Attorneys symptoms and conditions

I took my first pill of Levaquin 500 and started having abdominal pain.later I started feeling cold and shaking for about one hour. My arms and legs were so sore that I couldn't stand straight. Joints hurt a lot..My husband told me that my eyes were rolling and he was scare. Next day I had red dots in my whole body.mostly my legs. I went to the doctor for a blood test and my platelets were 35. Put me on prednisone. week before were 220. Almost sure was the levaquin. Shoud be taken out of market.

I was prescribed this medicine for a breast abscess. I have a bad reaction to penicillin and levaquin was given to me as an alternative. I took the first pill at 11:00 pm. I woke up about every 30 minutes drenched in sweat until 2:00 and then could not go back to sleep. I took drinks of water when I woke up in order to keep hydrated. I have a lap band, and I noticed that the water wasn’t going down easily which let me know the medicine had made my stomach swell. I finally fell asleep around 3:30 and had evil nightmares until 5am. I was afraid to go back to sleep so I decided I'd just stay awake until time for me to get up for work. I will be calling my doctor's office as soon as they open to let her know this medicine is not for me. After reading your stories, I refuse to take it another day.

This is not a new side effect, but the same day I started taking Levaquin for sinusitis, I suspected something was wrong. Within hours, ears were roaring. First night, NO sleep, and that's WITH Ambien CR. Day 2.....depression! Immediate. This is in spite of having a severe depression under control for over a year. Sudden. I really started suspecting Levaquin then, but thought it was a coincidence. Took it this morning. Deep, dark depression. After reading these posts, I knew my suspicions were correct. The depression is getting better after 10-12 hours after the dose. This is really scary stuff. Really scary. Oh, yes, and I had the stomach pains, also. Told my husband it was just hurting like a bruise, not like indigestion or gas. I will report it to my doctor so they will no it's a "no-no" for me....in spite of all the websites that said how safe it was. Glad I found this website. Thank God.

i ave a friend who has just had a bad case of the flu which has turned into pneumonia. her doctor out her on levaquin! i almost had a heart attack, called her and begged her to stop it. i sent her a bunch of info about it. why not put her on augment, something with less chance of adverse effects.
now i find she had a stroke over the weekend and is in the hospital! has anyone heard of anything like this on levaquin?

In addition to all I mentioned in my posting before, I am now having burning skin feeling and my shirt can't touch my skin sometimes without it burning, hurting.

Has anyone heard if this drug leaves your system or not???

so far, no side effects for me. I've been taking Levaquin for 8 days, 2 more to go. Scary stuff you're all experiencing. That's awful!!!

I am a few days away from my 19th birthday and i've been taking Yasmin since the age of 11. I was diagnosed with PCOS when i was 11 and Yasmin has been what's keeping my period regular and more or less pain free since then. In May of 2008 i was switched to the generic version of Yasmin called, Ocella and started to notice more and more symptoms and side effects. My stomach pain in the mornings grew greater by the day and when i was on my sugar pill i would gain an unbearable migraine. Thinking it was just part of being a woman i ignored it and went about my life. It wasn't until December of 2008 while out with a group of friends i came into some serious stomach pain. thinking it was just a typical stomach ache that i normally got i ignored it. when i came to be about 4 am and the pain hadn't stopped i started to worry. first thing in the morning i went to the doctor who referred me to get an ultrasound. The ultrasound showed that i had gall stones and that i should have my gall bladder removed before more complications were to occur. Being a college student only a week away from returning to my second semester i opted to wait until spring break to have the surgery. During the 3 month wait i experience extreme diarrhea whenever something was put in my mouth, extreme stomach pain, heartburn, nausea, headaches, sore muscles, the list goes on and on i felt like i had been hit by a truck every day and i still had to go to class. in March of 2009 i had my gall bladder removed thinking that the symptoms would finally stop i returned to school only to find that nothing got better. It's been 7 months since my gall bladder has been removed and i'm still having the same symptoms as before and now i've added depression, stress, lack of energy and interest and many other things to the list. I'm still taking Ocella because i've never been advised otherwise but the symptoms are taking over my life. I am a sophomore majoring in electrical engineering at college and it's just become harder and harder to focus on my work or to enjoy the aspects of college that i should be with the frequent trips to the bathroom or having to opt out of a fun activity because of stomach pain. I was wondering if anyone can help me, maybe point me in a direction where i can get better and get back to enjoying what a 19 should be. Thanks.

