Package Insert: Information for the Patient
Urorec 8 mg Hard Capsules
Urorec 4 mg Hard Capsules
Silodosina
Read this package insert carefully before starting to take this medicine, as it contains important information for you.
What is Urorec
Urorec belongs to a group of medications called alpha1A adrenergic receptor blockers.
Urorec is selective for receptors located in the prostate, bladder, and urethra. By blocking these receptors, it causes relaxation of the smooth muscle in these tissues. This makes it easier for you to urinate and alleviates your symptoms.
What is Urorec used for
Urorec is used in adult males to treat urinary symptoms associated with benign prostatic hyperplasia (BPH), such as:
Do not take Urorec
if you are allergic to silodosin or any of the other ingredients of this medicine (listed in section 6).
Warnings and precautions
Consult your doctor or pharmacist before starting to take Urorec
When taking Urorec, you may experiencedizzinessand, occasionally, asyncope, especially when starting treatment or taking other medications that lower blood pressure. If this occurs,sit or lie downimmediately until the symptoms disappear andinform your doctor as soon as possible(see also the section “Driving and operating machines”).
If your kidney problems are moderate, your doctor will start treatment with Urorec with caution and possibly with a lower dose (see section 3 “Dose”).
If your kidney problems are severe, do not take Urorec.
Sodium
This medicine contains less than 1 mmol of sodium (23 mg) per capsule; it is essentially “sodium-free”.
Children and adolescents
Do not administer this medicine to children and adolescents under 18 years of age, as there are no relevant indications for this age group.
Urorec with other medications
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Inform your doctorin particular if you take:
Pregnancy and breastfeeding
Urorec is not indicated for use by women.
Fertility
Urorec may reduce semen volume and temporarily affect your ability to conceive a child. If you intend to have a child, consult your doctor or pharmacist before using this medicine.
Driving and operating machines
Do not drive or operate machines if you feel dizziness, dizziness, or somnolence or have blurred vision.
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
The recommended dose is one Urorec 8 mg capsule per day taken orally.
Take the capsule always accompanied by food, preferably at the same time every day. Do not break or chew the capsule; swallow it whole, preferably with a glass of water.
Patients with kidney problems
If you have moderate kidney problems, your doctor may prescribe a different dose. For this purpose, the Urorec 4 mg hard capsules presentation is available.
If you take more Urorec than you should
If you have taken more than one capsule, inform your doctor as soon as possible. If you experience dizziness or feel weak, notify your doctor immediately.
If you forget to take Urorec
You can take the capsule later the same day if you forgot to take it earlier. If it is almost time for the next dose, do not take the missed dose. Do not take a double dose to make up for the missed capsule.
If you interrupt treatment with Urorec
If you interrupt treatment, it is possible that symptoms may reappear.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
Immediately contact your doctor if you experience any of the following allergic reactions, as their consequences could be severe: swelling of the face or throat, difficulty breathing, feeling of fainting, itching on the skin or urticaria.
The most common side effect is a reduction in the amount of semen expelled during sexual intercourse. This side effect disappears after stopping treatment with Urorec. Inform your doctor if you are planning to have children.
You may experiencedizziness,including dizziness when standing up, and, occasionally,fainting.
If you feel weak or dizzy,sit or lie downimmediately until the symptoms disappear. If you experience dizziness when standing up or fainting,inform your doctor as soon as possible.
Urorec may cause complications duringcataract surgery(eye surgery for cloudy lens; see "Warnings and precautions").
It is essential thatyou inform your ophthalmologist immediatelyif you are using or have previously used Urorec.
The possible side effects are listed below:
Very common side effects (may affect more than 1 in 10 people)
Common side effects (may affect up to 1 in 10 people)
Uncommon side effects (may affect up to 1 in 100 people)
Rare side effects (may affect up to 1 in 1,000 people)
Very rare side effects (may affect up to 1 in 10,000 people)
Unknown frequency (the frequency cannot be estimated from available data)
Reporting side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through thenational notification system included in theAppendix V. By reporting side effects, you can contribute to providing more information about the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the box and on the blister pack after “CAD”. The expiration date is the last day of the month indicated.
Do not store at a temperature above 30°C.
Store in the original packaging to protect it from light and moisture.
Do not use this medication if you observe that the packaging is damaged or shows signs of having been improperly handled.
