Micafungin
Brand names: Mycamine
Micafungin is an intravenous echinocandin antifungal used for invasive and oesophageal candidiasis and for prophylaxis of Candida infection in certain at-risk patients such as stem cell transplant recipients.
Adult dose
Paediatric dose
Dose adjustments
No dose adjustment is necessary in patients with renal impairment. However, micafungin may cause kidney problems, renal failure and abnormal renal function tests - monitor closely for worsening renal function.
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.
Structured value is for treatment of invasive candidiasis in children 4 months of age and over up to adolescents under 16 years, body weight 40 kg or less. Children in that band weighing over 40 kg: 100 mg/day (may increase to 200 mg/day). Prophylaxis of Candida infection in that band: 1 mg/kg/day (40 kg or less) or 50 mg/day (over 40 kg). Children (including neonates) under 4 months of age: treatment of invasive candidiasis 4-10 mg/kg/day; prophylaxis of Candida infection 2 mg/kg/day. Micafungin dosed at 4 mg/kg in children under 4 months approximates drug exposures achieved in adults receiving 100 mg/day for invasive candidiasis; if CNS infection is suspected a higher dosage (e.g. 10 mg/kg) should be used due to dose-dependent CNS penetration. Safety and efficacy of the 4 and 10 mg/kg doses for invasive candidiasis with CNS involvement in children (including neonates) under 4 months has not been adequately established. Experience in patients under 2 years of age is limited. Paediatric patients under 1 year of age may be more prone to liver injury. Treatment duration as for adults. Oesophageal candidiasis dosing is not stated for the paediatric population in this SPC. Verify all paediatric doses against a children's formulary before prescribing.
Contraindications
- Hypersensitivity to the active substance, to other echinocandins, or to any of the excipients
Side effects
- Nausea (2.8%), vomiting (2.5%), diarrhoea, abdominal pain (common)
- Blood alkaline phosphatase increased (2.7%), aspartate aminotransferase increased (2.3%), alanine aminotransferase increased, blood bilirubin increased, abnormal liver function test (common)
- Phlebitis (2.5%, primarily in HIV-infected patients with peripheral lines) (common)
- Leukopenia, neutropenia, anaemia (common); haemolytic anaemia and haemolysis (rare)
- Hypokalaemia, hypomagnesaemia, hypocalcaemia (common); headache, pyrexia, rigors, rash (common)
- Anaphylactic/anaphylactoid reaction including shock, and exfoliative cutaneous reactions (Stevens-Johnson syndrome, toxic epidermal necrolysis) (uncommon to rare)
Interactions
- Amphotericin B desoxycholate - co-administration only when benefits clearly outweigh risks, with close monitoring for amphotericin B desoxycholate toxicity
- Sirolimus - monitor for sirolimus toxicity; reduce sirolimus dose if necessary
- Nifedipine - monitor for nifedipine toxicity; reduce nifedipine dose if necessary
- Itraconazole - monitor for itraconazole toxicity; reduce itraconazole dose if necessary
- Concomitant hepatotoxic and/or genotoxic medicines - conduct micafungin treatment on a careful risk/benefit basis
Clinical monograph
How it works
It non-competitively inhibits beta-(1,3)-D-glucan synthase, an enzyme essential for synthesis of a key fungal cell-wall component absent from mammalian cells, leading to fungal cell death.
Prescribing in practice
- Liver function should be monitored as hepatic effects can occur, and regulatory advice notes liver tumours were seen in long-term animal studies, so prolonged use is weighed against benefit.
- Infusion-related reactions, including histamine-mediated symptoms, can occur and are reduced by appropriate infusion rates.
- It is given intravenously only and, unlike azoles, has comparatively few cytochrome P450-mediated interactions, though the SPC should still be checked.
Monitoring
Monitor liver function and review for infusion reactions, haemolysis and renal effects during therapy.
Counselling the patient
- Report any rash, flushing or breathlessness during the infusion.
- This treatment is given by a drip and your blood tests will be checked during the course.
- Mention any history of liver problems to your team.
Evidence & guidelines
Efficacy in invasive and oesophageal candidiasis is established in randomised trials and reflected in the SPC.
Reference: ESCMID Candida Guidelines; EMA Micafungin Hepatotoxicity Review 2012; PEDIATRIC Micafungin Studies; 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.
- Caprini Score for VTE Risk (2005) · VTE Risk
- Caprini VTE Risk Assessment · Venous Thromboembolism
- FIB-4 Index · Liver Fibrosis
- AST to Platelet Ratio Index (APRI) · Hepatology
- EVendo Score for Predicting Esophageal Varices · Portal Hypertension
- SAFE Score for Significant Fibrosis in NAFLD/MASLD · Liver Fibrosis