Left ear symptoms and conditions

No hearing loss in family history. Doctor put my father on 80 mg Lipitor, 1-1/2 years latter he started having trouble hearing. I was taking 40 mg Lipitor after 2 years my left ear went bad, 9 months latter my right ear went bad the same exact way. The ears went bad with a tinny sound to all when the hearing came back the 3 kHz area was very low. I have just put this together the recently. This is not a coincidence, I am sure Lipitor caused this. I also think this caused me to go through Hell from hard bump break outs on my body, had me spend thousands hunting for a parasite that was not there. It was not a rash, small bumps with a hard center.

I am a 49 year old female I took Cymbalta for 3 days and on the 4th morning I woke up with severe blurred vision and roaring in my ears that was April 26,2008. My ears are still ringing. I clenched my teeth so hard in my sleep I traumatized one of my upper molars which resulted in a root canal and crown. I have been to a ENT to have my ears checked, he said I had minimal hearing loss and gave me lipo flavonoid to take for the ringing. I just went to a neurologist today who is requesting an MRI on my brain to rule out a tumor. I don't know if this is a coincidence or not ,I know the clenching caused the damage to my tooth. The neurologist said ringing in the ears is not a side effect of Cymbalta. My life has been a nightmare since I took it.

Ear busing, pain and swelling on my left ear down and a golf ball un my throat, short pin pain on my kidneys and legs first noticed swelling of my lower lip with small blisters after one pill SMZ/TMP DS 800 –160 TAB QUAL
biolence, headache,

I had Mirena inserted one week ago and there was some minimal cramping directly after the insertion but I have had nothing ever since and I am hoping it remains that way. I am so sorry to hear of all the negative side effects that Mirena is causing some women but I am interested in hearing some of the more positive feedback.

Adderall has been an excellent drug for the treatment of ADD. It took me from a lethargic, disorganized adult, to a more productive one who finally could finish her work and leave her desk organized at the end of the day. Unfortunately...
...there are many side effects to this drug which has, reluctantly forced me to quit taking it. The weight loss was a welcome side-effect as was getting rid of the lethargy I have experienced on a daily basis since the age of 11 (anti-depressants did nothing). However, my infrequent migraines became daily and excruciating after starting Adderall and its generics. My insurance could not keep up with the coverage of the migraine meds I needed. I began experiencing ear problems (primarily in my left ear) that felt like I constantly had the pressure associated with a cold. After visiting my doctor (who told me nothing was wrong), an ENT doctor, getting a hearing test, and an MRI of my ear canals and Eustachian tubes, I finally found out it was due to the Adderall. The worst side effects, however, was a gradual increase in dermatitis (dry, itchy, scaly, skin). My complexion looked sallow and my back and neck broke out in horrible cyst-like acne (not typical AT ALL for me). My eyes became so dry (not to mention the cotton mouth), that I began trying to reverse this effect with pills from a Lasik eye center (helped, but didn't solve the problem). Perhaps the worst side effect, however, has been the hair loss. Long, beautiful blond hair, has been replaced by very thinning hair (comes out tons at a time in my shower), which is now brittle and breaks all the time. I have finally decided to quit this medication despite its benefits. I only took 15mg 2/day. Once my body recovers, I hope to take on an as-needed basis for important work projects or hectic weeks where productivity is necessary. Other than that, I won't take it any more. The side effects are too severe, even for me.

I had my parotid glands washed out with saline and because they were still dirty the surgeon decided to swab them with Betadine. When I came around from the operation I was panicking in the recovery room. Later, I was put into a side ward, luckily with my sister in attendance, and took a minute sip of water. This caused me to choke and I could not catch my breath. Assistance was sought and I was taken away to get help with my breathing. My whole face swelled up and my eyes had huge sort of blisters under them, which affected my sight for about 3 days; my hearing was also affected temporarily. The sides of my face, where the parotid glands are, were absolutely solid, my lips were distorted and I looked like I had been in a fight. My vocal cords were also swollen, which resulted in very poor speech for 24/36 hours. I had to be put on continuous oxygen, and have frequent nebulisers. I was given steroids, antihistamines, antibiotics and other treatments which I am not sure of. What should have been a 45 minute operation and 2-3 hour recovery resulted in a week's stay in hospital. When I was discharged, I had to return the following day, as the swelling had come back up again and I had to have the steroid medication I was sent home with doubled and Piriton and Omeprazole prescribed as well. I had intense pain at the top of my head, over my left ear, at various times during the week, resulting in me having to take Oramorph. All of these effects caused my diabetes to go out of control, with my blood sugars running over 20 for the first 2 days and well over 10 for the rest of the week. All in all I was very unwell.

