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Solifenacin Succinate/tamsulosin Hydrochloride Torrent 6 mg/0.4 mg modified release tablets – patient leaflet, side effects, dosage

Updated:
Key facts
Status:
Prescription only (POM)
Medicine strength:
6 mg/0.4 mg
Contains active substances:

Patient leaflet - Solifenacin Succinate/tamsulosin Hydrochloride Torrent 6 mg/0.4 mg modified release tablets

1. What Solifenacin succinate/Tamsulosin hydrochloride is and what it is used for

Solifenacin succinate/Tamsulosin hydrochloride is a combination of two different medicines called solifenacin and tamsulosin in one tablet. Solifenacin belongs to a group of medicines called anticholinergics and tamsulosin belongs to a group of medicines called alpha-blockers.

Solifenacin succinate/Tamsulosin hydrochloride is used in men to treat both moderate to severe storage symptoms and voiding symptoms of the lower urinary tract which are caused by bladder problems and an enlarged prostate (benign prostatic hyperplasia). Solifenacin succinate/Tamsulosin hydrochloride is used when previous treatment with a monoproduct for this condition did not relieve symptoms adequately.

As the prostate grows, it can lead to urinary problems (voiding symptoms) such as hesitancy (difficulty to start urinating), difficulty urinating (poor stream), dribbling and feeling of incomplete bladder emptying. At the same time, the bladder is also affected and contracts spontaneously at times you do not want to void. This causes storage symptoms such as changes in bladder sensation, urgency (having a strong, sudden desire to urinate without prior warning), and having to urinate more frequently.

Solifenacin reduces the undesired contractions of your bladder and increases the amount of urine that your bladder can hold. Therefore you can wait longer before you have to go to the toilet. Tamsulosin enables urine to pass more readily through the urethra and facilitates urination.

2. What you need to know before you use Solifenacin succinate/Tamsulosin hydrochloride

Do not use Solifenacin succinate/Tamsulosin hydrochloride if:

  • you are allergic to solifenacin or tamsulosin or any of the other ingredients of this medicine (listed in section 6).
  • you are undergoing kidney dialysis.
  • you have a severe liver disease.
  • you suffer from severe kidney disease AND if, at the same time, you are being treated with medicines that may decrease the

    removal of Solifenacin succinate/Tamsulosin hydrochloride from the body (for example ketoconazole, ritonavir, nelfinavir, itraconazole). Your doctor or pharmacist will have informed you if this is the case.

  • you suffer from moderate liver disease AND if, at the same time, you are being treated with medicines that may decrease the

    removal of Solifenacin succinate/Tamsulosin hydrochloride from the body (for example ketoconazole, ritonavir, nelfinavir, itraconazole). Your doctor or pharmacist will have informed you if this is the case.

  • you have a severe stomach or bowel condition (including toxic megacolon, a complication associated with ulcerative

    colitis).

  • you suffer from a muscle disease called myasthenia gravis, which can cause an extreme weakness of certain muscles.
  • you suffer from increased pressure in the eyes (glaucoma), with gradual loss of eye sight.
  • you suffer from fainting due to reduced blood pressure when changing posture (going to sit up or stand up); this is called

    orthostatic hypotension.

Tell your doctor if you think that any of these conditions apply to you.

Warnings and precautions

Talk to your doctor or pharmacist before using Solifenacin succinate/Tamsulosin hydrochloride if:

  • you have an inability to pass water (urinary retention).
  • you have some obstruction of the digestive system.
  • you are at risk of your digestive system slowing down (stomach and bowel movements). Your doctor will have informed

    you if this is the case.

  • you have a stomach tear (hiatus hernia) or heartburn and/or if, at the same time, you are taking medicines that can cause

    or worsen oesophagitis.

  • you suffer from a certain type of nervous disease (autonomic neuropathy).
  • you suffer from severe kidney disease.
  • you suffer from moderate liver disease.

Periodic medical examinations are necessary to monitor the development of the condition you are being treated for. Solifenacin succinate/Tamsulosin hydrochloride can affect your blood pressure which can make you feel dizzy, light headed or rarely can make you faint (orthostatic hypotension). You should sit or lie down if you experience any of these symptoms until they disappear.

If you are undergoing or have been scheduled for eye surgery because of cloudiness of the lens (cataract) or increased pressure in the eyes (glaucoma), please inform your eye specialist that you have previously used, are using or are planning to use Solifenacin succinate/Tamsulosin hydrochloride. The specialist can then take appropriate precautions with respect to medication and surgical techniques to be used. Ask your doctor whether or not you should postpone or temporarily stop taking this medicine when undergoing eye surgery because of a cloudy lens (cataract) or increased pressure in the eye (glaucoma). Children and adolescents

Do not give this medicine to children and adolescents.

Other medicines and Solifenacin succinate/Tamsulosin hydrochloride

Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines. It is especially important to inform your doctor if you are using:

  • medicines like ketoconazole, erythromycin, ritonavir, nelfinavir, itraconazole, verapamil, diltiazem, and paroxetine which

    decrease the rate at which Solifenacin succinate/Tamsulosin hydrochloride is removed from the body.

