Fwd: Re: ATSDR Registry Procedures for Ionized Platinum

[Guest guest]

Adverse Event report problem! . . . Please read!

--- Carolyn Wolf <carwol@...> wrote:

From: " Carolyn Wolf " <carwol@...>

" Rogene S " <saxony01@...>

Subject: Re: ATSDR Registry Procedures for Ionized

Platinum

Date: Mon, 18 Apr 2005 22:19:12 -0400

Hi Rogene,

The only thing we are asking people to do is to send

in an Adverse Event Report to the FDA... www.fda.gov

go to Medwatch, print out a copy of the report, fill

in and send in .. also might help if they sent a copy

to their Congresspeople -- senators and

representatives..

I have just sent mine in, all went well, but my name

and address for the " Reporter " section at the end did

not " take " -- so I'll fax it tomorrow...Good way for

the FDA to claim they did not receive it -- at whose

instigation, I'd wonder...

When you print the report, the 2nd page has a

coversheet, when, if folded correctly, provides the

address of the FDA -- and you don't even have to buy a

stamp!!

We urge everybody who has not filed reports on

ruptures, explantation, and for each disease with

which they are diagnosed, to immediately fill out

these reports and send them in. If the FDA does not

receive the reports, they can heed the manufacturers

claims that there is nothing wrong with the

implants...The proof exists in the numbers of reports

filed..

Carolyn