VENORUTON DIOSMIN 500 mg FILM-COATED TABLETS
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How to use VENORUTON DIOSMIN 500 mg FILM-COATED TABLETS
Introduction
Package Leaflet: Information for the User
Venoruton Diosmin 500 mg Film-Coated Tablets
Diosmin
Read the entire package leaflet carefully before starting to take this medication, as it contains important information for you.
Follow the administration instructions for the medication contained in this package leaflet or as indicated by your doctor or pharmacist.
- Keep this package leaflet, as you may need to read it again.
- If you need advice or more information, consult your doctor or pharmacist.
- If you experience side effects, consult your doctor or pharmacist, even if they are side effects not listed in this package leaflet. See section 4.
- You should consult a doctor if your condition worsens or does not improve after 1 or 2 weeks, depending on the indication.
Contents of the Package Leaflet:
- What Venoruton Diosmin is and what it is used for.
- What you need to know before taking Venoruton Diosmin.
- How to take Venoruton Diosmin.
- Possible side effects.
- Storage of Venoruton Diosmin.
Contents of the pack and additional information.
1. What Venoruton Diosmin is and what it is used for
Venoruton Diosmin is a venotonic medication: it increases the tone of the veins and the resistance of the capillaries (small blood vessels).
Venoruton Diosmin is indicated, in adults, for the relief of symptoms related to mild venous insufficiency of the lower limbs, such as pain, feeling of heaviness, tightness, tingling, and itching in legs with varices or swollen legs.
It is indicated for the relief of symptoms related to hemorrhoids, such as pain or inflammation in the anal area in adults.
You should consult a doctor if your condition worsens or does not improve after 2 weeks of treatment in case of venous insufficiency, or after 1 week of treatment in case of hemorrhoids.
2. What you need to know before taking Venoruton Diosmin
Do not take Venoruton Diosmin
- if you are allergic to the active substance or to any of the other components of this medication (listed in section 6).
Warnings and Precautions
Consult your doctor or pharmacist before starting to take Venoruton Diosmin.
Do not use for prolonged periods without medical supervision.
Children and Adolescents
Venoruton Diosmin is not intended for use in children and adolescents (under 18 years of age).
Other Medications and Venoruton Diosmin
Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication, including those purchased without a prescription.
No interactions with food or other medications are known. In any case, never take another medication on your own initiative without your doctor's recommendation.
Use of Venoruton Diosmin with Food, Drinks, and Alcohol
No interactions of this medication with food, drinks, or alcohol are known.
Pregnancy, Breastfeeding, and Fertility
If you are pregnant or breastfeeding, or think you may be pregnant or plan to become pregnant, consult your doctor or pharmacist before using this medication.
No harmful effects on humans have been reported. However, caution should be exercised when using diosmin during pregnancy, weighing the potential benefits of this medication during pregnancy.
It is not known whether the medication passes into breast milk, so its use is not recommended during breastfeeding.
Driving and Using Machines
No effects of diosmin on the ability to drive and use machines have been described.
3. How to Use Venoruton Diosmin
Follow the administration instructions for the medication contained in this package leaflet or as indicated by your doctor or pharmacist. In case of doubt, ask your pharmacist.
Adults
Venous Insufficiency:
The recommended dose in adults is 2 tablets per day, divided into two doses, one tablet at midday and another at night, with meals.
Relief of symptoms usually occurs within the first 2 weeks of treatment. If you do not feel relief after 2 weeks or your symptoms worsen, you should consult your doctor.
On medical indication, treatment can be continued with the same daily dose (2 tablets per day) for up to 2 to 3 months.
Hemorrhoids:
The recommended dose is:
For the first 4 days: 2 tablets, 3 times a day.
For the next 3 days: 2 tablets, 2 times a day.
After this, treatment can be continued with a dose of 2 tablets per day.
If your symptoms do not improve or worsen within the first week of treatment, you should consult your doctor.
Use in Children and Adolescents
The safety and efficacy of diosmin in children and adolescents have not been established.
If You Take More Venoruton Diosmin Than You Should
No cases of overdose with diosmin have been reported.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, go to a medical center, or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medication and the amount ingested.
If You Forget to Take Venoruton Diosmin
It is important to take this medication every day. However, if you forget to take one or more doses of Venoruton Diosmin, take another as soon as you remember and then continue with the prescribed treatment. Do not take a double dose to make up for the missed doses.
If you have any other doubts about the use of this product, ask your doctor or pharmacist.
4. Possible Side Effects
Like all medications, Venoruton Diosmin can cause side effects, although not everyone will experience them.
The frequencies of side effects have been listed below according to the following definitions:
Very common: May affect more than 1 in 10 people
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
Common: Gastrointestinal disorders (diarrhea, indigestion, nausea, vomiting).
Uncommon: Colitis
Rare: Nervous system disorders (dizziness, headache, malaise) and skin reactions (rash, pruritus, urticaria).
Frequency not known: Abdominal pain, isolated edema of the face, lips, and eyelids (swelling). Exceptionally, Quincke's edema (rapid swelling of tissues such as the face, lips, mouth, tongue, or throat that can cause difficulty breathing).
These side effects have been reported without the need to interrupt treatment.
Reporting Side Effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect not listed in this package leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.
5. Storage of Venoruton Diosmin
No special storage conditions are required.
Keep this medication out of sight and reach of children.
Do not use this medication after the expiration date shown on the box after "EXP". The expiration date is the last day of the month indicated.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE collection point in the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
6. Contents of the Pack and Additional Information
Composition of Venoruton Diosmin
- The active ingredient is diosmin (500 mg per tablet).
- The other components are: microcrystalline cellulose (E460i), gelatin, sodium glycolate starch (potato starch), talc (E553b), magnesium stearate, sodium lauryl sulfate, and orange opadry (hydroxypropyl methylcellulose (E464), glycerol, titanium dioxide (E171), yellow iron oxide (E172), red iron oxide (E172), polyethylene glycol 6000, magnesium stearate).
Appearance of the Product and Contents of the Pack
Venoruton Diosmin are orange, oblong, and scored film-coated tablets. The tablets are presented in blister packs in boxes of 30 or 60 tablets.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Laboratorio STADA, S.L.
Frederic Mompou, 5
08960 Sant Just Desvern (Barcelona), Spain
Manufacturer
Kern Pharma, S.L.
Venus, 72 – Pol. Ind. Colón II
08228 Terrassa - Barcelona
Spain
or
Laboratori Fundació Dau
c/ C 12-14,
Polígono Industrial de la Zona Franca,
08040 Barcelona
Spain
Date of the Last Revision of this Package Leaflet: November 2024
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
- Country of registration
- Active substance
- Prescription requiredNo
- Manufacturer
- This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
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