Drug Landscape ›
PIPERACILLIN 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: 8,870
Most-reported reactions
Off Label Use — 1,632 reports (18.4%) Drug Ineffective — 1,442 reports (16.26%) Acute Kidney Injury — 1,020 reports (11.5%) Pyrexia — 982 reports (11.07%) Diarrhoea — 730 reports (8.23%) Condition Aggravated — 670 reports (7.55%) Pneumonia — 616 reports (6.94%) Neutropenia — 612 reports (6.9%) Thrombocytopenia — 593 reports (6.69%) Febrile Neutropenia — 573 reports (6.46%)
Source database →
PIPERACILLIN 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 PIPERACILLIN SODIUM approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for PIPERACILLIN SODIUM in United States?
Marketing authorisation holder not available in our data.