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ATC Code

A13A (General tonic preparations)

Active Substance

Red deer antler extract (Grouping name)

Clinical-Pharmacological Group

A drug used for asthenic conditions

Pharmacotherapeutic Group

General tonic agent

Pharmacological Action

Adaptogenic agent. It has a stimulating effect on the central nervous system and the cardiovascular system, increases the tone of skeletal muscles, and intestinal motor activity.

It contains phospholipids and trace elements, increases working capacity, and normalizes blood pressure in arterial hypotension, stimulates the activity of the gastrointestinal tract organs.

Indications

Use this preparation for the treatment of asthenic conditions and as a general tonic to increase physical and mental working capacity.

• Administer as part of a complex therapy for diagnosed neurasthenia to alleviate symptoms of fatigue and irritability.
• Employ in the management of arterial hypotension to help normalize low blood pressure levels.

ICD codes

Dosage Regimen

Take orally, 30 minutes before meals, 2-3 times per day for a duration of 2-3 weeks. Maintain an interval of 10 days between treatment courses.

Repeat the course after a 5-7 day break if necessary, typically up to 3 times per year. For subcutaneous or intramuscular administration, inject 1-2 ml daily over a 15-20 day period, conducting 2-3 courses with a 10-day interval between them.

Adverse Reactions

Monitor for allergic reactions, including skin itching and rash. Be aware of the potential for increased blood pressure and the occurrence of headache.

Discontinue use immediately and consult a physician if any severe or persistent adverse effects develop during the treatment course.

Contraindications

• Do not use in patients with severe atherosclerosis, chronic heart failure, or angina pectoris due to the risk of cardiovascular complications.
• Avoid administration in conditions of hypercoagulation, severe forms of nephritis, diarrhea, arterial hypertension, and malignant neoplasms.

Use in Renal Impairment

Contraindicated in nephritis (severe forms).

Drug Interactions

Avoid concurrent use with anticoagulants due to potential interference with their therapeutic effect. Do not co-administer with calcium salts or medications that stimulate intestinal peristalsis.

Inform your physician about all concomitant medications before initiating therapy to prevent potential interactions.

Overdose

Symptoms of overdose may include a significant increase in blood pressure, severe headache, tachycardia, and nervous agitation.

Immediately discontinue the medication and initiate symptomatic and supportive treatment. There is no specific antidote; manage manifestations according to clinical presentation.

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.