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Package Leaflet: Information for the User
Vizarsin 50 mg Orodispersible Tablets
sildenafil
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack and other information
Vizarsin contains the active substance sildenafil, which belongs to a group of medicines called phosphodiesterase type 5 (PDE5) inhibitors. It works by dilating the blood vessels of the penis, allowing blood flow when sexually stimulated. Vizarsin will only help you to get an erection if you are sexually stimulated.
Vizarsin is indicated for the treatment of erectile dysfunction in adult men, sometimes also called impotence. This occurs when a man cannot get or maintain an erection firm enough for satisfactory sexual activity.
Do not take Vizarsin
Warnings and precautions
Consult your doctor or pharmacist before taking Vizarsin:
It is not recommended to use Vizarsin at the same time as any other oral or local treatment for erectile dysfunction.
You must not take Vizarsin with treatments for pulmonary arterial hypertension (PAH) that contain sildenafil or any other PDE5 inhibitor.
You must not take Vizarsin if you do not have erectile dysfunction.
The use of Vizarsin is not indicated in women.
Special considerations in patients with kidney or liver problems
You should inform your doctor if you have kidney or liver problems. Your doctor may decide to reduce your dose.
Children and adolescents
The use of Vizarsin is not indicated in persons under 18 years of age.
Using Vizarsin with other medicines
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
Vizarsin tablets may interfere with some medicines, especially those used to treat chest pain. In case of a medical emergency, you should tell your doctor, pharmacist, or nurse that you are taking Vizarsin and when you last took it. Do not take Vizarsin with other medicines unless your doctor tells you to.
You must not take Vizarsin if you are taking medicines called nitrates, as the combination of these medicines can lead to a dangerous decrease in your blood pressure. Always tell your doctor, pharmacist, or nurse if you are taking any of these medicines, often used to relieve angina pectoris (or "chest pain").
You must not take Vizarsin if you are taking medicines called nitric oxide donors, such as amyl nitrite ("poppers"), as the combination of these medicines can also lead to a dangerous decrease in your blood pressure.
Tell your doctor or pharmacist if you are taking riociguat.
If you are taking medicines known as protease inhibitors, such as those used to treat HIV, your doctor may recommend that you start with the lowest dose (25 mg) of Vizarsin.
Some patients who are taking an alpha-blocker, a medicine used to treat high blood pressure or prostate enlargement, may experience dizziness or lightheadedness that can be caused by low blood pressure when sitting or standing up quickly. Some patients have experienced these symptoms when taking Vizarsin with alpha-blockers. This is more likely to happen within 4 hours after taking Vizarsin. To minimize the chance of these symptoms, you should be on a regular daily dose of the alpha-blocker before starting Vizarsin. Your doctor may advise you to start with the lower dose (25 mg) of Vizarsin.
Using Vizarsin with food, drinks, and alcohol
Vizarsin can be taken with or without food. However, you may notice that Vizarsin takes a little longer to work if you take it with a large meal.
Drinking alcohol can temporarily impair your ability to get an erection. Therefore, to get the maximum benefit from the medicine, it is recommended not to drink large amounts of alcohol before taking Vizarsin.
Pregnancy, breastfeeding, and fertility
The use of Vizarsin is not indicated in women.
Driving and using machines
Vizarsin can cause dizziness and affect vision. You should know how you react to Vizarsin before driving or operating machinery.
Vizarsin contains lactose and sodium
If your doctor has told you that you have an intolerance to some sugars, consult him before taking this medicine.
This medicine contains less than 1 mmol sodium (23 mg) per tablet; this is essentially "sodium-free".
Follow exactly the instructions of administration of this medicine given by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended starting dose is 50 mg.
Do not take Vizarsin more than once a day.
You should take Vizarsin about one hour before you plan to have sex. Swallow the tablet whole with a glass of water.
If you notice that the effect of Vizarsin is too strong or too weak, tell your doctor or pharmacist.
Vizarsin will only help you to get an erection if you are sexually stimulated. The time Vizarsin takes to work varies from person to person, but it normally takes between 30 minutes and 1 hour. The effect of Vizarsin may be delayed if you take it with a large meal.
In the event that Vizarsin does not help you to get an erection or if the erection does not last long enough to complete sexual intercourse, consult your doctor.
If you take more Vizarsin than you should
You may experience an increase in side effects and their severity. Doses above 100 mg do not increase efficacy.
Do not take more tablets than your doctor has recommended.
Contact your doctor if you have taken more tablets than you should.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them. The side effects reported in association with the use of Vizarsin are usually mild to moderate and of short duration.
If you experience any of the following serious side effects, stop taking Vizarsin and seek medical attention immediately:
Symptoms include sudden wheezing, difficulty breathing or dizziness, swelling of the eyelids, face, lips or throat.
If they occur during or after sex:
If you have an erection that lasts more than 4 hours, you should contact your doctor immediately.
Symptoms can include severe skin peeling and swelling of the skin, blistering of the mouth, genitals, and around the eyes, as well as fever.
Other side effects:
Very common(may affect more than 1 in 10 people): headache.
Common(may affect up to 1 in 10 people): nausea, facial flushing, hot flush (including a feeling of warmth), indigestion, abnormal color perception, blurred vision, visual disturbance, nasal congestion, and dizziness.
