I am new on here after a recent and very unexpected diagnosis of Heart Failure.
I was sent for an ECG to be safe during a pre op assessment for some minor day surgery when I complained about tingling arm and tight painful chest. Been told for decades it was stress/anxiety related so wasn't concerned.
I had tried to get fit last few years, running 5K several times a week, but could never figure why I was not getting faster, just out of breath... now I know!
The test showed abnormalities as did 2 previous which were flagged 'further investigation' but not done. Within 2 weeks I had an Echo and another week later was medicated for Left Ventricular Dysfunction.
First drug, Enalapril, caused dairy intolerant me to get very ill so was changed to Ramipril 2.5mg. Two weeks in and on 5mg daily but feeling awful, dizzy, light headed, off balance, have whooshing in my ears, bloated and lost sense of taste.
On Monday was told to take tablet at night to see if this helped but by last night some 38 hours from last dose I was feeling so much better, almost back to where I was before being diagnosed and medicated!
I was loathe to restart as I don't want to feel ill for rest of my life - I'm only 45 - but did and now anticipating the side effects once more.
Any suggestions?
Thanks
Written by
CraftyGirl72
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I take Ramipril 1.25 at around 7pm and I have no issues with it. If Ramipril is an issue for you I think you need to try something else. Unfortunately not all drugs work the same in all people so a certain amount of ‘experimentation’ is quite common, until you find something that works and you can tolerate. Another trip to the GP sounds in order.
Hi, I'm 52 with Heart failure diagnosed about 3-4 years ago, they had me on rampril and I was getting to feel worse and worse then my gp stopped them, as with you feeling much better I'm now on Candesartan which is a group of meds alternative to ACE inhibitors (i'm on a very low dose because of low blood pressure), see the BHF main book on Heart failure, all the meds are listed, I would not stay on a med making me feel bad there are lots of others to try, good luck,
Definitely talk to your gp again. I was put on Ramipril and developed a really irritating dry cough, gp stopped me to Losartan and problem solved. There are several different drugs that do the same thing, so for your sake, kick up a fuss.
Thanks for the suggestions. I finally took tablet at midnight last night after an internal debate and felt not too bad earlier today but as day wore on started to feel unsteady again. Will keep persisting another few days and if no better head back to GP.
Take this at night this happened to me, this made a huge differnce to me. If then it still causing problems gp can change it. There are many drugs in this group and it is just a matter of trial and error. Hope this helps.
Hi....I've just started on Ramipril and they told me to take at night. Hoping I will settle in on it but would go back to GP if I get any side effects. Make sure you do if it doesn't suit you. I'm only 46 and will not let this take over my life! 💪 Good luck! X
It won't take over mine either... just struggling as I felt fine before diagnosis and only ill since taking the meds! Typical of my life but I have #innerstrength on my side. Take care x
hi .. i was diagnosed last year from having a heart attack caused by a blood clot aged 38 with heart failure and dilated cardiomyopathy .. i was on rampril and i was on it for a month and my hair started to fall out and the skin on my feet were just constantly peeling (they were a mess, it was coming of in sheets).. they changed me to valsartan and my skin and hair are back to normal ...
Hi I take mine at night as I get the same issues of dizziness and light headedness. It's because it lowers my already very low bp. You may need a lower dose. Get it checked out
Thanks but they are still working on increasing my dose!
Had 2 weeks on 2.5, been a week on 5 so far with plans to up again after another 3 as still fairly high BP. I fear it's only going to get worse. First medication was better for me but killed my stomach because of the lactose.
Hi Craftygirl ...... can I just say a huge thank you for your post. I read your symptoms and thought... that's me!
I have been on ramipril since may last year... they gradually upped my tablets and I am now on 10mg. I had all sorts of troubles last year with dizziness.. near fainting spells... but no cough.
I was just told take the tablets at night and if I didn't have a cough I would be fine.
Over time I thought the dizziness was due to my heart condition... I got bloated... and at night the swooshing in my ears got so. Had started getting memory loss too.
