Guest guest Posted April 2, 2006 Report Share Posted April 2, 2006 Dear PROVE Members, The AAPS (Association of American Physicians and Surgeons) has asked for our members' immediate help to write the FDA (Food and Drug Administration) before the comment period closes at the end of the day on April 4th! One of the pharmaceutical companies that is also a major vaccine manufacturer (Wyeth) has filed a complaint with the FDA to prod the FDA to essentially stop compounding pharmacies from compounding natural hormone therapies for women because Wyeth doesn't like the competition this poses to their potentially toxic synthetic chemical hormones. While this does not directly relate to vaccines, we are sending it out for a couple of reasons: 1) AAPS publicly opposes mandatory vaccines and is a direct friend of PROVE having helped us numerous times with our legislative efforts and it is our turn to help them 2) This is just another example of a big bad vaccine manufacturer trying to corner people by limiting treatment options and force them to use their toxic products - they have to be stood up to by the public! Many organizations have gotten together asking their members to submit comments to the FDA to oppose these restrictions. Below are some sample comments and simple directions how to submit them by clicking on a link and cutting and pasting. In addition, if you are really interested in this topic, AAPS is also involved in this issue in the courts and has submitted an amicus brief IN THE UNITED STATES DISTRICT COURT WESTERN DISTRICT OF TEXAS MIDLAND-ODESSA DIVISION posted at: http://www.aapsonline.org/judicial/fda-amicus-305.pdf that you can read explaining why the federal government should leave regulation of compounding pharmacies to the states – the FDA is overstepping its bounds outside of their directive from Congress and needs to be reminded where their authority stops. Thank you! Dawn , PROVE ==================================================================== DRAFT COMMENTS: I oppose the " Citizens Complaint " filed by Wyeth Pharmaceutical with the FDA on October 16, 2005, because it would take away my right to choose my own medical treatments. The 2002 Women's Health Initiative (WHI) showed that Wyeth's products, Premarin and Prempro, caused a significant increase in breast cancer, blood clots to the lungs, heart attacks and strokes. Since then Wyeth has apparently seen a dramatic decline in the sales of these products, known as " counterfeit hormones. " Wyeth's financial reports, which are available online at www.wyeth.com, indicate the following significant decline in sales of Premarin Family products; 2002 - $2,072,000,000; 2003 - $1,275,000,000; 2004 - $880,000,000. This represents a 68% decline in sales of Premarin Family products between 2002 - 2004. Wyeth's profits have likewise declined; 2002 - $4,447,000,000; 2003 - $2,051,192,000; 2004 - $1,234,000,000, a 72% decline in profits. Apparently competition is working, as tens of thousands of women have forsaken Premarin family drugs for bio-identical hormones made by compounding pharmacies. Competition and choice in health care are good for patients. Wyeth doesn't like competition, and its " Complaint " is an attempt to get the FDA to shut down Wyeth's competitors: compounding pharmacies that sell natural hormones. To boost its effort, Wyeth enlists the support of medical societies whose leaders may be seeking funding from Wyeth. FDA, please listen to real patients for a change. We want more competition and more choice in our medical treatments. I urge you to reject Wyeth's " Complaint " and its attempt to restrict patients' rights to choose safe, effective and natural medical treatments. ======================================================= INSTRUCTIONS and NOTE: The comment filing period ends on April 4, 2006 at which time the FDA will make its decision. To stop Wyeth and the FDA we need at least 20,000 comments opposing the Wyeth complaint. So please write your comment online today! Please forward this information to any one who will support this effort. Go to: http://www.accessdata.fda.gov/scripts/oc/dockets/comments/commentsmain.cfm?EC_DO\ CUMENT_ID=794 & SUBTYP=NEXT & CID= & AGENCY=FDA (you may need to cut and paste the entire URL in 2 sections next to each other depending on if your browser cuts it in half) After entering the requested information (zip code, name, etc.), hit the continue button to get the comment screen. Comments can be up to 4,000 characters. Hit the continue button to get to the next screen, where attachments can be filed. Hit the button “save comments” to submit (doesn’t make sense, but I tried it with my comments and that's what you have to do). This only takes a few minutes and can make a difference! THANK YOU! ------------------------------------------------------------------- Dawn PROVE(Parents Requesting Open Vaccine Education) prove@... (email) http://vaccineinfo.net/ (web site) ------------------------------------------------------------------- PROVE provides information on vaccines, and immunization policies and practices that affect the children and adults of Texas. Our mission is to prevent vaccine injury and death and to promote and protect the right of every person to make informed independent vaccination decisions for themselves and their family. ------------------------------------------------------------------- This information is not to be construed as medical OR legal advice. ------------------------------------------------------------------- Subscribe to PROVE Email Updates: http://vaccineinfo.net/subscribe.htm Tell a Friend about PROVE: http://vaccineinfo.net/subscribe/friends.shtml ------------------------------------------------------------------- Removal from PROVE Email Updates: Click here: http://vaccineinfo.net/unsubscribe.htm You are currently subscribed as texas-autism-advocacyegroups .. ------------------------------------------------------------------- Quote Link to comment Share on other sites More sharing options...
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