
I’ve had long term lower levels of nausea but the last week of school before graduating when I was finishing up a few huge projects, I had a ear infection, but after it was done I still had trapped liquid and it was making me nauseous and otc Dramamine wasn’t enough. And I had to BEG for 7 tablets of zofran to just survive until it was done. I have similar feelings about pain management options tbh. I think our healthcare system is bad at handling chronic health issues for a variety of reasons.
They seem to be under the impression I use it a lot because I’ve been needing it almost every morning the past two weeks. I also get asked about other options. But all they can do is manage nausea. The only other med for gastroparesis I had a severe reaction to. But the only reason I needed a refill was because my prescription was expired. BECAUSE I HARDLY NEED TO FILL IT
For some drs it was the qt risk (usually psych drs, bc some psych meds increase the risk) but they usually just say it’s not something to be taken long term. I get some patients need medication education. But why mess with what other specialists have deemed appropriate (I also had my as needed migraine med prescription cancelled on me bc I “didn’t fill it often enough”)