Blown away symptoms and conditions

Good evening everyone. I'm just blown away from the comments on this message board. I've been taking Lisinopril since Thursday and I've been tired and feeling like nausea just today. I've noticed how tired I am too. I was walking this morning; about a 3 mile walk and it was hard for me to finish up. I'm a 39 year old African American male, very active as well. So, when this happened, I wanted to check out the side effects of this medicine to see if I'm the only one......I plan to consult with my Dr, to change as well; excuse I just vomited. I will be changing ASAP. Have a bless day./

I am totally blown away by what I've read here because I have one Avelox pill left and now I know the source of all these symptoms I'm having. I"ve got the blurred vision in my right eye; feel like my body's on fire episodes--esp hot hands and red palms; achey feeling in my joints; headache that comes and goes; neck pain; fatigue; disoriented fog feeling and decreased mental capabilities; anxiety attacks and depression; dry mouth and eyes (and I'm drinking lots of water); waking up sweating; ears ringing from time-to-time; pain in kidney area that comes and goes; and not wanting to eat. The fever in my hands thing is the worst. Never had anything like it. The anxiety side effect got me thinking that I was dying. After reading this, I'm glad I can pinpoint it to Avelox. I won't ever take this again and I'll tell others about my reaction so they can avoid this experience. I can only hope and pray that these symptoms are not long-lasting.

I'm really upset that my doctor didn't forewarn me about the potential side effects.

I had my Mirena IUD inserted two weeks ago today. I had it inserted on day three of my normally five-day period. My period stopped for 2 days following insertion and then I spotted for one day. After that one day, I have been bleeding heavily ever since, and I'm talking super jumbo tampon every 2-3 hours bleeding. Before receiving Mirena, I talked to my GYN, read the pamphlet and researched online. Each resource told me to expect spotting - so I expected spotting for 3-4 weeks after and I am completely blown away by the constant heavy bleeding that I am now being told could potentially last 3-4 months.

I normally do not use oral contraceptives because of my problems with High Blood Pressure, but my doctor felt the low dosage of hormones in Mirena was "ok" for me. Since insertion, I've experienced a slight raise in my blood pressure but the doctor doesn't seem too concerned about it because I am supposedly "adjusting" to the Mirena. I am slightly worried that my constant bleeding and increased blood pressure are not going to subside in the 3-4 months the doctor is recommending I wait it out.

Not to mention how the constant, constant bleeding is ruining my sex life.

I honestly have no idea what kind of standards or limits I need to be setting here for myself. It has only been two weeks, but how much is too much..? I also have to say I am worried as well since I have to have minor surger in 4 weeks and would hate to have HBP/Anemia complications because of this.

WOW! My jaw is on the floor. I have been taking Simvastatin for 4 years! At around that time I started feeling ill. I ended up in the infection clinic. There they did 6 spinal taps since they could not understand why I had this major headache, and stablike pains.
I was hospitalized for 2 weeks and during the last 4 years I have been in and out of hospitals and doctors.
After they found 'nothing' they told me that I might have LUPUS/RA. So they started me on drugs to treat reumatism. I was on 2000mg per day! Complained and said that the meds where not working and I needed help and someone to listen to what I was saying. Then one of the many doctors I had was telling me to shut up and go see a psychiatrist. That got to me and so I started writing letters. I got a 'new' doctor and he said odd. Told me he was only interested in my joints. After the second time w him he passed away and so I met a fresh doctor, on that was right out of med school.
She looked at me and said...*You cant go on living like this, this is no life.* she sent me to the hospital for 2 weeks so that I could get the right treatment. There they realized that I have no sings of reumatisum but rather a connection w Simvastatin.
They right away told me to stop taking all the reumatisum medication and they will now focus on removing Simvastatin.
I am blown away.... I was so sick, so may hours lost from work, family and friends. I almost left my husband because I felt like I was just 'there' not ever being able to do things. I was so sick all the time.
Wow is the only word I have in my head right now- I am in a shock.

