Levaquin and good luck

I am taking Levaquin one time a day, 500 mg. for diverticultis. I have fibromyalgia so attributed symptoms of EXTREME FATIGUE to that but this is fatigue like I've never known. I can't do much of anything. I don't work outside the home so will just deal with it if it cures my infection. I'm using sleep meds too...but that could be fibromyalgia kicking in too. But fatigue is much worse. I hope it kills those bad bacteria!

I was prescribed 7 days 750mg of Levaquin on 9/10 and finished 9/16. I was originally diagnosed with bronchitis but went back to the Dr. yesterday cause I was not doing any better and he now says it's viral. I've gone to the hospital because I passed out on 9/13 and continue to faint at least once a day. I have tingling/numbness in my hands, ankles, toes, my knees hurt, my lower back is in a lot of pain, almost to where it is not tolerable, I'm dehydrated (I'm drinking and eating, just not as much) it is extremely painful to eat, my tongue and my gums hurt terribly. Last night I had a horrible dream (I don't dream usually, not nightmares) and today I started to hallucinate (mildly) A week ago I was functioning normally, a mother of 3, playing with my kids and now I can hardly walk without assistance, I can't go to work, I'm in constant pain. Someone please give me some kind of guidance. Will these feelings ever go away? What should I do? Thank you!!!!

I was prescribed an 11 day supply of Levaquin - 500 mg. I'm on day 7 and struggling to make it 4 more days. The first day I took the tablet around 5 pm. I was up all night. Since taking in the morning, I've been fine. Now, I'm suffering from very sore biceps, heels and stiff knees. The fatigue is overwhelming. I also experience extreme dizziness as well. I may call the doctor tomorrow to see if I can stop this. I've taken various antibiotics throughout my lifetime and never have experienced the side effects such as this one.

I'm on day 3 of 750mg of Levaquin for walking pneumonia, and I feel awful. I've been so nauseous that I feel like I have the flu now. It started yesterday, but is definitely much worse today. I'm not taking any more of this medication. I'm calling my Dr. in the morning. I feel lucky after reading all these other posts.

I took levaquin for 2 weeks to treat a infection, i am 26 years old and have never had muscle pain for longer than a couple days after working out...now i have moderate pain in my rib area and muscles near the groin area and even upper leg, and have done hardly any physical activity while being treated...i have seen no improvement for a few weeks now, but think my infection is gone... going back to my doctor tomorrow...need help

My 10 year old was prescribed levaquin for a sinus and ear infection, he has been "dizzy and lightheaded" and started having "horrible" nightmares. That was only after 1 dose. I don't think he'll be taking anymore. Thank You for this website! :) very informative.

I was hospitalized about four months ago for a total of three days due to a massive kidney infection, during three days in the hospital I was pumped full of Levaquin. I began suffering what the doctor believed was a migraine on the second day, let me tell you it was far worse than any other migraine I had ever had. So not only did they send me home with a prescription for Levaquin they sent me home with a migraine prescription. I took Levaquin for a week after my departure from the hospital, I am young and very naive when it comes to doctors and hospitals and I had faith in my doctor that the medicine they prescribed me was good for me. After suffering from a migraine for almost two straight weeks I began to suffer from blind spots in my eyes, and a kind of slowing down effect. I would get up and it would cause my head to feel like it take my mind and my eyes a couple minutes to catch up to my body, vertigo. Well I returned to the hospital and was told I was suffering a migraine, once again, no migraine I had ever had caused blind spots. They referred me to a neurological ophthalmologist who took the time to look at my eyes, and diagnosed me with Pseudotumor Cerebri. He told me that the medicine had caused pressure to build up in my head and caused hemorrhaging in the back of my eyes, hence the blind spots. I have a scheduled MRI to validate the doctors concerns, but the treatment he is telling me may reverse the affects is a long term treatment, and has a possibility of not being successful. So for a medicine I was given to treat one thing I acquire something far worse and all for trusting a doctor to have my interests in mind

UPDATE from Yesterday)))>>> well thanks to everyone i quit taking it yesterday BUT!!!---> today when i woke up i had a horrible head ache and it seemed to be coming from my left eye. i looked in the mirror and i have a really weird yellowish glazed tint in both my eyes and in my left eye a blood vessel has burst. i also noticed ive developed a skin rash on my right side of my stomach and on my left calf. My joints kept me up all night in constant pain which felt like someone was ripping apart my ligaments. I had a minor anxiety attack last night (Ive NEVER had anxiety before) and my body just feels weak, drained, and i keep getting really weird muscel spasms in my upper thigh. I tried to go out to the store earlier and as soon as i stepped into the sunlight a migraine hit me, and ive never been sensitive to light....Ive had a feeling of helplessness and worthlessness more in the past 24 hours than i have in a year. Im also experiencing horrible lower back pain and stomach pain around where my kidneys are.... I did have a small amount breast tenderness when i woke up and im not sure if that's another side effect...(no im not pregnant, had multiple urine tests in the last week)...I think ive only went potty maybe once today...and that was at like 9am...its now almost 9pm. Im pretty sure if this isn't over with or doesn't improve by 10pm im going to the hospital.....i cant drink water and im pretty sure im getting dehydrated....my skins turning pale, i have dark rings around my eyes.....etc.......has anyone else suffered with these things? Levaquin is by far the MOST painful, riskful, antibiotic ive been on...They should definitely take this sh*t off the market!!! =[[

