Left eye symptoms and conditions

I've had polyps removed and was prescribed Rhinocort. Shortly after I began experiencing major anxiety & panic attack that were terrifying. I stopped taking it & told my doctor who basically told me these side effects were impossible. He then put me on Nasonex. Within a very short time the symptoms returned and now include difficulty breathing properly. It constantly feels as though I can't get enough air. I've stopped taking it (about 4 days off now) and my panic attacks seen to be reducing. My left eye hasn't stopped twitching yet and I still feel uncomfortable when breathing but I think it's getting better. It makes me angry that doctor's really ignore this & make you feel like an idiot, but it has to be related.

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 ?

I was taking lisinopril and having optical migraines, pain behind my left eye, continued high blood pressure and had lost half the vision in my right eye. Went into the hospital bp was 240/138 having tia. After 10 years of fighting the BP problems and going from med to med, I finally figured out my problem was really with Aspartame, the artificial sweetener. Aspartame and MSG are both excitations that do terrible things to your brain. After cutting out diet soda and all other sources of the aspartame, and reading labels and staying away from MSG, and cutting out caffeine. I am off all of my meds and starting to feel normal again. It sure cuts down one the quick things you can eat, but better than being a slave to the BP meds forever. with all their side effects. Search the web for Aspartame side effects. You'll be surprised

September 8,2009
I took Niaspan 500mg on September 8, 2009 and begin to feel as if my body was on fire. I was scared, nervous, and panicked. It lasted about 20 minutes. I was considering going to the emergency room, but then it ended. The next day I saw blood in my left eye. I contacted my physician and he suggested to disregard the Niaspan and try to use Zetia 10mgs for only 4 weeks to lower my cholesterol and continue to a pursue a healthier diet with fruits, vegetables, and less fatty foods.

Very useful information by readers and writer on the drug I use for the last many many years i.e. Lisinopril I had laser treatment done to both eyes and my left eye is giving problem and that is BLURRED VISION as mentioned by many patient on the board. I am pleased to learn that it causes the blurred vision because I get this problem in the morning when I take the does. By the afternoon my vision is absolutely clear 100%. Thanks to you all who mentioned the problems and its a great help for me as well. Next step is to see GP and discuss with him and explain my condition. Thanks you all.

My husband stumbled across this website and first I would like to thank everyone who have posted their experiences on the NuvaRing. Because of you guys I now know I'm not losing my mind.

I started the NuvaRing March of 2008 and I started getting dizzy spells May 2009. I actually got my first dizzy spell when I was driving. Everything started to spin very fast!! My husband had to grab the wheel and tell me how to slow down and how fast to do it. That was the scariest thing ever!! My head felt a numbing sensation in my head. I had a pain above my left eye and it would shoot up my head and down my neck. The dizzy spells would come whenever, once every 8 days to twice in one day. I have had an MRI and an MRA done and nothing. The docs have had me on so many migraine meds to try to get a handle on this and nothing has helped. My longest migraine lasted for 14 days, that was in May. This month (July) I got a migraine on the 13th, took the ring out on the 21st, and had a dizzy spell this morning but this afternoon and especially this evening I feel amazing.

Since getting on the NuvaRing, like so many of you, my sex drive does not exist. It has caused so many fights between my husband and I. Its hard to tell him that he is still attractive but I can't explain why I'm not excited. So thank you for writing your experiences. He got to read that I'm not the only one and I wasn't making it up.

These last three months have been hell for my family and I. I have been like Dr. Jekyll and Mr. Hyde. So much tension has caused everyone to walk on pins and needles when they are around me.

So lets sum it up here, after being on the NuvaRing for 14 months I started getting dizzy spells, migraines, nausea, neck pain, twice I've puked because of the room spinning so damn fast, and very very VERY low sex drive.

I'M NOT CRAZY!!!! :)

I've used NuvaRing for over 4 years ~ LOVE IT! I always had a light period with no cramps or anything like that. The ring hasn't changed that. I think the only noticeable side effect I experienced recently is the inability to continue to wear contact lenses. My left eye has become extremely dry and no eye doctor could figure out why... I assume it's from the NR, though hard to imagine since I've been using it for over 4 years.

