VetSheet

Fluconazol

Fluconazole

Fluconazole (UK-49858)

Antifúngico - TriazolPOIVPerrosGatosPequeños mamíferosAvesCaballos

También conocido como: Diflucan · UK-49858 · Fluconazolum

Revisado por el equipo veterinario de VetSheetActualizado 5 abr 2026Referencia veterinaria basada en la evidencia

2.5-5 mg/kg PO or IV q12-24hPO/IV· q12-24h· 56-84 days
🐕

Las dosis son una referencia clínica para profesionales veterinarios autorizados. Confirme siempre con el prospecto actual y cada paciente individual.

Dosis por especie

🌎 NA — North America🌍 EU — Europe

Perros

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Cryptococcosis, candidiasis, systemic mycoses, nasal aspergillosis2.5-5 mg/kg PO or IV q12-24hPO/IVq12-24h56-84 days🌎 NA
Fungal meningitis5-8 mg/kg PO or IV q12h OR 8-12 mg/kg PO or IV once daily (q24h)PO/IVq12h or q24h56-84 days🌎 NA
Urinary candidiasis5-10 mg/kg PO q24hPOq24h21-42 days🌎 NA
Urinary Candida glabrata infection12 mg/kg PO once dailyPOq24h21-42 days🌎 NA
Cryptococcosis5 mg/kg PO once or twice dailyPOq12h or q24hAt least 2 months beyond resolution of clinical signs🌎 NA
Blastomycosis5 mg/kg PO q12hPOq12h60 days🌎 NA
Cryptococcosis5-15 mg/kg PO q12-24hPOq12-24h6-10 months🌎 NA
Treatment of Malassezia (may be safer than itraconazole or ketoconazole in dogs with hepatic disease)5 mg/kg PO once dailyPOq24h🌎 NA
Systemic treatment of Malassezia dermatitis5 mg/kg PO once dailyPOq24h🌎 NA
Recurrent Malassezia dermatitis5 mg/kg PO 3 times per weekPO3 times per week🌎 NA
Systemic treatment of Malassezia dermatitis2-5 mg/kg PO once daily (q24h)POq24h🌎 NA
Nasal aspergillosis (alternative to itraconazole or terbinafine)2.5-5 mg/kg PO q12hPOq12h3-6 months🌎 NA
  • Cryptococcosis, candidiasis, systemic mycoses, nasal aspergillosis: Often treat neurologic ocular cryptococcosis for at least 12 weeks or 2 weeks after CSF exam shows resolution
  • Nasal aspergillosis (alternative to itraconazole or terbinafine): Cure rates up to 60%

Gatos

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Nasal or dermal cryptococcosis5-10 mg/kg PO q12-24h, or 10 mg/kg PO q24hPOq12-24h🌎 NA
CNS, intraocular, or multisystemic cryptococcosis50-100 mg/cat PO or IV q12hPO/IVq12h🌎 NA
CNS, intraocular or multisystemic mycoses50 mg/cat PO once daily (q24h)POq24h🌎 NA
Cryptococcosis50 mg (total dose) PO twice dailyPOq12h1 month beyond resolution of clinical signs🌎 NA
Cryptococcosis50 mg (total dose) PO twice dailyPOq12hAt least 2 months beyond resolution of clinical signs🌎 NA
  • Nasal or dermal cryptococcosis: For most infections, 50 mg/cat PO once daily achieves adequate therapeutic levels
  • CNS, intraocular, or multisystemic cryptococcosis: Often treat neurologic ocular cryptococcosis for at least 12 weeks or 2 weeks after CSF exam shows resolution

Pequeños mamíferos

IndicaciónDosisVíaFrecuenciaDuraciónRegión
General (Rabbits)25-43 mg/kg slow IV q12hIVq12h🌎 NA

Aves

IndicaciónDosisVíaFrecuenciaDuraciónRegión
Candidiasis (cockatoos, parrots)20 mg/kg PO q24-48h or 10 mg/kg PO q24hPOq24-48h🌎 NA
Candidiasis (cockatiels)10 mg/kg fluconazole PO suspension and 100 mg/mL fluconazole treated drinking waterPO🌎 NA
Alternate treatment of aspergillosis5-10 mg/kg PO once dailyPOq24hup to 6 weeks🌎 NA
  • Candidiasis (cockatoos, parrots): Likely effective for C. albicans. C. galabrata and C. papasilosis may have higher MICs.
  • Candidiasis (cockatiels): Maintained plasma levels above the MIC for most strains of Candida albicans
  • Alternate treatment of aspergillosis: With or after amphotericin B

