Drug Landscape ›
TAZOBACTAM SODIUM ›
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: 8,603
Most-reported reactions
Off Label Use — 1,632 reports (18.97%) Drug Ineffective — 1,463 reports (17.01%) Acute Kidney Injury — 990 reports (11.51%) Pyrexia — 893 reports (10.38%) Diarrhoea — 700 reports (8.14%) Condition Aggravated — 658 reports (7.65%) Neutropenia — 601 reports (6.99%) Pneumonia — 577 reports (6.71%) Thrombocytopenia — 568 reports (6.6%) Febrile Neutropenia — 521 reports (6.06%)
Source database →
TAZOBACTAM SODIUM 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 TAZOBACTAM SODIUM approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for TAZOBACTAM SODIUM in United States?
Marketing authorisation holder not available in our data.