🇺🇸 aMIL in United States
20 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: 20
Most-reported reactions
- Alanine Aminotransferase Increased — 2 reports (10%)
- Alopecia — 2 reports (10%)
- Anaemia — 2 reports (10%)
- Anxiety — 2 reports (10%)
- Application Site Exfoliation — 2 reports (10%)
- Aspartate Aminotransferase Increased — 2 reports (10%)
- Asthenia — 2 reports (10%)
- Back Pain — 2 reports (10%)
- Blood Creatinine Increased — 2 reports (10%)
- Blood Disorder — 2 reports (10%)
Other Oncology approved in United States
Frequently asked questions
Is aMIL approved in United States?
aMIL does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for aMIL in United States?
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins is the originator. The local marketing authorisation holder may differ — check the official source linked above.