Drug Landscape ›
Heparin solution ›
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: 12
Most-reported reactions
Cardiac Arrest — 2 reports (16.67%) Hypotension — 2 reports (16.67%) Blood Creatinine Increased — 1 report (8.33%) Blood Urea Increased — 1 report (8.33%) Colitis — 1 report (8.33%) Coronary Artery Thrombosis — 1 report (8.33%) Cytomegalovirus Infection — 1 report (8.33%) Disease Recurrence — 1 report (8.33%) Dizziness Postural — 1 report (8.33%) Enteritis — 1 report (8.33%)
Source database →
Heparin solution 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 Heparin solution approved in United States?
Yes. FDA has authorised it.
Who is the marketing authorisation holder for Heparin solution in United States?
Nadezhda Women's Health Hospital is the originator. The local marketing authorisation holder may differ — check the official source linked above.