• Welcome to Crohn's Forum, a support group for people with all forms of IBD. While this community is not a substitute for doctor's advice and we cannot treat or diagnose, we find being able to communicate with others who have IBD is invaluable as we navigate our struggles and celebrate our successes. We invite you to join us.

Mercaptopurine long term side effects

Hi all,

I am new to this forum. I have been on mercaptopurine for 10 years now 75mg daily. 18 months ago my specialist confirmed i was in remission i am 44.

I have 2 questions.1 is anyone concerned about the long term side effects of taking this drug? Ie liver damage.
And 2 how do people deal with the fatigue?

Any feed back would be great. Thank you eldrickw
 
Welcome. Congratulations for being in remission. As far as fatigue, have you had your blood levels checked? If not, you may want to ask your doctor to have them checked. I have never been on mercaptoptopurine myself but there will be others on here who have been.
 
Hi I Was on mercaptopurine for 3 years, when in February of this year my consultant informed me that you should not be taking mercaptopurine for this long continuously, so I weaned myself off gradually. After a few months without it I started getting flare up to the extent where I now have multiple fissures and tears. I am now back on mercaptopurine and on a course of steroids which after 3 weeks don't seem to be helping much. I try to carry on working but when I get home all I can do is lie on settee or go to bed as I am exhausted.
 
Hi I Was on mercaptopurine for 3 years, when in February of this year my consultant informed me that you should not be taking mercaptopurine for this long continuously, so I weaned myself off gradually. After a few months without it I started getting flare up to the extent where I now have multiple fissures and tears. I am now back on mercaptopurine and on a course of steroids which after 3 weeks don't seem to be helping much. I try to carry on working but when I get home all I can do is lie on settee or go to bed as I am exhausted.
I hope you feel better soon.
 
Welcome. Congratulations for being in remission. As far as fatigue, have you had your blood levels checked? If not, you may want to ask your doctor to have them checked. I have never been on mercaptoptopurine myself but there will be others on here who have been.
Thank you for your reply. I get my bloods checked every 3 months but spoke to my Dr and next time will do a more extensive cgeck up.
Cheers
 
Hi I Was on mercaptopurine for 3 years, when in February of this year my consultant informed me that you should not be taking mercaptopurine for this long continuously, so I weaned myself off gradually. After a few months without it I started getting flare up to the extent where I now have multiple fissures and tears. I am now back on mercaptopurine and on a course of steroids which after 3 weeks don't seem to be helping much. I try to carry on working but when I get home all I can do is lie on settee or go to bed as I am exhausted.
Hi and thank you for your story. I was worried about liver damage but i do not want to go back to flare ups again. I will kepp your information in mind. Thank you.
Cheers.
 
Top