🇺🇸 Compound sodium lactate solution in United States

10 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.

• Window: 20 April 2025 – 20 April 2026
• Total reports: 10

Most-reported reactions

1. Hyperkalaemia — 2 reports (20%)
2. Confusion Postoperative — 1 report (10%)
3. Electrocardiogram Qt Prolonged — 1 report (10%)
4. Exposure During Pregnancy — 1 report (10%)
5. Mental Status Changes Postoperative — 1 report (10%)
6. Metabolic Alkalosis — 1 report (10%)
7. Rectal Abscess — 1 report (10%)
8. Unevaluable Event — 1 report (10%)
9. Unresponsive To Stimuli — 1 report (10%)

Source database →

Frequently asked questions

Is Compound sodium lactate solution approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Compound sodium lactate solution in United States?

Belfast Health and Social Care Trust is the originator. The local marketing authorisation holder may differ — check the official source linked above.