Drug Landscape ›
Sea water ›
Regulatory · United States
Marketing authorisation
FDA
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: 20 April 2025 – 20 April 2026
Total reports: 554
Most-reported reactions
Hypertension — 59 reports (10.65%) Asthma — 55 reports (9.93%) Blood Test Abnormal — 55 reports (9.93%) Burning Sensation — 55 reports (9.93%) Cardiac Disorder — 55 reports (9.93%) Fibromyalgia — 55 reports (9.93%) Gastrooesophageal Reflux Disease — 55 reports (9.93%) Headache — 55 reports (9.93%) Hypothyroidism — 55 reports (9.93%) Sensitisation — 55 reports (9.93%)
Source database →
Sea water in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Frequently asked questions
Is Sea water approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Sea water in United States?
University Ghent is the originator. The local marketing authorisation holder may differ — check the official source linked above.