🇺🇸 liquid lactulose in United States

9 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. Cardiac Failure Congestive — 1 report (11.11%)
  2. Fall — 1 report (11.11%)
  3. Hip Fracture — 1 report (11.11%)
  4. Hypoaesthesia — 1 report (11.11%)
  5. Intestinal Mass — 1 report (11.11%)
  6. Non-Hodgkin^S Lymphoma — 1 report (11.11%)
  7. Off Label Use — 1 report (11.11%)
  8. Urinary Tract Infection — 1 report (11.11%)
  9. Weight Decreased — 1 report (11.11%)

Source database →

liquid lactulose 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 liquid lactulose approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for liquid lactulose in United States?

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