Mirtapazine?
Hey guys! Just a little update, as I’m looking for any new information or people who have had similar experiences.
I was diagnosed with vestibular neuritis (VN) this summer. It was confirmed on July 22nd through caloric testing, which showed a 39% deficit in my right ear. Initially, in June, the doctors thought it was BPPV, but I continued to experience nausea and some dizziness, so I underwent further testing and was eventually diagnosed with VN.
My doctor prescribed Betaserc twice a day for two months and scheduled a follow-up appointment. Yesterday, I had another caloric test, and the deficit had decreased to just 8%, meaning there has been significant improvement in my vestibular function. My doctor said that the remaining nausea and dizziness shouldn’t be caused by the VN anymore.
Since I’m still experiencing symptoms, I was referred for a gastroscopy, but they couldn’t find anything wrong. After that, I was sent for an MRI of my brain and neck to check whether anything in the cervical spine could be contributing to my symptoms. I’ve had the MRI, and I’m waiting for the results next week.
In the meantime, we’ve also discussed a Plan C. If the MRI comes back clear, my doctor has prescribed mirtazapine, an antidepressant, to see if it helps with my symptoms. The plan is to start with half a tablet daily for the first month and then increase to one tablet daily for the second month, as prescribed by my doctor.
I’m wondering if anyone here has been through something similar, especially if you’ve experienced ongoing nausea and dizziness even after your vestibular function improved. Has anyone tried mirtazapine for these kinds of symptoms, and did it help?
I’d really appreciate hearing about your experiences. Thanks so much! ❤️