Loss of vision symptoms and conditions

i was prescribed cytomel as an adjunct to noretriptlin 25mcg twice daily/ I do not have any thyroid problems. Both above drugs were prescribed by a psychiatrist. I began to have brief loss of vision followed by extreme weakness and sweating. these symptoms occur I am currently undergoing a series of cardiological tests because my primary physician found an irregular heart beat via ekg. I have always had an irregular heart beat. All my physicians are aware of all the medications I take which includes a blood thinner. Most unfortunately, am having difficulty connecting the time frame to the "side effect" and datae of beginning the cytomel. I realize I can make the connection by calling the pharmacy tomorrow. I also have an eye disorder with no cure and have lost much of my peripheral vision so at first I thought there may that relationship. But I went to the doctor when I realized I was also experiencing the fatigue, shortness of breath and something quite akin to hyperventilation. I will have my 69th birthday this month and thought my body and mind had a close relationship, but I am beginning to think they have become arch enemies,bent on just confusing the hell out of me.The tests with the cardiologists have been on going for almost two months with no results or diagnosis given.that important phase is due August 27. It is a good thing that patience is one of my virtues although brevity is not. Any comments please and thank you

Symptoms: joint pain, blisters on tongue, low blood pressure, dizziness, loss of vision. I started Levaquin 750 mg orally 11 days ago for diverticulitis, along with Flagyl. I had taken Levaquin in the past for this same condition without any side effects. I am also on Benicar 25 mg for high blood pressure. This time after spending $106 dollars AFTER insurance, I started having problems with dizziness where I would lose my vision for a few seconds every time I stood up from a sitting position, or sat up from laying down. My arms and legs felt very heavy and I was exhausted and felt like I could hardly walk. Since I had taken this drug before without complications, it didn't occur to me that this might be a side effect of the Levaquin. My doctor recommended I stop taking the Flagyl, which I did. Nothing improved. After several days of this I finally went to an after hours clinic and found that my blood pressure was 90/50. The nurse told me to stop taking my blood pressure med for a few days, that maybe there was a reaction. (She stated she had never heard of blood pressure being affected by an antibiotic). I stopped taking my blood pressure medication and it came up to normal within about 36 hours. Approximately 4 days ago my tongue broke out with little blisters all over, top and bottom and my lips are cracking. Yesterday my joints started aching and I feel like I'm 75 every time I take a step. (I'm 46) I took my last Levaquin yesterday and I still have the blisters and the joint pain is worse. This morning my blood pressure was back to my normal "mild high" range of about 130/83. I took my blood pressure med and it came back down to what is normal for me, 122/77. I haven't done anything different (meds, food, products, etc.) that should be causing these blisters, and I don't feel sick other than the joint pain, so I'm assuming these are side effects related to the Levaquin. I'm hoping they will clear up now that I'm done with the medication. I find it interesting that I spoke with two different pharmacists and two different physicians and none of them indicated there might be contra-indications with Levaquin and my blood pressure med. The good news is that the diverticulitis seems to be gone!

Have any of you developed Leukemia after taking Yasmin? Or do you know some one who has developed it and they just happened to be taking it at the time? Any feedback would be appreciated.

I had the Mirena put in six weeks after having our daughter, on June 30th, 2006. I never was able to loose weight, and felt very bloated, moody, with pains in my sides (ovary level), and then in the Fall of 2007, I noticed a significant loss of vision in my left eye. I went through $40,000 worth of hospital visits, and one 8-day stay, to figure out that the Mirena had caused a rather large blood clot to form on the outside of my brain in the main vein that crosses over the top outside brain. I have suffered from multiple ER visits with migraines lasting up to 72 hours, even after shots and meds. I have been going to the University of Colorado Hospital for treatment and it has taken over six months to get me on a medication regiment that will hopefully alleviate my debilitating headaches and now am living with the possibility that my vision may never get better in my left eye. The Dr.'s I have seen: an eye surgeon, a Neurologist, a Neuro-ophthalmologist, a Retinal Specialist, and the multiple local MD's. The tests run on my body and head have been very extensive, including blood tests, multiple MRI's and the final MRVenagram that tests the flow and drainage of and around my brain that found the blood clot and have ruled out everything from MS, to Pseudotumor Cerebri (which is a lifelong disease offering only pain management for the most part), as well as a macular deterioration related with people over fifty, not 24, they have also ruled out any pre-existing tendency for being prone to blood clots . This has been the scariest thing of my life and so consuming and debilitating, that I would never recommend the Mirena to anyone. I have missed so much work and the traveling to doctors have been a drain on our financial situation. This kind of information needs to get out there because Dr's are denying any relation to the Mirena. My Dr's have definitely diagnosed my problem as the Mirena. The swelling of spinal fluid was my body trying to protect itself and that swelling caused such great pressure on my optic nerve that my macula, where a person has central and fine detail and focusing, wrinkled in a layer of my eye that cannot be operated on. I can no longer read out of my left eye and the stress that created for my right eye is a contributor to the migraines. I also see double at night, when lights or signs are illuminated by the headlights of my car. I am seeing two images! This is very hard to accept and not being able to read for very long also upsets me. The likelihood of my vision repairing on its own is slim to none. Thanks Mirena. SO please, please help the word get out!!!! Also caution anyone you know who is planning on getting the Mirena, or who has one in to be aware of any changes. My experience has been very extreme but maybe women out there are going through the same things I have been and no one will recognize the relation to the Mirena. I am only glad my Dr. was willing to admit the Mirena was the cause.

