Guest guest Posted January 3, 2012 Report Share Posted January 3, 2012 Does anyone have any input? Carol, I was wondering if we could start the letter off like this;My name is Jeanie Ward and I would like to petition the FDA to require that ALL the Nations Neurologists, Gastorinterologist, Urologists, Nephrologists, Endocrinologists, Pharmacologists, Microbiologists hold a review on the subject of the safety and effectiveness of polyethylene glycol in pediatric and adult patients and the possibility of pulling the medication or black box warning. It appears that there are many parents who have told their medical professionals of their concerns but the medical professionals seem to stand behind the protocol of it being poorly absorbed. This protocol needs to be reevaluated as the number of adverse reactions and deaths are on the rise. If the protocol is incorrect, our own medical professionals will determine that the long list of side effects reported must be coming from some other underlying condition. In our investigation we've studied the FDA adverse reactions (FOIA AERS reporting system) for a decade and created a yahoo group titled, "Miralaxgroups@..." as a support group and to find others with similar stories, and enclosed is our findings................. Quote Link to comment Share on other sites More sharing options...
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