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Antifungal (Azole) Pregnancy: Should not be used in pregnancy in standard doses and short-term treatments unless clearly necessary; high-dose and/or prolonged regimens should not be used during pregnancy except for potentially life-threatening infections. Observational data suggest an increased risk of spontaneous abortion with first/second trimester exposure, a small increased risk of musculoskeletal malformations (greater with cumulative doses over 450 mg), and a possible increased risk of cardiac malformations. Women of childbearing potential should be informed of the potential risk to the fetus; a washout period of 1 week is recommended after single-dose treatment before becoming pregnant, and contraception may be considered during longer courses and for 1 week after the final dose. Breast-feeding may be maintained after a single 150 mg dose but is not recommended after repeated use or high-dose fluconazole.

Fluconazole

Brand names: Diflucan

Fluconazole is a triazole antifungal for candidal infections (including vaginal and oral thrush) and some systemic fungal infections.

Auto-extracted from the source labelling — not yet independently clinician-verified. These values were distilled from the UK SPC (or the US label where noted) but have not had a clinician sign-off. Confirm against the current SmPC before prescribing.

Adult dose

Dose: Genital candidiasis (acute vaginal candidiasis; candidal balanitis): 150 mg as a single dose
Route: Oral (capsule). Fluconazole may alternatively be given by intravenous infusion; on transferring from the intravenous to the oral route, or vice versa, there is no need to change the daily dose.
Frequency: Single dose
Max: No single adult ceiling is stated. The highest adult regimens in this SPC are 800 mg daily (life-threatening cryptococcal infection; coccidioidomycosis, especially meningeal disease). A maximum dose of 400 mg daily should not be exceeded in the paediatric population.
The dose should be based on the nature and severity of the fungal infection; treatment requiring multiple dosing should continue until clinical parameters or laboratory tests indicate the active fungal infection has subsided. Treatment and prophylaxis of RECURRENT vaginal candidiasis (4 or more episodes a year): 150 mg every third day for a total of 3 doses (days 1, 4 and 7), followed by a 150 mg once-weekly maintenance dose for 6 months. Other adult regimens in the same SPC — Cryptococcal meningitis: loading 400 mg on day 1 then 200 to 400 mg once daily, usually at least 6 to 8 weeks (daily dose may be increased to 800 mg in life-threatening infection); maintenance to prevent relapse 200 mg once daily indefinitely. Coccidioidomycosis: 200 to 400 mg once daily for 11 to 24 months or longer; 800 mg daily may be considered for some infections, especially meningeal disease. Invasive candidiasis: loading 800 mg on day 1 then 400 mg once daily (for candidaemia, generally 2 weeks after the first negative blood culture and resolution of symptoms). Oropharyngeal candidiasis: loading 200 to 400 mg day 1 then 100 to 200 mg once daily for 7 to 21 days. Oesophageal candidiasis: loading 200 to 400 mg day 1 then 100 to 200 mg once daily for 14 to 30 days. Candiduria: 200 to 400 mg once daily for 7 to 21 days. Chronic atrophic candidiasis: 50 mg once daily for 14 days. Chronic mucocutaneous candidiasis: 50 to 100 mg once daily for up to 28 days. Prevention of relapse of oropharyngeal or oesophageal candidiasis in HIV: 100 to 200 mg once daily or 200 mg three times per week, indefinitely in chronic immune suppression. Dermatomycosis (tinea pedis, corporis, cruris, candida infections): 150 mg once weekly or 50 mg once daily for 2 to 4 weeks (tinea pedis may need up to 6 weeks). Tinea versicolor: 300 to 400 mg once weekly for 1 to 3 weeks, or 50 mg once daily for 2 to 4 weeks. Tinea unguium (onychomycosis): 150 mg once weekly until the infected nail is replaced. Prophylaxis in prolonged neutropenia: 200 to 400 mg once daily, starting several days before the anticipated onset of neutropenia and continuing for 7 days after the neutrophil count rises above 1000 cells/mm3. Fluconazole should not be used for tinea capitis. Elderly: adjust dosage based on renal function. Hepatic impairment: administer with caution (limited data). Capsules should be swallowed whole, independent of food; the capsule formulation is not adapted for infants and small children. Interaction entries below are drawn from the SPC §4.3/§4.4 and from the US labelling's drug-interaction section — the UK SPC §4.5 text was not captured in this fetch. Source: eMC SPC for Fluconazole 150 mg capsules (§4.2).

