Ears symptoms and conditions

This is not a new side effect, but the same day I started taking Levaquin for sinusitis, I suspected something was wrong. Within hours, ears were roaring. First night, NO sleep, and that's WITH Ambien CR. Day 2.....depression! Immediate. This is in spite of having a severe depression under control for over a year. Sudden. I really started suspecting Levaquin then, but thought it was a coincidence. Took it this morning. Deep, dark depression. After reading these posts, I knew my suspicions were correct. The depression is getting better after 10-12 hours after the dose. This is really scary stuff. Really scary. Oh, yes, and I had the stomach pains, also. Told my husband it was just hurting like a bruise, not like indigestion or gas. I will report it to my doctor so they will no it's a "no-no" for me....in spite of all the websites that said how safe it was. Glad I found this website. Thank God.

I've been on prednisone for nearly 3 years continuously for Ulcerative Colitis. I've been on 60 mgs for quite a while but I am now down to 4 mgs. Once I went below 10 mgs. I started experiencing severe itching on my entire scalp and then upper back, ears and collar bone. I went to a dermatologist but she can't see any reason for the itching. Has anyone else had this side effect while tapering? It's making me crazy!

im a 28 yr old male taking this med for 3 weeks i developed a rash type thing on my balls and penis they are itchy and red kinda raw ive also had swollen lips that cracked in the corner of my mouth. ive also developed a allergic rash on my face that made my face swell to the point i almost cant see out of my left eye my ears are red hot swollen and f ing itchy my doctor told me to take a couple bennies and stop the LISINOPRIL to see if that was the issue at hand ill come back to reply to let you know if this is my allergic reaction any body know a good bp med that doesn't suck ?

Hi all,
I am a 47 male and was prescribed this drug for depression at 60 mg per day, and here goes:
Couldn't laugh, cry, no emotion at all
Numbness in my fingers, and was getting worse
No sexual desire, if I could get it up, nothing would come out
Prostate pain
Constant brain zaps
Raised my blood pressure, even taking 160 mg of Diovan per day; negated the high blood pressure med
Thumping in my ears because of the high blood pressure
Blurry vision
Constant diarrhea and dark
Pain in my left side of my stomach
Could not sleep
Constant headache
Shakey
Nausea all day
Sleepy during the day
Grinding my teeth
Greater thoughts of killing myself
Lost 14lbs in a week
Could not deal with large crowds, and I am in sales; that is not like me
Wanted to be isolated from all people, as I had no social skills
So then I went on Zoloft, and the hell gets even worse
Don't go off these horrible drugs cold turkey like I did, several weeks of pure hell, but I am back and feeling myself again
These doctors who prescribe these drugs need to go on them for a couple of months, and go off them cold turkey. They will never prescribe them again.
Best to all, and I welcome your comments

I had a severe upper respiratory infection and regular well known antibiotics wouldn't kick it. I went back to the physician who prescribed Avelox. Within less than 2 minutes of taking the first pill out of the bottle I started getting sensations of bee's stinging my tongue everywhere and my lips were tight, purple and swollen. Within just minutes I started having a hard time breathing and the whites of my eyes were really bloody. Next thing I knew I could literally feel and hear my heart beat in my ears and everything sounded like I was in a tunnel. Within 5 minutes of taking the pill an ambulance was called and by the time they arrived my blood pressure was 70/16 with over 240 pulse.

When I got to the ER they said I wasn't the only one with the same issue to this drug and 3 were within the week prior to my being there. When I said I had SVT Supra Ventricular Tachycardia the doctor said people with SA Node (Natural pace maker of the heart) issues which control the magnetic aspect of your heart biting it sends something in there to screw it up and make it a big mess. I wouldn't suggest this med to anyone as I did some other research on it through the web and their reports from the FDA and there were some pretty NASTY side and long term effects of it.

Needless to say; since this happened I've developed a panic disorder and my nervous system isn't working correctly. Again; be careful what you take.