Caballos

IndicaciónDosisVíaFrecuenciaDuraciónRegión
C. immitis infection or Candida bacteremiaLoading dose of 14 mg/kg followed by 5 mg/kg PO once dailyPOq24h🌎 NA
Fungal keratitis1 mg/kg PO q24hPOq24h🌎 NA
  • Fungal keratitis: Anecdotal reports of successful treatment

Las dosis son una referencia clínica para profesionales veterinarios autorizados. Confirme siempre con el prospecto actual y cada paciente individual.

¿Atendiendo una consulta? La IA de VetSheet escribe el fármaco, la dosis y la duración directamente en una nota de visita estructurada.Descubre cómo funciona VetSheet

Resumen

El fluconazol es un agente antifúngico triazol sistémico. A diferencia de los azoles de primera generación (como el ketoconazol), es altamente hidrofílico, lo que permite una excelente penetración en el ​sistema nervioso central (LCR)​, ojos y tracto urinario.

​Perla clínica:​ El fluconazol no requiere un ambiente gástrico ácido para su absorción, lo que hace que su biodisponibilidad oral sea altamente confiable incluso en pacientes que reciben terapia antiácida. Además, tiene una afinidad significativamente menor por las enzimas citocromo P450 de los mamíferos en comparación con el ketoconazol, lo que significa que tiene un impacto mínimo en la síntesis de hormonas esteroides mamíferas y, por lo general, menos efectos secundarios.

Mecanismo de acción

Fluconazole acts by inhibiting the fungal cytochrome P450-dependent enzyme lanosterol 14-α-demethylase.

Lanosterol → (blocked by fluconazole) → Ergosterol

This depletion of ergosterol disrupts the synthesis of the fungal cell membrane, increasing its permeability and causing leakage of essential cellular contents. It also impairs the uptake of purine and pyrimidine precursors. Fluconazole is primarily fungistatic.

Seguridad y advertencias

Contraindicaciones

  • Hypersensitivity to fluconazole or other azole antifungals
  • Budgerigars (reportedly toxic)
  • Pregnant animals
  • Lactating animals

Efectos adversos

  • Inappetence
  • Vomiting
  • Diarrhea
  • Hepatotoxicity (rare)
  • Headache (humans)
  • Increased liver enzymes (humans)
  • Exfoliative skin disorders (humans)
  • Thrombocytopenia (humans)
  • Nausea
  • Diarrhoea

Precauciones

Use with caution in patients with hepatic impairment. Because fluconazole is eliminated primarily by the kidneys, doses or dosing intervals may need to be adjusted in patients with renal impairment. Safety during pregnancy has not been established (FDA Category C); use with caution in nursing dams as it is excreted in milk. Reportedly toxic to budgerigars.

Interacciones farmacológicas

Amphotericin B

May be antagonistic against Aspergillus or Candida; clinical importance unclear

Buspirone

Plasma concentrations of buspirone may be elevated

Cisapride

May increase cisapride levels and the possibility for toxicity

Corticosteroids

May inhibit the metabolism of corticosteroids; potential for increased adverse effects

Cyclophosphamide

May inhibit the metabolism of cyclophosphamide and its metabolites; potential for increased toxicity

Cyclosporine

Increases cyclosporine levels; dosage of cyclosporine may need to be decreased by 29%-51%

Diuretics, Thiazides

Increased fluconazole concentrations

Fentanyl/Alfentanil

May increase fentanyl levels

Midazolam

Increased midazolam levels and effects

NSAIDs

May increase NSAID plasma levels; increased risk for adverse effects

Quinidine

Increased risk for cardiotoxicity

Rifampin

May decrease fluconazole efficacy; fluconazole may increase rifampin levels

Theophylline/Aminophylline

Increased theophylline concentrations

Tricyclic Antidepressants

May exacerbate the effects of tricyclic antidepressants (e.g., clomipramine, amitriptyline)

Sulfonylurea Antidiabetic Agents

May increase levels of agents like glipizide or glyburide; hypoglycemia possible

Vincristine/Vinblastine

May inhibit vinca alkaloid metabolism

Warfarin

May cause increased prothrombin times

TheophyllineModerate

Fluconazole inhibits cytochrome P450-dependent liver enzymes, which may increase plasma theophylline concentrations.

