Aztreonam
Brand names: Azactam, Cayston
Aztreonam is a monobactam antibiotic active against aerobic Gram-negative bacteria, including Pseudomonas aeruginosa, and is also available in an inhaled form for cystic fibrosis.
Adult dose
Paediatric dose
Dose adjustments
Injection (US label, Renal Impairment in Adult Patients, verbatim): 'Prolonged serum levels of aztreonam may occur in patients with transient or persistent renal insufficiency. Therefore, the dosage of aztreonam for injection should be halved in patients with estimated creatinine clearances between 10 and 30 mL/min/1.73 m 2 after an initial loading dose of 1 or 2 g... In patients with severe renal failure (creatinine clearance less than 10 mL/min/1.73 m 2 ), such as those supported by hemodialysis, the usual dose of 500 mg, 1 g, or 2 g should be given initially. The maintenance dose should be one-fourth of the usual initial dose given at the usual fixed interval of 6, 8, or 12 hours. For serious or life-threatening infections, in addition to the maintenance doses, one-eighth of the initial dose should be given after each hemodialysis session.' There are insufficient data on dosing in paediatric patients with renal impairment. Inhaled Cayston (UK SPC §4.2, verbatim): 'No dose adjustment is necessary in cases of renal impairment since the systemic concentration of aztreonam following inhaled administration of Cayston is very low (approximately 1% of the concentration resulting from a dose of 500 mg aztreonam for injection)', but 'administration of Cayston in patients with renal impairment (serum creatinine > 2 times upper limit of normal) should be undertaken with caution.'
Injection: not stated — no hepatic impairment dosing statement appears in any fetched section of the US injection label. Inhaled Cayston (UK SPC §4.2, verbatim): 'There are no data on the use of Cayston in patients with severe hepatic impairment (ALT or AST greater than 5 times the upper limit of normal). No dose adjustment is necessary in cases of hepatic impairment.'
Dose independently re-sourced from UK Summary of Product Characteristics (SPC) via the eMC; US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — clinician-reviewed. Always confirm against the product SmPC and your local formulary before prescribing.
Per-dose figure. VERBATIM (US label, Table 3, Aztreonam for Injection Dosage Guidelines for Pediatric Patients): 'Mild to moderate infections 30 mg/kg [every] 8 [hours]; Moderate to severe infections 30 mg/kg [every] 6 or 8 [hours]'. The table footnote states '* Maximum recommended dose is 120 mg/kg/day' — that ceiling is recorded here rather than in maxDose because a per-kilogram quote must not be placed in the maxDose field. AGE RANGE (US §Pediatric Use, verbatim): 'The safety and effectiveness of intravenous aztreonam for injection have been established in the age groups 9 months to 16 years... Sufficient data are not available for pediatric patients under 9 months of age or for the following treatment indications/pathogens: septicemia and skin and skin-structure infections (where the skin infection is believed or known to be due to H. influenzae type b). In pediatric patients with cystic fibrosis, higher doses of aztreonam for injection may be warranted.' INHALED ROUTE (UK SPC §4.2): 'The dosing in children aged 6 years and older is the same as for adults' (75 mg three times per 24 hours for 28 days); 'The safety and efficacy of Cayston in children younger than 6 years of age have not been established... no recommendation on posology can be given.' Pyrexia was observed at a higher incidence in paediatric patients aged 6 to 17 years than in adults (UK SPC §4.8). concentration is null — no reconstitution or infusion concentration appears in the fetched sections of either label. These paediatric figures are US labelling; verify any under-18 use against a children's formulary and local antimicrobial guidance before prescribing.
Contraindications
- Injection (US label): 'This preparation is contraindicated in patients with known hypersensitivity to aztreonam or any other component in the formulation.'
