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Homeostres® (Tablets) Instructions for Use

Marketing Authorization Holder

Boiron (France)

Contact Information

BOIRON (France)

ATC Code

V30 (Not assigned)

Dosage Form

Bottle OTC Icon Homeostres® Homeopathic sublingual tablets: 40 or 90 pcs.

Dosage Form, Packaging, and Composition

Homeopathic sublingual tablets are white, round, biconvex in shape, with the engraving “SEDATIF P.C.” on one side, odorless or with a faint odor.

1 tab.
Aconitum napellus C6 0.5 mg
Belladonna C6 0.5 mg
Calendula officinalis C6 0.5 mg
Chelidonium majus C6 0.5 mg
Jequirity C6 0.5 mg
Viburnum opulus C6 0.5 mg

Excipients: sucrose – 225 mg, lactose – 72 mg, magnesium stearate – 3 mg.

18 pcs. – blisters (5) – cardboard packs.
20 pcs. – blisters (2) – cardboard packs.

Clinical-Pharmacological Group

Homeopathic preparation used for anxiety disorders and sleep disturbances

Pharmacotherapeutic Group

Homeopathic agent

Pharmacological Action

A multicomponent homeopathic remedy, the action of which is due to the components included in its composition.

Indications

  • Anxiety disorders;
  • Restlessness;
  • Sleep disturbances.

ICD codes

ICD-10 code Indication
F41.9 Anxiety disorder, unspecified
R45.1 Restlessness and agitation
F51.2 Nonorganic disorders of the sleep-wake schedule
ICD-11 code Indication
6B0Z Anxiety or fear-related disorders, unspecified
7B2Z Sleep-wake cycle disorders, unspecified
MB24.F Restlessness

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. 2 tablets should be slowly dissolved under the tongue 3 times a day.

For children under 6 years of age, the tablets should be dissolved in water before administration.

The duration of treatment is 7-14 days as recommended by a doctor. The use of the drug should not exceed 2 weeks. It is necessary to consult a doctor if symptoms worsen or do not stop after 7 days of treatment.

Adverse Reactions

To date, there is no information on the adverse reactions of the drug. If side effects occur, you should consult a doctor.

Contraindications

  • Severe anxiety disorders;
  • Children under 3 years of age;
  • Increased individual sensitivity to individual components of the drug.

Use in Pregnancy and Lactation

The drug is used after consultation with a doctor.

Pediatric Use

The use of the drug is contraindicated in children under 3 years of age.

Special Precautions

It is necessary to consult a doctor if there is no improvement in the condition while taking the drug.

In case of diagnosed fructose, sucrose or galactose intolerance, glucose-galactose malabsorption syndrome or sucrase/isomaltase deficiency, the drug should not be taken due to the presence of sucrose and lactose in its composition.

Information for patients with diabetes: each tablet contains less than 0.02 XE (Bread Units).

Effect on the ability to drive vehicles and operate machinery

No effect.

Overdose

Cases of overdose have not been reported to date.

Drug Interactions

To date, there are no data on interactions with other medicinal products.

The use of homeopathic medicines does not exclude treatment with other medicines.

Storage Conditions

The drug should be stored out of the reach of children at a temperature not exceeding 25°C (77°F).

Shelf Life

Shelf life – 5 years. Do not use after the expiration date printed on the packaging.

Dispensing Status

The drug is available without a 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.

Medical Disclaimer

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