Im only 16 years old and ive been on levaquin for about 3 days now. My doctor told me off the bat that the only thing wrong with the drug were some "theories" on cartilidge damage, how ever, now i see for myself, and for many other people that is not the only side effect. He told me that no one under 18 is supposed to have it but i caught a severe case of sinutitus, and a uti which ive had for 2 months and nothing was working, so he put me on levaquin, once a day for 7 days. Ive now been having the following symptoms and im extremely scared!!
1. Constant fatigue
2. Extreme Migraines
3. Nausea, vomiting
4. Rapid heart beat (and chest pain)
5. Stiffness in joints and horrible pain...
6. Constant anxiousness, to where i cant get to sleep
7. Dizziness

Is there anyone i can talk to who's had these same problems? please email me or something im scared and i don't know what to do my mother doesn't believe me and she says its just a head cold....

******

Please help me!!

My wife is experiencing severe muscle pain in the back and rib area after taking this drug. Has anyone gotten better after they stopped taking the medication or is everyone still suffering?

I too have been on a regimen of 750mg of Levaquin for an infection on my leg. On day 2 I could not figure out why my upper keft arm was hurting me so much. I as so many others, wrote it off to hanging drapes and cleaning out my pantry. Four days later the pain started in my right arm and again, I was trying to figure out what in the world was going on. It's an intense pain like I've never had before. I have Crohn's disease so I wrote some of it off to that as well. I saw my Doctor today and didn't even think about telling her about the Levaquin (different Doctor prescribed it). As I lay in bed this evening unable to sleep I decided to do some research on Levaquin as it was the only thing I could think of that was causing problems. Boy, did I discover something. Thank you all for posting your issues on this website. I will be seeing the prescribing doctor tomorrow and will let her know the outcome of the drug and will make sure that I will never be taking Levaquin again. Too bad we can't get this word out to everyone being prescribed this drug. It's dangerous and hardly worth it. There has to be something else out there that we can take. .

I have taken Cipro & levaquin or several occasions for several years. I DID NOT KNOW OF THE POSSIBLE EFFECTS OF THESE DRUGS ON TENDONS AND OTHER MUSCULOSKELETAL EFFECTS. A FEW DAYS AGO I HEARD A LEGAL AD ON TV WHICH CAUGHT MY ATTENTION: ' IF YOU OR A LOVED ONE HAS TAKEN LEVAQUIN AND SUFFERED A RUPTURED TENDON, CALL....... ' OVER THE PAST FOUR YEARS , I HAVE HAD THREE ROTATOR CUFF INJURIES, TWO OF WHICH REQUIRED SURGERY AND A LONG REHAB, AND A "PROBABLE" TENDON TEAR OF MY FOREARM FOR WHICH I WAS ON LIGHT DUTY FOR SEVERAL MONTHS, REHABBING W/ PT, STEROIDS, BOTH ORAL AND INJECTIONS, ANTI-INFLAMMATORY MEDS. AS MOST OF THESE INJURIES OCCURRED AT WORK- I AM A CCU NURSE- AND WAS TREATED BY OCC MED DOCTORS, AND THEN REFERRED TO SPECIALISTS WHEN I WASN'T GETTING BETTER, I WAS MADE TO FEEL AS IF THESE INJURIES WERE SOMEHOW MY FAULT, THROUGH POOR LIFTING TECHNIQUES,ETC. AT NO TIME DURING ALL THESE TREATMENTS FOR INJURIES DID ANY HEALTHCARE PROVIDER PUT THESE TWO THINGS TOGETHER AND ASK QUESTIONS, AND NOR DID MY OWN PHYSICIAN. THIS WOULD LEAD ME TO BELIEVE THAT THE POSSIBLE SIDE EFFECTS OF THIS DRUG HAS NOT BEEN WELL DISSEMINATED TO THE MEDICAL PROVIDERS.

I've been on Levaquin for only 2 days, combined with Prednisone... Taking them due to a nasty sinus infection. One of these two meds is making every joint in my body hurts, as well as me having lost almost every bit of my sense of taste. I ate general tso's chicken today for lunch and could not taste anything, so as an experiment I ate one of those little red Chinese peppers that I normally throw out because they are WAY too hot - I couldn't taste a thing. Last night I had to drop the air condition down to 68 degrees as one of these two meds made me sweat very heavily and uncomfortably hot.

