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Experiences with
Adoport
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Any decline in kidney function after changing from prograf to adoport
He was changed in the spring from prograf to
adoport
. Since then his kidney function seems to be declining. Has anyone else found this the case as well. He was perfectly fine before
He was changed in the spring from prograf to
adoport
. Since then his kidney function seems to be declining. Has anyone else found this the case as well. He was perfectly fine before
Adoport
Prograf used for immune suppressant but now been told I’ve to change to
Adoport
to save money. Cannot find any real info on
adoport
which is new product offered. I got hep c because government wanted to save money and very wary about these reasons being given for this change.
Prograf used for immune suppressant but now been told I’ve to change to
Adoport
to save money. Cannot find any real info on
adoport
which is new product offered. I got hep c because government wanted to save money and very wary about these reasons being given for this change.
Unexpected liver transplant due to unexplained liver failure
My biopsy was last month and although my alts were still deranged my
adoport
was reduced. Two weeks later and alt increased again so
adoport
was increased. At clinic today and if bloods dont improve I've to get another biopsy (im hoping the increase in
adoport
will hopefully sort bloods out).
My biopsy was last month and although my alts were still deranged my
adoport
was reduced. Two weeks later and alt increased again so
adoport
was increased. At clinic today and if bloods dont improve I've to get another biopsy (im hoping the increase in
adoport
will hopefully sort bloods out).
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Some really good news and some really bad news.
At the moment the only medication I take for my liver is 2mg of
Adoport
(tacrolimus) daily. As things are going so well I am to have my
Adoport
reduced again (all being well) at the next clinic in 3 months time.
At the moment the only medication I take for my liver is 2mg of
Adoport
(tacrolimus) daily. As things are going so well I am to have my
Adoport
reduced again (all being well) at the next clinic in 3 months time.
Memory loss
Does
adoport
cause memory loss. Please help
Does
adoport
cause memory loss. Please help
Steroids and BK virus
Six months after my 2nd kidney transplant I started rejecting and they discovered I had the BK virus so they took mr off MMF and kept me on
Adoport
and added Prednisolone which is now at 10mg per day and have been on this now for 18 months and have been told I will have to stay on this dose always .
Six months after my 2nd kidney transplant I started rejecting and they discovered I had the BK virus so they took mr off MMF and kept me on
Adoport
and added Prednisolone which is now at 10mg per day and have been on this now for 18 months and have been told I will have to stay on this dose always .
4 months post transplant and aching and breathless
I am on 75mg of Aza and 5mg of
Adoport
. Has anyone else suffered with aches( particularly neck ache) and/or breathlessness.
I am on 75mg of Aza and 5mg of
Adoport
. Has anyone else suffered with aches( particularly neck ache) and/or breathlessness.
Stressed
Im having to travel to the drs about 3 or 4 times a week theirs always a problem for instance i need 70
Adoport
for the week but the pharmacy can only give out 50 or100 because of the packaging but my dr only prescribes 50 at a tim.
Im having to travel to the drs about 3 or 4 times a week theirs always a problem for instance i need 70
Adoport
for the week but the pharmacy can only give out 50 or100 because of the packaging but my dr only prescribes 50 at a tim.
Change of anti rejection meds
My transplant was 19 weeks ago and I was on
adoport
tacrolimus but get severe reaction to it with the tremors while in hospital. I was weaned off, flushed and switched to ciclosporin. It was always decided I would switch back to tacrolimus once lots of the other drugs were out of my body i.e.
My transplant was 19 weeks ago and I was on
adoport
tacrolimus but get severe reaction to it with the tremors while in hospital. I was weaned off, flushed and switched to ciclosporin. It was always decided I would switch back to tacrolimus once lots of the other drugs were out of my body i.e.
4 months and feeling good 👍🏻
I am on ciclosporin and MMF (I was on
adoport
/tach) but had a very bad reaction to tach with the tremors and had to be weened off it while in hospital and switched to ciclosporin. I was wondering if anyone has experienced a bad rash whilst on the medication?
I am on ciclosporin and MMF (I was on
adoport
/tach) but had a very bad reaction to tach with the tremors and had to be weened off it while in hospital and switched to ciclosporin. I was wondering if anyone has experienced a bad rash whilst on the medication?
Me Again with more questions.!
Also his
Adoport
has to be increased. Just wondered if anyone else has been faced with this ? Probably me thinking the worst & I really won't know the full outcome 'til we go back next week. Thanks anyway.xx
Also his
Adoport
has to be increased. Just wondered if anyone else has been faced with this ? Probably me thinking the worst & I really won't know the full outcome 'til we go back next week. Thanks anyway.xx
How to reduce the drugs???
My
Adoport
was reduced from 3.5 x 2 to 1mg X 2 - & my creatinine finally broke the 200 barrier for the first time in 16 months since the transplant - and I felt great. My consultant just had to put it up again to 1.5 x 2 & it's probably coincidence, but I don't feel as great as a few weeks ago!
My
Adoport
was reduced from 3.5 x 2 to 1mg X 2 - & my creatinine finally broke the 200 barrier for the first time in 16 months since the transplant - and I felt great. My consultant just had to put it up again to 1.5 x 2 & it's probably coincidence, but I don't feel as great as a few weeks ago!
Adoport side effects
Hi, I am 11 weeks post transplant and have been having my dose reduced from 8mg x 2 a day from when I left hospital to 3mg & 2mg a day now as my tacro level has still not come down to the level that is best (8 - 10) as I understand, but I am now having really hot fingers that feel like they are burning
Hi, I am 11 weeks post transplant and have been having my dose reduced from 8mg x 2 a day from when I left hospital to 3mg & 2mg a day now as my tacro level has still not come down to the level that is best (8 - 10) as I understand, but I am now having really hot fingers that feel like they are burning
questions after transplant
hi everyone,had my transplant on 24/6/2013 since then my meds have been up an down,now on 6mg
adoport
,750 mycrophenelat,10 mg penniselone,,and i feel great but had my phone call today from transplant team,and they said my kidneys were struggling a bit and put my steroids up,and wonderered if anyone could
hi everyone,had my transplant on 24/6/2013 since then my meds have been up an down,now on 6mg
adoport
,750 mycrophenelat,10 mg penniselone,,and i feel great but had my phone call today from transplant team,and they said my kidneys were struggling a bit and put my steroids up,and wonderered if anyone could
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