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MICAFUNGIN IN SODIUM CHLORIDE 0.9%

MICAFUNGIN IN SODIUM CHLORIDE 0.9%

Clinical safety rating

safe

No significant drug interactions Can cause hypernatremia and fluid overload.


Mechanism of Action

Micafungin is an echinocandin antifungal that inhibits the synthesis of 1,3-beta-D-glucan, an essential component of the fungal cell wall, leading to osmotic instability and cell death.

What the body does with it

MetabolismMicafungin is metabolized by arylsulfatase and catechol-O-methyltransferase (COMT) to the M1 metabolite, and further metabolized by CYP3A4 to M2; however, CYP3A4 plays a minor role. The drug is not a significant inhibitor or inducer of CYP enzymes.
ExcretionPrimarily biliary/fecal (≈71% of administered dose recovered in feces as parent drug and metabolites); renal excretion accounts for ≈15% (urine: <1% as unchanged drug).
Half-lifeTerminal elimination half-life is approximately 13-20 hours in adults; supports once-daily dosing. Half-life is prolonged in moderate-to-severe hepatic impairment (Child-Pugh B/C) but no dosage adjustment is required.
Protein bindingHighly protein-bound (≥99.8%), primarily to albumin; slight binding to α1-acid glycoprotein.
Volume of DistributionVolume of distribution at steady state (Vss) is approximately 0.2-0.3 L/kg in adults; indicates limited tissue distribution, primarily confined to plasma and interstitial fluid.
BioavailabilityOnly available as intravenous infusion; oral bioavailability is negligible (<0.1%) due to poor gastrointestinal absorption.
Onset of ActionIntravenous administration: onset of antifungal activity is rapid; steady-state concentrations achieved after 4-5 daily doses (loading dose not required per US labeling).
Duration of ActionDuration of antifungal effect persists for at least 24 hours with once-daily dosing; clinical response typically assessed after 48-72 hours of therapy.
Molecular Weight1270

Classification & Brands

Dosing & administration

100 mg intravenously once daily for invasive candidiasis; 150 mg intravenously once daily for esophageal candidiasis.

Dosage formSOLUTION
Renal impairmentNo dosage adjustment required for any degree of renal impairment.
Liver impairmentIn moderate hepatic impairment (Child-Pugh B), reduce dose to 100 mg once daily; no data for severe impairment (Child-Pugh C). No adjustment for mild impairment.
Pediatric useFor invasive candidiasis: 2 mg/kg (max 100 mg) intravenously once daily for patients ≥40 kg; 2 mg/kg once daily for patients <40 kg. For esophageal candidiasis: 3 mg/kg (max 150 mg) once daily.
Geriatric useNo specific dose adjustment; use standard adult dosing based on renal and hepatic function.

Use during pregnancy

1st trimesterAnimal studies show fetal harm; no adequate human studies. Use only if potential benefit justifies potential risk.
2nd trimesterAnimal studies show fetal harm; no adequate human studies. Use only if potential benefit justifies potential risk.
3rd trimesterAnimal studies show fetal harm; no adequate human studies. Use only if potential benefit justifies potential risk.

Clinical note

No significant drug interactions Can cause hypernatremia and fluid overload.

FDA categoryAnimal
Placental transferLimited human data; animal studies indicate placental transfer. Molecular weight (~1270 Da) suggests potential transfer.
BreastfeedingMicafungin is excreted in animal milk; unknown in humans. Caution advised due to potential adverse effects in nursing infants.
Lactation RatingL3 (Moderately Safe)
Teratogenic RiskMicafungin is classified as FDA Pregnancy Category C. In animal studies, embryotoxicity and skeletal abnormalities were observed at doses 0.04 times the human dose. No adequate human studies exist. First trimester: Theoretical risk based on animal data; use only if benefit justifies risk. Second/third trimester: Limited data; may be used if clearly needed due to lack of alternative therapy.
Fetal MonitoringMonitor liver function tests (ALP, AST, ALT, bilirubin) due to potential hepatotoxicity; renal function tests (serum creatinine, BUN) as micafungin is cleared in part renally; complete blood count (CBC) for possible hemolytic anemia; and signs of infusion-related reactions (rash, pruritus, hypotension). Fetal monitoring: standard fetal growth and well-being assessments if used during pregnancy.
Fertility EffectsNo human data on fertility impact. Animal studies: no impairment of male or female fertility at systemic exposures similar to human therapeutic exposures.

Warnings & precautions

■ FDA Black Box Warning

There is no FDA black box warning for micafungin.

Side Effect Profile

Common Effectsfluid replacement
Serious Effects

Absolute Contraindications

Hypersensitivity to micafungin or any component

Clinical Precautions

PrecautionsHypersensitivity reactions, including anaphylaxis and anaphylactoid reactions, Hepatic effects: elevations in liver enzymes, bilirubin, and rare cases of hepatic necrosis or hepatitis, Renal effects: elevations in serum creatinine and BUN, Hematologic effects: hemolytic anemia, leukopenia, thrombocytopenia, Injection site reactions: phlebitis, thrombophlebitis, Photosensitivity and risk of skin malignancies in patients with prolonged exposure
Food/DietaryNo known food interactions. Grapefruit and grapefruit juice do not interact with micafungin.

Clinical Tips & Counseling

Clinical PearlsMicafungin is an echinocandin antifungal that inhibits beta-(1,3)-D-glucan synthase. Administer IV only; do not bolus. Monitor hepatic function due to risk of elevated transaminases. Caution in patients with moderate to severe hepatic impairment (Child-Pugh B/C). Use with caution in patients with hypersensitivity to other echinocandins. May increase sirolimus and nifedipine levels; monitor levels. No renal dose adjustment needed. Do not mix with other drugs in same infusion line.
Patient AdviceThis medication is given intravenously to treat serious fungal infections. · Report any signs of allergic reaction: rash, itching, difficulty breathing, swelling of face or throat. · Monitor for symptoms of liver problems: jaundice, dark urine, abdominal pain, unexplained fatigue. · Inform your doctor about all medications you take, including over-the-counter drugs and supplements. · You may have blood tests to monitor liver function during treatment. · Do not drive or operate heavy machinery if you experience dizziness or confusion.

MICAFUNGIN IN SODIUM CHLORIDE 0.9% Interactions

Loading safety data…

This overview is compiled from peer-reviewed clinical sources and FDA labeling. It's here to support — not replace — clinical judgment. Always verify dosing against your institution's current protocols before prescribing.

On this page

Mechanism of ActionDosing & administrationUse during pregnancyWarnings & precautionsDrug interactions

Compare with

ACETATED RINGER'S IN PLASTIC CONTAINERACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREEAMIKACIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINERAMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINERAMINOPHYLLINE IN SODIUM CHLORIDE 0.45%

External sources

DailyMed (NIH) PubMed OpenFDA