I've been taking Yasmin for 7 months now...at first it was brilliant! i have had trouble with other pills in the past and Yasmin seemed totally different.
however, after settling down with it, i am starting to experience some side effects. i appreciate that obviously they may not be related to Yasmin but after reading other people's experiences I'm thinking that they probably are!

my hair falls out more than is normal...i used to have really thick hair and now it's getting pretty thin.
i have developed a cyst on the side of my head?!
i get weird pains in the right of my chest and stomach as if I've been exercising too much or sitting balled up for hours.
i have gone off food.
my sex drive is none existent! my boyfriend and i used to do it pretty much every day and now i never want it. we haven't really had any proper sexual contact in over a month.
i had complete loss of vision in one eye.
I'm getting seriously anxious about things that are important, but overly so.
i feel permanently tired and drained no matter how much sleep i get.
i cry 24/7 over absolutely anything... songs, adverts... its ridiculous!?

if i come off Yasmin it'll be the 3rd pill that doesn't agree with my body. I'm gonna have to try something new i think...

27 yr old healthy male. Have red-irritated eyes, occasional sneeze and runny nose, live in Denver (highly polluted). Come to think about it, never started having symptoms until after about 1 yr of living here. Symptoms have persisted for 2 yrs now. Maybe I should move?

doctor thought was allergies, so tried: Patanol, Singulair, Claritin, Duramist = no help. Eyes are still itchy, eyelids are embarrassingly red (I look like I'm high all the time). After 4 months on Singulair, noticed significant weight gain, dehydration, and sensitivity to light. Couldn't work out, play paint ball. Urine was always dark yellow. Singulair seemed to help at first, but as time went on, symptoms were worse and had additional problems, weight gain, etc. Things seemed to be spiraling out of control, and I am really depressed b/c there seems to be no solution.

I complained of some loss of vision (i.e. blurriness, hard to focus), so doctor sent me to ophthalmologist. They prescribed glasses and said I have dry eye like that person posted on Nov 18th. They told me to wash my eyes with baby soap. No help! These people have no idea what to do, I got fed up and quite taking Singulair after reading this website. I hope to lose weight and start working out again. I can't believe that doctors prescribe Singulair and have no idea (NO IDEA!) of all of us who must suffer from this terrible drug.

I don't do drugs, drink occasionally and have really cut down trying to get this problem solved. I have become sensitive to caffeine, if I drink coffee, my eyes hurt so bad, I can hardly keep them open. I'm going to do as much research as I can to find a solution. I trusted my doctors - bad idea!

Headaches, extreme nausea, virtigo, flashes of loss of vision.

