Nephrolyt (Drops) Instructions for Use

Marketing Authorization Holder

Talion-A, LLC (Russia)

Dosage Form

Nephrolyt

Homeopathic oral drops: 25 ml dropper bottle.

Dosage Form, Packaging, and Composition

Homeopathic oral drops are transparent, light yellow in color, with a faint alcoholic odor.

Excipients: ethanol about 20 % (by volume).

25 ml – dark glass dropper bottle (1) – cardboard packs.

Clinical-Pharmacological Group

Homeopathic preparation used for cystitis

Pharmacotherapeutic Group

Homeopathic agent

Pharmacological Action

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

Indications

• As part of the complex therapy of acute cystitis or exacerbation of chronic cystitis.

ICD codes

Dosage Regimen

Administer orally. Dilute 8 drops in 1/4 glass of water.

Take in small portions, holding the solution in the mouth for a while before swallowing; do not drink anything immediately after.

Take 3 times a day, following a schedule of 5 days on and 2 days off.

Administer 30 minutes before or 30 minutes to 1 hour after a meal.

The standard treatment course is 1 month. Repeat courses are possible based on medical evaluation.

Adverse Reactions

Allergic reactions are possible.

Discontinue use immediately and seek medical attention if signs of hypersensitivity, such as rash, itching, or swelling, occur.

Report any unexpected effects to a healthcare professional.

Contraindications

• Hypersensitivity to any component of the preparation, including active ingredients or excipients.
• Use in patients under 18 years of age.
• Administration during pregnancy and lactation due to ethanol content.

Use in Pregnancy and Lactation

Not recommended due to the presence of ethyl alcohol (ethanol).

Use in Hepatic Impairment

Use with caution in liver diseases.

Pediatric Use

Contraindicated in children under 18 years of age.

Special Precautions

When taking homeopathic medicinal products, a temporary exacerbation of symptoms is possible. If this exacerbation occurs, you should consult a doctor and take a break from taking the preparation for 5-7 days.

The maximum daily dose of the preparation contains about 0.24 g of absolute alcohol.

Effect on the ability to drive vehicles and mechanisms

The preparation does not affect the performance of potentially hazardous activities requiring special attention and quick reactions (driving a car and other vehicles, working with moving mechanisms, work of a dispatcher and operator, etc.).

Overdose

No cases of overdose have been reported.

Symptoms are not expected to differ from the preparation’s known adverse reactions.

In case of suspected overdose, discontinue use and consult a physician; treatment should be symptomatic and supportive.

Drug Interactions

No specific drug interactions are known.

Concomitant use with other medicinal products is possible.

Inform your physician about all medications you are taking.

Storage Conditions

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

Shelf Life

The shelf life is 3 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.