I took Levaquin several months ago and have had on going foot pain. I was recently diagnosed with Complex Regional Pain Syndrome following a Stress Fracure in my heel. I have had muscle aches, all ove pains, bone pain, insomnia, depression, irregular heart beat, headaches. irritability, dizziness,stiffness in my joints, stomach aches. This has all been a terrible ordeal. Do you think it is related to Levaquin. I have also taken Cipro several times for UTI and Diverticulitis. Thanks for listening.

I am a 34 yr old registered nurse and I was given Levaquin for a kidney infection. I was very pleased that by the next day my symptoms from the infection were gone. Unfortunately, after 5 out of 7 days of taking Levaquin I developed pain in my knees, wrists,shoulders,ankles and hands. My hands are swollen and difficult to use even to type this. I am very familiar with Levaquin and give it to patients all the time without even considering these symptoms because they are dismissed as "very rare"! Obviously they are under reported because doctors don't attribute these complaints to the drug side effects. I pray that this pain goes away soon for myself and everyone else. I have learned in my career and in my own experience that though doctors are the ones with the ability to diagnose and treat, WE are the ones that must be our own advocates! I will definitely never give Levaquin without warning patients of potential side effects.

I went to the doctor on 9/11/09, having been sick for a couple of weeks w/ nasal congestion and then developing muscle aches, fatigue, and a fever, along with the new symptom of a cough. My doctor was on maternity leave, so saw someone else in the practice, who hastily diagnosed a sinus infection and prescribed penicillin. Got the beginnings of hives on Sunday early in the a.m., called the pharmacy, discontinued the penicillin. Still had a fever and was miserable, called the doctor on Monday to document the hives for my medical chart, and said I thought it was flu, not an infection. Finally was called back, and they called in levaquin, despite my thought it wasn't infection. Fever had broke finally, and I was making some progress, but figured the doctor knows best and took one dose of levaquin before bedtime. Had horribly vivid daymares/hallucinations and kept telling myself, "Its not real!" Woke the next morning, and could barely move. Couldn't get from the couch to the tv a few steps away and knew I was in serious trouble. Called the doctor and the nurse said they wouldn't see me, no appointments, so my husband took me to the ER. ER doctor said it was a reaction to levaquin, discontinue use, and it would take probably a day to pass through my system. Also said I had a virus, not an infection to begin with. (Horribly ironic, huh). It is now Thursday, 9/17, and I move like a snail. I have no stamina, and can barely walk. I went to work (I'm a teacher) and cried after walking my kids down to art. Am I ever going to feel normal again? This is really depressing. I was a healthy, active person before I took a dose of this poison.

I was give Levaquin when I had a Prostate Biopsy and had a reaction to it , Hives, muscle pain oral thrush ,I told the doctor about it so he gave me another anti biotic,CIPRO which made things worse, then I find out they are both from the same family of antibiotics, these doctors don't know what they are giving you and he said all that I should have gotten from them was a little stomach problem, Its two years now and I still have skin
problems, joint pain and pain in my neck amd the doctors say it can't be from the Levaquin, Well how come I was healthy until I took it

Hi,
I am just looking for a web site that can help me with Levaquin side effects.
I had some of the listed side effects however within 4 days of starting the medication my taste and smell was totally gone. That was in Feb. 09, its now Sept.09 and i got back some smell and taste back but nothing like I
used to. In fact a lot of things taste different than they used to. Can
anybody help or point me in the right direction?

