inforMED
InjuryFTC

PUVA

Received Feb 21, 2020

Report MW5093226 · MDR key 9744949

Device

Generic name

Light, Ultraviolet, Dermatological

Manufacturer

Unk

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

Not reported

  • Therapeutic Response, Decreased
  • Therapeutic Response, Decreased

Narrative

Description of Event or Problem

LACK OF EFFICACY.