Tysabri msds
Common Questions and Answers about Tysabri msds
tysabri
I recently worked with an epoxy that I had thought was an MSDS Health rating 2, which means:
"Intense or continued exposure could cause temporary incapacitation or possible residual injury unless prompt medical attention is given."
The warnings on the package suggest to avoid eye/skin contact, avoid breathing vapors and to work in "adequate ventilation" (note that no one ever explains what this means).
http://www.atsdr.cdc.gov/toxfaqs/tf.asp?id=255&tid=47
~ Dr. Parks
This answer is not intended as and does not substitute for medical advice. The information presented in this posting is for patients’ education only. As always, I encourage you to see your personal physician for further evaluation of your individual case.
Hi I am not a doctor but I would think that there would be an MSDS sheet that would explain the dangers. You already know that everything you we eat breathe and put on the body has to be processed by the liver. I will try to find something. and come back.
They found out the reason people contracted PML was because they were taking Avonex/and the other MS medications with Tysabri. I think the Tysabri has given me a second chance at helping slow my disease progress, but with out it I would be on no MS medications to slow the disease. I did alot of research before I decided to start the medication and the one resource that helped me make my decision was reading the Tysabri diaries on line.
www.msrc.co.uk/index.cfm?
I have had MD for 18 years. Been on Avonex, Betaseron, Tysabri, and now Tecfidera. Unfortunately, I'm also on lots of other medications, mostly due to terrible central pain. My neurologist made me stop the Tysabri after 24 infusions because of safety concerns. I felt my overall best while on Tysabri and have asked him if and when I might be able to go back on the monthly infusions. He does not have an answer for me at this point.
Are any of you on Tysabri? My doctor has suggested that I consider starting Tysabri treatment. His neurology practice runs a TOUCH infusion center. I've been on Copaxone for four years and have just had my first flareup. My recent MRI shows progression of MS with T2 hyperintense white matter lesions in the pons of the brainstem and the frontal lobe. Several of the older lesions have increased in size. Five years ago I was on Avonex. I had multiple flare-ups the whole year on this med.
I would like some information/details from anyone who has had (or seen) the rash you can get from Tysabril and/or PML?? I have been on Tysabri 10 years so far without any major issues. I was outside after my treatment for 10 minutes or so. After taking my shirt off, my husband gasped and asked what was wrong with my back.
So now he wants to take me off of the Copaxone, I have been on for a month and a half, and put me on Tysabri. I started the application process and now waiting for them to call me and get the ball rolling on that. Now he mentioned that this is the top of the line MS medication so that does give me some relief.
P.S. I did test negetive for the JC Virus.
Any thoughts, experiences etc on this Tysabri??!!
They keep on telling me that all i was exposed to was general purpose oil, used in the vacuum pump of the GCMS. There was no extraction from the GCMS instrument. I looked up the MSDS for that chemical but my symtoms are not consitent with there findings.
I sent off a hair sample to the US for mineral analysis. It stated that i had high levels of tin. I know inorganic tin is more or less harmless, or is it?, but can organotin cause these type of symtoms?.
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