Well, seeing as that's my only complaint, I still think it's so worth it. I never used BC pills because I know I'd forget. The NR works great and I have never had any problems with it.

I have used Nasonex for about two years. Last spring, I developed vision problems which I didn't attribute to the Nasonex. In the fall, I was diagnosed with a cataract and glaucoma in my left eye.
I did not have any known risk factors and take very few medicines, so I believe the Nasonex caused the cataract and glaucoma. The first eye doctor never mentioned that the Nasonex could be causing my eye problems so I continued to take it until recently when I discovered it was probably to blame. I am now facing cataract surgery and the new eye doctor I went to told me I have the eye of someone 20 years older.

Return of my sense of smell that had mysteriously been lost almost 10 years earlier! I had a small dry patch at the outer edge of my left eye that just wouldn't go away. My husband has psoriasis and uses MG217 Ointment with success so I tried a very small amount on the area at night for a couple of weeks. Smell returned off and on. I didn't make the connection until I stopped using it and my sense of smell diminished...only to return when I used it again in the same way. I have had a few days beginning January 1, 2009 when I have had a complete, accurate sense of smell. Wow!

Took it for a week. During the time I developed a sinus headache that would not go away. Sinus pressure, pain, congestion. Today had rapid heart palpitations and anxiety. I called my doctor and he said to stop taking it. I haven't felt like this since before I started taking Wellbutrin. I wonder if it interferes with it. I've read others who take Wellbutrin and after taking Singulair started having depression and anxiety. My boyfriend told me to stop taking it. I'm glad he did! He said when he took it, all his friends noticed major personality changes. It took it 2x/day for 3 months!

Doctors can be quacks and will throw any script your way. Be conscious of whats being given to you and if your Doctor really listened to your symptoms.

I had my Mirena put in back in June of 2008 right after I got married. I, too, was lead to believe that the effects of the progesterone were purely "localized" to the uterus and would not cause any symptoms at all.

Since then I've experienced SEVERE migraines and dizziness, loss of libido, greasy skin and hair, weight gain (size 6 to size 10/12), numbness/tingling in my feet, crying, irritability, and SEVERE brain fog. For the migraines, I went to a neurologist who wanted to prescribe me topamax and said the only major side effect is cognitive difficulties! HA!!! I already have the worst brain fog, can't remember anything, am tired.... rather..... exhausted all the time, and can't function.

This Mirena surely works well as birth control, seeing as I have NO SEX DRIVE at all! LOL. But seriously, it's great not to have a period, but I knew something was wrong when I was needing medication (antidepressants for the mood swings, provigil for the fatigue, botox nerve injections for the menstrual migraines) for this medication IUD!

Since no OBGYN believes me when I say I think it's the Mirena, I've began to think I was crazy and this was all in my head. So I started on the internet and all my symptoms sounded like MS. So I had thousands of dollars in testing including a full body MRI/MRA. Negative. Had ENT see me for the vertigo. Lots of tests. Negative. Anemic? No. Thyroid? Normal.

HOW MUCH MORE DO WE HAVE TO SPEND ON HEALTH CARE TO FIND OUT WE ARE "FINE" WHEN WE FEEL THE WORST WE'VE EVER FELT???

Then I found this site!!! I think it's the Mirena now! So I want to get it out. But then on the other hand, I feel SO GUILTY that my husband paid $900 for it and I only kept it 1 year. That's expensive birth control! But then again, all the tests, doctor's bills, and feeling lousy cost more! (Not to mention that my doctor cut my strings too short so we can't "check" them each month so to be certain that my IUD is in place he makes me get an ultrasound every 6 months for $250!!!)

My ONLY FEAR is that I will have this out and the symptoms WON'T go away and it was NOT the Mirena after all. Then I will have gone through the pain of putting it in, taking it out, and the cost of "throwing one away" and then what am I supposed to do? I'm 29 but in school and can't get pregnant for a few more years. I don't want to go back on the pill because the mood swings were terrible. But I never had migraines or anything on those, so why is the Mirena causing problems?