I can't believe this!! I was searching the internet to see if there were any side effects from the mirena as one gets closer to the end of the Mirena life and I came across this site. I'm so blown away. I am getting my Mirena taken out in a week because it's been 5 years that I've had it in and I NEVER realized all the problems I've been having in my life was because of the IUD!! This whole time I thought it was just me and I was going crazy. So looking back on the last five years it's all making sense to me! Not only was the pain so unbearable getting it in, but the pain in my abdomen was so bad for 2 weeks straight, and no let up with the pain, that I almost passed out from it. My horrible boyfriend at the time told me suck it up. I said a prayer one night praying for the pain to go away and that if wasn't gone by the morning I was going to go get it taken out! I woke the next day and the pain was gone. But this wasn't the end. I developed depression ( I thought it might have been because of the crazy relationship I was in) which I'm STILL prescribed for and I also severe anxiety attacks,which I NEVER had before in my life! dizziness, lower backaches, crying fits, extreme fatigue and copious amount of hair loss, right around my hairline. I used to have lustrious hair which I had to have two hairties in to hold it up, now I can use a tiny little jaw clip to hold it all up!!. Never in my wildest dreams did I think it was because of the Mirena. I thought how great it was that I got it put in and didn't have to worry about it for another 5 years, since I have a terrible time taking regular contraceptive pills ait the same time every day. My memory has definitely been affected and another symptom I never thought would be possible is the weight gain. A year ago I was diagnosed to be Pre-Diabetic and have had to change my diet and exercise. You think I would have lost the weight, NO, quite the opposite I have actually gained more weight. I have little to NO sex drive and I USED to have a very high sex drive. Now this is all making sense to me. I really wish I had found this site sooner! Like 5 years ago!!! So thank god I am getting this thing taken out of me next week. I am opting to get a diaphragm fitted and getting all these harmonies out of my system, maybe I'll go back to being my old self! (tears in eyes as I am typing this!!! ) All these years....who would've known. I am still in shock!!!!!

I had my 2nd child in June '08 and had Mirena placed on 8-8-08 with no discomfort or problems of any kind. I had already heard great things about it from two co-workers who LOVE theirs. This past weekend I finally started poking around on the computer because of my husband's constant complaints of the "whiskers" poking the head of his penis when we have sex. Lo and behold, I find this page and am BLOWN AWAY. I felt so relieved. I have never been one to have headaches, nausea, back pain or low sex drive. I had been attributing those things to a combination of being significantly overweight, having two babies under the age of 19 months and being on Prednisone (for rheumatoid arthritis). I also have been experiencing a lot of fatigue, night sweats/hot flashes, weight gain, swollen breasts, dizziness, swollen hands/feet, and crazy mood swings. I know that all of these symptoms can probably be explained away as being due to the prednisone, my weight, my life right now (two babies and working full-time) and any number of other things, but there are so many women who have Mirena who are reporting the EXACT SAME SYMPTOMS. I can't just be a coincidence. So anyway, I went to my doc today to have it removed and he, of course, told me that he doesn't believe that any of my symptoms are due to Mirena. I had it removed anyway, but he did tell me something I didn't know: the tiny amount of hormone is delivered locally, as opposed to oral contraceptives' systemic delivery in a larger amount. Go figure. In any case, I am disappointed and have mixed feelings, but I cannot wait to see if my sex drive returns and my lower back pain subsides. I also want control of my moods, weight and breasts again! We discussed the Essure, but I'm just not sure I'm ready to put something foreign in my body again right now. I don't want anymore kids (I'm 40 and have two already), but the options for 98%+ are limited. Everything seems to have a drawback. Oh well. I'll just be glad to see if the symptoms were related to Mirena. If not, I'll get it put back in.

I'm officially blown away. My 10 yr old son has been on Advair for a couple of months and strange things have started happening, so I thought I would surf the internet. HOLY $#!^!!!! I am now convinced that Advair is the cause for his headaches, fatigue, sleeplessness, and now the strange sores on his mouth and nose that NO 10 year old should have to be dealing with!!!!! How can the medical community continue to advocate the use of a medication that causes such significant side effects???? Oh wait, don't answer that...I really don't want to know the real answer do I?? Right now I'm just angry....

I went in on a Monday for some ear/throat pain, and was diagnosed with sinusitis and prescribed Avalox 400MG. By Thursday, I had an unrelenting headache, SEVERE anxiety and tremors, and decided to Google "avelox side effects". It's Friday morning, and I'm blown away by the amount of negative feedback this drug is getting. Obviously I've stopped taking it.

Worst part? I called my Dr on Thursday morning, told the receptionist that I was having side effects.....NEVER HEARD BACK FROM HIM. And this goddamn drug has a black box warning from the FDA about severe risk or tendon rupture, etc. I f*cking hate Western medicine.

