GlobalRPh Renal Dosing Masterv6.6
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Aztreonam

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Professional source

UCSF - systemic aztreonam

Product / population
Adults; single-agent systemic IV aztreonam. Combination-use comments are specialist-specific.
Renal measure
CrCl in mL/min where specified; no equation inferred.

Dosing / renal protocol and limits

IV regimen by CrCl: above 50, 2 g every 8 hours; 10-50, 2 g every 12 hours; below 10, 1 g every 12 hours. IHD: 2 g initially, then each evening. CVVHD: 2 g every 12 hours.

Selected meningitis or resistant Gram-negative cases may require 2 g every 6 hours under specialist direction. When combined with ceftazidime/avibactam for selected resistant infections, both may be infused over 3 hours; simultaneous dosing is preferred when intervals coincide. This is a systemic aztreonam protocol, not inhaled aztreonam or fixed-combination EMBLAVEO.

Source revision: Revision date not stated in the reviewed page. | Retrieved: 2026-09-05. Retrieval date is not the revision date.

Source: https://idmp.ucsf.edu/content/aztreonam

Scope: Locally included source-specific summary. Regimen differences are not automatically resolved. GlobalRPh v6.6.

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Retrieved: 2026-09-05

Professional guidance

UCSF - systemic aztreonam

Adults; single-agent systemic IV aztreonam. Combination-use comments are specialist-specific.

Renal method: CrCl in mL/min where specified; no equation inferred.
Retrieved: 2026-09-05

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Renal dosing and precautions

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Important source distinctions

Systemic aztreonam only; not inhaled aztreonam lysine. The original 125 mg dialysis comment is not one-eighth of every possible initial dose; the source paragraph specifies one-eighth of the initial dose. Both are preserved as a source discrepancy.

Locally stored source content

Original GlobalRPh protocol

Clinical facts and comments transcribed into a structured reading format. This is not a byte-for-byte HTML archive. Original source: https://globalrph.com/renal/aztreonam/

Usual Dosing (Adults)

[Mild infection] (i.e. UTI): 500mg to 1 gram IV q8-12h.

[Usual dose]: 1-2 grams IV q8-12h.

[Severe/life threatening infection]: 2 grams IV q6-8h. [Maximum dose]: 8 grams/day.

DOSAGE AND ADMINISTRATION - Dosage in Adult Patients

AZACTAM may be administered intravenously or by intramuscular injection. Dosage and route of administration should be determined by susceptibility of the causative organisms, severity and site of infection, and the condition of the patient. The intravenous route is recommended for patients requiring single doses greater than 1 g or those with bacterial septicemia, localized parenchymal abscess (eg, intra-abdominal abscess), peritonitis or other severe systemic or life-threatening infections.

The duration of therapy depends on the severity of infection. Generally, AZACTAM should be continued for at least 48 hours after the patient becomes asymptomatic or evidence of bacterial eradication has been obtained. Persistent infections may require treatment for several weeks. Doses smaller than those indicated should not be used.

AZACTAM DOSAGE GUIDELINES - ADULTS

Type of infectionDoseFrequency (hours)
Urinary tract infections500 mg or 1 g8 or 12
Moderately severe systemic infections1 g or 2 g8 or 12
Severe systemic or life-threatening infections2 g6 or 8

Maximum recommended dose is 8 g per day.

Because of the serious nature of infections due to Pseudomonas aeruginosa, dosage of 2 g every 6 or 8 hours is recommended, at least upon initiation of therapy, in systemic infections caused by this organism in adults.

GRPH-aztreonam-01 · Source section: Usual Dosing (Adults)Renal section finder

Renal Dosing

IV:

[CRCL >30 ml/min]: no change.

[10-30 ml/min]: Loading dose: 1-2 grams x 1, then give 50% of the usual dose (e.g. 0.5-1 gm) q6-12h.

