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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DENTAL AMALGAM FILLING

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DENTAL AMALGAM FILLING Back to Search Results
Patient Problems Emotional Changes (1831); Anxiety (2328); Depression (2361); Weight Changes (2607); Suicidal Ideation (4429)
Event Type  Injury  
Event Description
You all are criminals and belong in jail for what you do to people regarding dental amalgams.I've been sick for 30 years.Tons of mental health issues including depression, anxiety, suicidal ideations, anorexia, bulimia, and much more.Got my fillings safely removed last (b)(6) 2022 and my lifetime of mental health issues seemingly vanished overnight.You stole 30 years from me.I lived at doctors offices.Went to so much therapy and psychiatrists.Was tired all the time.Never dated.Was miserable and prayed to die.All b/c you covered up the effects of mercury.And it's been known since before the ada's conception that mercury was dangerous.Hell, the use of mercury in making felt hats stopped in the 1940s.I'm beyond disappointed what the usa has come to.I naively thought govt organizations were here to protect the people.Now i know they are puppets for big pharma.You have no desire to see people heal.Shame on you.If you follow the doctors who the fda has disbarred, you'll see they are telling the truth.I can only wish that the people who head these gov't and pharm organizations one day may become as sick as i was.I pray karma is real.Probably that schein company.I'm off all prescription medication after 20 years.B/c of the mercury i've been a lab rat most of my life.
 
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Brand Name
DENTAL AMALGAM FILLING
Type of Device
DENTAL AMALGAM
MDR Report Key17710794
MDR Text Key322954736
Report NumberMW5145366
Device Sequence Number1
Product Code OIV
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 09/02/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Was Device Available for Evaluation? No
Initial Date Manufacturer Received Not provided
Initial Date FDA Received09/08/2023
Patient Sequence Number1
Patient Outcome(s) Disability; Life Threatening; Other; Required Intervention;
Patient SexFemale
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