Experiences with

Chlorthalidone

It took almost three years to get myself halfway back together and I know once you had ckd you STILL have it even if your numbers are better has anyone taking Chlorthalidone with good results with their kidneys?

The only medication I am still taking is Acyclovir and Chlorthalidone. Anyone else having these issues? I have reached out to my doctor this morning.

Houston emphasized, by JNC reports 1 through 8: thiazide diuretics (hydrochlorothiazide), thiazide-like diuretics (chlorthalidone), and the older beta blockers like metoprolol and most other “ols.”

so now on two metoprolol a day my top number is beautiful so is the pulse but the bottom number is still 95 to 110 I'm afraid to try anything new because I think I just have severe allergic reactions as I have a lot of allergies so to have medicine allergies is really not shocking. now she tried chlorthalidone

I've been stable on these two medications since losing approximately 5 stone in 2016. According to the BMI estimator, I still have about 5 stone more to lose, which has and continues to be a challenge for me at the age of 62. I've been taking at least one BP med. since I was 20 years' old, so

Currently taking Olmesartan ( Benicar ) 40mg. and Chlorthalidone ( water pill ) 25mg. Tried adding Amlodipine in the past but it did not agree with me.

Hospital put me on lasix for it but my husband takes chlorthalidone and it says it’s from estrogen fluid retention he takes for high blood pressure. This is a person that use to only take herbs now I’m on all these drugs and not thrilled about it but you have to do what you have to do.

Been put on atenolol-chlorthalidone and it has helped control pretty much all the sever symptoms. Been a stress full 3 months. Anyone else with a similar tale? Any help or suggestions is appreciated.

I am on 25mg a day and I think I should be on 50mg per day. I am Stage 3 CKD