Amiodarone Wreck My Thyroid For Life?
Jan 12, 2016
In 2007, apparently for a prolonged QT I was hospitalized, given 1600 mg amiodarone and then 200 daily.Only one test was made, after five months. Ten months later I had a TSH of 38. A new cardio brought it down to normal in three months with levothyroxine and put me on Rythmol instead of amiodarone..Did the amio wreck my thyroid for life? Ever since, tests have been normal but with FT3 in the 20's. Doctor after doctor for six years have continue the levo never suggesting a T3 med (In guatemala where I live there is no Cytomel).On my own, I have tried levo doses from zero to 150 over two years with no notable change in TSH and T4 test levels but FT3 still below 30). I cannot pinpoint low FT3 symptoms among side effects from Rythmol 150, coreg 6.25, crestor 10, aspirin 100. I have not slept one night through for six years without two or three hour-long sweats/chills, nauseas, dizziness, weakness, fatigue etc.Daytime too. I'm 87 and tired of it. One stent 2010, RCA. Never felt angina or tachycardia. Any way out of this?
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my TSH was 38 after a year on amiodarone without tests.A second cardio brought this down to normal in three months with levothyroxine,My question: does an excess of amiodarone wreck a thyroid for life, am I on Levo for good?
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I have been on amiodarone for most of the last 20 years. I have a heart rhythm problem that killed my mother at age 25 and a sister at age 21. Initially I had problems with sleep and other symptoms until I got used to the drug. Nowadays I have to take care with the sun but have no other symptoms and ensure I have regular blood tests etc. If it were not for amiodarone I would probably not be here today.
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I have been on amiodarone 200/ day for 2 months after the initial loading doses. I left it because of side effects and want to restart sotalol 160 mg twice a day, the medication I was on before I started amiodarone. My cardiologist told me to start sotalol one week after discontinuing amiodarone. My concern is that the half life of amiodarone is 58 days. This means my body is loaded with amiodarone resulting in continued low heart rate of about 65 bpm and starting sotalol might further lower the heart rate to dangerous levels. Does anybody have a suggestion as to how many days I should wait before I start sotalol.
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I have been taking Amiodarone for 2 months now for cardioversion as I have AF. I have been told that it is unlikely to be successful but that I might as well give it a go. So far I have had no problems at all - I take 200mg daily. I will be on it for a maximum of 4 months so my specialist says that I am unlikely to run into problems which he says are usually connected with much longer term use. My message to others is - please don't be afraid of this medicine - it's at least worth a go in the short term to see if you can tolerate it. The chance of getting rid of AF is just too important not to take it. As I say, so far, I am lucky in being able to tolerate it amongst at least 8 other meds which I take. I was very afraid to start with but now I just see it as "another pill to take".
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I have taking Amiodarone 200mg for about 35 days for my AF .However, I still get irregular occasional especially after taking hot food. The improvement to my condition is marginal. Can anyone advise me if I should continue with Amiodarone. Also,I have been on warfarin for the past 3 years . Due to the interaction of Amiodarone with Warfarin, my doctor has reduced my Warfarin dosage from 4.5 to 3.5 to maintain my INR between 2 to 3.
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Has anyone been prescribed Amiodarone for Atrial Flutter/Fibrillation. I have been on this for 9 Days and am finding the side effects dreadful . I don't know if I should persevere for a bit longer or see my Dr.to see if there is anything else I can try.
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My son has been on amiodarone for four months now following an atrial flutter which required DC Cardioversion. He takes other drugs for his heart such as furosemide, ramipril and warfarin. He seems to have frequent throat infections which lead to flu symptoms (hot and cold shivers, aches and pains) these have forced him to bed for 6 days at a time. We have been told that these are not a side effect by the consultant but we were managing to keep on top of infections before amiodarone with some wonderful natural supplements. I am interested that none of the comments that I have read on this site have really mentioned similar side effects. Has anyone experienced the same? He has been free of atrial flutters and has declined an ablation on the grounds that they cannot guarantee a total success rate.
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i was put on this awful med, prior in for a Cardioversion , i have never been so ill in my life, it was strong dose, three a day, then two a days for second week then one every day after that. Since the first day I was nauseated,ulcers in my mouth, old sores at the corners of my mouth I lost 1 stone in weight,and couldn't, I persevered, with the Cardioversion at end. I went to get bloods and ECG prior getting the procedure, and I got a phone from the cardiac nurse to say my renal is only about 50 per cent,so cancelled and go to my Dr, I had more bloods, then later in the day I got to say go to the renal ward in hospital, probably for a few days. Might say I had routine bloods taken in April and no problem. Apparently my kidney's function is now at 29 percent. I am now waiting for a biopsy from my kidney!!! It's galling to think I have never drank and never smoked in my life and now this.Strangely they took me off the needs immediately, but theŷ never admit it was the Amiodarone. I am left with probably irreversible renal function, and still have PAF.....
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I've been on Bisoprolol 10mg for 3 months with no effect on my Paroxysmal AF episodes so was started on Digoxin, now at 187.5mcg also with minimal effect. My Cardiologist and GP are pushing me to take Amiodarone but reading stories of side effects I'm terrified. I live in NZ so don't have the choice of Dronedarone. Have others refused Amiodarone and if so what were they then put on? I feel backed into a corner with not many choices left.
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I post this to alert anyone checking these boards about the dangers of amiodarone. My father was given this drug for a minor arrhythmia, while he was hospitalized with bronchitis. It killed him in just 4 weeks as a result of sudden, irreversible pulmonary toxicity. If you or anyone you love is taking this drug, you need to know just how dangerous it is. The pharmaceutical companies have dodged responsibility for its many toxic effects for years, and doctors are woefully ignorant of its potential life-threatening complications. By doing an internet search under "amiodarone toxicity" you can find a wealth of information and a vast support system of people determined to stop this drug from killing anyone else.
