🇺🇸 Spiromax Budesonide/formoterol in United States

11 US adverse-event reports

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. Arthralgia — 2 reports (18.18%)
  2. Abdominal Pain — 1 report (9.09%)
  3. Angina Pectoris — 1 report (9.09%)
  4. Anxiety — 1 report (9.09%)
  5. Appendicitis — 1 report (9.09%)
  6. Asthma — 1 report (9.09%)
  7. Cardiac Failure — 1 report (9.09%)
  8. Cerebrovascular Accident — 1 report (9.09%)
  9. Covid-19 — 1 report (9.09%)
  10. Discomfort — 1 report (9.09%)

Source database →

Other Respiratory approved in United States

Frequently asked questions

Is Spiromax Budesonide/formoterol approved in United States?

Spiromax Budesonide/formoterol does not currently have US marketing authorisation in our dataset.

Who is the marketing authorisation holder for Spiromax Budesonide/formoterol in United States?

University Medical Center Groningen is the originator. The local marketing authorisation holder may differ — check the official source linked above.