🇺🇸 IC in United States

220 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: 23 April 2025 – 23 April 2026
• Total reports: 220

Most-reported reactions

1. Product Substitution Issue — 36 reports (16.36%)
2. Headache — 32 reports (14.55%)
3. Drug Ineffective — 29 reports (13.18%)
4. Nausea — 21 reports (9.55%)
5. Insomnia — 20 reports (9.09%)
6. Anxiety — 18 reports (8.18%)
7. Pain — 17 reports (7.73%)
8. Arthralgia — 16 reports (7.27%)
9. Diarrhoea — 16 reports (7.27%)
10. Abdominal Pain Upper — 15 reports (6.82%)

Source database →

Frequently asked questions

Is IC approved in United States?

IC does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for IC in United States?

Alliance for Clinical Trials in Oncology is the originator. The local marketing authorisation holder may differ — check the official source linked above.