🇺🇸 HuMax-IL8 in United States

7 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: 28 March 2025 – 28 March 2026
• Total reports: 7

Most-reported reactions

1. Bile Duct Stenosis — 1 report (14.29%)
2. Cholecystitis — 1 report (14.29%)
3. Colitis — 1 report (14.29%)
4. Dehydration — 1 report (14.29%)
5. Multiple Organ Dysfunction Syndrome — 1 report (14.29%)
6. Sepsis — 1 report (14.29%)
7. Supraventricular Tachycardia — 1 report (14.29%)

Source database →

Frequently asked questions

Is HuMax-IL8 approved in United States?

HuMax-IL8 does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for HuMax-IL8 in United States?

Bristol-Myers Squibb is the originator. The local marketing authorisation holder may differ — check the official source linked above.