Angiotensin II Receptor Blockers :: Losartan - Joints Hurt
May 8, 2015
I am 60 yr old been diagnosed with high blood pressure ,doctor has given me losartan 12.5mg been taking them for 2 month's now, felt dizzy at first so I take them at night instead of morning I feel tired all the time and my joints hurt everyday especially my knees I used to walk my dogs daily , out for at least an hour now after walking for 15 mins I ache so badly don't seem to have much energy these day's is it the tablet's has anyone else felt like this
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Does anyone out there on Losartan (25mg) have a very dry mouth caused by lack of saliva? Also a feeling that the skin was coming off the inside of my mouth. My dentist says this may be caused by Losartan and it might result in gum disease. Anybody with the same symptoms?
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Was originally on 2 mg candesartan and moved doctors and when my blood pressure was checked it was high 146 over 110 which is the highest i've seen it so been put on 50mg losartan and i've been getting bad headaches is this a side effect am back seeing the nurse next week and i intend to mention this and see if they can change my medication
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I was originally taking ramipril but as I was experiencing uncontrollable coughing fits and itchy hands and feet, I am now taking Losartan.
Thankfully the cough has gone, but I still have slightly itchy hands. Does anyone else experience this?
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Have changed from Amlodipine to Losartan as they gave me swollen ankles and dizziness, have been on Losartan for 4 month but have many side affects. I have a constant muzzy feeling, transient dizziness and a queasy feeling all of which come and go but feel extremely tired when experiencing the feeling. I get the feeling my GP is fed up as I keep getting side effects . Does anyone else get these side effects?
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I am on Losartan for about 3 years and i am 63 years old I had to cut my medication in half because of the very bad side effects I went to the dr and ask him to change my medication because of the side effect he just told me to continue with 25mg instead of 50mg but when I had my blood result my blood sugar was pretty high and i'm not diabetic and nobody in my family are and I have the reputation to eat healthy more the everybody and I exercise I read on the internet that losartan can affect your blood sugar is it true because I'm thinking to change to dr.
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Hi my GP has just prescribed Losartan, after 3 days I am experiencing headaches , tension in face and jaw ache,
He suggested I stop for 3 days but said it was not side effects of the drug but my fibromyalgia condition. I'm not convinced as after 3 days without the drug I began to feel better.
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Hi I'm female 60 years old recently put on meds for high BP. I also have Fibromyalgia I mention that because it seems whatever tablets I'm given for BP (,Losartan being the 4th tablet) my joint and muscle pain become some bad I struggle to even do the housework and where I used to walk the dog's for at least an hour I can only manage 15 mins also I could walk round the shops for hour's now can't wait to get my weekly food shop done and get back home . My BP when I take it at home is anything from 116/71 ,to 133/77 on the meds , I have stopped taking Losartan for 2 week's now and BP is 136/76 to 149/74 when I go to the docs the readings are always high 162/84 for example. I really can't cope with the pain when taking these tablet's especially in my knees has anyone else experienced this , is there even a tablet for BP that doesn't make you feel ill .I have stopped these but not told the doc yet as can't face being put on another tablet I am feeling so well at the moment I take my BP daily it's usually 140 something over 82 is that really too high for my age.
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I am taking beta blockers. I have had a heart attack couple of days ago and I guess beta blockers I have to take as prevention. No one needs a heart attack, right? But, even in that short period of time, some side effects occurred, I had trouble sleeping. Although, I have to admit that I am not sure if this was because of the stress or because of the beta blocker.
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My experienced with ramipril for high blood pressure was that I had a very bad cough, not a dry cough, but a very congested cough which I suffered for about three months. Although I returned to the Doctor after having the cough for about 6 weeks they still didn't take me off the ramipril - but gave me antibiotics this was despite me saying I felt it might be the ramipril - sometimes they don't listen. I was told to come back after 3 weeks which I did the anti biotics has done nothing - what a surprise and I was beginning to think I had developed some sort of severe Lung problem. I could hardly speak without coughing, I could not sleep for coughing, my chest felt like it would burst, I was physically sick from coughing. Doctor then thought it may be a good idea to stop taking ramipril I am now taking Atenolol - watch this space.
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I was diagnosed with overactive thyroid 6 weeks ago, i was put on carbimazole and beta blockers. Initially i felt loads better and could actually function nearly as normal. the beta blockers were stopped after 4 weeks. after check up 3 days ago they have stopped the carbimazole completely and put me back on beta blockers as my thyroid is nearly underactive but my heart rate is far too high. Im now back to how i was before. tired, giddy, nauseous, sweating and shaking. I have a 15 month old son and struggling to function. Can this be good just stopping carbimazole just like that i m back to square one!
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I was taking 100mg for 3 years and had tremendous weight gain and began getting numb toes and fingers. My GP reduced the dose to 50 mg and within the first month I lost a whole kilo and my bp dropped. Now trying to stop smoking too and with Zyban, and sleeping tabs I am getting night sweats and feel generally wiped out, so with gp's consent we are dropping the Atenolol totally and see what happens. Good luck to all out there who have found problems and I hope you find suitable solutions without the side effects.