  • other anticholinergic medicines, as effects and side effects of both medications can be enhanced if you are taking two

    medicines of the same type.

  • cholinergics, as they can reduce the effect of Solifenacin succinate/Tamsulosin hydrochloride.
  • medicines like metoclopramide and cisapride, which make the digestive system work faster. Solifenacin succinate/

    Tamsulosin hydrochloride can reduce their effect.

  • other alpha-blockers, as this may cause an unwanted decrease in blood pressure.
  • medicines such as bisphosphonates, that can cause or exacerbate inflammation of the gullet (oesophagitis). Solifenacin succinate/Tamsulosin hydrochloride with food and drink

Solifenacin succinate/Tamsulosin hydrochloride can be taken with or without food, according to your preference. Pregnancy, breast-feeding and fertility

Solifenacin succinate/Tamsulosin hydrochloride is not indicated for use by women.

In men, abnormal ejaculation has been reported (ejaculation disorder). This means that the semen does not leave the body via the urethra, but instead goes into the bladder (retrograde ejaculation) or the ejaculation volume is reduced or absent (ejaculation failure). This phenomenon is harmless.

Driving and using machines

Solifenacin succinate/Tamsulosin hydrochloride might cause dizziness, blurred vision, tiredness and, uncommonly, sleepiness. If you suffer from these side effects, do not drive or operate machinery.

3. How to use Solifenacin succinate/Tamsulosin hydrochloride

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

The maximum daily dose is one tablet containing 6 mg of solifenacin and 0.4 mg of tamsulosin, taken by mouth. It can be taken with or without food, according to your preference. Do not crush or chew the tablet.

If you take more Solifenacin succinate/Tamsulosin hydrochloride than you should

If you have taken more tablets than you have been told to take or if someone else accidentally takes your tablets, contact your doctor, pharmacist or hospital immediately for advice.

In case of an overdose your doctor may treat you with activated charcoal; emergency stomach washout may be useful if performed within 1 hour of overdose. Do not induce vomiting.

Symptoms of overdose may include: dry mouth, dizziness, and blurred vision, perceiving things that are not there (hallucinations), over-excitability, seizures (convulsions), difficulty breathing, increased heart rate (tachycardia), inability to completely or partially empty the bladder or pass urine (urinary retention) and/or an unwanted decrease in blood pressure. If you forget to take Solifenacin succinate/Tamsulosin hydrochloride

Take your next tablet of Solifenacin succinate/Tamsulosin hydrochloride as normal. Do not take a double dose to make up for a forgotten tablet.

If you stop taking Solifenacin succinate/Tamsulosin hydrochloride

If you stop taking Solifenacin succinate/Tamsulosin hydrochloride, your original complaints may return or worsen. Always consult your doctor, if you are considering stopping the treatment.

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

4. Possible side effects

Like all medicines, Solifenacin succinate/Tamsulosin hydrochloride can cause side effects, although not everybody gets them. The most serious side effect that has uncommonly (may affect up to 1 in 100 men) been observed during treatment with solifenacin succinate/tamsulosin hydrochloride in clinical studies is acute urinary retention, which is a sudden inability to pass urine. If you think you may have this, see a doctor straight away. You may need to stop taking Solifenacin succinate/Tamsulosin hydrochloride.

Allergic reactions could occur with Solifenacin succinate/Tamsulosin hydrochloride:

  • Severe allergic reaction (anaphylactic reaction) can occur with not known frequency
  • Uncommon signs of allergic reactions can include skin rash (which can be itchy) or hives (urticaria).
  • Rare symptoms include swelling of the face, lips, mouth, tongue or throat which may cause difficulty in swallowing

    or breathing (angioedema). Angioedema has been reported rarely on tamsulosin and very rarely with solifenacin. If angioedema occurs, Solifenacin succinate/Tamsulosin hydrochloride should be stopped immediately and not started again.

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If you experience an allergic attack, or a severe skin reaction (e.g. blistering and peeling of the skin), you must inform your doctor immediately, and stop using Solifenacin succinate/Tamsulosin hydrochloride. Appropriate therapy and/or measures should be taken.

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

  • Constipation
  • Indigestion (dyspepsia)
  • Dizziness
  • Blurred vision
  • Tiredness (fatigue)
  • Abnormal ejaculation (ejaculation disorder). This means that semen does not leave the body via the urethra, but instead goes into the bladder (retrograde ejaculation) or the ejaculation volume is reduced or absent (ejaculation failure) This phenomenon is harmless.
  • Feeling sick (nausea)
  • Abdominal pain
  • Dry mouth

Other uncommon side effects (may affect up to 1 in 100 men)

  • Sleepiness (somnolence)
  • Itching (pruritus)
  • Urinary tract infection, bladder infection (cystitis)
  • Impaired sense of taste (dysgeusia)
  • Dry eyes
  • Dry nose
  • Reflux disease (gastro-oesophageal reflux)
  • Dry throat
  • Dry skin
  • Difficulty in passing urine
  • Accumulation of fluid in the lower legs (oedema)
  • Headache
  • Fast or uneven heartbeat (palpitations)
  • Feeling dizzy or weak especially when you stand up (orthostatic hypotension)
  • Runny or blocked nose (rhinitis)
  • Diarrhoea
  • Being sick (vomiting)
  • Tiredness (asthenia)

