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Dutor 20 mg gastro-resistant capsules hard – patient leaflet, side effects, dosage

Text from the MHRA, as of · About this document

Medicine status: No longer supplied Details

Medicine strength:
20 mg
Still supplied:
The same active substance, strength and form in the NHS Dictionary of Medicines and Devices (dm+d). Ask your pharmacist or doctor before changing to another make.
Contains active substance:
ATC code:

Patient leaflet - Dutor 20 mg gastro-resistant capsules hard

1. What Dutor is and what it is used for

Dutor contains the active substance duloxetine. Duloxetine increases the levels of serotonin and noradrenaline in the nervous system.

Dutor is a medicine to be taken by mouth to treat Stress Urinary Incontinence (SUI) in women.

Stress urinary incontinence is a medical condition in which patients have accidental loss or leakage of urine during physical exertion or activities such as laughing, coughing, sneezing, lifting, or exercise.

Dutor is believed to work by increasing the strength of the muscle that holds back urine when you laugh, sneeze, or perform physical activities.

The efficacy of Dutor is reinforced when combined with a training program called Pelvic Floor Muscle Training (PFMT).

2. What you need to know before you take Dutor

Do not take Dutor if you:

  • are allergic to duloxetine or any of the other ingredients of this medicine (listed in section 6).
  • have liver disease.
  • have severe kidney disease.
  • are taking or have taken within the last 14 days, another medicine known as a monoamine oxidase inhibitor (MAOI) (see ‘Other medicines and Dutor’).
  • are taking fluvoxamine which is usually used to treat depression, ciprofloxacin or enoxacin which are used to treat some infections.

Talk to your doctor if you have high blood pressure or heart disease. Your doctor will tell you if you should be taking Dutor.

Warnings and precautions

The following are reasons why Dutor may not be suitable for you. Talk to your doctor before you take Dutor if you:

  • have depression or other conditions and are taking medicines to treat depression (see ‘Other medicines and Dutor’).
  • are taking St. John’s Wort, a herbal treatment (Hypericum perforatum).
  • have kidney disease.
  • have had seizures (fits).
  • have had mania.
  • suffer from bipolar disorder.
  • have eye problems, such as certain kinds of glaucoma (increased pressure in the eye).
  • have a history of bleeding disorders (tendency to develop bruises), especially if you are pregnant (see ‘Pregnancy and breast-feeding’).
  • are at risk of low sodium levels (for example if you are taking diuretics, especially if you are elderly).
  • are currently being treated with another medicine which may cause liver damage.
  • are taking other medicines containing duloxetine (see ‘Other medicines and Dutor’).

Dutor may cause a sensation of restlessness or an inability to sit or stand still. You should tell your doctor if this happens to you.

Medicines like Dutor (so called SSRIs/SNRIs) may cause symptoms of sexual dysfunction (see section 4). In some cases, these symptoms have continued after stopping treatment.

Thoughts of suicide and worsening of depression or anxiety disorder

Although Dutor is not indicated for the treatment of depression, its active substance (duloxetine) is used as an antidepressant medicine. If you are depressed and/or have anxiety disorders you can sometimes have thoughts of harming or killing yourself. These may be increased when first starting antidepressants, since these medicines all take time to work, usually about two weeks but sometimes longer.

You may be more likely to think like this if you:

  • have previously had thoughts about killing or harming yourself
  • are a young adult. Information from clinical trials has shown an increased risk of suicidal behaviour in adults aged less than 25 years with psychiatric conditions who were treated with an antidepressant

If you have thoughts of harming or killing yourself at any time, contact your doctor or go to a hospital straight away.

You may find it helpful to tell a relative or close friend that you are depressed or have an anxiety disorder, and ask them to read this leaflet. You might ask them to tell you if they think your depression or anxiety is getting worse, or if they are worried about changes in your behaviour.