Right after I started taking Lisinopri in May 2007, I had a major flare-up of my Psoriasis. I have had Psoriasis for over 35 years and it was only in certain areas, now it has completely spread over my entire body. I also have constant ringing in my ears, never thinking it could be related to the Lisinopril. Sometimes it works to lower my blood pressure and other times it seems not to help. Occasionally I experience dizziness. These are all symtoms I never had before, I am not overweight and do not smoke. I had been healthy except for borderline hypertension prior to taking Lisinopril. I am not taking any other medications. My dermatologist is pressuring me to start Raptiva and I have agreed, not realizing that maybe just stopping the Lisinopril might ease the symptoms of my psoriasis. I just started researching Lisinopril in the last few days when someone I work with casually mentioned that there may be a link between Lisinopril and Psoriasis flare-ups.

I would like to share this information with everyone. First, I would like to caution all that it does not prove anything regarding the negative side effect of Singulair but it does suggest that there might (only might) be a physiological cause for any side effect that could be attributed to brain function.

A Chinese team has been studying the receptor (Cysteinyl leukotrienes receptor 1) that is targeted by Singulair and is responsible for the method of action that makes Singulair successful. Here is one of their studies.

1: Neurosci Lett. 2004 Jun 17;363(3):247-51. Links
Expression of cysteinyl leukotriene receptor 1 in human traumatic brain injury and brain tumors.Zhang WP, Hu H, Zhang L, Ding W, Yao HT, Chen KD, Sheng WW, Chen Z, Wei EQ.
Department of Pharmacology, School of Medicine, Zhejiang University, 353, Yan An Road, Hangzhou 310031, PR China.

Cysteinyl leukotrienes (CysLTs) are potent proinflammatory mediators. CysLT receptor 1 (CysLT(1)) is one of the two CysLT receptors that has been cloned. Although the expression of CysLT(1) in the brain has been demonstrated by Northern blot and RT-PCR analyses, the location of CysLT(1) in the brain remains unknown. The objective of this study was to examine the distribution of CysLT(1) by immunohistochemical analysis in human brains with traumatic injury or tumors. CysLT(1) was expressed intensely in the microvascular endothelial cells in both normal and abnormal conditions. At 8 days after traumatic injury, microvascular regeneration was found and all of the endothelial cells highly expressed CysLT(1). In gray and white matters of the normal regions of the brain, CysLT(1) was expressed weekly or not at all. However, the CysLT(1) expression increased in the neuron- and glial-appearing cells in gray and white matters after traumatic brain injury. CysLT(1) was also detected in astrocytoma, ganglioglioma and metastatic adenocarcinoma, and the expression in the neuron- and glial-appearing cells around brain tumors increased robustly.

PMID: 15182953

Here is the relevant part of the study.

"Although the expression of CysLT(1) in the brain has been demonstrated by Northern blot and RT-PCR analyses, the location of CysLT(1) in the brain remains unknown."

That sentence says that these scientists believe that CysLT1 exists in the brain but they don't know what the location in the brain is.

It is logical to assume that if a receptor exists in any part of the body that it has a function in other words it does something or tells some other part of the body to do something. So we don't know what part of the brain or what the receptor does in the brain or what the effect on the body is if the receptor does not do it's job.

We do know that Singular (montelukast, Cysteinyl leukotriene receptor 1 antagonist) blocks this particular receptor so if the receptor exists in the brain that it COULD BE POSSIBLE that Singular prevents this receptor in the brain from doing it's job whatever that is.

I know that it is difficult to argue with doctors. This drug has been around a long time. It would be difficult to understand why we are just learning about problems after so long a period of time. I can see from all of these responses that these problems are very real. Of course, we have no idea if Singulair is related or not. But if you need something supportive to show that it is not impossible for them to be related even though there is no proof that they are related, you could print this out and discuss it with your doctor.

