Due to the fact that the incidence of influenza is seasonal in nature, it is recommended annually vaktsinatsiyuv autumn and winter, when flu risk is maximal.
The vaccine leads to the development of immunity only against 3 influenza virus strains contained in the product or against strains similar to those indicated. VAXIGRIP does not trenbolone enanthate provide immunity against the formation of influenza vaccination in the incubation period of the disease, as well as against influenza caused by other strains of the virus. VAXIGRIP not generate the development of immunity against diseases of similar symptoms with the flu, but caused by other pathogens. Vaccination against influenza, carried out during the previous epidemic season, can not provide reliable protection for the next season, because for each epidemic season is characterized by its most common strains of influenza virus.
The doctor should be informed of the presence of the patient immunodeficiency, allergy or unusual reactions to previous vaccinations as well as any treatment to coincide with the vaccination or previous vaccination.
The vaccine should not be used in uncharacteristic coloring suspension or the presence of foreign particles in it.
The use of this vaccine does not affect the ability to drive a motor vehicle or other machinery.
The doctor should be informed about all the cases of adverse reactions, not limited to those listed in these instructions. Within a few days after vaccination may be instances of false positives in the determination of antibodies to HIV-1, hepatitis C and, particularly, human T-lymphotropic virus type 1 enzyme immunoassay (EIA) method. In these cases, the evaluation result obtained by ELISA, performed by Western blotting. When vaccination must be available medicines needed to provide emergency assistance in case of an anaphylactic reaction.
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