I took my son off the end of March & come back once in awhile to read & I'm blown away by all the stories that I still keep reading :(

I just told his GI doc today that this might sound crazy.. but I have reason to believe that Singulair was making my son's reflux worse because now he only needs halk of his reflux med & is doing fine

My son like so many others on here had every side affect listed & it took almost a year to figure it all out He still has ADHD & other issues which I already knew about but all the stuff that was happening while he was on singulair Has Stopped!!!

GL to everyone I try to spread the word about this drug as much as I can

I had my Mirena put in a month ago. My OBGYN said it was a much better option than the pill, which I had taken for more than 10 years before I had my son four years ago. My body didn't react the same way to the pill anymore so I thought I would try an IUD. The insertion was awful! I had severe cramping and severe faintness immediately afterward. It took about 5 days for the cramping to go away and I got a light period 2 1/2 weeks later which lasted over 5 days (I suddenly felt that THAT was how it prevented pregnancy...it's hard to get knocked up if you're bleeding all the time!) I've had almost consistent low grade cramping ever since...it always feels like those first couple days before my period starts...kinda achely like you know it's coming. What is now starting to bother me is the acne that's COVERING my face. They're tiny little bumps and my face is always greasy. I'm 36 and I haven't had an acne problem in almost 20 years. Now I'm reading about all the problems with weight wain that other women have posted about. I gain about 10 pounds with the pill and that's exactly why I wanted to try the IUD!! I have a hard enough time keeping my weight in check and the idea of gaining more is enough to make me cry right now! I am blown away by the number of posts on this site and I wish I had found it before I had it put in. The information that I was given didn't mention most of these complaints and I know that if I call my doctor she'll tell me to give it a few months (the same advice she gave me with the three different birth control pills I tried). I'm 99% sure that I don't want anymore children but I don't want to commit to a more permanent form of birth control yet. I hope this post helps anyone who's considering an IUD...I would NOT recommend it!!!

My husband is in Nepal right now with a sinus infection. His doc gave him Avelox to take with him 'just in case'. So, with the blessing of the nurse practioner via phone, he took the Avelox. He called me in tears. I've been married for 7 years and believe me, my husband is never 'in tears'...he experienced an initial, intense flush on nausea and then became panicked, hyperventilating, paranoid, dizzy, and weak. I thought he was having a complete nervous breakdown. Then, the more I thought about it...it somewhat echoed a reaction that I had in the past to epinephrine...at the dentists office I was given a beta blocker with epinephrine in it, and immediately began to feel extreme panic, tears, shakiness, shortness of breath yada yada...and I'm someone who really could care less about the dentist. So. it turns out I'm "epi-sensitive" - anyway, upon recalling this...I mentioned to husband that perhaps he is not going insane, and instead is a having a reaction to the Avelox. So I checked online and am blown away by all of the horror stories. WTF? Why is this even being prescribed to people???? Why aren't we getting together a major class action lawsuit? I am just enraged. I called the emergency line to the doc's office...got a different doc, who said he never would have prescribed this antibiotic for sinus/ear infection.
WTF?!
That is specifically what is was prescribed for!!!
He said to take a benadryl and monitor symptoms - and that if there was ANY swelling to get to a hospital, pronto.
Spread the word! We are being experimented on with this drug.
What a nightmare.

im 14 and take 50 mg of adderal a day for ADHD and Bipolar, and i am unsure of it. I weight 96 lbs.... and i am almost 5 1/2 feet tall... so i am very underweight... and i do notice that when i take it, after it kicks in i seem more aditated, and cranky, and i obvleisuly dont eat.. and my mouth is always dry. i am just unsure about the whole crankyness change after i take it... does anyone else seem more agitated when they take this meds and it kicks in.../ plz reply. thanks

