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Candistat (Itraconazole)
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Itraconazole

Candistat (also called Candistat) is used to treat fungal infections. It is available as a 100-mg blue-and-pink capsule and as a clear yellowish liquid taken by mouth. It is also active against all skin fungi. It is not active against Mucorales or Fusarium spp. and a few other rare fungi. Until the development of posaconazole, it was the most active against black moulds, including Bipolaris, Exserohilum etc. Resistance to Candistat is described in Candida spp. and in Aspergillus fumigatus and A. niger.

Other names for this medication:
Itraconazole, Sporanox, Fulcover, Icoz, Candistat,

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Successful treatment of rifampicin-resistant intraocular tuberculosis. Comparison of the effect of two sugar-substituted chewing gums on different caries- and gingivitis-related variables: a double-blind, randomized, controlled clinical trial. Efficient ex vivo inhibition of perforin and Fas ligand expression by chimeric tRNA-hammerhead ribozymes. Role of mothers in the acquisition of tool-use behaviours by captive infant chimpanzees. Hot spot formation in the nuclear envelope of oocytes in response to steroids.

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Increasing maternal age is independently associated with specific adverse outcomes. The population as grouped into those having amalgam fillings (39 males and 10 females) and those without (41 males and 11 females). We compared outcomes between subjects that underwent selective laser coagulation using the Solomon technique (cases) and those that underwent selective laser coagulation without this procedure (controls). Over longer periods, insulin mRNA levels are modulated through effects on the rate of transcription of the insulin gene, and also through changes in the rate of decay of insulin mRNA. This dose was found to induce in vitro up-regulation of the glucocorticoid receptors (GcR) of peritoneal macrophages following 24 h of treatment.

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An examination of human prostate tissue augmentin generic name and classification of computers revealed significantly increased stromal staining of CathD in malignant prostate tissue. Genotoxicity and inactivation of catechol metabolites of the mycotoxin zearalenone.

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