Spiriva and mucus
Common Questions and Answers about Spiriva and mucus
spiriva
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?
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.
Is there anything I can avoid, which would help me, to produce less mucus, I live in a very damp part of England, and recently,2002! I was diagnosed as having Bronchiectasisis. Daily I produce Mucus, but recently it has got a lot worse,and is now continuous, It's very Anti Social.
Spiriva is extremely drying and it will make for thick mucus that is hard to cough up. Advair is also drying and I note that your extremely high dose of that inhaled steroid is not generally recommended.
I got rid of Spiriva because it was drying. It didn't help anyway. I got rid of Advair because I developed adrenal fatigue, osteoporosis, and it gave me a hacking cough which exhausted me and could not have been good for my lungs.
since the lost of his job i hav only been able to get my albuterol nebulizer meds, Theophylline, spiriva inhaler,. and numerous packs of Musinex 1200mg daily, to keep the mucus at bay!!!, but cant get the advair any longer, and which is a good thing after reading what i just read on this updates,. I don't want to take it anymore!...I think I wll purchase the B-5 for real!
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.
It is used primarily for the prevention of motion sickness. It can cause dryness of saliva and mucus and might help reduce the amount of mucous. You state that your asthma is, "...always out of control because of all this mucus". That could be true, especially if the mucus originates in the upper airways, rather than your lungs. However asthma is not infrequently characterized by excessive mucus and the mucus could be caused by your asthma.
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?
Common COPD inhalers that contain steroids are Advair, Symbicort, Breo and Dulera.
after checking, this bladder problem is a side effect of Spiriva...I had used Spiriva for over a year and the infections/non-infections got more frequent until I had to go to the urologist...I was on Azo Standard most of the time. I alerted my pulmonologist as to my problem and he took me off the Spiriva. Since being off the Spiriva, my breathing has gotten worse....my Dr said there was no replacement for Spiriva...I'm writing to find out what others might know.
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.
Well thank u he does the breathing exerciises I sit up with him patting his back he's got nebs ventolin spivira but they just don't seem to help him at all. It was very nice of u to give me some advice to me I'm just feeling a bit down with it all. Social services suppose to have helped but that was a year ago.
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 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 heard "not" I was diagnosed with acid reflux and yet I also have asthma, so they put me on spiriva and activar (something like that) and it didn't bother my so called acid reflux. It's just suppose to help with breathing. It can however bring on thrush, so be sure to wash the inhaler each time after use.
He is prescribed 16 hrs oxygen daily (we have machine)but only uses this when he feels he needs it (some days as little as 3 hours). He daily takes spiriva, symbicort and sabutamol inhalers and calcichew tablets also mucodyne capsules occassionally. These are prescribed by his doctor. He also takes Nytol (over the counter) herbal sleep tablets quite often. For the past 18months he has suffered from a tingling, burning feeling in his skin.
At my six-monthly checkup at my local hospital here in Spain there was a replacement doctor and since he was young I thought he might be willing to hear why I was not taking spiriva and steroids. He confirmed that a person with severe COPD MUST use these medicines. But - I objected - they do not cure, they’re only supposed to make you feel a little better and have nasty adverse effects.
Thanks for the input. My MD put me on Spiriva, and during the summer I experienced what felt like about 2/3 lung capacity. Symptoms improved when I went to the coast to get some "clean" air. When I got back to the valley I had a lung function test conducted, and the MD said Spiriva was not medically indicated. So now I'm not sure if I actually have COPD or not. Will take your advice and get a second opinion.
Recommended