Any feedback or encouragement would be helpful right now. I need advise!

I've been on Topamax (100 mg 2x per day) for 5 years as mono therapy for epilepsy. I switched over from Depakote which was a *nightmare* and it has been great, no seizures. I've had the pins and needles, diminished vocabulary and memory, and intermittent eye twitching but this week my right eye (why is it always the right eye?) has started twitching almost constantly. It is frightening and embarrassing and I am not sure what I should do.. I guess it's back to the neurological drawing for me because I am not sure why it's happening now. Has anyone else had the eye twitching occur after long term use?

My symptoms started with aches in my ankles and I thought I should stop wearing heals for a while. But then the tingling pain moved up into my lower legs and then my arms/wrists over a period of a few days. I felt like I was having constant shin-splints. I was heavy joint/muscle pains. Then the back of my head hurt really bad on the left side, just at the top of my neck/bottom of my head, and was also really sore to the touch. Then massive headaches. Probably migraines, although I have never had them before. My MD immediately put me on celebrex, which did nothing. I was eating Advil and Tylenol like candy and couldn’t sleep. So the doc put me on steroids (prednisone). That took the pain away. After a few days, while at work, the vision in my left eye went in and out (perfect vision to completely gone). I have never had any issue with my eyesight before - perfect vision. Then at one point (actually while I was in for my first MRI) my vision never came back. No one thought it was serious enough until I demanded to go to the hospital. I spent three days in the hospital, where they ran tests after tests (including MRI, Lumbar Puncture, blood work, neurological tests, echogardiogram, dobblers, etc). Upon leaving the hospital actually diagnosed me with Optic Neurosis, and gave me a 15% chance of getting MS later in life. We were all relieved it was not MS, like they originally suspected. After going to the Eye Dr, they told me that was not the case. This kind of eye stuff only happens to people in their 80’s! I will never regain my vision. If my diagnosis had been optic neurosis, it would not explain the joint pain. I have seen specialist after specialist over the last two months, and they still have no idea. Every test I have undergone has come back clear and I am perfectly healthy. My doc said we might have to go with the retinal specialists theory - which was a piece of cholesterol that clogged the artery in my eye. I just don’t get why a piece of cholesterol would have caused me so much pain over the rest of my body. After viewing this site and the Mirena pamphlet that I found online they give to the doctors, I really think it was the cause. The packet even notes, if you have symptoms like visual loss and headaches/migraines for the first time, to remove it immediately! I did not get mine removed until a month after my vision loss. Every doc I have seen I have asked if it was Mirena and not one of them thinks that could be the cause. But it is ironic, that when you see someone for the first time, the first question they ask is if you are on birth control or any other medications! I think I need to show them this site, so they can read other women’s symptoms. I did also have all the other symptoms as well - weight gain, irritable, oily skin, cramps, moodiness, vaginal odor, gross discharge, headaches, nausea, low sex drive, hot flashes, anxiety, restlessness at times, fatigue, and the list could really go on and on.

