Experiences with

Advair

So now she changed it to advair discus 500 . She said that this was comparable to Breo. I am really scared to try advair because of it being 500 that maybe it will be strong also. I also have paroxysmal A Fib and I don’t want to get an episode of A Fib.

I am on Advair.

Seems like I have had a reaction to Advair and now Spiriva. He told me to use the drops for 1 week and see if I feel better. I am so scared that this is from the Spiriva. What next?? Will Ifind an inhaler that I will not have a reaction to?

So the Dr. recommended advair discus 500 which she said it was compatible to Breo . I haven’t started it because I am scared that being it 500 that it might cause me an episode of A Fib. Is there anybody that has A Fib and asthma been successful with a combination inhaler ?

I just got new health insurance and they will only approve Advair Diskus. Should I be worried about it not working as well or getting sick from switching? Does anyone have any experience or advice? Thank you!

Today was my first time using 60 mg of prednisone and advair. I feel like my breathing was better during the day, but it got worse in the evening. I feel like my throat and my chest are tight and air is heavy. Duoneb helps a little bit.

I was prescribed advair, singular, cough medicine with antihistamine, and claritin, and or zrytec. It wasn't much help.

My take on it is that ever since I was hospitalized and sent home and taking first Advair, then Breo and now Symbicort everyday, that medicine alone has possibly contributed to my not feeling right.

I have advair inhaler, administer breathing treatments, allergy meds, prescription cough meds, but it is a constant battle. It started over two years ago. I am so tired of struggling every day. The lung specialist I have seen seem to think it is asthma, but I am not convinced it is?

.Hello, I was diagnosed with PBV stage 2 9 years ago. Now early stage 4 , been taking Urso which worked for years but now going to also start on Ocaliva next month. Recently I was in a major car accident and have a ruptured spleen, which is on the mend, but a huge hematoma beside it which is causing

My wife (age 58) has been diagnosed w/ PMR. She is down to 15mg of prednisone, but her symptoms are already getting worse. She is on Dapsone (antibiotic), Prednisone, Gabapentin, calcium and vitamin D suppliments, and Advil (which she says does nothing). It is really hard to watch her condition deteriorate

After a prolonged period of sleep deprivation, I'm talking 1.5+ years of horrible sleep I started feeling this sensation in my head that feels like a pressure build up, or a burning sensation all throughout my head. It's extremely unpleasant and chronic for me. Advil, Tylenol, Aleve and other over the

Hello - I have really bad neck pain about everyday. I try to message as well as stretch yet the pain continues. It's from my shoulders, neck to my head/headache. I try taking Ibuprofen and Advil yet they don't help Can you please give me any pointers. Thank you :)

If anybody hasnt been told benadryl makes RLS worse any meds that are like advil pm or tylenol pm have benadryl.Also carbs, sugar and caffeine make rls worse. I have done my research i had it since 2005 .mirapex helps at 1st but becomes the nightmare drug. They say klonipin works..we will see im waiting

Its 2:39AM and I can't sleep again. I had a klonapin. 3 Advil, 1-300 mg of neurotin ,not all at once, and still can't sleep. The pain is in my back and abdomin, arms burning, legs numb like pins and needles. This is almost every day. Nobody really gets how bad fibro can be. I think covid long haulers

Good Evening Everyone. I hope everyone had a wonderful Christmas!! As promised I am giving you my update on Kesimpta. I started with my first injection on Christmas evening. It was very easy injectable pen too operate, the injection took approximately 10 seconds too complete. I only experienced

Effects of commonly prescribed nonsteroidal anti-inflammatory drugs on thyroid hormone measurements Author links open overlay panelAlkaBishnoiM.D.abKennethLidonniciM.D.c Show more Outline Share Cite https://doi.org/10.1016/0002-9343(94)90148-1 Get rights and content Abstract purpose: To assess the effects

Started ivig 6 months ago. For 4 months I had a relatively lose dose but continued to get infections so cll specialist increase dose for #5 .I didn't feel great for the whole 4 weeks, tired many many headaches and nausea so she cut that dose down by 1/3…I had #6 on Friday and by Sunday my headache was

Looking for advice on Bayer aspirin. Is it safe to take once in a while. I know Advil is a no no and Tylenol is a better option but wasn't sure about simple aspirin. Thanks.

Hi all, haven’t been on here in short while but thought I’d share an update and ask a question. It seems my new neurologist found I have positive ganglioside antibodies. I was able to get the results from the lab and posted a picture here. Does anyone else have these antibodies? After doing some research