Have I Developed (Permanent) Reactive Tinnitus & Hyperacusis from Exposure to Security Alarm?

[NBH]

Hello everyone.

I'm twenty six years old, and for most of my life, I could recall hearing a faint "eeee" whenever I was in a quiet room, but it never really bothered me. I always assumed it was what everybody else heard in complete silence.

Fast forward to Sunday, May 16th (just over two weeks ago); I was exposed to an ear-piercing security alarm (it was tripped by one of my parents on accident). A few days later, I began to notice that the ringing in my ears had become more audible. I did some research and discovered that I had tinnitus, and sank into a deep depression that I'm still struggling with.

For what it's worth, I've actually been exposed to this same alarm on numerous occasions before (the security terminal indicates that it's been tripped nineteen times since we had it installed last May), and I can't recall my tinnitus worsening after any prior incident, but I digress.

Over the last several days, I've noticed a couple of things:

The first is that my tinnitus seems to become louder in direct response to certain noises (running water, car engines, leaf blowers) and immediately dies down once the sound is absent. In addition, certain musical instruments have a "tinny" sound to them, and some musical pitches are completely obscured by a sudden high-pitched ringing (as it were apart of the composition itself, although this seems to occur more often with low quality speakers).

The second thing I've noticed is that I've developed an increased sensitivity to sound. I find myself reacting to sudden noises with a heightened sense of awareness that I didn't have before, and a few noises (like a very loud sound through a phone speaker) are legitimately painful to listen to.

Looking back, I can recall having many of these symptoms after I got my ears cleaned at the doctor's office years ago, but they seemed to subside after a few days.

With all of that being said, would it appear that I have developed reactive tinnitus and hyperacusis as a result of loud noise exposure? And if so, is there any hope that I might recover from these conditions in the coming months?

Thank you for your time.

 

[Chris S.]

It is still very early to tell if your spike is a new reality or not. At least from my experience, it takes several (4-5) days for spikes induced by loud noises to subside. Hopefully, in a few days your tinnitus increase will abate and that may also change the pitch back to normal.

What you are describing sounds like hyperacusis (which I also have to a certain extent) - reactive tinnitus is another name for it that we use on this forum. Many sounds (not loud enough to do damage) make me uncomfortable. I also get muffled hearing for a time from some.

My word of warning - be very careful from now on around medications and supplements. If your tinnitus has become elevated, medications/supplements, rather than loud noises, are what may make it even more elevated. I am sorry if this sounds scary - but please check the following list for any common medications that you know or take.

 

[NBH]

It is still very early to tell if your spike is a new reality or not. At least from my experience, it takes several (4-5) days for spikes induced by loud noises to subside. Hopefully, in a few days your tinnitus increase will abate and that may also change the pitch back to normal.

What you are describing sounds like hyperacusis (which I also have to a certain extent) - reactive tinnitus is another name for it that we use on this forum. Many sounds (not loud enough to do damage) make me uncomfortable. I also get muffled hearing for a time from some.

My word of warning - be very careful from now on around medications and supplements. If your tinnitus has become elevated, medications/supplements, rather than loud noises, are what may make it even more elevated. I am sorry if this sounds scary - but please check the following list for any common medications that you know or take.

I actually started taking Prozac (fluoxetine) for my obsessive compulsive disorder at the beginning of May. I began with a daily dose of 10 mg for two weeks, then increased my dosage to 20 mg on May 14th; roughly four to five days before I started to notice my symptoms.

With that being said, I don't necessarily believe the medication is the culprit since I took it for several years before with no issues.

On another note; are reactive tinnitus and hyperacusis one and the same? I assumed they were different conditions.

 

[Chris S.]

I actually started taking Prozac (fluoxetine) for my obsessive compulsive disorder at the beginning of May. I began with a daily dose of 10 mg for two weeks, then increased my dosage to 20 mg on May 14th; roughly four to five days before I started to notice my symptoms.

With that being said, I don't necessarily believe the medication is the culprit since I took it for several years before with no issues.

On another note; are reactive tinnitus and hyperacusis one and the same? I assumed they were different conditions.

You will find some members here arguing this issue a lot - but, they are generally regarded as the same thing by many who post here. Or, some say - reactive tinnitus is in fact "ordinary" tinnitus + hyperacusis.

In my case, I have a tinnitus that reacts to the environment - what I eat, what I hear, how I sleep, etc. I also have mild hyperacusis that is mostly the result of using earplugs often when I am out.

Unfortunately, tinnitus is not a forgiving condition. Medications that previously did not affect you may worsen a newly developed tinnitus. That being said, however, I've been on SSRIs before (still take Mirtazapine, in fact) and know that getting off those is not easy at all. Prozac and Mirtazapine are both on the list of drugs that are ototoxic. That being said, before a single Aspirin pill made my tinnitus quite bad, it had been mild for nearly a year, during which time I was taking regularly Mirtazapine. So - perhaps Prozac is not responsible for your tinnitus spike. Be especially careful with antibiotics, including antibiotic ointments. As far as I know, only Augmentin and Amoxicillin are regarded as generally safe among the more frequently prescribed antibiotics. I had the bad luck of applying a Bacitracin/Neomycin sulfate ointment on a burn wound for nearly two weeks. I am still dealing with the tinnitus spike that it caused.

