Anginit-GF (Granules) Instructions for Use

Marketing Authorization Holder

Homeopathic Pharmacy, LLC (Russia)

Dosage Form

Anginit-GF

Homeopathic granules: 8 g jars or tubes

Dosage Form, Packaging, and Composition

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

Excipients: nonpareil sugar pellets 100 g.

8 g – polymer jars (1) – cardboard packs.
8 g – polymer tubes (1) – cardboard packs.

Clinical-Pharmacological Group

Homeopathic preparation used for acute and chronic tonsillitis

Pharmacotherapeutic Group

Homeopathic agent

Pharmacological Action

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

Indications

• As part of complex therapy for exacerbation of chronic tonsillitis.

ICD codes

Dosage Regimen

For acute symptom management, dissolve 5 granules every 30 minutes until condition improves. Do not exceed 16 doses per day.

After initial improvement, transition to a maintenance dose of 5 granules 3-4 times daily. Administer doses 20 minutes before or 1 hour after meals.

Complete the full treatment course of 10-14 days as directed.

Adverse Reactions

No specific adverse reactions have been formally reported for this preparation.

Be aware that homeopathic aggravations, characterized by a temporary intensification of existing symptoms, may occur. Discontinue use and consult a physician if this occurs.

Monitor for any signs of allergic reactions or individual intolerance to the components.

Drug Interactions

Formal drug interaction studies have not been conducted with this homeopathic preparation.

Avoid concurrent use with strong aromatic substances, including camphor, menthol, and eucalyptus, as they may theoretically antagonize the homeopathic effect.

Maintain a consistent time interval between administering this preparation and consuming food, beverages, or other medications to ensure optimal absorption.

Contraindications

• Hypersensitivity to any component of the formulation, including Apis mellifica, Belladonna, or Mercurius solubilis.
• Pregnancy due to the absence of adequate safety data for use during this period.
• Lactation due to the unknown excretion of components in breast milk and potential risk to the infant.
• Pediatric patients under 18 years of age because clinical data establishing safety and efficacy in this population are lacking.

Overdose

No cases of overdose have been reported to date. Due to the nature of homeopathic dilutions, the risk of toxicological effects from the active ingredients is considered low.

In the event of accidental ingestion of a significantly large quantity, the primary concern may be related to the sucrose excipient.

Discontinue the product and manage any gastrointestinal discomfort symptomatically. Seek medical attention if unusual symptoms occur.

Use in Pregnancy and Lactation

Contraindicated during pregnancy and lactation.

Pediatric Use

Contraindicated for children under 18 years of age due to the lack of sufficient clinical data.

Special Precautions

When using homeopathic medicines, a temporary exacerbation of symptoms may occur. In this case, you should stop taking the drug and consult a doctor.

If there is no therapeutic effect, as well as if side effects occur, you should consult a doctor.

Information for patients with diabetes: the carbohydrate content in a single dose of the drug (5 granules) corresponds to 0.01 bread units.

Effect on the ability to drive vehicles and operate machinery

No effect.

Storage Conditions

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

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.