Spiriva and kidney disease
Common Questions and Answers about Spiriva and kidney disease
spiriva
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Finally there are many causes of fluid retention including but not limited to heart disease (to rule this out may require further heart testing such as an echocardiogram) kidney disease, liver disease, and insufficiency of the large leg veins.
You might want to discuss these possibilities with your doctor.
I've been using Spiriva nearly 10 years and this year my PSA results spiked from less than 1 to above 6. Where did you get your info regarding the statistics on prostate cancer, as I would much like to study it.
Although I get good (better) results from the combination than Symbicort alone, since starting the Spiriva, I am experiencing very dry mouth, and nasal passages to the extent that I occasionally experience light bleeding when I blow my nose.
My questions are, How serious is this side effect, Should I continue using the Spiriva, Continue the Spiriva but stop the Symbicort, or Drop both and just take Combivent which I currently use as my emergency inhaler?
I'll try to be brief. My dr. ordered a pft last week (following three ct scans over 16 months). I had been using Spiriva for three years. My question is how long should I have been off the Spiriva for the test to show accurate results? Shouldn't I have had the test before being given Spiriva? Thanks in advance.
You are obviously doing the right things, including mouth washing after drug use and you are correct that the Spiriva and Duo-neb do not contain any steroid.
Unfortunately, some individuals develop allergy to the ipritropium in the Duo-neb or to Spiriva and the drug simply irritates the membranes of the mouth allowing the thrush to take hold.
That you also develop candidiasis under your breasts suggests that you might, for some reason be predisposed to this infectious agent.
I read that roflumilast is a new drug that controls the inflammation that causes copd to get more severe. I currently use Spiriva and this article said that there was a higher rate of sudden death with the mist inhalers in people with vascular disease. So I am thinking about switching up after talking it over with my doctor.roflumilast is a pill you take daily.So I guess your answer would be anti-inflammatory.
I have emphysema. i use advair twice a day and spiriva one a day. The biggest problem for me is that I always seem to havemucus build up in the mornings. My doctor has told me to try mucinex, but that doesn't seem to work all the time. So i try using albuterol in the morning to help loosen up the mucus so that I can breath better.
If you are taking Duoneb there is no point in taking Spiriva because Spiriva is related to the ipratropium that is a consitituant of Duoneb. Also Spiriva is extremely drying which may be why you are feeling so uncomfortable.
To be using Duoneb five or six times a day you would have to be close to death. Obviously you aren't, so you can cut back without any problem. I have serious COPD and my use of Duoneb averages 3.5 vials daily.
The big question is - how bad is your COPD?
Common COPD inhalers that contain steroids are Advair, Symbicort, Breo and Dulera.
Spiriva is very gritty and irritating. Also it is very drying. I stopped using it. And I got off all inhaled steroids because of the serious problems they caused. Now I use only natural anti-inflammatories and am all the better for it (as well as richer). By the way, my COPD is as bad as yours.
I was taking acetylcysteine (Mucomyst) by nebulizer for congestion. This is not always available so I had to make do in some other fashion.
I was told to stop my spiriva in Aug. that I had been using for about 3 yrs. This was after I had a PFT for the first time. I've had three ct scans over the past three yrs. Shows granulomata and calcified nodules..no change. For the past couple of days I've been very SOB and my arms feel weak and heavy. My chest doesn't hurt it just feels tight/full. Today has been worse. I was also put on neurontin 1 1/2 weeks ago for headaches and wonder if that could have anything to do with it.
I am 22 and have just found out I have kidney disease. I do not want to tell my family, because I know they wouldn't deal with it very well. Is it likely to be easy keeping this from them (I live with them)? I am considering not receiving any treament for now to make extra certain family don't find out.
i have kidney disease my creantine 2.12 my gfr 33.5 my normal is 1.
Hi there, about a month and a half ago I started feeling like something was always under both my ribs and it has been persistently like this and it's really uncomfortable, I'm also always itchy at night and have been feeling really dizzy and lightheaded constantly. I've went to my doctors and they took my bloods and all that came up was that my potassium levels were slightly high.
Hi there, about a month and a half ago I started feeling like something was always under both my ribs and it has been persistently like this and it's really uncomfortable, I'm also always itchy at night and have been feeling really dizzy and lightheaded constantly. I've went to my doctors and they took my bloods and all that came up was that my potassium levels were slightly high.
Hi recently I had pain on my adominal, usually the pain is on the right upper abdomen and the pain seem to move to lower left and right. I haven't did my kidney function test yet but I already did liver function test and my ALT is 9 U/L does this low ALT indicate that I have kidney issues?
Im very sick and cant get anyone to help. Ive even had a dr tell me he wont diagnose me with kidney disease until I get insurance so I got insurance and they denied coverage before he even diagnosed me. I then had to quit working due to illness. Now Ive got no job and no insurance and no help. What do all these results mean? Whats the next step? Who will help me?
Hello,
The symptoms are definitely suggestive of kidney disease. You should get an ultrasound kidneys and kidney function tests done to confirm the diagnosis.
It is very difficult to precisely confirm a diagnosis without examination and investigations and the answer is based on the medical information provided. For exact diagnosis, you are requested to consult your doctor. I sincerely hope that helps. Take care and please do keep me posted on how you are doing.
Obviously, he has severe anemia and no amount of iron will fix this kind. I have never heard of chemotherapy for kidney disease or kidney damage. I have kidney damage (kidney disease) due to an autoimmune disease. Kidney function is at 26% now, up from 20%. Autoimmune disease is in remission since I had all the mercury fillings removed from my teeth.
I would encourage both of you to talk with his endocrinologist about looking into possible changes that can bring his a1c levels well down below 7. That truly is his best protection not only against kidney disease, but against other complications. If sugar levels are maintained at near normal levels, damage cannot happen.
I have a 14 year old cocker spaniel who was recently diagnosed with kidney disease. She originally got sick a few weeks ago with pacreatitis, and when she recovered her lab work showed the kidney problems. We have been giving her fluids every other night as well as the epakitin powder with her food. Her blood report was better this last time. However she seems pretty good, has a good appetite ect and I'm wondering if there is anything else that could be causing this disease?
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