Levaquin and 4 months

My name is Heather I am now 32 years old I took levaquin when i was 29. After i took levaquin I went on a roller coaster ride I have yet to be able to get off of. First when i took it I had the worst night mares i have ever had only to wake up to a splitting headache and a very sore body. took another one the next day same reaction.I figured it was the bronchitis that was causing the problem. on the third day i was worse still I could hardly move. I stopped taking the drug. after another two days i felt better. two weeks later I was out with my father and he noticed a rash on my legs. I was also starting to get little blood blisters. I started to become concerned and the next day after going to the zoo with my family i came home and my legs were swollen three times there normal size and very sore. I put them up just to find the felt like play dough had been stuffed in to them and I had blood blisters the size of pencil erasers. I made an appointment to see the doctor. he said and i Quote " Heather I have No idea what the Hell you have" he sent me to a specialist. between the time of my first appointment and the appointment with the specialist my legs stopped working from the hips down i was 90% paralyzed (not spelled right ) they just wouldn't work right. My ten year old daughter was helping me get to the bathroom. I was soooo sick i had a headache all the time couldn't eat or sleep and when i did it was only for a few hours I couldn't move very well and to get up out of bed hurt so bad i almost fell every morning. by the time i had gotten to the specialist I had gone to the E.R. three times for the pain.and the last time was because my toes stopped moving altogether. at the appointment the doctor ran all kinds of tests checking me for everything from S.T.D.s (which i have been happily married for years) to Lupus. I felt Like and 80 year old Lady And like i said i was only 29. after the extensive tests and everything coming back normal the doctor put me on a steriod. for 4 months i was told i had to take prednisone After the first dose i could move again I still hurt but i could move.But now i had the side effect from that. i was gaining weight like it was going out of style, but at least i could move. after the 4 months things seemed normal kinda. I could move but if i sit still to long my legs go numb not fall sleep go completely numb even if i am standing to long. I am still afraid that i will wake up again feeling like i did that Fall three years ago. I still have problems but im not sure they are tied in but it wouldn't surprise me in the least. I only took three Pills of Levaquin three years ago!!!! How long does this stuff hang on really??????

I was just prescribed Levaquin (500 mg.) for bronchitis. I received a 10 day supply. The second night, I had trouble sleeping and felt quite anxious. By the 4th night I literally thought I was going to have a heart attack and had trouble swallowing. I called my doctor who blamed the bronchitis and gave me an additional prescription for an inhaler. That evening I slept a total of perhaps 20 minutes. My heart was racing and I felt as if I were choking. Another call to my doctor was placed. She advised I stop using the inhaler. I was becoming increasingly anxious, paranoid and began to have leg cramps. I haven't slept for more than a few minutes at a time for 3 days and the feeling of choking was so bad I had to go to the emergency room. They found it is from the Levaquin. I have never felt so desperate, paranoid, anxious, and horrid in my life. I actually had serious thoughts of ending my life to get away from this feeling. Even though I have been off it for two days, I am still feeling the effects, especially at night and was told I may feel effects for a week.

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 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.

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.

I was prescribes Levaquin 500mg for 10 days for sinusitis. On the second day, I woke up with a migraine and took Aleve. The headache accompanied by dizziness lasted 10 days or so. As time has passed, I have pain in my right shoulder and bicep and stiff/swollen joints in the back of my neck. It has been 4 months since I took Levaquin and my symptoms have only gotten worse. I have been on bed rest for a week just after a simple 5 minutes on an elliptical machine. Additional problems along the way have been anemia, my vision got extremely worse with retinal degeneration, anxiety, diarrhea, fatigue, irritability, and numbness in my hands and feet. My doctor says he believes me but mentioned fibromyalgia. My symptoms don't even fit that disease. Friends don't believe me either. I am a pharmaceutical rep. The FDA needs to pull this drug off the market. Why won't they do it? Someone has a connection someone. I am almost 31 years old and I don't know how much more my body can take. I miss my friends, tennis, and even normal daily tasks like opening a car door and sitting for an extended period of time. DO NOT TAKE LEZAQUIN EVER.

Took two courses of Levaquin. Got a rash in the groin area and left armpit.
Also, lymph nodes in the left armpit became swollen. Now after 4 months, the rash is gone, but the lymph nodes swell about every 3-4 weeks and then subside.

I have taken several rounds of Levaquin, and recently Avelox. After taking 2 rounds of levaquin for a sinus infection last spring I experience many of the myalgia type symptoms, and was tested for Rheumatoid Arthritis, and Lyme's disease, all negative... eventually felt better. I never attributed to the medication. Last fall I again had a sinus infection levaquin again, 2 rounds of 5 days in February, and then Avelox early April. I have never been sicker in my life. I have had many of the CNS effects, and the joint and muscle pain. Agonizing pain that I had never experienced. worse than passing a kidney stone. I am feeling a bit better, and heading back to work today after being unable to go for 10 days. I have also developed some eye problems, that are being managed with drops. I am trying to eat naturally and drinking lots of water. I pray this will go away, and want to warn everyone not to take this medication! Still have back and hip pain, pain in my feet, insomnia, headaches, and anxiety...but is not as severe as 10 days ago. My prayers are with all of you suffering from the side effects of these dangerous drugs.

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 prescribed Levaquin 500, because of bronquitis for one week, in that time I experienced:

diarrhea
nausea
numbness in arms, hands, fingers
extreme swelling in joints
insomnia
difficulty to stand up, walk
bruses in eyes and arms
no strength
tingly or electric sensation in hands

I went to many doctors, but none of them knew what was happening, until one of them told me this was called Serum Sickness, which is an extreme reaction to the drug. TWO MONTHS HAVE PASSED AND I STILL HAVE THE SYMPTOMS. It is affecting my life, because I depend of others to do certain things for me, because of the extreme pain, and weakness.