Drug Landscape ›
IV Furosemide ›
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: 11
Most-reported reactions
Pulmonary Oedema — 2 reports (18.18%) Acute Kidney Injury — 1 report (9.09%) Aortic Valve Incompetence — 1 report (9.09%) Atrial Fibrillation — 1 report (9.09%) Blood Creatinine Increased — 1 report (9.09%) Blood Pressure Systolic Increased — 1 report (9.09%) Cardiovascular Disorder — 1 report (9.09%) Hypokalaemia — 1 report (9.09%) Metabolic Acidosis — 1 report (9.09%) Mitral Valve Incompetence — 1 report (9.09%)
Source database →
IV Furosemide 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 IV Furosemide approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for IV Furosemide in United States?
Rambam Health Care Campus is the originator. The local marketing authorisation holder may differ — check the official source linked above.