Glasses symptoms and conditions

I have been on prednisone continuously now for 15 years. I was put on it in March of 1995 for a lung condition called chronic eosinophilic pneumonia. I was 122 pounds when I first started prednisone. Now 15 years later I am 197 pounds. I am 35 years old with osteoporosis. I have dealt with depression, terrible headaches, stomach ulcers, hormonal imbalance, hair loss, swollen feet and ankles, I now wear glasses when I didn't before, I have thin skin now that looks older than my 35 years, I deal with night sweats, and in the summer out in the heat my very round moon face turns red as a beet. But, no one can get me off the prednisone. I have seen many specialists, and within 1-2 days of starting to wean past 10mg I get so sick I have to be hospitalized, I literally can't breathe or live without it. I hate this stuff and what its done to me, but I have no choice but to take it or I will die. Doctors have tried alternate medications, nothing but prednisone works. If there is ANYONE who has had to be on it as long as I have or have had success in getting off it after being on it for so long, I would love to hear from you.

Began taking 500mg of niaspan after 81 mil of Bayer 30 minutes prior (at 11:00 in the am) about 3 weeks ago. Recommended at this time since I do enjoy my 2 glasses of red wine at night. I then take 10mg of Lipitor before bed. Side effects have been swollen lips that keep peeling, after many OTC lip balms, racing heart and unbelievable insomnia. Only had flushing the first day before nurse, not doctor, told me about aspirin. I don't know whether my allergic reaction is the Niaspan or the Lipitor. I also had mild nausea and foot cramps at night. The nausea has subsided but not my lip problem.

For one year prior to taking these drugs, I was on 10/40 of Vytorin but since all the negative results of that drug, my doctor has taken all his patients off of it.

I am a 56 year old man who has been on zocor for a few months. A few weeks ago after going out to a party, the next day I was ok in the AM, but then became increasingly dizzy to the point of having to stay in bed.

Last Saturday, I had a two hour drive and felt dizzy driving and got worse as the drive went on. I had several anxiety attacks and had to stop several times. On the way back Sunday, I was so dizzy and disoriented, I had more anxiety attacks and had to stop several times again. That night, I went to a birthday party and had several glasses of white wine, which made me feel a little better.

Ever since then, I have had severe dizziness and numbness almost sending me to the emergency room. This site keeps me out.

After 5 days of no zocor, and limited alcohol and caffeine intake, I am feeling much better.

Also, over the last few months, I have been getting weird flaking of skin on my face.

Don't take zocor. If you do, don't drink, and limit the caffeine.

PLEASE HELP! My father, age 74, was on lipitor for a year or so and then was switched to zocor a few weeks ago to help control his cholestorol. In the past week, the tightening he experienced in his leg, while on lipitor, has become debilitating leg pain now while he is on Zocor. Ultrasounds have ruled out a blood clot. He has no pain when he sits, but he describes the pain has his calf wanting to explode when he stands and he cannot walk with out the help of a cain. The pain radiates from his leg up to his hip.

His cardiologist has taken him off the zocor for a few weeks to see if there is an improvement. It has been 3 days and he feels a bit of relief. SO here is the million dollar question: His labs indicate his cholestorol is normal now, most likely thanks to the statins.....can anyone suggest another form of meds that will help regulate his cholestorol....say COeq10 and fish oil? Any help is SO appreciated!!! Thanks to each of you for your posts. It is so comforting for my dad to know he isn't developing a new issue and that it can be resolved with the removal of zocor!

Topamax is off label for weight loss. I was put on it after gaining about 35lbs from Seroquel. It took the weight off like it was supposed to. My dose has recently been stepped down because I'm back at my normal weight of 135 (I'm 5'11").

When I first started taking Topamax diet soda and other sugary things tasted really strange, which my doctor says he's never experienced before. I also had a numbness and tingling in my face and hands for about an hour or so after taking the pill for a while.

One more thing that I noticed about this drug is that while on it my vision went from perfect to needing to be corrected by glasses. I have read a few things about vision problems associated with Topamax but I am not sure if it caused my nearsightedness or not.

Thanks for letting me share my thoughts.
M.

