Hi, I'm super new here so I really appreciate if anyone reads this!
I'm 27 and developed unilateral tinnitus after 1 month on Venlafaxine (SNRI antidepressant). Before that I was on Fluoxetine (SSRI) for ~1.5 years before stopping a few months earlier. About a month into having the tinnitus, my GP and I realised it could be a side effect of the Venlafaxine and took me off it cold turkey. However, she thought it was unlikely to be the cause because a) I was on the lowest dose for a short period of time and b) my tinnitus was unilateral. I was checked for anything obvious like an ear infection. One thing with the Venlafaxine that I didn't get with SSRIs is the severe 'brain zaps', vertigo and dizziness when starting and ending it - these all are balance/ear related side effects, so I'm almost not surprised it could have manifested into tinnitus.
It's been 2 months since being off and I still have tinnitus. I've just started a new antidepressant now (Mirtazapine) because I was not doing well without anything. It's an atypical antidepressant and unlike the SNRI, it doesn't have tinnitus listed as a side effect on the BNF (I'm in the UK) so I'm quite hopeful it won't make things any worse. My tinnitus is always there, but it comes in waves as to how much I notice it. I saw an ENT this week who ordered an MRI just in case because of the unilateral nature of it, did a simple fork hearing test which was fine, and is thinking it is caused by the medication. What they couldn't tell me (understandably) is whether it will ever go away or get better. We'll have a review after the MRI and if it's negative, well, that's obviously good news but leaves me with nothing to go off but 'wait and see'. He has already just pointed me to online tinnitus organizations and some local support groups which, the fact he did that, honestly felt more dismissive than supportive.
So some questions...
Honestly, any advice or similar experiences would be so useful, especially if your tinnitus is one-sided. Thanks so much in advance!
I'm 27 and developed unilateral tinnitus after 1 month on Venlafaxine (SNRI antidepressant). Before that I was on Fluoxetine (SSRI) for ~1.5 years before stopping a few months earlier. About a month into having the tinnitus, my GP and I realised it could be a side effect of the Venlafaxine and took me off it cold turkey. However, she thought it was unlikely to be the cause because a) I was on the lowest dose for a short period of time and b) my tinnitus was unilateral. I was checked for anything obvious like an ear infection. One thing with the Venlafaxine that I didn't get with SSRIs is the severe 'brain zaps', vertigo and dizziness when starting and ending it - these all are balance/ear related side effects, so I'm almost not surprised it could have manifested into tinnitus.
It's been 2 months since being off and I still have tinnitus. I've just started a new antidepressant now (Mirtazapine) because I was not doing well without anything. It's an atypical antidepressant and unlike the SNRI, it doesn't have tinnitus listed as a side effect on the BNF (I'm in the UK) so I'm quite hopeful it won't make things any worse. My tinnitus is always there, but it comes in waves as to how much I notice it. I saw an ENT this week who ordered an MRI just in case because of the unilateral nature of it, did a simple fork hearing test which was fine, and is thinking it is caused by the medication. What they couldn't tell me (understandably) is whether it will ever go away or get better. We'll have a review after the MRI and if it's negative, well, that's obviously good news but leaves me with nothing to go off but 'wait and see'. He has already just pointed me to online tinnitus organizations and some local support groups which, the fact he did that, honestly felt more dismissive than supportive.
So some questions...
- Has anyone else heard much or done research about -specifically- unilateral tinnitus caused by antidepressants? It does seem odd it would only affect one ear but hey, I'm no scientist.
- Does anyone have experience with antidepressant-induced tinnitus and did it ever get better or completely resolve? Or are SNRIs/SSRIs truly ototoxic and can actually damage your ear permanently? I'm seeing conflicting things online for whether the tinnitus they cause is because of (permanent) cochlea hair cell damage or something more complicated to do with serotonin in the brain.
- Could the medication be a red herring and should I push for more tests/investigations into the cause?
Honestly, any advice or similar experiences would be so useful, especially if your tinnitus is one-sided. Thanks so much in advance!