I'm taking Stahist because I have been very dizzy due to having fluid in my ears. Stahist is supposed to dry me up. So far I have felt......different. I take one in the morning and one at night. I toss and turn during the night. I am now taking half a pill at night so it doesn't keep me awake. During the day, I feel like I'm drunk or something. Very relaxed. My pharmacist said the medicine is going off the market....WONDER WHY?? Maybe because it makes people feel crazy! :)

****KENALOG CLASS ACTION LAWSUIT****
Need a list of people that want to join Kenalog class action lawsuit A.S.A.P Please email me with name,state and all side effects. Include if you were treated for the side effects from a Doctor and/or hospitalized.
******

How could I forget the day and night sweats and terrible loose bowel movements and related vicious wind !!!!!!!!!!!!! The only parts of my body that have not increased in size are my ears and nose, I feel like someone has just pumped me up. In fact I feel really awful almost to screaming point.

I am really sorry if anyone else is suffering the same effects of this EVIL drug,

I am trying to just stay away from my husband so that he doesn't leave me.

From D. in Santa Barbara 26th August 2009

I had my Mirena placed in the first of may, it was very very very painful. The following months I had spotting and bleeding EVERY day, I had no energy what so ever. Some days I even felt pregnant, and not to mention my face, I looked like a teenager again, horrible acne!

Then I started having this tingling and stinging sensation in my hands and feet, I googled it and all I could find was MS(multiple sclerosis)! In shock I did a search in English(I'm from Norway) and found that I was NOT the only one having MS symptoms with the Mirena! I had the Mirena removed this week, but I still have the symptoms, but I guess it takes a little time for the hormones to leave the body completely!! My boyfriend said to me "let`s hope you didn't get MS from the Mirena".. And I am of course terrified... I have an appointment with the doctor at the end of the week!

I just don't think that this is a coincident!

Wow, I was amazed to find this site! and glad I did. I went to my doctor about 3 months ago, and I had some reflux coming up and he prescribed me the omeprazole. I didn't do any research on the drug and thought it was just a stronger version of tums or rolaids because I've never had to deal with this before. Well, I started on the Omeprazole and I felt like I was in another world. After I started taking it, I honestly feel many other things have happened, such as after I would eat, I couldn't breathe! It's not that I felt the food was getting stuck, but was moving slower or something and I couldn't take air through my nose or mouth...not once did I blame it on this meds...anyhow, My neck started hurting VERY bad! I thought it was just stress....next, my memory feels like it's really slacking and I'm only 38. I can't concentrate. So, I ended up in the ER and was having very bad chest pains...thought it was a heart attack, but everything turned out to be ok and they said I had GERD. They prescribed me Nexium. That's when the true hell began. The first day wasn't bad,but a lot of gas and chest pain, along with the shortness of breath continuing. By day 2 on nexium, I was having severe, and I mean severe anxiety and panic attacks...I ended back up at the ER, again, they said everything was ok and they gave me ranitidine to take too. If I'm not mistaken, nexium and prilosec are almost the same thing? Tonight was the worst of my life.....my panic attacks were horrible, felt like something was stuck in my throat, my neck hurts so bad and my mouth was so dry I couldn't even spit, I was so dizzy I couldn't walk, my ears were cramping from the anxiety and my eyes were blurry...I honestly feel crazy. I have taken prilosec on and off for 3 months, and now I know why my anxiety was so bad for so long, but the nexium topped it off. I heard that 40 mg of prilosec is actually 20 mg of nexium....this drug is BAD and I will never take it again. I will try the apple cider vinegar method w/ some honey. My grandparents swore by it and just start watching what Im eating. I heard its 72 hours before this crap gets out of your system..I can't wait!