So glad I found this site!! i just went to the Mirena website to check side effects. i had this inserted a few weeks after i had my first daughter in December of 07. The last two months or so of my pregnancy i noticed my sex drive was slowing down, but it mostly was just the thought of the discomfort(I put on 50 pounds lol) So for months now, I have had the same decreased sex drive-it brings me to tears! I was never like this in my life, and I finally thought that maybe something was up with this Mirena. Once I read the posts, ans saw some of others side effects, i think thats whats going on. I have had Horrible leg cramps in my lower legs, severe shooting pain when I stand up, and I could not figure that out either. I even just last week, went out and bought expensive new sneakers and have been trying to where them thinking maybe all my other shoes were messing something up. Now I doubt it! Luckily my periods have not been bad, except the fact that they are beyond irregular(just light) and my cramps are about the same, but I do get some sharp cramps like i never felt in my abdomen. AND!!! I have lost all but about ten ponds of baby weight, but I have been on Phentermetrizine (same as Phentermine diet pill) from the doc, and have only been able to lose about 3 pounds in a month, so I am thinking this thing is def. holding some weight on me. Hope I can get it out, I don't have any insurance anymore!!!

I have a 26-month old grandson who has been on Singulair for "27 DAYS". His pediatrician knows that his immune system is already compromised due to some developmental delays. However, before he started taking his Singulair he was a very happy, funny and loving child. Within 2 weeks on this medicine we started to notice a few changes in him. He started waking up at night "screaming" and he has been sleeping through the night for at least a year now. And when his mother would go in to get him out of his crib, he would be so frightened and afraid to leave her side. It would take her a very long time to settle him down and put him back down for the night. At the same time, he started not wanting to drink his normal daily glasses of milk or eat his regular meals. He was simply a mess most of the day and would fuss, cry, bang his head and we were having a very hard time trying to figure out what was wrong with him. He is not yet talking due to his delayed speech, so he could not tell us what was going on. Yesterday, I told my daughter let's look at the side effects of Singulair since it was the only thing that had changed within the last few months. When I found this site, I could not believe what the parents/grandparents were saying about their children on this drug. We immediately took him off Singulair. This will be his second day without being on the drug. According to my pharmacist, it will take approximately 50 hours for it to get out of his little system. The pharmacist had not heard the latest that aired on the TV station, so she asked me to call her back in a few days to tell her how my grandson is doing. Parents should be able to trust the medications that are prescribed by their Pediatricians, especially at such young ages. My daughter is REALLY UPSET and has a call into my grandson's doctor. Thank God I found this website. I simply searched on "side effects of Singulair in children" and this site came up. I do believe the Lord is watching over my grandson. Thanks.

I am a healthy female with little to no history of adverse reactions to medications. I was prescribed a 10 day dose of Levequin (500 mg) for a minor but stubborn skin abscess. After the third day, I woke up with significant joint soreness in my fingers. Progressively the soreness spread daily to my wrists, elbows, ankles, knees, hips, etc. I did not suspect the antibiotic at first, but I know my body, and I know something was WRONG.
After my 8th dose I decided to look online...it is at least good to know that what I'm experiencing is definitely from Levequin. Thank you all for sharing your stories.

I especially found MERCEDESLANE posting on April 15th interesting. I guess this person works in the health care system. Considering this uncompassionate individual, who apparently wants everythone to know he has a Mercedes, can't spell (whine), and does not have basic grammar skills. Wow...my faith in the our health care system is stronger than ever. But what do I know, I'm just an "IDIOT" with shingles that needs to have a couple of glasses of whine while I pop my remaining Levequin.

I'm 19 years old and have been on NuvaRing for 3 months. I am AWFUL at remembering the pill, so my gyno put me on it. I have not experienced any of these side effects...until i read this site! It's odd because I feel like I just shook a lot of things off to normality or just simple bodily changes, but now that I read and think about it, it's made a lot of changes in me too!
I have had blurred vision with distance and kept telling my mom I really think I may need glasses! It was weird because up until recently, I had perfect vision! Not only that, I have had MAYBE five headaches in my lifetime! I find I get AT LEAST one a day now. Not only that, but my sex drive...oooh...it is completely non-existent now! I feel so horrible because my boyfriend asks me more and more if I am not attracted to him anymore. It makes me so sad because he definitely turns me on, but my body doesn't seem to react the way my mind does. It is painful to have sex more than about five minutes because it's dry and just becomes painful friction so we have to stop. I am so mad at EVERYTHING all the time! I feel like I nit-pick everything my boyfriend does and I just get so mad and frustrated over NOTHING! Just one wrong thing said and I'm to boiling point in about .2 seconds! I also have a crazy rash in the last month that I shook off to changing laundry detergent and having a reaction, but it's not gone yet. It's all the way from half way up my sides to my knees and everywhere in between! Including my elbows, forearms, neck, I'm miserable with it! I have to get off this after finally having something bring this to my attention! I am going to the gyno the next open chance! Thanks ladies!

