Spiriva how supplied
Common Questions and Answers about Spiriva how supplied
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
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.
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.
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 was told that one of these breathers cannot be used with Proventil. Please tell me if it is Advair or Spiriva. I can't remember which one the doctor told me.
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.
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.
For 6 mths. after diagnosis, I did have insurance. So, I was prescribed Advair, Spiriva and ProAir. While having insurance, I did get a second opinion on the COPD by a pulmonary doctor as well. But, between my family doctor and the pulmonary doctor, I was prescribed these meds for my COPD. Three months after being on all these meds, I spent the sickest winter of my life. Pneumonia, bronchitis and pleurisy. I had never had pneumonia in my life. And the pleurisy lasted 3 long painful months.
i went wks and wks on inhalers after inhaler, prednazone , which in fact i needed antibiotics . how i found out is i went to the E.R. and they told me , then i scheduled myself an apt with a pulmonary doc. and he said he didnt see any indacation of asthma or copd ! I would get a second opinion if i were you !
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..
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.
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.
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.
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.
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 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 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.
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 agree. They still work for me but a part of me still misses my old white buddy, rather than this new blue imposter!
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