reported with the use of Flagyl®:

  • SJS/TEN can appear initially as reddish target-like spots or circular patches often with central blisters on the trunk. Also, ulcers of the mouth, throat, nose, genitals and eyes (red and swollen eyes) can occur. These serious skin ra-shes are often preceded by fever and/or flu-like symptoms. The rashes may progress to widespread peeling of the skin and life-threatening complications or be fatal. • AGEP appears at the initiation of treatment as a red, scaly widespread rash with bumps under the skin and blisters accompanied by fever. The most common location: mainly localised on the skin folds, trunk and upper extremities. The highest risk for occurrence of serious skin reactions is within one week, typically, within 48 hours

after start of treatment. If you develop a serious rash or another of these skin symptoms, stop taking Flagyl® and contact your doctor or seek medical attention immedia-tely.

Other medicines and Flagyl®

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines. This in-cludes medicines you buy without a prescription, including herbal medicines. This is because Flagyl® can affect the way some other medicines work. Also some medicines can affect the way Flagyl® works. In particular, tell your doctor if you are taking any of the following medicines:

  • Medicines used to thin the blood such as warfarin • Lithium for mental illness
  • Phenobarbital or phenytoin for epilepsy
  • 5-fluorouracil for cancer
  • Busulfan for leukaemia (cancer of the blood cells) • Ciclosporin – to prevent rejection of organs after a tran-splant
  • Disulfiram for alcoholism
  • Medicines that may cause heart rhythm disturbances (so-called QT prolongation which can be seen on ECG) such as:

    • certain anti-arrhythmics (medicines for heart rhythm di-sorders)
    • certain antibiotics
    • medication primarily used to manage psychosis (inclu-ding delusions, hallucinations, paranoia or disordered thought)

If you are not sure, talk to your doctor or pharmacist before using Flagyl®.

Flagyl® with alcohol

Do not drink any alcohol while you are using Flagyl® and for 48 hours after finishing your course. Drinking alcohol while using Flagyl® might cause unpleasant side effects, such as feeling sick (nausea), being sick

(vomiting), stomach pain, hot flushes, very fast or uneven he-artbeat (palpitations) and headache.

Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before using Flagyl® if:

  • You are pregnant, might become pregnant or think you may be pregnant. Flagyl® should not be taken during pre-gnancy unless considered absolutely necessary.
  • You are breast-feeding. It is better not to use Flagyl® if you are breast-feeding. This is because small amounts may pass into the mother’s milk.

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

While using Flagyl® you may feel dizzy or experience vertigo (spinning sensation), confusion, hallucinations (seeing or hearing things that are not there), convulsions (fits) or temporary eyesight problems (such as blurred or double vi-sion). If this happens, do not drive or use any machinery or tools.

Tests

Your doctor may wish to carry out some tests if you have been using this medicine for more than 10 days.

If you are going to have a blood test, tell the doctor or nurse performing the test that you are using Flagyl®. Flagyl® can af-fect the results of some blood tests.

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

3. HOW TO USE FLAGYL®

How to remove your suppositories from the pack

  1. 1. Tear off a

section containing

one suppository

  1. 2.

    Pull apart the plastic flaps

    1. 3. Use the

flaps to peel

the plastic

away from the

suppository

Using your medicine

Always use this medicine exactly as your doctor or pharmacist has told you.

It is important to finish a full course of treatment. The length of a course will depend on your needs and the illness being treated.

Check with your doctor or pharmacist if you are not sure. • Remember to wash your hands before and after you insert the suppository.

  • Flagyl® suppositories are used by putting them into your back passage (rectum).
  • The dose of Flagyl® will depend on your needs and the illness being treated.
  • The length of your treatment will depend on the type of infection you have and how bad it is. The recommended dose is:
  • Suppositories are normally used for 3 days. • As soon as possible after starting treatment with the suppositories, your doctor will suggest changing to a medicine taken by mouth.
  • However, after 3 days, if your doctor wants you or your child to carry on using the suppositories, you will pro-

    PACKAGE LEAFLET: INFORMATION FOR

    THE USER

    Flagyl® 500mg and 1g Suppositories

    (Metronidazole)

    1 2 IST13000073076-B - 54002099

    bably be told to use the suppositories every 12 hours.