Paediatric dose

Dose: 3 mg/kg
Route: Oral or intravenous infusion
Frequency: Once daily (single daily dose)
Max: A maximum dose of 400 mg daily should not be exceeded in the paediatric population
Infants, toddlers and children (28 days to 11 years) — mucosal candidiasis: initial dose 6 mg/kg, then 3 mg/kg once daily (the initial dose may be used on the first day to reach steady state more rapidly). Invasive candidiasis or cryptococcal meningitis: 6 to 12 mg/kg once daily depending on severity. Maintenance to prevent relapse of cryptococcal meningitis: 6 mg/kg once daily. Prophylaxis of Candida in immunocompromised patients: 3 to 12 mg/kg once daily depending on the extent and duration of neutropenia. Term newborn infants 0 to 14 days: the same mg/kg dose as for infants/children given every 72 hours, not exceeding 12 mg/kg every 72 hours. Term newborn infants 15 to 27 days: the same mg/kg dose given every 48 hours, not exceeding 12 mg/kg every 48 hours. Adolescents 12 to 17 years: the prescriber must judge whether adult or child posology is appropriate, based on weight and pubertal development. Safety and efficacy for the GENITAL CANDIDIASIS indication have not been established in the paediatric population; if treatment for genital candidiasis is imperative in adolescents 12 to 17 years, the posology should be the same as the adult posology. Doses of 100, 200 and 400 mg in adults correspond to 3, 6 and 12 mg/kg in children for comparable systemic exposure. Oral liquid formulations are more suitable than capsules in this population. Verify all paediatric dosing against a children's formulary.

Dose adjustments

Renal

No adjustment is necessary for single-dose therapy. For multiple-dose therapy (including in the paediatric population), give an initial dose of 50 mg to 400 mg based on the recommended daily dose for the indication, then adjust the daily dose by creatinine clearance: CrCl >50 mL/min — 100% of the recommended dose; CrCl ≤50 mL/min (no haemodialysis) — 50%; haemodialysis — 100% of the recommended dose after each haemodialysis session, with a reduced dose according to creatinine clearance on non-dialysis days.

Dose auto-extracted from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.

Paediatric weight-based calculator

Infants, toddlers and children (28 days to 11 years) — mucosal candidiasis: initial dose 6 mg/kg, then 3 mg/kg once daily (the initial dose may be used on the first day to reach steady state more rapidly). Invasive candidiasis or cryptococcal meningitis: 6 to 12 mg/kg once daily depending on severity. Maintenance to prevent relapse of cryptococcal meningitis: 6 mg/kg once daily. Prophylaxis of Candida in immunocompromised patients: 3 to 12 mg/kg once daily depending on the extent and duration of neutropenia. Term newborn infants 0 to 14 days: the same mg/kg dose as for infants/children given every 72 hours, not exceeding 12 mg/kg every 72 hours. Term newborn infants 15 to 27 days: the same mg/kg dose given every 48 hours, not exceeding 12 mg/kg every 48 hours. Adolescents 12 to 17 years: the prescriber must judge whether adult or child posology is appropriate, based on weight and pubertal development. Safety and efficacy for the GENITAL CANDIDIASIS indication have not been established in the paediatric population; if treatment for genital candidiasis is imperative in adolescents 12 to 17 years, the posology should be the same as the adult posology. Doses of 100, 200 and 400 mg in adults correspond to 3, 6 and 12 mg/kg in children for comparable systemic exposure. Oral liquid formulations are more suitable than capsules in this population. Verify all paediatric dosing against a children's formulary.

