Escizane (Tablets) Instructions for Use
Marketing Authorization Holder
Evalar, CJSC (Russia)
ATC Code
C05CX (Drugs reducing capillary permeability, other)
Active Substance
Aescine
Dosage Form
| Escizane | Film-coated tablets, 110 mg: 20, 30, 40, or 60 pcs. |
Dosage Form, Packaging, and Composition
| Film-coated tablets | 1 tab. |
| Dry extract of horse chestnut fruit | 110 mg |
| With a content of triterpene glycosides calculated as Aescine | Not less than 19% |
30 pcs. – polymer bottles (1) – cardboard packs.
40 pcs. – polymer bottles (1) – cardboard packs.
60 pcs. – polymer bottles (1) – cardboard packs.
30 pcs. – polymer jars (1) – cardboard packs.
40 pcs. – polymer jars (1) – cardboard packs.
60 pcs. – polymer jars (1) – cardboard packs.
20 pcs. – contour cell blisters (1) – cardboard packs.
20 pcs. – contour cell blisters (2) – cardboard packs.
20 pcs. – contour cell blisters (3) – cardboard packs.
Clinical-Pharmacological Group
Herbal preparation, used for disorders of venous circulation
Pharmacotherapeutic Group
Venotonic agent of plant origin
Pharmacological Action
A triterpene glycoside (saponin) from horse chestnut fruit (seeds). It has a pronounced capillary-protective activity and exerts anti-exudative and venotonic effects.
It reduces the concentration of lysosomal enzymes, thereby decreasing the breakdown of mucopolysaccharides in the capillary wall area. It significantly reduces vascular permeability, preventing the filtration of low-molecular-weight proteins, electrolytes, and water into the intercellular space.
When applied topically, Aescine has an anti-inflammatory effect, mainly in the initial phase of the inflammatory reaction, by reducing the permeability of the capillary wall, which is increased during inflammation.
Aescine also has a positive effect on capillary wall fragility and increases the tone of venous walls when it is weakened. All this leads to a reduction in venous stasis and fluid accumulation in tissues, preventing the appearance of edema.
Pharmacokinetics
After oral administration of 50 mg of horse chestnut fruit extract, the Cmax in blood plasma is reached after 2.35 hours and is 25.31 ng/ml.
Plasma protein binding is 84%.
T1/2 is 19.87 hours. After oral administration, 0.11% of the horse chestnut fruit extract is excreted by the kidneys in the form of escin.
Indications
Post-thrombophlebitic syndrome and individual symptoms of chronic venous insufficiency of various etiologies (including edema, calf muscle cramps, pain and heaviness in the legs), varicose veins, trophic disorders. Post-traumatic or postoperative soft tissue edema.
ICD codes
| ICD-10 code | Indication |
| I83 | Varicose veins of lower extremities |
| I87.0 | Postthrombotic syndrome |
| I87.2 | Venous insufficiency (chronic) (peripheral) |
| R60.0 | Localized edema |
| ICD-11 code | Indication |
| BD74.1Z | Varicose veins of lower extremities, unspecified |
| BD74.Z | Chronic venous insufficiency of lower extremities, unspecified |
| MG29.0 | Localized edema |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Administer orally or topically as appropriate for the clinical presentation.
For oral administration, take one 110 mg tablet three times daily with meals to enhance tolerability and absorption.
Continue the oral treatment course for a minimum duration of four weeks to achieve a stable therapeutic effect.
For topical application, gently rub the corresponding dosage form into the affected skin area several times per day until fully absorbed.
Adjust the total duration of therapy individually based on the severity of symptoms and clinical response.
Do not exceed the recommended oral dosage without medical supervision.
Discontinue use and consult a physician if symptoms persist or worsen after several weeks of treatment.
Adverse Reactions
Allergic reactions skin rash, urticaria, itching, redness, feeling of heat.
From the digestive system when taken orally – nausea, heartburn.
Contraindications
Hypersensitivity to escin.
Use in Pregnancy and Lactation
Oral administration during pregnancy, while breastfeeding, and in women of childbearing potential not using contraception is not recommended.
The necessity of topical application during pregnancy and breastfeeding is determined by the doctor individually.
Use in Renal Impairment
With long-term use, periodic monitoring of kidney function is recommended.
Pediatric Use
Use is possible according to the dosing regimen.
Special Precautions
Use topically with caution in patients prone to thrombosis.
Contraindications for oral preparations containing ethyl alcohol should be taken into account.
Drug Interactions
Concomitant use with escin may enhance the activity of anticoagulants and other drugs with antithrombotic action.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Over-the-Counter
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer
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