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How my joints are left after having reactive arthritis
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For about 7 or 8 months I have been cracking the joints and knuckles in my fingers. Now when I lower my middle finger on my left hand there is a little pop and the finger moves down a bit. And since i had also been cracking my toes the toes on my right foot make a pop too. I am kinda worried because I am only 13.
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I had unprotected sex with girl Unknown her status , then after 85 days i had AB test Cobas roche , and it was Negative , then i had some problems lymph nodes in neck and fatigue and joints pain , then all gone away But now red pimples start on My arms and neck and chest.
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My symptoms are severe pain in joints and sometimes muscles that always come with high fever, sore throat and weird cough (small but forced cough) a salmon colored rash and weakness in my joints. The pain is so bad that I scream. I am unable to care for myself. I am so stiff for hours. The pain has progressed throughout the year. I am at a loss. I live in Idaho and my rheumatologist is sending me to Salt Lake City Utah because they have a university hospital with more specialist. I swear to her that I have Stills Disease but she sais I have the symptoms but not necessarily all of the blood results to match.
My cbc always shows an infection, I am always slightly anemic but ferritin is good, not low nor high.
Here is my recent lab work. This is how desperate I am
C-REACTIVE PROTEIN 60
UNITS = ML/MIN/1.73m2
If patient is African-American, multiply result by 1.21.
ALBUMIN 3.5 - 5.0 GM/DL 3.5
AST(SGOT) 15 - 46 U/L 37 45
TOTAL BILIRUBIN 0.2 - 1.3 MG/DL 0.3
CALCIUM 8.4 - 10.6 MG/DL 8.8
PROTEIN TOTAL 6.3 - 8.2 GM/DL 6.1
ALK PHOS 38 - 126 U/L 37 78
ALT(SGPT) 9 - 52 U/L 37 50
ANION GAP 7 - 15 MMOL/L 8
CK 30 - 135 U/L 37 24
I do not like being on the prednisone because of the side effects but I can not handle the non stop pain when I don't have it. Such a little 5 mg dose saves my life. The pain is so bad that all I can do is pray to pass out. I can not take pain pills because they cause severe depression.
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I am due to have an op on my hallux valgus next week, the mtp joint us going to be fused, I do a lot of walking & am worried I will not be able to keep this up once I've recovered. I walk up to 8-10 miles, anyone any experience of this?
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I got diagnosed with ibs earlier this year, at the beginning it was dreadful. Their was no clear signs for me because one day the food that was giving me pains wouldn't the day after so it was all confusing. I tried healthy eating but that just made me worse so now I eat like I normally would but just lesser portions and I feel alright most of the time. Still haven't got used to my bowel movements yet, sometimes I'm really uncomfortable but this happens about twice a week now which I can handle if I take my buscopan regularly. Since I got diagnosed, my muscles and joints have been really weird and I read some information about ibs and the different symptoms and it did say about weakness of joints and muscles. I tore the ligaments in my big toe in both feet 3 times without even doing anything to them. Then I lost my balance in the shower because of my ankle pain and I sprained my wrist and that just feels weak all the time. Then Saturday last week, I was out with mates and my leg just gave way from under me, I was only standing there and it felt like it was cramp in my knee. Got rushed to the hospital and they sent me to the fracture clinic on Thursday, thank god it was just torn ligaments in my knee but the pain was so bad. I was just wondering has anyone else had an increase in muscle/joint/bone weakness since being diagnosed with ibs? I really need to find someone else to relate to with this because I'm only 20 years of age and I don't think my bones and stuff should be this weak.
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I've just had a blood test which showed vitamin D deficiency. I have very little energy, my muscles and joints are stiff and painful, and my feet really hurt when I try to walk any distance. I've always been very fit and active so I'm wondering whether I should push myself to exercise even though I don't feel like it or whether I risk making my condition worse by pushing myself too hard. I'm taking vitamin D supplements but I've seen from other posts on this forum that it might take months to get better. I find swimming less painful than walking or cycling so maybe that is okay?
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Was put on 80mg atorvastatin following a heart attack last October. Have had constant pain and muscle stiffness in both shoulders and cannot fully extend both arms. The cardiac nurse suggested I come off them for 2 weeks last xmas to see and ALL the pain went! After seeing the doctor he advised me to continue with Atorvastatin "and see". After one week I was in agony again. I reduced the dose to 40mg a month ago and it made no difference. Other side effects I have are twitchy eyelids, on and off loose stools and tiredness. I saw a different GP today as I cannot carry on like this. He has told me to stop Atorvastatin and has arranged for me to have an extensive blood test next Wednesday. He did say that there are risks with Atorvastatin re muscle and joint problems, liver etc. SO I will see what the tests say and how I am off the Atorvastatin.
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I have been suffering really painful joints particularly in my feet and legs. I get a sharp burning sensation on top of my feet every so often - what could this be? Also can black cohosh help as I really feel that it has calmed down my moods
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