Instruction for use: Ridostin

Dosage form: Lyophilizate for the preparation of solution for intramuscular and subcutaneous administration

Active substance: Natrii ribonucleas

ATX

L03A Immunostimulants

Pharmacological group:

Interferon Inductors

Composition and release form

1 ampoule with lyophilized porous mass for the preparation of the injection contains mixtures of sodium salts of double-stranded and single-stranded RNA 5 mg, sodium chloride 3 mg; In a cardboard pack of 10 ampoules.

Pharmachologic effect

Mode of action - antiviral, anti-inflammatory, immunomodulating, antibacterial.

It induces the production of interferon, stimulates the phagocytic activity of macrophages and neurophiles. It has antimutagenic, anti-carcinogenic, antimetastatic activity.

Indication of the Ridostin

Rabies, flu, herpes simplex, genital and shingles, tick-borne encephalitis, HIV and other viral infections; Urogenital chlamydia, recurrent prostatitis, Reiter's disease.

Contraindications

Hypersensitivity, severe damage to the liver and kidneys.

Application in pregnancy and breastfeeding

Contraindicated.

Dosing and Administration

SC and IM. The contents of the ampoule (8 mg) are dissolved in 2 ml of 0.5% novocaine solution or water for injection. With simple, genital and herpes zoster - 8 mg once every three days (course - 3 injections); With urogenital infections - 8 mg once every 2 days (course - 4 injections). To prevent recurrence - 4 injections with an interval of 2 days.

Storage conditions of the drug Ridostin

At a temperature of 12-8 ° C.

Keep out of the reach of children.

Shelf life of the drug Ridostin

2 years.

Do not use after the expiry date printed on the package.