🇺🇸 H2O in United States

12 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: 12

Most-reported reactions

1. Electrolyte Imbalance — 2 reports (16.67%)
2. Gastritis — 2 reports (16.67%)
3. Abdominal Discomfort — 1 report (8.33%)
4. Abdominal Pain — 1 report (8.33%)
5. Acute Kidney Injury — 1 report (8.33%)
6. Anaemia — 1 report (8.33%)
7. Application Site Erythema — 1 report (8.33%)
8. Application Site Rash — 1 report (8.33%)
9. Asthenia — 1 report (8.33%)
10. Atrial Fibrillation — 1 report (8.33%)

Source database →

Frequently asked questions

Is H2O approved in United States?

H2O does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for H2O in United States?

Montefiore Medical Center is the originator. The local marketing authorisation holder may differ — check the official source linked above.