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Fluconazole is an inhibitor of the human cytochrome P450 system, particularly the isozyme CYP2C19 (CYP3A4 and CYP2C9 to lesser extent) [31] In theory, therefore, fluconazole decreases the metabolism and increases the concentration of any drug metabolised by these enzymes.
By mouth: ibrexafungerp, fluconazole as a single dose. [4] For severe disease another dose after 3 days may be used. [27] Short-course topical formulations (i.e., single dose and regimens of 1–3 days) effectively treat uncomplicated candidal vulvovaginitis. The topically applied azole drugs are more effective than nystatin.
Unlike fluticasone furoate, which is approved in children as young as two years of age when used for allergies, fluticasone propionate is only approved for children four years and older. [12] [13] Fluticasone propionate was patented in 1980, and approved for medical use in 1990. [14] It is available as a generic medication. [10]
Fosfluconazole (INN Tooltip International Nonproprietary Name) is a water-soluble phosphate prodrug of fluconazole [1] — a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections.
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Studies have demonstrated the safety of inhaled fluticasone propionate in children. A systematic review published in 2013 found no significant adverse effect on the function of the hypothalamic–pituitary–adrenal axis , growth, and bone mineral density in asthmatic children when inhaled fluticasone is used for up to three months.
The drug comes in the form of creams, shampoos, and tablets. Other than treating the infection, ketoconazole may cause skin reactions at the site of application, including skin rash and itching. Ketoconazole is contraindicated in patients with acute porphyrias , where patients may present with shortness of breath and seizures .
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