Wow, I got on the internet this morning looking got side effects of advair b/c I mail ordered my script so i've been without for a few days. i have been experiencing severe neck pain, thought I slept on my neck wrong, but it's still here after 3 days. I have been on Advair 100/50 for 6 years, and have now worn glasses for 3 years, on nerve blocker medication for neck and shoulder pain, horrible heart palpitations, but I've never thought these things related to the Advair until recently. I've been asthmatic all my life and thought Advair was a lifesaver, but always had some concerns. I knew any medication could not be safe for life, and after 6 years. I'm really starting to pay a price.

My 17 yr old daughter received her first Gardasil on April 17,08 with only pain at the injection site on June 16th 08 she received the 2nd within days she started complaining of severe headaches and eye pain so I scheduled a routine eye exam thinking that her glasses may need to be updated. After her exam her optomatrist called me intot he room telling me that she had severe swelling of her optic nerve and scheduled her for an MRI before we could get that done she went to the ER for severe pain in the eye and headaches there they did the MRI and it was normal no tumors or anything that would cause such headaches. On July 3 she called me from work asking to be picked up because the pain was so bad she could not function at all she was weak, dizzy and overall just not feeling good. I took her to the ER again where they performed a spinal tap and tons of bloodwork and admitted her for pain control on July 5th she had a 2nd spinal tap and every day more bloodwork was performed so far ALL tests ran have come back normal. She was in the hospital 5 days. She seen her ophthalmologist a week after being released and we talked to her about the Gardasil and she felt there was enough "coincidence" to have my daughters pediatrician file a adverse reaction form. That has been done and my daughter has learned to live with the pain since nothing seems to help it anymore. Also the last 6 weeks she has had bad insomnia and nose bleeds.

Thank you so much for your website. I cannot begin to tell you what this drug has done to ruin my life.

I had been on it for over 4 years on a misdiagnoses (Never should have been on it) and was told
“It was no worse than Tylenol.” Ok I thought as I was suffering from a few swollen joints every
now and then but was fine otherwise.

Then one day I was working and someone noticed my face was swelling. I looked in the mirror and
low and behold my face was rubbing my glasses. I asked my doctor and he said “it will go away soon.”
I am very athletic so I continued to run and work out as I slowly went from a 30” waist to a 50” inch waist!!
People at my office thought I was on a food binge like no other. My wife was stunned on how fast this
happened as was my family. Now the problem had gotten much worse. Constant body aches and swollen ankles.
After a year I went from jogging, to walking, to using a cane to using a walker…how sad my family felt
for me and no friends insight. my company then laid me off as I used the walls as a walker and simply could
“perform up to par.”

Next came the extremely high sugar, blood pressure, Glaucoma and I suddenly noticed I was having problems
seeing. Went to the eye doctor and was told I was getting cataracts but it would take a couple of years to form.
90 days later I could not drive and could barely see in both eyes, now I was almost blind.
Now 80lbs overweight almost blind with Glaucoma, high blood pressure, diabetes and cataracts. not to mention severe depression and mood swings that were unbearable, and yes still using a walker from severe muscle pain.

Well the time came where I lost my health insurance and was unemployed. I was out of Prednisone
one day and called my doctor. He said come in for $320.00. I said I didn’t have it and pleaded for them to call
in a 30 day supply, I was told that they “weren’t a charity” and “go to the emergency room” click!! My wonderful
doc was gone. Well I went to the emergency room the next day and was told “they don’t give refills.” I had been
off prednisone for a day and as some people know if you stop that high of dose for that long you may die from
adrenal crisis. So I stood in the emergency room for 12 hours waiting to go into this crisis! Finally a nurse convinced
a doctor to see me for 30 seconds, gave me a refill and a list of welfare clinics and booted me out the door. They
hated my appearance and hated me for no cash.

One day I decided to end this nonsense and tread everything I could from sources I hadn’t read that were very old
regarding what was wrong with me. I went on self imposed diet of 1000 calories a day and lost 60 lbs…yes!!
I stated weaning from the Prednisone and took a ton of supplements I had read about. I got down to 7.5mg every
other day. Yes, suffering tremendous total body aches, severe mood swings, dizziness, severe hunger and
confusion but I plowed though. By the way I don’t recommend this but I couldn’t get a refill for a prescription from anyone
because I ‘had made to much money.” So I turned to the Internet for everything. I bought 500 5mgs for $23.00 screw the doctors I don’t need their prescriptions. I am now totally off for 6 weeks I do have some bad stiffness, muscle aches and mood swings but after 4 years of pure hell I am truly thankful to be off this dangerous drug, it ruined my life.

