🇺🇸 Flovent Diskus in United States

2,981 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. Dyspnoea — 406 reports (13.62%)
  2. Device Use Error — 392 reports (13.15%)
  3. Wrong Technique In Device Usage Process — 355 reports (11.91%)
  4. Drug Ineffective — 353 reports (11.84%)
  5. Asthma — 350 reports (11.74%)
  6. Wrong Technique In Product Usage Process — 326 reports (10.94%)
  7. Cough — 218 reports (7.31%)
  8. Wheezing — 196 reports (6.57%)
  9. Off Label Use — 194 reports (6.51%)
  10. Underdose — 191 reports (6.41%)

Source database →

Flovent Diskus 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 Flovent Diskus approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Flovent Diskus in United States?

Johns Hopkins University is the originator. The local marketing authorisation holder may differ — check the official source linked above.