Long distances symptoms and conditions

I was prescribed levaquin back in May for a sinus infection. Have suffered from severe side effects, worst of which being joint and muscle pain, stomach pains, weakness and hives (last dose was taken 10 days ago). This has been the most physical discomfort and pain that I've ever been in. In addition, my ability to concentrate and recall easy things has lessened.
The "Bafoon" of a doctor that prescribed this claimed he didn't know what was wrong with me after a normal blood test. My new knowledgeable doctor told me that some people can't even walk after taking Levaquin. She says it takes on average 7 days to 6 weeks to feel improvement. Being a 36 yr old woman, having to move turtle speed, and feeling like I'm in a 90 year old body is very depressing.
If anyone has any information on any class action or mass tort litigation lawsuits please send me the information. This drug is poison and should not be prescribed for minor infections!!!

I have had my mirena since June 2004. I've told a zillion people how great it was & how I want another one 5yrs from now because it is so great. Here is how my story goes my second child was born the last of May 2004 with a cleft lip & palate. In the first 6mo he either had 3 or 4 surgeries never sleep & still trying to pump breast milk to feed him. I go Nov 2004 to the Dr with panic attacks, anxiety, depression, they wanted to admit me & I would not let them. The looked at me & said your bipolar take your meds. I am still unable to take my kids in the movie theater or drive long distances in the car by myself . Feb 2005 I gained 45ibs always wore a size 3 in clothes but now then a Size 13! Took diet pills off & on to lose that. I now weigh 124 but my stomach always is bloated to where I look 3 or 4mo preg. summer 2008 till now I now double up in pain & tears it fills like laber pains, extreme mood changes worse than every because I'm on a mood stabilizer & it doesn't seem to help much, Very bad back ache, hands & feet always going numb, headaches. always tired no energy, I feel bad because I've been really angry with everybody around me & I feel that know one understands. I 've be going from doctor to doctor but for 6mo to try to get a answer. Even my husband noticed something must be wrong because I'm just not myself. I had just came up with I'm getting Old & falling to pieces even though I'm just 29yrs old. I go see a gyn today & I'm telling them to remove it now. The joy of life has been took from in the last 4yrs & 9mo. Please don't let this happen to you no the risk early

I am so glad that I found this site and to see that there are other women out there who are having problems with the Mirena. I thought it was just all in my mind! I had the Mirena inserted in February 2008. Started having problems with high BP when pregnant with first baby and when I went back on pill after his birth BP wasn't doing any better. After having my second child, I contemplated about Mirena vs. having tubes tied. My OB said the Mirena was the perfect thing for me and was pretty much like tubal ligation, but without the surgery. I had no problems when Mirena was inserted..just bleeding (seemed like forever for me to stop bleeding) and the normal dizziness. For the first three months, I never knew when my period was going to be, but I just kept remembering what my OB said "your periods will be like nothing after the first three months." My periods did get a little better...however not the "light" or spotting periods. After the first three months, I started noticing that my hair was starting to fall out more but thought it was part of postpartum. I started feeling really tired, skin started to break out, felt depressed, my mind was racing, couldn't sleep, had problems remembering things (simple things), migraines got worse and more frequent than what they used to be before, moody, agitated, had chest pains, nausea in the morning (at one point I thought I was pregnant again!), stomach pains, diarrhea/constipation, kept having vaginal discharge (like when you are pregnant), came down with bacterial vaginosis, UTI's were somewhat common,no sexual desire and my BP was out of control. Seven months after having Mirena inserted, I started having sharp pains near right ovary. I had problems with cysts in right ovary before and had them removed so when the pains started, I had a hunch that most likely it was another cyst. My OB closed her practice so when I went to new OB for annual pap, I mentioned all the things I was experiencing including suspicion of cyst. I told her I had been experiencing all symtoms since Mirena was put in. She told me that she has never heard of the Mirena to cause symptoms like these. Told me that perhaps I was still having effects of postpartum and that my body was trying to get "back to normal" and get used to Mirena. Had all these blood test done and everything came back normal. I did have a cyst on right ovary and was told that it should go away within 2 months. Just had a follow-up ultrasound today (2 months later) and cyst is still there along with other cysts on right AND NOW left ovary. Most of the time, I am in a lot of pain especially on the right side. I was told to just take Motrin for the pain, but that nor heat packs work at all. I am really considering to have the Mirena taken out. I REALLY believe that the Mirena is the cause of my cysts. Is there anyone out there who have gotten cysts while with the Mirena? And has anyone experienced having no problems with cysts after the Mirena was taken out? Since finding out that I have multiple cysts on both sides and knowing that my doctor will probably tell me they will eventually go away on their own (first one is less than 2cm and others are smaller), I don't know if it is even worth keeping the Mirena in. I hate having all these symptoms...I just want to be "normal" again. BUT, IT IS VERY COMFORTING TO KNOW THAT THERE ARE OTHERS WHO ARE OR HAVE EXPERIENCED THE SAME. Now I can tell myself that it is not all in my mind and I am not going crazy!

