VAN BI (Capsules) Instructions for Use

Marketing Authorization Holder

Lupin, Ltd. (India)

ATC Code

A13A (General tonic preparations)

Dosage Form

VAN BI

Capsules: 10, 20, 30, or 50 pcs.

Dosage Form, Packaging, and Composition

10 pcs. – PVC/aluminum foil blisters (1) – cardboard packs.
10 pcs. – PVC/aluminum foil blisters (2) – cardboard packs.
10 pcs. – PVC/aluminum foil blisters (3) – cardboard packs.
10 pcs. – PVC/aluminum foil blisters (5) – cardboard packs.

Clinical-Pharmacological Group

Herbal preparation of general tonic action

Pharmacotherapeutic Group

Herbal general tonic agent

Pharmacological Action

The combined drug Van Bi is developed based on the principles of Ayurvedic medicine. The pharmacological action of the drug is due to its constituent components (dry extracts of medicinal plants).

Asparagus racemosus has a general tonic effect and exhibits adaptogenic properties.

Withania somnifera helps reduce the severity of astheno-neurotic reactions and has an anti-stress effect.

Piper longum has anti-inflammatory and tonic effects, stimulates the body’s defenses.

Pueraria tuberosa activates metabolic processes in the brain and improves memory.

Mucuna pruriens stimulates appetite and normalizes gastrointestinal motility.

Dioscorea bulbifera has a moderately pronounced hypocholesterolemic effect.

Argyreia speciosa has a general tonic effect and enhances libido.

Mineral pitch (Shilajit) increases tolerance to physical exertion and activates mental activity.

The drug Van Bi increases endurance to adverse environmental influences, promotes rapid recovery after heavy physical exertion, and exhibits moderate anti-stress activity.

Indications

• Asthenic syndrome of various origins, during mental and physical fatigue, stress.

ICD codes

Dosage Regimen

Take orally with a sufficient amount of water.

Administer 1 capsule once or twice daily.

Adhere to a minimum treatment course of 4 weeks to achieve the intended therapeutic effect.

For long-term use beyond the initial course, consult a physician for re-evaluation.

Do not exceed the recommended daily dosage.

Take the capsules at consistent times each day to maintain stable blood levels.

If a dose is missed, take it as soon as remembered unless it is nearly time for the next dose; in that case, continue with the regular schedule.

Discontinue use and seek medical advice if adverse reactions occur.

The duration of therapy may be adjusted by a healthcare professional based on individual patient response and clinical need.

A repeat course of treatment requires prior medical consultation.

Adverse Reactions

Possible allergic reactions to the drug components, stool disorder (diarrhea or constipation), dizziness, sleep disturbance.

Rarely tachycardia, increased blood pressure.

Contraindications

• Sleep disturbance;
• Arterial hypertension;
• Epilepsy;
• Hyperkinesis;
• Pregnancy;
• Lactation period;
• Children under 18 years of age;
• Hypersensitivity to the drug components.

Use in Pregnancy and Lactation

Contraindicated during pregnancy and lactation.

Pediatric Use

Contraindicated in children under 18 years of age.

Drug Interactions

Potentiation of the action of stimulants and analeptics (caffeine, camphor, phenamine, etc.) is possible.

The drug is an antagonist of agents that depress the central nervous system (including barbiturates, anticonvulsants, etc.).

Storage Conditions

Store the drug in a dry, light-protected place, out of the reach of children, at a temperature not exceeding 30°C (86°F).

Shelf Life

Shelf life – 3 years. Do not use after the expiration date printed on the packaging.

Dispensing Status

The drug is approved for use as an over-the-counter product.

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.