Paying attention symptoms and conditions

I was on Nuvaring for exactly 2 weeks and 1 day and for the first few days it was great. The only side effect I seemed to be getting was the breast swelling and tenderness. Then about a week in, I started getting cramps that were very short (5-20 seconds or so) but very painful, and then came mood swings. I was very depressed. I didn't want to go anywhere or be around anyone.I would get angry at my fiance and want him to shut up and go away if he tried to have a conversation with me, but then I would cry hysterically if he was on the computer or not paying attention to me for any longer than about 20 minutes. I didn't want to move from the couch. All I wanted to do was nap or eat. If I wasn't doing either of those I was yelling or crying. So, my fiance and I did some research and found that the nuvaring could cause all of that. I took it out, and my mood swings immediately became less severe, and now, after having it out a week are almost gone. The problem is, I just started my period this morning and I am just pouring blood like no one would ever believe, and I have cramps worse than I have ever felt before. I am wondering if I should go to the emergency room or wait this out and call my Gyno on Monday.

My daughter was prescribed Doryx for mild acne- 150mg a day. At Track Meets she is complaining that she is dizzy (seeing black spots) after races. Now she says she has tingling in her hands and lips. They feel like they are on fire also. I had her stop the meds immediately and am waiting for the dermatologist to call back. If anyone had these symptoms how long does it take for them to go away?? email me: ******

I must admit I am very surprised by all of the side effects of Advair. I have been taking Advair 250 for years and have NEVER had any problems. I'm 28, healthy, thin, and happy. I exercise several times a week. ALL drugs have side effects. I don't think it's fair for anyone to say "don't take Advair, it's a horrible drug" because it works for some of us. I was taking Flovent before but it didn't work for me. I needed a rescue inhaler several times a week. Since I've been taking Advair I don't even fill my prescription for my rescue inhaler! All drugs have side effects, but they don't effect all people!

I have been on Paxil for just over a year. I am on it strictly for PMDD, and I can not use regular hormones so Paxil was the next best thing. I LOVE how much better I feel as far as the PMS symptoms are concerned, but my memory is TERRIBLE! I thought it was just me, I thought maybe I had some sudden memory disorder at 35! I couldn't find anything listed in the side effects having to do with memory loss. Movies are thr worst for me, I can not remember a movie to save my life. I have started a new job that requires recall from a dvd as well as a manual. YIKES! It is hard. I have also experienced a harder time paying attention. Almost like I know someone is talking but I end up tuning them out, like there is a blocker or something. It is really hard to explain. Anyway I am a very healthy, no other medications person. I am POSITIVE Paxil is causing this especially with the time line of it. Now I am scared to death to get off of it as I don't want to experience the withdrawals and I feel so much better than I did before, but the memory loss is awful, so what is the balance?

WOW! I have been taking wellbutrin for two years now. The first three weeks were spent with nausea, vivid dreams, some jitters and being very tired. By the end of the first month that had all pretty much gone away and I was feeling more energetic, less anxiety and no depression. When I started exhibiting memory loss at first I really didn't notice it since was just articulation & range of descriptive words. Eventually it progressed to common words and sentence endings. Then I began to notice I could no longer do ANYTHING and listen to someone else at the same time, that progressed to not paying attention to what someone was saying period and the lack of ability to remember the plot of books I had read or some movies I had watched. I also began to notice moderate hair loss. Last but not least I was very slowly gaining weight, it was beginning to add up and I didn't seem to be getting the energy boost or feel that great anymore. So I decided I would quit. After a quick taper off I got to experience all the joys of withdrawal, nausea, sleeping fourteen hours and taking a nap in the afternoon, appetite swings, mood swings, diarrhea , sweetooth and the inability to get up and do anything or go anywhere. It was paralyzing. That went on for almost a month. Its been three months now and the improvement in my cognitive function and physical energy was so profound that it made me wonder if my problems over the past two years could be related to the wellbutrin, so I typed in memory loss and wellbutrin and here we are. I really didn't realize it was affecting me (or others)so seriously and I had zero initiative to investigate my condition until after I quit taking it. Dont get me wrong when I started taking wellbuterin I was at the mercy of my emotions and I needed something, but I feel the corruption of my facualtys was very insidious with this drug and by the time I realized I was having problems I didn't readily recognize it and and had no desire to do any thing about it anyway. My husband had even pointed these symptoms out to me and still I didn't/wasn't able to put it together until now. I don't know what the solution for others will be but I have found mine. I guess what bothers me most is that none of the symptoms caused by this drug was expounded upon by my doctor, the focus was all about how much better I would feel, He never once mentioned memory loss or concentration. And in the last two years he has never once mentioned the idea that I would ever be off antidepressants. For most of us it doesn't have to bee forever. I don't know if I had it all to do again if I would take wellbutrin again or ask for something else, but what I do know is that I would be more aware of what I was taking and not take it for nearly the length of time I did. The drug itself kept me from reacting to its effects and I was unable to gage when I was starting to do better emotionally. The process of getting off it made me wonder if I could do it and if I really was better, believe me I thought about reaching for that bottle every day for a month. Ask yourself where you are mentally, talk to your doctor, MAKE HIM TALK TO YOU, and taper off a lot slower than I did so your able to clearly differentiate between recurring depression and withdrawal. I am no longer in the same frame of mind that I was when I started taking wellbutrin and now that I am completely off of it I feel fine. Good Luck and be careful

