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Amtersol (Syrup) Instructions for Use

Marketing Authorization Holder

Yaroslavl Pharmaceutical Factory, CJSC (Russia)

ATC Code

R05CA10 (Expectorants in combination)

Dosage Form

Bottle OTC Icon Amtersol Syrup: bottle 100 g

Dosage Form, Packaging, and Composition

Syrup 100 g
Ammonium chloride 200 mg
Potassium bromide 1 g
Sodium benzoate 1 g
Thick extract of licorice root 600 mg
Thermopsis herb liquid extract (1:2) 200 mg

100 g – dark glass bottles (1) – cardboard boxes.

Clinical-Pharmacological Group

Herbal preparation with expectorant and anti-inflammatory effects

Pharmacotherapeutic Group

Expectorant

Pharmacological Action

Licorice root extract has an expectorant effect, primarily due to the presence of glycyrrhizin, which enhances the secretory function of the upper respiratory tract mucous membranes.

Thermopsis extract has an expectorant effect by exerting a moderate irritating effect on the gastric mucosa receptors, reflexively increasing the secretion of the bronchial glands.

The alkaloids contained in thermopsis herb (methylcytisine, pachycarpine, anagyrine, thermopsine, thermopsidine) have an excitatory effect on the respiratory center, and in high doses, on the vomiting center.

Potassium bromide reduces the excitability of the central nervous system.

Ammonium chloride has an expectorant and diuretic effect.

Indications

  • As part of the complex therapy of inflammatory diseases of the respiratory tract, accompanied by cough with difficult-to-expectorate sputum (tracheitis, bronchitis, tracheobronchitis).

ICD codes

ICD-10 code Indication
J04 Acute laryngitis and tracheitis
J20 Acute bronchitis
J37 Chronic laryngitis and laryngotracheitis
J42 Unspecified chronic bronchitis
R05 Cough
R09.3 Sputum
ICD-11 code Indication
CA05 Acute laryngitis or tracheitis
CA0G Chronic laryngitis or laryngotracheitis
CA20.1Z Chronic bronchitis, unspecified
CA42.Z Acute bronchitis, unspecified
MD10 Abnormal sputum
MD12 Cough

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.

The drug is taken orally, after meals.

Children from 3 to 6 years: 1/2 teaspoon 3 times/day.

Children from 6 to 12 years: 1 teaspoon 3 times/day.

Adolescents from 12 to 18 years: 1 dessert spoon 3 times/day.

Adults: 1 tablespoon 3 times/day.

The average course of treatment is 10-14 days. Increasing the duration and conducting repeated courses of treatment is possible on the recommendation of a doctor.

Adverse Reactions

Allergic reactions are possible.

Contraindications

  • Peptic ulcer of the stomach and duodenum in the acute phase;
  • Pregnancy;
  • Lactation period;
  • Children under 3 years of age;
  • Hypersensitivity to the drug components.

With caution alcoholism, epilepsy, liver diseases, brain diseases and injuries (due to the presence of ethanol in the drug), diabetes mellitus (due to the high sugar content in the drug).

Use in Pregnancy and Lactation

Contraindicated during pregnancy and lactation.

Use in Hepatic Impairment

With caution in liver diseases.

Pediatric Use

Contraindicated in children under 3 years of age.

Overdose

With prolonged use in doses exceeding the recommended ones, nausea and vomiting are possible.

Drug Interactions

Amtersol should not be used simultaneously with drugs containing antitussive medicinal products, as this makes it difficult to cough up liquefied sputum.

Storage Conditions

In a place protected from light and out of reach of children, at a temperature not exceeding 25°C (77°F).

Shelf Life

The shelf life is 2 years.

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

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