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cefiderocol

Siderophore cephalosporin (novel beta-lactam antibiotic) · Antibacterial, β-Lactam Antibiotic, Cell Wall Synthesis Inhibitor (Antipseudomonal Cephalosporin)

START
2 g IV over 3 h every 8 h
TYPICAL MAX
6 g/day (2 g q8h)
STOP IF
Severe hypersensitivity, C. difficile colitis, or seizures
WATCH
Renal function (dose-banding), C. difficile, seizures; resistance pattern
CDSCO approvedATC J01DI04
Dose laddermg/d
750low/dose2kper dose6kmax/day
Renal dose adjustmenteGFR mL/min/1.73m²
FULLS90REDUCE1.5 g q8h60REDUCE1 g q8h30REDUCE750 mg q12h; post-dialysis on HD90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
6minONSET3hPEAK2.5h8hDURATION
ONSET
6min · infusion start
PEAK
3h · end infusion
2.5h ·
DURATION
8h · q8h
EXCRETION
Renal — ~99% unchanged
route + CYP
INTERACTIONS
10 major
SEVERE in our sources
PREGNANCY
Use only if benefit outweighs risk; limited data.
FDA category + note
Top interactionssee all 12
  • BerotralstatSevereDatabaseDDInter
  • BupropionSevereDatabaseDDInter
  • ButorphanolSevereDatabaseDDInter
  • FentanylSevereDatabaseDDInter

Mechanism

Catechol-substituted siderophore cephalosporin actively transported across the Gram-negative outer membrane via bacterial iron-uptake systems; binds PBP3 to inhibit cell-wall synthesis; stable against carbapenemases (MBL, KPC, OXA, ESBL).

Indications

Complicated urinary tract infections / pyelonephritis (resistant Gram-negatives)Hospital-acquired / ventilator-associated bacterial pneumonia (resistant Gram-negatives)

Dosing

Adult
2 g IV every 8 h over 3 h.
Pediatric
≥3 months (weight-band; specialist).
Renal adjustment
Stepwise reduction per CrCl band (e.g., 1.5 g q8h CrCl 60–89; 1 g q8h CrCl 30–59; 750 mg q12h CrCl 15–29; 750 mg q12h on HD post-dialysis).
Hepatic adjustment
No specific adjustment.
Geriatric
Adjust for renal function.
Max dose
6 g/day (2 g every 8 h)

Pharmacokinetics

Onset
Bactericidal levels from infusion
Peak effect
End of infusion
Duration
Dose every 8 h
Half-life
~2–3 h
Bioavailability
IV 100%
Protein binding
~40–60%
Metabolism
Minimal
Excretion
Renal (~99% unchanged)

Contraindications

  • Severe hypersensitivity to cephalosporins / beta-lactams
  • Caution: history of seizures

Side effects

Common
DiarrhoeaInfusion-site reactionsConstipationRashIncreased liver enzymes
Serious
  • Severe hypersensitivity / anaphylaxis
  • C. difficile colitis
  • Seizures (high dose, renal failure)
  • Increased all-cause mortality in critically-ill HABP/VABP (CREDIBLE-CR observation)

Pregnancy & lactation

Pregnancy

Use only if benefit outweighs risk; limited data.

Lactation

Limited data; caution.

Drug interactions

Berotralstat
Severe
Database

Drug interaction classified as: excretion

Source: DDInter

Bupropion
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Butorphanol
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Fentanyl
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Hydrocodone
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Iohexol
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Iopamidol
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Oliceridine
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Oxycodone
Severe
Database

Drug interaction classified as: metabolism

Source: DDInter

Tramadol
Severe
Database

Drug interaction classified as: synergy

Source: DDInter

Anticoagulants
Moderate
Database

Possible INR change (cephalosporin class)

Monitor INR

Source: Kimi deep-research + Cla

Other Beta Lactams
Moderate
Database

Class cross-reactivity

Caution in severe beta-lactam allergy history

Source: Kimi deep-research + Cla

Related guidelines

Ask House about cefiderocol

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

Sources: Goodman & Gilman 14e, Harrison 22e·Verified: 2026-05-20 · House clinical team·Cockpit curated: 2026-05-20