🇺🇸 Krestin in United States

32 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: 32

Most-reported reactions

1. Interstitial Lung Disease — 7 reports (21.88%)
2. Anaemia — 4 reports (12.5%)
3. Platelet Count Decreased — 4 reports (12.5%)
4. Dyspnoea — 3 reports (9.38%)
5. Febrile Neutropenia — 3 reports (9.38%)
6. Rash — 3 reports (9.38%)
7. Alanine Aminotransferase Increased — 2 reports (6.25%)
8. Aspartate Aminotransferase Increased — 2 reports (6.25%)
9. Blood Creatinine Increased — 2 reports (6.25%)
10. Blood Lactate Dehydrogenase Increased — 2 reports (6.25%)

Source database →

Frequently asked questions

Is Krestin approved in United States?

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

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

Hokkaido Gastrointestinal Cancer Study Group is the originator. The local marketing authorisation holder may differ — check the official source linked above.