I had my mirena since 2002, I recently found this site and really started paying attention to my body, MOODY, definitely, IRRITABLE, definitely, DEPRESSED, for sure, NO SEX DRIVE, my husband hates it. BACK PAIN, is unbelievable. OMG, I’ve spoke with 2 Doctors about these being possible side effects of Mirena, OUT OF THE QUESTION. In Feb of 2008, I was diagnosed with FIBROMYALGIA, I wonder how much of that is really the MIRENA. Can some one post to my private email (******) to let me know the side effects AFTER having the Mirena removed and if you are better now. Thanks for saving a life.

i have been taking wellbutrin to help me deal with anxiety for a little more than a week. i thought it would take more time to have an effect, but i feel very calm. i even stopped smoking right off, which i didn't intend to do. The side effects are worse that i thought they would be. i have lost the ability to spell, my short-term memory is noticeably impaired, and i have trouble paying attention in class/at work. i feel very foggy and disconnected. i've also been having headaches, night sweats, and stomach pains, but they are mild.

This is an update to my experience. I got my Mirena IUD removed mid-May, and it has been amazing to see the difference in my body and health. My cycle has always been very predictable. I'm one of those every 28 or 29 days ladies. About every 2 weeks - coinciding with either ovulation or the onset of my period - my body heals a little more. For example, just this last ovulation a few days ago my joints quit hurting. I have seen my energy level, concentration/focus, and mood improve at about every 2 weeks. So for me, my body is getting back to normal by doing what it's supposed to do - Ovulate! Menstrate! No more hormone contraception for me!!! I'm still slowly losing weight (at first it was immediate weight loss of about 7 lbs). The last couple of weeks, since my joints aren't hurting anymore and my energy level has risen dramatically, I'm able to exercise like I used to prior to all my problems with the Mirena IUD. So at every event in my cycle my body is a purging of more and more of the artificial progesterone. My husband and I have grown closer through this too. We have decided to work together and respect my body's natural cycles. I'm aware now of when I ovulate by looking at the signs - mainly the time of the month, a twinge of pain (not uncomfortable at all) telling me I'm ovulating, and cervical music - when it's stretchy and looks like egg whites. By paying attention, I know. I can't believe I didn't trust myself before. We use condoms when I am ovulating (a few days before I predict it to happen and a few days after). I'm fortunate to be so regular, but even if I wasn't nothing could convince me to ever use hormone contraception again!!!

I've been taking Yaz for only a week, but life is more miserable than ever! I have PMDD and get totally insane two weeks before my period! I'm moody, suicidal, angry at all humanity, but I experience little pain or cramps once my bleeding starts. I bleed for 8 days, and I was hoping that Yaz would help with shorter bleeding and less mood disturbances. So far on this drug I have been crying for no reason, yelling at the computer when the internet is slow, wanting to kill myself, trouble focusing on a book or paying attention to a tv show, and shuddering when I talk! I had tummy issues throughout my teen years, but once I hit my late 20's they went away. Now that I take Yaz, I feel like I'm gonna throw up every day and my tummy hurt so much the second day that I couldn't sleep that night! I'm very anxious, and it's hard for me to express my thoughts or complete a sentence! I hate this drug! My sister has PMDD and is curious about taking this drug, but I would never recommend it to her or anyone!! I'm so frustrated! Are we women just supposed to suffer until menopause ends???!!!