Wow. I can't even express how blown away I am by all of this.My son is 7 and has been on singulair since he was 2. He was moved to the 5 mg last year in March. The only difference between my son and all of your stories is that when he was in kindergarten we discovered a rather large arachnoid cyst in his brain that had to be drained. It was easy to blame some if not all of his behavioral problems on the location of the cyst. It is in the left temperol lobe. Having something in that region of the brain can cause behavior problems. His cyst was also big enough to push on his pituitary gland making him think he needed to use the bathroom all the time. He had a slight case of diabetes insipidus. During all of this he was complaining of headaches, fatigue, leg pain, the boy could not walk from one end of the mall to the other, he would melt down at the slightest provocation and turn into an angry little monster at around diner time. We attributed it to low sodium levels messing with his head, but his blood work never reflected someone who was THAT bad. After his surgery he had some normal depression, but in March, four months after, he became a different person. He was full of rage and anger and almost got kicked out of school. He broke things at home and lashed out at people, he said awful things. He was put on Tegretol, (that made him very sick) and Wellbutrin. Since he couldn't tolerate the tegretol they switched him to abilify. He still takes this. The one time we tried to take him off he went completely nuts again. Same kind of aggressive behavior, lashing out, no self control, crying all the time, very moody, saying things like "nobody loves me." My son is the sweetest person you will ever know. Before all of this, he would melt your heart with his kind words. Now he has been diagnosed with ADD, Aspergers, and has all of one friend at school. I go every day to eat lunch with him so he doesn't have to sit alone. I completely understand that my son will continue to have problems once this medicine is out of his system, because he does have other issues, but this morning the first thing he said to me was, "Mom it's weird, I don't know why but I feel so happy."
He has been off the Singulair for 6 days now. I called his allergist and he was VERY interested in all of this and wants to meet with me. He has always been so heartbroken by how my son has struggled. Don't think all doctors are bad. This one isn't. He is going to help me report all of this. He is really upset too. Of course he is older, been around for ever. I don't know. He cares about his patients. His receptionist said she thought they would be getting a ton of calls about this and I was the only one. Hang in there everyone. Alone we are quite together we are LOUD.

my son is almost 4 and has been taking singulair since right before he turned 2! I am just blown away by all these things i've heard and now read about this med. I NEVER would have thought about this making him act the way he does! I thought it was just his terrible 2's and 3's! He has major anger issues, he screams out of nowhere for no apparent reason, when he gets in trouble he hits me or makes these horrible faces! he scares me sometimes! he has trouble falling asleep but once he is asleep he is out for like 11 hours sometimes! Here in the past yr when he plays with other kids he is very very mean to them... hitting them, beating them up, yelling at them.. i've NEVER seen my son act like that! It really sucks when other people just don't even wanna be around anymore b/c your kid is so mean! Which he has never been a mean kid! everyone loves him to death but can't understand why is so mean and has these outbursts sometimes! B/C that just isn't my Brayden!! sometimes i just think he is flat out crazy... like maybe i need to get him tested for some kinds of disorders! i just don't know what to do! the doc will tell me its normal 3 yr old behavior I'm afraid... and now if i take him he will think i am some crazy mother who is hearing all these stories and believing everything! Well hell ya I'm reading all this and believing everything cuz I'm sitting here experiencing the exact same thing other moms are who's children are on the same medications! I've even thought maybe its me i just had a baby 3 months ago so maybe its postpartum... so went to the doc and she has me on Zoloft which i DON'T need... I'm not a depressed person at all! But i have days where i just don't know what to do with my 3yr old i just cry i cant handle it it is entirely to much for me! it just blows me away to think that it may all be caused by a med that I give my child every night to help him! But is it really doing more goood than bad? I don't even wanna know whats gonna happen next... what is he gonna do?! I don't wanna even think about the possibilities... To know i may have an answer to his anger and everything else is kinda relieving, yet this whole thing scares me!! The med has seemed to help his breathing problem since hes been on it though! But if it makes him angry I'm sure the zyrtec and breathing treatments will do just fine!!

I've been blown away also. My son is 10 years old and was originally diagnosed with RAD (Reactive Airway Disease) when he was about 3 and has had allergy and mild asthma issues since. When he was 5 he was put on Singulair, Nasonex, and Zyrtec. My son has always been a beautifully happy child, but the last few years have been extremely emotional for him. He gets depressed, he's extremely hard on himself and is ultra-sensitive and scared about everything. He has never been frightened and was a baby that loved his room and always slept really well. Now I think that I understand why he’s been afraid to sleep in his room alone. Ever since he's been on Singulair he complains and complains of bad dreams. I can't believe that I'm hearing that he's been taking this medication like clock-work for 5 years and all of his problems may be related to this. His allergies are not severe and nor has his asthma ever been - but I was told constantly that he needs this medication. This is unbelievable - I've stopped giving Singulair to him and have made an appointment with a new allergist.

I have been crying for almost 24 hours now. I cannot believe what I am reading and hearing about Singulair. My son has been to hell and back again and again. I cannot say for sure the Singulair is the culprit. But after reading all of the other stories on this website, I am convinced it is a strong possibility.

