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Aztreonam — Membership Pricing

Aztreonam is not confirmed for no-additional-cost pricing. Membership pricing may be available; confirm the price with the dispensing pharmacy.

Aztreonam Pricing

Pricing typePrice
TheDrugClubMembership pricing may be available
Typical Retail$35.00

Membership pricing may be available; confirm the price with the dispensing pharmacy.

About Aztreonam

Aztreonam is a prescription medication. Ask your doctor if Aztreonam is right for you.

How to Check Aztreonam Pricing

  1. Join TheDrugClub for $19.95/month
  2. Receive your member card by email
  3. Present your card at a participating pharmacy
  4. Check active-formulary eligibility or available membership pricing

Aztreonam at Participating Pharmacies

Pharmacy participation and fulfillment options vary. Present your membership card and confirm current pricing before filling.

Other medications in Infections

What Aztreonam is approved for (FDA label)

AZACTAM is indicated for the treatment of the following infections caused by susceptible Gram-negative microorganisms: Urinary Tract Infections (complicated and uncomplicated), including pyelonephritis and cystitis (initial and recurrent) caused by Escherichia coli , Klebsiella pneumoniae , Proteus mirabilis , Pseudomonas aeruginosa , Enterobacter cloacae , Klebsiella oxytoca *, Citrobacter species*, and Serratia marcescens *. Lower Respiratory Tract Infections , including pneumonia and bronchitis caused by Escherichia coli , Klebsiella pneumoniae , Pseudomonas aeruginosa , Haemophilus influenzae , Proteus mirabilis , Enterobacter species, and Serratia marcescens *. Septicemia caused by Escherichia coli , Klebsiella pneumoniae , Pseudomonas aeruginosa , Proteus mirabilis *, Serratia marcescens *, and Enterobacter species.

Source: Read the full FDA label on DailyMed. Label effective date: December 15, 2025.

Excerpt from the FDA-approved prescribing information. This is not medical advice; talk to your doctor or pharmacist.

Adverse reactions for Aztreonam (FDA label)

Local reactions such as phlebitis/thrombophlebitis following intravenous administration, and discomfort/swelling at the injection site following intramuscular administration occurred at rates of approximately 1.9% and 2.4%, respectively. Systemic reactions (considered to be related to therapy or of uncertain etiology) occurring at an incidence of 1% to 1.3% include diarrhea, nausea and/or vomiting, and rash. Reactions occurring at an incidence of less than 1% are listed within each body system in order of decreasing severity: Hypersensitivity —anaphylaxis, angioedema, bronchospasm Hematologic —pancytopenia, neutropenia, thrombocytopenia, anemia, eosinophilia, leukocytosis, thrombocytosis Gastrointestinal —abdominal cramps; rare cases of C. difficile –associated diarrhea, including pseudomembranous colitis, or gastrointestinal bleeding have been reported.

Source: FDA prescribing information (DailyMed). Set ID: 9a105eaf-ee77-4016-beeb-d425a5565db2. SPL document ID: 1308cf65-8900-4fc3-8a41-47b766adbd3a. Label effective date: December 15, 2025. Read the full label.

Excerpt from the FDA-approved prescribing information. This is not medical advice; talk to your doctor or pharmacist.

Contraindications for Aztreonam (FDA label)

This preparation is contraindicated in patients with known hypersensitivity to aztreonam or any other component in the formulation.

Source: FDA prescribing information (DailyMed). Set ID: 9a105eaf-ee77-4016-beeb-d425a5565db2. SPL document ID: 1308cf65-8900-4fc3-8a41-47b766adbd3a. Label effective date: December 15, 2025. Read the full label.

Excerpt from the FDA-approved prescribing information. This is not medical advice; talk to your doctor or pharmacist.

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