Levaquin and yahoo

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!!!!

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!!

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. .

My husband was having gastrointestinal problems for about a week. The PA at his primary care physician's office prescribed Levaquin for 7 days. Blood taken ½ hr after Levaquin started showed liver levels to be a little high. By the 3rd or 4th day my husband was jaundiced. Blood taken on the 6th day revealed liver levels dramatically higher. He is still jaundiced and liver levels are still at the higher level. Had ERCP procedure, CT scan of abdomen and MRCP, but no conclusions other than stricture of bile duct and possibly pancreatic cancer, although a mass has not been seen on any film. Has this happened to anyone else on Levaquin? Doctors want to try ERCP again and if that does not work then the Whipple Procedure which is major surgery to remove a possible pancreatic cancer that they have not seen.

To all the people who are just starting to make the connection between their symptoms and Levaquin or other fluoroquinolone antibiotic: There is a lot of information available on the internet. Check out the following websites: fluoroquinolones.org, antibiotics.org, medicationsense.org, fqvictims.org, fqresearch.org. There are also support groups on yahoo for sufferers. Please don't forget to file a medwatch report with the FDA. Finally the FDA is starting to listen to the victims!

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?

In July 2007, I was put on Levaquin for pneumonia. I was 53 years old, working full-time, active. The pneumonia was caused by aspiration when vomiting. I had never had these problems - pneumonia or aspiration - before. I had gradually worsening generalized joint and muscle pain and stiffness, which I reported to my doctor after about 5 days on the Levaquin. The pain I was experiencing was worse than the pneumonia symptoms (mostly high fever). The course of levaquin was supposed to be 14 days. After 9 days, I could not tolerate it any longer. My doctor put me on a Z-pack (azithromycin) for the remainder of my treatment. It is a year later, and I am still plagued with muscle pain in my back, shoulders, arm, abdomen - and, at its worst, my legs. The only way I'm able to function is on prescription painkillers, which I detest having to take - but they're a lifesaver. I've been seeing a rheumatologist since December '07. He dosen't seem to believe the levaquin - pain connection. He thinks I may have Polymyalgia Rheumatica. I have consistently elevated blood levels of creatine phosphokinase, a muscle enzyme which indicates muscle damage. I was on prednisone 10 mg. from early March '08 which I have just weaned off of after suffering a depressive episode with a suicide attempt at the begining of this month. I can't work now. I'm terrified of becoming permanently disabled. Finding answers has been very difficult but I firmly believe that the Levaquin started all this.

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 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!!!

Hi guys.... Well I'm quite interested in this drug and I do prescribe it to my patients however I am surprised at the magnitude of side effects listed here. I am based here in south-east Asia and I do prescribe Yasmin to my patients and I rarely here of these side effects. Perhaps this can be contributed to the fact that it (Yasmin) is available here under a different brand name however consists of the same chemical position. I am interested in the ones available in the U.S. Does anyone know how I may go about purchasing them. You can contact me personally on ****** thank you.

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 took Leva-kill last November, 500mg for 10days due to a resistant ear infection. On the 3rd day, my back felt like it was on fire. Went to ER, did one blood test for muscle deterioration, came back fine.Told to keep taking. I thought I was going to die. I felt and still feel like I was poisoned. Seems to be permanent. Some days worse than others. Check out FQVICTIMS.ORG.Any doctors and dentist I have seen says not Levaquin {about ten]. One ENT said "I bet" when told levaquin made me feel like dying, but that was it. Has anyone heard of any hope? Is this really permanent?

i have been taking levaquin for a week now and i cant move my body it is too sore to move.also i have extreme stomache pain and diareah.i have yet to feel better and feel things are getting worst. now i feel like throwing up too. not really sure what it is but after seeing the sideaffects everyone is having i contribute it to this drug

I am a 36 year-old female, and in very good physical condition. I have been a runner for 15 years. I was prescribed levaquin for a recurrent sinus infection, 500mg x 7 days. On the second day I developed severe carpal tunnel syndrome (tendonitis of the forearms & hands); I could barely hold a pen in my hand, much less write. I refused to take the 3rd dose. On the 5th day (even though I am not taking it anymore) I woke up with severe hip pain (both hips). I can barely walk, much less run. I am a full-time physician and have a small child. I am not sure what will happen to my favorite hobby, running. This drug is extremely dangerous, and I will never prescribe it to anyone. It should be removed from the market!!

