🇺🇸 Subetta 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. Arteriosclerosis — 1 report (11.11%)
  2. Blood Pressure Increased — 1 report (11.11%)
  3. Chronic Kidney Disease — 1 report (11.11%)
  4. Diabetes Mellitus Inadequate Control — 1 report (11.11%)
  5. Diabetic Macroangiopathy — 1 report (11.11%)
  6. Diabetic Nephropathy — 1 report (11.11%)
  7. Diabetic Neuropathy — 1 report (11.11%)
  8. Hypoglycaemia — 1 report (11.11%)
  9. Non-Alcoholic Steatohepatitis — 1 report (11.11%)

Source database →

Subetta 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 Subetta approved in United States?

Yes. FDA has authorised it.

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

Materia Medica Holding is the originator. The local marketing authorisation holder may differ — check the official source linked above.