| Re: Lotronex?
Since Lotronex is back (like a bad dream) I feel the need to share my experience with the drug. I've had IBS issues for years, and it was so bad that I could never guess when it would hit, and had more than my share of embarrassing situations.
So when I first started on the drug, I thought it was fantastic. As my symptoms improved, I went to one pill every other day. I never realized just what the relative freedom (I would still get the occasional flare up, but not like before) cost me.
The drug was pulled from the market, but I had continued to take my remaining meds in what I thought was a very moderate schedule to maintain (one pill every three days). I still ended up with an impacted bowel. After that, the drug disappeared from my shelf.
Since then, with Weight Watchers, cycling and walking, I've dropped a fair amount of poundage (and this is also post cervical spinal surgery, folks) and try very hard to keep up the fiber intake. I still need to take something like Loperamide on occasion to still my bowels, but I would never suggest anyone take Lotronex after what I went through. What started out as a godsend ended up a nightmare.
I think doctors just push the current "in" pill, regardless of the cost to patients in money or health. I just had a nurse practioner prescribe Effexor (an antidepressant) for my incessant hot flashes. She gave me samples, and though the drug was never approved for that use I tried them. Ended up with nausea and cramping that convinced me I am never filling the script.
I am beginning to subscribe to the Public Citizen creed of not using any drug that hasn't been on the market for at least 7 years. I'm tired of feeling like Big Pharma's guinea pig. As for Lotronex, my advice is RUN AWAY.
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Nancy D-ACDF 6/02, bladder suspension 12/06, sarcoidosis 10/07
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