    The usual doses for adults and children using suppo-sitories are provided below:

    To treat infections

    Adults and children over 10 years

    • Use one 1g suppository, every 8 hours for 3 days. See above for dosing after 3 days.

Children aged 5 - 10 years

  • Use one 500mg suppository, every 8 hours for 3 days. See above for dosing after 3 days. Children aged 1 - 5 years
  • Use one half of a 500mg suppository, every 8 hours for 3 days. See above for dosing after 3 days.

Infants under 1 year old

  • Use one quarter of a 500mg suppository, every 8 hours for 3 days. See above for dosing after 3 days.

To prevent infections from happening after surgery Adults and children over 10 years

  • Use one 1g suppository 2 hours before surgery.
  • Repeat every 8 hours for up to 3 days. See above for dosing after 3 days.

Children aged 5 - 10 years

  • Use one 500mg suppository 2 hours before surgery.
  • Repeat every 8 hours for up to 3 days. See above for dosing after 3 days.

People having kidney dialysis

Your doctor may tell you to stop using Flagyl® during your dialysis and start using it again when your dialysis is finished.

People with liver problems

Your doctor may tell you to use a lower dose or to use the medicine less often.

If you use more Flagyl® than you should

If you have used more suppositories than you should or if you or a child swallow any suppositories, tell a doctor or go to a hospital casualty department strai-ght away. Take the pack and any suppositories left with you. This is so that the doctors know what you have used.

If you forget to use Flagyl®

If you forget to use a Flagyl® suppository, use it as soon as you remember. However if it is nearly time for the next dose, skip the missed dose. Do not use a double dose to make up for a forgotten dose. If you stop using Flagyl®

You should only stop using Flagyl® if your doctor tells

you to. It is essential to take the medicine and not stop and start as this could cause unwanted side ef-fects. 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 ef-fects, although not everybody gets them. Stop using Flagyl® and see a doctor or go to a hospital straight away if you notice any of the following serious side effects – you may need ur-gent medical treatment:

  • You have an allergic reaction. The signs may in-clude: swelling of the hands, feet, ankles, face, lips or throat which may cause difficulty in swallowing or breathing, an itchy, lumpy rash (hives) or nettle rash (urticaria).
  • A serious but very rare side effect is a brain di-sease (encephalopathy). Symptoms vary but you might get a fever, stiff neck, headache, or see or hear things that aren’t there. You might also have problems using your arms and legs, problems with speaking or feel confused.
  • You develop skin rashes including Stevens-John-son syndrome or toxic epidermal necrolysis. These can appear as reddish target-like spots or circular patches often with central blisters on the trunk, skin peeling, ulcers of the mouth, throat, nose, genitals and eyes and can be preceded by fever and flu-like symptoms. Stop using Flagyl® if you develop these symptoms and contact your doctor or seek medical attention immediately. See also section 2.
  • You develop a red, scaly widespread rash with bu-mps under the skin and blisters accompanied by fever at the initiation of treatment (acute generali-sed exanthematous pustulosis). Stop using Flagyl® if you develop these symptoms and contact your doctor or seek medical attention immediately. See also section 2.
  • Yellowing of the skin and eyes. This could be due to a liver problem (jaundice).
  • Unexpected infections, mouth ulcers, bruising, ble-eding gums, or severe tiredness.