I've been on NuvaRing for a year and I thought It was working great. After having two rings "disappear" I decided to talk to my doctor about a different form of b/c. I have not had a ring in this month and I cannot believe the sex drive I have now. I'm single so I hadn't really noticed it was gone but now that it's back I realize how much the NR had affected me. As I was reading posts here I was amazed at how many symptoms I share with others. I have always been prone to headaches but since starting this a year ago they got more frequent and more intense. I also had issues with fatigue, however, being a single parent of a one year old I just kept blaming the baby but so far this month without the ring I hardly ever need a nap anymore. I have also noticed my mood swings are not as severe...I won't blame NR for all my moodiness because I have always been a moody person but I can tell a difference. I never had problems with the nausea or charleyhorses or tender breasts but all hormones have a different effect on different people. NR may work well for some and to those I wish congrats. I am hoping that my new method of b/c works out for me but I will be paying attention this time to what the hormones are doing to my body.

Is there a potential explanation for the adverse psychiatric side effects of montelukast?

In my opinion, there are at least some very good clues based upon the work of the Chinese researchers.

A 2006 report indicated that they had localized (meaning found it was there) the CystLT1 receptor (same as the receptor that montelukast
Singulair blocks) in the neurons of the brain tissue of rats. In order to do that, they injected rat brain's with NMDA to cause a chemically induced state of excitotoxicity. Excitotoxicity is a common factor in Central Nervous System disease. They concluded that both 5-LOX and CystLT1 were upregulated by the excitotoxicity that they artificially created
with the NMDA. Therefore, there would be a potential link between neuron activity and CystLT1. Nerve cells are damaged by excitotoxicity. These researchers used NMDA to cause nerve damage which caused the CystLT1 to show up. NMDA was often used in human behavior studies to cause brain damage. They would then try to observe whether behavior was compromised to conclude what areas of the brain determined what behavioral response.

So I was thinking about the Chinese researchers as I was reading other posts. One post interested me particularly regarding the mother who described behavior that seemed like hypoglycemics when their snack doesn't arrive on time. So a light bulb went on. Glutamate, another excitotoxin, can build up in the brain to a level that is damaging if humans become excessively hypoglycemic. If glutamate concentration around the synaptic cleft reaches too high a level then neurons die. Clinically, it really does seem that many people experience things that sound like the effects of hypoglycemia. It could be only a coincidence. But then again, maybe not.

The Chinese researchers found the CystLT1 receptor in the rat brain neuron after brain damage. They found the CystLT1 receptor in the normal human brain in the microvascular endothelial cells and in neuron and glial-appearing cells in brain trauma or tumors.

What role does the CystLT1 play in brain function? If it exists in brain tissue, we can assume that it does have a function. If it plays a role in preventing or repairing neuron damage due to excitotoxins, then there would be a very direct link between Singulair and adverse psychiatric side effects.

http://www.chinaphar.com/1671-4083/27/1526.htm

The bottom line is that Merck owes people who take Singulair further research regarding it's effect on the brain.

I wrote an earlier post but I am now reading alot of your posts where you say your child experienced FEAR on Singulair. That is so interesting. When my son was on it for around 3 years he would never sleep alone in his own bed and he would have episodes every night that would last up to 3 hours at bed time because I would try to get him to sleep in his own bed, even at 8 years old. I thought he was possessed!!!! He would scream and fight me and I would literally have to hold him down to get him to stay in bed. It was horrible. I'm not sure how a hullicination would be described but maybe that was part of it. All I know is that he turned into a totally different child. It was something out of a horror movie. I eventually gave up and let him sleep in our bed cause it was exhausting. He would just make blood curdling screams and the terror in his eyes was horrific. Then the next morning he would be fine like nothing had ever happened.
Now that he is off of Singulair he will sleep in his own bed with the light off all night. It was an amazing turn around. He also told me he's not scarred anymore.. Who knew????? Has anyone else experienced anything like that with their child????

As a pediatrician I write for singulair every day.
The medication is for allergies.
Allergies cause adenoidal swelling, which cause sleep disturbances which makes the child tired the next day with makes him over weight, less attentive, hyper and eventually act out.
This in turn makes the child experience parental, peers and teachers criticism/ abuse, with leads to the child feel inadequate, embarrassed, frustrated and eventually depressed and suicidal.

