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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I have been taken off the bendroflumethiazide and put onto Ramipril. This is the third day and even though I am no longer totally fatigued as I was with the bendro, I am experiencing very dry mouth, Cough, cramp in lower legs, heartburn sensation in chest. Not due to see my GP for 3 more weeks. Hopefully will settle down
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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. ..
*Weakness in arms and legs
*Pain in both legs and arm, worse when walking/working
Also in my feet.
* Frequent bladder
*Random muscle twitching all over the body, especially feet
*Eye sight slightly worse (need glasses now)
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 am in my early 60s and have had facial paralysis (left side) and mini stroke in 2005. I have recently been diagnosed with Angina. I also have high blood pressure, diabetes and sciatic. Recently I have been getting lots of pain in my left arms, neck, both legs, shoulders, chest and ribs and pain has woken me up. I am due to have angiogram soon. Dr has given me GTN and Nicorandil. On my left side I get pain in my temple this side is affected by facial paralysis. I find it very difficult to walk and get very breathless. Just walking up the stairs I get very breathless. Does anyone else suffers from same symptoms? I feel I have no energy and I am housebound.
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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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my doctor put me on lisinopril and ever since i have had a dry cough. i thought it was due to post nasal drip but now that i read the side effects i have my doubts. i was wondering if it would be wise to try losartan.
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I have been on ramipril for about 8 months now. Have had a dreadful cough which has got worse the longer I have taken them. I also have asthma and the cough has been put down to that as it has triggered severe asthma attacks, which have caused me to go into hospital with blue light flashing. Not once has any doctor said this is down to Ramipril. I will be changing this medication before it kills me. BE VERY WARY IF YOU ARE ASTHMATIC!!!!!
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I wrote on this sight about a month ago, declaring that i dont really have any problems with ramipril, other than contracting a couple of nasty colds with very tickly coughs since starting on it. How wrong was I. Every bug going has got me, I ache pretty much all of the time and constantly feel as though im about to undergo an attack of the flu. The tickly cough has stayed, sometimes keeping me awake at night! Ive just finished a course of antibiotics for a chest infection and was amazed when my doctor told me that the ramipril worsens any kind of cold, cough or virus! the scary part is though, my bp has been higher than usual and my doctor is monitoring it with the intent of highering my dosage if it doesnt come down.
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My elderly husband has taken ramipril 5.0mg for many years with apparently no or minimal side effects. But over the last two years he has suffered increasingly from dizziness in the morning. I think he also coughs a great deal more than he ever did.
I've been measuring his blood pressure regularly recently and the diastolic measure is consistently on the edge of 'low' (around 60). The systolic is just into 'high' and it creeps up a bit if he forgets the ramipril however. I wonder if a reduced dose of ramipril might still control the latter with less risk of hypotensive dizziness. Does that make any sense?
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I was put on Amlodipine for severe hypertension and the first night i was in terrible pain with my chest and that brought on a anxiety attack, stayed on it for a week and still had spikes in my high blood pressure and chest pain, went back to the doctor and told her and she looked at me like i was lying, changed my medication to Ramipril and the chest pain and anxiety went but i have got a terrible dry cough with the Ramipril so need to come of them too, my blood pressure was very high and i was told it may lead to a heart attack or stroke so now i am in trouble as i don't trust any medications because of the side effects.
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Just spoken to my GP who has taken me off Ramipril because of the blasted cough. I'm now on Candesartan, which I've never heard of. Anyone out there have any experience of this drug?
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Prior to taking Ramipril I suffered from a persistent dry cough of which the cause had not been diagnosed.
On taking Ramipril the cough was very considerably aggravated particularly at night: codeine gave some relief ( as phoschol and 15mgm tablet) but sleep was reduced to snatches between coughing bouts.
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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I had a heart attack 5 weeks ago and since have been on various medicines one of which is 5mg Ramipril every night. I read the booklet which explained that a side effect is a cough but agree with other inputs here that the cough is very depressing. It constantly disrupts my sleep pattern and it's so dry ! Im off to the GPs Tomorrow and hopefully he can prescibe something else. Is there anyway else of stopping the cough ?
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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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have been taking Ramipril for 3 months now and at first didn't link the dreadful cough with this drug until I researched it on the web. I have developed a dreadful dry tickly cough which starts at the back of the throat and immediately starts to make my eyes water. The coughing then starts to go into a spasm and its worse at night - I haven't had a full night's sleep for weeks.
Also my chest is beginning to be sore due to all the coughing, its very distressing and I am going to be back at my gp.
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Been on Ramipril for 2 1/2 years, always suffered froma bad cough with it, most annoying. Saw new Dr few months ago whos took me off ramapril because of cough. New tablet (evil drug) called amlovasc terrible side effects, pins and needles to the face, legs, and arms, severe tiredeness, swelling to ankles and knees. Took myself off these tablets. Going back to GP tomorrow morning, prefer to put up with the cough
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At age 42, I'm starting to notice some loss of hair on my arms and legs. I'm a male, and of Mediterranean ancestry, so I've been quite hairy in those areas since I was a teen. My hair remains very full and thick on my head, so it seems odd I should be losing it in other places. Is this normal? I don't like the way it looks - like the skin of an old man, all bare and plain.
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Been taking ramipril 5mg for a year. And also bendroflumethiazide I have acid reflux daily and a dry tickling cough at night. Is this caused by the tablets does anyone know.
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Does anyone's arm and leg burn and ache? Do they feel hot and full with this diabetes?
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Last month i had a very bad bout with the flu. My whole body was paining. It started with my upper legs. Almost like someone gave me charlie horse in my muscles. Then my feet and bottom of my feet started paining. I could not even walk. I wore memory foam slippers on my feet the few times out of bed. My hands had the same painful sensitive sensations as my feet. a few days later my lungs started to hurt and I had something pneumonia. When i started recovering, the pain and numb sensations stayed on the bottom of my feet, my hands legs and arms. Not to mention the weakness that still exist in my limbs. Also, which is confusing and worrying me most now is the numbness on my face and in my mouth, it feels like dental freezing leaving my mouth. It's been at least a month since i recovered from the flu. I have seen my Dr. and have been scheduled for a CT scan. Has anyone had these symptoms before?
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