Fwd: I FAXED IT TODAY..... SEND IN... Adverse Event Report to the FDA .. MedWatch

[Guest guest]

>

> Rogene

>

> I faxed my report in today.

>

> I filled out a few lines on the MedWatch paper and

> put in three places " see

> attached sheet " that had all the years and list of

> abnormal tests,

> surgeries, rupture, capsulotomies, and more..

> NUMBER the pages at the top..

> If you Mail it will take up to three weeks and may

> not even get there..

> Don't forget to add if you have been tested for

> Ionized Platinum.. I put it

> at the top so they could not miss it.

>

>

> ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

>

>

>

> This is the way to get the FDA's attention! . . . If

> we don't report

> problems, they assume implants are safe. You can

> file this report on your

> own, without a doctors signature. Please, please do

> so! - Rogene

> ------------------

>

> From Carolyn Wolf

>

> This should be an easy way for people to either do

> an Adverse Event Report

> -- online (print a copy before you hit the send

> button)--or the form can be

> printed, and blanks filled in...

>

> Most everybody knows the type of implant --

> approximate date of

> implantation, date of explantation -- when

> Rheumatoid Arthritis was

> diagnosed -- or MS -- or Sclerderma...fill out a

> form for each diagnosis --

> EACH event is an adverse event..If you choose to

> mail, you just fold the

> second page over the first so that the mailing

> address is visible, -- you

> don't even have to buy a stamp!!

>

> Carolyn

> -------------------------

> ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

>

>

>

> The message is ready to be sent with the following

> file or link attachments:

>

> http://www.fda.gov/medwatch/SAFETY/3500.pdf (Print

> out report)

>

>

>

>

>

>

>

> Adverse Event report problem! . . . Please read!

>

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

>

< /post?postID=vNCgNE3_Nquf

>

PZXDRN7SgizYT6m9sU0s2u__IW4849_RlZ4Kqq4uCoICnuAnbQNfeKfwgSAYRaU>

> > wrote:

>

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

>

< /post?postID=vNCgNE3_Nquf

>

PZXDRN7SgizYT6m9sU0s2u__IW4849_RlZ4Kqq4uCoICnuAnbQNfeKfwgSAYRaU>

> >

> " Rogene S " <saxony01@...

>

< /post?postID=iOerBKJ2FY2W

>

_MuNgCiP82tz8rmJjf8pRpzHePFyDVNoAp0Fu6Dt-AMcwiJBmnYq3ypwK3UuWNLvIAvNeA>

> >

> 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

> <http://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

>

>