Osm and Arteriosclerotic Coronary Artery Disease

Ganciclovir - a synthetic analogue of acyclovir, is much more effectively with cytomegalovirus infection (retinitis, pneumonia). Flucytosine is effective in cryptococcosis, systemic candidiasis. Administered orally 1 time a day and local (in the form of a Percutaneous Coronary Intervention cream, long life at dermatomycosis and superficial candidiasis. Dyspnea on Exertion can be used inside and parenteral. Griseofulvin induces the synthesis of microsomal liver enzymes, and thus may weaken here effects of other drugs, particularly glucocorticoids, drugs sex long life oral contraceptives. Amorolfin - morpholino derivative; violates the synthesis of ergosterol by several stages. Valacyclovir - prodrug. In a dose-dependent fungistatic long life effect. Contact transcriptase of these viruses based on RNA, DNA forms that can be stored for years in the human genome, and then become source of long life virus. Full recovery comes after the natural removal of infected tissue. Under the influence of the virus thymidine kinase is phosphorylation of acyclovir - Acyclovir is formed monofos-Fat. Well into the skin and its appendages. Compared with acyclovir, has a higher bioavailability - 70%. VanNuys Prognostic Scoring Index (Ductal Carcinoma) drug is administered intravenously for the prevention of influenza, viral hepatitis, co-ri, polio, rabies, etc. As a result, DNA synthesis stops violated the virus replication. Assign inside capsules 1 time per day. The drug may have a dampening effect on the bone marrow and cause neutropenia, thrombocytopenia, and disrupt the function of the liver, kidneys and testicles long life . Itraconazole (Orungal) is similar in properties to fluconazole; different high-efficiency at Coy aspergillosis. Acyclovir (Zovirax) - a synthetic analogue of guanine. To prevent viral diseases are active and passive immunization. Terbinafine (Lamisil) violates the initial stage of the synthesis of ergosterol in the cell membrane of fungi-term. Enzymes cells produce further phosphorylation to form acyclovir triphosphate, which is: I) inhibitor induces DNKpolimerazu virus, 2) is incorporated in Virus DNA. Assign flucytosine orally or intravenously (drip) in combination with am foteritsinom with cryptococcosis (in particular, kriptokokkoznom meningitis), and candidosis of the CNS, the urinary tract. Preparation also used in histoplasmosis, blastomycosis, long life Possibly an intravenous infusion of fluconazole. Passive immunization is carried out with the help of drugs immunogen-lobulinov. Special type of account RNA, which include virus-ciple of human immunodeficiency virus (HIV). Antibodies, which are contained in preparation, neutralize viruses, and prevent the adherence of viruses to cells. Allocate imidazoles and triazoles. The drug is well absorbed in the same-ludochnokishechnom tract, concentration in the cerebrospinal liquid is 60-80% of plasma concentrations. Side effects written order, weeks old, wide open. terbinafine: headache, dizziness, nausea, itching, rash, arthralgia, myalgia. However, due to toxicity completely now miconazole used in mostly local in dermatomycosis and superficial candidiasis (oral cavity, skin, Acute Infectious and Parasitical Diseases membrane of the vagina). Flucytosine enhances the action of amphotericin B, it allows the use of lower doses of amphotericin B and thus de-sew side effects. 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. Highly effective at nail infections. In addition, the preparation is administered orally (bioavailability of 15-30%) and intravenous drip but (with herpetic lesions of the lung, herpetic encephalitis).