Experiences with

Flovent HFA

I’ve been on Flovent HFA for ever and recently the manufacturer is no longer making Flovent. I’ve had to resort to the generic Flovent which I feel it really is not working as the brand Flovent. I’ve been having more asthma exacerbation.

I have been on a steroid inhaler for along time ( Flovent HFA ). Recently I have had to resort to the generic Flovent because the manufacturer is no longer making it . I’ve noticed a big difference in my breathing, it’s not working as good as the brand. And I keep having an asthma exacerbation.

I also take Flovent hfa and Spiriva respimat . Yesterday, I used my nebulizer Levalbuterol first waited 2 hours then used Spiriva. Oh my gosh , after I used the Spiriva I started coughing and like I couldn’t breath for a few. Then it passed. Has this ever happened to anyone?

Hi everyone, I have asthma plus paroxysmal a fib. My normal inhalers are Flovent , Levalbuterol and I take montelukast. Also am on metoprolol Succinate Er for high blood pressure. Recently I had an episode of high blood pressure . The dr. Changed my metoprolol to cardivilol which is a non- selective

My asthma has been acting up lately. I take Flovent a steroid inhaler and Levalbuterol . Recently I asked my Dr. about adding another inhaler. I feel like I need something more. They recommended Spiriva respimat but my insurance won’t cover it. Then they recommended maybe adding Incruse Ellipta which

I know this med is posted a lot, and there are a ton of different side effects people experience but I am wondering if mine are related to Singulair or if it truly is anxiety. Sorry ahead of time for such a long post! I recently experienced heart palpitations while driving, was lightheaded, faint,

GCA and earache Hello you lovely people! Having been off pred for PMR since July 2023, after a near perfect tapering program since January 2022, according to NHS guidelines, I thought I would not be needing to post in this forum again. However, I did keep my membership going just in case! And the

Hi everyone , For thoses of you that have a fib and asthma. Have you been able to take combined inhalers without triggering an a fib attack ? I’ve been on Flovent for quite some time but recently needed something more to open me up. I’ve tried Spiriva Respimat which was great accept it dried my mouth

Hi - i have ETD (awaiting to see ENT) the fluctuation of this condition is extremely hard to bare - I have religiously for nearly a fortnight been trying things, gargling, Otovent balloon, lymphatic draining, steaming etc etc...,some days it feels like its improving but today its awful, blocked and

It is known that a symptom of difficulty swallowing is associated with B12 deficiency. How I experienced it was not accepted by the medics I hired. At times usually at night I would aspirate/choke on food and sometimes fluid my whole life. This is often called having go down the wrong tube. It was

I post here as some on this forum helped me discover a solution. It is my understanding that the problem was caused by the difficulty swallowing caused by B12 Deficiency. The Eustachian tube is closed the majority of the time. It opens in response to pressure changes including when swallowing. About

So I was DX with chronic swimmers ear and told all I could do was treat with alcohol and vinegar. I read here about blocked Eustachian tubes and did some reading. So far I have been able to self treat with trying to pop my ears and swallowing. If I can not keep up I know the next step is to buy Otovent

Hey All! A little bit of background on me. Early October I was infected with COVID-19, I’m 4 times vaxxed, and while it was only two days of symptoms, I ended up with SOB on day 3 which later turned into Long COVID. I was prescribed Flovent and Salbutamol by the ER Doctor, my NP then prescribed me Symbicort

I’ve posted this on SRUK forum too. Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and

Sorry this goes on a bit. Along with my UCTD with systemic sclerosis gut problems I’ve developed, I’ve had hearing problems for years. I’ve never really thought it could be another autoimmune problem but recently I couldn’t hear my own voice. I wear hearing aids and have just got new ones and thought

I have bad asthma and 95% of the time my regular colds turn into bronchitis. With wearing masks I have not had a cold or bronchitis for 2.5+ years. I am now on day 9 of bronchitis and was wondering if anyone can tell me how long the wheezing and lungs full of phlegm usually last with bronchitis? When

So it's been just over a month since I've had T caused by clarithromycin. Since I last posted I've seen a high street audiologist for a hearing test and to discuss the T. No hearing loss, which is good right? Hearing loss can make T caused by antibiotics permanent, I've read. The audiologist sent a

hi, I have bad asthma but Flovent keeps it under control in the summer months. I started having a sore throat and felt tired yesterday and tested positive for Covid. Today is the same. my question is for those who have had omicron specifically What days were the worst for you? The first few days

23F, 123lbs, 10 years daily smoking marijuana. For 3 years I've had chronic daily phlegm - like hocking up a loogie. I started getting chest pains and some shortness of breath after quitting smoking 2 months ago. I have been on Flovent inhaler for 2 months but nothing before this. My PFT seems indicative

23F, 123lbs, 10 years daily smoking marijuana. For 3 years I've had chronic daily phlegm - like hocking up a loogie. I started getting chest pains and some shortness of breath after quitting smoking 2 months ago. I have been on Flovent inhaler for 2 months but nothing before this. My PFT seems indicative