I was prescribed Levaquin by my Dr. for a sinus infection. There were 10 pills and I was to take one a day. No one mentioned any of the side effects or drug interactions except to not take antacids within 2 hours of taking the meds. During the coarse of me taking the medication I began having substernal chest pains which I thought was just horrible heart burn, but it got so bad that I woke up screaming multiple nights from the pain. I also started having pain in my ankles, legs and especially my knees. The pain in my knees gets so bad that I think my knee caps are going to shatter when I walk especially when going down the stairs. I didn't know any of the drug interactions and my father in law who is a physical therapist has always advised me to take ibuprofen for muscle and joint pain so that's what I did, but little did I know that was only increasing the effects on my central nervous system. I am also experiencing bouts of nausea, confusion, light headedness, difficulty sleeping, anxiety and I actually thought I was having a mental breakdown.. I was freaking out on my husband and very depressed even having suicidal thoughts. It wasn't until my mother randomly mentioned that she had heard about the FDA issuing the Black Box warning that I connected the dots and had already finished the meds. I called my doctor's office right away and was told that the symptoms I am having are not side effects of the medicine. Maybe the Dr. doesn't listen to the news either.

I have just finished taking Levaquin for a 10day treatment for pneumonia. In the last 5 days or so I have noticed stiffness in my achilles tendon (no pain) until I get moving. I have also notice a tremor in my hands and no muscle weakness and shaking in my triceps and quads. Of course I hadn't read the precautions to this drug before noticing these symptoms. I contacted both my pharmacist and physician and neither seemed concerned and told me if I was really worried to go to the emergency room. I am wondering if these symptoms will disappear since I am no longer on the drug, how long it will take, and how long I should worry about tendon damage----is the possibility of rupture forever???

Levaquin is a wonderful drug and one of a very few that help men with prostatitis. If you have ever suffered with a prostatitis infection you know what i mean. No problems here with Leviquin.

I was given a 750mg Levaquin rx for recovery from pneumonia on 7-17-08. I was sent home and lost all my appetite and forced myself to eat. Next I never slept at all for the following four days, it was like I was wired to the max and nothing I tried could induce rest of any kind. I called the doctor who switched me to a new antibiotic, my appetite returned the next day and finally I got some sleep. I would say this drug should not be on the market. My recovery was slowed by four days due to this drug and my head is still a little foggy at times as the drug wears off.

I had bladder surgery and was given levaquin 500 mg. I took 1 pill when I got home that day and my entire face was swollen and I was also sweating and definitely couldn't even think of falling asleep. My mind was going crazy and to try to tell you how I felt it was kinda like I was in someone elses body looking through their eyes, it's the weirdest feeling I have ever had, I didn't know that it was the medication at first because I just thought I was feeling bad from the surgery and them putting me to sleep. The next day I took another pill, same thing felt really really bad, got up on the third day went to work and left in an ambulance. They told me it's because of this medicine and what's in it. I still feel really weird and typing this letter is killing my wrist. I don't know why because I am on the computer a lot before all of this and never a problem. I wish I knew what was going on with me. I feel like I am going out of my mind, and my swelling is no better. My husband even ask me if I took my lasix and I already did and still swelled up in the face. Any feedback would be great. please help.

Began taking Levaqauin on/about 19Mar08. Became symptomatic (agitation + insomnia followed by a host of psychiatric ills) within eight weeks. I'm in a living hell now, which might or might not be related to flouroquinolone, e.g., levaquin poisoning. There are more than 2000+ posting on this site that go back five or so years. Most of the postings constitute one-way communiques from hell. (Go ahead, read a representative sampling of the postings.) Here's the question: what became of these people who wrote their awful posts? Are they still alive? Did they find cures? How does one contact some of the earlier posters?

Question for you all. I have been on levaquin for 6 days 750 mg. For the last 3 to 4 days my hands have been killing me and it is getting worse, my knees, and shoulders hurt now. After reading your remarks I am calling doc first thing in the morning. Please let me know if you have any advice for me.

Muscle weakness, pain, tingling

After taking levaquin, I still suffer from muscle weakness, pain, and tingling several years later. My doctor who is one of the top specialists in New York has seen what this drug has done to me and is doing research for an article in a medical journal to put the word out of the horrible side effects of this drug as well as increasing the knowledge to hopefully figure out how to counteract this.

If you are/have suffered similar results, please contact me at ****** and we can discuss how you can send your case information to my doctor for the study and medical journal article. We need more scientific studies and literature out there about this drug and the side effects.