This isn't proof of anything but at least it might be a clue.

My deepest, most heartfelt sympathy for all the horrific losses and suffering.
I wrote earlier, but I am so traumatized by all this... I can't write long now. Besides all the rest of the torture we've all endured, please let me know and do reply if tinnitus and/or hearing loss has been a major problem. Perfect a year and a half ago, I just had my hearing tested and have so hearing loss in my left ear only. Right ear is still perfect. Funny too... my newly developed tinnitus is also in my left ear only.
I am 50 with a bunch of problems from a head injury of 22 years ago and just within the last few year correctly diagnosed. My life is already destroyed, but about a year ago... it all started getting worse. Now, almost completely unable to function, I am trying to nail if the cause is the Singulair I stopped couple of nights ago and started maybe 2 years ago.
I need to determine (because they can find no cause) for the recent onset of the hearing loss and tinnitus... which someone described perfectly as a hissing sound, like someone is letting the air out of my head.
So please let me know if tinnitus and or a hearing loss seems a result of this miserable drug for you too... Thank you...
losthope18

I started on Lisinopril/hctz 10/12.5 mg ten days ago and within four days I had a severe hearing loss in my left ear. I thought it was plugged with wax, but when examined they found nothing. After being referred to a ENT specialist they found nerve damage to the ear and are unsure if I will regain my hearing or not. They are trying to treat the hearing loss with steroids but are unsure if it is reversible. Both the ENT and the internist did not think there was a connection with the Lisinopril. I think there is. I am a healthy 47 year old who has never had a health issuer before ten days ago.

I would love to hear from anyone else with this problem. We need a definitive link to this drug for hearing loss.

On 02-26-08 Tuesday my Dr. prescribed Lisinopril 10 mg 1 time per day, 14 days later on 03-11-08 at 2:30 am I woke up because I could not hear the fan we sleep with. When I sat up I heard the fan going w/my right ear and felt my left ear was plugged. I tried to unplug it but it wouldn't and I realized I had to go to sleep because I had to go to go for some fasting blood work for my diabetes.When I got up that morning my ear still felt plugged and I thought I must have an ear infection so I would go up to see my Dr. since I had to go to the lab. 16 days later 03-26-08 3 audio test, 1 MRI the Dr's don't know what happened. Lisinopril was the only new medication I had started taking. I believe it was the cause of my 100% hearing loss. I noticed that someone else wrote about hearing loss on 03-18-08 & I replied to them but I have not heard back to see if they have regained their hearing. They say I probably will not get my hearing back! Thanks A LOT Lisinopril!

I started taking 750mg of Levaquin last Thursday, March 20, 2008, for a strep throat infection that was not responding to 500 mg. of Penicillin. I took Levaquin last summer due to another bad throat infection and had absolutely no side effects. However, this time I am experiencing a raft of them, from awful insomnia and sluggishness and tiredness, to sever headaches and coughing. I suffer from depression and this is effecting my reaction to the depression medication. I am feeling more depressed.

A few days ago, my head started to hurt near my left eye, and my skull became very sensitive on the top left side, midway between the middle of the skull and my left ear. If I cough, it feels as if my head is about to explode. To make matters worse, whenever I try to speak, I start coughing , which in turn hurts my head. My head is painful to the touch.

This is awful. Can anyone help me out with some pain relief or something?

Mikal

I have been on Lisinopril-HCTZ 20/25 for about 5 weeks now and I have noticed a little dry cough recently and a constant runny nose. Since 3-15-08 I notice that my left ear has been losing some hearing and today the 18 of march it feels like I have something jammed in there and everything is severly muffled.I was just on Lisinopril at first and on 3-11-08 the Dr put me on Lisinopril-HTCZ 20/25 and this started 4 days after I started the drug I have not taken it today and don't plan on it after I I have read what I have just read. I am going back to see my Dr. this after noon.

