Solifenacin succinate
You should carefully read the contents of the leaflet before taking the medicine, as it contains
important information for the patient.
Solifenacin succinate, the active substance of Vesisol, belongs to a group of medicines called anticholinergics. These medicines reduce the activity of an overactive bladder. This action allows for longer intervals between visits to the toilet and increases the amount of urine retained in the bladder. Vesisol is used to treat the symptoms of an overactive bladder. These symptoms include: urgency, i.e. episodes of sudden, urgent need to urinate, frequent urination, and involuntary loss of urine, associated with a failure to reach the toilet in time.
Before starting treatment with Vesisol, you should inform your doctor if any of the above situations apply or have applied in the past.
Before starting to take Vesisol, you should discuss it with your doctor or pharmacist.
Before starting treatment with Vesisol, you should inform your doctor if any of the above situations apply or have applied in the past. Before starting treatment with Vesisol, your doctor will assess whether there are other causes of frequent urination (e.g. heart failure - insufficient strength of the heart muscle to pump blood - or kidney disease). If a urinary tract infection occurs, your doctor will prescribe an antibiotic (an antibacterial medicine that acts on specific bacteria).
Vesisol should not be used in children or adolescents under 18 years of age.
You should tell your doctor about all medicines you are taking or have recently taken, as well as any medicines you plan to take. It is particularly important to inform your doctor if you are taking:
Vesisol can be taken with or without food, depending on the patient's preferences.
If you are pregnant or breastfeeding, think you may be pregnant or are planning to have a baby, you should ask your doctor or pharmacist for advice before taking this medicine. You should not take Vesisol during pregnancy, unless it is absolutely necessary. You should not take Vesisol during breastfeeding, as solifenacin passes into breast milk.
Solifenacin may cause blurred vision, sometimes drowsiness, and a feeling of fatigue. If such side effects occur, you should not drive or operate any machinery.
If you have been told that you have an intolerance to some sugars, you should contact your doctor before taking this medicine.
This medicine should always be taken exactly as your doctor has told you. If you are not sure, you should ask your doctor or pharmacist. The usual dose is 5 mg, unless your doctor has recommended a dose of 10 mg. The tablet should be swallowed whole, with a glass of water. Vesisol can be taken with or without food, depending on the patient's preferences. The tablets should not be crushed.
If you have taken too many Vesisol tablets or if a child has accidentally taken Vesisol, you should immediately contact your doctor or pharmacist. Symptoms of overdose may include: headache, dry mouth, dizziness, drowsiness, and vision disturbances, seeing things that are not there (hallucinations), excessive excitement, seizures (convulsions), difficulty breathing, rapid heartbeat (tachycardia), urine accumulation in the bladder (urinary retention), and dilated pupils.
If you miss a dose of Vesisol, you should take the next dose as soon as possible, unless it is almost time for the next dose. You should not take Vesisol more often than once a day. If you are not sure, you should ask your doctor or pharmacist.
If you stop taking Vesisol, the symptoms of an overactive bladder may return or worsen. If you want to stop treatment, you should consult your doctor. If you have any further questions about the use of this medicine, you should ask your doctor or pharmacist.
Like all medicines, Vesisol can cause side effects, although not everybody gets them. If you experience an allergic reaction or a severe skin reaction (e.g. blistering and peeling of the skin), you should immediately inform your doctor or pharmacist. In some patients taking solifenacin succinate, angioedema (a type of allergic skin reaction that causes swelling of the tissue under the skin) with swelling of the airways (difficulty breathing) has been reported. If you experience angioedema, you should immediately stop taking Vesisol and start appropriate treatment and/or take appropriate measures. Vesisol may cause other side effects, including:
Common(may affect up to 1 in 10 people):
Uncommon(may affect up to 1 in 100 people):
Rare(may affect up to 1 in 1,000 people):
Very rare(may affect up to 1 in 10,000 people):
Frequency not known(frequency cannot be estimated from the available data):
If you experience any side effects, including those not listed in this leaflet, you should tell your doctor or pharmacist. Side effects can be reported directly to the Department of Post-Marketing Surveillance of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181 C, 02-222 Warsaw, Tel.: +48 22 49 21 301, Fax: +48 22 49 21 309, e-mail: ndl@urpl.gov.pl. Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
The medicine should be kept out of the sight and reach of children. There are no special precautions for storage. Do not use this medicine after the expiry date stated on the carton/blisters after EXP. The expiry date refers to the last day of the month stated. Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Coating:
Vesisol, 5 mg: Opadry yellow OY 32823 [hypromellose 6cP, titanium dioxide (E 171), macrogol 400, iron oxide yellow (E 172), iron oxide red (E 172)].
Vesisol, 10 mg: Opadry white 03B28796 [hypromellose 6cP, titanium dioxide (E 171), macrogol 400], Opadry brown 02F23883 [hypromellose 5cP, titanium dioxide (E 171), macrogol 6000, iron oxide yellow (E 172), iron oxide red (E 172)].
Vesisol, 5 mg: yellow, round, biconvex coated tablet with a diameter of 6 mm.
Vesisol, 10 mg: pink, round, biconvex coated tablet with a diameter of 7 mm.
Pack sizes: 30, 50, 60, 90, and 100 tablets.
Not all pack sizes may be marketed.
G.L. Pharma GmbH, Schlossplatz 1, 8502 Lannach, Austria
G.L. Pharma GmbH, Schlossplatz 1, 8502 Lannach, Austria
PRO.MED.CS Praha a.s., Telčská 377/1, Michle, 140 00 Prague 4, Czech Republic
G.L. PHARMA POLAND Sp. z o.o., Al. Jana Pawła II 61/313, 01-031 Warsaw, Poland, Tel: 022/ 636 52 23; 636 53 02, biuro@gl-pharma.pl
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