Prospect: information for the user
Dutasteride TecniGen 0.5 mg soft capsules EFG
Read this prospect carefully before starting to take the medicine because it contains important information for you.
1.What is Dutasteride TecniGen and for what it is used
2.What you need to know before starting to take Dutasteride TecniGen
3.How to take Dutasteride TecniGen
4.Possible adverse effects
5.Storage of Dutasteride TecniGen
6.Contents of the package and additional information
Dutasterida TecniGenis used in men to treat an enlarged prostate(benign prostatic hyperplasia) ,a non-cancerous growth of the prostate caused by excessive production of a hormone called dihydrotestosterone.
The active ingredient is dutasteride, which belongs to a group of medications called 5 alpha reductase inhibitors.
As the prostate grows in size, it may produce urinary problems such as difficulty in urinating and a need to urinate more frequently. It may also cause a smaller and weaker urine stream. If benign prostatic hyperplasia is not treated, there is a risk of complete blockage of urine flow(acute urinary retention). This requires immediate medical treatment. In some cases, surgery may be necessary to reduce the size of the prostate or remove it. Dutasterida TecniGen reduces the production of dihydrotestosterone, which helps to reduce the size of the prostate and alleviate symptoms. This reduces the risk of acute urinary retention and the need for surgery.
Dutasterida may also be used with another medication, tamsulosin (used to treat symptoms of an enlarged prostate)
Do not take DutasteridaTecniGen
-if you are allergic
If you think you are in any of these situations, do not take this medication until you have consulted with your doctor.
This medication is only for men.Women, children, or adolescents should not take it.
Warnings and precautions
Consult your doctor or pharmacist before starting to take this medication.
Consult your doctor or pharmacistif you have any questions about taking this medication.
Use of Dutasterida TecniGenTecniGenwith other medications
Inform your doctor or pharmacist if you are using or have recently used other medications.
Do not take dutasteride with these medications:
Certain medications may interact with dutasteride, which may cause you to experience adverse effects. Some of these medications are:
-verapamil or diltiazem(for high blood pressure)
-ritonavir or indinavir(for HIV/AIDS)
-itraconazole or ketoconazole(for fungal infections)
-nefazodone(an antidepressant)
Inform your doctor if you are taking any of these medications. You may need to reduce the dose of Dutasterida TecniGen
Taking Dutasterida TecniGenTecniGenwith food, drinks, and alcohol
Dutasterida TecniGencan be taken with or without food.
Pregnancy, breastfeeding, and fertility
Pregnant women (or those who may be pregnant) should avoid contact with broken dutasteride capsules. Dutasteride can be absorbed through the skin and may affect the normal development of the male fetus. This risk is especially important in the first 16 weeks of pregnancy.
Use a condom during sex.Dutasteride has been found in the semen of men taking this medication. If your partner is pregnant or thinks she may be pregnant, you should avoid exposing her to your semen.
Dutasteride has been shown to decrease sperm count, motility, and semen volume. This may reduce your fertility.
Consult your doctorif a pregnant woman has been in contact with dutasteride.
Driving and operating machinery
It is unlikely that dutasteride will affect your ability to drive and operate machinery.
Important information about some of the components of Dutasterida TecniGenTecniGenThis medication contains soy lecithin, so it may contain soy oil. Do not use this medication if you are allergic to peanuts or soy.
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
Always take this medication regularly. If you do not take this medication regularly, the control of your PSA levels may be affected (see section 2 “Warnings and precautions”).
What dose should you take
The usual dose is one capsule (0.5 mg) once a day.Dutasterida capsules should be swallowed whole with water. Do not chew or break the capsules. Contact with the contents of the capsules may irritate your mouth or throat.
The treatment with dutasterida is long-term. Some men may experience a rapid improvement in symptoms. However, others may need to continue treatment for up to 6 months or more before an effect begins to occur. Continue taking this medication for the time your doctor has indicated.
If you take more Dutasterida TecniGen than you should
In case of overdose or accidental ingestion, consult your doctor, pharmacist, or call the Toxicological Information Service, phone 915620420, indicating the medication and the amount ingested.
If you forgot to take Dutasterida TecniGen
Do not take a double dose to compensate for the missed doses. Take the next dose at the usual time.
If you interrupt treatment with Dutasterida TecniGen
Do not interrupt treatment with Dutasterida TecniGen without consulting your doctor first. You may need up to 6 months or more to notice an effect.
If you have any other questions about the use of this medication, ask your doctor or pharmacist
Like all medications, this medication may produce adverse effects, although not all people will experience them.
Allergic Reaction
The symptoms of an allergic reaction may include:
You should immediately contact your doctor if you experience any of these symptoms and stop taking dutasteride.
Frequent Adverse Effects (may affect up to 1 in 10 men)
Rare Adverse Effects (may affect up to 1 in 100 men)
Adverse Effects of Unknown Frequency
The frequency cannot be estimated from the available data:
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect not listed in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use. Website: www.notificaRAM.es.
By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging or in the bottleafter CAD. The expiration date is the last day of the month indicated.
Do not store above 86°F (30°C). Store in the original packaging to protect from moisture.
Medications should not be disposed of through drains or in the trash. Dispose of the containers and medications you no longer need at the SIGRE collection pointat 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.
Composition of Dutasteride TecniGen
The active ingredient is dutasteride. Each soft capsule contains 0.5 mg of dutasteride. The other components are:
Content of the capsule: Glycerol monocaprylate (type I) and butylhydroxytoluene (E-321)
Capsule coating: Gelatin, glycerol, titanium dioxide (E-171), iron oxide yellow (E-172), medium-chain triglycerides, lecithin (may contain soybean oil) and purified water.
Appearance of Dutasteride TecniGen and content of the container
Dutasteride TecniGen are soft gelatin capsules, oblong, opaque, yellow in color, and unprinted, containing a yellowish oily liquid. It is available in containers of 30 capsules.
Only some sizes of containers may be marketed.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Tecnimede España Industria Farmacéutica, S.A.
Avda. de Bruselas, 13, 3rd D. Edificio América. Polígono Arroyo de la Vega,
28108 Alcobendas (Madrid) Spain
Responsible for manufacturing
Cyndea Pharma S.L.
Polígono Industrial Emiliano Revilla Sanz
Avenida de Ágreda, 31
Olvega, 42110 Soria
Spain
or
Galenicum Health S.L.U.
Sant Gabriel, 50
Esplugues de Llobregat
08950 Barcelona.
Spain
or
Pharmadox Healthcare, Ltd.
KW20A Kordin Industrial Park,
Paola, PLA 3000, Malta
or
SAG Manufacturing S.L.U.
Ctra. N-I, Km 36
28750 San Agustín de Guadalix
Madrid, Spain
Last review date of this leaflet: August 2016
The detailed and updated information on 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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