I am a 49 year old male and took a 14 day course of Cipro for a UTI. By day four the souls of my feet were very sore, especially first thing in the morning but no other side effects. Mentioned sore feet to Dr after 7 days of Cipro but he did not believe it was from Cipro and had me complete the course. After 14 day course of Cipro feet were now so painful that I could barely walk on them especially after resting or getting out of bed. Also burning sensation on skin of feet and hands and some minor tremor. Saw a specialist and he immediately confirmed Cipro as the culprit and advised never to take that drug family again. Have since done the whole web search thing and discovered the whole saga of these drugs. Other symptoms have also appeared, some pain in middle of back, sharp pain in middle of back of both knees, hot and cold flushes, pain in left bicep, fingers that are very susceptible to joint injury and feelings of weakness and anxiety. Has been over three weeks now since I stopped Cipro and condition shows no improvement, may even be slightly worse. About to try a shotgun approach with treatment as there appears little documented evidence of anything conclusive on line. Starting course of anti-inflams (Voltaren) and these have already reduced the pain in my feet. Also magnesium and calcium supplements (theory goes that it may mop up any remaining Cipro and there is plenty of reports from sufferers saying that symptoms continue to appear for some months after stopping Cipro), Vitamin B6 (can apparently help with some types of nerve pain and tingling) and Fish Oil (omega 3's can help reduce inflammation). Not very scientific I know and can't be sure that all these are compatible with each other but am a bit desperate at this stage. Bracing myself for a three to six month recovery (just based on experience of many others). At this stage I am just hoping that damage is not irreversible as this appears to be a real risk. As everyone here will agree it is amazing how this situation is being allowed to continue. I could have stopped my Cipro on day two or three if I had been made fully aware of the risks and what to look out for. I am no expert by any means on this but from what I can gather Cipro and its relatives do nerve damage by the very way they work. It appears that anyone taking these drugs will inflict some nerve damage but for many it will not manifest to a degree that is a problem or at least a noticeable problem. So in some ways we are all sufferers, just to varying degrees. Another point mentioned often is that the symptoms may not appear for some months after the Cipro is stopped and therefore is not always associated with the drug. Also some say there is an accumulative affect with using the drug a second or third time. Symptoms may appear only after multiple use or symptoms may get much worse and more likely irreversible with multiple use. It's all scary reading. At this stage I am just hoping I can make a full recovery. Do damaged nerves repair themselves, does the Cipro eventually leech out of our systems .... I don't know. I will post in this forum again in a few months or sooner if I make a recovery.

LEVAQUIN SIDE EFFECTS - As I posted yesterday, after taking one Levaquin - 750 mg, I had hallucinations, sleeplessness, extremely severe headache, and now today I woke up with "thrush mouth/yeast infection" in my mouth - plus aching gums and teeth.

Please, FDA or drug company that makes this, read these boards. This is the TIP of the ICEBERG. Think of the thousands or millions who don't take time to report the side effects of this drug. It would not surprise me if suicides and death are not brought on from LEVAQUIN.

I am thankful I had the good sense to stop this drug after one dose or I might be dead. The hallucinations and headache were the most horrific of my life. I can't imagine what I would be like if I had taken all 7 pills.

I took this antibiotic for 2 days. I have no history of mental illness whatsoever and I thought I was losing my mind for 2 days. I had a panic attack 2 nights in a row and stayed up all night starring at front door afraid that someone was going to break into my home and hurt my children. I can not believe that this "antibiotic" is even on the market. This is an extremely dangerous drug. I called the doctor and he sounded like he didn't believe me- maybe I should share some of this stuff with him so he can experience the crazy too!

I have been taking Levaquin for sinus infection after Augmentin didn't keep it from coming back. All I can say is that I am completely exhausted. I wonder if it is the drug or something else. No muscle pain. I don't know if I should stop taking it or continue. Tonight I was walking for exercise and couldn't finish because I thought I might faint. My heart was beating and I was shaking. Do you think it is the drug? HELP!

I started taking Levaquin last Monday, today is Saturday the 17th of May. I have a chronic sinus infection which i was given Augmentin that did not work. The Augmentin was taken for 10 days. Then I was told to wait 5 or 6 days to see if the infection would clear up. No it did not. So my doctor gave me 10 days of 750mg of Levaquin. I started taking Levaquin last Monday, today is Saturday the 17th of May. I decided to get back to walking for exercise to loose a little extra weight gained this past winter. I walked about 1 mile. I am used to walking and that is nothing. I usually try to walk 5 to 6 miles each evening. Today, I can hardly move. My hips are sour and my shoulders are killing me. I thought I must be really out of shape, but why are my arms and shoulder hurting. After reading the postings here, I am sure it is the Levaquin. I was fine Monday as far as muscle aches and pains just the sinus infection. Now I can hardly move. I will call my doctor first thing Monday morning. Thanks to you all for your postings and good luck.

I am a 54 year old, very active female. Had a UTI and was given 750 Levaquin. I have taken 10 days worth and began having a sore swollen ankle, followed by right knee pain, followed by shoulder and arm pain. I have never experienced muscle pain to this degree before. I am scheduled for a doctor appt in 3 days. I started trying to imagine what could be causing this. I took a shot and looked up Levaqin side effects this morning, after another night of no sleep and severe shoulder pain. Well guess what, from everything I just read I think I found the source. The problem now is how do I get my life back???? The one thing I am sure of is it's time to stop taking the poison!!!

I had a viral infection and was put on Levaquin 750 mg. After being on it for 5 days my joints began to hurt. I didn't think the medicine caused it and I continued to take it. Until the 7th day I began to research and found this web site. I quit taking it. I was unable to stoop down and it hurt really bad to walk up or down stairs. Regular walking was some painful. I also had some pain in my wrist. I've been off the medicine for 6 or 7 weeks and I'm still having bad joint pain in my knees. I'm unable to perform normal activities. I'm not saying Levaquin caused it; but it's just that when this started was while on it. If anyone knows how long this might last or if it causes permanent damage, please let me know! I will be going to a specialist in 1 week to get this checked.

