Search
Search
About
Log in
Join
Experiences with
Tacrolimus
Posts
Communities
237 public posts
Filter results
Tacrolimus
Hi anyone on this drug? I have started it this week. Just wondered anyone on it and side effects?
Hi anyone on this drug? I have started it this week. Just wondered anyone on it and side effects?
Seashoreshanty
in
NRAS
6 years ago
Treatments for C3G
These drugs include: o Glucocorticoids (corticosteroids, steroids) o Rituximab o Cyclophosphamide o Mycophenolate mofetil (MMF) o
Tacrolimus
o Sirolimus o Azathioprine
• Plasma exchange (plasmapheresis):
Plasma
These drugs include: o Glucocorticoids (corticosteroids, steroids) o Rituximab o Cyclophosphamide o Mycophenolate mofetil (MMF) o
Tacrolimus
o Sirolimus o Azathioprine
• Plasma exchange (plasmapheresis):
Plasma
DavidF_NKF
Administrator
in
C3 Glomerulopathy
6 years ago
HRT for early onset menopause caused by meds. I have SLE & Lupus Nephritis. Is this a recipe for flares, flares, flares or ???
Also discovered that I am allergic to Mycophenolate so... ...two cycles of 3 months each of cyclophosphamide, 2 yrs on
Tacrolimus
and 5 months of methotrexate, Iand finally I am sort of in remission. I remain on Plaquinel and 5mg of Pred, with occasional pulse doses of methylprednisone.
Also discovered that I am allergic to Mycophenolate so... ...two cycles of 3 months each of cyclophosphamide, 2 yrs on
Tacrolimus
and 5 months of methotrexate, Iand finally I am sort of in remission. I remain on Plaquinel and 5mg of Pred, with occasional pulse doses of methylprednisone.
lil_darling
in
LUpus Patients Understanding and Support
6 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
6months
that I started back at work after 3months albeit on a phased back but I’ve been full time for last 5 weeks for me personally I’d say the hardest part of this journey has been the medication after as it really hit me hard but over time they lower in strength and the body gets used to them am on 4mg of
Tacrolimus
that I started back at work after 3months albeit on a phased back but I’ve been full time for last 5 weeks for me personally I’d say the hardest part of this journey has been the medication after as it really hit me hard but over time they lower in strength and the body gets used to them am on 4mg of
Tacrolimus
1football
in
British Liver Trust
6 years ago
Great success with oral tacrolimus in 3 Hailey Hailey patients!
Recalcitrant Hailey-Hailey Disease Responds to Oral
Tacrolimus
and Botulinum Toxin Type A Cutis. 2015 December;96(6):E14-E16 Author(s): Monica Bedi, MD Andrea Lowery Taylor, MD
Recalcitrant Hailey-Hailey Disease Responds to Oral
Tacrolimus
and Botulinum Toxin Type A Cutis. 2015 December;96(6):E14-E16 Author(s): Monica Bedi, MD Andrea Lowery Taylor, MD
Dermatologist
in
Hailey-Hailey Disease Worldwide Support Community
6 years ago
20/20! Plus Paris centre closing 😢
GGT of 29, kidneys 91%, myfortic snd
tacrolimus
residues great. Fibroscan of 4.8. He said he gave me a 20/20. Next appointment in 3 months, 14.5 months post tx here in France. Only bad news is my tx centre is closing as they have too many in Paris area.
GGT of 29, kidneys 91%, myfortic snd
tacrolimus
residues great. Fibroscan of 4.8. He said he gave me a 20/20. Next appointment in 3 months, 14.5 months post tx here in France. Only bad news is my tx centre is closing as they have too many in Paris area.
Isabelle2
in
British Liver Trust
6 years ago
Antibiotics
Then on contacting my GP regarding my awareness of the drug interaction I had to spell out “
tacrolimus
” and my knowledge of the interaction. Sadly the GP was obviously not aware of my drug or my even taking it as it wasn’t on their drug list that I was taking this!
Then on contacting my GP regarding my awareness of the drug interaction I had to spell out “
tacrolimus
” and my knowledge of the interaction. Sadly the GP was obviously not aware of my drug or my even taking it as it wasn’t on their drug list that I was taking this!
Denise15
in
British Liver Trust
6 years ago
Treatment going ahead for antibody mediated rejection!!
So lady’s and gents, some may remember my post a few weeks ago about being treated with a form of dialysis for antibody mediated rejection, the docs decided to send me home and watch how I go with my
tacrolimus
levels being high, this has caused a bit of damage to my kidneys and my bloods are much worse
So lady’s and gents, some may remember my post a few weeks ago about being treated with a form of dialysis for antibody mediated rejection, the docs decided to send me home and watch how I go with my
tacrolimus
levels being high, this has caused a bit of damage to my kidneys and my bloods are much worse
littleleah86
in
British Liver Trust
6 years ago
Immune suppression mix
Is anyone else on Prograf (
Tacrolimus
) Mycophenalate Mofetil & Zentiva (Hydrochloroquine) recently added to the mix by my dermatologist? Just seems an awful lot. I have loads of other types of meds too. I hate to think of the chemical mix in my poor system. 😣 No wonder mozzies don't bite me 😂
Is anyone else on Prograf (
Tacrolimus
) Mycophenalate Mofetil & Zentiva (Hydrochloroquine) recently added to the mix by my dermatologist? Just seems an awful lot. I have loads of other types of meds too. I hate to think of the chemical mix in my poor system. 😣 No wonder mozzies don't bite me 😂
MandaM
in
LUPUS UK
6 years ago
Tacrolimus?