Hello everyone..I have many great things to say about Neurontin. It has been a miracle medication for me. I was in a car accident in 2000 as a passenger my face and head hit the windshield at 80mph. my jaw was broke and the back of my teeth were broken.
Little did I know it was extremely traumatic! My MRI's came back fine and I moved on with my life. About 6 months later my life began to change a brown spot covered my eyesight in the left eye. I began falling all the time and having seizures.
I had another MRI's of by brain done it came back negative. Not one Doctor could seem to understand what was wrong with me. I was put on Topamax for bad headaches that seemed to help. I began loosing weight and continued having seizures(Granmal) where you lose ur vision and it began to effect my speech and i would become confused.
My life was like this for 5 long years. Life didn't get better, I began to be soo tired and felt exhausted all the time. One day out of no where , I couldn't raise my head to get out of bed for work, my whole right side was burning and i was in pure agony!!! i will never forget that day. I had to have my Daughter help me up and i could barley walk...I pushed myself to keep going thinking this is all in my mind!! theres nothing wrong with me.. The MRI's are negative. I proceeded with my day in so much pain and limping all day.
It finally went away and I was fine again fo a small amount of time, I started not being able to remember things ....and forgetting from one second to the next and getting lost when I would drive...i began to panic and have anxiety, I felt like my life was out of control. I called my Mom and she said she had noticed a change in me, things I guess I didn't even know. She said I couldn't hold a conversation as before and i would slur my words and I couldn't recall what she would tell me.
My attacks moved to 4-5 times a week sometimes having seizures 2-3 times a day. I ended up having to be taken care of and moving where my Mother was so she could watch over me. I didn't get better. I couldn't work and I couldn't do much of anything.
My Mother took me to a MS specialist and he was the one who noticed there was something wrong! My face and legs would jerk and I couldn't sit still ..I had so much going thru my mind what could be wrong? I had 2 Sets of MRI's this time and it wasn't fine this time...My Spinal Cord was barley attached to my Brain Stem and CV 5-6 in my neck.
I was at the stage of being in a wheelchair not that I hadn't been using one from time to time and needing a cane.
I was sent to ER Surgery and had a stay in the Hospital and really thought I was a lucky Person to have made it for 5yrs without dying. It has been 4years and I still have soo many problems, I'm held together with a steel plate in my neck that holds mt together.
I'm now 41 years old and I wonder what my future holds. I'm not the same girl I used to be and probably never will be. I have to have Neurontin 600mgx4 a day and 1000mg Keppra a day...Without it I would not want to live the pain is unbearable for me! The only negative side affect is my hair falls out and I have severe Insomnia. Neurontin is a Miracle for me!

I wish all of you the BEST! Prayers for all of you.....

Back in October last year i was having really bad pain behind my eyes - they hurt on movement. I went to my doctors 8 times within two weeks - he kept giving me pain killers saying it was a tension headache. The last appointment i had with him id lost the vision in my right eye - they eventually referred me to the hospital. After loads of tests and questions they finally put me on Steroids and strong antibiotics via drip and i had MRI scans but by then i had lost my sight completed and was told i would never regain my sight as my nerves were severely damage. After a week or so on Prednisone my sight was getting slightly better in the left eye which was great i could think about seeing my son again. I have been taking Prednisone along with loads of other tables one for my bones and nerves and folic acid and very strong painkillers etc for months. I tried to reduce my dose as directed and my condition got worse the pain behind my eyes came back and they they said i had C.R.I.O.N so now im back on a high dose and im also taking azathioprine. I have experienced all the side affects of this drug - Round Face (moon face) server muscle cramp - i was unable to walk for 8 hours a few weeks ago i was in so much pain. Terrible bad back - shoulder blades hurts. Terrible spots. Really bad heaches. Eye pain. Water retention. Sleeping problems. Mood swings. Theres to many to list. This drug helped me regain my sight but i cant wait for the azathioprine to get into my system so i can start to reduce the steroid and start loosing some weight and get rid of all the other side affects.

I am generally classed as an active, happy and positive person, loving life.... but the last 4 months have been a blinking nightmare....
It seems we all pretty much have the same symptoms, horrid shoulder pain, muscle soreness, spasms, feet and generally feeling like "what the??" is where we are all at..horrid thoughts of MS? Motor Neurons, Parkinsons, etc. all sorts of possible sinister problems.
I too have stopped taking Lipitor only a week ago (and I only started back in October 2008 after "arguing with my doctor for many years not wanting to take it...and i didn't even know about the horror side effects, i just thought it was totally unnatural to strip the body of something almost totally,).. within 2 months I started showing signs of chronic neck C5/6/7 and left shoulder. Maybe I had injured myself once before and suffered pinched nerves, but the pain eventually went, but this is not normal or should I say usual...... I have constant buzzing of left thumb/forefinger and hand and my right leg. NEVER NEVER have I suffered from this type of symptom before in my entire 50 years... Even some days when the spasms are at their worst I get an itchy nose and tingling lips. The scariest symptom of a white flash in my left eye convinced me...So fed up with it and after stumbling on all the negative comments and side effects with this drug I made to decision to take control of my own life. It is too uncanny....As I said, it's only a week now free of Lipitor, I have increased my Vitamin C intake and making sure I take a Mega Multivitamin daily too. There is some interesting reading in various websites of Vitamin C vs Statins...