Sorry for the long post! I started taking Levaquin in mid Feb and I'm still feeling the effects. I am a 37 year old female who has never had any kind of reaction to any drug. When I say never - I mean not even slight nausea. I was prescribed Levaquin for bronchitis - 500 mgs for 10 days. I took it for 5. My bronchitis cleared up but I experienced feelings of depression after 3 pills. No nausea, headaches or loss of appetite at all. After the 5th day, I experienced numbness and tingling in my hands and feet. I went back to the doctor that same day because I was terrified. I was prescribed prednisone. 5 days after that, I started experiencing full body pain. It hurt to even lay down. Went back to the doctor that same day was prescribed vicoprofen. It didn't really help. I was given a muscle relaxer to take w/vicoprofen and that helped me get through the day at work but the pain was always there and that caused many sleepless nights. I went back to the doctor because the pain had left my torso and pretty much my legs too but settled in my arms and hands and was even more intense than when it was all over my body and prescribed Cymbalta. The pain was so intense, I was crying the whole weekend. Since my doctor didn't believe the intensity of my pain, I was desperate for a moment of relief and felt very ashamed to have to call a friend who's an RN and she had her doctor prescribe vicoprofen for me. I was able to semi-function again. 1 week later went to a rheumatologist and was told I had swelling in my nerves in both wrists and it may be carpal tunnel, fibromyalgia, nerve damage or rheumatoid arthritis and given Lyrica. Had an EMG/NCV(Horrible) and the results were negative. I also had extensive blood work and was told on 4/21 that I tested positive for drug induced Lupus possibly caused my Ibuprofen. I stopped taking Motrin and my doctor prescribed Vicodin and I'm finally starting to feel better(the pain is not as intense) but I don't believe for one minute that Ibuprofen was the cause of the Lupus. I believe Levaquin broke my system down( I have Vitiligo - an auto immune disease) and made me even more susceptible to other auto immune diseases. Levaquin is finally starting to leave my body. My calves are stiff when I get up in the morning and my hands still hurt, but it's nothing compared to how I felt the previous 10 weeks. Sleep is still disrupted by pain.

I am going back for a blood test next week to see if the Lupus is still in my system. I'm happy for the people that have used this drug and have been fine, but for my body, it's toxic. Hopefully, there will be a blood test in the future that will show if you are prone to have severe side effects to this drug before it's prescribed.

For All of you suffering, you are not alone.I have found great comfort on this board knowing that I'm not alone.

I was given a 10 day dose of LEVAQUIN for a mild bronchitis/respiratory ailment on Jan. 29, 2008. I took 1 500mg pill for the full ten days. Three days after I stopped taking this medication, I experienced incredibly painful swelling in both knees. I could barely walk, and couldn't bend my knees. I was scared, upset, and in absolute misery. I spent a week literally throwing myself backwards onto chairs. It was unbelievable. When I could finally get to my normal health care provider 5 days later, she immediately identified the culprit as the Levaquin I had taken. She said she knew it to cause people's tendons to burst. It was obvious since it was both knees that it was not an injury and I never had any other problem with my legs. I am, or shall I say I was an avid walker. I was told to see an orthopedic doctor if I had not improved in one week. I had not improved in a week. The orthopedic doctor sent me for an MRI which showed irreversible, permanent cartilage damage in my left knee. The right knee he didn't MRI at the time, saying he could determine what he needed to know from the one knee and would only be able to do corrective surgery on my knees in 6 week intervals. This horrible drug has permanently altered my way of life. I was a 53 year old active, ambulatory adult who would walk miles a day. Two months later, I still have constant knee pain, cannot stand for long periods of time without leaning on something and can no longer kneel, etc. I can only walk around a bit and if I'm on my feet for long periods of time I experience knee, ankle pain and swelling. I sent a report to the FDA who obviously cares nothing about this situation, since I'm not the only unsuspecting person to have this happen. I've been studying this drug now and there was evidence in animal clinical trials of joint and tendon damage, To me it would have been no different an experience if someone had come up and hit me with a baseball bat across both knees. I am permanently damaged from Levaquin. I think it's criminal this drug is given to younger ambulatory adults at all.

My adult son was put on Levaquin and by the 5th day was severely depressed to the point of thinking of sucide and he has never been depressed and the Dr said he never heard of Levaquin causing this but the pharmacy said yes it does cause depression only people are not telling the Doctors.My son ended up bleeding rectally 7 days after he started Levaquin???This clearly should be monitored and people should be told of this side effect because some people do not connect depression with taking an Antibiotic

I am a 32 year old sane woman with a degree in Psychology. I was prescribed levaquin for walking pneumonia. This is day 7, and I am in tears because I truly thought I was having a psychotic break for the past 5 days. My roller-coaster of symptoms include emotional instability, paranoia, violent thoughts, thoughts of hopelessness and suicide, overwhelming gloom, facial numbness, insomnia, and the feeling of tingling in my mouth and throat. I am going to stop taking this medicine right now, and I've already called my doctor. I just wish I would have linked this to the only medicine I'm taking much sooner.

