Name:
Nazoferon spray naz.dozir. 5000 IU/dose, 100 doses (5 ml) in a vial. in pack. â„–1
Description:
Transparent colorless liquid. NAZOFERON is a recombinant human interferon alpha-2b. The main active ingredient is recombinant human interferon alfa-2b 100,000 IU/ml Product form Dosed nasal spray Dosage 5 ml Pharmacological propertiesPharmacodynamicsRecombinant alfa-2b interferon, which is the active component of nasal spray Nazoferon, has antiviral immunomodulatory properties. The antiviral effect of interferon alfa-2b is mediated by the activation of a number of intracellular enzymes that inhibit viral replication. The immunomodulatory effects of interferon are also due to the influence on the production of a number of cytokines (interleukins, interferon gamma). All these effects of interferon may mediate the therapeutic activity of nasal spray Nazoferon. Pharmacokinetics Not studied. Indications for use Prevention and treatment of acute respiratory infections (ARVI) in adults and children older than 1 year. Method of application and doses 1 spray-dose = 1 short press on the dispenser. At the first signs of ARVI disease (for 5 days) Children from 1 to 3 years old – 2 spray doses in each nasal passage 3-4 times a day (single dose – 20,000 IU, daily dose – 60,000-80,000 IU); Children from 3 to 14 years old – 2 spray doses in each nasal passage 4-5 times a day (single dose – 20,000 IU, daily dose – 80,000-100,000 IU); Children from 14 to 18 years old – 2 spray doses in each nasal passage 5-6 times a day (single dose – 20,000 IU, daily dose – 100,000-120,000 IU); Adults – 3 spray doses in each nasal passage 5-6 times a day (single dose – 30,000 IU, daily dose – 150,000-180,000 IU). For the prevention of respiratory viral infections In contact with the patient and hypothermia – in accordance with the age dosage 2 times a day for 5-7 days. If necessary, repeat preventive courses. With a single contact, one injection is sufficient. With a seasonal increase in the incidence – in accordance with the age dosage once in the morning with an interval of 1-2 days. Precautions The drug contains methyl parahydroxybenzoate, which can cause allergic reactions, including delayed ones, in exceptional cases, bronchospasm. Do not use the drug in case of violation of the integrity and labeling of the package, with a change in physical properties (color or transparency of the liquid) and after the expiration date. Individual use is recommended to avoid the spread of infection. Use during pregnancy or lactation. Application is contraindicated. Children. Apply to children from 1 year. The ability to influence the reaction rate when driving vehicles or working with other mechanisms. Does not affect. Interaction with other drugs The simultaneous use of intranasal vasoconstrictor drugs is not recommended, since they contribute to the dryness of the nasal mucosa. Contraindications Hypersensitivity to interferon alfa-2b and other components that make up the drug, a history of severe forms of allergic diseases. The period of pregnancy or lactation Active ingredient: human recombinant interferon alfa-2b 100,000 IU/ml; excipients: trometamol, trometamol hydrochloride, hypromellose, disodium edetate, lysine hydrochloride, potassium chloride, methyl parahydroxybenzoate (E 218), water for injection. 1 spray-dose contains: active ingredient: recombinant human interferon alfa-2b not less than 5000 IU; excipients: trometamol, trometamol hydrochloride, hypromellose, disodium edetate, lysine hydrochloride, potassium chloride, methyl parahydroxybenzoate (E 218), water for injection. Overdose Not studied Side effectsIn isolated cases – a rash on the skin. In case of adverse reactions, you should consult your doctor. Storage conditions Store in a place protected from light at a temperature of 2 ºС to 8 ºС. Keep out of the reach of children! Shelf life after opening the vial, if stored at a temperature of 2 ºС to 8 ºС (in the refrigerator) – 10 days. Best before date. 2 years. Do not use the drug after the expiration date indicated on the package. Buy Nasoferon nasal spray dosed 5000m/dose 100 doses (5ml) No. 1
Nasoferon nasal spray dosed 5000 IU / dose 100 doses (5 ml) No. 1
$28.00
INN | INTERFERON ALFA-2B |
---|---|
The code | 73 964 |
Use during pregnancy and lactation | Forbidden to use |
Composition Means | active ingredient: recombinant human interferon alfa-2b 100, 000 IU/ml; excipients: trometamol, trometamol hydrochloride, hypromellose, disodium edetate, lysine hydrochloride, potassium chloride, methyl parahydroxybenzoate (E 218), water for injection. 1 spray-dose contains: active ingredient: recombinant human interferon alfa-2b not less than 5000 IU; excipients: trometamol, trometamol hydrochloride, hypromellose, disodium edetate, lysine hydrochloride, potassium chloride, methyl parahydroxybenzoate (E 218), water for injection. |
Main Active Substances | interferon alfa-2b recombinant human 100, 000 IU/ml |
Release Form | Spray nasal dosed |
Application Gender | Any |
Age category | 1+ |
Volume (ml) | 5 |
Side effects | In isolated cases – a rash on the skin. In case of adverse reactions, you should consult your doctor. |
Barcode | 4, 82E+12 |
Contraindications | Hypersensitivity to interferon alfa-2b and other components that make up the drug, a history of severe forms of allergic diseases. Period of pregnancy or lactation |
Indications Applications | Prevention and treatment of acute respiratory infections (ARVI) in adults and children older than 1 year. |
Scope of application | For the nose |
Manufacturer | Farmak PAO, Ukraine |
Active substance | Interferon alfa 2v |
Dosage | 5000IU/dose |
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