🇺🇸 Actidose Aqua in United States

9 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: 21 April 2025 – 21 April 2026
• Total reports: 9

Most-reported reactions

1. Accidental Exposure — 1 report (11.11%)
2. Agitation — 1 report (11.11%)
3. Blood Glucose Increased — 1 report (11.11%)
4. Drooling — 1 report (11.11%)
5. Eye Rolling — 1 report (11.11%)
6. Lip Swelling — 1 report (11.11%)
7. Miosis — 1 report (11.11%)
8. Mood Altered — 1 report (11.11%)
9. Somnolence — 1 report (11.11%)

Source database →

Frequently asked questions

Is Actidose Aqua approved in United States?

Actidose Aqua does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Actidose Aqua in United States?

National Institute of Allergy and Infectious Diseases (NIAID) is the originator. The local marketing authorisation holder may differ — check the official source linked above.