Yes, singulair does cause behavioral change but they appear within the first couple of peels, the rest is due to allergies, lack of medical care, i.e. sleep, singulair, and zyrtec deficiency.
Allergy shots cause 4 times the incidence of suicidally than singulair, and Ritalin 10 times more.
They say in hebrew "once a stone is thrown into a well, thousands of smart people won't find it".
Check it, it's true.

Hi. My eight year old daughter has been on singular for 6 months. She has had chronic stomach pains that she says feel like pressure. Her appetite is terrible. She always says she isn't hungry. I have to search for anything I think she will eat. She is very tall and very thin for her age. She grew an inch in the last year but gained no weight. First time her growth just stopped. No surprise as she doesn't want to eat. I took her to the doc several times and they think she has acid reflux and have given her 2 different acid eliminators ( which freak me out as well) Said she should see a gastroenterologist. We have appointment in March . I started reading this site and thought well maybe it's the singular. So I called her allergist and told them I was taking her off to see if that's why she has the stomach problems. They said I could since it wasn't a big trigger time(seasonal) and she wasn't sick with any cold or flu) She gets mild asthma when sick. Her allergist asthma doc thinks her stomach aches are related to the mucus dripping into her stomach. I have taken her off all meds to try to see if it could be the Singular. She also has been very tired and can't keep up in her dance classes. Her school teacher had to put her in the front of the class because she said she wasn't paying attention. She seems to lose it over anything that requires focus or attention.She also seems kind of depressed. She is worried that something is really wrong with her. This child used to eat normally and is gifted academically .Her tests results(taken while on the Singulair) went way down from last year. She was put in gifted pull out program from last year results but would have barley made it in this year based on her much lower scores. That does not make sense to me. Never has had attention or focus problems before. I will keep everyone posted. Does anyone know how long it might take to get this drug out of her system? Has anyone else had this kind of reaction to this drug? I also wonder whether she had reflux before but this made it worse? I had her blood tested for Celiac and general stuff and nothing showed up.I wanted to get the Singular out of her system before we see the G.I. doctor. anyway thanks, Elizabeth

My son was diagnosed w/ ADD/ADHD when he was 7. My husband and I were not advocates of giving drugs to a child and avoided it for some time. But as I watched him struggle and become depressed because he couldn't focus, etc .etc, I remembered what it was like when I was his age. (I am also ADD). You can say what you want about drugs but when my little boy was looking up at me crying and pleading for help "please help me, please...please come to school with me and tell me what to do, remind me because I forget what the teacher says right after she says it".... To see him struggle like that at such a young age we had to do something. He was a very confident and happy kid prior to starting school and after being in school for a few years being the kid that was always getting corrected by the teacher or being called out more than others for not paying attention was taking it's toll on his personality.
He did not start out on Adderall, but another Ritalin type drug. But it made a drastic change in his life - he was happier, able to focus and his self esteem came back. Later he was changed over to Adderall. He said it didn't make him feel nervous like the Ritalin type drugs. I am also on Adderall and it has made such a positive difference in my life as well. I didn't realize how much I had to struggle to stay focused, how much I procrastinated and how overwhelmed I used to feel on a regular basis until I stopped having those issues...what a relief!!! I don't have the stress eating issue anymore because I don't feel as stressed. The only side effect I noticed was my eyes getting red and a some dry mouth.
Adderall has a calming effect on me, I don't feel nervous, I don't feel detached, or any of that stuff several other folks wrote about. My son doesn't either, he is calm and happy and is doing great in school. Neither of us have any issues when we don't take the medication - as far as craving it, etc. In fact, from the initial research I've done and my own personal experience,many who are truly ADD and not misdiagnosed are less apt to become addicted than those who are not truly ADD. When we don't take it we might be a little less apt to remember that important thing we were supposed to do because we got distracted! But we don't seem to have any other withdrawal symptoms or tiredness, etc. So far it has been positive choice.

So for all you people having social issues, hearing voices, having chest pains, feeling strong urges to take the medicine even when you don't want to - YOU PROBABLY SHOULD NOT TAKE IT! All medications effect everyone differently and not all people can take or tolerate the same medicine. And for all you folks that are able to spend 10mins w/ your kids and get good results...well good for you, but DON'T JUDGE those of us for which that technique didn't work. During the summers we usually don't make him take any medication and we spend a lot of time talking through the issues that arise, practicing focus without medication, etc. We spend a lot of time reassuring him that it's OK to make mistakes when you're trying to change your behavior and that we love him just like he is. We hope that eventually as he matures that he will find it easier to do this on his own with out medication to help. However, if he doesn't, then I would rather see him be happy on medication than to struggle and be depressed without it.

