cellcept alternatives?

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Regular Member

Date Joined Dec 2005
Total Posts : 66
   Posted 10/1/2007 7:58 PM (GMT -6)   
It's been a long time since I've posted. 
Sorry if this question has already been addressed.
I just found out a bit ago, my RX for cellcept is going to cost over $171.00 and this is with insurance.  I have a 50% coinsurance for brand names.  Have any others experienced similar situations? And what did your rheumatologist recommend as alternatives?  I just can not afford that every month as a "maintenance"  medication.   I just can't believe the price. 
I hope you are all doing well.  For those going through rough times, warm hugs to you all. 

Veteran Member

Date Joined Mar 2006
Total Posts : 2570
   Posted 10/1/2007 9:16 PM (GMT -6)   
Wow, clogan, that's a real problem. Have you called your rheumy and asked her or him? I doubt if samples are available but maybe your doctor has a suggestion. Someone else here may have another idea. Please let us know if you find a solution to this. You won't believe how well pharmaceutical stocks are doing and I don't doubt that is partly because of the high prices of the drugs they manufacture. There is something wrong with the system and I'm sorry you're experiencing the effects of it.
Lupus, Sjogren's, osteoarthritis, fibro, renauds, restless leg, hiatal hernia, double vision, migraines.
cellcept, neurontin, prednisone, plaquenil, synthroid, triamterene, tramadol, actonel, tri-est, imitrex, cymbalta, multivitamin, calcium w vit D, fish oil, aspirin

Veteran Member

Date Joined Jan 2005
Total Posts : 8616
   Posted 10/2/2007 9:37 AM (GMT -6)   
Hi clogan,

Sorry you have such a gap in coverage for your meds. *phewwww!* That is rough.

Patty's idea of samples sounds like the best shot. And also her idea of asking about an alternative.

I don't know if it would be any help because you do have "some" insurance . . . but there is a list of web-sites that will help with meds for low-income households. My daughter has actually received free meds directly from the manufacturer . . . she just had to fill out forms. Anyway, the websites are listed in "Lupus Resources" topic (link included at the bottom of my signature).

Gosh . . . I hope you find some help with that. Don't be shy about contacting the manufacturer either. If you don't ask, they can't help!!


In His Grip

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UCTD, Hashimotos, Inflammatory Bowel, Inflammatory Arthritis

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