🇺🇸 aspart 30 in United States

20 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 Creatinine Increased — 2 reports (10%)
  2. Cerebral Infarction — 2 reports (10%)
  3. Chronic Kidney Disease — 2 reports (10%)
  4. Diabetes Mellitus Inadequate Control — 2 reports (10%)
  5. Fatigue — 2 reports (10%)
  6. Hyperkalaemia — 2 reports (10%)
  7. Hypertension — 2 reports (10%)
  8. Hypokalaemia — 2 reports (10%)
  9. Myositis — 2 reports (10%)
  10. Pruritus — 2 reports (10%)

Source database →

aspart 30 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 aspart 30 approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for aspart 30 in United States?

Huazhong University of Science and Technology is the originator. The local marketing authorisation holder may differ — check the official source linked above.