BUT it would really be nice to read any comments of people who have recovered from these rotten symptoms and what sort of time frame it took to get over them. Is there a light at the end of the tunnel for us all. Some indication of Recovery period is probably our greatest "want to know"... and also...when will i be able to enjoy cycling again. Thank you to everyone for the input and may our strength be returned, not only physically but spiritually as well. :-)

ent into cardiac arrest while being given carboplatin ,Had to be resusatated,was put on a ventilator my left eye and my hands and my tongue and my lips swelled twice their normal size,was in icu for 2 days and in isolation for 2 days due to this carboplatin ,I had to be resusatated twice in a short time period.I have anal carcinoma and it has metastasized to my intestines and liver.

Have been on Cymbalta 30mg daily for a year. Started on Wellbutrin 50mg daily about 6 weeks ago to help with attention deficit. About 4 weeks or so ago I started having occasional muscle cramping in hands and feet. Yesterday I started with twitching of left eye. Last time I had the eye twitching it was the beginning of an allergic reaction to Prozac. I'm thinking even the low dose Wellbutrin may be too much. anyone else had this experience? I'm also starting to notice an increase in anxiety. Not sure if it's due to worrying about the cramping and twitching or the Wellbutrin itself. Any thoughts?

hey everyone...reading every post makes me even more scared now. I was diagnosed with Bells Palsy on Jan. 13th. My doctor prescribed me prednisone and valtrex. 5 days, twice a day, 20 mgs. On the 18th i was finished with the pills. Very happy because the bells palsy went away. On my birthday, January 23rd. I washed my faced with Biore skin cleanser (which ive used for years) and it felt like as if my face was peeling off as i was washing it! I got so scared when i rinsed my face i actually felt my skin turning to leather. I got out of the shower and my face was round and beet red and my eyes were puffy and face was very very dry...The next day i woke up and my face was worse. I called my doctor and he told me go straight to the emergency room that i was having an allergic reaction to a skin chemical and get treated for an allergic reaction. I did just that. The hospital gave me another dose of prednisone. 60mgs the first day then again the same dosage that my other doctor prescribed me. Im scared to death now to take this pill. Yeah, my face went down and is not beet red anymore but what's going to happen next week once i come off??? i don't want to go against what the hospital gave me, but as im reading these posts, im up at 2:55 am and not sleeping..! help!

I've only been on topamax for about a month and a half and already I'm feeling some interesting side effects. In the first week of taking the medication I had such pressure behind my left eye I thought it was going to pop. It eventually went away and has not come back (thank the Lord). I also experienced some pretty nasty numbness, tingling, and uncomfortable pins and needles in my fingertips and toes/sole of my foot. The tingling in my hands usually lasted a few hours and the tingling in my feet only lasted for a couple of minutes. This tingling is never predictable.

Eventually the tingles went away and I was tingle free for a while. But in the past few days they came back. It actually coincided with my PMS. The tingles came back and with intensity about three days before my period started. I was wondering if it was common to have a side effect return or increase in intensity around your menstrual cycle? My hormones are pretty nutty and the reason I'm on topamax is to stop severe migraine auras and slight seizures that are tied to my menstrual cycle.

The feet tingles are the worst. It feels like I'm being jabbed with needles and I hate when it happens while I'm sleeping because it wakes me up and I can't fall back asleep again until they go away... they are that irritating. The hands I can deal with because I'm used to my left arm going numb when I was having the auras.

My sleep patterns have been disturbed because of topamax... I'm not too peeved about that. I still manage to get enough sleep. However there are times when I'm out with friends or having conversations and I'll know the word I want to say and I'll just bust out the wrong one. Like for example saying symphony instead of sympathy. My friends have gotten used to it and know what I'm trying to say. It cracks them up when my word salad produces sexual innuendos on accident when I really mean something else. BUT it's really messing up job interviews at the moment. I'm a bright and articulate person who is getting her BA in Anthroplogy and Archaeology, minor in History and am trying to get research assistant jobs at museums and universities. It's really hard to get a job when you are sitting there sounding like an uneducated moron high on crack.

