When did spiriva go on the market
Common Questions and Answers about When did spiriva go on the market
spiriva
You might want to read up on the side effects of Advair. There has been a movement away from the use of inhaled steroids. I stopped using Advair almost four years ago.after developing serious side effects. My condition actually improved when I got off it. You might be interested to know that inhaled steroids do not reduce mortality. I tried Spiriva but found it very drying and had to stop using it.
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.
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 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.
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. And knock on wood, I have been doing pretty good without them. No more constant illness. I still use a rescue inhaler.
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. And that was with treatment with antibiotics. I did not like Advair whatsoever. Stopped taking that.
Nobody knows. Vertex isn't going to make any claim and the FDA isn't going to taint their objectivity by offering a prediction.
It seems that the often repeated and repeated prediction is middle of next year.
It is a different question entirely what it will be priced at and what insurance companies will do with regard to paying for the triple therapy.
Many people think the cost will be too expensive.....
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?
Go to the doctor or ER. The only symptoms I had for a massive PE was SOB. I have, in the last two weeks been diagnosed with more DVT's and PE's in both lungs. Request a d-dimer test. It is the way they started to look for mine. Be persistant!! I know that it is hard to manage the finances of illness, but the alternative is not very appealing.
When I was first diagnosed with DVT's and PE's in January of this year I had let it go for 10 days. I am lucky to still be here.
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.
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.
Hello and hope you are doing well.
When using inhaled corticosteroids, some of the drug may deposit in your mouth and throat and cause laryngitis. This can cause coughing, hoarseness, dry mouth and sore throat. Gargling and rinsing the mouth after each puff on your corticosteroid inhaler, may help to prevent mouth and throat irritation.
Hope this helped and do keep us posted.
What Spiriva is a a capsule that you place in the device for delivery of the medicine. You place the capsule in a hole inside then when you close the top and press a button a little nail shaped metal piece stabs a hole in the capsule. You blow all of your breath out slowly then suck in slowly while it delivers a little at a time to your lungs. It really works to cut down on coughing because all that phleum doesn't come up like it use to.
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.
Thanks for the input. My MD put me on Spiriva, and during the summer I experienced what felt like about 2/3 lung capacity. Symptoms improved when I went to the coast to get some "clean" air. When I got back to the valley I had a lung function test conducted, and the MD said Spiriva was not medically indicated. So now I'm not sure if I actually have COPD or not. Will take your advice and get a second opinion.
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.
It is now called Insevik(SP?) The drug name they used in the trials was Telaprevir.
Recommended