So I went to a new Doctor finally and my diagnoses was a food allergy and simply had a small stint of bursitis a total mis- diagnoses from my first Doctor! Doctors aren’t gods so take it from me trust yourself first and do your research.

My prayers to all who suffer from this drug. Damn the incompetent doctors who wrongly prescribe it!

Dan

PS Does anyone know how long these severe body aches last after completely stopping. Its been 6 weeks and its just a little better. My doctor told me to fight it out or get back on pred. NO WAY!!

Thank you so much for your website. I cannot begin to tell you what this drug has done to ruin my life.

I had been on it for over 4 years on a misdiagnoses (Never should have been on it) and was told
“It was no worse than Tylenol.” Ok I thought as I was suffering from a few swollen joints every
now and then but was fine otherwise.

Then one day I was working and someone noticed my face was swelling. I looked in the mirror and
low and behold my face was rubbing my glasses. I asked my doctor and he said “it will go away soon.”
I am very athletic so I continued to run and work out as I slowly went from a 30” waist to a 50” inch waist!!
People at my office thought I was on a food binge like no other. My wife was stunned on how fast this
happened as was my family. Now the problem had gotten much worse. Constant body aches and swollen ankles.
After a year I went from jogging, to walking, to using a cane to using a walker…how sad my family felt
for me and no friends insight. my company then laid me off as I used the walls as a walker and simply could
“perform up to par.”

Next came the extremely high sugar, blood pressure, Glaucoma and I suddenly noticed I was having problems
seeing. Went to the eye doctor and was told I was getting cataracts but it would take a couple of years to form.
90 days later I could not drive and could barely see in both eyes, now I was almost blind.
Now 80lbs overweight almost blind with Glaucoma, high blood pressure, diabetes and cataracts. not to mention severe depression and mood swings that were unbearable, and yes still using a walker from severe muscle pain.

Well the time came where I lost my health insurance and was unemployed. I was out of Prednisone
one day and called my doctor. He said come in for $320.00. I said I didn’t have it and pleaded for them to call
in a 30 day supply, I was told that they “weren’t a charity” and “go to the emergency room” click!! My wonderful
doc was gone. Well I went to the emergency room the next day and was told “they don’t give refills.” I had been
off prednisone for a day and as some people know if you stop that high of dose for that long you may die from
adrenal crisis. So I stood in the emergency room for 12 hours waiting to go into this crisis! Finally a nurse convinced
a doctor to see me for 30 seconds, gave me a refill and a list of welfare clinics and booted me out the door. They
hated my appearance and hated me for no cash.

One day I decided to end this nonsense and tread everything I could from sources I hadn’t read that were very old
regarding what was wrong with me. I went on self imposed diet of 1000 calories a day and lost 60 lbs…yes!!
I stated weaning from the Prednisone and took a ton of supplements I had read about. I got down to 7.5mg every
other day. Yes, suffering tremendous total body aches, severe mood swings, dizziness, severe hunger and
confusion but I plowed though. By the way I don’t recommend this but I couldn’t get a refill for a prescription from anyone
because I ‘had made to much money.” So I turned to the Internet for everything. I bought 500 5mgs for $23.00 screw the doctors I don’t need their prescriptions. I am now totally off for 6 weeks I do have some bad stiffness, muscle aches and mood swings but after 4 years of pure hell I am truly thankful to be off this dangerous drug, it ruined my life.

So I went to a new Doctor finally and my diagnoses was a food allergy and simply had a small stint of bursitis a total mis- diagnoses from my first Doctor! Doctors aren’t gods so take it from me trust yourself first and do your research.

My prayers to all who suffer from this drug. Damn the incompetent doctors who wrongly prescribe it!

Dan V

I am a 39 year old man with peripheral neuropathy and migraines. When I was diagnosed 3 years ago, the pain in my right leg was horrible and headaches daily. My Dr. put me on Topamax and I was so happy, it seemed to help but one night( about three weeks into it) I went to bed and awoke in the morning legally blind. Topamax was stopped that day but it took 4 months ( and changing the prescription in my glasses 3 times) for my vision to return to 20/20. The doctors tell me I was lucky as some people have perminate lens damage from the optical pressure change.
My doctor said I could not take any thing in that class of medications as it would probably have the same effect on me. So he decided to put me on Cymbalta for the neuropathy. He said it was being tested as a possible use for neuropathy but had not been proven. It works great for the pain and oddly my migraines have gone down to about two a month.

