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AboutAboutPathogen CoveragePatient Risk FactorsAntimicrobial Subscription Model PilotDosingDosingDosingPreparation GuideShelf Life and StorageEfficacy & SafetyEfficacy & SafetyMechanism of ActionREPROVE Phase III trial(HAP/VAP)RECLAIM Phase III trial(cIAI)RECAPTURE Phase III trial(cUTI)REPRISE Phase III trial(cIAI and cUTI)Safety and TolerabilityEfficacy and Safety Data for Paediatric PatientsSupport & ResourcesSupport & ResourcesAMS ResourcesSepsisWebinars (Live and On-demand)KOL Videos - ZaviceftaKOL Videos - Gram-negativeKOL Videos - Clinical experienceVideosMaterials

Information on how to access prescribing information and adverse event reporting can be found towards the bottom of the page.

ZAVICEFTA® (ceftazidime - avibactam): For the management of serious infections in critically ill patients

ZAVICEFTA (ceftazidime and avibactam), for the treatment of patients at high risk of MDR Gram-negative infections with suspected or documented P. aeruginosa, CRE (KPC, OXA-48), and ESBL- and AmpC-producing pathogens1-4.

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ZAVICEFTA is indicated for the treatment of adult and paediatric patients aged 3 months and older with the following infections:1*

Complicated intra-abdominal infection (cIAI)
Complicated urinary tract infection (cUTI), including pyelonephritis
Hospital-acquired pneumonia (HAP), including ventilator-associated pneumonia (VAP)

Treatment of adult patients with bacteraemia that occurs in association with, or is suspected to be associated with, any of the infections listed above. ZAVICEFTA is also indicated for the treatment of infections due to aerobic Gram-negative organisms in adult patients with limited treatment options.
*Consideration should be given to the official guidance on the appropriate use of antibacterial agents.1

†Data support the use of ZAVICEFTA in adult patients with limited treatment options including in primary bacteraemia, cSSTI, BJI, meningitis, febrile neutropenia, cystic fibrosis, post-transplant patients due to KPC and OXA-48 resistance mechanisms, and MDR Pseudomonas.7-21

Access results of ZAVICEFTA Phase III clinical trials in adult patients with cUTI, cIAI or HAP/VAP View Phase III trial results Loading Learn more about the safety data of ZAVICEFTA from 4 Phase III clinical trials View safety profile Loading Learn about ZAVICEFTA dosing across patient populations, preparation & administration, and shelf life & storage Access dosing guide LoadingExplore more​​​​​​​

Patient Risk Factors

Identifying patients at risk of MDR Gram-negative infections is vital for appropriate selection of adequate, early antimicrobial therapy to reduce the risk of fatal outcomes5.


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Pathogen coverage

ZAVICEFTA has broad spectrum coverage against Gram-negative pathogens including in vitro activity against MDR P.aeruginosa, CRE, including KPC- and OXA-48 producing strains, and ESBL- and AmpC-producing bacteria1-4.


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Antimicrobial Stewardship

Access our resources for implementation of an Antimicrobial Stewardship Programme and learn more about Pfizer initiatives to fight AMR


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Abbreviations

BJI, bone and joint infection; cUTI, complicated urinary tract infection; cIAI, complicated intra-abdominal infection; cSSTI, complicated skin and soft-tissue infection; HAP, hospital-acquired pneumonia; VAP, ventilator-associated pneumonia; MDR, multi-drug resistant; BL/BLI, β-lactam/β-lactamase inhibitors; CRE, carbapenem-resistant Enterobacteriaceae; KPC, Klebsiella pneumoniae carbapenemase; MBL, metallo-β-lactamase; OXA, oxacillinase; ESBL, extended-spectrum β-lactamase, BSI, bloodstream infection; cSSTI, complicated skin and soft tissue.

Prescribing information

Click here for Prescribing Information for Zavicefta® (ceftazidime and avibactam)

Click here for prescribing information for Meronem® (meropenem trihydrate)

Tygacil® (tigecycline)
Great Britain
Tygacil® (tigecycline) 50mg powder for solution for infusion
Northern Ireland
Tygacil® (tigecycline) 50mg powder for solution for infusion

References

ZAVICEFTA. Summary of Product Characteristics​​​​​​Liscio JL, et al. Int J Antimicrob Agents 2015;46:266–7Nicolau DP, et al. J Antimicrob Chemother 2015;70:2862–9Mazuski JE, et al. Surg Infect 2017;18:1–76 Bonine NG, et al. Am J Med Sci 2019;357:102–10​​​​​​​Morris, AC. JECCM 2018;2:101-01.Caston JJ, et al. J Infect Dis 2017;59:118–23Van Duin D, et al. J Clin Infect Dis 2018;66:163–71Sousa A, et al. Antimicrob Chemother 2018;73:3170–5Temkin E, et al. Antimicrob Agents Chemother 2017;61:e01964-16Shields K, et al. Antimicrob Agents Chemother 2017;61:e00883-17Tumbarello M, et al. Clin Infect Dis 2019;68:355–64.Tumbarello M, et al. Clin Infect Dis 2021;ciab176.Tsolaki V, et al. Antimicrob Agents Chemother 2020;64:e02320-19.Rathish B, et al. Cureus 2021;13:e13081.Jabbour J-F, et al. Curr Opin Infect Dis 2020;33:146–54.Chen W, et al. Ann Transl Med 2020;8:39.Atkin SD, et al. Infect Drug Resist 2018;11:1499–510.Aguado JM, et al. Transplant Rev (Orlando) 2018;32:36–57.Soriano A, et al. Infect Dis Ther 2021;1–46.Mazuski JE, et al. Infect Dis Ther 2021;1–16
PP-ZVA-GBR-1906. February 2024
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