🇺🇸 Fluid bolus in United States

15 US adverse-event reports

Marketing authorisation

FDA

  • Status: approved

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.

Most-reported reactions

  1. Blood Creatinine Increased — 2 reports (13.33%)
  2. Cough — 2 reports (13.33%)
  3. Tachycardia — 2 reports (13.33%)
  4. Unresponsive To Stimuli — 2 reports (13.33%)
  5. Vomiting — 2 reports (13.33%)
  6. Abdominal Discomfort — 1 report (6.67%)
  7. Activated Partial Thromboplastin Time Prolonged — 1 report (6.67%)
  8. Blood Urea Increased — 1 report (6.67%)
  9. Bradycardia — 1 report (6.67%)
  10. Cardiac Arrest — 1 report (6.67%)

Source database →

Fluid bolus 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 Fluid bolus approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Fluid bolus in United States?

Domonkos Trásy is the originator. The local marketing authorisation holder may differ — check the official source linked above.