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Adalat retard
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Hello I'm elprof7557
Have had Ltd scleroderma for 7 yrs.Have Raynaud's above all when passing from warm environment to cold one and if outside temp. dips below 10°C. Have 4 or 5 digital ulcers similar to very small razor blade cuts each winter.Am on adalat 30 in winter and 20 rest of year.
Have had Ltd scleroderma for 7 yrs.Have Raynaud's above all when passing from warm environment to cold one and if outside temp. dips below 10°C. Have 4 or 5 digital ulcers similar to very small razor blade cuts each winter.Am on adalat 30 in winter and 20 rest of year.
elprof7557
in
Scleroderma & Raynaud's UK (SRUK)
6 years ago
Long time since I posted.
Hi everyone. After being diagnosed exactly 2 years ago, following a few months of ups and downs my afib actually settled down. I was feeling really good, started pilates, walking and actually lost about a stone and a half. During the summer months I had a little blip when my blood pressure occasionally
Hi everyone. After being diagnosed exactly 2 years ago, following a few months of ups and downs my afib actually settled down. I was feeling really good, started pilates, walking and actually lost about a stone and a half. During the summer months I had a little blip when my blood pressure occasionally
Hidden
in
AF Association
6 years ago
Help
Can’t get
Adalat
retard
is any one els having a problem
Can’t get
Adalat
retard
is any one els having a problem
123-456-789
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
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Levodopa Medications and Vitamin B6
Introduction
Vitamin B6 is a cofactor in over 100 enzymatic reactions. In the process it is converted from the active form, principally P5P (pyridoxal-5-phosphate), to the inactive form, pyridoxine. An excess of pyridoxine is toxic because it occupies sites that require the active form. For this
Introduction
Vitamin B6 is a cofactor in over 100 enzymatic reactions. In the process it is converted from the active form, principally P5P (pyridoxal-5-phosphate), to the inactive form, pyridoxine. An excess of pyridoxine is toxic because it occupies sites that require the active form. For this
park_bear
in
Cure Parkinson's
7 years ago
Adalat 🤔
So I was on them for 8 months and no issues, was able to exercise and walk miles. Then developed headaches and doctor took me off them and said no one is on them now, there are better ones to take, was put on bisoprolol and can no longer take them. Advised by a different doctor to go back on adalat -
So I was on them for 8 months and no issues, was able to exercise and walk miles. Then developed headaches and doctor took me off them and said no one is on them now, there are better ones to take, was put on bisoprolol and can no longer take them. Advised by a different doctor to go back on adalat -
Hidden
in
British Heart Foundation
7 years ago
Raynauds 😒
I have been taking
Adalat
Retard
for my Raynauds for about 2years with no side effects.
I have been taking
Adalat
Retard
for my Raynauds for about 2years with no side effects.
Banker123
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Raynauds medication.
Hello, I hope this finds you all well. I started Adalat two weeks ago and have been mostly ok. I've had an increase in headaches, flushes and urination. Hoping with time on them things would improve. I take 5mg three times a day. The whitening of my fingers has indeed decreased, but the rate they go
Hello, I hope this finds you all well. I started Adalat two weeks ago and have been mostly ok. I've had an increase in headaches, flushes and urination. Hoping with time on them things would improve. I take 5mg three times a day. The whitening of my fingers has indeed decreased, but the rate they go
TiccingBat
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Drug availability
My GP surgery has put me on a substitute
Adalat
retard
until they can get the original one again. Anyone else on it and how do you find it good or bad?. Would love your experiences. Hope your all as well as possible. Many thanks MistyX
My GP surgery has put me on a substitute
Adalat
retard
until they can get the original one again. Anyone else on it and how do you find it good or bad?. Would love your experiences. Hope your all as well as possible. Many thanks MistyX
misty14
in
LUPUS UK
7 years ago
Steroid injections or treatment assessment?
I wanted to have some thoughts from you lovely people on here. I was diagnosed 3 years ago with RA and have been having Mxt 15mg weekly since. My RA has greatly improved since the early days but I still have a lot of flares and can't do many of the things I used to enjoy. A year ago my rheumatologist
I wanted to have some thoughts from you lovely people on here. I was diagnosed 3 years ago with RA and have been having Mxt 15mg weekly since. My RA has greatly improved since the early days but I still have a lot of flares and can't do many of the things I used to enjoy. A year ago my rheumatologist
Downtime
in
NRAS
7 years ago
Anyone tried or on any of these medications need some advice
Have received letter from my rheumatologist stating how my thermography showed significant peripheral vasospasm which is consistent with a diagnosis of primary raynauds.She has listed a few medicines if I want to try 1st is Adalat xl at 20 mg a day,or losartan at 25mg or fluoxetine at 20 mg daily. I
Have received letter from my rheumatologist stating how my thermography showed significant peripheral vasospasm which is consistent with a diagnosis of primary raynauds.She has listed a few medicines if I want to try 1st is Adalat xl at 20 mg a day,or losartan at 25mg or fluoxetine at 20 mg daily. I
littleones
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Anyone else have Raynauds in their 30's
I keep being told that Raynauds is very common but in older people. (Sorry not calling u all old!!). But I'm 33 and have got hit with severe Raynauds 9 months ago and no treatment is working. I have got Iloprost drip for 5 days which worked for 6 weeks, then Adalat 5, then Adalat 20 and now my Rheumatologist
I keep being told that Raynauds is very common but in older people. (Sorry not calling u all old!!). But I'm 33 and have got hit with severe Raynauds 9 months ago and no treatment is working. I have got Iloprost drip for 5 days which worked for 6 weeks, then Adalat 5, then Adalat 20 and now my Rheumatologist
mc_clean_david
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Getting help from GP? - what questions to ask?
