60, polysorbate 80, propylene glycol, purified water, sorbitan monostearate and stearyl alcohol. L level in ketoconazole cream dosage over a 72-hour period.

Development of resistance to ketoconazole has not been reported. It is postulated that the therapeutic effect of ketoconazole in seborrheic dermatitis is due to the reduction of M. Carcinogenesis, Mutagenesis, Impairment of Fertility A long-term feeding study in Swiss Albino mice and in Wistar rats showed no evidence of oncogenic activity. However, these effects may be related to maternal toxicity, which was seen at this and higher dose levels. There are no adequate and well-controlled studies in pregnant women. Ketoconazole should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nevertheless, a decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother. Pediatric Use Safety and effectiveness in children have not been established. 208 patients treated with placebo reported side effects consisting mainly of severe irritation, pruritus and stinging. One of the patients treated with Ketoconazole Cream developed a painful allergic reaction. In worldwide postmarketing experience, rare reports of contact dermatitis have been associated with Ketoconazole Cream or one of its excipients, namely propylene glycol. Patients with tinea versicolor usually require two weeks of treatment. Patients with tinea pedis require six weeks of treatment.

If a patient shows no clinical improvement after the treatment period, the diagnosis should be redetermined. Keep this and all medications out of the reach of children. By clicking Subscribe, I agree to the Drugs. Privacy Policy and understand that I may opt out of Drugs.

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