🇺🇸 DHA (Docosahexaenoic Acid) in United States
38 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: 38
Most-reported reactions
- Off Label Use — 6 reports (15.79%)
- Dyspnoea — 5 reports (13.16%)
- Fatigue — 5 reports (13.16%)
- Gastrooesophageal Reflux Disease — 4 reports (10.53%)
- Arthralgia — 3 reports (7.89%)
- Condition Aggravated — 3 reports (7.89%)
- Covid-19 — 3 reports (7.89%)
- Death — 3 reports (7.89%)
- Diarrhoea — 3 reports (7.89%)
- Intentional Product Use Issue — 3 reports (7.89%)
Other Neurology approved in United States
Frequently asked questions
Is DHA (Docosahexaenoic Acid) approved in United States?
DHA (Docosahexaenoic Acid) does not currently have US marketing authorisation in our dataset.
Who is the marketing authorisation holder for DHA (Docosahexaenoic Acid) in United States?
Alzheimer's Disease Cooperative Study (ADCS) is the originator. The local marketing authorisation holder may differ — check the official source linked above.