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

ZAVICEFTA®: As effective as a carbapenem in hospitalised patients with aerobic Gram-negative cIAIs15, cUTIs16 or HAP, including VAP17

Overall Risk Factors

HAP/ VAP Patient Profile

cIAI Patient Profile

cUTI Patient Profile

Identifying patients with cUTI at high-risk of MDR Gram-negative infections

"In the face of increasing rates of antimicrobial resistance in complicated urinary tract infections (cUTIs), clinicians need to understand cross-resistance patterns among commonly encountered pathogens." Zilberberg M D, et al (2020)24

Patient Profile: Rosa – 56-year old female*

*The example described here is not an actual patient, but rather a fictious representation of a scenario for which ZAVICEFTA could be considered. 

​​​​​​​Risk Factors in a cUTI Patient2-5

Patient History:
  • Undergoing chemotherapy following mastectomy for node-positive, left-sided breast cancer
  • Neutropenic (chemotherapy related)
  • Immunosuppressed
  • Recent carbapenem treatment

Symptoms:
  • Presented with frequent urination and loin pain 
  • Dysuria
  • Fever
  • Disorientation/ confusion
  • ​​​​​​​Symptoms ongoing for >36 hours

Diagnosis:
  • cUTI with sepsis

Suspected Pathogens:
  • K. pneumoniae, including those resistant to carbapenems (KPC). 

Learn about ZAVICEFTA dosing across patient populations, preparation & administration, and shelf life & storage.

Access dosing guide

Access results of ZAVICEFTA Phase III clinical trials in adult patients with cUTI, cIAI or HAP/VAP​

View Phase III trial​

Abbreviations:

​​​​​​​​​​​​​​cUTI, complicated urinary tract infection, cIAI, complicated intra-abdominal 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; K. pneumoniae, Klebsiella pneumoniae;  MBL, metallo-β-lactamase; OXA, oxacillinase; ESBL, extended-spectrum β-lactamase; P. aeruginosa, Pseudomonas aeruginosa;  CrCl, creatinine clearance; AMR, Antimicrobial Resistance; CVC central venous catheter; ICU intensive care unit. AE, adverse event; CE, clinically evaluable; CI, confidence interval; cMITT, clinically modified intention-to-treat; TOC, test of cure;

Prescribing information​​​​​​​

Zavicefta (ceftazidime and avibactam) 2g/0.5 g Powder for Concentrate for Solution for Infusion

Meronem® (meropenem triydrate) IV 1g

Meronem® (meropenem triydrate) IV 500mg

References
  1. ZAVICEFTA. Summary of Product Characteristics
  2. Bassetti M, et al. Exp Rev Anti Infect Ther 2017;15:55–65
  3. Miller BM, et al. Am J Infect Control 2016;44:134–7
  4. De Waele J, et al. Intensive Care Med 2018;44:189–96
  5. Albur M, et al. Ann Clin Microbiol Antimicrob 2016;15:23
  6. Harris AD, et al. Emerg Infect Dis 2007;13:1144–9
  7. Timsit JF, et al. Intensive Care Med 2019;45:172–89 
  8. Bonine NG, et al. Am J Med Sci 2019;357:102–10
  9. Raman G, et al. BMC Infect Dis 2015;15:395
  10. Kang CI, et al. Clin Infect Dis 2003;37:745–51
  11. Scheuherman O, et al. Infect Control Hosp Epidemiol 2018;39:660–7
  12. Daikos GL, et al. Antimicrob Agents Chemother 2014;58:2322–8
  13. Navarro-San Francisco C, et al. Clin Microbiol Infect 2012;19:E72–9
  14. Zarkotou O, et al. Clin Microbiol Infect 2011;17:1798–803
  15. Mazuski JE, et al. Clin Infect Dis 2016;62:1380–9
  16. Wagenlehner FM, et al. Clin Infect Dis 2016;63:754–62
  17. Torres A, et al. Lancet Infect Dis 2017;Epub
  18. Micek ST, et al. Crit Care 2015;19:219
  19. Sartelli M, et al. World J Emerg Surg 2017;12:22
  20. Flores-Mireles AL, et al. Nat Rev Microbiol 2015;13:269–84 ​​​
  21. Torres A, et al. European Respiratory Journal 2017 50: 1700582;
  22. Sartelli, et al.  CIAO study. World J Emerg Surg 2012;5-6
  23. Gomila A, et al. Infection and Drug Resistance 2018:11 2571–2581
  24. Zilberberg M D, et al. Antimicrob Agents Chemother 2020;63:e00346-20
PP-ZVA-GBR-0840. June 2021

Learn more about the tolerability data of ZAVCEFTA from four Phase III clinical trials. 

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View safety profile 

** This is an optional area where footnotes can live.

KOL Video 2019

Professor Francesco G. De Rosa, Prof. of Infectious Diseases (Italy, Professor Philip Montravers, Anaestheisa and Critical Care Medicine (France) and Dr Paula Ramirez, Critical Care Department (Spain) discuss high-risk patients and early treatment of patients with suspected MDR Gram-negative infections in their clinical practice, and their experience using ZAVICEFTA.

Card CTA

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Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in Google Play or Apple App Store

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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PP-PFE-GBR-3863. November 2021

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