inforMED
InjuryEMA

FUJI PLUS CAPSULE

Received Dec 4, 2014 · Event occurred Oct 27, 2014

Report 1410097-2014-00005 · MDR key 4337068

Device

Generic name

Unk

Catalog number

425030

Lot number

UNK

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

Not reported

  • Hypersensitivity/Allergic reaction

Narrative

Description of Event or Problem

PT EXPERIENCED ALLERGIC REACTION AFTER RECEIVING FUJI PLUS FROM HER DENTIST DURING A DENTAL PROCEDURE. WITHIN 24 HRS PT HAD A REACTION AND WENT TO HOSP BECAUSE OF SWELLING OF HER TONGUE AND CHIN. PT WAS HOSPITALIZED AND RECEIVED STEROID TREATMENT.