🇺🇸 ChAdOx1 nCoV-19 in United States
44 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: 44
Most-reported reactions
- Back Pain — 5 reports (11.36%)
- Dry Skin — 5 reports (11.36%)
- Nasopharyngitis — 5 reports (11.36%)
- Skin Ulcer — 5 reports (11.36%)
- Abdominal Distension — 4 reports (9.09%)
- Constipation — 4 reports (9.09%)
- Diarrhoea — 4 reports (9.09%)
- Gastrointestinal Disorder — 4 reports (9.09%)
- Neuropathy Peripheral — 4 reports (9.09%)
- Rash Papular — 4 reports (9.09%)
Other Immunology / Infectious Disease approved in United States
Frequently asked questions
Is ChAdOx1 nCoV-19 approved in United States?
ChAdOx1 nCoV-19 does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for ChAdOx1 nCoV-19 in United States?
EuBiologics Co.,Ltd is the originator. The local marketing authorisation holder may differ — check the official source linked above.