Universal reference book for medicines
Name of the preparation: POLIMURAMIL В® (POLIMURAMIL)

Active substance: nonappropriate

Type: Immunostimulating drug

Manufacturer: KORUS FARM (Russia) manufactured by COMBIOTECH NPK (Russia) manufactured by GRITWAK (Russia)
Composition, form of production and packaging
Solution for the / m introduction
as a colorless, clear liquid.

0.5 ml

Polymuramil 200 Ојg

0.5 ml - ampoules (5) - packings cellular cardboard (1) - packs cardboard.

0.5 ml - ampoules (5) - packs of cardboard.

0.5 ml - ampoules (10) - packings of cellular cardboard (1) - packs cardboard.

0.5 ml - ampoules (10) - packs of cardboard.

INSTRUCTION FOR THE SPECIALIST.

Description of the drug approved by the manufacturer for the printed edition of 2014.

PHARMACHOLOGIC EFFECT

Polymuramil is a natural immunostimulant.
It enhances the absorption of bacteria and bacterial killing by phagocytic cells. This increases the ability of monocytes, macrophages and dendritic cells to produce cytokines (interleukin-12, tumor necrosis factor-, granulocyte-macrophage colony-stimulating factor, etc.) that activate cellular and humoral immunity. Polymuramil enhances the synthesis of antibodies and increases the functional activity of natural killers, which play an important role in antiviral and antitumor immunity. Polymuramil does not have teratogenic, embryotoxic, mutagenic and carcinogenic properties.
INDICATIONS

Polymuramil is used in adults simultaneously with antibacterial drugs in complex therapy:

- secondary immunodeficiency states, manifested in the form of chronic, sluggish, recurrent infectious and inflammatory processes of any localization (skin and soft tissues, ENT organs, urogenital tract, etc.);

- with acute and chronic purulent-inflammatory diseases of the skin and soft tissues, including all kinds of pyoderma, incl.
furunculosis, carbuncles; abscesses, phlegmon;
- for the treatment and prevention of surgical infections, incl.
purulent-septic complications.
DOSING MODE

Polymuramil is administered intramuscularly at a dose of 200 Ојg / 0.5 ml daily.
The duration of administration is determined by the clinical picture. Recommended duration of administration is from 5 to 7 days.
SIDE EFFECT

Perhaps a temporary increase in temperature to 37.5 В° C, chills, tenderness at the injection site.

CONTRAINDICATIONS

- Pregnancy;

- lactation;

- Children under 18 years.

PREGNANCY AND LACTATION

Polymuramil is contraindicated in pregnancy and lactation.

APPLICATION FOR CHILDREN

Contraindicated for children under 18 years.

SPECIAL INSTRUCTIONS

Impact on the ability to drive vehicles and manage mechanisms

The drug does not affect the ability to drive vehicles and other mechanisms.

OVERDOSE

In case of an overdose, an increase in temperature is possible, with febrile temperature values, symptomatic treatment should be performed.

DRUG INTERACTION

The drug is compatible with all antimicrobial and anti-inflammatory drugs.

TERMS OF RELEASE FROM PHARMACY

The drug is released by prescription.

TERMS AND CONDITIONS OF STORAGE

Store in a place protected from light, out of reach of children, at a temperature of 2 to 8 В° C.
Do not freeze. Shelf life - 2 years.
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