🇺🇸 Phytolacca decandra in United States
2 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: 2
Most-reported reactions
- Osteonecrosis Of Jaw — 1 report (50%)
- Stomatitis — 1 report (50%)
Other Immunology approved in United States
Frequently asked questions
Is Phytolacca decandra approved in United States?
Phytolacca decandra does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for Phytolacca decandra in United States?
Universidade Federal do Rio de Janeiro is the originator. The local marketing authorisation holder may differ — check the official source linked above.