 

[Matchbox]

SSRIs might not be inherently toxic but they can put your brain into a less forgiving tinnitus state.

Serotonin does play a role in the hippocampus and then the gating system. So messing with that might sway your tinnitus threshold, allowing a signal to pass and potentiate that shouldn't.

I took an SSRI briefly, seemed to actually help a lot. Coming off of it made me spike hard. There's definitely something going on.

Lowest dose for shortest time is always a good rule of thumb with mind altering drugs. Ironically, for me, that might include coffee.

 

[NBH]

I won't be able to see my doctor for the next two months, but I'll be sure to ask them about the medication during my next appointment in early August.

In the meantime, have there been any reports of people recovering from reactive tinnitus/hyperacusis induced by loud noise exposure?

I'm nearly three weeks into my condition, and I can't say I've noticed any improvements so far (although my stress levels, sleeping patterns, and appetite have improved considerably).

 

[danielthor]

In the meantime, have there been any reports of people recovering from reactive tinnitus/hyperacusis induced by loud noise exposure?

A bunch. Try looking through the threads of "reactive tinnitus". I'm currently going through them and taking screenshots.

Are you still dealing with it?

 

[Tau]

Yes, people do recover, just protect your ears: no headphones (or extremely low volume, but some people swear by not using headphones at all - look into that), no loud venues (or protective earplugs in those). Try to get enough sleep.

I could not manage my anxiety and made my condition much worse.

 

[Stacken77]

A bunch. Try looking through the threads of "reactive tinnitus". I'm currently going through them and taking screenshots.

I'm also aware of the fact that quite a few actually recover. Would you mind somehow sharing those screenshots somewhere later? Would be nice to maintain the hope for better days.

 

[Tau]

On a side note, has anyone heard of people with hidden hearing loss improving? That would be a great motivator for me.

 

[Stacken77]

On a side note, has anyone heard of people with hidden hearing loss improving? That would be a great motivator for me.

I have a hard time believing hearing loss overall can improve once the damage is done, but tinnitus and hyperacusis in its many shapes and form seems to improve for a lot of people with time, loads of time. While tinnitus may be a symptom of peripheral damage, it ultimately is a issue of the brain, and the brain can adapt and change with time, both ways.

 

[Tau]

I have a hard time believing hearing loss overall can improve once the damage is done, but tinnitus and hyperacusis in its many shapes and form seems to improve for a lot of people with time, loads of time. While tinnitus may be a symptom of peripheral damage, it ultimately is a issue of the brain, and the brain can adapt and change with time, both ways.

That's what I am thinking, unlucky for me.

 

[NBH]

A bunch. Try looking through the threads of "reactive tinnitus". I'm currently going through them and taking screenshots.

Are you still dealing with it?

My baseline tinnitus is more or less the same, but my sound sensitivity seems to have improved a bit as I find myself experiencing less discomfort in the presence of certain noise levels.

One thing I forgot to mention is that feelings of aural fullness in both ears subsided after one week following onset (although I still experience some mild pain in my left ear from time to time).

I should also note that I may be suffering from sound distortions resulting from dysacusis rather than reactive tinnitus/hyperacusis as the phantom noises that accompany certain sounds immediately die down once the sound is absent (they also sound quite different from my baseline tinnitus).

With all that being said, I'm doing much better today than I was five weeks ago.

 

[NBH]

My doctor examined my ears today and discovered a buildup of fluid behind both eardrums along with a minor bacterial infection in one ear.

I was prescribed Ofloxacin otic (ear drops) and am already feeling a lot less pain in both ears after a single dosage (although my aforementioned symptoms are more or less the same).

My doctor also informed me that if my symptoms don't improve within a month's time then she'll refer me to an ENT.

 

[NBH]

I took the ear drops for seven days as prescribed by my doctor, and began noticing improvements a week after stopping treatment.

Some sound distortions became quieter while others disappeared altogether. Sound sensitivity seems to have improved as well.

I went back to the doctor yesterday for a follow-up appointment and had my ears examined again. She said that they looked much better than they did a month ago but are still somewhat infected. As a result, she prescribed me more Ofloxacin otic and suggested that I resume taking it for the next two weeks.

Overall, I'd say I'm doing really well right now. Hopefully, my symptoms will continue to improve within the coming weeks.

 

[NBH]

I took the ear drops for ten days this time (I ran out of droplets on the tenth day of treatment), and began to notice further improvements to my condition a week afterwards. Just like before, some sound distortions became quieter while others disappeared altogether.

I went back to my doctor today, and was surprised to discover that my ears are still somewhat infected. Once again, I was prescribed more ear drops, but this time in a much larger bottle to ensure that I don't run out of doses before my treatment is over.

At this point, it would seem that my symptoms are closely related to the infection in both ears, but I've also decided to stop taking Prozac due to its potentially ototoxic side effects. I'm curious to see if the absence of Prozac will bring further improvements to my condition.