Hats symptoms and conditions

My Avelox experience has been hellish! I took 10 days of Avelox in the first part of May, 2009. Today is July 12.

By day 3 of taking this drug, I had severe welts all over my face, I tried to get an emergency appointment with my HMO doctor. He was on vacation. I had an emergency appointment with my HMO dermatologist, who gave me an alternative rosecea cream. (this WAS NOT rosecea.!)

Ever since I have taken this drug, my skin gets blotchy, itchy, swollen and extremely red. It begins one day, stays a second day and starts to subside the third day. It all happen again about a week later.

I've tried many different face sun tan lotions, as I have to be outside part of the day for my job. I do use hats and an umbrella. Any solution or similar experiences would be appreciated, if shared

J.F. , Manhattan Beach , CA

Oh yeah - another thing - a couple of weeks ago a friend was putting my hair up and she said, "do you realize you have a bald spot in the back of your head?" I have noticed hair falling out (especially when I'm cooking despite tying it back - ugh). Must go - time to go to eBay to shop for hats :)

I can agree with so many of you who've shared your experiences - for about a year I felt more like 'the old me' on Wellbutrin, but in the last six months I've become progressively more fuzzy-minded. It scares me that there are times that I worry that I won't be able to finish a coherent sentence... like I'm speaking in slow motion waiting for individual words to filter through the fog of my brain so that they can be spoken. OK, it's certainly not always like this - and so far only my husband seems to have noticed, but I dread muttering the wrong thing in a business setting. Perhaps worse than this, in the vanity that is our present reality, I've seen significant hair loss from the top of my head - my squeaking clean pate is SHINY in the mirror and I hate it!!! It's winter now, but I can't wear hats all the time, and I just don't happen to work in a 'fashion forward' industry where I might hope to make hats a trend for all to follow. I will be weaning myself off of Wellbutrin and looking into oral and topical arnica b/c I'm nervous about trying Rogaine and begging stuck with that regimen for the rest of my life. The women in my family all have lovely hair; I'm 40, not 80!!

I take Lamictal for seizures for 3 years. I had my first unexplained seizure at 25 and another 6 moths later. Both times I had drank heavily two nights in a row. After the second seizure I was put on the Lamictal. I was slowly ramped up to 100mg in the morning and 200mg at night. On occasion, I get horrible "poop pains" as I call them. It feels like my insides are being ripped apart. I can sit on the toilet and poop incredibly runny stool, then I have to wait up to 15 minutes for the second batch. The pain doesn't subside until the second batch but it is immediately gone. It usually only happens when I wake up in the middle of the night. I have tried to correlate it to foods that I have eaten and can't match anything up. I also have horrible short term memory. I sometimes tell the same person the same story twice and they will be like "you just told me that." Also, golfing is the best example. I have a hard time remembering my strokes. My long term memory is fine. As fair as hair loss, I was already on track to lose my hair before I was on the meds so I don't know if they made it any worse or if this is a natural progression. It seems somewhat rapid but I never loose it in quantities or clumps. I just notice it in my hats and beanies every once in a while. I also have a hard time falling asleep on occasion and if I wake up in the middle of the night I have troubles falling back asleep as well. The bottom line is that this drug WORKS. I can live with the side affects cause they are random and not that often. I am a volunteer Fireman and cannot risk loosing that again so I am too hestitant to change meds as the doctor said Lamictal has the least side affects of the seizure drugs.

I have had EXTREME hair loss and I did not know what from. I never thought it was my advair. I checked all of my other medications and only one other one said there was a possibility of hair loss (PREVACID) so I went off of that but my hair was still falling out. I have been so desperate that I scheduled and appointment to see a dermatologist tomorrow. Today I happened to google "advair/hair loss" and I cannot believe all of the articles that came up with people expressing the correlation.
I have been so depressed from this hair loss. I had the thickest, shiniest hair and now I barely have a pony tail. I wear hats all of the time because I am embarrassed.It has been totally devastating.
What I need to know is which other asthma medication will NOT cause hair loss so I can switch? Too bad I just dropped $100 on a 3-month supply of Advair and now cannot use it.
Also, those of you who went off the Advair, how long did it take for you to experience hair growth or it not falling out?

I read these posts and regarding my being quoted as saying that it is unclear whether there are leukotriene receptors in the brain, that isn't true, there are leukotriene receptors in the brain and the relationship between neural systems involved in inflammation and mood is well established. I don't think the misquote was deliberate, I wasnt that definitive when I commented to the reporter on the 'breaking' story (she called me because I had just blogged about it and I updated the blog after I got off the phone). There are a number of parallels with other drugs used to treat medical conditions that have been associated with psychiatric side effects, you can follow the links from the March 27 post "If they dont kill us they will drive us crazy" at
http://www.beforeyoutakethatpill.com/blog.html

Doug Bremner MD