Konium-Plus (Granules) Instructions for Use

Marketing Authorization Holder

Doctor N, LLC (Russia)

Dosage Form

Konium-Plus

Homeopathic granules: 20 or 40 g bottles, 5 g cases, 10, 15 or 20 g jars.

Dosage Form, Packaging, and Composition

Homeopathic granules uniform, of regular spherical shape, white or white with a gray or cream tint, odorless.

Excipients : sucrose granules 100 g.

20 g – orange glass bottles (1) – cardboard packs.
40 g – orange glass bottles (1) – cardboard packs.
5 g – cases (1) – cardboard packs.
10 g – jars (1) – cardboard packs.
15 g – jars (1) – cardboard packs.
20 g – jars (1) – cardboard packs.

Clinical-Pharmacological Group

Homeopathic preparation used for menstrual cycle disorders, mastopathy and premenstrual syndrome

Pharmacotherapeutic Group

Homeopathic agent

Pharmacological Action

A multicomponent homeopathic medicine, the action of which is due to the components that make up its composition.

Indications

• Benign fibrocystic mastopathy;
• Mastodynia;
• Premenstrual syndrome.

ICD codes

Dosage Regimen

Administer 8 granules sublingually 5 times a day.

Allow granules to dissolve completely under the tongue.

Continue treatment for a duration of up to 8 weeks.

Subsequent treatment courses are permissible if clinically indicated.

Adverse Reactions

Monitor for signs of allergic reactions, which may include skin rash, pruritus, or urticaria.

Discontinue use immediately upon the appearance of any hypersensitivity reactions.

Report any unexpected adverse events to a healthcare professional.

Drug Interactions

No specific pharmacokinetic or pharmacodynamic drug interactions are currently known or have been reported.

Concomitant administration with other medicinal products is not contraindicated.

Inform your physician about all medications you are taking to ensure comprehensive therapy management.

Contraindications

• Do not use in patients with a known hypersensitivity to any of the active or excipient components of the granules.
• This product is contraindicated in individuals under 18 years of age due to the absence of sufficient safety and efficacy data in this population.

Overdose

No cases of overdose have been reported to date, and the clinical presentation of an overdose is unknown.

Given the composition, significant toxic effects are considered unlikely.

In the event of suspected overdose, provide symptomatic and supportive care as there is no specific antidote.

Use in Pregnancy and Lactation

The drug can be taken if the expected benefit to the mother outweighs the potential risk to the fetus and child.

Consultation with a doctor is necessary.

Pediatric Use

Contraindicated for use in children under 18 years of age.

Special Precautions

If there is no therapeutic effect, as well as if side effects not described in the drug instructions appear, you should consult a doctor.

Information for patients with diabetes mellitus – taking the recommended daily dose of the drug in sucrose granules corresponds to 0.13 bread units.

Effect on ability to drive vehicles and operate machinery

No effect.

Storage Conditions

In a dry place, protected from light, at a temperature not exceeding 25°C (77°F).

Keep out of reach of children.

Shelf Life

Shelf life – 5 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.