Children and adolescents under 18 years of age

Dutor should not be used for children and adolescents under 18 years. Also, you should know that patients under 18 have an increased risk of side-effects such as suicide attempt, suicidal thoughts and hostility (predominantly aggression, oppositional behaviour and anger) when they take this class of medicines. Also, the long-term safety effects concerning growth, maturation, and cognitive and behavioural development of Dutor in this age group have not yet been demonstrated.

Other medicines and Dutor

Please tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription.

The active substance of Dutor, duloxetine, is used in other medicines for other conditions:

  • diabetic neuropathic pain, depression, anxiety and urinary incontinence

Using more than one of these medicines at the same time should be avoided. Check with your doctor if you are already taking other medicines containing duloxetine.

Your doctor should decide whether you can take Dutor with other medicines. Do not start or stop taking any medicines, including those bought without a prescription and herbal remedies, before checking with your doctor.

You should also contact your doctor:

If you experience signs and symptoms of restlessness, hallucinations, loss of coordination, fast heart beat, increased body temperature, fast changes in blood pressure, overactive reflexes, diarrhoea, coma, nausea, vomiting, as you might be suffering a serotonin syndrome.

In its most severe form, serotonin syndrome can resemble Neuroleptic Malignant Syndrome (NMS). Signs and symptoms of NMS may include a combination of fever, fast heart beat, sweating, severe muscle stiffness, confusion, increased muscle enzymes (determined by a blood test).

You should also tell your doctor if you are taking any of the following:

Monoamine oxidase inhibitors (MAOIs):

You should not take Dutor if you are taking, or have recently taken (within the last 14 days) an antidepressant medicine called a monoamine oxidase inhibitor (MAOI). Examples of MAOIs include moclobemide (an antidepressant) and linezolid (an antibiotic). Taking a MAOI together with many prescriptions medicines, including Dutor, can cause serious or even life-threatening side effects. You must wait at least 14 days after you have stopped taking an MAOI before you can take Dutor. Also, you need to wait at least 5 days after you stop taking Dutor before you take a MAOI.

Medicines that cause sleepiness:

These include medicines prescribed by your doctor including benzodiazepines, strong painkillers, antipsychotics, phenobarbital and sedative antihistamines.

Medicines that increase the level of serotonin:

Triptans, tramadol, buprenorphine, tryptophan, SSRIs (such as paroxetine and fluoxetine), SNRIs (such as venlafaxine), tricyclic antidepressants (such as clomipramine, amitriptyline), pethidine, St John’s Wort and MAOIs (such as moclobemide and linezolid). These medicines increase the risk of side effects; if you get any unusual symptom taking any of these medicines together with Dutor, you should see your doctor. These medicines may interact with Dutor and you may experience symptoms such as involuntary, rhythmic contractions of muscles, including the muscles that control movement of the eye, agitation, hallucinations, coma, excessive sweating, tremor, exaggeration of reflexes, increased muscle tension, body temperature above 38°C. Contact your doctor when experiencing such symptoms.

Oral anticoagulants or antiplatelet medicines:

Medicines which thin the blood or prevent the blood from clotting. These medicines might increase the risk of bleeding.

Dutor with food, drink and alcohol

Dutor may be taken with or without food. You should take extra care if you drink alcohol while taking Dutor.

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.

  • Tell your doctor if you become pregnant, or you are trying to become pregnant, while you are taking Dutor. You should use Dutor only after discussing the potential benefits and any potential risks to your unborn child with your doctor.
  • Make sure your midwife and/or doctor knows you are on Dutor. When taken during pregnancy, similar medicines (SSRIs) may increase the risk of a serious condition in babies, called persistent pulmonary hypertension of the newborn (PPHN), making the baby breathe faster and appear bluish. These symptoms usually begin during the first 24 hours after the baby is born. If this happens to your baby you should contact your midwife and/or doctor immediately.
  • If you take Dutor near the end of your pregnancy, your baby might have some symptoms when it is born. These usually begin at birth or within a few days of your baby being born. These symptoms may include floppy muscles, trembling, jitteriness, not feeding properly, trouble with breathing and fits. If your baby has any of these symptoms when it is born, or you are concerned about your baby’s health, contact your doctor or midwife who will be able to advise you.
  • If you take Dutor near the end of your pregnancy there is an increased risk of excessive vaginal bleeding shortly after birth, especially if you have a history of bleeding disorders. Your doctor or midwife should be aware that you are taking duloxetine so they can advise you.
  • Available data from the use of Dutor during the first three months of pregnancy do not show an increased risk of overall birth defects in general in the child. If Dutor is taken during the second half of pregnancy, there may be an increased risk that the infant will be born early (6 additional premature infants for every 100 women who take Dutor in the second half of pregnancy), mostly between weeks 35 and 36 of pregnancy.
  • Tell your doctor if you are breast-feeding. The use of Dutor while breastfeeding is not recommended. You should ask your doctor or pharmacist for advice.

