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Atenolol / Nifedipine
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Think I forgot my atenolol last night never done that before, just hoping I dont pay the price - doh !
Its my daughters wedding day today so here I am in my finery complete with big hat taking time out from the mayhem around me to relax. I think, in the madness surrounding me last night that I forgot to take my evening atenolol. I opted to risk missing a dose rather than risking doubling up. Not had
Its my daughters wedding day today so here I am in my finery complete with big hat taking time out from the mayhem around me to relax. I think, in the madness surrounding me last night that I forgot to take my evening atenolol. I opted to risk missing a dose rather than risking doubling up. Not had
meadfoot
in
AF Association
11 years ago
First step
Hi all I've finally been diagnosed as having Raynauds today after struggling to get a "routine" appointment with our GP. I guess I've always known I've got Raynauds but now its official. The doctor must also be pretty concerned as I've ben prescribed Nifedipine which I have to take three times a day
Hi all I've finally been diagnosed as having Raynauds today after struggling to get a "routine" appointment with our GP. I guess I've always known I've got Raynauds but now its official. The doctor must also be pretty concerned as I've ben prescribed Nifedipine which I have to take three times a day
Hidden
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Taking atenenol and Digoxin....
I have had persistent af for around 10 years, taking Digoxin,atenolol and warfarin, does anyone take digoxin and atenolol together , as I keep getting remarks from other doctors that it should not be taken together. I suffer from chronic fatigue on some days, wondering which drug is likely to be causing
I have had persistent af for around 10 years, taking Digoxin,atenolol and warfarin, does anyone take digoxin and atenolol together , as I keep getting remarks from other doctors that it should not be taken together. I suffer from chronic fatigue on some days, wondering which drug is likely to be causing
Mercman
in
AF Association
11 years ago
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Finally People who are like me
Hi everyone, I am new to this site and I am so grateful to Nicola Whitehill who told me about this site. I have suffered for years with Raynaud's but have only just found out I have it after my wonderful new GP finally listened and knew what was wrong right away. I am 29 years old at the moment and feel
Hi everyone, I am new to this site and I am so grateful to Nicola Whitehill who told me about this site. I have suffered for years with Raynaud's but have only just found out I have it after my wonderful new GP finally listened and knew what was wrong right away. I am 29 years old at the moment and feel
plum3010
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Intro by new reynards sufferer and IVF question
Hi all, My name is Dan and i am 39 and have just been diagnosed with primary reynards, I have it in my fingers only so far which went white especially outdoors and having visited my supportive doctor a few times I was prescribed nifedipine which did make the attacks less and for shorter duration
Hi all, My name is Dan and i am 39 and have just been diagnosed with primary reynards, I have it in my fingers only so far which went white especially outdoors and having visited my supportive doctor a few times I was prescribed nifedipine which did make the attacks less and for shorter duration
Hidden
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
****UPDATE 15/04/2013**** Diagnosed - official Raynauds sufferer, but can't thank my GP enough!
***UPDATED 15 APRIL 2013*** Thank you all for your comments. A quick update from Friday when I started taking the Nifedipine - amazing difference! As soon as I took the first tablet I could tell the difference, my feet became warm for a start off and my hands and nose have been
***UPDATED 15 APRIL 2013*** Thank you all for your comments. A quick update from Friday when I started taking the Nifedipine - amazing difference! As soon as I took the first tablet I could tell the difference, my feet became warm for a start off and my hands and nose have been
marshall-williams
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Rheumatologist had just recommended another session of Iloprost. Does anyone know the minimum time you need to come off nifedipine as it is
so very cold I dread not taking the nifedipine prior to going to hospital. I forgot to ask the Rheumatologist this question. In Oct I had gone blue and it certainly wasn't this cold. I have normal blood pressure.
so very cold I dread not taking the nifedipine prior to going to hospital. I forgot to ask the Rheumatologist this question. In Oct I had gone blue and it certainly wasn't this cold. I have normal blood pressure.
creditcrunchie
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Adalat retard instead of Nifedipine ?
I have been on Nifedipine three times a day for about two years for Raynaurds and had no side effects as far as I am aware, unless my lack of appitite or anxiety is one. But my doctor has told me I won't be able to continue with Nifedipine as it is no longer available, I have been given Adalat retard
I have been on Nifedipine three times a day for about two years for Raynaurds and had no side effects as far as I am aware, unless my lack of appitite or anxiety is one. But my doctor has told me I won't be able to continue with Nifedipine as it is no longer available, I have been given Adalat retard
Bernadette309
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Does anyone suffering from Raynauds and Scleroderma have headaches caused by the cold weather?
Since the arctic weather conditions that have been sweeping across the country I have been suffering from bad headaches......At first I thought I had a head cold......but I have noticed every time I leave the house in the bitter freezing cold I end up complaining of headache across my forehead, around
Since the arctic weather conditions that have been sweeping across the country I have been suffering from bad headaches......At first I thought I had a head cold......but I have noticed every time I leave the house in the bitter freezing cold I end up complaining of headache across my forehead, around
wartsandall
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Diltiazem...hello all..is there any1 taking this med..ive been on nifedipine my doc wants me to change to diltiazem is it okay to take??
fruitpastle
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
I have had Raynauds for 20 years and never taken medication (my choice) Raynauds really affecting me now.
G.P suggesting to repalce existing dose of Adalat 30mg with Nifedipine to use for my high blood pressure and the Raynauds . I have researched Nifedipine and is described as Adalat.. So I am rather confused. I do read blogs etc on this site so maybe someone could shine some light on my confusion.