My 16 year old son took Levaquin 6 months ago and had a bad reaction to it. His symptoms were severe muscle weakness (he would get exhausted walking from the parking lot to a store and back, severe joint pain (in thumbs, wrists, elbows, knees, and ankles), dizziness (he felt like the room was moving away from him and would lose balance), and headaches (a severe pressure in the back of his head that was constant and then shooting pains in his his head that would come and go for no reason). I should say he was in top shape before this and wrestling in the 125 pound category. He took Levaquin to prevent an infection after sinus surgery.

Now 6 months later, his joint pain is completely gone except for his knees. They still hurt when he does squats and they are not good enough for him to go back to wrestling, but he can walk around pain free. His dizziness is also gone as well as his muscle weakness. His headaches are still there and still constant, but not as bad as they once were; however, he has had them 24 hours a day, 7 days a week for 6 months. He is on Lyrica which has helped make the headaches subside.

I have taken him to more than 16 medical doctors of all specialties, had multiple MRIs, CT Scans, blood tests, spinal tap, and an MRA. All come back negative. Thankfully, despite all of this, he still remains happy and positive that he will once again be 100% healthy; it will take lots of time, but he will get better. I know the first three symptoms (joint pain, dizziness, weakness) are clearly Levaquin related, but I haven't heard much about the headaches from people. Anyone else out there that has suffered from a constant headache after Levaquin? I REALLY want to hear about headaches from others!!!!

By the way, we have filed a medwatch already. I also know that Levaquin is not approved for anyone under 18 years old and he never needed such a powerful drug to prevent an infection, but there is nothing I can do about that now except to warn others. One of his UCLA doctors wants to write a case study on him to make this more known to others and I am helping him with that.

If anyone has questions, please feel free to ask. If you have had a headache from Levaquin, please let me know where in the head the pain was, if it is constant, what it feels like (pressure, shooting, throbbing), how long you have had it, and what, if anything, helped. THANKS.

I was prescribed Levaquin 1000 mg. for 5 days for pneumonia the last week of December 2006. I was also prescribed Prednisone. Everything I ate tasted like metal. A couple of days after I started taking the Levaquin I started experiencing muscle cramps in my rib cage which are so severe it makes me double over in pain. After more than a year I still have the muscle cramps which now include not only my rib cage, but the arch of my feet and sometimes legs. I have a torn tendon in my left arm which didn't happen until about a month ago, but I am sure it is caused from muscle damage from the Levaquin. I am also on Advair Discus 250 which I didn't take before using the Levaquin. I didn't require inhalers or other medication before the pneumonia. My doctor now says I have COPD caused from asthma and chronic bronchitis. I used an Albuterol inhaler when I first got sick because the pneumonia was so bad. I thought after taking the Levaquin I would get back to normal. But even after the infection was cleared up I would get out of breath, so I returned to my doctor. She did an x-ray and said I had COPD and prescribed the inhalant. What I don't understand is that I didn't have breathing problems before the Pneumonia. I didn't have joint pain and muscle cramps either. I have had to quit working this past year because of it. I cannot go without the Advair, I can no longer walk long distances without pain. I have constant muscle pain just trying to do normal housework. How long do the effects last? Must be a lifetime.

I took 500 mg Levaquin daily for 5 days during the first part of Oct. 07. Tendon pain developed on the third day. Today, after four and a half months, three doctors and a dozen sessions of physical therapy, I still can't walk more than a few feet without a walker. Any thoughts regarding how I might proceed will be greatly appreciated.
David M.