I have been on Levaquin over 6 times in the past 2 years for upper respiratory infections. I just came off another levapak 750mg for 10 days and my biceps were feeling really tight. I mentioned this to my doctor but he said it was a common side effect. After researching this today I am shocked about the tendon damage. I have had distal bicep tendon surgery on each arm on separate occasions in the past two years. Now I am terrified this is going to happen again. None of the surgeons could figure out why someone my age (41) could do this twice in under 2 years. Has anyone found a way to reverse this? I am terrified to go back to the gym or even lift anything. My biceps are so sore and I have been off the Levapak for 3 days and my biceps seem to be getting more tight and sore each day. I can't face having another surgery. This drug should be taken off the market.

Started Levaquin 500 mg for 14 day treatment 4 days ago for chronic ethmoid sinusitis (15 months of battles!). Within 1 day, my symptoms were significantly better - and now 3 days later are about 95% gone. Only strange side effect happened on day three (3rd pill), got severely nauseated and dizzy and felt disoriented within 20 mins of taking the pill, but all subsided within 3 hours. Might have happened because I had taken a Zyrtec the night before - I believe that the 2 don't really mix well. Have been fine since (not taking Zyrtec with it again!).
Do also feel a little tendon pressure in my knees and elbows, but is very little and doesn't bother me at all.

I have never, ever responded to any of these "side effects" websites before! As a healthy person who very rarely requires medication, I had to find something on the web that would "explain" my suspected side effects for the Levaquin I've been taking for the last three days. This was prescribed for a UTI. The "new" side effect (that I didn't see addressed anywhere here) was what I can only describe as "asthma-like," to include wheezing, coughing, and shortness of breath. Anyone else with this symptom? I was also overcome with a great sense of futility that just scared me. I am normally a positive, "the-sun'll-come-up-tomorrow" type person, but this just knocked me for a loop!

I posted my experience with Levaquin back in January 2008. It's been three months since my initial reaction to Levaquin. I was in terrible pain then and I could barely walk. It has been three months now and I am still in a lot of pain and the pain in my lower back is worse. However, I can walk better now. I have yet to find a doctor who can help me or who even believes that Levaquin caused this. If anyone out there has a physician who believes that Levaquin can cause this damage and who is competent to treat this problem, PLEASE email me with his or her name. I am willing to travel to wherever I need to travel to to get some relief from this. If nothing else it would be great to have a doctor who understands the problem. Thanks. My prayers are with you all.

Chris

Wow, I had no idea that Levaquin affected so many people. My daughter had knee surgery a couple of years ago. They gave her vancomycin before the surgery. She had an allergic reaction to the stuff. She also found out from one of the nurses that levaquin is related to vancomycin.

I had a total hip replacement 3 years ago and they gave me vancomycin just before the surgery. I was laid up in the hospital for a week. When I arrived home I noticed that my skin was really itchy (mostly my arms). Whenever I scratched it left whelps and turned extremely red. Now after 3 years my skin is still itchy, but not as frequent as it used to be. Has anyone had this problem with their skin?

I wanted everyone to be aware of the relation between vancomycin and levaquin.

Good luck to all.

I was taking Levaquin for a sinus infection. After taking the first dose of 750 mg, I noticed that I started having tingling and numbness in my hands and arms. After the second dose, I started feeling the same tingling and numbness in my arms, hands, and legs. Because I had been having severe headaches anyway, I started wondering if I had some kind of neurological problem and my headaches were linked to the strange sensations. However, I noticed that I didn't have any problems with my arms and legs until after I started taking Levaquin. Some of my other symptoms were: tightness in my neck muscles and sore muscles. I also remember seeing a flashing light from the corner of my left eye and floaters. I stopped taking Levaquin after just 2 doses because it began scaring me and I feared what might happen after my third dose. I can't afford to take any chances with my health. That's why I appreciate this post, and I see that I wasn't just imagining these side effects. Since I've stopped taking this medication I still have problems with my arms. They feel heavy like I've been lifting weights and the ache. A couple of times, I've had to take pain medicine for the pain in my arms because they've hurt so bad, it feels kind of like when you hit your funny bone and you try to figure out why they call it a "funny bone" because it's definitely not funny! My arms hurt so bad I couldn't lift them, and I could type or write so I just took some medicine (tremadol) and laid down. It's been weeks since I've taken levaquin, but I still I have sensations and aching and heaviness in my arms. Has anybody been off of Levaquin for a considerable amount of time and found that the symptoms go away? Please give me some hope! :) Thanks.

Levaquin actually worked great when I took it. I was diagnosed with epididymitis after a urine culture was analyzed and the doc gave me a 10 day supply of Levaquin to take once a day. The side effects I felt were pain in the abdominal area, headaches, anxiety, confusion, and dizziness. Those I could live with, because the epididymitis problem had more side effects than the drug. The trade off was worth it. I'm on my 7th day of Levaquin and I feel a whole lot better than without it. But do beware some people do react badly to the Levaquin family of drugs including cipro. This is some powerful stuff not to be messed around with, it is also used to treat HIV patients and people who had post inhalation of Anthrax. Yes it is powerful enough to treat those dangerous conditions. When you take Levaquin just get plenty of rest drink lots of water AND Cranberry juice which prevents unitary tract infections. Do not exercise while on this medicine for it will cause tendon damage, just take it easy for the whole time you are on it with plenty of fluids. Get better and stay healthy.