I was prescribed Cipro for a UTI on 1/25/08. I took 500 mg for 7 days. About day four I began to experience intermittent "little pains" in my hands and feet. I thought it could be a side effect of Cipro but no big deal and would subside when I finished the prescription. Boy was I wrong. It has been two months and every week that goes by I feel worse. I have pain and mild cramping in my arms, hands, legs and feet on and off all day. The muscles in my neck and the back of my head tighten up and I get very lightheaded. When I get up in the morning I am extremely stiff and do not feel like myself most of the time. I have read many comments by others who have used this drug on several websites and I am quite worried at this point. Can I expect these symptoms to gradually subside or am I on the road to becoming an invalid? Sorry to sound dramatic but this is very upsetting. Has anyone found anything to help with these sort of symptoms or does anyone have any suggestions? Thanks.

Started Januvia 08/07. Constant runny nose. Ear congestion. Experienced sudden hearing loss in left ear from infection. Had to get a tube put in. Ears and hearing still not normal. Headaches once in a while. Lost 30 pounds in 5 months. Sugar levels in the 80's most of the time. Hair has gotten thinner, was already thin to begin with.

I have suffered with chronic sinusitis for about 8 years, and concurrent asthma for about 6 years. I am a 46 year old male.

I have worked with highly noted ENT in the area, and he tried many (non-prescription) recommendations over the course of a few months, but nothing worked. I had a CT scan that showed profound sinusitis in all regions, especially the ones that nasal corticosteroids cannot reach. In an attempt to avoid surgery, which he described as risky and not particularly effective with the type of widespread sinusitis I had (my orbital lobes were involved), he then suggested I get a single intramuscular corticosteroid shot, which he administered about 10 days ago. I was not advised of any potential side effects.

I called today to ask what it was, and was told Kenalog 60mg - I was getting a prescription for something else and wanted to make sure the pharmacist knew what I already had in my system. No comment from the pharmacist.

First of all, the Kenalog has worked like a miracle drug on my sinusitis. I can breathe normally, I can fly without intense ear pain, my sense of smell and taste has returned after an absence of almost a year, and my asthma seems to have improved. Also, and perhaps strangely, I had a noticeably enlarged lymph node below my left ear on the lower part of my neck for many, many years. It felt like a pea under the skin. None of the doctors in any of my physicals expressed concern about it over the years. Since receiving the Kenalog, this node has returned to normal and I cannot feel it unless I really search for it. I thought it has just calcified and was going to remain that way forever, but perhaps it was permanently inflamed from permanent sinusitis.

The only side effect while on Kenalog that I have noticed is that following Albuterol inhalation (for the asthma), my lungs burn a little and I have a productive cough for a few hours. I suspect that two things are going on: the Kenalog has decreased bronchial inflammation, and increased a vast amount of sinus drainage, some of which is going into my lungs to be expectorated.

My doctor is an older, seasoned pro, and I trust him. I just found and read online the BMS prescribing leaflet (the one for doctors) and it is very explicit that unless the injection is given as a DEEP intramuscular injection, then local atrophy is LIKELY to occur (their words, not mine). It does appear, therefore, that the side effect of atrophy is potentially dependent on the skill of the administering doctor.

I know I will get about 2-3 months relief from this medication, but with all the very tragic tales of side effects listed here, with which I sympathize deeply, I will be reluctant to take it again.

I am hoping the skill of my doctor - and my body's own system - cope with injection without some of the more serious side effects that the people here have been experiencing, though I expect I will have to wait a couple of months to see what happens. For some of us, the drug has (so far) saved us from a life of constant misery and fatigue. I am keeping my fingers crossed and will report back.

Wishing you all well.

