Experiences with

Adoport

Anyone taking Envarsus after being on Adoport after liver transplant and had any side effects.

Had liver transplant 8yrs ago, taking 1.5mg of adoport and mofetil am & pm but the doctors want me to put me on Envarus but don't know why, but they have said that my kidneys are not has good has they should. Any replies would be great.

I had a liver transplant in 2016 now last few years health isn't going great, and Dr wants to change my adoport to envarus, but my story is long. But just for now does envarus stop bad headaches, cause weight gain. Plus suffer low sodium levels and type 3c diabetic. That's me for now

I had a t/plant just over 5yrs ago through pbc I've been doing fine a few little things but not really bad now the consultant is changing tabs from traclamus to adoport just wondering if anyone out there has had this happen to them and if so did you have any side effects

Kidneys now struggling with Adoport. Level reduced & yesterday told I’m going through bout of rejection but can’t increase Adoport due to kidneys. So, now going to duo suppression with MMF. Read so many awful side effects. Sickness, diarrhoea, hair loss.

I’m on Immuran ( Azathioprine) and Adoport ( Tacro) and have diarrhoea that isn’t unbearable but would be nice if I didn’t have it. Sore co sultans today who said he’d like it not to be there , and is thinking if a solution …. Anyone any sugg

I’m on Immuran ( Azathioprine) and Adoport ( Tacro) and have diarrhoea that isn’t unbearable but would be nice if I didn’t have it. Saw my consultant today who said he’d like it not to be there , and is thinking of a solution …. Anyone any suggestions .

My partner is taking Adoport after a transplant 5 years ago. He has had both Pfizer doses & thought he was quite safe. After reading said post I am now worried that he should be continuing to take extra precautions . If this is the case why hasn't his medical team advised him of this?

Others that i have met on the liver unit that were transplanted around the same time as me, December 2019, or later are prescribed Prograf and Adoport, both slow release. Curious to know why? Many thanks.

Does anybody know what the average dose is of adoport post transplant ?

Hi there everyone 👋

Hi, I take 5 mg prednisolone and 250mg MMF at around 7.00 after breakfast and 6mg Tacro at 9.0 am. Around 11.00 am I’m wiped out, interval shakes and trembles ... nearly 1 year post transplant . This is a recent thing and I’ve just had Tacro reduced from 7mg to 6mg in last month. Any suggestions

I feel fine apart from constant headaches which they had hoped that reducing my Adoport would sort out.

I just accidentally took my tomorrow's anti-rejection medicines (adoport , prednisolone) 7 hours early (instead of my vitamins) I plan to take next scheduled dose 14 hours later (instead of 12) , and each thereafter one hour later until back on schedule . . .

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.

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

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).

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.

Does adoport cause memory loss. Please help

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 .