Peace.

Was on Vytorin for 3 mos before I started developing serious health issues. First it was pneumonia. While trying to recover from that, I started experiencing pain in my thigh muscle which caused me to have difficulty walking and sitting. Each day the intensity of pain was increasing, so much so that by day 5 my husband took me to the emergency room at 4 in the morning because the pain wouldn't stop. I was put on bed rest for a week and had to take a narcotic for the pain, anti-inflammation and muscle relaxer meds. I missed 2 weeks from my job in 2 months. After paying attention to the commercials (something I never do) I realized that Vytorin could have caused my problems.

I've been off the drug for 30 days now. It has also caused damage to my liver. I have to have blood drawn bi-weekly to see if my liver is healing properly. The pain in my thigh has gone away to the point where I can walk normally but I'm still stiff when trying to stand up after sitting for a while. I tried to go back to exercising but the damage to my muscle isn't allowing that to happen. I'm praying that this won't be permanent.

I am currently on my 3rd NuvaRing. I had been on approximately 8 different pills since 2004 and could not find a solution for my CONSTANT bleeding. I have Endometriosis and I was only having about 5 days of the month that I was not bleeding. This has actually been going on for about 14 years but getting a lot worse since I came off of the Norplant in 2004. Since being on the NuvaRing, this is the first time I have gone more than one month with a completely normal period. I have noticed a decrease in my sex drive but not a complete death, I am paying attention. I am having slight heart palpitations for the first time since coming off of the Norplant, so I know those are from the NR, but not too badly or frequently. Headaches on the last 3 days before it comes out but otherwise. And absolutely NO pain or bloating associated with my period (I used to look 4 months pregnant most of the time). So far I am happy but am watching carefully. I have noticed a negative change in my attitude also but am not convinced yet that it's the NR since I have been through a lot recently. I will keep you posted.

I might have mild FIBROMYALGIA, but on this drug I felt like I got hit by a truck. I am on my 3RD WEEK. Terrible pain/weakness in all my muscles, the trigger points for FM were very tender. It may be that FM is getting wose due to stress, but this all happened on Yasmin.

"Spacy" and not paying attention. I blamed things on my stress level. No interest is sex due to the pain and hurting.

Very depressed and not wanting to do much (mostly because I hurt!) I can't ride my horse w/o pain afterwards.

No nausea, some stomach trouble. Acne is not better or worse.

I am getting off it this weekend and going to see if it in fact the pill.

Women with CHRONIC FATIGUE AND FIBRO be warned to keep an eye on things.

After by-pass heart surgery in 2002, my cardilogist put me on 40mg of zocor.
I was in good health with no physical limitations. I had no heart damage. The restriction of heart arteries were found due to my stress test that was performed each year as a part of my annual Physical. After surgery I was on zocor for three years, during that time I experienced a little tiredness, little weakness, a little muscle aches. some tingling in my right arm and shoulder. I went to my heart doctor Jan. 2006 and he changed me to vytorin (10mg zetia and 40mg zocor). about 6 months all of the about symptoms got worse.
By Jan. 2007, my muscles became so stiff, I could not walk, had balance problems, severe muscle aches and cramps, numbness and tingling in both arms and hands, also stifness and pain in my hands, stiffness and pain in both feet, stifness and pain in my back and weird nerve sensations over my entire body. During Jan. and Feb 2007, I was seen by my family doctor, a neurologist, and a muscle doctor. Thanks to the internet, I found info on zocor and zetia, which is the drug vytorin. Warnings described the same symptoms I am experiencing. I stopped vytorin, I am not taking any statins drugs now. My doctor order a blood test to check for muscle damage, It indicated severe damage, a Creatine level of 770. This level should not be over 200. After being off the drugs for 30 days the creatine level dropped to 645. My condition has improved by 25%. I am walking a little better, but I still having muscle problems, there is improvement. I think there will be a very long recovery. There seems to be some evidence that these Statins affect people of age much more than the young. I am 70 years old. PLEASE PEOPLE, IF YOU ARE TAKING STATINS DRUGS, STOPPED NOW! SLOVE YOUR CHOLESTROL PROBLEMS BY OTHER MEANS. Since I stopped my cholestrol has gone from 157 to 280, but I am not going back taking these drugs. I am trying the natural way now. I have read post after post on many web-sites of people with the same symptoms that were using these drugs. The drug companies and the FDA are responsible for the the degradation of people's health taking these statin drugs.

