BRAND NAMES
 MECHANISM OF ACTION
Sertaconazole is an antifungal agent of the imidazole class. It inhibits lanosterol 14α-demethylase, a cytochrome P-450 enzyme that converts lanosterol to ergosterol.
Ergosterol is an essential component of the fungal cell membrane. The inhibition of its synthesis results in accumulation of toxic 14α-methylated sterols and the production of a defective cell membrane with altered permeability and leakage of cellular contents.
Candidal vulvovaginitis (vaginal thrush)
300 mg vaginal suppository: A single dose introduced deeply into the vagina, preferably while lying down, at night. The vaginal suppository can be used during menstruation. In general, 1 vaginal suppository suffices to eradicate the vaginal mycosis. However, if it persists, a second vaginal suppository can be applied alter 7 days..
- Patients who have a known or suspected sensitivity to sertaconazole
- Pregnancy and lactation
 PREGNANCY AND LACTATION
- Pregnancy and lactation: generally not recommended during pregnancy and lactation
 SIDE EFFECTS
Rarely, slight local and transient erythematous reaction.
 RELATED LINKS
|Ergosterol target : Cell membrane target||Azoles (lanosterol 14 alpha-demethylase inhibitors) : Ergosterol inhibitors||Imidazoles||Topical: Bifonazole • Clotrimazole • Econazole • Fenticonazole • Ketoconazole • Isoconazole • Miconazole • Sertaconazole • Tioconazole|
|Triazoles|| Topical: Fluconazole • Terconazole|
Systemic: Fluconazole • Itraconazole • Posaconazole • Voriconazole
|Polyene antimycotics (ergosterol binding; they form pores in the membrane)|| Topical: Nystatin |
Systemic: Amphotericin B
|Allylamines (squalene epoxidase inhibitors) : Ergosterol inhibitors|| Topical: Amorolfine • Naftifine • Terbinafine |
|Echinocandins (β-glucan synthase inhibitors) : Cell wall target||Anidulafungin • Caspofungin • Micafungin|
|Pyrimidine analogues / Thymidylate synthase inhibitors : Nucleic acid inhibitors||Flucytosine|