🇺🇸 Lantus in United States

90,071 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 Glucose Increased — 27,415 reports (30.44%)
  2. Off Label Use — 9,285 reports (10.31%)
  3. Blood Glucose Decreased — 7,791 reports (8.65%)
  4. Nausea — 7,708 reports (8.56%)
  5. Inappropriate Schedule Of Product Administration — 7,492 reports (8.32%)
  6. Drug Ineffective — 7,338 reports (8.15%)
  7. Product Storage Error — 6,369 reports (7.07%)
  8. Visual Impairment — 5,981 reports (6.64%)
  9. Hypoglycaemia — 5,481 reports (6.09%)
  10. Diarrhoea — 5,211 reports (5.79%)

Source database →

Lantus in other countries

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

Other Metabolic approved in United States

Frequently asked questions

Is Lantus approved in United States?

Yes. FDA has authorised it.

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

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