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Pfizer MedicinesTherapy AreasExplore ContentEventsVideosMaterialsFeatured ArticlesLet’s ConnectSupplyAlliance HealthcareOff-contract claims

Adverse event reporting can be found at the bottom of the page

About Zinforo

About Zinforo

OverviewExtended spectrum coverage
Dosing

Dosing

Adult & adolescent dosingNeonatal & paediatric dosing
Efficacy & Safety

Efficacy & Safety

EfficacyFOCUS Phase III Trial (CAP)CANVAS Phase III Trial (cSSTI)ASIA CAP Phase III TrialPaediatric EfficacyAdult safetyPaediatric Safety
Clinical & Scientific Data

Clinical & Scientific Data

Patient Risk FactorsCAP patient profilescSSTI patient profilesCAPTURE study
Support & Resources

Support & Resources

Videos & case studiesVideos
Materials

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

Identifying a CAP patient who may benefit from Zinforo®Listen to Professor Antoni Torres as he discusses the challenges involved in treating community-acquired pneumonia.In CAP patients, initial antimicrobial therapy failure is associated with up to 5 days longer in hospital and 3x higher mortality2,8,9George, 70-year-old nursing home resident presented with fever, cough and sputum production*

Severity

  • PORT score IV (severe)​​​​​​​
    • 70-year-old male
    • RR >30/min
    • Temperature >40°C
    • Nursing home resident

History/comorbidities

  • History of smoking

Risk factors for difficult-to-treat infection

  • Age >65 years
  • Recurrent infection (hospitalised for pneumonia 3 months ago)
  • Previous antibiotic use
Marco presented with fever, cough and pleuritic chest pain and there has been no improvement with ceftriaxone*

Severity

  • PORT score IV (severe)
    • 78-year-old male
    • Chronic renal disease
    • Pulse >125 bpm
    • RR >30/min
    • No clinical improvement within 72 hours of ceftriaxone initiation

History/comorbidities

  • Renal insufficiency
  • Recent alcoholism

Risk factors for difficult-to-treat infection

  • Age >65 years
  • Medical comorbidities
  • Alcoholism
Marie presented with fever, dyspnoea and cough*

Severity

  • PORT score III (moderate)
    • 56-year-old female
    • PO2<90% (upon admission)
    • Blood glucose >250 mg/dL
    • Increasing oxygen requirements to maintain oxygen saturation

History/comorbidities

  • Mild asthma
  • Diabetes

Risk factors for difficult-to-treat infection

  • Recent antibiotic exposure for URTI within previous 3 months
When there’s no time to wait, clinical trial evidence supports the use of Zinforo in your CAP patients§3,4​​​​​​​

Learn about proven efficacy in CAP patients

Explore More Read several cSSTI patient profiles describing potential scenarios where Zinforo could be a treatment of choice. Access cSSTI patient profilesLoading To learn more about the efficacy of Zinforo in a real-world setting, explore the CAPTURE study.  View CAPTURE study profileLoading

*The examples described here are not actual patients, but fictitious representations of scenarios for which Zinforo could be considered.
§ Refer to SmPC for further information on Zinforo1

Abbreviations​​​​​​​

CAP, community-acquired pneumonia; cSSTI, complicated skin and soft tissue infections; ICU, intensive care unit; RR, respiratory rate; URTI, upper respiratory tract infection; PORT, Pneumonia Patient Outcomes Research Team.​​​​​​​

Prescribing Information​​​​​​​

Zinforo® (ceftaroline fosamil)
Great Britain
Zinforo 600 mg powder for concentrate for solution for infusion
Northern Ireland
Zinforo 600 mg powder for concentrate for solution for infusion 

References

ZINFORO. Summary of Product CharacteristicsOtt SR, et al. Eur Respir J 2012;39:611–18File TM, et al. Clin Infect Dis 2010;51:1395–405Eckburg P, et al. Infect Dis Clin Pract 2012;51:1395–405Laudano JB. J Antimicrob Chemother 2011;66(Suppl.3):iii11-iii18Garrison MW, et al. Expert Rev Anti Infect Ther 2012;10:1087-103Drusano, GL. J Antimicrob Chemother 2011;66(Suppl3):iii61–7Ostermann H, et al. BMC Pulm Med 2014;14:36.Menéndez R, et al. Thorax 2004;59:960–5.
PP-ZFO-GBR-0231. September 2021

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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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