Drug Landscape ›
Sterile Water Injection ›
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: 10
Most-reported reactions
Agonal Respiration — 1 report (10%) Agonal Rhythm — 1 report (10%) Chest Discomfort — 1 report (10%) Chest Pain — 1 report (10%) Cough — 1 report (10%) Discomfort — 1 report (10%) Granulocytopenia — 1 report (10%) Hypoxia — 1 report (10%) Myelosuppression — 1 report (10%) Off Label Use — 1 report (10%)
Source database →
Sterile Water Injection 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 Sterile Water Injection approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Sterile Water Injection in United States?
Suez Canal University is the originator. The local marketing authorisation holder may differ — check the official source linked above.