Ramipril (cough) And Losartan (pain In Arms And Legs)


Apr 4, 2016

reading the effects of above on other guests. I just wanted to confirm that I was put on 2.5mg ramipril last year , having suffered from Coughs for 3 months, asked my GP to change the drug ( as my mother had suffered 2 years before it was diagnosed and the doctor changed her ramipril, what a nightmare it was) and I was put on 25 mg Losartan, However I must admit  I am having aches and pains in my legs and my right arm and have been going to Physio every couple of months , assuming it was age related ( male 65).

I noted that one of the guests used candesartan so i will take it up with my GP next time I go and see him. many thanks for everyone's comments. I hope that the GP's are reading these columns too.

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Legs, Arms And Thighs - Intermittent Pain Cause ?

I was wondering if anyone has experienced any kind of pain like this:

For the past couple years or so I have had this intermittent type of pain (it usually happens about a couple times a week, for instance it happened in the beginning of the week for at least two consecutive days and not at all today; each episode usually consists of a series of acute attacks, maybe several of them in a row, and then they would just stop). This would happen in several areas: mainly now my thighs and legs (almost always the back of them, though a couple times it has been along the front); sometimes it is in the arms too; for a little while it was in the back (though it hasn't happened there for a while now).

I'm not sure how to describe the pain (I wish there was some sort of questionnaire I could find that might help me in that area); it's definitely not severe, but then I'm known to have a high tolerance for pain. I would say it is more sharp than dull and it seems to be a kind of stabbing pain though maybe not exactly shooting, though I guess it could be thought of that way (I don't know that it's radiating either--I can't see how it can be radiating anywhere; it seems, if I am remembering correctly, it is moving along the length of some specific area; that doesn't seem like it would fit the description of radiating). It is definitely not tingling or numbness (except when it happens in the arms--then there is a definite weakness that results after it in which I have less of an ability to grasp anything with much strength).

I'm just curious as to what can be causing this, or maybe it's just normal when you age, though I wouldn't consider myself to be too old at just 33.

Well, if anyone has any ideas I would appreciate hearing them. I would say for sure the pain in the arms sounds like some sort of nerve pain but I'm not sure about the other areas. I went to the doctor once about it, but he wasn't able to help much, just called it "fibromyalgia" which is basically what they say when they don't know what it is. For a while I was sure it was nerve pain but then I keep hearing how nerve pain is more of a tingling, numbness or loss of sensation more than actual pain; and then the doctor calls it fibromyalgia which from what I gather is thought to be muscle pain. I do not participate in any rigorous exercises, just walks for a mile or more a few times a week so it shouldn't be due to any sort of injury.

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Symptoms I been having. ..

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Also in my feet.

* Frequent bladder
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A doctor I saw was just at a regular clinic and he did blood work and it came back fine beside that my Vit D level was at 7 which he had the nurse call me and immediately gave a prescription over the phone for V2 vitamin 10,000unit pills and been working on that. Anybody know if my symptoms sound like a legit cause of the vitamin d deficiency? Could it really cause pain and muscle twitching?

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I was a raving hypochondriac, have suffered cs for 5 years,had mr scans,ct scans,myelograms and lumbar punctures,see my specialist regularly and just given different medication,vi suffer neck pain, headaches,numbness in arms and hands,but also have severe numbness in legs and feet,my hands and feet are permanently icy while the rest of my body burns up,feel permanently dizzy and nauseous,i have vision problems and incontinence problems,for past few months i have got steadily worse and not able to walk more than few yards,and cant get outdoors without aid of wheelchair,as pain in my joints and muscles is so bad,the nerves that are trapped have moved down my spine which is causing the leg pain,i have seen 3 specialists and a professor of m.s,i have meltdowns every so often as i always have been so active and cs can just bring you to your knees,i find that the specialists i see seem to think i am neurotic,i asked him to have my pain for a week and then come back and tell me how he feels...i feel people just don't understand how debilitating cs is and because outwardly you look ok and you do your hair and put some slap on your face,but walk a mile in my shoes when at 3am im walking the floor counting the hours till can have another pain killer,my last visit to my specialist i was given morphine patches,but suffering from ibs and gall stones was warned by my doctor that they would have adverse effects and they were so addictive.

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This lasted for 3/4 months until I was advised to stop its use.

Within a week I retrurned to the status quo ante with considerable relief.

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