Now starting on
Tacrolimus
but worried about long term. Anyone else?
Now starting on
Tacrolimus
but worried about long term. Anyone else?
patient165
in
LUPUS UK
6 years ago
Hrdroxychloroquine
Im also on
Tacrolimus
and Mrcophenalte Mofetil for my Lupus and to protect my renal transplant. The chemist just gave me the cheapest Quinoric. I've just read on here that Quinoric is bad for lupus and for skin.
Im also on
Tacrolimus
and Mrcophenalte Mofetil for my Lupus and to protect my renal transplant. The chemist just gave me the cheapest Quinoric. I've just read on here that Quinoric is bad for lupus and for skin.
MandaM
in
LUPUS UK
6 years ago
Creatinine is 0.86 but protein in Urine found
I was told that my creatinine and
tacrolimus
numbers are great but they are concerned about protein in the urine. Has anyone experienced this before? May I ask how it unfolded or progressed from there? Thanks! ~Clarissa~
I was told that my creatinine and
tacrolimus
numbers are great but they are concerned about protein in the urine. Has anyone experienced this before? May I ask how it unfolded or progressed from there? Thanks! ~Clarissa~
ClarissaR_12032016
in
Kidney Transplant
6 years ago
Update
Hi every one and I hope everyone is doing much much better.my ppps is in sleeping mode probably so it’s all fine.i have mild eczema on my feet which is maintained with marigold/calendula balm very good results.i saw derm. for check up and was given protopic/
tacrolimus
in case of any flare up .does anyone
Hi every one and I hope everyone is doing much much better.my ppps is in sleeping mode probably so it’s all fine.i have mild eczema on my feet which is maintained with marigold/calendula balm very good results.i saw derm. for check up and was given protopic/
tacrolimus
in case of any flare up .does anyone
Tgdn
in
Beyond Psoriasis
7 years ago
Drugs to Avoid with CMT
Colchicine (extended use) Dapsone Didanosine (ddI) Dichloroacetate Disulfiram Gold salts Leflunomide Linezolid (extended use) Metronidazole/misonidazole (extended use) Nitrofurantoin Nitrous oxide (inhalation abuse or vitamin B12 deficiency) Perhexiline* Pyridoxine (high dose) Stavudine (d4T) Suramin
Tacrolimus
Colchicine (extended use) Dapsone Didanosine (ddI) Dichloroacetate Disulfiram Gold salts Leflunomide Linezolid (extended use) Metronidazole/misonidazole (extended use) Nitrofurantoin Nitrous oxide (inhalation abuse or vitamin B12 deficiency) Perhexiline* Pyridoxine (high dose) Stavudine (d4T) Suramin
Tacrolimus
Hidden
in
Charcot-Marie-Tooth UK
7 years ago
Reflecting on my RA journey.........
Was a year without meds’ with Rheumys blessing but commenced on
Tacrolimus
in March 2017 due to some bone erosion in little finger and a toe. My main problems with RA are teno-synovitis (inflammation of tendons and tendon sheaths) in my fingers and wrists (so not the typical presentation of RA).
Was a year without meds’ with Rheumys blessing but commenced on
Tacrolimus
in March 2017 due to some bone erosion in little finger and a toe. My main problems with RA are teno-synovitis (inflammation of tendons and tendon sheaths) in my fingers and wrists (so not the typical presentation of RA).
Braecoon
in
NRAS
7 years ago
Tacrolimus Test
How often should
Tacrolimus
level be checked?
How often should
Tacrolimus
level be checked?
Huzaif
in
Kidney Transplant
7 years ago
Update - in case anyone else is in a similar position!
I've been put on
tacrolimus
. Wondering if anyone else with hypo has had or tried this? I'll update in a month or so even if no one has, just in case it helps anyone else down the line. :)
I've been put on
tacrolimus
. Wondering if anyone else with hypo has had or tried this? I'll update in a month or so even if no one has, just in case it helps anyone else down the line. :)
brilliantbobbie
in
Thyroid UK
7 years ago
Tacrolimus for inflammatory arthritis
Has anyone had any experience of
Tacrolimus
? Thanks E
Has anyone had any experience of
Tacrolimus
? Thanks E
Elaine777
in
NRAS
7 years ago
Change of anti rejection meds
I am changing over my anti rejection drugs at next appt at beginning June and was just wondering if anyone is taking Envarsus (slow releasing
tacrolimus
) ? 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 am changing over my anti rejection drugs at next appt at beginning June and was just wondering if anyone is taking Envarsus (slow releasing
tacrolimus
) ? My transplant was 19 weeks ago and I was on adoport
tacrolimus
but get severe reaction to it with the tremors while in hospital.
nickiwj
in
British Liver Trust
7 years ago
Tacrolimus toxicity?
Has anyone experienced this? So the last time I went into hospital for clinic my level was 9. I could feel that it was too much because my tremors had returned. Recently I've been having a lot of anxiety attacks and continuous anxiety throughout the whole day with severe tremors. My GP practice is really
Has anyone experienced this? So the last time I went into hospital for clinic my level was 9. I could feel that it was too much because my tremors had returned. Recently I've been having a lot of anxiety attacks and continuous anxiety throughout the whole day with severe tremors. My GP practice is really
Jahida
in
British Liver Trust
8 years ago
1
...
9
10
11
12
Next page
10
Filter results
Clear filters
Posted in
All communities
Kidney Transplant
76 results
British Liver Trust
43 results
LUPUS UK
30 results
View top 10 communities
Sort by
Most Relevant
Newest