My son is 11 years old. He has severe allergies and asthma. He takes many, many medications for this including Singulair. He as been on Singulair for about 8 years now (my best guess because he has been on it for sooooo long.)

My son was diagnosed with ADHD in pre-school. He has taken many medications for the ADHD, but none have ever done any good at all. We thought some of the medications even made things worse. Now, I'm not so sure.

After exhausting all the ADHD medications, our pediatrician sent my son to a psychiatrist and a counselor. The psychiatrist put him on 2 different antipsychotic medications. Again, neither one did any good and seemed to make matters worse. The psychiatrist sent my son to a psychologist to be tested for Asperger's. For those of you who don't know Asperger's is a high functioning form of autism. The psychologist ruled out Asperger's by diagnosed ADHD and Anxiety Disorder. He did not prescribe any medication.

For some unknown reason, I've only given my son the Singulair off and on for the last year. My son had the best year in school ever. However, his pediatrician was still not satisfied. He sent him to see another psychiatrist at Children's Hospital in Pittsburgh. We were told he is believed to have more than one disability. He is believed to have ADHD, Aspergers, Teurettes and a possible 4th medical problem that has not yet come to light.

We are scheduled to see a neurologist at Children's Hospital on the 15th of April to rule out any medical reasons for his tics. We see the psychiatrist again on the 18th of April.

I am so tormented by this recent news. Has all of these problems been caused from him taking the Singulair for so long? Although he has had his best year in school yet, he still has a lot of problems. Are the side effects of the Singulair permanent.

The other side of the coin is this: It is also very scary to watch my son not be able to breath. Asthma can also be life threatening. What is a parent supposed to do.

Also, I now don't know whether to keep these appointments that are coming up. I hate so much to put him through more. He has endured enough doctors and tests to last him a lifetime. However, what if it is not the Singulair and there is help out there for him that I am not aware of.

Please if anyone else has had a similar experiences e-mail me. I would love to hear from you.

God Bless everyone who has been through this kind of hell.

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona

I am freaking out!! I just found this site and can't believe what I'm reading. I have a huge crater in my right buttock as well. This is the second time it has happened to me. After the first incident, I went to the doctor and she said she didn't know what it was, that it must have been due to trauma. This is the same doctor who prescribed the Kenalog shot for my allergies. It started out as a large bruise, so I assumed I must have hit something really hard and damaged the tissue. Now, a couple of yrs later, I have another, larger crater. I thought something really bad was wrong with me, so I decided to google and see what I could find. I am truly blown away by this and VERY upset that they did not warn me of this. I called the doctor, but they haven't returned my call yet. I'm concerned is this going to continue to get deeper? I also believe it affected my period as well. I have always been very regular, but for several months after the shot I would start my period every couple of weeks.

Wow. I am blown away by what everyone has said. I am 27 and got my Mirena put in June 2007. I thought I had hit gold finding a form of BC that didn't require any work on my part and that didn't have side effects. YEAH right! A week after getting it inserted I began having migraines on a daily basis to the point where I had to go and see a specialist. I have gained about 15lbs, my sex drive is almost non existent (when I should be at my peak) and I am crabby all the time. However, the cherry on top of all of this is that my darn period has gotten longer and heavier. I went to see my GYN yesterday only to find out that the Mirena was in the wrong place! HUNCH!! That means it wasn't working and I have a possibility of being pregnant right now. Not cool at all. To say the least I had the darn thing removed and have chosen to go back to the NuvaRing. I never had side effects and it's as easy to use as putting in and taking out a tampon. If you have Mirena I would say get rid of it!

My 2 year old son was prescribed Singulair for eczema yesterday and gave him his first dose last night. His bedtime is at 8 and since he is two years old and fights sleep, it normally takes him 30 to 60 minutes to actually fall asleep. He was still awake at 10:30. He couldn't seem to wind down. I knew it was from the Singulair immediately. I woke up this morning and got the prescription literature to see if this is even prescribed for eczema. It didn't say. So I got on Singulair's ...... and nothing about eczema. I then searched ...... and found this website and I am completely blown away by everyone's stories. I think I will take the 30 bucks for next months prescription and buy a humidifier for the apartment and use some Cetaphil lotion. He didn't have breakouts this summer due to the humidity, so I will just make my apartment humid. The doctor not only prescribed Singulair, but also Clarinex. The pharmacy had to order it and I was supposed to pick it up today, but I am going to search the side effects for it first. I will probably just save my money and see what I can do with home remedies.