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I had an ultrasound today and it says that there is "a homogeneous appearance to the echotexture of the thyroid gland. Bilateral thyroid nodules are observed. There is evidence of a complex cystic and solid lower pole right thyroid nodule measuring 1.8 x 1.0 x 0.9 cm. Within the left thyroid lobe there is evidence of a hypoechoic midpole left thyroid nodule measuring 0.6 x 0.4 x 0.7 cm. Bilateral thyroid nodules. Dominant nodule is a complex cystic and solid lower pole right thyroid nodule measuring up to 1.8 cm. what does this mean?
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I have 3 thyroid nodules and 1 cyst. I have been advised to have a thyroidectomy. I do not want to go this route yet and am searching for some natural remedies. I have heard of using iodine but to be careful do to the fact that that might enlarge the nodules. I recently found out that I am very iodine deficient from a lab result. I have heard of iodine trapping, whereby the iodine taken in when their is a severe deficiency is immediately 'trapped' and held in the gland in order to preserve some iodine for the use of the thyroid. I would like to proceed with caution and try the iodine therapy.
Does anyone on this board have any experience with successfully dissolving or at least reducing the nodules/cysts?
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It wasn't long after I moved to an area within 10 miles of a nuclear power plant that I was diagnosed with an enlarged thyroid with nodules. And after a surgery I had, I became extremely depressed and I still am, this was three years ago. Also a feeling of not being myself.
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I am new to this site. I have been diagnosed as Euthyroid (antithyroid antibodies with a fully functioning thyroid) and I also have Anti-nuclear antibodies - Speckled 1:640.
I don't have Lupus as have been tested for that.
I am currently undergoing IVF and have had 2 failed rounds. I have been put on Aspirin (100 mg), Prednisolone 7.5mg a day and CoEnzyme Q10, folate and Vit B12 with no success.
I am desperately looking for anyone in my situation that can offer any sort of guidance, maybe a drug regime you are on or just anything at all. I desperately want children but it isn't looking too good. I'm terribly sad about the prospect of never having children.
Ive been trying for 3 years now and was pregnant once and miscarried at about 5 weeks back in 2011 and have never been pregnant since indicating a problem but I don't have any other issues except a low egg reserve which is from these other issues
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I really feel like I'm beginning to feel more and more mentally ill..rather people say it's going to pass..it's really not..having faith doesn't help..don't nothing helps or work..I pray and get no answers..sure it might be a test but it's really a test I'm failing at..do people ever think about others who have been praying for years and never go a answer?
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I have a benign 1.4 cm cyst in the middle part of my thyroid (isthmus). It is visible in my neck. The doctor said to remove it would require to take out my thyroid and since it is benign he wants to watch to see if it gets bigger. Currently it is not causing me any problems. Has anyone had this same thing, and if so, what did you do? Also, do the cysts ever get smaller or go away on their own?
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47 year old sufferer and worried. Do i have these for life and it's all down to managing them, short of surgery of course?
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I have been on meformin for about a year now. I became diabetic about 5 years ago but was able to do the diet and exercise thing until I was put on metformin. I asked the doctor about getting off of it now that my sugars have been doing good. He said that once diagnosed with diabetes I can never come off of meformin??? I cannot believe that. He can't be for real. I don't want to be on metformin for the rest of my life. I would like to be able to get off of it and just control my diabetes on my own. I did it before so I would like to do it again. How do I convince him to let me go off of metformin?
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I'm a 24, soon to be 25 year old. I know I'm really young, and that's the biggest ''encouragement'' people give me generally. You haven't lived much, there's still so much ahead, etc. But the thing is, I've been depressed for almost 10 years now. I've been on and off with meds, had some ''brighter'' episodes in between the years, but basically I've accomplished nothing. I have no education degrees, no work experience. I can barely function on my own. My family lives far away, and doesn't understand my depression at all. In fact, my sister tells me I'm depressed simply because I'm just that lazy. Maybe that's true? I don't know. I live alone, and have no friends. I have just recently cut off my last tie to a person by managing to tick off my ex so badly he almost suffocated me by strangling to get his point of wanting me out of his life through. He's the father of my son, who's another point of depression. Just can't seem to be able to love the kid like I should. What good is someone like me anyway? I have no right to call myself a mother.
I've gone through abortion, abusive boyfriend, neglect and abuse from my dad, losing all my friends, being homeless, attempting a suicide through slicing my wrists open... Something bad, you name it and it's probably happened. So far, anything I've tried turns to ash soon. Relationships, jobs, even normal day to day life... I can't get a grip of any of it and I just end up failing.
I'm honestly hanging on to life by the tiniest possible thread simply for the sake of being so stubborn I can't give up. But every day is torture, and I just keep waiting on something to change, yet it doesn't. I can't find the will to live but I'm too stubborn and too much of a coward to go through with ending it. Also don't want to go through the experience of laying in a hospital bed listening to the nurses go on how ''it's another of those attention seekers''. That was devastating for me. But I'm at my wits end. How long will it go on? When does one get a happy end? How do you find a will to live through all the sh*t?
I want to die, but I can't. I want to live, but I don't know how or why. I want to move on, do something, but I don't have the strength. What should I do, really?
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I am about to marry and want to make sure circumcision won't affects my marriage life. I used to get irritations in my foreskin and advised to remove it.
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