Drug reference directory
Drug reference

Aztreonam

Monobactam (β-lactam) antibiotic · Antibacterial

START
1–2 g IV/IM every 8–12 h (severe Gram-negative)
TYPICAL MAX
8 g/day
STOP IF
Severe hypersensitivity, C. difficile colitis, or hepatotoxicity
WATCH
Renal function (dose-banding), LFTs, ceftazidime allergy history
CDSCO approvedATC J01DF01
Dose laddermg/d
1klow/dose2kusual/dose8kmax/day
Renal dose adjustmenteGFR mL/min/1.73m²
FULLStandard dosing30REDUCEReduce dose 50%10REDUCEReduce 75%…≥90

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
6minONSET30minPEAK1.7ht½8hDURATION
ONSET
6min · infusion start
PEAK
30min · end infusion
t½
1.7h · t½
DURATION
8h · q8h
EXCRETION
Renal — 60–70% unchanged
route + CYP
INTERACTIONS
—
none in our sources
PREGNANCY
Considered acceptable when indicated (β-lactam class).
FDA category + note

Mechanism

Binds penicillin-binding protein 3 of Gram-negative aerobes, inhibiting bacterial cell-wall synthesis; selective for aerobic Gram-negatives (including Pseudomonas) with no Gram-positive or anaerobic activity.

Indications

Complicated urinary tract infectionsLower respiratory tract infections (including cystic fibrosis Pseudomonas, inhaled form)SepticaemiaIntra-abdominal infections (combined with anaerobe coverage)Skin/soft-tissue infections (Gram-negative)Pelvic inflammatory disease

Dosing

Adult
1–2 g IV/IM every 8–12 h (severe: 2 g q6–8h). Inhaled (CF): 75 mg nebulised three times daily for 28-day cycles.
Pediatric
≥9 months: 30 mg/kg every 6–8 h; CF inhaled per protocol.
Renal adjustment
CrCl 10–30: reduce dose 50%. <10: reduce 75%; dose after HD.
Hepatic adjustment
Caution; reduce dose in severe disease.
Geriatric
Adjust for renal function.
Max dose
8 g/day

Pharmacokinetics

Onset
Bactericidal levels from infusion
Peak effect
End of infusion
Duration
Dose every 6–12 h
Half-life
~1.7 h (~6 h in severe renal failure)
Bioavailability
IV/IM 100%; inhaled local
Protein binding
~56%
Metabolism
Minimal
Excretion
Renal (60–70% unchanged)

Contraindications

  • Severe hypersensitivity to aztreonam
  • Generally tolerated in penicillin allergy (no cross-reactivity except ceftazidime)
  • Caution: severe ceftazidime allergy (shared side chain)

Side effects

Common
Injection-site phlebitisRashNausea/vomitingDiarrhoeaTransaminase elevation
Serious
  • Severe hypersensitivity (rare)
  • C. difficile colitis
  • Hepatotoxicity (rare)
  • Seizures (high dose, renal failure)

Pregnancy & lactation

Pregnancy

Considered acceptable when indicated (β-lactam class).

Lactation

Compatible with breastfeeding.

Drug interactions

Aminoglycosides
Moderate
Database

Synergistic Gram-negative coverage (intended)

Standard combination; monitor renal function

Source: Kimi deep-research + Cla

Ceftazidime
Moderate
Database

Shared side chain

Avoid if severe ceftazidime allergy

Source: Kimi deep-research + Cla

Other Nephrotoxins
Moderate
Database

Renal stress

Monitor renal function

Source: Kimi deep-research + Cla

Probenecid
Moderate
Database

Reduced renal tubular secretion

Monitor; usually no adjustment

Source: Kimi deep-research + Cla

8 additional unreviewed or low-confidence interactions hidden because their provenance or source detail is insufficient.

Related guidelines

Ask House about Aztreonam

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Textbook-sourced·Sources: KD Tripathi 7e, Goodman & Gilman 14e, Harrison 22e, Katzung·Updated: 2026-05-20·Cockpit curated: 2026-05-20