Adaptocon (Solution) Instructions for Use

Marketing Authorization Holder

Pharmakon, JSC (Russia)

ATC Code

A13A (General tonic preparations)

Active Substances

Tocopherol (Ph.Eur. European Pharmacopoeia)

Laminaria (BP British Pharmacopoeia)

Dosage Form

Adaptocon

Oral solution, alcohol-based: bottle 100 ml

Dosage Form, Packaging, and Composition

Oral drops (alcohol-based).

25 ml – dark glass bottles (1) – cardboard packs.
40 ml – dark glass bottles (1) – cardboard packs.
50 ml – dark glass bottles (1) – cardboard packs.
100 ml – dark glass bottles (1) – cardboard packs.

Clinical-Pharmacological Group

Drug with general tonic action

Pharmacotherapeutic Group

General tonic agent

Pharmacological Action

General tonic agent. It increases the body’s resistance to adverse factors during physical and mental fatigue.

Indications

• Asthenic conditions and states of general fatigue and weakness.
• As a supportive treatment during the convalescence period following illness or medical procedures.
• For use in situations involving intense physical exertion or demanding mental stress to support adaptive capacity.

ICD codes

Dosage Regimen

Administer orally. Dilute the required number of drops in 50 ml of water immediately prior to ingestion.

For adults, use 20 to 40 drops per dose. Adjust the exact number of drops within this range based on the severity of the asthenic condition and individual patient response.

Take the prepared solution three times daily, preferably with meals.

The maximum daily dosage is 120 drops. Do not exceed this limit.

The typical treatment course is 3 to 4 weeks. The duration of therapy can be repeated as directed by a physician, with intervals between courses.

Adhere strictly to the prescribed dosage, frequency, and duration of administration. Do not adjust the regimen without medical consultation.

Adverse Reactions

Monitor for systemic hypersensitivity reactions.

Discontinue use immediately and seek medical attention if signs of an allergic reaction occur, such as rash, pruritus, urticaria, or angioedema.

Contraindications

• Contraindicated in patients with a known hypersensitivity to any component of the formulation, including iodine or tocopherol.
• Do not use in patients with cardiosclerosis, history of myocardial infarction, acute nephritis, or severe renal failure.
• Avoid use in patients with hemorrhagic diathesis, thyroid diseases, or diagnosed hypervitaminosis E.
• Contraindicated during pregnancy and throughout the lactation period. Do not administer to individuals under 18 years of age.

Use in Pregnancy and Lactation

Contraindicated during pregnancy and lactation (breastfeeding).

Use in Hepatic Impairment

With caution: liver cirrhosis, viral hepatitis.

Use in Renal Impairment

Contraindicated in severe renal failure.

Pediatric Use

Contraindicated under 18 years of age.

Geriatric Use

With caution in elderly age.

Special Precautions

When using, the daily requirement and therapeutic doses of vitamin E should be considered to avoid overdose.

The daily requirement of vitamin E for an adult is on average 10 mg.

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

Rx Only

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.