Experiences with

Flovent

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.

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.

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 beta blocker .

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 have Flovent and albuterol already (which worked fine before the Singulair I just had asthma flare up from a cold and was out of Flovent which is why she presumably prescribed Singulair).

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 out too much. So now my pulmonologist wants me to try Trelegy Ellipta or Breo Ellipta.

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?

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 - 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 was prescribed Flovent and Salbutamol by the ER Doctor, my NP then prescribed me Symbicort and I’ve been on that until early March.

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

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

Below are a few things to know; I take 4 puffs of Flovent a day(2 when I get up and 2 when I go to bed and have been on it for years), I take montelukast daily(since August) and take lots of vitamin C, D, B,K,zinc,echinacea, elderberry etc.

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?

I have been on Flovent inhaler for 2 months but nothing before this. My PFT seems indicative of copd (chronic bronchitis) but I have been told it is "probably" asthma. I am so confused and unsure what to think.

I have been on Flovent inhaler for 2 months but nothing before this. My PFT seems indicative of copd (chronic bronchitis) but I have been told it is "probably" asthma. I am so confused and unsure what to think.