Drug interaction classified as: metabolism
Source: DDInter
Antifungal
Clotrimazole is an imidazole antifungal that inhibits lanosterol 14-α-demethylase (CYP51), a fungal cytochrome P450 enzyme essential for converting lanosterol to ergosterol. This depletes ergosterol from fungal cell membranes and causes accumulation of toxic 14-α-methylsterols, disrupting membrane fluidity and function. As an imidazole (rather than triazole), it has less selectivity for fungal over mammalian P450 enzymes, limiting its use primarily to topical applications for vulvovaginal candidiasis and dermatophyte infections.
Can be treated with vaginal application during pregnancy; oral antifungal treatment should be avoided.
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism.
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism.
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Drug interaction classified as: metabolism.
Source: DDInter
Drug interaction classified as: metabolism
Source: DDInter
Continue into a citation-backed clinical answer with the drug context already attached.
Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-10 · House clinical team