Driving and using machines

Dutor may make you feel sleepy or dizzy. Do not drive or use any tools or machines until you know how Dutor affects you.

Dutor contains sucrose

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

Information on sodium content

This medicine contains less than 1 mmol sodium (23 mg) per capsule, that is to say essentially ‘sodium free’. Colour Black

3. How to take Dutor

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

The recommended dose of Dutor is 40 mg twice a day (in the morning and late afternoon/evening). Your doctor may decide to start your treatment with 20 mg twice a day for two weeks before increasing the dose to 40 mg twice a day.

Dutor is for oral use. You should swallow your capsule whole with a drink of water. Dutor may be taken with or without food.

To help you remember to take Dutor, you may find it easier to take it at the same times every day.

Do not stop taking Dutor, or change your dose, without talking to your doctor. Treating your disorder properly is important to help you get better. If it is not treated, your condition may not go away and may become more serious and difficult to treat.

If you take more Dutor than you should

Call your doctor or pharmacist immediately if you take more than the amount of Dutor prescribed by your doctor. Symptoms of overdose include sleepiness, coma, serotonin syndrome (a rare reaction which may cause feelings of great happiness, drowsiness, clumsiness, restlessness, feeling of being drunk, fever, sweating or rigid muscles), fits, vomiting and fast heart rate.

If you forget to take Dutor

If you miss a dose, take it as soon as you remember. However, if it is time for your next dose, skip the missed dose and take only a single dose as usual. Do not take a double dose to make up for a forgotten dose. Do not take more than the daily amount of Dutor that has been prescribed for you in one day.

If you stop taking Dutor

DO NOT stop taking your capsules without the advice of your doctor even if you feel better. If your doctor thinks that you no longer need Dutor he or she will ask you to reduce your dose over 2 weeks.

Some patients who suddenly stop taking Dutor after more than 1 week of therapy have had symptoms such as:

  • dizziness, tingling feelings like pins and needles or electric shock-like feelings (particularly in the head), sleep disturbances (vivid dreams, nightmares, inability to sleep), fatigue, sleepiness, feeling restless or agitated, feeling anxious, feeling sick (nausea) or being sick (vomiting), shaking (tremor), headaches, muscle pain, feeling irritable, diarrhoea, excessive sweating or vertigo.

These symptoms are usually not serious and disappear within a few days, but if you have symptoms that are troublesome you should ask your doctor for advice.

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 some side effects, although not everybody gets them. These effects are normally mild to moderate and often disappear after a short time.

Stop taking Dutor and seek urgent medical treatment, if you experience any of the following serious but very rare side effects:

  • allergic reactions
  • serious allergic reaction which causes difficulty in breathing or dizziness with swollen tongue or lips
  • vomiting blood, or black tarry stool (faeces)
  • inflammation of the liver that may cause abdominal pain and yellowing of the skin or whites of the eyes
  • liver failure, yellowing of the skin or whites of the eyes (jaundice)
  • suicidal behavior, suicidal thoughts
  • syndrome of inappropriate secretion of anti-diuretic hormone (SIADH)
  • coughing, wheezing and shortness of breath which may be accompanied by a high temperature
  • Steven-Johnson syndrome (serious illness with blistering of the skin, mouth, eyes and genitals), serious allergic reaction which causes swelling of the face or throat (angioedema).

