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@kudzu

I should add it’s important to do our own research because unfortunately drs don’t always tell us everything. I’ve had many wonderful drs but enough negative experiences to convince me this is essential.

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Replies to "I should add it’s important to do our own research because unfortunately drs don’t always tell..."

Thanks for your comments and your story. That was my first episode of AFib. I saw my cardiologist (At that time I had never heard the term "electrophysiologist"). I just accepted what he said about needing a blood thinner to prevent a stroke and the Amiodarone for the AFib. At that time I did very little research - thought AFib was like diabetes - something you had and treated (like taking insulin). Then I started researching and found that most people are started on Amiodarone in the hospital to make certain they tolerated it and not just given 400 mg twice a day! In the years since, I have become much smarter! I research everything, won't take a new medication, unless I have learned everything I can, and generally get the opinion of other doctors. My next 3 episodes of AFib I approached very differently and saw an electrophysiologist, not a cardiologist. My EP wants to do an ablation; today I saw another EP for a second opinion. My amiodarone experience has made me very cautious. I have permanent scarring in my lungs; the four months of steroids reversed some of the damage - but not all. Like you, I have had many wonderful doctors, but enough negative experiences to convince it is essential to do my own research and question EVERYTHING!