Valocormid (Drops) Instructions for Use

Marketing Authorization Holder

Yaroslavl Pharmaceutical Factory, CJSC (Russia)

ATC Code

N05CM (Other hypnotic and sedative drugs)

Dosage Form

Valocormid

Oral drops: 25 ml bottle or dropper bottle.

Dosage Form, Packaging, and Composition

Excipients : ethanol.

25 ml – bottles (1) – cardboard packs.
25 ml – bottles.
25 ml – dropper bottles.
25 ml – dropper bottles (1) – cardboard packs.

Clinical-Pharmacological Group

Herbal preparation with cardiotonic and sedative effects

Pharmacotherapeutic Group

Sedative

Pharmacological Action

A combined preparation of plant origin, which includes: belladonna tincture, valerian rhizomes with roots tincture, lily of the valley herb tincture, Sodium bromide, racemic menthol.

Valocormid is available as oral drops. It has a sedative, cardiotonic, and antispasmodic effect.

Preparations containing valerian and Sodium bromide reduce the excitability of the central nervous system.

Lily of the valley tincture, containing cardiac glycosides, has a cardiotonic effect.

Belladonna alkaloids have an m-cholinolytic effect.

Indications

• Functional disorders of the cardiovascular system (as a sedative).

ICD codes

Dosage Regimen

Administer orally.

Use 10-20 drops per single dose.

Take 2-3 times daily.

Administer before meals.

Measure the dose precisely using the dropper provided.

Dilute the required number of drops in a small amount of water immediately before administration.

Do not exceed the recommended dosage.

The duration of use is determined by the physician based on clinical indications and treatment response.

Discontinue use and consult a physician if symptoms persist or worsen.

Adverse Reactions

Gastrointestinal system: nausea, vomiting, diarrhea.

Cardiovascular system: arrhythmias.

Nervous system: headache, myasthenia.

Special senses: accommodation paresis.

Immune system: allergic reactions.

Drug Interactions

Exercise caution with central nervous system depressants (alcohol, sedatives, hypnotics) due to risk of additive sedative effects.

Belladonna alkaloids may interact with other anticholinergic drugs, increasing adverse effects.

Monitor for enhanced effects when combined with other cardiac glycosides.

Sodium bromide may interact with diuretics and lithium.

Contraindications

• hypersensitivity to any component of the preparation;
• Severe cardiosclerosis;
• endocarditis;
• myocarditis;
• Hepatic and/or renal failure;
• respiratory failure;
• Closed-angle glaucoma.

Overdose

Symptoms may include severe nausea, vomiting, diarrhea, cardiac arrhythmias, marked sedation, confusion, and visual disturbances.

Immediately discontinue the preparation.

Provide symptomatic and supportive treatment.

Gastric lavage and administration of activated charcoal may be considered.

Seek immediate medical attention.

Use in Hepatic Impairment

Contraindication — hepatic failure.

Use in Renal Impairment

Contraindication — renal failure.

Special Precautions

Effect on the ability to drive vehicles and operate machinery

During treatment, caution should be exercised when driving vehicles and engaging in other potentially hazardous activities that require increased concentration, rapid psychomotor reactions, and good vision.

Storage Conditions

Store at 15°C (59°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.

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.