Grippferon - instructions for use, dose, side effects, contraindications

Excipients: disodium edetate dihydrate 0.5 mg, sodium chloride 4.1 mg, sodium hydrogen phosphate dodecahydrate 11.94 mg, potassium dihydrogen phosphate 4.54 mg, povidone-8 thousand 10 mg, macroline 4000 100 mg, water purified to 1 ml.

Description:Transparent colorless or light yellow solution.

Pharmacotherapeutic group:Cytokine

ATX: & nbsp

L.03.A.B.05 Interferon alfa-2b

Pharmacodynamics:The drug has an immunomodulatory, anti-inflammatory and antiviral effect.

Pharmacokinetics:With intranasal application, the concentration of the active substance reached in the blood is well below the detection limit (the limit of determination of interferon alpha-2b -1-2 IU / ml) and has no clinical significance.

Indications:Prevention and treatment of influenza and ARVI in children and adults.

Contraindications:

Individual intolerance to interferon preparations and components that make up the drug.

Severe forms of allergic diseases.

Pregnancy and lactation:Grippferon® is approved for use throughout the pregnancy period according to the age-appropriate dose.

Dosing and Administration:

At the first sign of the disease, Grippferon® is used for 5 days:

- at the age of 0 to 1 year, 1 drop in each nasal passage 5 times a day (single dose 1000 ME, daily dose 5000 ME)

- at the age of 1 to 3 years, 2 drops in each nasal passage 3-4 times a day (single dose 2000 ME, daily dose 6000-8000 ME)

- at the age of 3 to 14 years, 2 drops in each nasal passage 4-5 times a day (single dose 2000 ME, daily dose 8000-10000 ME)

- adults 3 drops per each nasal passage 5-6 times a day (single dose 3000 ME, daily dose 15000-18000 ME).

In order to prevent ARVI and influenza:

- when in contact with a patient and / or when supercooled, the drug is instilled in a single age dose 2 times a day. If necessary, preventive courses are repeated;

- with a seasonal increase in the incidence of the drug is instilled in the dose once in the morning with an interval of 24-48 hours.

After each instillation, it is recommended to massage the wings of the nose with your fingers for several minutes to distribute the drug evenly in the nasal cavity.

Side effects:

Allergic reactions.

Interaction:The use of intranasal vasoconstrictor medications in conjunction with Grippferon® is not recommended, as this contributes to the additional drying of the nasal mucosa.

Form release / dosage:Nasal drops of 10,000 IU / ml.

Packaging:5 ml or 10 ml in plastic bottles with a dispenser-dropper. Each bottle, together with the instructions for use, is placed in a pack of cardboard.

Storage conditions:At a temperature of 2 to 8 ° C. Keep out of the reach of children.

Shelf life:

2 years. The opened vial should not be stored for more than 30 days.

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

Terms of leave from pharmacies:On prescription

Registration number:P N000089 / 01

Date of registration:05.01.2011 / 13.08.2013

Expiration Date:Unlimited

The owner of the registration certificate:FIRN M, ZAO FIRN M, ZAO Russia

Manufacturer: & nbsp

FIRN M, ZAO Republic of Belarus

Information update date: & nbsp10.05.2017

Illustrated instructions

Instructions

Grippferon® (Grippferon®)