- Inhaled Cayston (UK SPC §4.3): hypersensitivity to the active substance or to any of the excipients
- Not a contraindication but an absolute administration bar (UK SPC §4.4): 'Aztreonam for injection must not be used in the Altera or other nebulisers' — it is not formulated for inhalation and contains arginine, which can cause pulmonary inflammation
- Not a contraindication but a §4.4 caution: history of beta-lactam allergy (penicillins, cephalosporins, carbapenems) — cross-reactivity may occur, although animal and human data show a low risk
- Not a contraindication but a §4.4 caution: active haemoptysis — inhaled therapy should be given only if the benefits are considered to outweigh the risk of inducing further haemorrhage
Side effects
- Injection (US §Adverse Reactions): local reactions — phlebitis/thrombophlebitis after intravenous administration (about 1.9%) and discomfort/swelling at the injection site after intramuscular administration (about 2.4%)
- Injection: systemic reactions at 1% to 1.3% — diarrhoea, nausea and/or vomiting, and rash
- Injection, incidence less than 1%: anaphylaxis, angioedema, bronchospasm; pancytopenia, neutropenia, thrombocytopenia, anaemia, eosinophilia, leukocytosis, thrombocytosis; abdominal cramps and rare cases of Clostridioides difficile-associated diarrhoea including pseudomembranous colitis, or gastrointestinal bleeding; toxic epidermal necrolysis, purpura, erythema multiforme, exfoliative dermatitis, urticaria, petechiae, pruritus, diaphoresis; hypotension, transient ECG changes (ventricular bigeminy and PVC), flushing
- Inhaled Cayston (UK SPC §4.8): most frequent adverse reactions in the placebo-controlled studies were cough (58%), nasal congestion (18%), wheezing (15%), pharyngolaryngeal pain (13.0%), pyrexia (12%) and dyspnoea (10%)
- Inhaled Cayston (UK SPC §4.8): common — bronchospasm, chest discomfort, rhinorrhoea, haemoptysis, rash, arthralgia, decreased lung function test; uncommon — joint swelling
- Bronchospasm, defined as an acute reduction of 15% or more in FEV1, is a complication associated with nebulised therapies including Cayston (UK SPC §4.4, §4.8)
- The UK SPC notes that toxic epidermal necrolysis, anaphylaxis, purpura, erythema multiforme, exfoliative dermatitis, urticaria, petechiae, pruritus and diaphoresis have been reported after parenteral use of other aztreonam-containing products
Monitoring
- Estimate creatinine clearance and adjust the dose accordingly, particularly in the elderly and in transient or persistent renal insufficiency (US label, Renal Impairment and Dosage in the Elderly)
- Watch for Clostridioides difficile-associated diarrhoea and pseudomembranous colitis, whose onset may occur during or after antibiotic treatment (US §Adverse Reactions)
- Watch for allergic reactions — 'If an allergic reaction to aztreonam does occur, stop administration of the medicinal product and initiate treatment as appropriate. The occurrence of rash may be indicative of an allergic reaction to aztreonam' (UK SPC §4.4)
- Inhaled therapy: give a bronchodilator before each dose and watch for bronchospasm (an acute reduction of 15% or more in FEV1) and for haemoptysis (UK SPC §4.4)
- Monitor lung function — a decreased lung function test result is a common adverse reaction with the inhaled product, though it was not associated with a sustained decrease in FEV1 (UK SPC §4.8)
- Monitor for emerging resistance and superinfection: 'The development of antibiotic-resistant P. aeruginosa and superinfection with other pathogens represent potential risks associated with antibiotic therapy' (UK SPC §4.4)
- Continue treatment for at least 48 hours after the patient becomes asymptomatic or bacterial eradication has been demonstrated (US label)
Clinical monograph
How it works
It binds penicillin-binding protein 3 in Gram-negative bacteria, inhibiting cell wall synthesis and causing bacterial death.
Prescribing in practice
- It has a low rate of cross-reactivity with other beta-lactams, making it a useful option in many penicillin-allergic patients, though caution is advised with ceftazidime allergy due to a shared side chain.
- It has no useful activity against Gram-positive bacteria or anaerobes, so additional cover is needed for mixed infections.
- The inhaled formulation is used to manage chronic Pseudomonas infection in cystic fibrosis.
Monitoring
Monitor clinical response and, with prolonged therapy, renal and hepatic function and full blood count.
Counselling the patient
- Report any rash, swelling or breathing difficulty.
- With the inhaled form, use a bronchodilator beforehand if advised and follow the prescribed inhalation technique.
- Complete the full course as directed.
Evidence & guidelines
Aztreonam is an established option for Gram-negative infections, and inhaled aztreonam is supported for chronic Pseudomonas infection in cystic fibrosis.
Reference: BSAC; CF Trust; UKHSA AMR; SmPC; 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.
- Centor / McIsaac Score for Strep Pharyngitis · Throat
- Acute Otitis Media — Antibiotic or Observation (AAP 2013) · Otitis Media
- FeverPAIN Score for Strep Throat · Throat
- Jarisch-Herxheimer Reaction Severity Assessment · Treatment Reactions
- PID Diagnosis and Hospitalisation (CDC Criteria) · Gynaecological Infections
- Gustilo-Anderson Classification (Open Fractures) · Fracture Classification
- Infective Endocarditis · ESC 2023 Infective Endocarditis Guidelines; NICE NG41
- Eczema Herpeticum · BAD; NICE CKS
- Suspected Bacterial Meningitis (Adult) · NICE NG240 (2024); NICE NG143 (paeds)
- Clostridioides difficile Colitis · NICE NG199 (2021); IDSA/SHEA 2021
- Returning Traveller — Fever · NaTHNaC; PHE; ESCMID 2018
- Malaria — Diagnosis & Management · PHE 2016; WHO 2023