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Daflon film-coated tablets 500 mg

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1. What are Daflon 500mg film-coated tablets and what are they used for? The substances contained in Daflon 500 mg film-coated tablets act on the large veins and the fine capillaries. They reduce both the excessive extensibility and the pathologically increased permeability of the vessel walls for blood fluid. At the same time, the capacity of the veins for blood is reduced. This prevents the symptoms of blood congestion, such as a feeling of heaviness or pain in the legs or nocturnal calf cramps. At the same time, complaints caused by hemorrhoids are also favorably influenced. Areas of application Complaints in chronic venous diseases of the legs, especially a feeling of heaviness, pain and nocturnal calf cramps. Complaints caused by hemorrhoids. If you do not feel better or even worse, contact your doctor.

Application

What should you consider before taking Daflon 500 mg film-coated tablets? Daflon 500 mg film-coated tablets must NOT be taken, - if you are hypersensitive (allergic) to the active substance or any of the other ingredients of Daflon 500 mg film-coated tablets. - Please refer to the section "Contents of the pack and further information". Warnings and Precautions Please talk to your doctor or pharmacist before taking Daflon 500 mg film-coated tablets. If sudden swelling, redness, tension, heat or pain occur, especially if only one leg is affected, please consult your doctor immediately. Children and adolescents The use of Daflon 500 mg film-coated tablets in children and adolescents is not recommended. Taking Daflon 500 mg film-coated tablets together with other medicines Inform your doctor or pharmacist if you are taking/using, have recently taken/used or intend to take/use any other medicines. Interactions are not known for Daflon 500 mg film-coated tablets. Pregnancy, breastfeeding and fertility If you are pregnant or breastfeeding, or if you suspect you may be pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before taking this medicine. Pregnancy For reasons of special caution, this medicine should not be used during pregnancy. Breastfeeding Daflon 500 mg film-coated tablets should not be used during breastfeeding as there is no data on the passage of the drug into breast milk. The occurrence of pregnancy must be reported to the doctor. Ability to drive and operate machinery Daflon has no or negligible influence on the ability to drive and use machines. Always take Daflon 500 mg film-coated tablets exactly as described in this leaflet or exactly as agreed with your doctor or pharmacist. Check with your doctor or pharmacist if you are not sure. The recommended dose is: 1 film-coated tablet twice a day (morning and evening). Alternatively, 2 film-coated tablets can be taken once a day (morning or evening). In the case of acute hemorrhoidal complaints, a temporary increase to 2 x 2 to 3 film-coated tablets per day is possible. The film-coated tablets are taken with meals without chewing and with sufficient liquid. Use in children and adolescents The use of Daflon 500 mg film-coated tablets in children and adolescents is not recommended. If you have taken more Daflon 500 mg film-coated tablets than you should If you have taken more Daflon than you should, contact your doctor or pharmacist immediately. Experience with overdoses of Daflon is limited, symptoms such as diarrhea, nausea, abdominal pain, itching and rash have been reported. If you forget to take Daflon 500 mg film-coated tablets Continue taking the next time. Do not take a double dose if you have forgotten the previous dose. If you have any further questions about the use of the medicine, ask your doctor or pharmacist.

Ingredients

What Daflon 500 mg film-coated tablets contain - Active ingredient: 1 film-coated tablet contains 500 mg purified, micronized flavonoid fraction, consisting of 450 mg diosmin and 50 mg flavonoids, shown as hesperidin. - The other ingredients are: sodium starch glycolate, microcrystalline cellulose, gelatin, magnesium stearate, talc, glycerin, sodium lauryl sulfate, hydroxypropyl methylcellulose, polyethylene glycol 6000, titanium dioxide (E 171), yellow iron oxide (E 172) and red iron oxide (E 172).