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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

DURLOBACTAM\SULBACTAM: 11 Adverse Event Reports & Safety Profile

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11
Total FAERS Reports
7 (63.6%)
Deaths Reported
2
Hospitalizations
11
As Primary/Secondary Suspect
1
Life-Threatening

Active Ingredient: DURLOBACTAM SODIUM\SULBACTAM SODIUM ·

First Report: 20250216 · Latest Report: 20250509

What Are the Most Common DURLOBACTAM\SULBACTAM Side Effects?

#1 Most Reported
Off label use
4 reports (36.4%)
#2 Most Reported
Death
4 reports (36.4%)
#3 Most Reported
Condition aggravated
2 reports (18.2%)

All DURLOBACTAM\SULBACTAM Side Effects by Frequency

No side effect data available.

Who Reports DURLOBACTAM\SULBACTAM Side Effects? Age & Gender Data

Gender: 0.0% female, 100.0% male. Average age: 45.7 years. Most reports from: US. View detailed demographics →

Is DURLOBACTAM\SULBACTAM Getting Safer? Reports by Year

YearReportsDeathsHosp.
2025 3 2 0

View full timeline →

What Is DURLOBACTAM\SULBACTAM Used For?

IndicationReports
Acinetobacter infection 5

Official FDA Label for DURLOBACTAM\SULBACTAM

Official prescribing information from the FDA-approved drug label.