I used it for 2 months
it was hardly effective, pressure went down from 23 to 22
many sever side-effects which all persist to this day, even though I stopped using it 17 months ago,
they include: severe pain in the eyeball, macular edema, blurred vision, loss of vision from 90% to 25%, headache, severe back pain,

Two weeks after taking Levaquin for a urinary tract infection, I developed a rash/hives that covered my entire body. I had frequent violent itching attacks and wanted to scratch my skin off. After two days of the hives, I went to Urgent Care and was given a steroid shot and Prednisone. The next day I had severe chest pains and shortness of breath. I went to the emergency room and and EKG came back abnormal. My white cell count had shot off the charts to 35.0 I was admitted to the cardiac unit and was put through a battery of heart tests. All came back unremarkable. After three days of blood tests, CT scans and nitro tablets, I was released with no conclusion as to what I was experiencing. The rash continued, just not as bad and I've experienced joint pain. One week after the intial symptoms, I began experiencing dizziness and loss of vision. It has now been two weeks. I've had a MRI on my head to determine the cause of the dizziness and the vision loss and results from the MRI are pending. I was a healthy 46 year old before taking Levaquin. Currently, I cannot work a full day without vision loss or dizziness. I've been so perplexed as have the five doctors I've seen as to what the cause of my symptoms could be. After reading many comments from Levaquin patients, I now believe that I've found the cause.

I have been on advair 250/50 for about a year and a half. II am 48 years old. I cannot believe how many side effects i have had and did'nt even realize it. I have had alot of problems with my eyesight since I have been on this medication but did'nt realize it. I had my eyesight checked and it was fine. I also have had alot of dizziness and I have had alot of sinusitus and choking especially every morning. I finally called the doctor aboot the side effects and he agreed so he put me back on my original treatment which was Q-var and I can't tell you how much better I feel. I have no more dizziness or eye blurriness that I had before and I feel so much better and I have so much more energy that it makes me wonder what I was thinking just so I could breathe better.

Tetracycline is directly affected to a condition known as Idiopathic Intercranial Hypertension or more commonly known as Pseudotumor Cerebri. It is a very rare neurological condition. It causes Cerebral Spinal Fluid to build up on the brain and therefore causes servere headaches and permanent loss of vision due to pressure built up on the optic nerves. I had taken Tetracycline off and on for many years as a treatment of acne and was always told that the headaches that I had were migraines until I was hosptialized and finally diagnosed correctly by a Neurologist who promptly took me off of the medication. After learning all of this I have done much research and I was already in a high-risk category for this condition and Tetracycline is directly listed on every website as a cause of this condition. I SHOULD HAVE NEVER BEEN PRESCRIBED THIS MEDICATION!!! There are no warnings on the medication to indicate that it causes this condition and my healthcare provider was not aware or she never would have prescribed it to me. Now I live with a VP shunt, blood clots in my brain and constant headaches. What a price to pay to get rid of acne!

I took predisone for only a few months and I can take it no more. Other things work far better. The side effects were, loss of vision, swelling, headaches, dizzy, run into things and
others.

I took it for breathing, and I am breathing far better since I quit it. It is probably one of the worst medicines ( if you can call it that ) on the market.
I would question any doctor that subscribes it, when many
people quit it, use other things and get well.

Inherited high cholesterol. Recent blurred vision in left eye that started with a vitreal detachment but led to loss of vision prompted the eye specialist to contact my primary physician. After MRI, etc., determined vascular disease. Immediately place on Zocor 40 mg per day along with low dose aspirin. That was 2 months ago. I now have ankle swelling, heart palpatations, weight gain all in the middle, night sweats, hot flashes and awful dreams. Had a fasting cholesterol test done on Monday. Results - Satisfactory (whatever that may mean) since the doctor did not bother to quote the levels on the small postcard sent to me to give results. I WILL be telephoning his office first thing Monday morning!

My Lupron experience has been mixed.

I had 3 Lupron injections--7 months worth of the drug--before my November 2003 myomectomy for a grapefruit-sized fibroid. I consulted 4 doctors (including a family member) before taking the Lupron plunge, and opted not to read too many scare stories online. I'm 32 and I want very much to have children, and everyone told me that my surgery would be most effective if we could use Lupron to cut the blood flow to the fibroid. The good news is that it seems Lupron (and a very good surgeon) did the trick--my surgery was without complications and declared a success. (Now we just have to get me pregnant!)

Now I'm just waiting for the effects of Lupron to go away. I had my last (3 month dose) shot in September 2003, and my most severe symptoms were in the weeks after that shot--especially severe and frequent hot flashes, night sweats, the works. For the entirety of the injection, my libido was utterly shot. For me, these were all annoying, but not unbearable. I figure it's just a taste of what's to come when the real menopause happens in another decade or so.

