Experiences with

Relvar Ellipta

My peak flows were 325-300-300 The nurse said that these were fine and to continue taking my Relvar Ellipta but change from Salbutamol to Bricanyl This nurse was also the diabetic, thyroid, HTN and HF specialist. I don’t doubt her qualifications but even I know that my peak flows are not fine.

Relvar ellipta 184 and spirive in capsules. Always rinsing out the mouth and throat. I don't know what else can I do anymore? Is this normal after inhalers? Or maybe I should go to the doctor with this problem? Thanks in advance for all answers. Regards

Ellipta high dose .tiotropium high dose an ventolin .and lots of courses of steriod tabs .just wondered if anyone is on the injections

I have been taking Relvar ellipta 184/22 for three weeks. feels good during the day and night. But I need salbutamol every morning. Only once in the morning. It worries me very much. Is it normal? Thanks for all the answers.

How long does Relvar ellipta take to work? Thank you

I received a new Relvar ellipta inhaler. After all, something new. I hope to help. Regards.

Given Relvar Ellipta suffered severe headaches. Changed to Seratide seems fine but get night cramps. Now given Salbutamol not tried yet anyone similar experience?

Hi I have been using Relvar ellipta 184 for seven days. I got a rash on my face, redness under my eyes. Could this be a problem with the new inhaler? I don't know what to do. Thanks for all the answers.

I use Ventolin, Relvar Ellipta and Montelukast. I am also on Prednisolone for GCA/PMR and I have reduced to 7mg a day from 80mg initially.

I have a question about the Incruse Ellipta inhaler. It was written for me for the treatment of asthma, I read the leaflet and it says it is intended for the treatment of COPD. It worried me because I have asthma and not COPD. Have any of you been prescribed this asthma inhaler? Thanks for all the

Had a chat with my Consultant on this Bronchiectasis, I don,t bring up much phlegm so he thought that was good, it meant it is not too bad. He said increase my Asthma inhaler from 100/6 to 200/6. Try to be active, up to a point, in other words do not go overboard. Keep on with Incruse Ellipta, although

I managed to get a face-to-face appointment with a doctor yesterday but unfortunately other events changed the outcome. As I’ve detailed in my Profile I also have an autoimmune illness and, due to a type of flare, I’d had to increase my steroids (from 6mg of Prednisolone to 60mg per day). I seemed to

I was diagnosed with COPD about 4 years ago. I had another lung function test the following year but have only had “telephone lung function tests” since then😩. The respiratory nurse at my doctor’s surgery retired last month and has not been replaced so I’m finding it difficult to get advice. Just before

Hello everyone, I’m a newbie to posting on here but I have followed some of the chats and everyone seems so friendly and knowledgeable, I wondered if I could pick your brains. I had mild Covid in April 2020 and it left me with long covid, the worst effects of which for me are fatigue and shortness

Has anyone been prescribed Incruse Ellipta 55mg for lung fungus? If they have, how did they find it? All answers gratefully received!!! Thank You..x

I'm currently on 184/22 Relvar Ellipta and Salbutamol after trying every other inhaler available. They didn't work and made it even worse; Relvar now works but the GP says it's the strongest medication they have that works for non-allergic asthma.

Finally, after several weeks of agony my Relvar Ellipta started to kicks in. I'm on the highest dose possibile right now and i'm feeling waaaay better than before. The breath is perfect. I still have occasional chest pain and mucus especially with movements but i can finally live a normal life.

As I wrote last week, I started taking Spiriva again following problems with Trelegy Ellipta. Spiriva had been my first inhaler four years ago, followed by Anoro and eventually Trelegy. I’ve been really short of breath since re-starting Spiriva so I really feel I need to change. As I have no idea how

First of all, thank you for your comments and support. One thing I probably should have included in my post is that, although I was a member of this group during my late husband’s illness, I feel very much like a “new” member, in that I really need to be refreshed into the symptoms/progressions of this

I first joined this forum some 10 years ago when my husband became very ill with COPD plus various cardiac issues. He sadly passed away almost 6 years ago so my contact with the forum stopped. My own health was reasonable - just high BP - but was constantly stressed because of trying to help my husband