<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="billres.xsl"?>
<!DOCTYPE resolution PUBLIC "-//US Congress//DTDs/res.dtd//EN" "res.dtd">
<resolution dms-id="H440E809C863A4150AFB82D6E90D0F66" key="H" public-private="public" resolution-stage="Introduced-in-House" resolution-type="house-concurrent" star-print="no-star-print">
<metadata xmlns:dc="http://purl.org/dc/elements/1.1/">
<dublinCore>
<dc:title>110 HCON 342 IH: Expressing the sense of Congress that the
</dc:title>
<dc:publisher>U.S. House of Representatives</dc:publisher>
<dc:date>2008-05-06</dc:date>
<dc:format>text/xml</dc:format>
<dc:language>EN</dc:language>
<dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
</dublinCore>
</metadata>
	<form>
		<distribution-code display="yes">IV</distribution-code>
		<congress display="yes">110th CONGRESS</congress>
		<session display="yes">2d Session</session>
		<legis-num>H. CON. RES. 342</legis-num>
		<current-chamber>IN THE HOUSE OF REPRESENTATIVES</current-chamber>
		<action display="yes">
			<action-date date="20080506">May 6, 2008</action-date>
			<action-desc><sponsor name-id="R000573">Mr. Ross</sponsor> (for
			 himself, <cosponsor name-id="E000172">Mrs. Emerson</cosponsor>,
			 <cosponsor name-id="B001230">Ms. Baldwin</cosponsor>,
			 <cosponsor name-id="B001248">Mr. Burgess</cosponsor>,
			 <cosponsor name-id="F000030">Mr. Farr</cosponsor>, <cosponsor name-id="C001051">Mr. Carter</cosponsor>, and <cosponsor name-id="G000554">Ms.
			 Giffords</cosponsor>) submitted the following concurrent resolution; which was
			 referred to the <committee-name committee-id="HIF00">Committee on Energy and
			 Commerce</committee-name></action-desc>
		</action>
		<legis-type>CONCURRENT RESOLUTION</legis-type>
		<official-title display="yes">Expressing the sense of Congress that the
		  Food and Drug Administration’s (FDA) new policy restricting women’s access to
		  medications containing estriol does not serve the public
		  interest.</official-title>
	</form>
	<preamble>
		<whereas><text>Whereas menopause is often a challenging transition for
			 millions of women that requires specialized medications and medical
			 treatments;</text>
		</whereas><whereas><text>Whereas physicians prescribe a variety of pharmaceutical
			 treatment options to treat women experiencing the symptoms of menopause;</text>
		</whereas><whereas><text>Whereas individual women respond differently to different
			 treatment options;</text>
		</whereas><whereas><text>Whereas women’s physicians determine on a case-by-case
			 basis which treatment option is optimal for each woman;</text>
		</whereas><whereas><text>Whereas many physicians prescribe compounded estrogen and
			 other bioidentical hormone treatments for patients for a variety of
			 reasons;</text>
		</whereas><whereas><text>Whereas many physicians prescribe compounded estrogen
			 treatments that contain estriol to treat menopausal and perimenopausal
			 women;</text>
		</whereas><whereas><text>Whereas estriol is one of three estrogens produced by the
			 human body;</text>
		</whereas><whereas><text>Whereas estriol has been prescribed and used for decades
			 in the United States;</text>
		</whereas><whereas><text>Whereas Congress has long recognized active pharmaceutical
			 ingredients meeting standards set by the United States Pharmacopeia as
			 permissible options for physician prescribing and pharmacy compounding;</text>
		</whereas><whereas><text>Whereas the Food and Drug Administration (FDA) has
			 announced that it will no longer permit compounding pharmacists to prepare
			 medications containing estriol pursuant to a doctor’s prescription;</text>
		</whereas><whereas><text>Whereas insurers are now denying women reimbursement for
			 compounded medications containing estriol as a result of the FDA’s
			 announcement; and</text>
		</whereas><whereas><text>Whereas the FDA has acknowledged that it is unaware of any
			 adverse events associated with use of compounded medications containing
			 estriol: Now, therefore, be it</text>
		</whereas></preamble>
	<resolution-body id="H9CF231AAA7B5459897AF423C4BA91CF4" style="traditional">
		<section display-inline="yes-display-inline" id="H018EC98507B34A90BD79C990E38ED6C" section-type="undesignated-section"><enum></enum><text display-inline="yes-display-inline">That it is the sense of the Congress
			 that—</text>
			<paragraph id="HFF58199E2BC147D782CB4D33D114B6C7"><enum>(1)</enum><text display-inline="yes-display-inline">physicians are in the best position to
			 determine which medications are most appropriate for their patients;</text>
			</paragraph><paragraph id="HE45936526F6A4CB6B6E2E82D9BEECF32"><enum>(2)</enum><text display-inline="yes-display-inline">the Food and Drug Administration (FDA)
			 should respect the physician-patient relationship; and</text>
			</paragraph><paragraph id="H3BE7DC4C5DA04303924F8E593E9720AE"><enum>(3)</enum><text>the FDA should
			 reverse its policy that aims to eliminate patients’ access to compounded
			 medications containing estriol that their physicians prescribe for them.</text>
			</paragraph></section></resolution-body>
</resolution>


