Hi I've been taking your drug for 16 years with no side effects - would advise you to contact your Doctor or COPD nurse as others are available. Good luck!
Hi Dollysdream, I have tried at least 10 inhalers, all of which have had side effects, some serious. You need to get in touch with your doctor/respiratory nurse and ask for a different inhaler. At present I am on Spiriva respimat mist inhaler, which has some side effects but bearable for now. You shouldn't have to put up with side effects. I usually give each inhaler two weeks for my body to adjust, before asking for a change, but you must judge if the side effects are bad enough to stop taking it.
You can google the inhaler to find out side effects that people have suffered.
I wish you well in your search for an inhaler that works for you.
Hi Dollysdream, I hope you find one that is suitable, I always rinse my mouth out after using inhalers, as some inhalers can give you a bad stomach if swallowed.
I can't take tiotropium inhalers, it freezes my peristalsis causing continuous bloating belching gerd & associated IBS.
I take Formoterol (1 puff twice daily). It's not as effective as Spiriva, measured with a peak flow meter, but it works without intolerable sides - I think it may be the cause of a little bit mucous in my throat & sinuses, which a saline gargle & rinse helps.
How does symbicort work? My consultant has given me Anoro & Spiolto as my only options with a separate Budesonide inhaler - looking to change to Trelegy 3in 1 in August if deemed beneficial. I kind of understand LAMA LABA inhalers which is what I have to have apparently but where does Symbicort fit in?
Hi....symbicort is made up of.... Budesonide & formoterol fumarate dihydrate. It is suitable for Asthma or as in my case COPD. There are two strengths. I have a feeling the 200/6 is the most popular.. I take two puffs night & morning. .......great stuff. 😁
Jo.
I'd ask your pharmacist, they're the drug experts. Tiotropium (nebulised at the moment) has been a lifesaver for me, god knows where I'd be without it, so I'd put up with a lot of side effects (providing they weren't dangerous) before I'd give it up.
Cheers, I’ll pop into the Chemist tomorrow to check with the Pharmacist.... Tiotropium does work well for me, so really just a case of checking if the side effects I’m having are acceptable .... thanks
I can't take tiotropium, I had the most awful allergic reaction to it. It's disappointing because it's so easily absorbed but don't dismiss side effects because they can be significant even if they are just from a small inhaled dose.
ADVAIR although I also use Spiriva. I use both for close to a decade and while I smoke for 37 years I stop at age 53 and at 63 was ID with COPD Those two drugs stop the disease from getting worst. I am rated moderate and never needed an emergency enhaler. I also do breathing exercises on my own. At age 71, I also having PAD, I do exercise and would shock many people on my physical fitness with all my garbage diseases like diabetes that i have. I've been fighting my mother's health issues she pass along to me for decades, including 75 operation. I live with pain and I fight to live.
I was on Spiriva with the pill you put into the inhaler. I had dreadful side effects. I tried Anora ellipta, but that made my stomach very bad, so I then tried Spiriva Respimat, as the dose is lower. I started on one puff a day for about a month and then increased it to two. This seems to work well, without as many side effects. It can make you tremble a bit, just after you have taken it. My mother has just been given Trimbow - the new 3 in 1 inhaler. She seems to be finding it beneficial, at the moment and it has got some good reviews, but it has only been about, in England, since last October.
Hi just read your post , funny enough I was thinking about seeing my Dr because I have had tingling in my feet for quite a while now. I last time I mentioned it to my Dr I had Vitamin B12 injections and that helped but it has come back again . I use Tiotropium and Symbicort and Nebs and I have the easi breathe inhaler too. And the hospital has just said they are willing to give me oxygen now . No one has ever suggested that inhalers might cause tingling.
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.