Other Side Effects

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

  • feeling sick (nausea), dry mouth, constipation
  • fatigue

Common side effects (may affect up to 1 in 10 people)

  • lack of appetite
  • trouble sleeping, feeling agitated, less sex drive, anxiety, difficulty sleeping,
  • headache, dizziness, feeling sluggish, feeling sleepy, tremor, numbness, including numbness, pricking or tingling of the skin
  • blurred eyesight
  • feeling of dizziness or “spinning” (vertigo)
  • increased blood pressure, flushing
  • diarrhoea, stomach pain, being sick (vomiting), heartburn or indigestion
  • increased sweating
  • weakness, shivering

Uncommon side effects (may affect up to 1 in 100 people)

  • throat inflammation that causes a hoarse voice
  • decreased thyroid gland activity which can cause tiredness or weight gain
  • dehydration
  • grinding or clenching the teeth, feeling disorientated, lack of motivation, difficulty or failure to experience orgasm, unusual dreams
  • feeling nervous, difficulty concentrating, changes in sense of taste, poor sleep quality
  • large pupils (the dark centre of the eye), problems with eyesight, eyes feel dry
  • tinnitus (hearing sound in the ear when there is no external sound), ear pain
  • feeling the heart pumping in the chest, fast and/or irregular heart beat
  • fainting
  • increased yawning
  • stomach bug (gastroenteritis), inflammation of the mouth, burping, difficulty swallowing, breaking wind (flatulence), bad breath
  • (itchy) rash, night sweats, hives, cold sweats, increased tendency to bruise
  • muscle pain, muscle tightness, muscle spasm, contraction of the jaw muscle
  • difficulty to start urinating, painful urination, needing to pass urine during the night, frequent urination, abnormal urine odour
  • abnormal vaginal bleeding, menopausal symptoms,
  • chest pain, feeling cold, thirst, feeling hot
  • weight loss, weight gain
  • Dutor may cause effects that you may not be aware of, such as increases in liver enzymes or blood levels of potassium, creatine phosphokinase, sugar, or cholesterol

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

  • low levels of sodium in the blood (mostly in elderly people; the symptoms may include feeling dizzy, weak, confused, sleepy or very tired, or feeling or being sick, more serious symptoms are fainting, fits or falls), syndrome of inappropriate secretion of anti-diuretic hormone (SIADH)
  • mania (over activity, racing thoughts and decreased need for sleep), hallucinations, aggression and anger
  • “Serotonin syndrome” (a rare reaction which may cause feelings of great happiness, drowsiness, clumsiness, restlessness, feeling of being drunk, fever, sweating or rigid muscles), fits, sudden involuntary jerks or twitches of the muscles, sensation of restlessness or an inability to sit or stand still, difficulty controlling movement e.g. lack of coordination or involuntary movements of the muscles, restless legs syndrome
  • increased pressure in the eye (glaucoma)
  • dizziness, lightheadedness or fainting on standing up, cold fingers and/or toes
  • throat tightness, nose bleeds
  • passing bright red blood in your stools, inflammation of the large intestine (leading to diarrhoea)
  • sensitivity to sunlight
  • muscle twitching
  • difficulty or inability to pass urine, needing to pass more urine than normal, having a decreased urine flow
  • abnormal periods, including heavy, painful, irregular or prolonged periods, unusually light or missed periods, abnormal production of breast milk
  • excessive vaginal bleeding shortly after birth (postpartum haemorrhage)
  • falls (mostly in elderly people), abnormal gait

Very rare side effects (may affect up to 1 in 10,000 people)

  • inflammation of the blood vessels in the skin (cutaneous vasculitis)

Frequency not known (cannot be estimated from the available data)

  • Signs and symptoms of a condition called “stress cardiomyopathy” which may include chest pain, shortness of breath, dizziness, fainting, irregular heart beat

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 Dutor

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 and blister/bottle pack. The expiry date refers to the last day of that month.