Please can someone give me advice so I can help my mum. She is 84 years old and had her parathyroids out about 14 years ago and has really struggled with her health since. I think that my mum feels she doesn't have the knowledge or 'power' to challenge her GP's with their treatment of her condition
Please can someone give me advice so I can help my mum. She is 84 years old and had her parathyroids out about 14 years ago and has really struggled with her health since. I think that my mum feels she doesn't have the knowledge or 'power' to challenge her GP's with their treatment of her condition
piggyporkpie
in
Thyroid UK
7 years ago
Should I be referred by GP?
I have been prescribed
Adalat
Retard
by my GP. Recently my symptoms have gotten worse, both my feet are affected as are both hands.
I have been prescribed
Adalat
Retard
by my GP. Recently my symptoms have gotten worse, both my feet are affected as are both hands.
Debic75
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
Still no answers....I just don't care anymore
retard
20mg day,Statins 20mg day.
retard
20mg day,Statins 20mg day.
Danworg
in
Pain Concern
7 years ago
PSA treatment
Hi, I was diagnosed with seronegative R A 2 years ago. Initially prescribed 15mg Methotrexate and folic acid which was moderately successful. 8 months ago it seems that I probably have a form of Psa as I've had patches of psoriasis and it runs in my family as does R A. Although my rheumatologist didnt
Hi, I was diagnosed with seronegative R A 2 years ago. Initially prescribed 15mg Methotrexate and folic acid which was moderately successful. 8 months ago it seems that I probably have a form of Psa as I've had patches of psoriasis and it runs in my family as does R A. Although my rheumatologist didnt
Downtime
in
NRAS
7 years ago
Doing OK
Hi, as the title says I am actually doing o.k on my medication, Apixaban and Zemtard. They appear to be keeping things fairly well under control with only a few minor hic cups now and again. However there are a couple of things I would appreciate some advice with please if anyone can help. Have been
Hi, as the title says I am actually doing o.k on my medication, Apixaban and Zemtard. They appear to be keeping things fairly well under control with only a few minor hic cups now and again. However there are a couple of things I would appreciate some advice with please if anyone can help. Have been
Hidden
in
AF Association
7 years ago
My racing heart saga.
Hi all just in from work sorry it's late.Saw cardiologist today he can give me medication that shouldn't make my Raynaud's worse but won't until I have a repeat stress test and checking blood pressure at the same time.Also a heart monitor for 48 hours.😭 He wants to see what's going on.He also said the
Hi all just in from work sorry it's late.Saw cardiologist today he can give me medication that shouldn't make my Raynaud's worse but won't until I have a repeat stress test and checking blood pressure at the same time.Also a heart monitor for 48 hours.😭 He wants to see what's going on.He also said the
Circles
in
LUPUS UK
8 years ago
Crest
I'm on
Adalat
Retard
for Raynaud's should I be on any other meds ? TIA
I'm on
Adalat
Retard
for Raynaud's should I be on any other meds ? TIA
Banker123
in
Scleroderma & Raynaud's UK (SRUK)
8 years ago
Recently Diagnosed with Systemic Scleroderma.
Any help or advise please. I was admitted to hospital with shortness of breath & chest pain, after being unwell for the past 6 months. I spent 12 days in hospital where I had CAT scans, MRI, lung function, & many blood-tests, I received the diagnosis not knowing anything about the disease which I have
Any help or advise please. I was admitted to hospital with shortness of breath & chest pain, after being unwell for the past 6 months. I spent 12 days in hospital where I had CAT scans, MRI, lung function, & many blood-tests, I received the diagnosis not knowing anything about the disease which I have
GillSuffolk
in
Scleroderma & Raynaud's UK (SRUK)
8 years ago
Possible Psa diagnosis now
My original diagnosis was RA 18 months ago but MXT has never been very successful. I was in pain every day. The only thing that helped was NSAIDs but the doc said I shouldn't be taking them along with the MXT. The last appointment with rheumy I showed him what I thought was psoriasis on one leg . Very
My original diagnosis was RA 18 months ago but MXT has never been very successful. I was in pain every day. The only thing that helped was NSAIDs but the doc said I shouldn't be taking them along with the MXT. The last appointment with rheumy I showed him what I thought was psoriasis on one leg . Very
Downtime
in
NRAS
8 years ago
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