Post-Lupron recovery:
The hot flashes finally went away about 5.5 months after my last shot, and I've been gradually feeling more and more normal, though my libido is still not back to normal. Most worryingly, and this is why I'm writing today, is what happened to me this last week. Noone ever seems to write about the hormonal hell that your body goes through when it's trying to return to it's pre-menopausal state. I'm 90% sure that my symptoms are in fact attributable to these hormonal fluxes, and not to something worse (like abdominal adhesions from my surgery).

Three evenings ago, I got extremely dizzy and nearly passed out. It took me over 20 minutes to get back to my office, since I was so dizzy (loss of vision, balance, and nauseaI had to sit down three times in the couple dozen yards. I also had a pain in my abdomen. I barely made it the final steps to my office, where it took me at least 45 mintues to get to the point where I could make it to the car to go home. I had strong stomach pain, tingling hands, and gradually decreasing dizzyness. At this time I also noticed that my entire abdomen was very swollen. While the other symptoms have not returned, I have continued to have a very swollen abdomen, which has been very tender to the touch. I have been unable to walk at my usual vigorous pace, and have spent much of the last 3.5 days sitting quietly or lying down. The whole experience has been very frightening--and NOTHING like any PMS I have ever had before. But then again, I've never been menopausal for a year before!

So, I'm writing this post so that others might be aware that the hormonal changes the body goes through while getting OFF Lupron can be even more severe and frightening than the ones you experience going ON the drug.

Took it for a month. Being a person who was prone to depression and panic attacks in my younger years i wish I had read this first.
Constant head aches, diorreah, Pain in legs, chronic leg cramps, Very severe depression, putting my self at saftey risks due to sever depression, diziness, feelings of "out of this world", neck pain, tierdness, insomnia, joint pain everywhere, loss of vision, loss of sex drive, loss of loving emotion for boyfriend, unreasonable fits of crying, and general feeling of crap.

This pill is dangerous!

I've also had more trouble seeing after using 1 spritz of Nasonex in each nostril once a day (for several months). I've also felt progressively more tired. Most concerning, and my reason for being here, is that I developed a Rosacea-like condition. My dermatologist dx'd me with mild Rosacea, which is unbelievable to me, as my family line has nothing like this in it. When I did a Net search on Rosacea, it mentioned that steroids can cause this condition. Also, Rosacea is progressive and can damage the eyes and even cause loss of vision. So, if you suspect that this nasal steroid is affecting your vision, I'd recommend getting off of it. Oral and nasal steroids can become systemic if taken for long periods of time. This is common knowlege in medical circles. I took myself off of Nasonex today and am already starting to feel better.

Straight from the Yasmin booklet that comes with the pack of pills:
Warning signals:
Sharp chest pain, coughing of blood, sudden shortness of breath, pain in the calf, crushing chest pain or heaviness in cheast, sudden severe headache - vomiting - dizziness - or fainting, disturbances of vision or speech, weakness, or numbness in an arm or leg, sudden partial or complete loss of vision, breast lumps, severe pain or tenderness in the stomach area, difficulty in sleeping, weakness, lack of energy, fatigue, change in mood, jaundice of skin or eyeballs, irregular bleeding, fluid retention, Melasma (spotty darkening of the skin - particularly in the face) and other side effects may inclue change in appetite, headache, nervousness, depression, dizziness, loss of scalp hair, rash and faginal infections.

It makes me furious that some of you have told your doctors outright that you've been experiencing some of the above effects from this pill and yet they tell you to your face that it's not the pill.....(fuming)

The other poster is right - call Berlex and tell them what's happened to you and that Yasmin sucks!!

My mother is currently using Alphagan-P to lower her IOP. Her doctor has recommended that she switch to Xalatan or add it as a second drop at bedtime. I want to be especially cautious given that she is monocular and 90% of her optic nerve is damaged ( she seem to be progressively losing her perpheral vision despite an IOP of 13-17 ), and she has some macular degenerative problems. I understand with Xalatan, there could potentially be macular side effects. I would appreciate it if anyone has used Xalatan or Alphagan-P to comment on side effects that they may have experienced or efficacy and also if anyone may have some insight or perhaps personal experience related to this. I would be so very, very thankful for your help.

lance67@bellsouth.net
I have experienced blurred vision and a shadow of objects and letters that is faint and just below the object or letter. For example, people will appear to have two sets of eyes. My Doctor stopped the Xalatan and assured me that the blurred vision would clear up, but it has been approximately 3 years and it seems to be getting worse. How many others have experienced this problem?? Nancy Dunaway, Oak Ridge, Tenn.