[<10 ml/min]: 1-2 grams x 1, then 25% of usual dose (e.g. 250-500 mg) q6-12 hours.

Renal Impairment in Adult Patients

Prolonged serum levels of aztreonam may occur in patients with transient or persistent renal insufficiency. Therefore, the dosage of AZACTAM should be halved in patients with estimated creatinine clearances between 10 mL/min/1.73 m2 and 30 mL/min/1.73 m2 after an initial loading dose of 1 g or 2 g. When only the serum creatinine concentration is available, the following formula (based on sex, weight, and age of the patient) may be used to approximate the creatinine clearance (Clcr).

The serum creatinine should represent a steady state of renal function.

Males: Clcr = [weight (kg) x (140-age)] / [72 x serum creatinine (mg/dL)]

Females: 0.85 x above value

In patients with severe renal failure (creatinine clearance less than 10 mL/min/1.73 m2), 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.

GRPH-aztreonam-02 · Source section: Renal DosingRenal section finder

Hemodialysis

Hemodialysis:

1-2 grams x 1, then 25% of usual dose q6-12h. (e.g., 250-500 mg q6-12 hours).

For serious or life-threatening infections, give an additional 125mg after each hemodialysis session (1/8th of the usual dose).

PD: 1-2 grams x 1, then 25% of usual dose q6-12h. (e.g., 250-500 mg q6-12 hours).

GRPH-aztreonam-03 · Source section: HemodialysisRenal section finder
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Professional

UCSF - systemic aztreonam

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UCSF Infectious Diseases Management Program · Adults; single-agent systemic IV aztreonam. Combination-use comments are specialist-specific.

Renal method: CrCl in mL/min where specified; no equation inferred.
Source date: Revision date not stated in the reviewed page.
Retrieved: 2026-09-05

Locally included source-specific summary. Regimen differences are not automatically resolved.

Dosing / renal protocol and limits

IV regimen by CrCl: above 50, 2 g every 8 hours; 10-50, 2 g every 12 hours; below 10, 1 g every 12 hours. IHD: 2 g initially, then each evening. CVVHD: 2 g every 12 hours.

Selected meningitis or resistant Gram-negative cases may require 2 g every 6 hours under specialist direction. When combined with ceftazidime/avibactam for selected resistant infections, both may be infused over 3 hours; simultaneous dosing is preferred when intervals coincide. This is a systemic aztreonam protocol, not inhaled aztreonam or fixed-combination EMBLAVEO.

RDM30-003-aztreonam-1 · Source locator: UCSF - systemic aztreonam; renal/dosing sections and stated qualifiers

Source identity and provenance
Source
https://idmp.ucsf.edu/content/aztreonam
Retrieved
2026-09-05
Renal-function method
CrCl in mL/min where specified; no equation inferred.
Source date/version
Revision date not stated in the reviewed page.
Hash meaning
Locally authored summary text; not original SPL, HTML or PDF bytes
Local summary SHA-256
9365c1f0040a336429593cb3cb7adbcdee676e02dd584559897afb2532007056

Provenance and preservation

Additional summaries stored on this page: 0 official-label, 0 RX List, 1 professional, 0 handbook. Empty additional-source groups are not shown. A missing layer is not a no-adjustment recommendation.

Original source
https://globalrph.com/renal/aztreonam/
Source retrieval
2026-09-05. This is not the source publication or label revision date.
Original source type
globalrph individual
Local text SHA-256
7bffacfa7543698e7753f5cc3bf44699069aadf6ba664e31920d14a8100a683e
Import versus clinical validation
Source-section locators identify where retained content came from. A source-section identifier does not assert that every numeric statement has been independently corroborated. The local text hash is not a hash of original HTML, an FDA PDF or SPL XML.

The original individual GlobalRPh pages commonly cite NIH/NLM DailyMed and instruct readers to review the applicable package insert for updates. That historical reference is preserved as context; it is not counted as an independently retrieved current label.

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