Amorolfin - morpholino derivative; violates the synthesis of ergosterol by several stages. In addition, the preparation is administered orally (bioavailability of 15-30%) and Surgery drip but (with herpetic lesions of the lung, herpetic encephalitis). Assign inside capsules 1 time per day. Therefore, treatment usually lasts 3-12 months. Side effects of acyclovir: headache, dizziness, nausea, vomiting, diarrhea, skin rashes, liver problems hyperuricemia, violations of blood after intravenous injection - des-orientation, excitation, hallucinations, tremor. This is manifested acquired immunodeficiency syndrome (AIDS). Applied topically as a cream, solution for external use in dermatomycosis. Antifungal agents of this pullback are effective in systemic mycosis, dermatomycosis and candidiasis. Used acyclovir for herpes simplex 1 pullback 2 (orofacial and genital-LIMITED herpes) and herpes zoster. In onihomikozah apply nail polish 'Batrafen. Assign flucytosine orally or pullback (drip) in combination with am foteritsinom with cryptococcosis (in particular, kriptokokkoznom meningitis), and pullback of the CNS, the urinary tract. Highly effective at nail infections. Fluconazole (Diflucan) designate inside capsules 1 time per day for the crypto-coccosis (in particular, for kriptokokkoznom meningitis), systemic candidiasis, oral candidiasis, food, water, vagina, and dermatomycoses. Antibodies, which are contained in preparation, neutralize viruses, and prevent the adherence of viruses to cells. Tsiklopiroks similar in effect to the azole. Ketoconazole (Nizoral) appointed interior 1 per day in the form of pellets current suspension, as well as externally in the form of cream, shampoo. Prevents penetration into the cells of the influenza virus A2 and is used mainly for prevention of this disease. Side effects of terbinafine: headache, dizziness, nausea, itching, rash, arthralgia, myalgia. Terbinafine (Lamisil) violates the initial stage of the synthesis of ergosterol in the cell membrane of fungi-term. Griseofulvin side effects: headache, stomatitis, taste disturbances, nausea, vomiting, diarrhea, liver damage, photosensitization of the skin, skin rash, proteinuria, peripheral neuro-patii. Full recovery comes after the natural removal of infected tissue. Administered orally 1 time a day and local (in the form of a solution, cream, spray) at dermatomycosis and superficial candidiasis. Side effects of flucytosine: nausea, vomiting, diarrhea, liver damage, bone marrow suppression (may be offset by the appointment of agents colony-stimulating factor), alopecia. Compared with acyclovir, has a higher bioavailability - 70%. Acyclovir penetrates into cells infected with the virus, with the participation of timidinkina-za virus. Triazoles compared to the imidazoles act on lanosterol mushrooms more selectively, and in general more effective (effective fungicide) and less toxic (do not affect significantly on pullback function). Flucytosine is effective in cryptococcosis, systemic candidiasis. This group of compounds are synthetic derivatives of nucleotides (guanine, adenine, thymidine), breaking the DNA synthesis or RNA viruses. As a result, DNA synthesis stops violated the virus replication. The drug used for histoplasmosis, blastomycosis, koktsidioido-fungal, as well as dermatomycosis and surface candidiasis. Under the influence of the virus thymidine kinase is phosphorylation of acyclovir - Acyclovir is formed monofos-Fat. Passive immunization is carried out with the help of drugs immunogen-lobulinov. Possibly an intravenous infusion of fluconazole.
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