Navigation

oxiconazole (Oxistat)

 

Classes: Antifungals, Topical

Dosing and uses of Oxistat (oxiconazole)

 

Adult dosage forms and strengths

cream/lotion

  • 1%

 

Fungal Infections

Apply qDay-BID to affected & surrounding area

Tinea pedis: x4 weeks

Tinea cruris & corporis: x2 weeks

 

Pediatric dosage forms and strengths

cream/lotion

  • 1%

 

Fungal Infections

Apply qDay-BID to affected & surrounding area

These infections rarely occur in <12 years old

 

Oxistat (oxiconazole) adverse (side) effects

1-10%

Pruritus (1-2%)

Burning (1-2%)

 

<1%

Irritation

Stinging

Erythema

Rash

Folliculitis

Papules

Nodules

Maceration

Fissuring

 

Warnings

Contraindications

Hypersensitivity

Not for ophthalmic or intravaginal use

 

Pregnancy and lactation

Pregnancy category: B

Lactation: distributed into milk; use with caution in nursing women

 

Pregnancy categories

A: Generally acceptable. Controlled studies in pregnant women show no evidence of fetal risk.

B: May be acceptable. Either animal studies show no risk but human studies not available or animal studies showed minor risks and human studies done and showed no risk.

C: Use with caution if benefits outweigh risks. Animal studies show risk and human studies not available or neither animal nor human studies done.

D: Use in LIFE-THREATENING emergencies when no safer drug available. Positive evidence of human fetal risk.

X: Do not use in pregnancy. Risks involved outweigh potential benefits. Safer alternatives exist.

NA: Information not available.

 

Pharmacology of Oxistat (oxiconazole)

Absorption: minimaL

Excretion: urine (0.3%) within 5 days

Enzymes inhibited: hepatic CYP3A4

 

Mechanism of action

Fungistatic in action but may be fungicidal in high concentrations or against very susceptible organisms

Presumably exerts its antifungal activity by altering cellular membranes, resulting in increased membrane permeability, secondary metabolic effects, and growth inhibition

Appears that the antifungal activity of the drug results from interference with ergosterol synthesis, probably via inhibition of C-14 methylation of sterol intermediates (e.g., lanosterol)