🇺🇸 Photodynamic Therapy in United States

124 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. Wrong Technique In Product Usage Process — 39 reports (31.45%)
  2. Erythema — 19 reports (15.32%)
  3. Drug Ineffective — 15 reports (12.1%)
  4. Product Complaint — 11 reports (8.87%)
  5. Pain — 10 reports (8.06%)
  6. Nonspecific Reaction — 8 reports (6.45%)
  7. Off Label Use — 6 reports (4.84%)
  8. Skin Exfoliation — 6 reports (4.84%)
  9. Application Site Pain — 5 reports (4.03%)
  10. Application Site Reaction — 5 reports (4.03%)

Source database →

Photodynamic Therapy 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 Photodynamic Therapy approved in United States?

Yes. FDA has authorised it.

Who is the marketing authorisation holder for Photodynamic Therapy in United States?

Roswell Park Cancer Institute is the originator. The local marketing authorisation holder may differ — check the official source linked above.