Arthritus symptoms and conditions

I took Levaquin on multiple occasions for a severe prostate infection. I took a 15 day supply...then off for 1 week...another 15 day supply...off for two weeks...and then a 30 day supply. I took another 30 day supply when the infection resurfaced about a year later. During the time I was on it I experienced extreme "arthritis like" pain in my ankles, wrists, shoulders, and especially my back. The infection was over 3 years ago and I have not taken Levaguin since. However, the joint pain has never went away. I can barely climb stairs as my right knee feels like it is going to pop out of socket. The bone pain in my neck and between my shoulder blades is horrible. I visited a doctor (I never even considered the Levaguin as a possible antagonist) and was told that I had spinal degeneration and needed physical therapy. Protect yourself and your family from this drug.

hello again ladies. i'm 3 weeks 4 days post removal of mirena and i'm just having my first proper period. it is heavier than normal, but bearable. i was just wondering if anyone else has really bad headaches after removal. i'm not usually a headache sufferer, i was wondering if it could be hormone related.
the heartburn i was previously experiencing has completely cleared up, (so far) the pregnancy feeling has gone and i'm no where near as agitated or moody. i'm so glad i had the evil device removed i do feel better but not completely yet.

also i don't know if anyone else has the the same problem, but i've been having blood tests because i was feeling ill and having joint pain. i had blood tests which showed a raised esr level. i had the test repeated 3 weeks post removal and its the level has dropped quite a lot. it was 20 which is the lowest result i've had so far. i've been tested for lupus arthritis etc, could mirena have been the culprit all along? hmmmmmm..........

I share the scare - I developed a bacterial infection after surgery and had an allergic reaction to first two antibiotics so was given Avelox. About an hour after the 1st dose my eyes became bloodshot, my joints ached like I had the flu or severe arthritis and I started having jolts of pain in different places, legs, groin, neck. I became disoriented and developed tiny blisters on bottom of feet, behind knees, on neck they faded, and at base of my fingers. The second dose caused severe joint and neck pain, disoriented feeling and again blisters. My doctor had me break the pills in half to take twice a day with benadryl. I also took large dose of Ibuprofen an hour after taking Avelox. That helped lessen severity of side effects. Final straw was the fifth dose - took before sleeping, woke at 4am and could not move from neck pain. My husband pulled me up so I could use the bathroom with me crying from pain. Sitting on the commode, I threw up and started to pass out. I managed to get downstairs and take an 800 mg. Ibuprofen and passed out for about 30 seconds. We went to ER. The attending physician decided I was having a muscle spasm and dismissed my fear it was the drug. They gave me a muscle relaxer and sent me home. I slept like the dead. My doctor called me that afternoon and told me to stop the Avelox immediately. You can imagine after missing 5 weeks of work for surgery, then having to miss three days last week and who knows this week how bummed I am. I am 46, have a wonderful family (a husband and 4 kids), a job I love, and life is good. I hope my body can recover soon as I am not used to inactivity. I cannot seem to function normally anymore.

I tried taking Lipitor on two occations for several weeks each. About a week into each attempt at using Lipitor I began having sustantial pain in my left shoulder. This was severe enough I also began taking nsaids for arthritus with limited relief. After discontinuing Lipitor for about 3 weeks my shoulder pain slowly dimminished. The following month I made another attempt to take Lipitor for several weeks with the same results. Currently I am not taking Lipitor or Artritis medicine and am pain free.

I had been taking Lipitor for well over six years to help lower my Cholesterol count with no know side affects. A problem developed about two and a half years ago with nerve damage that gave me excruciating pain in my shoulder and arm. After an MRI and three cortisone shots I was referred to a neurologist for help. He had no idea what was causing the problem.

About six months after many doctors could do nothing for me, and referring me to a physical therapist, my wife showed me a story in a magazine, which I can no longer find, that talked about problems with Lipitor that had not been properly documented. The article talked about exactly the side effects I was having. The article said there was a problem with nerve damage. It had been well documented that some people had muscle problems, but it was not know there could also be a problem with nerve pain.

I contacted my doctor and stopped taking Lipitor. Two months later, the pain just disappeared. The very day the pain ceased, I had a visit from a good friend of mine who is a Radiologist and who had studied Lipitor because of a problem he was having.

He explained that Lipitor was doing the job it was supposed to do, namely keeping the liver from producing all fats. The problem I was having was that I had injured a nerve and Lipitor was keeping the liver from producing a particular fat needed to help heal that nerve. It seems that the myelin sheath around the nerve needs that fat to help the nerve heal itself, and Lipitor was preventing the production of that particular fat.

Once I quit taking Lipitor it took about two months for the healing fat production to do it's thing. Recovery of the nerves in that arm has been very slow, but they do seem to be healing now.

I thought this was such an important finding that I notified all the doctors I had seen about this problem. To my great surprise I heard from no one. Not even a thank you. I guess that since they didn't find the solution, they just were not interested.

I hope this discussion helps someone else. Thanks for listening.

I've been taking Januvia for 8 weeks, and have experienced muscle cramps with shock-like pain running down my leg into my heel; upper and lower GI spasms; night sweats with sleep interruption; and I gained 5 pounds in the first 4 weeks which I can't attribute to anything else. I've also taking metformin and glyset for several years, and although I've experienced the night sweats, they've greatly increased in intensity.

