🇺🇸 Ionolyte in United States

8 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. Abdominal Pain — 1 report (12.5%)
  2. Amylase Increased — 1 report (12.5%)
  3. Drug Interaction — 1 report (12.5%)
  4. Drug Level Increased — 1 report (12.5%)
  5. Lipase Increased — 1 report (12.5%)
  6. Nausea — 1 report (12.5%)
  7. Pancreatitis — 1 report (12.5%)
  8. Procalcitonin Increased — 1 report (12.5%)

Source database →

Ionolyte in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Other approved in United States

Frequently asked questions

Is Ionolyte approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Ionolyte in United States?

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