Kenalog and adverse events

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK THIS LINK AND COMPLETE THE FORM: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities.

Here's my case: I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is over a year later and the indent remains and continues to cause discomfort. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch and strongly urge others to report their adverse event to the FDA (see link above).

I was having Kenalog injections into my knee. On the ninth injection within a years time,with a few Aristospan injections in between, my knee to my foot blew up. Tripled in size, and the skin was bright red with purple marks all over the skin from my upper shin to the ankle bone. I had a big depression in the shin too, which I can not figure out because the injection was into my knee.
I went to my GP who sent me to the ER to rule out a blood clot-ultrasound.
NO blood clot. I was given no medication, nothing, and it was very painful.
Actually, I saw three doctors and not one of them seemed to care. One doctor said, "Steroids are Powerful Drugs" I do not know if this reaction was do to an infection, some side effect, I have no idea. The swelling eventually went down within six months=long time. I still get purple round marks on the skin at the shin, and sometimes my ankle swells. The skin gets red and white marks mixed into the already rash looking skin.
I asked many times what the cause was to this all, and it was like no doctor would say anything negative about the doctor that gave me the injection.
I also discovered that Kenalog is used off label for Epidural Steroid Injections and can cause Meningitis, Arachnoiditis, bowel and bladder dysfunction and more adverse events, because neurotoxins are added to the steroid to make the compound that is injected into the epidural space. Asking other people if their doctor ever told them the drug name they were getting injected by their doctor before this procedure and each and all said "NO."
This is also true for the drugs Depomedrol and Celestone Soluspan. All three drugs are used off label for epidural injections. Neurotoxins do not belong in the spine! If one gets a dura puncture-FOR GET IT!

Post your side effects at www.fda.gov/medwatch, on the Food and Drug Administration's (FDA) MedWatch site, which is under FDA's Center for Drug Evaluation and Research (CDER). According to someone from that office, CDER is supposed to report adverse events to their Drug Safety Oversight Board, and then the Board is supposed to decide if the drug should be pulled. FDA can claim they do not know about the claims if no one calls them. See staff below:

Steven Galson
Deputy Director
(301) 594-5400

Randy Levin
(301) 824-7784

Safety Policy and Communication Staff can be reached at (301) 594-0104. Staff include:

Paul Seligman
Norman Marks of MedWatch
Susan Cummins of Drug Safety Oversight Board