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A year ago an ICD was implanted. Recent data from the ICD (over a 6 month interval) indicated a couple of events that were properly converted. The cardiologist who did the implant recommended taking amiodarone. This started in early May. Amiodarone involves taking large amounts during the "loading phase" followed by the target dosage (200 mg in my case). I got through the loading phase with a few problems. But by mid-May I was experiencing very low BP in the mornings. The cardiologist suggested greatly decreasing the amount of Toprol-XL. Then the problems began.
My BP starting running high... very high... in the afternoons.
After I ended up in an ER the cardiologist (who did the implant) suggested returning to 50 mg Toprol-XL.
The dramatic increases in BP in the afternoon continued.
These increases (to a systolic 160, 179, 180, and even 190) would begin about 2:00 p.m. Then they started earlier. And earlier. Until the beginning of this upward trend was starting even at 10:00 a.m.
The net from this was that I'd begin the day with systolic near 125 and by mid-morning it was more than 150. I'd never seen such numbers in the past. It was suggested that I "time taking the lisinopril" to counter the increases. That worked sometimes, but not for extended periods of elevated BP.
The cardiologist who has cared for me since 1984 prescribed catapres... 1 mg 2X a day. Those doses made me faint and dizzy, so this was changed to one-half of 1 mg three times a day. That's where I am now. But there's the matter of timing when to take the catapres, frequently measuring BP, etc.
In the meantime I've developed tremors in my hands. Much more in my right hand than in my left hand. When my BP goes up those tremors become unacceptable. There are times when I cannot put a cap on a tube of toothpaste.
I cut the amiodarone dosage from 200 mg daily to 100 mg daily (with permission from my cardiologist). This has not solved the problem. It's reached the point at which the Toprol-XL doesn't seem to be doing much of anything and I'm running strictly on catapres. Without catapres my systolic would go to 180+ and stay there. I'm about ready to reduce amiodarone to 50 mg daily.
The warnings that come with amiodarone describe a lot of side effects. But increased BP is not in the list of warnings. The effect of changes in amiodarone dosage are slow to take place because there's a lot of it stored in the body.
The basic question here is this. Has anyone else experience increases in BP (especially dramatic and almost uncontrollable increases) when taking amiodarone?
All of my Drs. find it difficult to believe my high BP problems are caused by amiodarone. But the fact is that I never experience such a problem before taking it.
My GP has prescribed some tests to learn where there's a restriction in arteries that supply blood to the kidneys. That will be done on Monday. In the meantime, when I woke up this morning my systolic was 167. The usual does of catapres brought it down to as low as 129. It will increase and another does will be required... and another... and another. This is no way to live!!
I was given amiodarone following my ablation in December. Almost immediately I noticed the same symptoms--hand tremors. My handwriting which has always been poor, became illegible. I had a very difficult time writing a check and often had my wife do it for me. With permission, I cut the dose in half--but no change. Because during the healing process from the ablation I seemed to be having no other rhythm problems, he allowed me to quit altogether. It took six to eight weeks due to the half life of the drug, to work out of my system. Regarding BP issues? I could not detect any changes.
Hopefully there are some alternative medications for you.
I have been using 200mg of amiodarone daily for more than 8 years to control my A-Fib. The only side effect has been that my skin has become more sensitive to sunlight.Have taken care of this with sun block.Fortunately I have not had any BP issues.
Rgs Ian
Hopefully there are some alternative medications for you.
Rgs Ian