Channel Blockers. Anyone have any info on these?

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RobThatsMe

Well-known member
Joined
Jun 11, 2001
Messages
1,457
Location
USA - TN
Hi Everyone,

My cardiologist did suggest that I could switch from taking a Beta Blocker to a Channel Blocker.

Anyone have any first hand information or studies on these? Side effects... ?

Thanks,
Rob
 
Yeah. Blasted channel blockers. Make it so you can't see the porno channels on cable... :rolleyes:

Calcium channel blockers block some of the calcium from entering the heart cells. The heart is a muscle, and the calcium is what causes the heart's contractions (muscle contractions). The walls of your arteries also have muscle-type tissues to contract them, and they are also affected by the lower amount of calcium, and stay more open.

Cedars-Sinai has a pretty good site about these: http://www.cedars-sinai.edu/6497.ht...OVKEY=calcium channel blockers&OVMTC=standard

Best wishes,
 
Rob,

Be careful w/ CCB's. They can worsen your symptoms. My personal experience was very negative.

Good luck,
 
John is on ccb's

John is on ccb's

for ph,cardiomyopathy....for a while only verapramil would work..we have switched to norvasec recently to see if he can maintain his #'s. His last echo was about 3 months ago, and the #'s hadnt changed. So we hope.. :eek:
 
Hey Rob - Jay here. I have had direct dealings myself with a cacium channel blocker. I have aortic insufficiency (regurgtitation). I was originally diagnosed May of 2004. At the time my LVD was 5.0. I was asked by my cardio to come back in every three months, just as a percautionary measure. At my next 3 month checkup I was at 5.4. That was in September. The next in December was 5.6, and it was looking like I might be on the fast track to surgery with my cardio suggesting that we begin to discuss the possibility of surgery around 6.0. Mind you all of this time I was pretty much asymptomatic. At the time of my echo in December (5.6) my doc said that she had just gotten back from a seminar in Atlanta with one of the "top valve guys" in the country from California. She said that she thought of me directly in regards to a certain topic he was discussing. That topic was about a drug called Procardia (generically called Nefedical or Nefedipine). This is a calcium channel blocker which works as described in an above post, in lamentss terms it makes the workload on the heart decrease by blocking the calcium of the heart and by doing this may relieve a certain level of the regurgitation, etc.

My Cardio suggested that I begin to take Procardia and to see how I tolerated it. It is given in doses of 30,60,90, and the most being 120 mg. Side effects can be lightheadedness or swelling of the ankles ( among a list of a dozen almost never occuring side effects, just like any bottle of tylenol :)) both of which occur very minimally. At least from my own experience, Procardia is a wonderful therapy that has helped me. A short bit of information, I started out on 30 mg for the first 30 days, then went to 60 mg for the next 30, and the last 30 before my echo I went to 90. the highest it is prescribed at is 120. That is the reason that I started out on the low end, to see if I could tolerate it. I have to date had NO side effects. In hindsight I wish I had started on a higher dose, but of course wouldnt feel that way unless the facts were that I have had no side effects. Went back for my most recent echo about 4 weeks ago (late Feb. 05') and my LVD had not only levelled off but had actually regressed back to 5.3. This could of been within the margin of error of course for echo's, but my feeling, as well as my cardio's, is that it was the therapy from the Procardia. Upon the results of my last echo, my doctor bumped me up to 120 mg, which I have been taking for a month now and still no side effects.

I had read one of the posts above where the woman had bad side effects from calcium channel blockers (the two she had mentioned I had never heard of). I would have to say from my own personal experience that I have had great results from my therapy with them. I would highly reccomomend ANYONE who is in the same situation as me to at the very least contact their cardiologist about Procardia and if the doctor doesn't have all the details then demand they look into it for you. Hope this has helped.

Jay
 
I took a ccb before they knew the extent of what was going on. I had a very negative reaction to them. Ended up the the ER because of them. The ER doc even tried to correct what was going on with another ccb and that didn't work. I was then put back an a beta blocker and was just fine. Just be cautious when using ccb and ask a lot of questions first.

Take Care!
Gail
 
I have first hand experience with Cardizem and Verapamil. Every time I have been on these drugs I have had increased problems with swelling of my legs and shortness of breath. I do have a history of cardiac vasospasm and also migraines and these drugs are also used for those conditions. I also felt like I was in a fog sometimes. The cardizem was helpful in preventing chest pain for me.

My husband was on Cardizem for years and his only complaint with it was he thought it made him feel tired.
 
WOW.... Thanks everyone for so much information...

Now all I have to do is process it.

Just to give you a short history of this with me. I am on Atenolol, and told my cardiologist at my last visit, that taking a beta blocker seems to have blocked all the highes and lows in life... I mean... I can be on a treadmill walking at a 4.2 mph pace, and my pulse will be 98.

I like experiencing life's reactions..and don't care to be in a limbo kind of state. So,,, my doctor suggested channel blockers..

It seems though that from some folks I talked with and from other on here, that the side effects may be even worse than the beta blockers..


hmmm..... perhaps that is why I am back to drinking more coffee.......

Take care....

Happy spring... It's finally here!!

Rob
 
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