Uncommon(may affect up to 1 in 100 people): vomiting, skin rash, eye irritation, eye discharge/red eyes, eye pain, flashing lights, increased light sensitivity, light sensitivity, tearing, palpitations, rapid heartbeat, high blood pressure, low blood pressure, muscle pain, somnolence, reduced tactile sensitivity, vertigo, ringing in the ears, dry mouth, blocked or stuffy nose, inflammation of the nasal mucosa (including symptoms such as runny nose, sneezing, and nasal congestion), upper abdominal pain, gastroesophageal reflux disease (including symptoms such as heartburn), blood in urine, pain in arms or legs, nosebleeds, feeling hot, and feeling tired.
Rare(may affect up to 1 in 1,000 people): fainting, stroke, heart attack, irregular heartbeat, temporary decrease in blood flow to some parts of the brain, feeling of tightness in the throat, numbness in the mouth, bleeding in the back of the eye, double vision, decreased sharpness of vision, abnormal sensation in the eye, eye swelling or eyelid swelling, small particles or spots in the eye, seeing halos around lights, dilation of the pupil, change in color of the white of the eye, bleeding from the penis, presence of blood in semen, dry nose, swelling inside the nose, feeling irritable, and sudden decrease or loss of hearing.
During post-marketing experience, rare cases of unstable angina (heart disease) and sudden death have been reported. It should be noted that most men who experienced these side effects, although not all, had pre-existing heart disease before taking this medicine. It is not possible to determine whether these side effects were directly related to Vizarsin.
Reporting of side effects
If you experience 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 national reporting system listed in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.
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 and blister after EXP. The expiry date refers to the last day of the month shown.
This medicine does not require any special storage conditions.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Vizarsin
Core of the tablet:
microcrystalline cellulose (E460), hydrogenated calcium phosphate, sodium croscarmellose, hypromellose (E464), magnesium stearate (E470b).
Film coating:
lactose monohydrate, hypromellose (E464), titanium dioxide (E171), triacetin (E1518).
See section 2 "Vizarsin contains lactose and sodium":
Appearance and packaging of the product
Vizarsin 50 mg film-coated tablets are white, oblong, and engraved with "50" on one side.
Vizarsin 50 mg film-coated tablets are available in packs of 1 film-coated tablet in a blister pack and also in packs of 4 x 1, 8 x 1, or 12 x 1 film-coated tablets in unit-dose blister packs.
Not all pack sizes may be marketed.
Marketing authorization holder and manufacturer
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
For further information on this medicine, contact the local representative of the marketing authorization holder:
Belgium/Belgique/BelgienLithuania
KRKA Belgium, SA. UAB KRKA Lietuva
Tel: +32 (0) 487 50 73 62 Tel: +370 5 236 27 40
BulgariaLuxembourg/Luxemburg
KRKA Bulgaria EOOD KRKA Belgium, SA.
Tel: +359 (0) 2 962 34 50 Tel: +32 (0) 487 50 73 62 (BE)
Czech RepublicHungary
KRKA CR, s.r.o. KRKA Magyarország Kereskedelmi Kft.
Tel: +420 (0) 221 115 150 Tel: +36 (1) 355 8490
DenmarkMalta
KRKA Sverige AB E. J. Busuttil Ltd.
Tel: +46 (0)8 643 67 66 (SE) Tel: +356 21 445 885
GermanyNetherlands
TAD Pharma GmbH KRKA Belgium, SA.
Tel: +49 (0) 4721 606-0 Tel: +32 (0) 487 50 73 62 (BE)
EstoniaNorway
KRKA, d.d., Novo mesto Eesti filiaal KRKA Sverige AB
Tel: +372 (0) 6 671 658 Tel: +46 (0)8 643 67 66 (SE)
GreeceAustria
KRKA ΕΛΛΑΣ ΕΠΕ KRKA Pharma GmbH, Wien
Tel: +30 2100101613 Tel: +43 (0)1 66 24 300
SpainPoland
KERN PHARMA, S.L. KRKA-POLSKA Sp. z o.o.
Tel: +34 93 700 25 25 Tel: +48 (0)22 573 7500
FrancePortugal
KRKA France Eurl KRKA Farmacêutica, Sociedade Unipessoal Lda.
Tel: +33 (0)1 57 40 82 25 Tel: +351 (0)21 46 43 650
CroatiaRomania
KRKA - FARMA d.o.o. KRKA Romania S.R.L., Bucharest
Tel: +385 1 6312 100 Tel: +4 021 310 66 05
IrelandSlovenia
KRKA Pharma Dublin, Ltd. KRKA, d.d., Novo mesto
Tel: +353 1 293 91 80 Tel: +386 (0) 1 47 51 100
IcelandSlovakia
LYFIS ehf. KRKA Slovensko, s.r.o.
Tel: +354 534 3500 Tel: +421 (0) 2 571 04 501
ItalyFinland
KRKA Farmaceutici Milano S.r.l. KRKA Finland Oy
Tel: +39 02 3300 8841 Tel: +358 20 754 5330
CyprusSweden
KI.PA. (PHARMACAL) LIMITED KRKA Sverige AB
Tel: +357 24 651 882 Tel: +46 (0)8 643 67 66 (SE)
LatviaUnited Kingdom
KRKA Latvija SIA Consilient Health (UK) Ltd.
Tel: +371 6 733 86 10 Tel: +44 (0)203 751 1888
Date of last revision of this leaflet:
Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu.
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