I haven't had problems with memory, thank the Lord. Even though I've got the word salad going on (and it's strange... the word jumbles are only when I'm speaking... I'm super coherent when typing) I'm not forgetful. I was able to make it through finals week perfect, while juggling a full work load. I hope I don't start losing my memory.

I haven't lost any weight (AW SHUCKS!!!!!). I was looking forward to that one. How soon should I expect to lose weight by, if I do in fact lose weight? I'm a difficult duck when it comes to weight loss. I've been at a stable weight since I was 13. I'm an athlete so my body is my temple sort of thing. But in the past two years I've put on a little bit of unwanted weight in certain areas when I stopped hitting the weight machines :( My question is, if I haven't lost it yet... will I lose any?

I'm also classified as type II bipolar, obsessive compulsive, and anxiety disordered. I've noticed my mood has stabilized. I'm not as all over the place as I used to be. My highs could get pretty high and when they would get up there my obsessive compulsive would almost go on a little joy ride. And when I was low, I was super low and my anxiety would take the depression out for a spin. But now I feel a calmness and a zen that I never felt previously. It's not an apathy I can certainly tell you that. I feel like I am in control of my life. I thank topamax for that.

Reading all of these posts I just worry that the honeymoon period of my medication maybe over. I worry about other side effects cropping up. I think that I can deal with my tingling extremities and that I can manage my word salads. I don't want the pressure in my eye to come back. I also don't want to start exhibiting the other side effects. What is the possibility that I will start exhibiting more side effects or are you generally stuck with what initially presents in the first month or so? My doctor also does NOT intend on increase my dosage. He thinks 50mg once a day will do me just fine. Oh and one last question, anyone else experiencing the side effect increase coinciding with PMS?

Sorry for the super long post! All replies are welcome!

Hi: I've been on Lisinopril for over a month. It has dropped my blood pressure which was getting really high down to, say, 135/70 varying by day.

However, I keep experiencing issues while taking the drug. I woke up the other day with blurred vision in my left eye. I keep getting mild headaches after awakening. I felt ok for 5 days last week. Normal actually, then Sunday I felt tired, headache, fatigued. I don't know if it's my BP causing the issues or the medication.

I never had HBP until I had to stop running due to foot problems and leg problems. Now, I can't get any good cardio exercise and I think it's affected my BP.

Regards, P.

Hi: I've been on Lisinopril for over a month. It has dropped my blood pressure which was getting really high down to, say, 135/70 varying by day.

However, I keep experiencing issues while taking the drug. I woke up the other day with blurred vision in my left eye. I keep getting mild headaches after awakening. I felt ok for 5 days last week. Normal actually, then Sunday I felt tired, headache, fatigued. I don't know if it's my BP causing the issues or the medication.

I never had HBP until I had to stop running due to foot problems and leg problems. Now, I can't get any good cardio exercise and I think it's affected my BP.

Regards, P. in Charlotesville

I was diagnosed with Optic Neuritis in my left eye, at the time of diagnosis, I felt fine. Had an MRI to check for lesions on the brain, there were none. I was put on IV solu-medrol for 3 days, then 90 mg of prednisone for one week, with a rapid taper the second week. 6 days into the prednisone, I started have shortness of breath, etc. Went to the ER and my white count was 22,000. Had bronchitis and the beginnings of pneumonia. Because of the breathing problems, I only did 2 days of taper (doctor's advice). I have lost site completely in the left eye and now I have blurred vision in my right eye. Extreme fatigue, and a mental fog I just can't explain. A "twitch" in my left left hand and muscle weakness. I just don't feel "right". How long does it take for this drug to leave your system? Has anyone had a similar experience? My eye doctor was considering another round of prednisone for the optic neuritis, but I am not so sure I can survive it.