I have verapamil as I declined the beta blocker offered initially.
It is a calcium channel blocker. Lots of good info on the British Heart Foundation website (sorry link not posting properly).
Anyway I have found it has helped. It instantly relieved my chest pain and breathlessness and seems to have slowed by HR but not too much.
Crucially serious side effects are rare and the only.one my EP specifiacally mentioned was constipation. Magnesium supplements are great for your heart and also seem to help the bowels so. I've had no issues 😀. All the best.
I have taken Verapimil for many years - about 20. It was first prescribed at a very low dose for possible PVCs (only slight evidence with event recorder & nothing on echo), then the dose was bumped as my blood pressure rose, & now it has the function of keeping my HR I check. When AF was first diagnosed last March, the dose was doubled by my GP to lower heart rate, but now I'm back to the regular dose. It seems to work with few side effects. My EP thought that I should stay with what is working for now.
As a matter of interest I'm pretty certain it was a bad attack of COPD brought on my AF. I have never had AF before. Now I have PAF but it's very mild and I haven't had any COPD for a long time.
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