I live in Israel, and here in this country not only do the police do their duty incorrectly, but so do psychiatric officials.
I was in a bad state emotional, and that did not result in any obscene or out-of-the-order matter, but me having chosen to move on with my life was a bad idea since moving on meant letting go and kicking out of my life a she-devil that posed as a girlfriend.
she had connections and accused me wrongfully of stuff i didn't do, and since she had friends in the police force, I ended up being admitted to a psychiatric hospital, there I was forced to take 10 mg of ZYPREXA, every day, for a little more than a month and a half, after a couple of weeks i developed a rash on my head, and vibrations with palpitations.
when i stopped taking ZYPREXA, the rash continued, the vibrations when i go to sleep with the palpitations continue but are even worse,
I cant sleep, and when i do fall asleep I wake up every hour, if lucky i sometimes manage to sleep for 2 hours and then only wake up, and i keep waking up until i give up on sleeping, i get headaches, nausea, dizziness, i eat, and after 30 minutes to 1 hour i go the the toilet and diarrhea..
my left eye sees blurry, i hear much less in my left ear, and not to mention that i have no tinnitus, - all day long i hear an electric pulse in my ears, i am disconnected from emotions, cant concentrate, my memory is impaired, i cant seem to make myself do anything, i cant even figure out what i am feeling, my teethes health has gone bad, get mood swings which are not extreme at all, resulting in me not knowing what it is I'm going through, i think this Zyprexa ordeal as resulted in multiple sclerosis which hasn't been diagnosed yet, and i don't know what more else there is, since i am quite handicapped mentally emotional and physically i can do stuff, but for some reason i don't do anything.
bad dreams (when i do manage to get several minutes of sleep), and i feel stoned all the time. and this is not all, but seriously, here in Israel or overseas, who really gives a damn? and who can help these things go away??..Ive been told to wait (I've been waiting a little more that 3 months) for all this to go away, and nothing as gone away, instead more things slowly gather.
too bad there is no death sentence here in Israel, if there was I might try to get it, to end this suffering, though, what can i say, even dying is not something I can manage to get myself to do, I cant seem to actually decide to do anything, I just think of it, and in the meanwhile, my whole life is passing in front of my eyes, making me realize, this might be the ending of my life as I know it, and all i have to do about it is just sit and wait, either for things to change (cause i cant change them), or to die.

I have switched from Lotrel to the generic form of Lotrel. I have been taking Lotrel for about 2 years and the generic for about eight months. I have recently experienced a fullness in my left ear, at times hearing loss in only the left ear. It is very bothersome! I also have constipation and stomach pains.

I'm crying reading these posts. I thought there was something wrong with me. I'm 41 years old - and my family has a health history of "making" cholesterol. Both parents were on statins. My total cholesterol was 267 a few months ago - LDLs were 171 and my HDLs were 42. I started taking flaxseed meal every day - and within a few months, my cholesterol dropped to 193, my LDLs were 117 and my HDLs were the same.
My doctor's didn't think it was the flaxseed - they had prescribed Vytorin which I reluctantly took for about a week. They attributed my lowering numbers to the statin, not the flaxseed - so I followed their advice and started taking the Vytorin about 3 weeks ago......
Now I don't know if it's coincidence, but I have developed a severe left ear problem....and have taken 2 separate antibiotics, but to no avail. I have also developed a severe pain in my left shoulder, the back of my left arm and sometimes it shoots into my chest.
I suffer from anxiety attacks, so of course, to me, this is a heart attack, but since I've been tested so many times and I'm a healthy woman, I know that's not it. I thought I'd log onto google today and search out what could possibly be causing these troubles. I read these posts and I literally have been crying for about 15 minutes. My doctors have told me that Vytorin is almost a "magic" pill. They said if someone could tell you that you could take this pill and it would reduce your risk of heart attack and stroke by 50%, why wouldn't you take it? Given the history of your parents, it would be foolish to not.
I have also been given instructions to lose about 25 pounds (not bad), and I know that if I could just exercise, eat well and take my flaxseed as well as making sure I eat 2-3 meals of fish a week, then I have to be better, don 't you think?
Do you think statins are the only way to go? I'm so happy to know I'm not alone - I'm not going crazy - I'm not experiencing any heart attacks....my anxiety is ten-fold lately - I wake up after a full-night's sleep feeling exhausted. I have four wonderful children and a wonderful husband - I live for them - and I feel so sad and depressed lately.
Oh my gosh everyone - do you really think that the Vytorin would have such an incredible impact on all of our lives?????

I was on Levaquin for 6 of the 7 prescribed days, and as a result I have extreme joint pain. I am 37 years old and feel like I am 70 years old. I can't walk up or down stairs easily, it hurts when I get dressed, wash my hair...basically any movement hurts. After the first 2 days of taking the meds, I called the pharmacist since it was the weekend, and he told me that the Levaquin shouldn't cause this and it was OK to continue using it. So, I did through Sunday, then called my Dr. on Monday when I was instructed to discontinue its use. The only side effect remotely similar that was noted was "rupture of Achilles tendon" in rare instances. I've read some of the other messages that were posted and am glad to see that the pain some of you are having is subsiding. I sure hope mine does too. I go for blood work on Friday to see if any real damage has been done.

