POLIDENT TABLET *

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 2004-12-02 for POLIDENT TABLET * manufactured by Glaxosmithkline, Consumer Healthcare.

Event Text Entries

[17414567] A consumer's neighbor described the occurrence of bone cancer in a pt who used polident (polident denture cleanser tablets) for dental cleaning. The consumer's neighbor contacted the mfr to praise the product. A physician or other health care professional has not verified this report. Concurrent medications included polident overnight denture cleanser tablets. On an unk date, the pt started polident (dental), at an unk dosing. At an unk time after starting polident, the pt fell and was diagnosed with bone cancer. The pt was treated with cancer chemotherapy. The pt was hospitalized some time in 2004, had continued to use polident and died in 9/2004. The cause of death is unk. It is unk whether an autopsy was performed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1020379-2004-00011
MDR Report Key557615
Report Source04
Date Received2004-12-02
Date of Report2004-11-18
Date Mfgr Received2004-11-08
Device Manufacturer Date2003-09-01
Date Added to Maude2004-12-06
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 CityPARSIPPANY NJ 07054
Manufacturer CountryUS
Manufacturer Postal07054
Manufacturer Phone9738892494
Manufacturer G1GLAXOSMITHKLINE
Manufacturer StreetMEMPHIS FACILITY 2149 HARBOR AVE.
Manufacturer CityMEMPHIS TN 36113
Manufacturer CountryUS
Manufacturer Postal Code36113
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePOLIDENT TABLET
Generic NameDENTURE CLEANSER
Product CodeJER
Date Received2004-12-02
Model Number*
Catalog Number*
Lot NumberMI173
ID Number*
OperatorLAY USER/PATIENT
Device AvailabilityY
Device Eval'ed by MfgrN
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key547283
ManufacturerGLAXOSMITHKLINE, CONSUMER HEALTHCARE
Manufacturer Address* PARSIPPANY NJ * US


Patients

Patient NumberTreatmentOutcomeDate
101. Death; 2. Hospitalization 2004-12-02

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