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

  • Lodging of a large amount of hardened stool in the large intestine (faecal impaction), colonic obstruction
  • Feeling faint (syncope)
  • Skin allergy that results in the swelling that occurs in the tissue just below the surface of the skin (angioedema)Very rare side effects (may affect up to 1 in 10 000 men)

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

  • Hallucinations, confusion
  • Allergic skin reaction (Erythema multiforme)
  • Long-lasting and painful erection (usually not during sexual activity) (priapism)
  • Rash, inflammation and blistering of the skin and/or mucous membranes of the lips, eyes, mouth, nasal passages or genitals (Stevens-Johnson syndrome)

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

  • Decreased appetite
  • High levels of blood potassium (hyperkalaemia) which can cause abnormal heart rhythm
  • Increased pressure in the eyes (glaucoma)
  • Irregular or unusual heart beat (QT prolongation, Torsade de Pointes, atrial fibrillation, arrhythmia)
  • Faster heartbeat (tachycardia)
  • Shortness of breath (dyspnoea)
  • During an operation of the eye for cloudiness of the lens (cataract) or for increased pressure in the eye (glaucoma) the pupil (the black circle in the middle of your eye) may not increase in size as needed. Also, the iris (the coloured part of the eye) may become floppy during surgery.
  • Voice disorder
  • Liver disorder
  • Muscle weakness
  • Renal disorder
  • Impaired vision
  • Nose bleeds (epistaxis)
  • Delirium
  • Intestines disorder (ileus)
  • Abdominal discomfort
  • Severe skin allergy that results in peeling off the skin (exfoliative dermatitis)

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 Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App. By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Solifenacin succinate/Tamsulosin hydrochloride

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 or blister after EXP. The expiry date refers to the last day of that month.

This medicine does not require any special storage conditions.

Do not throw away any medicines via wastewater 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 Solifenacin succinate/Tamsulosin hydrochloride contains

  • The active substances are: solifenacin succinate and tamsulosin hydrochloride.

Each modified–release tablet contains 6 mg solifenacin succinate corresponding to 4,5mg solifenacin and 0.4 mg tamsulosin hydrochloride corresponding to 0,37mg tamsulosin.

  • The other ingredients are cellulose, microcrystalline; macrogol; silica, colloidal anhydrous; magnesium stearate; calcium hydrogen phosphate; silicified microcrystalline cellulose; hydroxypropylcellulose, low-substituted; hypromellose; iron oxide red (E172).

What Solifenacin succinate/Tamsulosin hydrochloride looks like and contents of the pack

Solifenacin succinate/Tamsulosin hydrochloride Torrent 6 mg/0.4 mg modified release tablets are round (9 mm diameter), biconvex, red, film-coated tablets, debossed with “6 04” on one side.

PA/Aluminium/PVC/Aluminium blister in outer carton box containing 30, 90 or 100 tablets. PA/Aluminium/PVC/Aluminium unit-dost blister in outer carton box containing 30 x 1, 90 x 1 or 100 x 1 tablets.

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.

Manufacturer

Adamed Pharma S.A.

ul. Marszałka Józefa Piłsudskiego 5

95-200 Pabianice,

Poland

This leaflet was last revised in 01/2025

8099743-7803

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 36687/0485

Last revision stated in the text: January 2025 · MHRA data as of 13 October 2026

What the sections and the side effect frequencies mean: How to read a patient leaflet

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 Solifenacin Succinate/tamsulosin Hydrochloride Torrent 6 mg/0.4 mg modified release tablets

What these facts mean

Prescription needed?? Yes, prescription-only medicine (POM)
Active substances? Tamsulosin, Solifenacin
Strength? 6 mg/0.4 mg
Pharmaceutical form? Modified-release tablet
Each tablet is red, film-coated, round, 9 mm diameter, biconvex, engraved “6 04” on one side.
How is it taken? Oral
Excipients? Tamsulosin layer – modified release layer Cellulose, microcrystalline Macrogol, high-molecular-mass, Macrogol, Silica, colloidal anhydrous, Magnesium stearate, Solifenacin layer- immediate release layer, Calcium hydrogen phosphate, Silicified microcrystalline cellulose, Hydroxypropylcellulose, low-substituted, Hypromellose, Iron oxide red (E172)
Pack sizes 30 tablet
Is it available?? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life? 36 months
Storage The medicinal product does not require any special storage conditions.
Drug group (ATC)? Alpha-adrenoceptor antagonists
  1. G Genito urinary system and sex hormones
    1. G04 Urologicals
      1. G04C Drugs used in benign prostatic hypertrophy
        1. G04CA Alpha-adrenoreceptor antagonists, benign prostatic hypertrophy
          1. G04CA53 tamsulosin and solifenacin
Marketing authorisation? PL 36687/0485 (first authorised 26 October 2023)
Marketing authorisation holder? Torrent Pharma (UK) Ltd.
Codes? GTIN 5060623373238 · BNF 07040100

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 11.1.0 of 9 November 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.