Hello Everyone ---
I just wanted to share my story and hope that it helps others. On December 20th I was prescribed Levaquin to help clear up a bad case of Bronchitis that I had taken a Z-Pac for a week earlier. I still had remnants and the doctor saw as fit to give me the Levaquin to help me get over what was remaining. I had a 10 day supply of the 500mg Levaquin prescribed to take once a day. After (2) two days of taking the medicine I noticed that I was having a slight amount of pain in my left knee, and by the 23rd of December it hurt to walk or stand or sit. The pain was just a dull ache however; it would also become sharp with any movement. Just to let you know I finished all of my 10 day supply, not knowing that the Levaquin was what was causing my problems. I am a healthy 31 year old male that has a 3 year old daughter, so I am always on the go. However, beginning the 24th & 25th of December the pain had spread from my left knee to my right knee, ankles, as well as hip bones. By the end of my prescription my pain was all over my body, it hurt to sleep, it hurt to move, however, taking 800 mg of Motrin every 6 hours seemed to help ease the pain but never seemed to knock it out. I tried everything from Tylenol to Aleve...however, Motrin was the best. Not knowing what had caused my problems, and getting tired of being in pain I went to see my family medical physician on the 7th of January. He ran me through the mill with test to figure out what was going on. Nothing out of the ordinary, I was a little anemic, however, that had nothing to do with my problems. We talked about the Levaquin, and he as most doctors dismissed the chance of that being the case. However, he did prescribe me 200 mg of Celebrex per day, and told me to take Tylenol as needed to help with the pain. After taking the combination of those drugs for 10 days, I called his office back and told him I was still having problems not as strong as before and I could tell I was getting a little better however movement was still bad, so he referred me to a Rheumatologist. I saw the Rheumatologist on Jan. 22nd and he seemed to help more than anyone else, he also did some blood work, however, nothing out of the ordinary once again, he also check for arthritis, and nothing came of that either. He believes that the medicine was the root of the problem, and until it is gone from my system nothing I am going to continue to have problems. He upped my Celebrex to 2 times per day, and told me to take Tylenol Arthritis 2 pills 3 times a day...this combination has almost knocked away all of the pain. I can still tell that I have problem areas such as my wrist when opening the car door; however, hopefully those will go away in time. Apparently, according to him there is a small amount of people in the world that is allergic to fluoroquinolone drugs and do not know it until they take one of these. I go back to see him again on the 12th of February hopefully I will be back to normal, however, I do have one burning question in my mind…what happens if I get off the Celebrex? Hopefully he will be able to answer that one for me. For anyone out there that is having these same problems as I have you might want to recommend for your Doctor to prescribe you Celebrex and see if will help you…

I am so upset just reading these posts! I started on a regimen of 500 mg of Levaquin on Tuesday, January 15, 2008 along with an Advair inhaler for treatment of a bronchial infection. On Thursday I started feeling twinges in my knees when I went up and down steps. By Sunday, I could barely bend my knees so I called the Pharmacist. She suggested it was the Advair so I discontinued using it but still called my MD in the morning. She prescribed massive doses of ibuprofen (800 mg) which in a 32 hour period did NOTHING to relieve the pain. If anything it has gotten worse. I spoke to a friend the same evening who said her husband had severe muscle/joint pain in his hands when he took Levaquin this summer. This morning I called my MD twice in tears (she didn't respond until 3:30 PM.) She still doesn't seem to think it's the Levaquin but told me to take Benadryl (after I told her that this is what my friend's husband's MD told him to do!) I am going in to see her on Thursday morning and I will go armed with these comments from all of you brave people who are suffering from the effects of this awful drug!

I can not believe I found this web-site. I honestly felt like I was going crazy and that this was in my head. I was prescribed Levaquin for a sore on my finger to fight infection. I was taking 750mg every morning, once a day. The morning of the 8th day, I woke up and felt like I had been ran over by a truck. I felt foolish telling my family even the "back of my knees hurt." By the evening of that day, after laying in bed for just 45 minutes, I couldn't put down my right leg or put any pressure on it. I haven't taken the Levaquin for 24 hours now and it still hurts to try to open doors because my hands are so cramped. Does anyone else feel dizzy? All of sudden I just won't beadle to focus and my head hurts, only last a few seconds, but it is definitely there. Does anyone feel they have long term pain or affects of this drug? This is unbelievable that so many of us fell this way. Just yesterday I was at the doctor because of the pain. He instructed my to stop taking the Levaquin and told me, he has never hear of anyone feeling this way, but it is listed as one of the side effects and is very rare. Apparently it isn't that rare!! Glad I found you guys.
Stacy

I was in the hospital for a bowel re-section. On the third day, they switched me to Levaquin because I spiked a fever. I was released four days later (after 2 doses of I.V. Levaquin per day) and sent home with three days worth of pills. Ever since I've taken the Levaquin, I've had horrible shoulder and back pain and feel somewhat neurotic. The doctor said that it's a side effect from Levaquin. I have one day left of the medication and will continue to take it, but I'm curious if anyone else has had mental side effects. All I've read about is the joint and muscle soreness. Please help! It's affecting my sleep and daily routine. I don't recommend this and will not take it in the future (not to mention the cost of the medication!)
thanks

I've been on Levaquin 500mg for almost a week. All of a sudden I have pain in my right arm, mainly from my shoulder to my elbow. It kind of aches/burns. I also have some pain behind my right knee and in my middle to lower back. Are these side effects of Levaquin? I didn't have any of this until I started taking this medication. I have a call into the doctor, hopefully something will help the discomfort.

