Similar drugsTo uncover
Dosage form: & nbsplyophilizate for the preparation of a solution for intramuscular injection
Composition:

Immunomax 100 ED or 200 units.

Sodium chloride 8.1 mg or 7.2 mg.

Description:Lyophilized powder of white color.
Pharmacotherapeutic group:Immunomodulating agent
Pharmacodynamics:

Immunomax enhances immune defense against viral and bacterial infections. Immunopharmacological mechanisms of action of the drug consist in the fact that Immunomax activates the following links of the immune system:

- NK cells, which in 2-3 hours, after exposure to Immunomax, intensively express the activation molecules of CD69. The cytolytic activity of NK cells increases 3-fold;

- circulating monocytes 2-4 hours after activation by Immunomax begin to secrete cytokines: interleukin-8, interleukin-1β and tumor necrosis factor alpha;

- neutrophilic granulocytes are activated by means of monocytes, the drug does not directly affect neutrophilic granulocytes. Secreted by monocytes, interleukin-8 induces activation of neutrophilic granulocytes, which is clearly manifested 24 hours after exposure to Immunomax;

- tissue macrophages, which is manifested in a change in the morphology of these cells, increased production of bactericidal substances, changes in the activity of 5'-nucleotidase;

- the formation of antibodies against foreign antigens, soluble and corpuscular;

Immunomax enhances protection against infections caused by viruses (human papillomavirus, herpes simplex virus, parvovirus, carnivorous plague virus, etc.) or bacteria (Escherichia coli, Salmonella, Staphylococcus, Chlamydia, Mycoplasma, Ureaplasma, etc.). This effect of the drug is manifested in adults and newborns with the introduction of Immunomax in various ways: intramuscularly, intravenously, intraperitoneally, re os.

Pharmacokinetics:
Pharmacokinetics of the drug has not been studied in connection with its peptidoglycan nature and very small acting doses.
Indications:

- Correction of weakened immunity;

- treatment of pathological conditions (condylomata, warts, dysplasia, etc.) caused by the human papillomavirus;

- treatment of infections caused by the herpes simplex virus, chlamydia, mycoplasma, ureaplasma, other bacteria and viruses.

Contraindications:Individual hypersensitivity to Immunomax. Children under 12 years.
Pregnancy and lactation:The application is only possible if the potential benefit to the pregnant woman exceeds the possible harm to the fetus.Immunomax is not recommended for use by nursing mothers. Features of the drug use by children and adults with chronic diseases, no.
Dosing and Administration:

Before use, the drug is dissolved in 1 ml of water for injection.

The recommended dose for adults and children 12 years and older is 100-200 / ED, depending on the severity of the disease. The drug is administered intramuscularly, once a day. The course of treatment-6 injections in 1,2,3, 8,9,10 days of treatment.

For the treatment of recurrent anogenital warts, a course of 6 injections of 200 units of Immunomax is combined with the destruction of warts by one of the most common methods: cryodestruction, electrocoagulation, laser destruction or solcoderm.

To treat infections caused by bacteria or viruses, a course of 6 injections of 100-200 units of Immunomax is administered.

For correction of weakened immunity, a course of 3-6 injections of 100-200 units of Immunomax is administered.

Side effects:Not detected.
Overdose:Symptoms of overdose are not described.
Interaction:Not described.
Effect on the ability to drive transp. cf. and fur:
The drug does not affect the ability to drive vehicles,moving mechanisms and engage in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions,
Form release / dosage:
Lyophilizate for the preparation of a solution for intramuscular injection of 100 units or 200 units.
Packaging:

For 100 units or 200 units per vial or ampoule.

- 3 vials or ampoules together with instructions for use in a cardboard box;

- 1 vial or ampoule with the drug, 1 ampoule with water for injection 2 ml, 1 disposable sterile syringe 2 ml, G preinjection wipe along with instruction for use in the pack (Kit);

- 3 vials or ampoules with the preparation, 3 ampoules with water for injection 2 ml, 3 disposable sterile syringes 2 ml, 3 preinjection wipes together with instructions for use in the pack (Kit);

- 30 bottles or ampoules with the drug with 5 instructions for use (For hospitals).

Storage conditions:Store at temperatures between 4 ° C and 8 ° C. Keep out of the reach of children.
Shelf life:2 years. Do not use after expiry date.
Terms of leave from pharmacies:On prescription
Registration number:P N001919 / 02
Date of registration:17.10.2011
Expiration Date:Unlimited
The owner of the registration certificate:IMMAPHARMA, LLC IMMAPHARMA, LLC Russia
Manufacturer: & nbsp
Information update date: & nbsp24.10.2017
Illustrated instructions
    Instructions
    Up