FDA Adverse Event Injury Summary report: N

POLIGRIP TOOTH CREAM

MDR report key: 1832352 · Received August 31, 2010

Report

Report Number
MW5017355
Event Type
Injury
Date Received
August 31, 2010
Date of Event
August 25, 2010
Report Date
August 31, 2010
Product Code
KOL
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
WV, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

I TOOK PRESCRIBED AMOX TRX CL 500-12 TAB (AUGMENTIN 500 TAB). I ALSO USED POLIGRIP TOOTH DENTURE CREAM AT THE SAME TIME. MY ALLERGIC REACTION WAS A HEADACHE, RUNNY NOSE, DRY THROAT, FEVER AND ACHES ALL OVER MY BODY. DOSE OR AMOUNT: TO LINE DENTURE, FREQUENCY: ONCE A MONTH. DATES OF USE: (B)(6)2010. DIAGNOSIS OR REASON FOR USE: TO LINE DENTURES. EVENT ABATED AFTER USE: YES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 POLIGRIP TOOTH CREAM NONE KOL

Patients

Seq Age Sex Outcome Treatment
1 75 YR Other