🇺🇸 AVA in United States
68 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: 21 April 2025 – 21 April 2026
- Total reports: 68
Most-reported reactions
- Pain — 10 reports (14.71%)
- Hypotension — 8 reports (11.76%)
- Constipation — 7 reports (10.29%)
- Fall — 7 reports (10.29%)
- Balance Disorder — 6 reports (8.82%)
- Blood Calcium Decreased — 6 reports (8.82%)
- Cognitive Disorder — 6 reports (8.82%)
- Creatinine Renal Clearance Decreased — 6 reports (8.82%)
- Depressed Level Of Consciousness — 6 reports (8.82%)
- Fatigue — 6 reports (8.82%)
Other Immunology / Infectious Disease approved in United States
Frequently asked questions
Is AVA approved in United States?
AVA does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for AVA in United States?
Emergent BioSolutions is the originator. The local marketing authorisation holder may differ — check the official source linked above.