Spiriva if swallowed
Common Questions and Answers about Spiriva if swallowed
spiriva
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?
my husband has copd he uses adviar spiriva and combivent and it doesnt work what can it be thak you
Yes! Spiriva is a long acting 24 hour broncho-dialator. So this means it will dialate your airway, make it bigger so air can pass thru it easier.
Adviar: is a cortico-steriod. This means it is a anti-inflammatory type med that will take the inflammed part and calm it down.
These are two very different medications. one holds it open and the other calms down the inflammed parts.
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.
I have wet macular degeneration as well as COPD and my ophthamalogist theorizes that the weird "blisters" that are appearing at the site of the oozing veins may be caused by the steroid content of my asthma medication ( namely Spiriva). So he has asked me to change to something that doesn't contain any steroids. My pulmonologist has suggested I add floridil to my albuterol nebulizer.
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.
m on Advair or oral steroids. So I try to avoid them if at all possible. I am currently using Spiriva HandiHaler which I believe is not suppose to have any steroids but I keep getting Thrush in my mouth ! It is a constant problem even just using the Duoneb, and especially if I have to take any antibiotics. I'm, constantly having to take Fluconazole tablets after a round of antibiotics for candidiasis under my breasts and in my mouth.
COPD Fev 45-50% , have been on Flovent,/Spiriva/ Proair 10 years and am sensitive to medications. I dont smoke.
Have had increasingly reactive airways for 3 years, had first Dxed exacerbation last fall triggered by woodsmoke. No congestion and did not take antibiotics. Pulmo said airways 'sounded just like asthma' but do not have that Dx. Airways felt raspy, swollen, inflamed. Have slowly recovered on a higher dose of Flovent.
The normal lining of the lung clears phlegm by lifting it up and delivering it down the esophagus (you can think of this as the food pipe). The normal situation then is that, phlegm is swallowed in small, regulated amounts that it is entirely automatic (there is no need to push it down voluntarily in the manner of swallowing a lump of food).
Smoking destroys the lining, and hence to clear phlegm – the lungs must cough it out. Hence, the cough may be persistent.
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.
Is there any history on how long these inhaded drugs (poisons) remain in the body. I stopped both five days ago and have noticed a marked improvement in joint aches. Still awaiting improvement to attitude to do things I totally enjoy, have energy to do basic housekeeping, limit naps to one a day instead of most of the day....
My lungs seem to be dispersing copious amounts of mucus...and sinus drainage has slowed. Without any exertion I can breathe normally...whatever the hell that tis..
coughing phlegm from lungs for the past six months, have taken antibiotics with no results, did take predrisone together with SPIRIVA 18 mcg and ADVAIR 500/50 for the past month. Still coughing up phlegm and have limited lung capacity. Any suggestions comments.
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.
Is it possible to be misdiagnosed with COPD if person is recovering from a "chest cold" at time of the X-Ray?
does spiriva or alvesco cause acid reflux?
This discussion is related to <a href='http://www.medhelp.org/posts/show/284791'>Asthmatic bronchitis, how long does it usually last? Could I have something else?</a>.
I use Albuterol, SPIRIVA and ADVAIR to control Asthma & COPD. I also take CRESTOR for cholesterol and ADVIL for arthritis.
In the last month (after starting SPIRIVA), when I first wake up in the morning, my eyes "roll" from right to left in an arcing motion when I attempt to focus on something. After a few attempts to focus on an object (the clock on the clock radio), the movement stops and I'm fine.
Any thoughts?
I also see a rheumotologist for UCTD and am on Placquenil and prednisone (5 mg or less QD during flares.) Was put on Spiriva and Symbicort. Had to stop Spiriva due to intolerable cholinergic effects. Am fine so far with just the Symbicort. Talked with Rheumy about value of CT scan and if it would change any of the treatments. He felt no. To me is just seems like a very expensive test and wouldn't really change anything. I don't have any clinical signs at this time of PH.
I currently take advair and Spiriva medication.. is this the one and only mediacation,since there are no genericand here in the united states unlike the rest of the world which has a free market, we are controlled by the drug industry.
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.
why do i cough up blood? my dr. has tried to explain it to me, something about air ways, air vents, etc. i do this the majority of the time maybe 2 days in between doing so. sometimes it's bright red and then sometimes a darker pink. i have 50% breathing capacity and am on oxygen. it's real scary even though i've been told not to worry about it. i take advair and spiriva and don't cough up that much but when i do and it is very little.
I just found out i have copd, on oxgen 24/7, feel ok but have trouble taking deep breathe, prednisone seem to help about six hours after i take it, but im getting scared that if i dont get relief soon ill die, im only 53 , i need to hear from other people with this problem, i feel so bad all the time
My husband and I were putting on one of those window kits to keep out the cold air out and I became very tired and my arms and legs felt like they were burning. I use 2 inhalers a day, Spiriva and Advair Diskus 250/50 and use Albuterol inhaler as needed. I am 70 years old. I have never been real athetlic but I find I am getting weaker all the time.
How do you tell if Afib converted on its own or if the medication did the conversion or if the medication was causing the Afib? I have been to the Primary doctor and Emergency room both said I was not in afib currently. Another words, when do you know when to stop taking the medications? In Nov 2013, I have Aortic heart valve replacement and a maze procedure. My old cardiologist wanted to do a cardioversion but I didn't want it, so I had to change Cardiologist.
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