Petition Opening statement 3 times is a charm!

[Guest guest]

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 from the market or adding a 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. Our own Primary Care Physicians seem to be unaware of what to do in this situation other than to tell us to contact the FDA.

These children are not receiving the correct medical attention if the medical professionals prescribing it to them are unaware of the side effects it's causing. This is my third attempt to petition the FDA with a correspondence letter from the FDA stating, "It needs more

research" In our investigation we've studied the FDA adverse reactions (FOIA AERS reporting system) with our Physician's, for a decade, and created a yahoo group titled, "Miralaxgroups@..." consisting of 1555 members as a support group and to find others with similar stories, and enclosed is our

findings.................