Oral antifungal medications may be required for fungal infection if:
- It is extensive or severe.
- It resists topical antifungal therapy.
- It affects hair-bearing areas (tinea capitis and tinea barbae).
The choice of oral antifungal medication, its dose and the duration of treatment depend on:
- The type of fungus i.e. candida, dermatophyte (tinea), malassezia, or mould.
- The site affected i.e. skin, mucosa, nails.
- Other co-existing diseases.
- Interactions with other medications.
Medication for both candida and dermatophyte infections (azoles)
The trade names of the medications sold in New Zealand are given in parentheses.
- Itraconazole (Sporanox® capsules).
- Ketoconazole (Nizoral® tablets).
- Fluconazole (Diflucan® capsules).
Some species of candida are resistant to azoles, and azole resistance is increasing especially in immunosuppressed patients who are prescribed long courses.
Medications only suitable for candida infections
- Nystatin (Mycostatin®, Nilstat®), a polyene. This is not absorbed into the bloodstream through the gut.
- Flucytosine (Alcobon® infusion), usually used with amphotericin. It can cause bone marrow depression.
- Amphotericin B (Ambisome® injection; Fungizone® infusion), a polyene. This is not absorbed into the bloodstream through the gut.
- Caspofungin, anidulafungin and micafungin (echinocandins)
Medications only suitable for dermatophyte infections
- Griseofulvin (no longer available in New Zealand), derived from Penicillium
- Terbinafine (Lamisil®, Terbafin® tablets), an allylamine.
Antifungal drug resistance
Extensive therapy-resistant dermatophyte infection should prompt this as a possible problem. Where available, fungal culture and estimation of drug minimum inhibitory concentration determined to guide appropriate medication
For more information, see antifungal drug resistance.
If you are not based in New Zealand, we suggest you refer to your national drug approval agency for further information about medicines (eg, the Australian Therapeutic Goods Administration and the US Food and Drug Administration) or a national or state-approved formulary (eg, the New Zealand Formulary and New Zealand Formulary for Children and the British National Formulary and British National Formulary for Children).