Here are some more side effects that I encountered during my ordeal with Lipitor. A week after I started the medication, I started experiencing blurry and decreased vision, this used to go away and come back sometimes, I could swear I always had 20/20 although I never went to eye doctor, but I never needed glasses all my life, if fact any type of glasses will blurry my vision and make me dizzy. I had my first eyes exam a couple days after I discontinued Lipitor, guess what? I have 20/20 vision.
More details about the back and right arm pain, not only the pain was unbearable, I felt my muscles sagging and they did not have any strength, this thing sucked the life out of my muscles, it made me very tired and easily irritable. My fist victim was my little baby ( my beautiful 4 year old), her daddy couldn’t hold her anymore, I even avoided staying close to her, because anyone who touches that right arm will make it feel like another deep stab to the arm deep into the bone. I have never experienced pain like this. I knew about toothache when I had a cavity at 23, but it was fixed and went away, I even experienced the pain of a broken arm at 16, but this thing was something else. The other victim is my wife, I stopped doing stuff, I used to be a very active dude, I do stuff on weekends with family and even every day after work ( you name it, park, boating, swimming pool, malls etc..). It felt like I was dying one piece at a time, going down the tubes fast with no clue of what was wrong with me.

I finally don't feel so alone. I got into poison ivy on June 1. On June 12th I finally went to my md to get something to take for it to go away. I had been treating it with calamine, topical stuff and taking Benadryl.... She gave me a shot which actually made it all go away within two hours. BUT, she also loves giving out pills, so she gave me the Dexpak. I took it for 7 days and my heart was beating uncontrollably. I didn't get REM sleep for 5 straight days. I took myself off. Cold turkey, yeah, I know you're not supposed to do that, but that stuff was killing me. So finally after having a meltdown in my office at home, my husband and I went back to her to see what she could do for me. She said oh, just go home, drink some wine and get some sleep.
I went home, drank two glasses of wine (which after doing research is NO combination with with high powered drug and she should have known better!!) Took a really hot bath, tried to get sleep. My husband took off work for three days to try to get me sleep.... finally we went to the ER because my heart wouldn't stop pounding so fast. The ER drugged me with some serious sedatives. I had a reaction to those and had a panic attack in the ER, so their solution: strap her down (bruised my wrist) and take her to a psychiatric unit for "symptoms of schzitophernia." So I was basically in a room with a bunch of people that can't control themselves. I did get 8 hours of sleep and regained all cohesive control. I was still groggy from the sedatives, but I knew what was going on. The nurses were the rudest people I have EVER been in contact with. No wonder the patients were in fits! After 5 hours of me and my husband (who was downstairs with my Mom) they finally released me. I talked to the discharge nurse and she said that if I sign a form releasing myself "against medical advice" that insurance might not pay for it. I said, are you kidding me? I would rather pay to get out of here than sit here one more minute with these people.

It was the worst medical experience I've EVER had. I have since fired my md. She doesn't know it though because she hasn't BOTHERED to call to check on me!! So, I am not going to a psychologist and my obgyn to make sure those steroids didn't screw up my brain or my endocrine system as we are trying to have a baby. Yeah, that was my first thought too... why would my MD who KNOWS we are trying to conceive do this to me?

Whew. Anyway, so my advice is to make sure you have someone around you at all times that can monitor your heart beat and write down EVERYTHING that happens in case you have a situation like mine. I journal all the time, so it was easy for me to explain to the shrink.

Okay, good luck out there!!!

I have had all the side effects mentioned in this column for about 14 years. I started on 10 mg of Lipitor.

I have looked for alternatives but found none. Lately I have started consuming about 2 to 3 glasses of red wine. I am finding that the adverse side effects of Lipitor get drastically reduced.

Anyone else experience the same thing!!

I've been on Xalatan for 10 months. At first I had only red eyes, but after two months my vision got blurred. So I got new glasses. One month later I needed new glasses again. The cornea began to swell and finally I had a macular edema. After having stopped using the drug, my vision still remained bad.
Why on earth do doctors still prescribe Xalatan???

