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Caspofungin

Echinocandin antifungal · Antifungal

Also known as Caspofungin acetate, Cancidas, Casporex

START
70 mg IV load day 1, then 50 mg IV once daily
TYPICAL MAX
70 mg/day
STOP IF
Serious hypersensitivity or significant hepatotoxicity
WATCH
LFTs, infusion reactions, response/cultures
CDSCO approvedSchedule HATC J02AX04
Dose laddermg/d
35start50titrate70ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLNo dose adjustment at any eGFR (not renally cleared; not dialysed)90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET1hPEAK10h1dDURATION
ONSET
1h · infusion
PEAK
1h · end of infusion
10h · beta t½
DURATION
1d · once-daily
EXCRETION
Hepatic hydrolysis; renal + faecal, low unchanged
route + CYP
INTERACTIONS
12 major
SEVERE in our sources
PREGNANCY
Use only if benefit outweighs risk — animal embryotoxicity; limited human data
FDA category + note
Top interactionssee all 12
  • CarbamazepineSevereDatabaseDDInter
  • CiclosporinSevereDatabaseKimi deep-research + Cla
  • DexamethasoneSevereDatabaseDDInter
  • EfavirenzSevereDatabaseDDInter
Available in India

51 branded formulations. Look up specific brands in the Drugs workspace.

Mechanism

Non-competitive inhibition of 1,3-beta-D-glucan synthase, disrupting fungal cell-wall synthesis → osmotic lysis; fungicidal against Candida, fungistatic against Aspergillus. No human cell-wall target → favourable safety.

Indications

Invasive candidiasis / candidaemiaEmpirical therapy of febrile neutropeniaInvasive aspergillosis refractory/intolerant to other therapyOesophageal candidiasis

Dosing

Adult
70 mg IV loading dose day 1, then 50 mg IV once daily; 70 mg/day maintenance if <80 kg inadequate response or with enzyme inducers.
Pediatric
70 mg/m² loading then 50 mg/m² daily (max 70 mg).
Renal adjustment
No adjustment (not renally cleared).
Hepatic adjustment
Moderate hepatic impairment (Child-Pugh 7–9): 35 mg/day maintenance after standard 70 mg load. Severe: no data.
Geriatric
No specific adjustment.
Max dose
70 mg/day

Pharmacokinetics

Onset
IV; antifungal effect over days
Peak effect
End of 1-h infusion
Duration
Once-daily
Half-life
Beta ~9–11 h (distribution-dominated PK)
Bioavailability
100% IV
Protein binding
~97% (albumin)
Metabolism
Slow hepatic hydrolysis/N-acetylation (non-CYP)
Excretion
Renal and faecal (low unchanged)

Contraindications

  • Hypersensitivity to caspofungin or echinocandins

Side effects

Common
Infusion-related (fever, phlebitis, histamine-like flushing)HeadacheNauseaRaised hepatic transaminases
Serious
  • Hepatotoxicity
  • Anaphylaxis/serious hypersensitivity
  • Severe skin reactions (rare)

Pregnancy & lactation

Pregnancy

Use only if benefit outweighs risk — animal embryotoxicity; limited human data

Lactation

Unknown excretion; caution

Drug interactions

Carbamazepine
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Ciclosporin
Severe
Database

Increased caspofungin AUC + raised transaminases

Use only if benefit outweighs risk; monitor LFTs

Source: Kimi deep-research + Cla

Dexamethasone
Severe
Database

Drug interaction classified as: metabolism.

Source: DDInter

Efavirenz
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Fosphenytoin
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Leflunomide
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Lomitapide
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Mipomersen
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Nelfinavir
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Nevirapine
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Pexidartinib
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Phenytoin
Severe
Database

Drug interaction classified as: metabolism.

Source: DDInter

Related guidelines

Other Echinocandin antifungal drugs

Ask House about Caspofungin

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Verified: 2026-05-19 · House clinical team·Cockpit curated: 2026-05-19