Verify in a children's formulary

US labelling (FDA)

Reference — US labelling, may differ from UK

DOSAGE AND ADMINISTRATION Dosage and Administration in Adults: Single Dose Vaginal candidiasis: The recommended dosage of fluconazole for vaginal candidiasis is 150 mg as a single oral dose. Multiple Dose SINCE ORAL ABSORPTION IS RAPID AND ALMOST COMPLETE, THE DAILY DOSE OF FLUCONAZOLE IS THE SAME FOR ORAL AND INTRAVENOUS ADMINISTRATION. In general, a loading dose of twice the daily dose is recommended on the first day of therapy to result in plasma concentrations close to steady-state by the second day of therapy. The daily dose of fluconazole for the treatment of infections other than vaginal candidiasis should be based on the infecting organism and the patient’s response to therapy. …

Source: US FDA prescribing information (openFDA / DailyMed), label dated 2025-11-17. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.

Contraindications

  • Hypersensitivity to the active substance, to related azole substances, or to any of the excipients
  • Co-administration of terfenadine in patients receiving fluconazole at multiple doses of 400 mg per day or higher
  • Co-administration of other medicinal products known to prolong the QT interval and metabolised via CYP3A4, such as cisapride, astemizole, pimozide, quinidine and erythromycin

Side effects

  • Headache (common); dizziness, somnolence, insomnia, taste perversion, paraesthesia (uncommon); seizures (uncommon)
  • Abdominal pain, vomiting, diarrhoea, nausea (common); constipation, dyspepsia, flatulence, dry mouth (uncommon)
  • Raised alanine aminotransferase, aspartate aminotransferase and blood alkaline phosphatase (common); cholestasis, jaundice, raised bilirubin (uncommon); hepatic failure, hepatocellular necrosis, hepatitis (rare)
  • Rash (common); urticaria, pruritus, drug eruption, increased sweating (uncommon); toxic epidermal necrolysis, Stevens-Johnson syndrome, acute generalised exanthematous pustulosis, exfoliative dermatitis, angioedema, alopecia (rare); DRESS (frequency not known)
  • QT prolongation and torsade de pointes (rare); anaphylaxis (rare); anaemia (uncommon), agranulocytosis, leukopenia, thrombocytopenia, neutropenia (rare); hypokalaemia, hypercholesterolaemia, hypertriglyceridaemia (rare)

Interactions

  • Terfenadine — contraindicated with fluconazole 400 mg/day or higher (§4.3)
  • Cisapride, astemizole, pimozide, quinidine, erythromycin — QT-prolonging CYP3A4 substrates; co-administration contraindicated (§4.3)
  • Amiodarone and other QT-prolonging medicines — QT prolongation may be amplified via inhibition of CYP3A4 (§4.4)
  • Prednisone — adrenal insufficiency has been reported in relation to concomitant treatment (§4.4, referring to §4.5)
  • Combined oral contraceptives — US labelling reports mean AUC increases of up to about 38% (ethinyl estradiol) and 25% (levonorgestrel) with fluconazole 200 mg daily; no significant change with 50 mg daily (US label, Drug Interaction Studies)

Clinical monograph

How it works

It inhibits fungal ergosterol synthesis (14-alpha-demethylase), disrupting the fungal cell membrane.

Prescribing in practice

  • It is a CYP inhibitor with interactions (e.g. warfarin, some statins) and can prolong the QT interval.
  • Hepatotoxicity can occur; reduce the dose in renal impairment for multi-dose courses.
  • Higher or repeated doses in pregnancy are associated with birth defects — avoid in pregnancy other than where specifically advised.

Monitoring

Monitor liver function with longer courses; review interactions.

Counselling the patient

  • Tell your clinician your other medicines.
  • Report yellowing of the skin or eyes.
  • Seek advice if you are pregnant or planning pregnancy.

Evidence & guidelines

Standard treatment for candidal infections (NICE CKS), with interaction and pregnancy cautions.

Reference: MHRA Drug Safety Update 2018 (Fluconazole in Pregnancy); Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.