FDA Adverse Event Summary report: N

*

MDR report key: 518650 · Received March 16, 2004

Report

Report Number
MW1031605
Date Received
March 16, 2004
Date of Event
February 27, 2004
Report Date
March 13, 2004
Manufacturer
*
Product Code
LEJ
Report Source
Voluntary report
Reporter Location
IN, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

STAPH INFECTION. RECEIVED IV ANTIBIOTICS, ORAL ANTIBIOTICS, PAIN MEDICATION AND ADMITTED TO HOSPITAL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * LEJ * * *

Patients

Seq Age Sex Outcome Treatment
1 *