Spiriva copd
Common Questions and Answers about Spiriva copd
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?
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.
Is it possible to be misdiagnosed with COPD if person is recovering from a "chest cold" at time of the X-Ray?
I was diagnosed with moderate COPD in Oct. 07. I too was put on Spiriva and Advair. About 3 mths. on these meds, I had the sickest winter of my life. Pneumonia, bronchitis and 3 months of painful pleurisy. I instantly stopped the Advair. Then, I stopped the Spiriva. And for almost 2 yrs. now, I am doing better without these meds, then when I was taking them. I don't suggest this stopping of meds for everyone. But, personally these meds made me much worse.
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.
http://www.nycomed.
I started Spiriva 2 years ago. I had mild COPD. I also had no prostate problems prior nor did I have a family history of Prostate cancer.Towards the end of last year I was diagnosed with stage 3 prostate cancer, gleason 10. My psa was 18.1. I have since had the DiVinci surgery (which I fully recommend) and I am not undergoing radiation. None of the existed before Spiriva!!!! I found out that if you are on Spiriva 2 years - 5 years your chances of getting prostate cancer is 50%.
I am 56 year old woman who was diagnoised with COPD 10 years ago. I am not taking any oral steroids at this time. I use Duo Neb Inhalation 2 times per day and oxygen on 2 L continously. The Pulmonary Doctor keeps having me try to use Advair but I get thrush in my mouth anytime I'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 !
I have moerate COPD. As to Spiriva, I used it briefly and it turned my lungs to glue. If any of you have thick sputum that is hard to expel (caused by all those drying medications), vitamin B5 is an outstanding mucolytic (mucus thinner). I take 1000 mg. daily. It is also specific for adrenal fatigue.
I take Spiriva Respimat (tiotropium bromide) 2.5 mcg/actuation, and Wixela (fluticasone propionate salmeterol inhalation powder) for my COPD. Is there a sequence I should be taking these meds in? Is there a time frame I should use between the two meds?
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 was diagnosed with copd 5 years ago,,had pulm,,test,,,,,recently , had another lung function test,,,the doctor showed me the lsit with all the numbers ,he said a gp would look and see nothing,,but he pointed out 1 number was 176 he said that shoud be below 100,,that number shows mild to moderate emphysema,,but said he could not tell me my lung capcity,it that number bad???
I was recently diagnosed with early copd. Since I do not have health insurance, i go to a clinic. The physician's assistant has prescribed singular for my copd, I don't feel that it is helping me very much. I mostly have shortness of breath & coughing in the evening. This disease frightens me because I don't feel I am getting the right medical advice. I asked about simbicor & spiriva and was told that those meds are for later stages of copd.
did the COPD show up immediately when the tests were done? or did it take a while before you figured it out?
Yes, there are. Spiriva® HandiHaler® (tiotropium bromide inhalation powder) is one and Serevent® Inhalation Aerosol (salmeterol xinafoate) another. Each is a bronchodilator and capable of giving good relief of shortness of breath.
I was diagnosed in Oct. 07 with moderate COPD. Was put on Advair, Spiriva and ProAir as my rescue inhaler. After being on the Advair and Spiriva for several months, I began to become ill. Spent the sickest winter of my life, while on these inhalers. Bronchitis, pneumonia and pleurisy that was so painful for 3 months. I was doing okay before the inhalers. At least not sick all the time. Then, I went off the inhalers. Personally, I said heck with them.
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.
I am taking Flovent, Spiriva and ProAir. Since I've been on the medication I've been Dxed with idiopathic neuropathy, cervical radiculopathy, carpel tunnel. I also have other entrapment symptoms, ulnar ,and I think in my legs as well.
Sometimes I get a burst of nerve pain in my arms and legs a few minutes after using the Flovent and it also causes some tendon swelling. I've shown over and over that I have less pain on lower doses of meds.
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?
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.
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