Neurocadiogenic syncope and IST
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My symptoms were mainly fatigue and brain fog, but when they put me on atenolol it was like I had my life back! I have a low tolerance to drugs, so I couldn't tolerate more than 12.5mg of atenolol which wasn't enough to control the tachycardia. My EP added verapamil 180mg and this seems to do the trick. We found that if I take the atenolol in the morning and the verapamil at bedtime I have fewer episodes of breakthru tachy. Later he started me on a 1g salt tablet. (I am now experiencing a good bit of fatigue again, but have other health problems, so I don't at this point know what the cause is).
I hope this helps you and that you can find something to work for you.
I haven't had a EP study, it's funny because all of my dr.s think I should have had one. I am glad I haven't and why should I? I am not willing to get my sinus node modified. A dr. from this forum (I think it was Dr. Cole) suggested looking into, but I am not interested, at least not yet. I don't know if I could get off of meds even with having it done, because of the NCS. It sounds like mine is better controlled than yours, also. I am not aware of any side effects with the atenolol being so low, nor with the verapamil.
I hope you can find something soon to help you!
Let me give you this link, it is a forum for autonomic dysfunction. Maybe you will find it helpful talking to others with these problems.
http://216.149.163.247/cgi-bin/forumdisplay.cgi?action=topics&forum=NDRF+General+Discussion&number=1&DaysPrune=20&LastLogin=
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