Glycyrrhizic Acid + Phospholipids (Capsules) Instructions for Use
Marketing Authorization Holder
Pharmstandard JSC (Russia)
ATC Code
A05BA (Drugs for the treatment of liver diseases)
Active Substances
Glycyrrhizinic acid (BP British Pharmacopoeia)
Phospholipids (Group Grouping name)
Dosage Form
| Glycyrrhizic acid + Phospholipids | Capsules 35 mg+65 mg: 50 pcs. |
Dosage Form, Packaging, and Composition
Capsules are soft gelatin, light brown in color, oval, with a seam, elastic, opaque; the capsule contents are a homogeneous mass from light yellow to dark yellow in color, with a consistency ranging from ointment-like to denser, with a specific odor; slight stratification of the capsule contents is allowed during storage.
| 1 caps. | |
| Sodium glycyrrhizinate (trisodium salt of glycyrrhizic acid) | 35 mg |
| Phospholipids | 65 mg |
Excipients: beeswax – 36 mg, sunflower oil – a sufficient quantity to obtain capsule contents weighing 450 mg.
Composition of the gelatin capsule shell: gelatin – 106.22 mg, glycerol – 48.93 mg, purified water – 13.6 mg, sodium benzoate E-211 – 0.25 mg, titanium dioxide E-171 – 0.22 mg, dyes: red iron oxide (E-172) – 0.13 mg, yellow iron oxide (E-172) – 0.51 mg, black iron oxide (E-172) – 0.14 mg.
10 pcs. – blister packs (5) – cardboard packs.
Clinical-Pharmacological Group
Hepatoprotective agent with immunomodulatory and antiviral action
Pharmacotherapeutic Group
Hepatoprotective agent
Pharmacological Action
Hepatoprotective agent, also possesses antiviral activity.
Glycyrrhizic acid suppresses virus reproduction in the liver and other organs due to its stimulating effect on interferon production, increasing phagocytosis, and enhancing the activity of natural killer cells. Due to its detergent action, it improves the emulsification of phosphatidylcholine in the intestine.
Phosphatidylcholine is the main structural component of the phospholipid layer of biological membranes (cellular and intracellular). It restores the structure and function of damaged hepatocyte membranes, thereby preventing the loss of enzymes and other active substances by the cells, normalizes protein, lipid, and fat metabolism, restores the detoxification function of the liver, suppresses the formation of connective tissue in the liver, and reduces the risk of fibrosis and cirrhosis of the liver.
Pharmacokinetics
The components of this combination are well absorbed in the small intestine both in the form of the original molecule and as biologically active products of their hydrolysis by digestive enzymes (unsaturated fatty acids, glycerol, inorganic phosphate and choline, glycyrrhetinic acid), which are transported through the intestinal wall into the lymphatic system, easily penetrate the liver, lungs, skin, and other organs.
Partial resynthesis of phosphatidylcholine from hydrolysis products occurs in the liver.
Indications
As part of complex therapy: acute and chronic hepatitis; fatty hepatosis and other degenerative liver lesions; drug-induced and alcoholic liver lesions; liver cirrhosis; intoxications; psoriasis; neurodermatitis; eczema.
ICD codes
| ICD-10 code | Indication |
| B15 | Acute hepatitis A |
| B16 | Acute hepatitis B |
| B17.1 | Acute hepatitis C |
| B18.0 | Chronic viral hepatitis B with delta-agent |
| B18.1 | Chronic viral hepatitis B without delta-agent |
| B18.2 | Chronic viral hepatitis C |
| K70 | Alcoholic liver disease |
| K71 | Toxic liver disease |
| K73 | Chronic hepatitis, not elsewhere classified |
| K74 | Fibrosis and cirrhosis of liver |
| K76.0 | Fatty (change of) liver, not elsewhere classified |
| L20.8 | Other atopic dermatitis (neurodermatitis, eczema) |
| L28.0 | Lichen simplex chronicus (circumscribed neurodermatitis) |
| L30.0 | Nummular eczema |
| L40 | Psoriasis |
| ICD-11 code | Indication |
| 1E50.0 | Acute hepatitis A |
| 1E50.1 | Acute hepatitis B |
| 1E50.2 | Acute hepatitis C |
| 1E51.0Z | Chronic hepatitis B, unspecified |
| 1E51.1 | Chronic viral hepatitis C |
| 1E51.2 | Chronic hepatitis D |
| 4A85.00 | Drug hypersensitivity-induced liver disease |
| 9A06.70 | Atopic eczema of the eyelids |
| DB92.0 | Non-alcoholic fatty liver disease without steatohepatitis |
| DB92.Y | Other specified non-alcoholic fatty liver disease |
| DB92.Z | Non-alcoholic fatty liver disease, unspecified |
| DB93 | Fibrosis or cirrhosis of liver |
| DB94.Z | Alcoholic liver disease, unspecified |
| DB95.Z | Drug-induced or toxic liver disease, unspecified |
| DB97.2 | Chronic hepatitis, not elsewhere classified |
| EA80.0 | Infantile atopic eczema |
| EA80.1 | Childhood atopic eczema |
| EA80.2 | Adult atopic eczema |
| EA80.Z | Atopic eczema, unspecified |
| EA82 | Nummular dermatitis |
| EA83.00 | Lichen simplex of vulva |
| EA83.01 | Lichen simplex of male genital organs |
| EA83.02 | Lichen simplex of perianal area |
| EA83.0Z | Lichen simplex of unspecified location |
| EA85.20 | Atopic hand eczema |
| EA90.Z | Psoriasis, unspecified |
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. |
Take the capsules orally with meals, swallowing whole with a small amount of water.
The standard adult dosage is 2 capsules taken three to four times daily.
For acute conditions, initiate therapy at the higher frequency of four times daily.
For chronic liver diseases, maintain the prescribed dosage for the full duration of therapy.
The duration of treatment is determined by the physician based on the disease severity and clinical response.
For parenteral administration, administer the solution intravenously and slowly.
The single IV dose is administered twice daily, in the morning and evening.
The typical course of IV therapy is 10 days.
Following the IV course, switch to oral administration of the capsules to continue treatment.
Do not adjust the dosage or frequency without medical consultation.
Adverse Reactions
Allergic reactions skin rash.
Contraindications
Hypersensitivity to the components of the combination.
Use in Hepatic Impairment
The drug is approved for use in liver dysfunction
Drug Interactions
The solution for parenteral administration should not be mixed with solutions of other medicinal products.
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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