FDA Adverse Event Injury Summary report: N

AVENOVA

MDR report key: 7689237 · Received July 13, 2018

Report

Report Number
MW5078373
Event Type
Injury
Date Received
July 13, 2018
Report Date
July 12, 2018
Manufacturer
NOVA BAY PHARMACEUTICALS INC.
Product Code
FRO
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
IL, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

AVENOVA: PRODUCT DID NOT WORK. AZITHROMYCIN: PRODUCT HAD NO AFFECT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
528325 AVENOVA WOUND DRESSING / DRUG FRO NOVA BAY PHARMACEUTICALS INC.

Patients

Seq Age Sex Outcome Treatment
1 AZITHROMYCIN