🇺🇸 PEG -Intron in United States

7,367 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: 7,367

Most-reported reactions

1. Fatigue — 975 reports (13.23%)
2. Nausea — 900 reports (12.22%)
3. Anaemia — 899 reports (12.2%)
4. Weight Decreased — 771 reports (10.47%)
5. Vomiting — 737 reports (10%)
6. Asthenia — 675 reports (9.16%)
7. Dehydration — 653 reports (8.86%)
8. Depression — 598 reports (8.12%)
9. Pyrexia — 587 reports (7.97%)
10. Headache — 572 reports (7.76%)

Source database →

Frequently asked questions

Is PEG -Intron approved in United States?

PEG -Intron does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for PEG -Intron in United States?

Beth Israel Deaconess Medical Center is the originator. The local marketing authorisation holder may differ — check the official source linked above.