This could be caused by a blood problem. • Severe stomach pain which may reach through to your back (pancreatitis)

Tell your doctor or pharmacist if any of the fol-lowing side effects get serious or lasts longer than a few days, or if you notice any side effects not listed in this leaflet:

Very rare (affects less than 1 in 10,000 people)

  • Fits (convulsions)
  • Mental problems such as feeling confused and seeing or hearing things that are not there (halluci-nations)
  • Problems with your eyesight such as blurred or double vision
  • Skin rash or flushing
  • Headache
  • Darkening of the urine
  • Feeling sleepy or dizzy
  • Pains in the muscles or joints
  • Liver problems including life-threatening liver fai-lure (hepatocellular liver injury)

Not known (frequency cannot be estimated from the available data)

  • Numbness, tingling, pain, or a feeling of weakness, in the arms or legs
  • Unpleasant taste in the mouth, furred tongue • Feeling sick (nausea), being sick (vomiting), upset stomach, stomach pain or diarrhoea
  • Loss of appetite
  • Fever
  • Feeling depressed
  • Pain in your eyes (optic neuritis)
  • A group of symptoms together including: fever, nausea, vo-miting, headache, stiff neck and extreme sensitivity to bright light. This may be caused by an inflammation of the mem-branes that cover the brain and spinal cord (meningitis)
  • Hearing impairment / hearing loss
  • Ringing in the ears (tinnitus)
  • Vertigo (spinning sensation)
  • You get a rash or skin discolouration with or without raised areas which often reoccurs at the same location each time the drug is used.
  • Acute liver failure in patients with Cockayne Syndrome (see section 2 ‘Warnings and precautions’)
  • Heart rhythm disturbances (so-called QT prolongation which can be seen on ECG), particularly when Flagyl® is used with other medicines that may cause heart rhythm disturbances.
  • PRES - A brain condition with symptoms such as headache, confusion, visual disturbance and seizures

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 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 FLAGYL®

Keep this medicine out of the sight and reach of chil-dren.

Store below 20°C in the original package in order to protect from light.

Do not use this medicine after the expiry date which is stated on the pack 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 any medicines you no longer use. These mea-sures will help protect the environment.

6. CONTENTS OF THE PACK AND OTHER INFORMATION

What Flagyl® Suppositories contain

Each suppository contains 500mg or 1g of metroni-dazole as the active substance.

Other ingredients are: suppository bases E75 and W35, which are vegetable fats.

What Flagyl® Suppositories look like and conten-ts of the pack

Flagyl® 500mg and 1g Suppositories are cream co-loured, smooth surfaced and torpedo shaped. They are available in blister packs of 10 suppositories Marketing Authorisation Holder and Manufacturer

Marketing Authorisation Holder

Fidia Pharma UK Ltd

170 Edmund Street, Ground Floor

Birmingham, B3 2HB, UK

Tel: 0121 468 2143

Email: medinfo@fidiapharma.uk

Manufacturer

Haupt Pharma, Livron, France

This leaflet does not contain all the information about your medicine. If you have any questions or you are not sure about anything ask your doctor or pharmacist. This leaflet was revised in November 2025.

3 4 IST13000073076-B - 54002099

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 56485/0002

Last revision stated in the text: November 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 Flagyl 500 mg suppositories

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Metronidazole
Strength 500 mg
Pharmaceutical form Suppository
A cream coloured, smooth, torpedo-shaped suppository.
How is it taken Rectal
Excipients Flagyl suppository also contain the following excipients: suppository base E75 and suppository base W35.
Pack sizes 10 suppository
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years
Storage Store below 20°C.
Store in the original package in order to protect from light.
Drug group (ATC) Anti-bacterials for systemic use
  1. P Antiparasitic products, insecticides and repellents
    1. P01 Antiprotozoals
      1. P01A Agents against amoebiasis and other protozoal diseases
        1. P01AB Nitroimidazole derivatives, antiprotozoal agents against amoebiasis and other protozoal diseases
          1. P01AB01 metronidazole
Marketing authorisation PL 56485/0002 (first authorised 10 September 1991)
Marketing authorisation holder Fidia Pharma UK Ltd
Codes GTIN 8055267240630 · BNF 05011100

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.