Medications should not be disposed of through drains or in the trash. Ask your pharmacist how to dispose of the packaging and medications that you no longer need. In this way, you will help protect the environment.
Composition of Urorec
Urorec 8 mg
The active ingredient is silodosin. Each capsule contains 8 mg of silodosin.
The other components are pregelatinized cornstarch, mannitol (E421), magnesium stearate, sodium lauryl sulfate, gelatin, titanium dioxide (E171).
Urorec 4 mg
The active ingredient is silodosin. Each capsule contains 4 mg of silodosin.
The other components are pregelatinized cornstarch, mannitol (E421), magnesium stearate, sodium lauryl sulfate, gelatin, titanium dioxide (E171), yellow iron oxide (E172).
Appearance of the product and contents of the package
Urorec 8 mg are hard gelatin capsules, opaque and white, size 0 (21.7 x 7.6 mm, approximately).
Urorec 4 mg are hard gelatin capsules, opaque and yellow, size 3 (15.9 x 5.8 mm, approximately).
Urorec is available in packages of 5, 10, 20, 30, 50, 90, 100 capsules. Only some package sizes may be marketed.
Marketing Authorization Holder
Recordati Ireland Ltd.
Raheens East
Ringaskiddy Co. Cork
Irlanda
Responsible for manufacturing
Recordati Industria Chimica e Farmaceutica S.p.A.
Via Matteo Civitali 1
20148 Milán
Italia
Laboratoires Bouchara-Recordati
Parc Mécatronic
03410 Saint Victor
Francia
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
België/Belgique/Belgien Recordati Ireland Ltd. Tél/Tel: + 353 21 4379400 | Lietuva Recordati Polska sp. z o.o. Tel: +48 22 206 84 50 |
Recordati Bulgaria Ltd. ??π.: + 359 2 829 39 37 | Luxembourg/Luxemburg Recordati Ireland Ltd. Tél/Tel: + 353 21 4379400 |
Ceská republika Herbacos Recordati s.r.o. Tel: + 420 466 741 915 | Magyarország Recordati Ireland Ltd. Tel: + 353 21 4379400 |
Danmark Recordati Ireland Ltd. Tlf: + 353 21 4379400 | Malta Focused Pharma Ltd. Tel: + 356 79426930 |
Deutschland Recordati Pharma GmbH Tel: + 49 731 70470 | Nederland Recordati Ireland Ltd. Tel: + 353 21 4379400 |
Eesti Recordati Polska sp. z o.o. Tel: +48 22 206 84 50 | Norge Recordati Ireland Ltd. Tlf: + 353 21 4379400 |
Ελλáδα Recordati Hellas Pharmaceuticals A.E. Τηλ: + 30 210-6773822 | Österreich Recordati Austria GmbH Tel: + 43 676 353 0 262 |
España Casen Recordati, S.L. Tel: + 34 91 659 15 50 | Polska Recordati Polska sp. z o.o. Tel: + 48 22 206 84 50 |
France Laboratoires Bouchara-Recordati Tél: + 33 1 45 19 10 00 | Portugal Jaba Recordati, S.A. Tel: + 351 21 432 95 00 |
Hrvatska PharmaSwiss d.o.o. Tel: +385 1 63 11 833 | România Recordati România S.R.L. Tel: + 40 21 667 17 41 |
Ireland Recordati Ireland Ltd. Tel: + 353 21 4379400 | Slovenija Recordati Ireland Ltd. Tel: + 353 21 4379400 |
Ísland Recordati Ireland Ltd. Sími: + 353 21 4379400 | Slovenská republika Herbacos Recordati s.r.o. Tel: + 420 466 741 915 |
Italia Recordati Industria Chimica e Farmaceutica S.p.A. Tel: + 39 02 487871 | Suomi/Finland SwanMedica Oy Puh/Tel: +358 17 3690033 |
Κúπρος G.C. Papaloisou Ltd. Τηλ: + 357 22 49 03 05 | Sverige Recordati Ireland Ltd. Tel: + 353 21 4379400 |
Latvija Recordati Polska sp. z o.o. Tel: +48 22 206 84 50 | United Kingdom (Northern Ireland) Recordati Ireland Ltd. Tel: + 353 21 4379400 |
Last review date of this leaflet
Other sources of information
The detailed information about this medication is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
Есть вопросы по этому лекарству или вашим симптомам? Свяжитесь с лицензированным врачом для получения помощи и персонализированного ухода.