Antraliv (Capsules) Instructions for Use
Marketing Authorization Holder
Nizhpharm JSC (Russia)
ATC Code
A05BA10 (Phospholipids)
Active Substance
Phospholipids (Grouping name)
Dosage Form
| Antraliv | Capsules 300 mg: 20, 30, 40, 50, 60, or 100 pcs. |
Dosage Form, Packaging, and Composition
| Capsules | 1 caps. |
| Phospholipids | 300 mg |
10 pcs. – blister packs (2) – cardboard packs.
10 pcs. – blister packs (3) – cardboard packs.
10 pcs. – blister packs (4) – cardboard packs.
10 pcs. – blister packs (5) – cardboard packs.
10 pcs. – blister packs (6) – cardboard packs.
10 pcs. – blister packs (10) – cardboard packs.
Clinical-Pharmacological Group
Hepatoprotective agent
Pharmacotherapeutic Group
Hepatoprotective agent
Pharmacological Action
Hepatoprotective agent; the Phospholipids included in the composition are the main elements in the structure of the cell membrane and mitochondria.
It regulates lipid and carbohydrate metabolism, improves the functional state of the liver and its detoxification function, promotes the preservation and restoration of the structure of hepatocytes; inhibits the formation of connective tissue in the liver.
Pharmacokinetics
Binding mainly to high-density lipoproteins, phosphatidylcholine enters, in particular, into liver cells.
The T1/2 of the choline component is 66 hours, and that of unsaturated fatty acids is 32 hours.
Indications
Fatty liver dystrophy (including in diabetes mellitus); acute and chronic hepatitis, liver cirrhosis, liver cell necrosis, hepatic coma and precoma, toxic liver lesions; pregnancy toxemia; pre- and postoperative treatment, especially for operations in the hepatobiliary area; psoriasis (as an auxiliary therapy); radiation syndrome.
ICD codes
| ICD-10 code | Indication |
| B15 | Acute hepatitis A |
| B16 | Acute hepatitis B |
| B17.1 | Acute hepatitis C |
| B18 | Chronic viral hepatitis |
| K71 | Toxic liver disease |
| K72 | Hepatic failure, not elsewhere classified (including hepatic coma, hepatic encephalopathy) |
| K73 | Chronic hepatitis, not elsewhere classified |
| K74 | Fibrosis and cirrhosis of liver |
| K76.0 | Fatty (change of) liver, not elsewhere classified |
| L40 | Psoriasis |
| O21 | Excessive vomiting in pregnancy |
| T66 | Unspecified effects of radiation (radiation sickness) |
| Z51.4 | Preparatory procedures for subsequent treatment or examination, not elsewhere classified |
| Z98.8 | Other specified postprocedural states |
| ICD-11 code | Indication |
| 1E50.0 | Acute hepatitis A |
| 1E50.1 | Acute hepatitis B |
| 1E50.2 | Acute hepatitis C |
| 1E51.Z | Chronic viral hepatitis, unspecified |
| 4A85.00 | Drug hypersensitivity-induced liver disease |
| 8E61.0 | Radiation-induced brain injury |
| 8E61.1 | Radiation-induced spinal cord injury |
| DB91.Z | Unspecified acute or subacute liver failure |
| 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 |
| DB95.Z | Drug-induced or toxic liver disease, unspecified |
| DB97.2 | Chronic hepatitis, not elsewhere classified |
| DB99.7 | Hepatic failure, not specified as acute or chronic |
| DB99.8 | Chronic hepatic failure |
| DB9Z | Liver diseases, unspecified |
| EA90.Z | Psoriasis, unspecified |
| JA60.Z | Excessive vomiting in pregnancy, unspecified |
| NF00 | Exposure to radiation, not elsewhere classified |
| QB6Z | Surgical or postprocedural conditions, unspecified |
| QB9A | Preparatory procedures for subsequent treatment |
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 with a meal. Swallow capsules whole with a sufficient amount of liquid. Do not chew.
For adults and adolescents over 18 years of age, the standard dosage is two capsules ( 600 mg) three times daily.
The maximum daily dose is six capsules ( 1800 mg). Do not exceed this dose.
The duration of therapy is determined by the physician based on the indication and severity of the condition. The typical course of treatment is up to three months.
For maintenance therapy, use one capsule ( 300 mg) three times daily.
In severe cases, such as liver cirrhosis, the initial dosage may be increased. Follow the physician’s specific instructions.
For psoriasis as adjuvant therapy, administer two capsules three times daily for at least two weeks, followed by one capsule three times daily for the subsequent at least two months.
For radiation syndrome, initiate treatment with two capsules three times daily for a 10-14 day course.
Adjust the regimen for pre- and postoperative care as directed. The dosage form is for oral use only.
Adverse Reactions
From the digestive system when used in high doses – diarrhea.
From the immune systemhypersensitivity reactions, including skin allergic reactions: skin rash, skin itching, exanthema or urticaria.
Contraindications
Age under 18 years; soy intolerance; hypersensitivity to the active substance.
Use in Pregnancy and Lactation
Use during pregnancy is possible only in cases where the expected benefit of therapy for the mother outweighs the potential risk to the fetus.
It is not recommended for use during breastfeeding due to the lack of data on safety of use.
Special Precautions
As the patient’s condition improves, parenteral administration is replaced by oral administration of a drug containing Phospholipids in the appropriate dosage form.
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