Does anyone know if penicillin can cause/or aggrevate tinnitus? If so please explain, any experience?

I’ll choose best answer
ive taken penicillin as i have swollen glands/lymph nodes. im a bit achey all over too, but no cold symptoms,

i had quite a severe build up of ear wax, which has never happened to me before, and since then i’ve got a loud ringing in that ear which i believe is tinnitus, i was wondering is this permanent? because i cannot concentrate and its causing me to lose sleep and get stressed, if it is permenant are there any ways of curing it???

Also when I’m stress or excited my tinnitus gets really bad.

I know there are alot of things that can cause tinnitus but anyone know why when I’m stress or excited my tinnitus gets worse.

Okay, so yesterday, I have developed a new tinnitus sound in my left ear and it’s never been a victim of ototoxicity. Okay, so, I wake up, and I notice the new sound in my left ear. I couldn’t believe it. It’s like my brain is filled with the Debrox ear drops I had accidentally used during a perforation. I went to the ENT on emergency and I was finally diagnosed with tinnitus from ototoxicity, but the doctor never told me anything about ototoxicity involving the brain. Instead, he warned me about the possible outcome of my hearing and my ears:

"I’m sorry, but I’m afraid the Debrox may have penetrated your round window membrane, entered your cochlea and caused your ototoxicity. I’m afraid you are going to lose all your hearing in a matter of months. There’s nothing I can do. I’m really sorry."

That’s what my ENT physician said when I saw him on emergency visit. I came home crying. There was no hope. I’m scared that my ears are dying. Can ototoxicity really involve both ears over time? I wish I could know, because I’m getting scared and I think I’m losing my hearing slowly on both ears.

I wanna ask you guys, am I going to lose all of my hearing just because I used Debrox during a perforation which according to my ENT physician, caused possible progressive ototoxicity? Because I’m really really scared right now. Should have NEVER have used Debrox during an eardrum perforation.

I’m really scared of getting my wisdom teeth out because I’m afraid it’s going to make my tinnitus louder and if that happens my life is over….
Does anyone know if this can happen?
Because I’m really afraid! But it seems like I have to take it out because it’s in the way of my other teeth.

I’ve had mild tinnitus for years but lately it’s been getting worse. I talked to my doctor (GP) about it and he shrugged and said there is nothing to do about it. Still I see ads and such about it now and then. Is it all nonsense or are there truly thing that can help?

How To Cure Tinnitus Fast and Naturally?

I’m 17, male. I have anxiety and depression, and I’m not on any medication, but undergoing therapy. I need to stress down, my anxiety evolves around my health, especially my heart, but I have found the best way to avoid disease is to live healthy, and not to be stressed. Which makes me more stressed. I’m really scared that my stress is going to give me Tinnitus, Chronic Fatigue Syndrome, Fibromyalgia and the likes. I am planning to take action by starting to exercise, but actually getting started is a challenge.

When I lay down at night I hear sort of a crackling and sizzling sound in my ear, and it sorta sounds like a heartbeat. And my ear feels warm inside when it makes that sound. Do you think there’s wax in it? When I sit up it goes away, but when I lay down I can feel and hear it

We are pretty sure that my dad has Chiari I. About TEN years ago he had a severe vertigo spell, along with ringing in the ears, headaches, and nausea. They gave him a MRI, but found nothing abnormal. And it didn’t happen anytime after that for a very long time, so they just assumed it was an abnormal spell. This January (first time in 10 years) , he had another similar spell. And in August he had another. They gave him another MRI this time since it seems to be happening more often, and they didn’t find anything really, except that she said (in a bunch of fancy medical terms..) that basically his brain looked a bit lower on one side that on the other (this is how he explained it to me). When he got home he typed in the details of what she said (in medical terms) into google and Chiari was the first thing that popped up. It makes a lot of since now though… because he has about half of the symptoms that are related to it: Vertigo, tinnitus, numbing hands, hearing loss, vision problems…etc.

So, I am wondering if anyone on here has ever had this before?
What symptoms did you have?
What did your neurologist suggest as a treatment? (I heard some people choose to do nothing about it)

She said that it was just barely hanging low, but that this may be the problem, since they’ve done dozens of tests and this has finally showed up.