I started NuvaRing on Thursday, June 15 2007 and Monday, November 5 was the final draw. I talked with my best friend and admitted to her that something was seriously wrong with me but I didn’t know what. I told my friend I need to talk to someone about how I’ve changed for the worst. Things has gotten so bad with me I actually thought I was Bipolar. So we did some research on NR and when I read the different stories I was blown away because I would have never linked what I was going through to NR.

I had no sex drive non-what so ever, the thought of my boyfriend touching me made me sick to my stomach. I would actually get into physical altercations with him which has never ever happened, my attitude had taken a turn for the worst, I would have thoughts of hurting people that made me angry, I had to wear a panty liner everyday because of the discharge, migraine headaches, pain in my right breast, nausea, abd cramping, feeling tired, waking up in night sweats, felt the need to be alone, and mood swings. Yesterday I called my Dr. and told her I need to get off NR ASAP so she said she would call me back but never did so I took it out for the final time last night. Before I start taking anything else my body will be free of any birth control until NR is totally out my system if this means slipping up and getting pregnant in the process then so be it, it will be a first for me anyway.

NuvaRing was wonderful and the thought of not having to take a pill everyday was even better but the side effects will make you become someone you don’t know and your life will take a turn for the worst and it will have you thinking you are loosing your mind. For those who had no side effects consider your selves lucky because I wouldn’t want anyone to experience what I’ve went through while on NR.

Hi, My name is Scott and I am 58 years old. I had a severe case of Bronchitis four years ago. I was so sick my Doc. sent me to have a chest x-ray thinking I might have pneumonia. He prescribed Levaquin...one tablet a day for 30 days. I immediately started taking the antibiotic. I was so sick I did not realize any reaction immediately. I just felt horrible, but attributed it to the bronchitis. The infection started to come under control, but I was starting to feel worst physically. I got so bad my wife took me to the emergency room. I was slurring my speech, my muscles ached, I had night sweats and I lost my coordination. It had also affected my memory...both short term and long term. The physician who saw me at the hospital was 99% sure that I had suffered a stroke. I was admitted to the hospital and spent 3 days undergoing blood-work and testing to see if they could determine what was happening to me. Upon release I was sent to a neurologist and had MRI's of my brain. All came back negative.

I took the medicine for 26 days before it dawned on me that it could be a reaction to the Levaquin. I went home and researched Levaquin and was blown away by what I read. All of the weird symptoms I had been experiencing were right there in front of me. I immediately stopped taking the antibiotic and within days started to feel better. I continued to get better until I was feeling almost normal. This took about three weeks. I still experienced problems with my memory and had residual effects with my coordination, but otherwise felt 100% better.

Approximately three months later I had a severe relapse. It came out of the blue. I was not taking any medicine, but was taken to the hospital and admitted with the same symptoms I had experienced before. Again the Doc's had no idea what the problem was. I did explain about my reaction to the prior use of levaquin, but that was dismissed as not probable and they released me after three days with no idea what was wrong.

I continued to have relapses for the next 2 1/2 years, every three or four months. Each time was not as bad as the last. Finally I traveled to Boston and saw a very well known neurologist who explained that he had seen this before. He called it a post infection syndrome. He was the first person who agreed that it was a reaction to my long-term use of levaquin. I finally felt vindicated!

If you check the manufacturer warnings online, you will see that they do know about these reactions. It a small percentage so they think the benefits out way the adverse reactions of some patients. As a person who has suffered with these reactions, no percentage is worth the risk!

For those of you that are experiencing adverse effects, there is hope at the end of the tunnel. It does take time, but it does get better. I can live with my memory problems and although I have some residual muscle and tendon problems in my legs, my life is almost back to normal. I have not had a relapse in the past year.

Good luck to everyone and keep the faith!

Scott

I am blown away that another woman had the exact same entry: anxious. I was also prescribed reglan to increase milk production and feel like I am losing my mind. I'd rather use formula than to feel like this.

Hi there everyone,

the more i read the more blown away i am with all these horrible symptoms that i thought i was doing it alone.
Can i ask anyone, i stopped the pill 10 days ago after finding this site and knowing i am like all of you but i was wondering if any of you still had the black spotsin front of the eyes and how long i could expect for this to continue, its on and off.