On 8/1/09 I entered the ER with unremitting high fever and was diagnosed with a UTI. My EKG was normal. The doctor wanted to give me Levaquin and said it was a broad-spectrum antibiotic and there "no side-effects." I said I wanted to be informed before I took the med- wanted to know the action and side-effects. The nurse said I could look up the drug on the Internet when I got home - their info was in the computer and they could not print out a fact sheet. The doctor said that I could take the prescription to a pharmacist after discharge, and he would explain everything in detail. I asked if he would substitute a different antibiotic - the answer was "No, this is what you need.This is a crowd-pleaser - you only have to take it once a day. " In desperation to feel better, I took the initial dose. Within 1/2 - 3/4 hour, I experienced an irregular heart beat, ringing in my ears and head "fullness." I was no longer hooked up to the monitor, so asked the nurse if she would reattach me. Her response - "Everyone has irregular beats, your EKG was normal." I would not let her take out my IV until my symptoms had abated (within 3/4 hour).
Having found out by the lab that I did NOT have a UTI, 2 days later I called the ER (to see what they would say),and they said to continue taking the Levaquin - that's what the doctor had wanted me to take Clueless, totally clueless.
Needless to say, I only took one dose and will never take another dose and now have it as an ALLERGY, to make sure I never get it!

I'm a 46 yr old white male that was prescribed Lisinopril, I took it for only 5 days (at night) the 5th dose sent me over the edge, I ended up in the ER with a swollen lip and tight throat. I stopped this med right then and there. I was also experiencing HIGH anxiety with this drug. I called my doctor and she said keep taking it (can you believe that?) because my body was just getting used to it, and that it would get better in time. Im in the medical field and couldn't believe my ears when she told me that. Im feeling better now that im off it, its only been 5 days now but im getting a lot better. PLEASE don't take this drug!!!

During a cold in late March 2009, I contacted a Doctor regarding my chest cough, running nose and wheezing when I slept at night. She prescribed Nasacort AQ one spray for each nasal passage in the evening; 10mg of Loratadine each day; and one tablet of singulair at bedtime for one week.

Because of my cold I could barely taste and smell. After taking these medications for one week, my cough stopped, my nose stopped dripping and my wheezing disappeared. However, I lost all taste and smell.

I returned to the doctor the following week and described my improved condition but that I no longer had any taste and smell. aaaaaaaaShe instructed me to continue administering the Nasacort and Loratadine for another week and then see my family doctor when I returned home. She also checked my ears and cleaned them out and took five (5) xrays of my sinuses and found no polps, blockages, etc.

Since April 1st I have not been able to taste or smell and this situation is now becoming aggravating since today is July 17th.

How can this situation be remedied ? HELP

It seems that everyone is having similar symptoms. I have been on Doxy for about 14 days now and I'm feeling worse every day. I am on it because i had been bitten by a tick and contracted Lyme disease. I don't know much about the disease but it has me freaked out. I started taking the antibiotic 2 weeks after being bitten; losing my balance and almost falling to the ground. I also had a couple of dizzy spells after eating. I seemed to feel a little bit better the first week of taking it but started feeling the side effects. It started out with the occasional dizzy spell then came the exhaustion, anxiety, depression, lower back aches, soreness in the back of my eyes, stiff neck, headache in the back of my head, flu like shivers, racing heart, and complete body aches. I also found out the hard way not to go out into the sun while on Doxy. Felt like the tops of my hands were being pricked with a million needles and burning. I wish I could stop taking the drug and be done, but I am already scared about the outcome of the Lyme disease. I hope I can feel normal again soon.

Hey Everyone...
I was really just reading... but it's all just to familiar. And now I'm questioning some things I thought were just stress or whatever.

Headaches, always tired no matter what... pain.... crazy crying episodes...

I know everyone has mentioned headaches... but is it in a certain spot or go into the ears ever? I had sever headaches for like two weeks and they would always be around the back of my head and in my ear. And reading all of this, I just realized that it started a couple days after getting the mirena put in... And although my ears have stopped hurting I still get headaches at least once a day.
Has anyone just felt achy too? Like I've got the always tired feeling and EVERYTHING hurts. But I am always achy on top of it... Like my body just went through a rigorous workout or I just got over the flu... only neither has happened.

