Hyporolam (Solution) Instructions for Use

Marketing Authorization Holder

Biopharmkombinat, LLC (Russia)

Manufactured By

Biopharmkombinat, LLC (Russia)

Or

Medkhimprom Pharmchemical Company, OJSC (Russia)

ATC Code

A13A (General tonic preparations)

Dosage Form

Hyporolam

Oral solution: bottle 50 ml or 100 ml

Dosage Form, Packaging, and Composition

Oral solution (alcoholic) in the form of a transparent liquid from yellow to yellowish-red in color, with a specific odor.

Excipients: ethanol 95% – up to 100 ml.

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

Clinical-Pharmacological Group

Herbal preparation with general tonic effect

Pharmacotherapeutic Group

Herbal general tonic agent

Pharmacological Action

A combined preparation, the action of which is due to the biological activity of its constituent components.

It increases the body’s resistance to adverse factors (in particular, to hypoxia), during physical and mental overwork.

Indications

• Asthenic conditions;
• Convalescence period after past illnesses;
• Increased physical and mental stress (as part of complex therapy in adults).

ICD codes

Dosage Regimen

Administer orally.

Use only for adults.

Take one teaspoon (5 ml) once daily.

Always dilute the dose in 50 ml of water prior to administration.

Take the dose in the morning.

Take after a meal.

The standard course of treatment is 2 weeks.

Do not exceed the recommended duration without medical consultation.

Any increase in duration or repeated treatment courses requires a doctor’s recommendation.

Adverse Reactions

Allergic reactions are possible.

Contraindications

• Hypersensitivity to the components of the drug, including iodine;
• Nephritis;
• Renal failure;
• Hemorrhagic diathesis;
• Thyroid diseases;
• Alcoholism;
• Traumatic brain injury;
• Brain diseases;
• Liver diseases;
• Hypervitaminosis A;
• Pregnancy, breastfeeding period;
• Age under 18 years.

Use in Pregnancy and Lactation

Contraindicated during pregnancy and lactation.

Use in Hepatic Impairment

Contraindicated in liver diseases.

Use in Renal Impairment

Contraindicated in renal failure and nephritis.

Pediatric Use

Contraindicated in children under 18 years of age.

Special Precautions

The preparation contains at least 90% ethyl alcohol.

The maximum daily dose of the preparation (5 ml) contains about 4.5 g of absolute alcohol.

When using Hyporolam simultaneously with multivitamin preparations, the content of carotenoids in its composition should be taken into account to avoid possible overdose.

One teaspoon (5 ml) of Hyporolam contains at least 0.04 mg of the sum of carotenoids calculated as beta-carotene.

Overdose

No cases of overdose have been reported.

Storage Conditions

In a place protected from light, at a temperature of 15-25°C (59-77°F). Keep out of reach of children.

Shelf Life

Shelf life – 2 years.

Dispensing Status

By prescription.

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.