If you would like to report the adverse effects you experienced
after Uterine Artery Embolization to the HERS Foundation and FDA
please fill out the following form:
* If you would like to know the name and manufacturer of the product
used to occlude your uterine arteries, (i.e. Polyvinyl alcohol particles
manufactured by Cook) go to the medical records department in the
hospital in which the surgery was performed and ask for an itemized
copy of your bill.
The adverse effects reported by women build our database
of the consequences of this surgery. All information is strictly
confidential unless you have specifically asked us to provide your
information to FDA.