And I know what you mean about sex drives! I haven't always had the best sex drive, but it was certainly a lot larger than it has been in the last month. (I got mirena put in just over a month ago) The sex drive thing just seems to get worse. Is it just not there for you guys or do you have the feeling but go dry anyway? That's what I keep doing. I want my husband so bad, but right in the middle of everything I'll go completely dry... And then of course he'll freak like it's his fault or like he really thinks I'm not interested.... And if we do manage to get further it hurts so bad I'm almost in tears... but I can't bare to tell him because the lights are out and I just want him to be able to finish and have faith in me again.
I thought mirena would be great because I have two kids already and would be scared to death about getting pregnant again throughout having sex instead of enjoying it. Now I'd do just about to be able to share that special time with my husband again.

When I was pregnant with my daughter I would cry over anything. From an argument with my husband to the sappiest of sappy movie scenes.... When I'm not pregnant I rarely cry. For the last week or so I've had tears welling up a couple times. It's driving me nuts. I don't think that I act much different other than that though... And no one has really noticed that I know of.

Are these like the symptoms you ladies are experiencing?

I am so glad to have found this site. We are taking my 2 1/2 year old son off Singulair immediately. He has been experiencing a rash on and around his ears, around his hairline, back of his neck and shoulders, down his arms to his wrists and on his face and below his chin - almost everywhere above the neckline. At first we thought it was a reaction Singulair and took him off the medication. When it didn't subside, we took him to his pediatrician's and they told us it was a heat rash due to a reaction to sunscreen and sweat. Since I have had that reaction myself, we agreed with the doctor's diagnosis. We restarted him on Singulair and the rash only got worse. We've taken him off the Singulair and will be contacting his allergy/asthma doctor immediately about this reaction. We are not sure if he has experienced other side effects - we have seen an increase in him crying when he goes down for bed and wanting to snuggle, as well as not wanting to be touched on the legs (not sure if that's due to his scraped knees or not). Unfortunately, it's difficult to get a 2 1/2 year old to tell you exactly where it hurts.
Thanks for the information - we now know that we were correct in the beginning and that our son does not have to go through this any longer and can enjoy his summer.

I had a cortisone injection into my left knee on Friday, June 5th and immediately started to react. Within an hour, I had extreme redness and heat in my face, neck and upper chest. Wheezing, hives in throat and mouth and behind my ears. Extreme headache that came on suddenly and started in the back of my head and stretched to the front. Dizziness, chest discomfort. I went to the ER and was given a nebulizer treatment, benadryl IV and prednisone because the doctors at the ER felt that I must have had an allergic reaction to some medication that was mixed with the cortisone injection, because they said that to be allergic to cortisone is very rare. About 20 minutes after they gave me 60mg of oral prednisone, they started my benadryl IV. I felt such a hot rush to my face, my ears were burning. Eventually, the reaction calmed down and they sent me home with a prednisone taper and benadryl every 4 to 6 hrs. Sunday morning, I took 60mg of the prednisone and within 20 minutes I knew that I was in trouble so I took 50mg of benadryl and on the advice of my doctor, called an ambulance. In the ambulance, I was given oxygen, a nebulizer and more benadryl IV. After that morning, I knew that my problem was the steroid. I hadn't had any sleep since Thursday, I had been nauseous ands been battling chest discomfort and a very bad headache. I spoke with my doctor on Monday and he wanted me to take Atarax,25mg, every 3 to 4 hours. I saw him on Tuesday and I went to an allergist on Wednesday. She started me on 50 mg of zyrtec twica a day and 25mg of Atarax at night to see if this would help the reaction that I continue to have. She said that it could be several weeks, at least, that I will continue to react, until the injectable steroid is out of my system. It had been 13 days, and Im still reacting.