I have Asmatic Bronchitis... nothing helped... Azithromyicin was my 1st. antibiotic....... didn't help... then the doctor put me on a 5 day Levaquin 750 mg no refills.... I took them faithfully along with 6 days od methylprednisolone..... All this started New Years eve... today. 1/14,2007 I am feeling a lot better and taking breathing treatments too..... there is not much medicines I can take so I was glad this one helped

I went back to my PCP today. Yes the one that gave me the Levaquin. He was very nice and even agreed it was the Levaquin I took back in December. He said that these types of side effects we all are describing are RARE (I would have kicked him for all of us, but my legs hurt to bad).

But he did acknowledge pain and my symptoms (listed in my December post) and prescribed me Prednisone for my ligaments and Lyrica for my nerve pain. He also said it was going to be a long haul. I know that some of you are dying to telling why these meds are bad too, but I am going to try it because I haven't really been out of my bed for two weeks.

I just wanted to let you all know, that maybe some doctors are starting to listen... and that we should keep speaking out and warning others about the HIGH risk of our side effects.

I was prescribed Levaquin for Chronic Sinusitis and ended up with gout like symptoms in my left big toe. It has made it very difficult to walk and carry out everyday responsibilities.I am only 29 years old and have two young children to tend to and this has made it very difficult. It is very difficult to walk and stand and I am unable to wear shoes due to the inflammation and swelling. Does it get better?

I have been on Levaquin for close to 4 weeks. 27 days at 500mg and the rest at 750. I have a severe open wound after a foot surgery. I started feeling like my shoulders had been hit by a bat. Slowly every single joint in my body is in pain. I cry with every move I make and dread going to sleep for fear of how painful and stiff my body will be in the morning. I begged the Dr. to remove me and he has agreed. i just pray it leaves quickly.

Struggling with a sinus infection that threatened to bore into my brain, resulting, ultimately, in seizures and death, I've been taking Levaquin now for three days. I'm experiencing anxiety and sleeplessness, however, it's not from the medication. It's from all the hyperbole on the internet.

Look, I understand that many have had adverse reactions to this medication. One dose of penicillin can kill you without warning. At anytime. No warning. I suspect that few of those labellings Levaquin "poison" would ever bother to consider that - or anything else. All wrapped up in your misery, you spout off with rhetoric that is really better left to lawyers and politicians.

If you were uninformed of the possible side-effects of this medication, blame your doctor. I see that the last post here is dated November 2007, and the bottom of this first page takes us to October 2006. Perhaps one could take a bit of responsibility for oneself and do some research on one's own before popping a pill handed out by a disinterested physician. This information is out there - and yes, your doctor could have seen it, too. But he didn't bother, did he? Neither did you.

So, yes, with my first dose, and despite the impact drill driving through my eye-socket, I waited for the seizures, swelling and signs of imminent demise. Nothing. Sorry. Oh, my sinuses feel better, I don't have a brain infection, and so I won't die frothing at the mouth on my living room floor.

I'm sorry you feel bad - and if you hadn't run off at the mouth calling what may be one of the last effective antibiotics "poison", I might mean that with some sincerity. Oh, and lest you forget, antibiotics are poison by definition - the idea being that they affect/poison/kill the source more than they do the host.

So let's stop the hyperbole, and simply say you had a bad reaction to this medication. Not everyone does. Your option might have been to skip the doctor and the meds altogether, and see how you'd fare. But that would leave the responsibility, and the blame, all on you, then, wouldn't it? Far better to spread it around some.

My son is 14 years old and was given two rounds of this drug for an infection (two weeks and one week respectively). Last round in the middle of September. The pain started with the first round and got worse the second time. Real bad. We had him tested for a multitude of diseases and x-rayed the knees - all came back normal. We finally stumbled onto the fact that the joint pain coincided with the drug - WE WERE NEVER WARNED!

Well, he's a heck of an athlete/student/good kid...and has been wrestling since he's 5 years old, has competed nationally and this sport is "his thing." Well, now he's finally in high school and can barely make it through practice - can't go live at all. The pain and stiffness ain't going away even though he's been off it since September!

What in the world can we do to treat this effectively (or t all)? Doctor prescribed anti-inflammatory meds and they did nothing. Physical therapy is doing nothing. Ultrasound treatment on knees is doing nothing.

How long will it last?

Help please anybody with any information - we're disparate.

Prayers are welcome too.

Thanks.

Craig V. (Dustins Dad)