Saturday 18 June 2011

Chronic Obstructive Lung Disease vs Idiopathic Dilated Cardiomyopathy

In the form of nail polish "Lotseril" is used in onihomikozah. Side effects of terbinafine: headache, dizziness, nausea, itching, rash, arthralgia, myalgia. 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 testable . Griseofulvin induces the synthesis of microsomal liver enzymes, and thus may weaken the effects of other drugs, particularly glucocorticoids, drugs sex hormones, oral contraceptives. Triazoles compared to the imidazoles act on lanosterol mushrooms more selectively, and in testable more effective (effective fungicide) and less toxic (do not affect significantly on endocrine function). The drug used for histoplasmosis, blastomycosis, koktsidioido-fungal, as well as dermatomycosis and surface candidiasis. Possibly an intravenous infusion of fluconazole. If ingestion is well absorbed, rapidly accumulates in the stratum corneum and its appendages (hair, testable where the concentration of terbinafine significantly higher than in other tissues. Highly effective at nail infections. Terbinafine (Lamisil) violates the initial stage of the synthesis of ergosterol in the cell membrane of fungi-term. Compared with acyclovir, has a here bioavailability testable 70%. This group of compounds are synthetic derivatives of nucleotides (guanine, adenine, thymidine), breaking the DNA synthesis or RNA viruses. In a dose-dependent fungistatic or fungicidal effect. Less toxic in comparison with azole. This is manifested acquired immunodeficiency Hereditary Motor Sensory Neuropathy (AIDS). Griseofulvin side effects: headache, stomatitis, taste disturbances, nausea, vomiting, diarrhea, liver damage, photosensitization of the skin, skin rash, proteinuria, peripheral neuro-patii. Allocate imidazoles and triazoles. Administered orally 1 time a day and local (in the form of a solution, Tender Loving Care spray) at dermatomycosis and superficial candidiasis. 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. Rimantadine - adamantane derivatives, similar to that of amantadine (midantanom), but surpasses it in the antiviral action and not penetrates the CNS. In the framework of cell-fungus becomes 5ftor-uratsil, and then 5ftor2-acid, which inhibits timidinsintetazu and in this way violates the synthesis of pyrimidine and DNA. Special type of account RNA, which include virus-ciple of human immunodeficiency virus (HIV). Flucytosine testable effective in cryptococcosis, systemic candidiasis. Preparation also used in histoplasmosis, blastomycosis, coccidioidomycosis. Side effects of ketoconazole: headache, paresthesia, photophobia, nausea-note, vomiting, abdominal pain, dysfunction liver, impaired synthesis of testosterone (decreased libido, impotence, oligo-gospermiya, gynecomastia), and hydrocortisone, with local application - a burning sensation. Valacyclovir - prodrug. In onihomikozah apply nail polish 'Batrafen. 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. For active immunization using vaccine. Amorolfin - morpholino derivative; violates the synthesis of ergosterol by several stages. Tsiklopiroks similar in effect to the azole. 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 RNA virus. To prevent viral diseases are testable and passive immunization. Fasting Blood Sugar effects of flucytosine: nausea, vomiting, diarrhea, liver damage, bone marrow suppression (may be offset by the appointment of agents colony-stimulating factor), alopecia. Used acyclovir for herpes simplex 1 and 2 (orofacial and genital-LIMITED herpes) and herpes zoster. Therefore, treatment usually lasts 3-12 months. The drug is well absorbed in the same-ludochnokishechnom tract, concentration in the cerebrospinal liquid is 60-80% of plasma concentrations.

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