SUPER POLIGRIP FREE DENTURE ADHESIVE CREAM *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2005-01-07 for SUPER POLIGRIP FREE DENTURE ADHESIVE CREAM * manufactured by Glaxosmithkline, Consumer Healthcare.

Event Text Entries

[313508] This case was reported by a consumer and described the occurrence of parkinson's disease in a pt who used poligrip (super poligrip free denture adhesive cream) for loose dentures. A physician or other health care professional has not verified this report. Concurrent medications included polident dentuare creme toothplaste. In 2004 the pt started using poligrip (dental). In the following month the pt was diagnosed with parkinson's case. This case was assessed as medically serious by gsk. Treatment with poligrip was continued. The event is unresolved. The lot number for this product is available and quality test is pending.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9681138-2004-00047
MDR Report Key564585
Report Source04
Date Received2005-01-07
Date of Report2005-01-05
Date of Event2004-11-01
Date Mfgr Received2004-12-13
Device Manufacturer Date2004-06-01
Date Added to Maude2005-01-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer Street1500 LITTLETON RD.
Manufacturer CityPARRISPANY NJ 07054
Manufacturer CountryUS
Manufacturer Postal07054
Manufacturer Phone9738892494
Manufacturer G1GLAXOSMITHKLINE,IRELAND
Manufacturer StreetCLOCHERANE, YOUGHAL ROAD
Manufacturer CityDUNGARVAN
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSUPER POLIGRIP FREE DENTURE ADHESIVE CREAM
Generic NameDENTURE ADHESIVE
Product CodeKCO
Date Received2005-01-07
Model Number*
Catalog Number*
Lot NumberX04252
ID Number*
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key554340
ManufacturerGLAXOSMITHKLINE, CONSUMER HEALTHCARE
Manufacturer Address* PARSIPPANY NJ * US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-01-07

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