Like several others, I truly believe God directed me to this website today. I have PCOS so w/o BC, I don't have a period. I thought it was just MY hormones being affected and my family suffering but after reading this - the ring is coming out and I'm calling my doctor!! I honestly feel like I am going cRaZy!! I feel like barbed wire is crawling under my skin and suddenly I have a million pet-peeves. Everything is making me either want to cry or go into a rage - there is NO happy medium. My hands and feet are swollen and achy - we seriously thought it was an early onset of arthritus! For the first time in weeks, these posts have made me feel normal. Please don't suffer needlessly, take the ring out and find another option. I know I am - I owe it to my husband and three boys!!

i am 22, and before the levaquin and tequin i was healthy and normal.
Last november while visiting family for thanksgiving, i came down with strepthroat. i couldnt get an appt with tricare so my mother gave me some tequin, she had used it for strep throat. Since then my life has been a living nightmare and it has been the worst year of my life. I took the tequin for 4 days. on the 4day, i left to go back to VA where i live. I got horribly sick that day, but thought nothing of it as my husband and son had gotten the 24 hr bug while we there. pretty soon i started having anxiety attacks and chest pain left and right. The came the stomache PAIN. I thought i was having appendicitis. I ended up going to the er once sometimes 2x a month for things like severe abdominal pain and chest pain, anxiety attacks going out of control, and unbearable migraines (which i had never had before.) i was diagnosed with lots of different things, IBS, Ulcer, pulled muscles, chest wall pain, and once even gall bladder dysfunction. So as a result of all that i have been perscribed all kinds of things for the pain the nausea the headaches the unbearable insomnia etc.
These things caused a major rift in my marriage. My husband has at a few times talked of divorce bc he couldnt stand the hypochondriac *as he put it* that i had become. I have thought i was going crazy, have contemplating hospitalitizing my self etc. Recently my PCM and I decided to try a perscription for depression. One of the major symptoms of depression is"persistand physical symptoms that DO NOT respond to treatment. Such as Headaches, digestive disorders and headaches." so i tryed it. Then a week ago i stepped on something outside and went to get a tetanus shot. They perscribed levaquin 750 mg a day for 5 days, and gave me a 750mg dose at the hospital. That was Monday. it is now 430 am on friday and this week has sucked. My side effects have included insomnia(even with my nightly ambien), nausea, burning/tingling in my entire right arm, chest pain, a sinus infection, knee pain, back pain, shoulder/neck stiffness, headaches, jitters, something kinda like blurred vision..like right on the verge of not being able to focus. Constipation, pain in my hands, and almost overwhelming fatigue.
regretably i had already taken todays dose, and i started feeling bad again so i decided to look up all my current meds online to see if maybe it was an interaction of sorts. I tried the levaquin last, as it is an antibiotic. After reading 9 pages of nothing but negative comments i decided to flush the remainder of the bottle of pills down the toilet. I plan on filing a compaint with the FDA. This is poisin and I cannot belive with all the side effects it is still on the market. I cannot believe that for almost a year my life has been a living, tormenting hell. And all b/c of something that is supposed to make things better? If you read this please stop taking the pills and see your doc about another alternative. I agree that the drug should be taken off the market and soon. i also agree that a class act lawsuit should be filed. These side effects LAST A LONG TIME, they interfere with your ability to function on a daily basis. I am very interested in talking with others about the problems with the side effect, and the longevity of them. My yahoo email/ID is ******* i would appreciate and be thankful for any advice, and i would also like to be in contact with others who have suffered as i have suffered.

I have arthritus in my left thumb from injections for psorsis onmy hands.

took levaquin for 10 days for broncidus. During treatment I developed severe soreness in my elbo neck and knee joints. My broncidus cleared up but I now feel Like a 90 year old man with arthritus. My doctors say that the medicine could not have caused it , I say bull , they are only covering thier ass. They probably win a trip for selling the stuff> Ill never take it again.

Some lady entered that we should all quit complaining about
the bad side effects because she loves this drug and to just
use something else. I now need an antidote to counter act it.
This site isn't for people who don't have a badside effect.
We arn't being selfish and trying to deprive her of this drug. I have serious joint and tendon and muscle tenderness. Have trouble sleeping from pain. Perhaps my fault, but I had mild arthritus when I took this drug, nothing really bad, within five days I couldn't get down the stairs. I thought ,what, after years of mild arthritis It had attacked me. Well I continued for another round and then it got worse. Yeah, I thought then. Its a reation! Antidote - I'm afraid it's going to get worse.

I have had severe pain in my right hip-joint area and difficulty sleeping on that side for several weeks now, and it is increasing in intensity. I have experienced the "fog" that many have discussed as well, leg and foot cramps are all too familiar as well as the dizziness periodically! I had noticed increased stiffness upon arising in the morning but attributed that to possible arthritus, hmmm, now makes me wonder. I also thought the increased hair loss (nothing creating baldness) that I found inconvenient, I feel like a shedding dog, was from aging! After reading so many comments about Lipitor, I am wondering if there is a link with this medication.

I do have one symptom I would like to inquire with others about...I had a bout with Hemoptysis (bleeding lungs) and recently nose bleeds, for no apparent reason other than minor activity. Also I have a feeling of being "Anxious" for no reason and it is not a normal feeling for me to experience even during duress circumstances. Are others experiencing similar reactions that may be related to taking Lipitor? Thanks. Tomball, Texas

had hbp 8 monthes ago no history in familie doc prscribed lisinopril 5mg hbp down dry cough sneezing fits dry eyes low erection coming of this to morrow when i get a bp monitor whish id read this page before thanks for the ifor also burning senseastion in legs at night thought this might be to do with my arthritus but will see when i come of this crap regards good luck to every one any better alternatives