🇺🇸 Fisiogen Ferro Forte in United States
40 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: 40
Most-reported reactions
- Aphonia — 4 reports (10%)
- Arthralgia — 4 reports (10%)
- Dizziness — 4 reports (10%)
- Dry Eye — 4 reports (10%)
- Eye Disorder — 4 reports (10%)
- Eye Pain — 4 reports (10%)
- Fatigue — 4 reports (10%)
- Frequent Bowel Movements — 4 reports (10%)
- Headache — 4 reports (10%)
- Hypersensitivity — 4 reports (10%)
Other Hematology approved in United States
Frequently asked questions
Is Fisiogen Ferro Forte approved in United States?
Fisiogen Ferro Forte does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Fisiogen Ferro Forte in United States?
Hospital Universitari Vall d'Hebron Research Institute is the originator. The local marketing authorisation holder may differ — check the official source linked above.