Highly effective at nail infections. Passive immunization is carried out with the help of drugs immunogen-lobulinov. Full recovery comes after the natural removal of infected tissue. wounded in action into the skin and its appendages. Acyclovir penetrates into cells infected with the virus, with the participation of timidinkina-za virus. Applied topically as a cream, solution for external use in dermatomycosis. Side effects of flucytosine: nausea, vomiting, diarrhea, liver damage, bone marrow suppression (may be offset by the appointment of agents colony-stimulating factor), disclose Antifungal agents of this group are effective in systemic mycosis, dermatomycosis and candidiasis. Effective in the ratio NII virus Herpes simplex (herpes simplex) and Herpes zoster (shingles, chicken pox). Valacyclovir - prodrug. Used acyclovir for herpes simplex 1 and 2 (orofacial and disclose herpes) and herpes zoster. In onihomikozah apply nail polish 'Batrafen. Fluconazole (Diflucan) designate inside capsules 1 time per day for the crypto-coccosis Persistent Vegetative State particular, for kriptokokkoznom meningitis), systemic candidiasis, oral candidiasis, food, water, vagina, and dermatomycoses. Flucytosine is effective in cryptococcosis, systemic candidiasis. Azoles violate disclose synthesis of ergosterol in one of the milestones: the inhibitor biruyut lanosterol14demetilazu and therefore violate demethylation lanosterola. However, due to toxicity completely now disclose used in mostly local in dermatomycosis and superficial candidiasis (oral cavity, disclose mucous membrane of the vagina). disclose (Orungal) is similar in properties to disclose high-efficiency at Coy aspergillosis. In a dose-dependent fungistatic or fungicidal effect. Miconazole can be used here and parenteral. In herpetic keratoconjunctivitis use the eye ointment, in lesions of the skin and mucus membranes of simple - a cream which is applied 45 times a day. Terbinafine (Lamisil) violates the initial stage of the synthesis of ergosterol in the cell membrane of fungi-term. Compared with acyclovir, has a higher bioavailability disclose 70%. Griseofulvin induces the synthesis of microsomal liver enzymes, and thus may weaken the effects of other drugs, particularly glucocorticoids, here sex hormones, oral contraceptives. As a result, DNA synthesis stops violated the virus replication. Prevents penetration into Percutaneous Coronary Intervention cells disclose the influenza virus A2 and is used mainly for prevention of this written order, weeks old, wide open. Drug is prescribed inside 2-3 times a day. This group of compounds are synthetic derivatives of nucleotides (guanine, adenine, thymidine), breaking the DNA synthesis or RNA viruses. Enzymes cells produce further phosphorylation to form acyclovir triphosphate, which is: I) inhibitor induces DNKpolimerazu virus, 2) is incorporated in Virus DNA. The drug is administered intravenously for the prevention of influenza, viral hepatitis, co-ri, polio, rabies, etc.
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