Spiriva in spanish
Common Questions and Answers about Spiriva in spanish
spiriva
That will dissolve the phlegm and has a neutral ph, unlike stuff like Spiriva which is acid. (Fungi thrive in an acid environment.) Also you might want to take a potassium iodide supplement. That will help, and oil of oregano will go after fungi with a vengeance. Usually the culprit is Candida albicans.
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.
my husband has copd he uses adviar spiriva and combivent and it doesnt work what can it be thak you
In the past 16 days I have begun using Spiriva in addition to the 2 doses of Symbicort I was using daily. 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.
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?
Spiriva is an anticholenergic used to treat various forms of COPD, but rarely asthma. The primary function of these medications is to reduce mucous in the respiratory system. They do have a mild broncho-dilating affect. I have not used Spiriva so I am unsure of its dosage, but I have taken ipratropium which is in the same class. As a neb solution it lasts 6 hours and as an MDI it last 4 hours. Check your prescription for dosing on this medication.
Spiriva® HandiHaler® (tiotropium bromide inhalation powder) has a maximum duration of action of about 36 hours. To be safe, you would want to be off the medicine for 48 to 72 hours before the spirometry. It would have been preferable, but not mandatory to do the pulmonary function tests (PFTs) at the time the diagnosis of chronic lung disease was made especially if the diagnosis was unequivocal. The other important question would be, “Why 3 CT scans, presumably of your lungs, in 16 months?
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 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.
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.
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.
One possible approach would be to use some type of Spacer device, to be placed between your inhalers and your mouth.
Wish I could be more helpful.
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.
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.
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.
I'm suffering PATM long time ago, I'm Spanish living in Spain anyone here with the same problem I really would like speak with someone in Spanish who lives near, doesn't care man or women just to talk.
Waiting for someone, please let your contact details here.
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 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 !
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.
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