Search
Log in
Join
Experiences with
Adalat LA
Posts
Communities
41 public posts
Filter results
Update on Nifedipine
Hi all, Thank you to everyone who responded to my previous post. Just to clarify it’s the Bayer Adalat Nifedipine that is no longer available. I’ve now been prescribed Coracten which is another brand of Nifedipine. They don,t do the 5mg ones so I’m on the 20mg moderate release so hopefully they will
Hi all, Thank you to everyone who responded to my previous post. Just to clarify it’s the Bayer Adalat Nifedipine that is no longer available. I’ve now been prescribed Coracten which is another brand of Nifedipine. They don,t do the 5mg ones so I’m on the 20mg moderate release so hopefully they will
Adalat retard
Please could anyone let me know if they are on
adalat
retard 20 mg I have been on
adalat
la
for a few years now the chemist can't get them , I feel very anxious and exhausted on these Meds l have no colour very pale , also muzzy headed .i also have underactive thyroid which is not helping .as my THS
Please could anyone let me know if they are on
adalat
retard 20 mg I have been on
adalat
la
for a few years now the chemist can't get them , I feel very anxious and exhausted on these Meds l have no colour very pale , also muzzy headed .i also have underactive thyroid which is not helping .as my THS
Adalat 20mg
Good afternoon, First time on this site and am asking a question on behalf of my husband if it is alright with all. He has Raynaulds together with arthritis and has been on Adalat 20 mg for a very long time for the Raynaulds, unfortunately our surgery is having problems getting anymore at this moment
Good afternoon, First time on this site and am asking a question on behalf of my husband if it is alright with all. He has Raynaulds together with arthritis and has been on Adalat 20 mg for a very long time for the Raynaulds, unfortunately our surgery is having problems getting anymore at this moment
Want to take advantage of all our features? Just log in!
Log in
or
Join
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.
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
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 -
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
Raynauds 😒
I have been taking Adalat Retard for my Raynauds for about 2years with no side effects. Last week I went to my rheumatologist I told her I was having a lot of pain in 3 of my fingers on my right hand she changed my medication from Adalat to Idipine MR 20 , since taking them I'm experiencing bad headaches
I have been taking Adalat Retard for my Raynauds for about 2years with no side effects. Last week I went to my rheumatologist I told her I was having a lot of pain in 3 of my fingers on my right hand she changed my medication from Adalat to Idipine MR 20 , since taking them I'm experiencing bad headaches
Drug availability
Hello all Just wondering if there's anyone who has also had problems getting nifedipine(Adalat) ?. It's such a common blood pressure pill that I'm surprised there are manufacture problems for it!. My GP surgery has put me on a substitute Adalat retard until they can get the original one again. Anyone
Hello all Just wondering if there's anyone who has also had problems getting nifedipine(Adalat) ?. It's such a common blood pressure pill that I'm surprised there are manufacture problems for it!. My GP surgery has put me on a substitute Adalat retard until they can get the original one again. Anyone
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
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
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
Should I be referred by GP?
Hello, I've suffered with Raynauds for almost 3 years now. I have been prescribed Adalat Retard by my GP. Recently my symptoms have gotten worse, both my feet are affected as are both hands. My hands are getting worse , very painful and turn from white fingers to a greyish black colour, this usually
Hello, I've suffered with Raynauds for almost 3 years now. I have been prescribed Adalat Retard by my GP. Recently my symptoms have gotten worse, both my feet are affected as are both hands. My hands are getting worse , very painful and turn from white fingers to a greyish black colour, this usually
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
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
Crest
I was diognosed with Crest Syndrome 2014 😒 My symptoms change every day. I'm not sure if it is Crest that is causing - hair loss - eyes stinging - painful fingers - pain in left thigh knee and ankle - severe fatigue- breathless- lots of problems with teeth (fillings ) dry mouth -bowel problems . I don't
I was diognosed with Crest Syndrome 2014 😒 My symptoms change every day. I'm not sure if it is Crest that is causing - hair loss - eyes stinging - painful fingers - pain in left thigh knee and ankle - severe fatigue- breathless- lots of problems with teeth (fillings ) dry mouth -bowel problems . I don't
Shocked by my very low thyroid TSH result. Help!
After reading posts on this forum I have, for the first time, requested a copy of my recent Thyroid function test results from my GP and I am shocked and confused. The shock comes from a Serum TSH reading of <0.01mu/L (0.27-4.2) and confusion that the unit measurement is mu/L rather than the unit mlU
After reading posts on this forum I have, for the first time, requested a copy of my recent Thyroid function test results from my GP and I am shocked and confused. The shock comes from a Serum TSH reading of <0.01mu/L (0.27-4.2) and confusion that the unit measurement is mu/L rather than the unit mlU
figlin
i have been given adalat 5 mg nifedipine for raynauds any comments from suffers and what are the side effects
i have been given adalat 5 mg nifedipine for raynauds any comments from suffers and what are the side effects
Dryness back
Hi not diagnosed yet but so far Raynaud's resting tachycardia chronic pancreatitis and all sjogrens symtoms. On plaqeunil and adalat. Felt a bit better since stating the plaqueil especially the dryness however all the dryness and especially the female dryness is back with a vengence. Any ideas was on
Hi not diagnosed yet but so far Raynaud's resting tachycardia chronic pancreatitis and all sjogrens symtoms. On plaqeunil and adalat. Felt a bit better since stating the plaqueil especially the dryness however all the dryness and especially the female dryness is back with a vengence. Any ideas was on
New to auto immune and a bit in awe of everyone's stories.
Misscarraiges ×3 in my twenties now fifty three. Rashes on and off for years.unbelievable fatigue on and off. Felt really sick for last six years started going to docs last two years. So far have chronic pancreatitis Raynaud's and resting tachycardia. All sjogrens dryness joint pain rashes worse in
Misscarraiges ×3 in my twenties now fifty three. Rashes on and off for years.unbelievable fatigue on and off. Felt really sick for last six years started going to docs last two years. So far have chronic pancreatitis Raynaud's and resting tachycardia. All sjogrens dryness joint pain rashes worse in
1
2
3
Next page
Filter results
Clear filters
Posted in
All communities
Scleroderma & Raynaud's UK (SRUK)
21 results
LUPUS UK
10 results
Thyroid UK
6 results
View more
Sort by
Most Relevant
Newest
