alternative blood thinners to warfarin
Posted , 7 users are following.
Hi Everyone,
I am about to speak to my GP and Cardiologist about having one of the alternative blood thinners as because of an underlying problem with my bladder I am often on Prophylactic antibiotics and they do not interact well with the warfarin, making it difficult for them to get my INR correct. can any of you on any of the alternatives let me know how you are on them, any any side effects related to them, don't want to jump out of the frying pan into the fire!!!! the good thing for me would be I understand they do not interact with other medication, the 3 I have found that are available are Dabigatran, Rivaroxaban and Apixaban.
Hope you are all relatively well.
L.
0 likes, 20 replies
betty47298 linda51222
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frank61666 linda51222
Posted
linda51222 frank61666
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madge07350 linda51222
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macas02 linda51222
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M.
linda51222 macas02
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I know Madge the antibiotics are not good, and as I suffer with autoimmune disease anyway its difficult, you keep hearing from NHS that GP's should not give them out unless absolutely necessary, and yet they give them to me like smarties. I think my immune system is intolerant of the warfarin as it is to many meds especially analgesics
but when you get diagnosed with AF they do the same for everyone without taking your past health history into consideration.
Thank you both
L.
cardiac_congo linda51222
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simon56380 linda51222
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i found it really tricky maintaining the acceptable range of warfarin in my system (was. Bouncing all over the place!)
Am really pleased to be back on Apixaban post procedure - so much easier.
However, my 84 year father-in - law doesn't like apixaban, he claim it makes him feel 'fuzzy' and 'dizzy'.
So I gues its not to everyone's liking, but I love it compared to warfarin.
(I'm a 50 yo male and 95 kgs)
Hope this is of some help to you?
betty47298 simon56380
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linda51222 simon56380
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I think I am going to ask to be tried on Apixaban, really am struggling with the warfarin. I have given it a good try I have been on it since August last year, I suppose I can exercise my patient choice, unless of course they give me a good clinical reason why I shouldn't.
Thank you
L.
linda51222
Posted
L
simon56380 betty47298
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I was diagnosed with heart failure (a tachycardia induced cardiomyopathy) in Dec 2014. my left ventricle had become severely enlarged & I had an ejection fraction of only 25 % .
first cardioversion only lasted a couple of days, was then put on amioderone and cardioverted again three weeks later. This worked really well for me. I stayed in rhythm for the next 11 months. My cardiomyopathy cleared up within the first 4-6 weeks, my left ventricle Ejection fraction returned to 58%. (within the normal range ).
All was going great until mid Jan. This year when I went into Afib again got cardioverted back in, and then again mid Feb. and then AGAIN at the end of Feb (3 times in 6 weeks).
Because of the increasing frequency of cardioversion, it's was suggested that I could be fit from having the ablation. Let's hope they're right.
Time will tell I guess?
betty47298 simon56380
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macas02 linda51222
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You say you have an Autoimmune problem , so do I . I have PMR and was told this could be perhaps the cause of my heart problems!!!!
linda51222 macas02
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I have Sjogren's Syndrome and Pallindromic Rheumatism, and chronic bladder disease.
L.