I have been on Levaquin 750mg for an infection in the bone of my toe. I am also on a daily IV drip of antibiotics. Since I have been taking the Levaquin, I ache all over. Every joint aches from my hands to my ankles.
I'm wondering if this is all a side effect of the Levaquin. I have nothing else to blame the aches upon.

I've been on seroquel since 1997. In periods of stress I sleep cook, sleep eat and sometimes sleep drive out to shop for groceries. I just got off the medicine about a week ago while hospitalized. I strongly suggest it be taken off the market. Are the attorneys aware of this side effect?

I cant Walk this crap disabled me! I have nerve damage to my left knee.Dont take this crap.Period It can Kill you.there are a bunch of greedy people making a ton of money on the sale of this crap.We seem to have no Rights??? I was i a lot of pain like someone shot my knee off pain.Plus my lower left leg too all the way from ankle to my Thigh joint.It really sucks too when doctor blows you off.I went and sen another one for second opinion he had never seen a Knee swollen 5 times the size of other right knee.Class action Lawsuit anyone.I,d sign on.I was forced to take this poison.by insurance company.I was on Benicar for last two years.that worked for me.But for costs I was told I had to change over or die was my choices.Well to save a couple bucks its going to cost a lot more getting my extra doctors bills.plus attorneys fees I hope.

I took Zocor for 9 months after I had a heart attack. After about 8 months I began having sever muscle spasm in my legs. I had a couple of episodes where when walking I couldn't pick up my feet and thought I was having a stroke and had to sit down and rest before walking on. I had to do this several times to get where I was going. I told my cardiologist and he had me stop the Zocor. The spasms stopped but I never regained the strength in my legs. Today I have had to put ramps in at home cannot climb steps. The ramp is difficult because of the incline but it is better than crawling up my steps to get in the house. I can only walk about 50 steps before my legs give out on me. I cannot walk on uneven ground without holding on to something or someone. I have now had 2 back surgeries because I have been told over and over it is my back with no relief for the legs. This last surgery my left foot drags and my big toe hangs down and I cannot pull it up. Now I fall a lot because of that and have to wear an AFO to keep my foot and toe up so it doesn't drag and trip me. The back doctor thinks it another pinched nerve and wants to open back up again. I am so tired of them trying to convenience me it is my back when I know it was the Zocor and the damage apparently is irreversible but no one wants to agree with me. I am sick of it and just wish they would say yes it was the Zocor and get you a scooter and live the best you can. I know I am headed for that road I use a walker and cane when I don't have someone with me to hold on to. Because I am so unstable on my legs.

This post is directed to anyone who has contacted me regarding a possible class action lawsuit, which I was trying to initiate, as stated in my Oct 17th, 2008 post.
After contacting as many as 10 law firms, from NY to San Francisco, I have virtually "thrown in the towel". In essence, what they are saying is, this will be too expensive to litigate. The pharmaceutical companies have "teams" of lawyers, and I believe they are reluctant to go up against them.
I find it diabolical that this drug Kenalog is causing so much suffering, some emotional, some esthetic and some, like myself, sheer physical pain...but nothing can be done about it.
For all of you who have emailed me and I was unable to return your ems, I apologize....but I have been waiting to hear something positive feedback to relay. Unfortunately, that was not the case. If anything does develop I have stored your information and will get back to you. I would hope you would do the same.

