Zavicefta
·
- Prescription status not stated
- Antibiotics, antivirals and antifungals taken into the body
- Active substance
- Ceftazidime;avibactam
- Made by
- Pfizer Ireland Pharmaceuticals Unlimited Company
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
- Zavicefta is indicated in adults and paediatric patients aged 3 months and older for the treatment of the following infections: Complicated intra-abdominal infection (cIAI) Complicated urinary tract infection (cUTI), including pyelonephritis Hospital-acquired pneumonia (HAP), including ventilator associated pneumonia (VAP) Treatment of 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 adults and paediatric patients aged 3 months and older with limited treatment options. Consideration should be given to official guidance on the appropriate use of antibacterial agents.
From the official label · 2026-09-30 · European Medicines Agency
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
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United StatesNo exact match for this strength and form
Details
| Made by | Pfizer Ireland Pharmaceuticals Unlimited Company |
|---|---|
| Active substance | Ceftazidime;avibactam |
| Used in | Antibiotics, antivirals and antifungals taken into the body |
| Classification | J01DD52 · Antibiotics, antivirals and antifungals taken into the body |
| Authorised on | 2016-06-23 |
| Last updated by the regulator | 2025-11-14 |
| EMA product number | EMEA/H/C/004027 |
Source: European Medicines Agency — medicine data · 2026-09-30 · not reviewed by a clinician
Source: European Medicines Agency (EMA). Product information as published by EMA. Reuse terms: EMA legal notice (reproduction authorised).