I had bacterial pneumonia a few weeks ago they gave me Levaquin as well, After the hospital I notice some pain in my left arm. A week later I was unable to straighten my arm now the pain has moved up to my neck and back and is slowly reaching my right shoulder. It seems that though you ask doctors question you never get answers and yes its true about this pain I have been in agony for almost a month now and can not find any type of relief. I was treated with a 7 day regimen of medication and I don't know what is worst the pneumonia or the pain. If there is any where to find relief as a natural source please post it

Thank you

Need some advice for my husband. He has been given Levaquin and he is in alot of pain. Headache, stomach, dizzy, lower back pain..and what ever else you can think of. So my question is, what did you do to get relief from taken the medicine and how long untill you felt better. I have told him not to take anymore, but what else if anything can he do to feel better? Please e-mail me at thetuggles@yahoo.com...thanks, trish

HOW ABOUT THIS MED. OH MY GOD I CANT BELIEVE THIS IS HAPPENING TO ME. I HAD BRONCHITIS,SINUSITIS,AND TONSILITIS,AND I FELT AWFUL, WELL I WAS PRESCRIBED THIS POISON AND NOW I FEEL 10X WORSE, IF ANYONE IS READING THIS THAT IS PRESCRIBED THIS PLEASE PLEASE DONT TAKE IT. YOU WILL BE SO GLAD YOU DIDNT. I HAVE EXTREME PAIN IN MY KNEES,WRISTS,ANKLES,HANDS,AND ARMS. I FEEL LIKE AN OLD WOMAN AND I AM 42.WHY ISNT THIS TAKEN OFF THE MARKET? HAS ANYONE GOT ANY LAW SUITS THAT ANYONE KNOWS OF. I AM GOING TO CALL MY LAWYER.THIS NEEDS TO BE STOPPED.PLEASE LET ME KNOW IF ANYONE HAS ANY INFO

Beware of cycling. That's what happens with this poison. You start to feel better and all of a sudden you're hit again. After a few weeks you start to blame it on something else because it's so hard to believe that this so=called medicine is still messing with your body. The dr. will blame it on something else for sure but the fact is that with some people the damage is done and it will go on for possibly years if not forever. Make sure you send it a medwatch report to the FDA and check out the forum that yahoo has on quinolones and side effects. There is help there.

Admitted to the hospital for diverticulitis. Was put on an IV of Levaquin. When I reminded the dr and nurse that I'm sensitive to meds I asked what side effects might come along with it. I was told that "it's just an antibiotic" and the most I could expect was nausea. That night I couldn't sleep and by morning the elbow tendons in my right arm were in severe pain but was told that it was most likely due to the IV entry point.

Was sent home with 7 days oral dosage. I began to experience spaciness, confusion, short term memory problems, burning and tingling in my feet and hands, pain in my wrist, my right arm was no longer usable having no grip strength and weakened muscles. A general feeling of exhaustion came along with it all. I stopped the meds on the 3rd day after reading the stories of others who experienced similar madness.

My GP was reluctant to agree that it could be Levaquin but I feel fortunate that she did indeed refer me to a neurologist. Tomorrow will be the full workup and blood tests for liver functions.

I would very much like to be involved in any project, legal action or otherwise, that is focused on bringing to light the dangers of this family of medicines. You can contact me at VFrancis@southbuffalo.net Good luck to everyone!

back in april 2006 I was give levaquin for brockitis. I have had leg and foot pain. now my right arm cannot be lifted above shoulder high with out pain. I have had pulpitations ever since and am being sent to see a cardialigist on the 26th of june. I had an e k g at my doctors office and it is not normal now. I don't get panic attacks any more and the head ache is much less, but I still cannot sleep more then 4 hours at a time. after reading all these posts, I know what caused it, but dose anybody know how to get better. my doctor just keeps sending me for more tests. i wonder how much money he makes by sending me for all these expensive tests..former---******

hello again, another week an a half and still not able to sleep with out help. my heart has not been racing as much and the blood pressure has come down some but now i have pain in my knees and my lower back is realy bad. i have a hard time getting dressed in the mourning because of the back pain. i saw my doctor yesterday and he said not to beleive what i read on the net and that i have arthridis. i may have to see a diferent doctor. dose any body know how long this knee and back pain is going to last. if so, please let me know----******