Welcome to Medications.com

I was diagnosed with Optic Neuritis in my left eye, at the time o...

Posted at 1:20 PM on Nov 28, 2008 by spammy08, #36935
I was diagnosed with Optic Neuritis in my left eye, at the time of diagnosis, I felt fine. Had an MRI to check for lesions on the brain, there were none. I was put on IV solu-medrol for 3 days, then 90 mg of prednisone for one week, with a rapid taper the second week. 6 days into the prednisone, I started have shortness of breath, etc. Went to the ER and my white count was 22,000. Had bronchitis and the beginnings of pneumonia. Because of the breathing problems, I only did 2 days of taper (doctor's advice). I have lost site completely in the left eye and now I have blurred vision in my right eye. Extreme fatigue, and a mental fog I just can't explain. A "twitch" in my left left hand and muscle weakness. I just don't feel "right". How long does it take for this drug to leave your system? Has anyone had a similar experience? My eye doctor was considering another round of prednisone for the optic neuritis, but I am not so sure I can survive it.
REPLY TO THIS POSTING | Private Message me | Add as friend | Flag as inappropriate
 
Reply 11 months ago on Nov 29, 2008 by 47140, #14905

This is my opinion-- You must be sure the diagnosis is correct and it is indeed Optic Neuritis. Next, research Prednisone. This is not a drug to fool around with.

Private Message me | Add as friend | Flag as inappropriate
 
Reply 11 months ago on Nov 29, 2008 by 47140, #14906

I want to stress the importance of a correct diagnosis. I have had medical experts tell me that optic neuritis is a condition basically without treatment and in general that is how steroids are used. Please contact me if more info is needed.

Private Message me | Add as friend | Flag as inappropriate
 
Reply 11 months ago on Nov 30, 2008 by cosmiccutie, #14915

I am so glad I decided to research this drug before continuing using it. Last night in the emergency room, I was given 40 mg of predisone for a severe skin disorder called Lichen Planus. After reading this and other posts, I will not be taking anymore. So far the only side effect I have had is a sense of well being. Sorry to hear about all the terrible side effects you and the others have been going through. I do hope things will get better soon. Good luck.

Private Message me | Add as friend | Flag as inappropriate

Make a reply to this posting:

Type your reply to this side effect post:


Medical advice disclaimer
© 2002-2007, Skylabs Inc.  |  About Us  |  Disclaimer/Terms of Use  |  Advertise  |  Contact Us  |  Site Map  |  Developed by: W3matter.com | Sleep Apnea