FDA Adverse Event Injury Summary report: N

POLYGRIP (SUPER)

MDR report key: 1842643 · Received September 20, 2010

Report

Report Number
MW5017502
Event Type
Injury
Date Received
September 20, 2010
Date of Event
February 15, 2000
Report Date
September 13, 2010
Manufacturer
PROCTOR & GAMBLE
Product Code
KOL
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I HAVE USED POLYGRIP FROM THE END OF (B)(6)2000 UNTIL NOW. I CANNOT HAVE MY BLOOD WORK TAKEN JUST BECAUSE I WANT IT CHECKED I'M IN PRISON. THE STUFF DOES NOT WORK WELL, IT GAGES ME AND CAUSE HEADACHES. NUMBNESS IN BUTT AND LEGS AND FEET SOMETIMES NECK AND HEAD. MEMORY LAPSE AND SOME INCREASED HEART RATE. BLURRED VISION AND RINGING IN EARS (ONLY AT TIME). NOTE: I HAD TO STEAL THIS BLACK INK PEN AND WE ARE NOT ALLOWED ANY TAPE. DOSE OR AMOUNT: DENTURE CREAM. FREQUENCY: TWICE DAILY. ROUTE: ORAL. DIAGNOSIS OR REASON FOR USE: DENTURE ADHESIVE CREAM. EVENT ABATED AFTER USE STOPPED OR DOSE REDUCED: NO.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 POLYGRIP (SUPER) FALSE TEETH KOL PROCTOR & GAMBLE UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 53 YR Other| S NONE AT THIS TIME