This medicine does not require any special storage conditions.

Shelf life after first opening of the HDPE bottle:

28’s container: 30 days

98’s and 100’s container: 100 days

Do not throw away any medicines via wastewater. 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 Dutor contains

The active substance is duloxetine.

Dutor 20 mg:

Each gastro-resistant capsule, hard contains 20 mg of duloxetine (as hydrochloride). Dutor 40 mg:

Each gastro-resistant capsule, hard contains 40 mg of duloxetine (as hydrochloride).

The other ingredients are:

Capsule content: Hypromellose 2910, hypromellose acetate succinate, sucrose, sugar spheres (consisting of sucrose, maize starch, (liquid) glucose, purified water), talc, titanium dioxide (E 171), triethyl citrate, macrogol 400

Dutor 20 mg:

Capsule shell: gelatine, sodium lauryl sulphate, titanium dioxide (E 171), indigo carmine (E 132)

Dutor 40 mg:

Capsule shell: gelatine, sodium lauryl sulphate, titanium dioxide (E 171), Indigo carmine (E 132), iron oxide yellow (E 172), iron oxide red (E 172)

Printing ink: shellac, black iron oxide (E 172), potassium hydroxide

What Dutor looks like and contents of the pack

Dutor is a gastro-resistant capsule, hard. Each capsule of Dutor contains pellets of duloxetine with a covering to protect them from stomach acid.

Dutor 20 mg: Size ‘4’ hard gelatin capsule having light blue cap and body, imprinted with ’20 mg’ on the body and ‘1109’ on the cap with black ink, containing off white to reddish brown coloured pellets.

Dutor 40 mg: Size ‘2’ hard gelatin capsule having light blue cap and orange body, imprinted with ’40 mg’ on the body and ‘1112’ on the cap with black ink, containing off white to reddish brown coloured pellets.

Pack sizes:

Dutor 20 mg is available in blister packs of 7, 28, 56, 98 capsules.

Dutor 40 mg is available in blister packs of 7, 28, 56, 98, 140 and 196 (2 x 98) capsules. Dutor 20 mg/40 mg is available in HDPE bottles with PP screw cap of 28, 98 and 100 capsules

Not all pack sizes may be marketed.

Marketing authorisation holder and Manufacturer Torrent Pharma (UK) Ltd.

3rd Floor, Nexus Building, 4 Gatwick Road, Crawley, West Sussex, RH10 9BG, United Kingdom

This leaflet was last approved in 09/2024.

8098050-7803

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 36687/0185

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 Dutor 20 mg gastro-resistant capsules hard

Active substance Duloxetine
Strength 20 mg
Pharmaceutical form Gastro-resistant capsule
Size ‘4’ hard gelatin capsule having light blue cap and body, imprinted with ’20 mg’ on the body and ‘1109’ on the cap with black ink, containing off white to reddish brown coloured pellets.
How is it taken Oral
Excipients Hypromellose 2910, Hypromellose acetate succinate, Sucrose, Sugar spheres (consisting of sucrose, maize starch, (liquid) glucose, purified water) Talc, Titanium dioxide (E 171), Triethyl citrate, Macrogol 400, Gelatine, Sodium lauryl sulphate,, Titanium dioxide (E 171),, Indigo carmine (E 132), Shellac, Black iron oxide (E 172), Potassium hydroxide.
Is it available? No, all its packs are listed as discontinued (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 2 years
HDPE bottles:
Shelf life after first opening of the bottle: 28’s container: 30 days
98’s and 100’s container: 100 days
Storage This medicinal product does not require any special storage conditions.
Drug group (ATC) Psychoanaleptics; Other antidepressants
  1. N Nervous system drugs
    1. N06 Psychoanaleptics
      1. N06A Antidepressants
        1. N06AX Other antidepressants
          1. N06AX21 duloxetine
Marketing authorisation PL 36687/0185 (first authorised 18 December 2019)
Marketing authorisation holder Torrent Pharma (UK) Ltd.
Codes BNF 07040200

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.