Drug Landscape ›
Cefazolin Injection ›
Regulatory · United States
Marketing authorisation
FDA
Safety signals — FAERS
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
Window: 20 April 2025 – 20 April 2026
Total reports: 64
Most-reported reactions
Infection — 24 reports (37.5%) Bacteraemia — 7 reports (10.94%) Treatment Failure — 7 reports (10.94%) Incision Site Infection — 6 reports (9.38%) Disease Progression — 4 reports (6.25%) Exposure During Pregnancy — 4 reports (6.25%) Clostridium Difficile Infection — 3 reports (4.69%) Disease Complication — 3 reports (4.69%) Drug-Induced Liver Injury — 3 reports (4.69%) No Adverse Event — 3 reports (4.69%)
Source database →
Cefazolin Injection in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Frequently asked questions
Is Cefazolin Injection approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Cefazolin Injection in United States?
Abdul El-Rabbany is the originator. The local marketing authorisation holder may differ — check the official source linked above.