Hello-
I am here to share my story about topamax in hopes that others may read this and not have to go through what I did. I went on topamax for the prevention of migraine headaches. It worked great to prevent my headaches but gradually I could not talk, I stuttered severely, and I have memory and other cognition problems. At my doctors recommendation I stayed on the medicine for about 6 months because he assured me that the stuttering would go away. I was in such awful pain that I agreed with him. Needless to say that 6 months was not me. I couldn't talk and I couldn't think. Now when I think back on it, I wish I had just endured the pain. When I went off of the medication I still stuttered. It was not quite as severe but it was bad. It effected my work, my personal life, and daily menial tasks. I could no longer communicate. I was devastated. My doctor was puzzled and said that he had never heard of this before. So to make a long story short I went to a speech clinic, bought casa futura techs small talk device, and tried some anti-stutter meds. My speech now, 2 years later, is much improved thanks to the smalltalk but guess what,? I still stutter. Manageable and not very noticeable to others at times but my speech has not returned to pre-topamax status. I looked into sueing the drug company to bring awareness about this issue but did not get much positive feedback from attorneys. IF YOU ARE ON TOPAMAX AND ARE STUTTERING, STOP TAKING IT. IT MAY NOT GO AWAY WHEN YOU DISCONTINUE THE MEDICINE. It is not worth it. You cannot put a price on speech. I don't care what the physicians desk reference says, what your doctor says, what the corrupt drug companies say. I know my experience and it has been a catastropohic effect from topamax. Find a different med if you have speech problems! Please, for your own sake. Thanks for letting me share my story.

DO NOT TAKE THIS POISON!! I have spent the last 4 years dealing with
adverse side effects of this medication. I have central nervous system damage, digestive disorders, anxiety, panic attacks, dizziness, achiness-it feels like a really really bad flu. My dad who is a doctor didn't believe that Levaquin was the cause at first however he had a chemist look up the compound makeup and was told to never prescribe this or any other fluoroquinolone again (cipro, avelox, etc!) Side effects can last long after you finish this medication. Also animals can get this stuff so it can be in the meat you eat which will make you feel worse or it could kill your beloved pets. Do your research. Warn friends and family-even strangers. Make a mediwatch report. Helpful sites if you are dealing with poisoning.
There is also a yahoo group.

As a Doctor myself I think drugs are NEVER the answer except in EMERGENT issues in Heroic life saving... YOU however and all individuals are and should be MORE accountable for your own health and STOP DEMANDING the Drugs and look to LIFESTYLE changes in DIET and EXERCISE to achieve the GOALS so necessary for quality and quantity of life.... The tools are at your fingertips ... The almighty internet ... And your OWN imaginative mentation is your TRUE limitation... So TAKE control of yourself and BE accountable .... Sorry so blunt but MORE tough love and Educating people is whats needed.... NOT more drugs....

MDG

I aged ten years in a month. My legs lost any muscular power and I needed help to get up our 3 steps to the front door. My eyes are sore and my balance is also affected. What I do not know is how long am I going to be affected like this. I began to think that I was starting with either motor
neurone disease or Parkinson's disease.
Muscle weakness, loss of balance, bad dreams,anxiety, irritability.joint pain.sore itchy eyes and difficulty focusing on printed pages.
A., Yorkshire, England.I am 69 years old and prior to Singulaire I was pretty fit for my age.

I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch. I urge others to report their adverse event to the FDA--just click on this link and complete the form: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities. Such documented cases and recognition by the FDA will provide leverage for attorneys in pursuit of a class action suit.

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

I had posted my case on May 17th on this blog--as I noted, I URGE others to report their adverse event to the FDA--just click on this link and complete the form: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities. Such documented cases and recognition by the FDA will provide leverage for attorneys in pursuit of a class action suit. Also wanted to see if anyone has contacted a lawyer on this issue?

-- By slmgator | Reply | (3) replies | Send Private Mail

This was a post from a lawyer back in April 2006 that I found. Please read:
"I am the lawyer that sweet Julie (below) was talking about. Anyone who is interested in talking with me, I would love to talk to. I too had Mirena and suffered terribly from it and would love to hear your story if you are willing to share. The more that we have, the more likely that something can be done about it!
Please write at ****** with any questions/comments."
No one responded to this post, unless they did it privately.

Then i found another page that ticked me off. It is below. If the link does not come up, I can email it to you.
******
back in the 80's and 90's, some IUD failed as well, causing sickness to many women. They settled but it was an extreme case of absolute malfunction. Since then, these types of lawsuits don't really go anywhere. I think they are stupid! No one listens about this Mirena being so terrible. I have been searching and have not found anything yet. I'm glad I took it out but I have to recuperate. I should not have to be recuperating from anything.
Anyone found anything on a class action suit???