4 weeks ago my aunt was prescribed Biaxin for a sinus infection. After finishing the meds she developed musical ear syndrome. She now hears music, wind and ringing in her ears. It never stops. She can't sleep because the music never stops. Has anyone heard of this?

I have been using Allegra for over 2 years. It worked for my allergy symptoms. There are side effects I experienced but didn't really make the connection until I started reading everybody else's experiences. I had headaches, ear aches and ear infections that wouldn't go away, leg cramps at night a foot cramps while driving. I was on several antibiotics for the ear infections. Severe headaches/brain fog at doses of 180. I tried an experiment by stopping the Allegra. Sure enough my ears have cleared up and no more leg & foot cramps. The down side is that my allergies are worse and I have been taking the old antihistamines Chlor-Trimeton & Benadryl.

I just began using Yaz about 4 months ago and I have had the weirdest thing happen. I have massive headaches (never had them before) and this weird pain in me face (right about my right cheekbone) At first I thought it was a sinus infection.. Major pressure and headaches are easy to diagnose. Then when it didn't go away I got scared. An emergency room visit and a neurology appointment later (everything is "normal") I have decided it HAS to be the Yaz. I have also been having weird ear "fullness" Out of nowhere my ears will just pop like i'm going up a mountain...The took me off that and put me on Yasmin. Isn't it the Same pill? Anyway.. has anyone experienced similar symptoms? If so, how long did it take to go away? Thanks!!

increased dosage from 2.5mg to 40mg ran up my blood pressure; my blood pressure has always been perfect. my head feels rather numb,ann my ears feel as though they are stopped up, and I feel lightheaded and dizzy.

Six hours after taking my first mobic pill my face turned beet red along with my ears. Then my back and chest broke out with either rashes or hives. Then my face started to swell. Had to start taking benadryl immediately. Fortunately my tongue did not swell so I did not have to go to the ER. Following day the itching and rash were gone and most of the swelling in my face. Still had terrible bags under my eyes. I have taken other anti inflammatories with no problems, but my body does not like this drug.

I was just put on prednisone due to a very strong sinus infection. I took 4 pills today of 10 mg each,and so far I have been feeling good,except of course of the normal discomfort of the sinuses dripping in my ears and shortness of breath. The Dr. also prescribed Amoxicillin, and so far so good. However I get really nervous when I hear what other people post about what has happened to them because I suffer from anxieties and don't wanna have another one of those EVER! I am 50 years old and have always been very healthy but as soon as I turn 50 booom! the next morning,aches and pains and irrational thoughts and fears and you name it! It is really awful:)

It has helped me a lot reading everyone's experiences with the "dreaded" Simvastatin. I have been off this poisonous drug for 7 weeks, and am still feeling rough, and thinking when is this all going to go away ! My doctor swears blind it is nothing to do with the Simvastatin, but I am a 100% sure it is , as I felt fine before I took these nasty tablets. I still have persistent buzzing in the ears , dizziness, palpitations, constantly tired , and generally feel as if I am on another planet. Ive had blood tests , ecg tests and nothing has been found. Im hoping one morning to wake up feeling "normal". I will never , ever, take Cholesterol drugs again , as I don't want to go through all this again. I really feel for everyone that is suffering, and would be interested if anyone is having the same after affects as myself.
Good luck to everyone who is suffering like me .

I found this page after searching for info about Helioplex and rashes.

I used Neutrogena Ultra Shear SPF 70 both last year and the year before without any problems. I have also used the moisturizer with Helioplex without any problems either.

However, this year the stuff has broken me out in the most terrible rash, both on my neck and on top of my wrists. Strangely enough I can smear the stuff on my face and no rash results, but this is really affecting my neck. It's itchy, scaly and looks a lot like hives.

I really think there is something up with this stuff - the fact that it didn't affect me until now suggests to me that perhaps it's changed my skin somehow over time. I wonder how many complaints they get?