My daughter is 5 years old and has been on singulair for 1 week. i have already noticed a dramatic change in her behavior. she has become irritable, mean, nasty, and emotional. she has had me in tears on a daily basis. she has turned into a monster. we will be calling the doctor in the morning!

My 6 year old son has had all of these more or less. He has been on Singulair for about 5 months. We took him off last Friday when he started having seizures. It is only now that we are connecting the things he has complained about. He is still going through testing but everytime a test is done it is negative. He is in perfect health. The dr.s are stumped. What happens is, he smells a wierd smell. Then he sees lights. After this he has a bad headache and becomes weak so he lays down. Shortly thereafter he stiffens and starts shaking his arms and legs while clinching his hands. He also grunts and makes a buzzing sound and appears as though he only breathes out. the dr.s say it is not seizures but movement disorder and if it is Singulair it should be out of his system within 3 days... He is still having the seizure type fits and its been a week since we took him off singulair. He is still losing his temper and having horrible dreams as well. Cat scan was normal, EEG was normal, blood work is ok, they want to do an MRI but does this sound familiar to anyone?

I am not cetain Advair is the cause of this but about year or so ago I started experiencing fainting feelings and almost passed a couple of times. The doctoer ran tests and everything seemed normal. One day I was paying attention to the side effects of Advair via an ad on tv and was stunned.
I stopped Advair a couple of months ago and have not had these "weak spells". Now it may be a coincidence but I won't be using it anymore so time will tell. Has anyone else experienced feelings like this?

hi everyone. I was put on yasmin in june for cramps. It works great on my cramps and my cycle. The only problem is my cycle is so light that i cant use tampons but i hate pads

The problem i am having is ever since i have been put on it i have no sex drive at all. I dont like it if my boyfriend touches me in a sexual way, but the minute he leaves for work i am all over him. Everytime we try to have sex it burns and is really painful for me. It got worse after i had kidney stones and surgerys. My boyfriend and i havent had sex in 4 months. I love my boyfriend and he is patient but i know he misses sex.

I get more sad for no reason and a medicine i was put on for paying attention in college it would only make me sleep 3 hours. My doctor is putting me on a medicine to control my anixous feelings.

My boyfriend wouldnt believe me until he read this site about yasmin and sex drive. I feel really bad that i dont like to be touched and all i want to do is sleep.

i was prescribed meprozine when i had my wisdom teeth removed. i only took two during the healing process because it didnt hurt hardly any. i saved the rest. i have taken a couple when i couldnt sleep for a long period of time and i got on here to see if it might help anything else.... sinuses, colds.... anything? i find some of the stories on here kind of scary. im sorry that those reactions happened to yall. hopefully next time the doctors will listen to you and prescribe what is helpful instead of harmful.
*tip- i wouldnt go back to a doctor that clearly ignored or wasnt paying attention to what i was saying about my medical history (seizures). thats YOUR life they are dealing with. find a doctoe whom you trust! :)

I am a 32 year old male who gets occasionally bad sinus infections. i found this site yesterday after 3 days on levaquin, and had numerous side effects, notably: light headedness, weakness in my legs and hands, headache, sleeplessness and a nigthmare that caused me to sleepwalk. ( which I had never done before!)

I planned on stopping this medication as I did not feel right and had a softball game in the evening. Well I only lasted 2 innings of the game when I chased a foul ball and crashed into the fench and went to the hospital with a severly sprained ankle. i blame this on the fact that i was out of sorts and not really paying attention to my location on the field due to the lightheadedness of the medication.

at the hospital I was asked if i was currently on medication. when i told the nurse i had been taking leviquin and was not feeling right, she responded by saying she did not like the drug and had similar effects herself. Another nurse agreed. When I told the attending doctor she stated that levequin was not normally a drug she would prescribe as it is very strong and recommended i talk to my physician and use something else.

Use caution when using this drug, do not plan on doing any strenuous activities as your degree of concentratioin could be altered. I will not take this drug again and have been drinking lots of water to get it out of my system. It seems to be helping .