G.P suggesting to repalce existing dose of Adalat 30mg with Nifedipine to use for my high blood pressure and the Raynauds . I have researched Nifedipine and is described as Adalat.. So I am rather confused. I do read blogs etc on this site so maybe someone could shine some light on my confusion.
babyblue
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Hi all, I have been on Nifedipine 30mg one a day for a few years now without a problem but recently after approx 3 hours of taking
it I start to feel jittery. I know its not sugar levels and wonder if it is a blood pressure drop from the tablets. Anyone else have this and why after years without a problem?
it I start to feel jittery. I know its not sugar levels and wonder if it is a blood pressure drop from the tablets. Anyone else have this and why after years without a problem?
newton
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
And the waiting continues..
Saw my favourite GP today. You know why she is my favourite? She actually turns away from her PC, moves closer to you and listens to what you want to say & asks you questions. Other GPs at the practice have a horrible habit of continually looking at their computer screen and click away as you try to
Saw my favourite GP today. You know why she is my favourite? She actually turns away from her PC, moves closer to you and listens to what you want to say & asks you questions. Other GPs at the practice have a horrible habit of continually looking at their computer screen and click away as you try to
tcogb
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Back to GP...again....
Still waiting for my appointment to come through since my referral to the Royal Free. Meanwhile it's so difficult to get to see a GP of my choice and I have to wait weeks sometimes so I give up and have an appointment with someone else which turns out to be a complete waste of time. Grrrr. I had a blister
Still waiting for my appointment to come through since my referral to the Royal Free. Meanwhile it's so difficult to get to see a GP of my choice and I have to wait weeks sometimes so I give up and have an appointment with someone else which turns out to be a complete waste of time. Grrrr. I had a blister
tcogb
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Joint pain - is it me? Please read and give me your views, am still awaiting def lupus diagnosis but I must say you have all know the answer
I get really achey cold feet, they throb and are freezing cold (I take nifedipine for the coldness), at night my elbows lock whilst im asleep but soom wakes me with excruitating pain I scream when trying to bend or straighten them, my finger joints are always hurting too, my knees, shoulders but not
I get really achey cold feet, they throb and are freezing cold (I take nifedipine for the coldness), at night my elbows lock whilst im asleep but soom wakes me with excruitating pain I scream when trying to bend or straighten them, my finger joints are always hurting too, my knees, shoulders but not
beckybooboo
in
LUPUS UK
11 years ago
I get Raynauds in my hands . I've tried Losartan but it made no difference and am wondering if nifedipine would help.
I read Sandycharlie's post and it seems a lot of people take it with success. What dose do you need to take and are there any side effects? Am 52 years old and get Raynauds all year round - usual symptoms - white fingers, pain and pins and needles etc. but fortunately no ulcers - any suggestions?
I read Sandycharlie's post and it seems a lot of people take it with success. What dose do you need to take and are there any side effects? Am 52 years old and get Raynauds all year round - usual symptoms - white fingers, pain and pins and needles etc. but fortunately no ulcers - any suggestions?
DeedeeP
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Skin rashes & large blister appearing overnight
After recent blood tests and years of various symptoms my GP has finally referred me to the Royal Free (just waiting for appointment to come through) after my Raynaud's has gone into overdrive and the recent blood test results (in conjunction with my clinical symptoms) indicate Mixed Connective Tissue
After recent blood tests and years of various symptoms my GP has finally referred me to the Royal Free (just waiting for appointment to come through) after my Raynaud's has gone into overdrive and the recent blood test results (in conjunction with my clinical symptoms) indicate Mixed Connective Tissue
tcogb
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Could these images be Livedo? (Sneddons, Antiphospholipid Syndrome (APS) & Livedo help!)
Hi there. Basically my question is, do the images below look like something that could be related to Sneddons, Antiphospholipid Syndrome or Livedo? Sorry to ask but I'm very confused with my symptoms! Pictures: *Hopefully link now working* https://plus.google.com/photos/110776790922857768864
Hi there. Basically my question is, do the images below look like something that could be related to Sneddons, Antiphospholipid Syndrome or Livedo? Sorry to ask but I'm very confused with my symptoms! Pictures: *Hopefully link now working* https://plus.google.com/photos/110776790922857768864
medsoph
in
LUPUS UK
11 years ago
nifedipine
been on this drug now for two wks, was ok at first but now feel terrible...hot sweats driving me made feel tired and the pain in me finger tips getting worse...going bk doc on Monday have to get another treatment......i have been keeping my hands warm as well as my body but still cold and in pain....
been on this drug now for two wks, was ok at first but now feel terrible...hot sweats driving me made feel tired and the pain in me finger tips getting worse...going bk doc on Monday have to get another treatment......i have been keeping my hands warm as well as my body but still cold and in pain....
sandycharlie
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
About to get confirmation that I am suffering from Raynauds
I am having a hard time typing this as the tips of my fingers are protesting at the pain and coldness. Tip of my nose too is starting to join in... See I normally sit with a hot water bottle at work when I'm having to be at the desk typing such that I alternate between typing and warming either the nose
I am having a hard time typing this as the tips of my fingers are protesting at the pain and coldness. Tip of my nose too is starting to join in... See I normally sit with a hot water bottle at work when I'm having to be at the desk typing such that I alternate between typing and warming either the nose
strained1
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
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