Fw: adverse reactions FDA FOIA AERS

[Guest guest]

There are 1,966 FDA adverse reactions now.......................they went up 563 reports since 2009. When it was prescribtion only, they went up around 100 per year, now that it went over the counter, it doubled just like my Physician said........................remember.............I started with 6 people in 2000. If this isn't happening, how could we have 2000 people who took the time to submit their adverse reaction to the FDA? Think about the people that don't take the time to submit or don't know how? A very smart woman once told me to take your number and X by 10,000 and there's your number. This is the calculation method used for census's......................I'll post them

soon.....................----- Forwarded Message ----To: "miralax " <miralax >Sent: Sat, May 28, 2011 10:00:54 AMSubject: adverse reactions FDA FOIA AERS

I resubmitted yesterday, it's costs me $67.00 for every submission and the price increases as the numbers increase. Should be here within the next two weeks. I was thinking about how this all transpired last night and it would take some digging to make exact, but this is how the PEG adverse reactions increased

They medical professional first started giving this medication to children in 1999, in 2000 there were 6 adverse reactions reported to the FDA

I resubmitted every 6 months for the first couple years.

6 - 2000

54

67

89

165

189

235

665

865

1403 - 2009

2011?

If you feel you or someone you know has had an adverse reaction to polyethylene glyco. Please call MedWatch at 1-800-FDA-1088 or contact www.fda.gov/medwatch to heighten their awareness.

According to our Medical Professionals, the protocol says that the molecule is too big and cannot be absorbed. If this were true, we wouldn't have even ONE person who submitted to the FDA OR even ONE person complaining of side affects on this group.

Thanks

Jeanie