I take Klonopin and Celexa and my mood and feeling are better than I remember before I started them. There are many other positive outcomes we have notices. I used to have many addictive behaviors and many of them have ceased. Now for the issues: I fall asleep every time I sit down. I have had arthritis since I was a young teen, so I do need to sit down for breaks anyway. I used to fall asleep from time to time, but now it is everyday. If I am in a meeting I nod off and start snoring. I was not able to work while depressed and anxious with panic attacks. I feel better, but I still am unable to work. I plan to stay on Klonopin as any other of the drugs would probably only be worse. When I was on Ativan about 17 years ago while I was in the hospital it only took me 5 - 15 minutes to fall asleep for at least 8 hours. I have friends that can drive long distances on these drugs, so it is not like this for everyone thank God!

i have been on topamax for 6 months... i was also on tegrotol at the time. the drug made me stupid, i couldn't visualize things or think clearly, my memory had gone and i was forgetting the most familiar things in my life, i felt unreal and as if i were just a pair of eyes watching the world, i could ever just relax and feel normal, riving made me feel weird and i cant drive long distances. iv now decided to come off the drug and live drug free... i really hope that these effects go away... its the worst thing my neurologist has ever done...

I was diagnosed at age 46 with osteopenia and being post-menopausal (altho I never had any symptoms). I was put on Fosamax 1X/week. After a couple of months I developed a painful locked left shoulder. X-rays revealed nothing, and the doctors could not give me any cause except "getting older." I was unable to hook my bra, raise my arm above my head, take an item down from a cabinet shelf, pull a shirt over my head, or put my hair up. I was referred to a physical therapist, and after four months of daily exercises with tension bands and light hand weights, most of the pain subsided and mobility resumed.

Now, a year later, I have developed terrible pain in my right shoulder along with pain in the upper arm, difficulty sleeping due to the pain, and recurring pain in the left shoulder. The right shoulder is not locked as was the left, but it is more painful.

I started doing the shoulder exercises on my own and found that the pain would be better for a few days, then resume with a vengeance--usually on the weekends. After reading this website and many others--voila! I have been taking Fosamax on Fridays. I've been off it now for two weeks and the pain is definitely better.

A few other things that have helped are a good massage to loosen the muscles around the shoulder joints, nighttime application of a heating rub (BenGay), and sleeping with a small pillow tucked under the armpit on the painful side (like holding a baby) to take the weight of the arm off the shoulder joint.

I have also been losing clumps of hair every day; I don't see any thinning or bald patches, but I am amazed at the two handfuls that come out every time I wash my hair. I feel so much weaker, especially in my arms, than I ever have in my life. I have always been quite strong for my small size, able to life heavy things, run long distances (three marathons), and have great physical endurance. Now I feel like a weakling; I have trouble getting up or down if I am seated on the floor or laying down, trouble lifting anything over my head, and trouble relying on the strength in my arms for ordinary tasks such as lifting or throwing.

I will check back on this site often and post an update if I see any significant changes after being off the Fosamax for a while longer. I want my shoulders, my hair, and my strength back!

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.

Fluoroquinolones interfere with thyroid hormones. IMany of us (from another site) have found that we have Hashimoto's, which is that our autoimmune systems are attacking our thyroids. Also, there's a possibility that your adrenals are shot too. Now that I am on Armour (pig thyroid) all of the horrible tendon issues, anxiety, fibromyalgia and chronic-fatigue-like symptoms have abated. I am walking long distances again. Suggest that you all have these tests done: FREE T3, FREE T4, and thyroid antibodies test in addition to the TSH test that they will always do. Also, be aware that your TSH test score should NOT be above 2.0. Your docs will erroneously insist that anything under 5.0 is ok. WRONG. My scores were in the 3's before being floxed and in the 4's after. I also take tiny amounts of Cortef for my adrenal fatigue.

I had a shot of kenalog in my knee for a problem I have when I run long distances. I was told that it would have a 50% chance of helping but it could prevent surgeries. He never mentioned side effects. After the injection- my period came a week late and lasted three days longer than normal. Four days after it ended I got another period. This one was accompanied by severe headaches(I never get headaches) This period lasted another nine days. I went for my follow up and questioned the doctor about it and he said he must have forgotten to mention it but that it can cause some hormone irregularities but that it should go away within a month. I have been so exhuasted and barely able to function. It was five days since my last period and now I got another one today! I am furiouse because I was trying to get pregnant! Now I am freaking out because I am seeing on this sight how long this can really last!

After all of us have had these same problems you think we would be able to sue the company. What can we do becuase I'm on board if you all want to have a class action law suit. How do we start it?

I've been using maxide now for over 5 years as a way to keep off unwanted water retention. For the past year I've been experiencing numbness and tingling in my feet and hands which has progressed to severe peripherial neuropathy. In the beginning, it was only brought on while running and I thought it was just a result of my running long distances and perhaps just an electrolite deficiency. I began taking a potassium supplement and continued to run (30- 60 miles per week) without much relief. At this point I am no longer able to run. My arms are numb much of the time and my feet and legs become numb while sitting. I am unable to stop using the drug as I blow up and cannot even wear my own clothes. I have not been able to go off the drug for more than a few days without intolerable side effects. It's changed my life. I'm depressed and frustrated that I can no longer enjoy running which was a major part of my life. Has anyone experienced any similar side effects or have any idea if this condition can be reversed?