Spiriva adverse effects
Common Questions and Answers about Spiriva adverse effects
spiriva
But - I objected - they do not cure, they’re only supposed to make you feel a little better and have nasty adverse effects. So he gave two new drugs: Seebri Breezhaler (glycopyrronium) 44 micrograms and Oslif Breezehaler (Indacaterol) 150 micrograms. I googled them quickly and they seem to be pretty similar both to spiriva and to one another. Can you please tell me whether you believe 1) these two new inhalers go well together and 2) it’s an improvement over spiriva.
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.
My guess would be if it is day 5 without the inhalers, then they should be out of your system. I too had problems with Advair and Spiriva. 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.
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 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.
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.
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 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.
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 still grapple with thought of having it but I just don't want to dwell on it......
Anyone have any thoughts about the value of this?
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.
of vitamin B5, plus mullein extract, and MSM daily. B5 will also counteract the drying quality of albuterol. There are absolutely no side effects. I got off Advair because of very serious side effects which actually made my breathing worse. Symbicort is probably just as bad. They are steroids that throw your adrenals out of whack. Because of Advair I suffered serious adrenal fatigue which I am being treated for. Stick to natural whenever you can.
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.
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.
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.
About 2 months ago I was prescribed Restasis Eye drops and after being on the dug for about 2-3 weeks I noticed that my mouth got extremely dry. So I looked up all the side effects and none included dry mouth. so I called the Dr. that prescribed it to me and I was told that 1% of patients get this dry mouth and I was told to discontinue use of the drug and come see the Dr in 1 month. It's been a month and I went to the Dr but the symptoms has gotten worse instead of better.
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