AMALGAM FILLINGS UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-02-22 for AMALGAM FILLINGS UNK manufactured by Unk.

Event Text Entries

[5527717] A 6 amalgam fillings placed many years ago. I am not sure of the dates. I have been to doctor after doctor who could not tell me what was wrong with a myriad of gi, neurological, endocrine immunological, joint complaints, thyroid goiter and other complaints. I have had a diagnosis of chronic fatigue. I recently had fillings removed by iomt protocol 4 in (b)(6) and 2 in (b)(6). (my regular dentist refused to use iomt protocol). My energy levels have improved to normal, but other complaints are not resolved. I am still having especially troublesome neurological effects. I am putting today's date on the date of event because this form is inadequate for chronic toxicity. It is designed for acute toxicities. I have been sick for years. Although the mercury from the amalgams is not the total cause, the improvement of symptoms after the removal, which also correlates with the data from studies about lowering of blood mercury levels, proves in my mind that the amalgams are partly causing the symptoms. Please convince ada to honour the minamata convention and stop routine use of amalgam!
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5040917
MDR Report Key4551491
Date Received2015-02-22
Date of Report2015-02-22
Date of Event2015-02-22
Date Added to Maude2015-02-27
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationPATIENT
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameAMALGAM FILLINGS
Generic NameAMALGAM FILLINGS
Product CodeEJJ
Date Received2015-02-22
Model NumberUNK
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device Sequence No1
Device Event Key0
ManufacturerUNK


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-02-22

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