🇺🇸 Liposomal Amphotericin B in United States
171 US adverse-event reports
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: 22 April 2025 – 22 April 2026
- Total reports: 171
Most-reported reactions
- Drug Ineffective — 49 reports (28.65%)
- Respiratory Failure — 19 reports (11.11%)
- Acute Kidney Injury — 16 reports (9.36%)
- Drug Interaction — 16 reports (9.36%)
- Pneumonia — 14 reports (8.19%)
- Aspergillus Infection — 13 reports (7.6%)
- Multiple Organ Dysfunction Syndrome — 13 reports (7.6%)
- Bronchopulmonary Aspergillosis — 11 reports (6.43%)
- Condition Aggravated — 10 reports (5.85%)
- Drug Level Increased — 10 reports (5.85%)
Other Infectious Disease approved in United States
Frequently asked questions
Is Liposomal Amphotericin B approved in United States?
Liposomal Amphotericin B does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Liposomal Amphotericin B in United States?
Taiwan Liposome Company is the originator. The local marketing authorisation holder may differ — check the official source linked above.