I am sure glad I found this sight. I was trying to find out if the Prilosec OTC may be why I have had sharp pains in my right side, where my liver is located, and after reading the effects that Prilosec has had on other people I am throwing mine away. I am scheduled to see a doctor in regards to bad dizzy spells, pains that run from my left shoulder, up my neck, my left ear rings terribly, and tremendous pressure behind my left eye. I was fearful that I have a blockage in a vein to my brain. My left leg from above my knee has gone numb, I can't wiggle my toes, I get tremendous cramps in my left calf at least 6 times a night. I feel like a basket case and I have done nothing to make any of these things start happening. A year after having my gall bladder removed and adhesions cut away from my stomach the doctor gave me Prilosec to see if it would help with some very minor stomach pains I was having. As a matter of fact I took a Prilosec an hour ago because of the pain in my liver area and as I write this I have a bad headache, my left arm is tingly, the left side of my neck is tight, I am dizzy, and feel like I want to vomit. No more Prilosec for me and I am definately telling my friend who is on it after he had his esophogus removed 5 years ago due to cancer about what I have read here tonight. He can't figure out why he felt so much better 4 years after his cancer was removed but feels so terrible now. They gave him Prilosec 6 months ago to help him with a phlegm problem. I thank you all for your input on this message board. You helped me out tremendously. I have only been on it for a couple weeks and as of right now I am not going to take it again.

I have been taking lisinopril now for about a year. Previously I was on a diuretic. My doctor says I have to take BP meds for the rest of my life. The pains in my body are getting so bad I can hardly function. They began between the shoulder blades. Now it is pressure in my left ear, pain down my neck to shoulder, down left arm, and the left side of my body seems to go to sleep. Even my hip complains. I'm in the process of moving and as soon as I get to my new location I'm off this stuff. ronni9@netzero.net

im tore all to pieces my 22 month old had a sandpaper feeling type rash thats been there 4 2 weeks . a few days prior to the rash he had a slight caugh and stuffy nose. his dr said it was a viral rash. then a few days later developed a temp of 103. we took him back to the ped. she said he had a upper respitory infection and fluid in his left ear, she prescibed omnicef. the rash seems to be more prominent now. im very worried. she did a cbc and the white count was 15000 and the platelets were slightly elevated. she wasnt worried though and said it was a viral rash, let it run its course. so? i dont know if i should be worried or not>help

I've only been on singulair for 6 days and it is now 4:23am. I just couldn't sleep tonight. I've been having the strangest dreams and I commented to my wife about them. We just laughed it off. Anyway, at this time of the morning, my EARS are "Hissing" so loudly, not ringing, however I do detect a slight pulsating tonal sound in my left ear, that I just couldn't sleep anymore. I've a history of Tinnitus but something has exacerbated my tinnitus dramatically, so much so it is keeping me awake. I think I'll be needing something to help me sleep now. Perhaps I will stay off the Singulair for now just to see if life returns to some kind of normalcy. Could it be a side effect of Singulair. I don't know but I felt like driving something through my head to stop all the loud noise. Has anyone else experienced elevated levels, or a new development of "Ringing in the Ears", commonly known as Tinnitus?

I can't believe what I'm reading tonight on this page, I decided that today was the day I needed to check up on side effects of singulair, since my 5yro, needs his 3rd refill. Three weeks ago I took my boy to the doctor, because of severe weeknes,fatigue. irritability,lose of interest in studying, in sports, in home works, and lose of appetite one of my main concern, I ask his ped if maybe these could be side effects from his singulair, She said no way she hasn't heard of such effects from this drug, and that the side effects form singulair was realy mild, I took her word on it and continue my poor lillte boy in the hell he is living in, oh. she send him to the lab and draw blod for a series of exams, but find nothing so I continue my days wondering and suffering for my child, My mother-in-law even recomended counseling for my boy since we have a new baby at home, tonight I decided before getting his reffill why not do some research and find out what other people are saying? this is the first page i ran in to and I know that I dont need to read much more to take my boy off of this singulair.
ps. we can not rely on our doctors to talk bad of any drug.