FDA Adverse Event Death Summary report: N

EUFLEXXA

MDR report key: 12280536 · Received August 4, 2021

Report

Report Number
MW5103002
Event Type
Death
Date Received
August 4, 2021
Date of Event
June 6, 2021
Report Date
August 3, 2021
Manufacturer
FERRING PHARMACEUTICALS INC.
Product Code
MOZ
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Description of Event or Problem · 1

PATIENT'S HUSBAND REPORTED THAT PATIENT PASSED AWAY ON (B)(6) 2021.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1169753 EUFLEXXA ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS INC. NOT REPORTED

Patients

Seq Age Sex Outcome Treatment
1 68 YR Death