BrooksK
08-26-2009, 07:51 PM
I'm on a beta blocker (nadolol) and disopyramide. My most recent blood tests indicate an elevated PSA. In Dr. Sherrid's presentation "Evaluation and Selection for Symptomatic LV Outflow Obstruction" given at the HCMA conference, he noted that disopyramide has "vagolytical side effects, dry mouth and exacerbation of prostatism."
I have a follow-up appointment with a urologist in a week, but are there any words of wisdom about the disopyramide/prostate connection?
Probably unrelated, but I also have continuing hypertension. When I started the beta blocker in January, I discontinued Benicar and amlodipine (which exacerbated the HCM SOB symptoms), but my pulse is really low (40 - 50), but BP in Stage I Hypertension. Various side effects with other BP meds (including cough and increased uric acid/gout). Again, any words of wisdom as to which drugs help with HBP, but don't exacerbate HCM symptoms? (Yes, I do have calls into my HCM doc, but my local doc seems determined to do whatever is needed to lower BP since there's the nice objective, measurable standard of what the numbers should be while the HCM symptoms are a bit more subjective . . .)
Does anyone ever take fewer drugs? Anyone note any difference with HCM with low Vit D levels? That, too, showed up on the blood test, so I'm also taking Vit D supplement now . . .
I have a follow-up appointment with a urologist in a week, but are there any words of wisdom about the disopyramide/prostate connection?
Probably unrelated, but I also have continuing hypertension. When I started the beta blocker in January, I discontinued Benicar and amlodipine (which exacerbated the HCM SOB symptoms), but my pulse is really low (40 - 50), but BP in Stage I Hypertension. Various side effects with other BP meds (including cough and increased uric acid/gout). Again, any words of wisdom as to which drugs help with HBP, but don't exacerbate HCM symptoms? (Yes, I do have calls into my HCM doc, but my local doc seems determined to do whatever is needed to lower BP since there's the nice objective, measurable standard of what the numbers should be while the HCM symptoms are a bit more subjective . . .)
Does anyone ever take fewer drugs? Anyone note any difference with HCM with low Vit D levels? That, too, showed up on the blood test, so I'm also taking Vit D supplement now . . .