Newly diagnosed - azathioprine help
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I was diagnosed with UC in December following severe food poisoning from chicken in summer last year.
I've had several different cameras - most recently colonoscopy the weekend before easter. Come easter weekend I was away for the weekend and had a flare up. Having no idea what to do (any suggestions if this happens would be grateful).
I went to hospital and my nurse said she wants to change my medication from pentasa to azathioprine. I've read leaflets and it looks like last resort before surgery and quite an aggressive drug. Reading about it suggest side effects have made people very ill.
Does anyone have experience of azathioprine?
As all this is new to me any advise would be grateful.
Thanks Carrie
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tony33900 carrie303
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carrie303 tony33900
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kate21881 carrie303
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mzmcgee1231 carrie303
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sillip2007 carrie303
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Like most of the replies on here I also agree that AZA tends to presribed when other drugs are not working. I am on 150mg of AZA and have been since Jan 2014. I still have flare ups and am then placed on steroids, which like James mentioned, are great as you do feel like you get part of your life back.
Aza is definitely not a replacement for steroids. I started on enemas and steroids when I flared up and then but have now become drug dependant. (I did not have any side effects from the Aza, just the steroids which gave me bad heartburn). I have had infliximab which is given when you are exhausting most drug options and no longer repsonding to them. This happens to a few people but most patients seem to be okay on Aza and symptoms start to be alleviated.
I hope Aza works for you. You do have regular blood tests so you are kept an eye on, so I would not worry too much.
Good luck