And then I read your post....... and it was like a switch coming on... it's not my heart.... I am not getting dementia...its the ramipril!!!
I called my doctor yesterday went through the symptoms... all of them...amd my dizziness and wooshinge in my ears has been awful recently, and he has immediately taken me off the ramipril and offered the Candestral( sure I have spelt this wrong)
I didn't take any tablets last night... and although I had a little wooshing in my ears at night, it was not nearly as bad, and no dizziness. So thank you for your post which made me realise that these symptoms are the tablets... not my condition .
I would say that although I was told to persevere.... and I did... the symptoms had got much worse as time went on... so do take heed of how you are feeling and ask for them to be changed if you are having too many side effects.
And many thanks for your post... I love this forum 😀
I am so glad I posted asking advice letting you see what others endure. I hope you have better luck on the new drug...
I am still perservering on the Ramipril for now in hope it settles or untill I can see a cardiologist (12 week wait list) and get him to look at my medication.
I can assure you I won't stay on something making me ill long term.
Hi Avril.... yes I agree give it a chance to work.. . But know that there are alternatives. Interestingly my GP did say this week that a lot of people don't tolerate ramipril. The reason I didn't go before is i hadn't twigged that it could be the drug causing my symptoms. I thought it was my heart getting worse.
So it's even more good news that the ticker is not that bad after all 😀
Good luck with your medication and take in a list of any questions you want to ask the cardiologist as you don't get much time and so it's good to have a list so you don't forget to ask anything. X
I never had any symptoms before diagnosis, dodgy ticker wasn't even on my radar! I just though uphill/running breathlessness was me as an unfit old bird 😳 That's why I knew how I was feeling was side effects not symptoms.
Started a list already as it was suggested in some of the literature I was sent by BHF.
Glad your heart is better than you thought... that is always good news! 😉x
Just saying hi as I missed your post initially. Hope you are making some progress with your medication now. Feel free to message me if you ever want to chat. My specialist subjects are craft and heart failure
I'm having a paper crafting afternoon with friends for my birthday next month. Nothing like getting folks round to use up your stash! (though I may have purchased a few new items for the occasion... 😳) I'm a jack of all craft trades so have an unruly stash for every occasion - fabric, paper, beads, wool...
Hope it's not too long before you see your cardiologist and get some replacement medications. Rampiril is one I've never taken but it seems to disagree with a lot of people. Hopefully an alternative will have you feeling better than you were pre-diagnosis x
Then natural green drinks I make myself have done more good for me in the last year then any medicine, I have taken in the 5 years since I was diagnosed with diabetes type 2.
Glad my inner debate helped you (and a few others), I was taken off Ramipril, eventually put on Bisoprolol and taken off it too... I was unmedicated from May, discharged from cardiology in October but forced back on medication after another stress attack in January. 4 weeks of Losartan and I'd rather have been dead! Off again and although BP not quite where it should be I feel better, decided just to play Russian Roulette unmedicated.
Can I ask what green drinks you refer to? My doctors, although accepting of my refusal to take drugs which make me ill, are not offering help for me go natural with diet and exercise.
So glad I read this!!! I have experienced all of the side effects mentioned. The sensation of constantly being on a round about (spinning) is not good for your mental health.. and the memory loss is horrible.
I am only on 3.75mg raised from 2.5 two months after my heart attack and haven’t started on 5 as suggested because the first step knocked it out of me.
I will be going to my GP tomorrow, I didn’t realise there was other options...
Glad this has made you realise the drugs can be cause of more misery than the illness. Speak to doctors and try others, there are many! I went through over a dozen in 18 months each one making me feel awful in some way to point I chose to stop them to enjoy what was left of my life. A year or two feeling ok with risk was better than 15 feeling horrendous by my reckoning.
I am absolutely fine, unmedicated at almost 3 years, even my BP is normal (unless going to see doc - white coat syndrome).
Everyone's body is different and remind doctor of that when you speak to them... me I'm off out to do another 5K run (term used loosely but nowt to do with heart just rubbish at exercise)! Take care.
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