Warnings and precautions
Consult your doctor or pharmacist before starting to take Silodosina Alter.
When taking this medication, you may experience dizziness and, occasionally, fainting, especially when starting treatment or taking other medications that lower blood pressure. If this occurs, sit or lie down immediately until the symptoms disappear and inform your doctor as soon as possible (see also the section “Driving and operating machines”).
If you have moderate kidney problems, your doctor will initiate treatment with Silodosina Alter with caution and possibly with a lower dose (see section 3 “Doses”).
If you have severe kidney problems, do not take Silodosina Alter.
Children and adolescents
Do not administer this medication to children and adolescents under 18 years of age, as there are no relevant indications for this age group.
Combining Silodosina Alter 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
Silodosina Alter is not indicated for use by women.
Fertility
This medication 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 medication.
Driving and operating machines
Do not drive or operate machines if you experience dizziness, drowsiness, or blurred vision.
Silodosina Alter contains sodium
This medication contains less than 1 mmol of sodium (23 mg) per capsule; it is essentially “sodium-free”.
The recommended dose is one Silodosina 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 Silodosina Alter 4 mg hard capsules presentation is available.
If you take more Silodosina Alter 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.
In case of overdose or accidental ingestion, consult your doctor or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If you forget to take Silodosina Alter
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 compensate for the missed capsule.
If you interrupt treatment with Silodosina Alter
If you interrupt treatment, it is possible that the symptoms will reappear.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
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 frequent side effect is a reduction in the amount of semen expelled during sexual intercourse. This side effect disappears after discontinuing treatment with Silodosina. Inform your doctor if you are planning to have children.
You may experiencedizziness, including dizziness when standing up, and, occasionally,fainting.
If you notice weakness or dizziness,sit or lie downimmediately until the symptoms disappear. If you experience dizziness when standing up or fainting,inform your doctor as soon as possible.
Silodosina 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 Silodosina.
The possible side effects are listed below:
Frequent 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)
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 the Spanish System for the Pharmacovigilance of Medicines for Human Use:https://www.notificaram.es.By reporting side effects, you can contribute to providing more information on 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.
Store in the original packaging to protect it from light.
Do not use this medication if you observe that the packaging is damaged or shows signs of having been manipulated improperly.
Medications should not be disposed of through drains or in the trash. Deposit the containers and medications you no longer need at the SIGRE collection pointof the pharmacy. If in doubt, ask your pharmacist how to dispose of the containers and medications you no longer need. By doing so, you will help protect the environment.
Silodosina Alter 4 mg
The active ingredient is silodosina. Each capsule contains 4 mg of silodosina.
The other components are pregelatinized cornstarch, mannitol (E421), glyceryl dibehenate, sodium lauryl sulfate, gelatin, titanium dioxide (E171), yellow iron oxide (E172), and printing ink components (shellac, propylene glycol, concentrated ammonia solution, black iron oxide (E172), potassium hydroxide).
Silodosina Alter 8 mg
The active ingredient is silodosina. Each capsule contains 8 mg of silodosina.
The other components are pregelatinized cornstarch, mannitol (E421), glyceryl dibehenate (E471), sodium lauryl sulfate, gelatin, titanium dioxide (E171), and printing ink components (shellac, propylene glycol, concentrated ammonia solution, black iron oxide (E172), potassium hydroxide).
Appearance of the product and content of the container
Silodosina Alter 4 mg are hard gelatin capsules with an opaque yellow body, size 3, and a marked cap with “4” in black ink.
Silodosina Alter 8 mg are hard gelatin capsules with an opaque white body, size 0, and a marked cap with “8” in black ink.
Silodosina Alter is available in PVC/PE/PVDC-aluminum blisters. Containers of 30 capsules.
Marketing authorization holder
Laboratorios Alter, S.A.
C/ Mateo Inurria 30
28036 Madrid
Spain
Responsible for manufacturing
Rontis Hellas Medical and Pharmaceutical Products, S.A.
Larisa Industrial Area, P.O. Box 3012,
Larisa, 41500, Greece
Last review date of this leaflet May 2024
The detailed information of this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es
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