Tick-E-Vac, 0.5 ml/dose 0.5 ml 10 pcs

Specific prophylaxis of tick-borne encephalitis for persons aged 16 years and older in a dose of 0.5 ml and for children from 1 to 16 years in a dose of 0.25 ml;

The immunization of donors in order to obtain specific immunoglobulin.

Contingents subject to specific prophylaxis:

1. Population living in areas enzootic for tick-borne encephalitis.

2. Persons arriving in these areas who perform the following work:

– agricultural, hydromelioration, construction, excavation and relocation of soil, procurement, fishing, geological, surveying, expeditionary, deratization and disinfestation.

– on logging, clearing and improvement of forests, recreation and recreation areas.

3. Persons visiting areas endemic for tick-borne encephalitis for recreation, tourism, work in summer cottages and garden plots.

4 Persons working with live cultures of tick-borne encephalitis pathogen.

Active ingredient

Composition

How to take, the dosage

The general vaccination schedule is presented in the table:

Type of vaccination

Primary vaccination

First revaccination

Subsequent

revaccinations

Second

day 0

vaccination

/p>

1-7 months after the first vaccination

Every 3 years

Emergency

2 weeks after the first vaccination

Dose for persons 16 years and older

0.5 ml

0.5 ml

0.5 ml

0.5 ml

Dose for children from 1 year to 16 years

0.25 ml

0.25 ml

0.25 ml

0.25 ml

Interaction

Special Instructions

Vaccinations are carried out with strict adherence to asepsis and antisepsis rules. The room must be equipped with anti-shock and anti-allergic therapy.

Before opening the ampoule a visual inspection must be carried out. The drug in ampoules with broken integrity, labeling, foreign inclusions, large unbreakable conglomerates, expired shelf life, violation of temperature conditions of storage or transportation shall not be suitable.

Immediately prior to injection the vaccine in an ampoule shall be shaken until a homogeneous suspension is obtained. The drug is injected immediately after opening the ampoule intramuscularly into the deltoid muscle of the shoulder.

The vaccinations administered shall be recorded in the established record forms indicating the name of the drug, date of vaccination, dose, series number, manufacturer, reaction to vaccination.

The drug cannot be administered intravenously!

Inoculation of children and adults with chronic diseases in the acute stage is carried out not earlier than 1 month after recovery (remission).

The vaccine is not used in children under 1 year of age.

Impact on the ability to drive vehicles and machines:

The marked general reactions to administration of the vaccine (significant fever, severe headache) are contraindications to driving vehicles and machinery.

Contraindications

Side effects

Overdose