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RE: Draft FDA Guidance document on the use of KI



Does anybody else see inconsistencies here?  Most of the thyroid cancers
were caused by ingesting milk products, but we want you to take KI
immediately (or within 4 hours) when the accident occurs for protection
against inhaled radioiodines??  It seems we are spending a lot of time and
resources for protection against the inhaled radioiodines when it is the
ingested products that are the real culprits.

My thoughts alone.

Cindy Ledbetter
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TVA Mechanical-Nuclear Design / Engineering / Watts Bar
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Cynthia M. Ledbetter
EQB 2N-WBN
P. O. Box 2000
Spring City, TN 37381-2000
Phone:  (423) 365-1582  Fax:  (423) 365-1750
E-mail:  cmledbetter@tva.gov


> ----------
> From: 	Jim Hardeman[SMTP:Jim_Hardeman@mail.dnr.state.ga.us]
> Reply To: 	radsafe@romulus.ehs.uiuc.edu
> Sent: 	Wednesday, January 03, 2001 2:39 PM
> To: 	Multiple recipients of list
> Subject: 	Draft FDA Guidance document on the use of KI
> 
> Colleagues -
> 
> The Food and Drug Administration (FDA) has published a draft document
> titled "Potassium Iodide as a Thyroid Blocking Agent in Radiation
> Emergencies" (Issued 1/2001, Posted 1/3/2001) on its website at
> http://www.fda.gov/cder/whatsnew.htm. The document is found close to the
> bottom of the page under the "Guidance Documents" section, in either HTML
> or PDF format.
> 
> I apologize in advance to those of you who may received multiple copies of
> this message ... I broadcast it as widely as possible, and some of you are
> one 2-3 of my e-mail lists.
> 
> 
> 
> 
> Jim Hardeman, Manager
> Environmental Radiation Program
> Environmental Protection Division
> Georgia Department of Natural Resources
> 4244 International Parkway, Suite 114
> Atlanta, GA 30354
> (404) 362-2675  fax: (404) 362-2653
> Jim_Hardeman@mail.dnr.state.ga.us
> 
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