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Ceftazidime

Generic Name
Ceftazidime
Brand Names
Avycaz, Fortaz, Tazicef, Zavicefta
Drug Type
Small Molecule
Chemical Formula
C22H22N6O7S2
CAS Number
72558-82-8
Unique Ingredient Identifier
DZR1ENT301

Overview

Bacteria possess a cell wall comprising a glycopeptide polymer commonly known as peptidoglycan, which is synthesized and remodelled through the action of a family of enzymes known as "penicillin-binding proteins" (PBPs). β-lactam antibiotics, including cephalosporins, are PBP inhibitors that, through inhibition of essential PBPs, result in impaired cell wall homeostasis, loss of cell integrity, and ultimately bacterial cell death. Ceftazidime is a third-generation cephalosporin with broad-spectrum antibacterial activity, including against some treatment-resistant bacteria such as Pseudomonas aeruginosa. Ceftazidime was approved by the FDA on July 19, 1985, and is currently available either alone or in combination with the non-β-lactam β-lactamase inhibitor avibactam to treat a variety of bacterial infections.

Indication

Ceftazidime is indicated for the treatment of lower respiratory tract infections, skin and skin structure infections, urinary tract infections, bacterial septicemia, bone and joint infections, gynecologic infections, intra-abdominal infections (including peritonitis), and central nervous system infections (including meningitis) caused by susceptible bacteria. Ceftazidime is indicated in combination with avibactam to treat infections caused by susceptible Gram-negative organisms, including complicated intra-abdominal infections (cIAI), in conjunction with metronidazole, and complicated urinary tract infections (cUTI), including pyelonephritis, in patients aged three months and older. This combination is also indicated to treat hospital-acquired and ventilator-associated bacterial pneumonia (HABP/VABP) in patients aged 18 years and older. In all cases, to mitigate the risk of bacterial resistance and preserve clinical efficacy, ceftazidime should only be used for infections that are confirmed or strongly suspected to be caused by susceptible bacterial strains.

Associated Conditions

  • Bacteremia
  • Bacterial Infections
  • Bacterial Septicemia
  • Bone and Joint Infections
  • Bronchopulmonary Infection
  • Central Nervous System Infections
  • Complicated Intra-Abdominal Infections (cIAIs)
  • Complicated Skin and Soft Tissue Infection
  • Complicated Urinary Tract Infection
  • Complicated Urinary Tract Infections caused by susceptible Gram-negative microorganisms
  • Fever caused by susceptible bacteria
  • Gynecological Infection
  • Intraabdominal Infections
  • Lower Respiratory Tract Infection (LRTI)
  • Meningitis, Bacterial
  • Nosocomial Pneumonia
  • Peritoneal Dialysis Associated Peritonitis
  • Skin and skin structure infections
  • Urinary Tract Infection
  • Ventilator-associated Bacterial Pneumonia caused by susceptible Gram-negative microorganisms
  • Chronic suppurative Otitis media
  • Hospital-acquired bacterial pneumonia caused by susceptible Gram-negative microorganisms
  • Malignant Otitis Externa
  • Susceptible Intra-Abdominal Infection caused by susceptible Gram-negative microorganism

Research Report

Published: Aug 5, 2025

An Expert Monograph on Ceftazidime (DB00438)

1.0 Executive Summary

Ceftazidime is a parenteral, third-generation cephalosporin antibiotic that has been a significant component of the antimicrobial armamentarium since its patenting in 1978 and subsequent commercial introduction in 1984.[1] Classified as a small molecule drug, it is recognized for its essential role in medicine and is included on the World Health Organization's List of Essential Medicines.[1] The bactericidal action of Ceftazidime is achieved through the inhibition of bacterial cell wall synthesis, which it accomplishes by binding to and inactivating essential penicillin-binding proteins (PBPs), with a particularly high affinity for PBP3 in Gram-negative organisms.[3]

The drug possesses a broad spectrum of activity, but its clinical value is most pronounced in its potent efficacy against a wide range of Gram-negative pathogens. It is especially noted for its activity against Pseudomonas aeruginosa, an opportunistic pathogen frequently associated with multi-drug resistance.[1] This makes Ceftazidime a critical agent for the treatment of severe, life-threatening infections, including hospital-acquired and ventilator-associated pneumonia (HAP/VABP), meningitis, sepsis, complicated urinary tract infections (cUTIs), and bone and joint infections.[1] Furthermore, it holds the status of a first-line therapy for melioidosis, a serious infection endemic to tropical regions.[1]

The pharmacokinetic profile of Ceftazidime is characterized by its parenteral route of administration (intravenous or intramuscular), minimal plasma protein binding of less than 10%, and excellent penetration into a wide variety of body tissues and fluids, including inflamed cerebrospinal fluid.[5] It undergoes no significant metabolism and is eliminated almost entirely unchanged via renal glomerular filtration.[5]

Continue reading the full research report

Clinical Trials

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Title
Posted
Study ID
Phase
Status
Sponsor
2015/06/04
Phase 4
UNKNOWN
2013/02/07
Not Applicable
Completed
2013/02/05
Phase 4
Completed
University Hospital Rijeka
2012/08/17
Phase 4
UNKNOWN
The Alfred
2012/07/19
Phase 3
Completed
2012/05/16
Phase 3
Completed
2012/05/10
Phase 3
Completed
2011/10/19
Phase 2
Terminated
University of Padova
2011/09/09
Phase 1
Completed
2011/04/29
Not Applicable
Completed
University Hospital, Bordeaux

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