TerfenadineMajor

Co-administration has led to terfenadine toxicity in humans.

CiclosporinMajor

Fluconazole increases ciclosporin blood levels.

Monitorización

  • Clinical efficacy
  • Liver function tests (occasional, with long-term therapy)
  • Liver enzyme panel (ALT, AST, ALP, Bilirubin) prior to and during prolonged therapy
  • Renal function (BUN, Creatinine)
  • Resolution of clinical signs of fungal infection
  • Therapeutic drug monitoring for concurrent medications like ciclosporin or theophylline

Farmacocinética

Absorción

Rapidly and nearly completely absorbed (90%) after oral administration. Gastric pH or the presence of food do not appreciably alter oral bioavailability.

Distribución

Low protein binding and widely distributed throughout the body. Penetrates well into the CSF, eye, and peritoneal fluid.

Metabolismo

Minimal hepatic metabolism compared to other azole antifungals.

Eliminación

Eliminated primarily via the kidneys and achieves high concentrations in the urine.

Sobredosis

There is limited information on acute toxicity in domestic animals. In rodents, massive overdoses (1-2 g/kg) caused respiratory depression, salivation, lacrimation, urinary incontinence, and cyanosis, leading to death within several days.

​Treatment:​ If a massive overdose occurs, consider gut emptying (emesis or gastric lavage) if recent, and provide supportive therapy as required. Fluconazole may be removed by hemodialysis or peritoneal dialysis.

Productos disponibles

Formulaciones

  • Tablets
  • Powder for oral suspension
  • Injection
  • 150 mg oral capsule
  • 200 mg oral capsule
  • 40 mg/ml oral suspension
  • 2 mg/ml injectable solution

Etiquetado para humanos

  • Fluconazole Oral Tablets: 50 mg, 100 mg, 150 mg, & 200 mg
  • Fluconazole Powder for Oral Suspension: 10 mg/mL & 40 mg/mL (when reconstituted)
  • Fluconazole Injection: 2 mg/mL in 100 mL or 200 mL bottles or Viaflex Plus
  • Diflucan 50 mg, 150 mg, 200 mg capsules
  • Diflucan 40 mg/ml oral suspension
  • Diflucan 2 mg/ml injectable solution

Estado regulador

European Union✓ AprobadoMedicamento de prescripciónEMA
🐕 Dogs🐈 Cats

POM (Prescription Only Medicine)

United Kingdom✓ AprobadoMedicamento de prescripciónVMD
🐕 Dogs🐈 Cats

POM-V (Prescription Only Medicine - Veterinarian)

Sin datos reguladores para: 🇺🇸 US · 🇭🇰 HK · 🇹🇼 TW · 🇯🇵 JP · 🇰🇷 KR · 🇦🇺 AU

Almacenamiento y estabilidad

Tablets should be stored at temperatures less than 30°C in tight containers. Injection should be stored at 5-30°C (5-25°C for Viaflex bags); avoid freezing. Do not add additives to the injection.

Información para el cliente

  • ​La paciencia es clave:​ Las infecciones fúngicas tardan mucho tiempo en curarse. El tratamiento a menudo dura de varias semanas a meses. No suspenda la medicación antes de tiempo aunque su mascota parezca estar mejor, ya que la infección puede reaparecer.
  • ​Administración:​ El fluconazol se absorbe muy bien tanto si se administra con comida como con el estómago vacío.
  • ​Esté atento a los efectos secundarios:​ Aunque generalmente es muy seguro, vigile si presenta pérdida de apetito, vómitos o diarrea. Comuníquese con su veterinario si estos ocurren.
  • ​Costo:​ Debido a que el tratamiento es prolongado, el costo puede acumularse, aunque las opciones genéricas lo han hecho más asequible.

La referencia de medicamentos de VetSheet está destinada a profesionales veterinarios autorizados como ayuda para la toma de decisiones clínicas, no como sustituto del criterio profesional ni del prospecto actual del fabricante.