I am on my first pack of Loestrin 24 Fe. I was doing okay except for constant breakthrough bleeding. This past weekend I was at a rehearsal dinner and wedding where I did a fair amount of drinking. On Monday I started feeling weird. By Monday night I was so weak and tired feeling that I couldn't lift my head. I've been laying on the couch for 24 hours and I still feel like the life has drained out of me. I"ve also had a stuffed nose and post-nasal drip since I started the pill. I went to the doctor this morning and they decided I needed iron pills to counteract the bleeding and an antihistamine and singlulair for the nasal symptoms. I'm now totally afraid of this pill!

I have been taking 40mg of Lisinopril daily for over 5 years, which has successfully lowered my blood pressure. I thought the drug was fine - however, I do occasionally experience ED, and to be sure of successful performance, I need to take 50 mg of Viagra. My testosterone levels are fine. My doctor has ascribed the ED to my 3 - 4 glasses of wine each evening - saying that if I reduced the wine intake to 2 glasses, the problem would go away. After reading these accounts, I'm not sure it is the wine. I did experience severe leg cramps at night for 2 - 3 years - but those have stopped, and I have not had any of the other symptoms mentioned.

I have experienced many of the same issues with Loestrin, bloating, random spotting, weight gain, moodiness, and loss of sex drive. However the side effect that I haven't heard but one person mention is what happens when you drink alcohol while on this pill. I have a low tolerance to begin with, yet now that I am on this pill I will get a hangover after 1 or 2 glasses of wine. It really has varied but at one point I only had two drinks and the following morning proceeded to throw up three times. I am changing to Yasmin because of insurance reasons but am happy to try something new as this pill has only greatly complicated my life.

red eyes, itchiness, occasional pain behind the eye, blurred vision, loss of visual acuity (I have to have new glasses every 2 months) and rapid development of cataract.

I took Toprol for 4 years. I gained 50+ pounds, had the worst dreams ever. They were so real, I would get out of the bed and put on my glasses to make sure I was seeing what I thought. Sometimes I would see actual performances. If I wake up and see a light, any light, even on the alarm clock, some figure would appear. I and my family thought I had lost my mind. I sweated like a maniac for no reason, you would think that I had just ran a marathon. My body ached, legs would be so heavy, especially upon waking. Sometimes I had to lay in bed longer because my legs were achy and too heavy to get up. I had brain fog, couldn't concentrate and my night vision was almost zero. I never felt like doing anything, the only thing I wanted to do was sleep. I never got a good night sleep, sometime I didnt sleep at all.
Being on Toprol was HELL!!!!!!!!! I am off now and I feel like a different person.

50 yr old female ( gasps @ 5-0 still)

I've been on ToprolXL for some time now. I started with Tenormin and felt FINE! The doctor then decided it was not the 'right medicine' for me and changed me to a 'new and better medication' names TOPROL XL, He started me on 50mg a day. I had experienced rapid heart beat of at least 150 bpm up to 200! My heart had to be stopped in the ER to get it back to being a normal rhythm. At the time I was 39 yrs old :( SCARY! I had every test imagined. Heart tests, lung and leg scans. You name it, I had it done to me ( thankfully, to make sure it was nothing serious). Although I do consider a heart beating that high to be serious! I already have a anxiety disorder, I noticed that my panic attacks are worse now more than ever! I am very very lethargic. Just thinking about doing ANYTHING makes me tired. I even getting tired when I talk too much! My mouth is always excessively dry. I put on weight and even paid for a diet that consisted of 2 'shakes' and one meal per day. Followed it to the "T"! and nothing ?! I've recently read that ToprolXL can lead to all kinds of diseases. One of them being Lou Gehrig's (ASL) :( I am SO very upset that medication is prescribed supposedly to make a person feel better AND I don't think I've physically felt this depleted and depressed in years! I want medical answers and I need support and words of encouragement from everyone that has been on this drug , most especially those weaned off ot it and are on a better drug. Most of the people I notice taking TOPROL XL are taking it fro HBP or symptoms other then the one's I have. I am SO confused now :(

I work in a health care system and we have used levaquin for this last cough, cold and flu season. It has worked wonders for the various upper respiratory infections.

No one has developed rashes, boils, or bone/muscle pain. After reading the first response, her abnormal reaction sounds more like a bad case of shingles.

Then, I read the last post where the person drank two glasses of whine to help with the blah blah blah. Mixing alcohol with any type of medication will not help with Your sypmtoms were a "full fledged panic attack" as you stated from the beginning.

Nothing but idiots posting here!