Class action lawsuit symptoms and conditions

OMG!!!!! I am a Registered Nurse and still didn't know so many women (including myself) had these extreme side effects from this awful thing. I had a miscarriage back in March and chose Mirena as my birth control afterwards. Every since then I have felt like I was going (or already gone) insane. Like the original poster, I have EVERY SINGLE SIGN AND SYMPTOM!!!!! I haven't slept more than 2 hours at a time since, My bra size before was a 36C, I am now back up to 40E. Which is larger than they got after I had my son and was breast feeding him. I have the pregnant belly, mood swings from hell, hot flashes, off and on cramping (especially after sex), acne that has scared my face, bouts of awful depression, unable to concentrate on anything, lower back pain, nausea, and I always have this feeling that I'm pregnant. I also gained a whooping 25 lbs which is impossible since I had gastric bypass surgery 6 yrs ago. Just like many of you I stepped up the exercise and modified my already limited diet. I truly wish that I had stayed on Depo-Prevera. I plan on having this thing taken out of me this week. This awful "demon" needs to be taken off the market. I guess all of us that have had these extreme side effects need to be on the look out for a class action lawsuit. No woman should have to go through what all of us have been through. To those of you that have already had it removed: Did you lose all the weight that was gained after the Mirena placement? If so, how long did it take??? I'm so ready to be normal again!!

I finally stopped taking Topamax because of the side effects. But the worst was getting kidney stones from it. I only drink water and drink a lot, but I still got stones. The first time I was in so much pain that I could barely stand it. The second time, I had the pain and with it a kidney stone that was too big to pass. I could barely urinate. Had to have emergency lithotripsy to remove it. The doctor did a CT scan recently and it showed I still have many stones in both kidneys. I can't take another one of these attacks because they are so painful. My neurologist gave me a natural remedy for migraines called Petadolex. This stuff works! It has made my headaches much less severe when I have them which is not very often and my daily low level headaches are gone. This stuff is made in Germany and can be found in most health food stores and pharmacies. It also cost a lot less than Topamax.

When the generic Topamax (topiramate) came out, my insurance company wouldn't cover the real Topamax and it was costing me $400 a month if I wanted it over the generic. The generic was the worst drug I have ever taken. It is NOT the same as Topamax. I got so ill off of it that I had to get back on Topamax. I am finally off of Topamax completely after decreasing the dosage over many weeks. I was on 200 mg a day. I had all the side effects too like tingling hands, cognitive impairment and depression along with some others. This drug is poison and I am so angry the manufacturer didn't state all the possible side effects when they knew damn well it had them. There is a class action lawsuit against this manufacturer for not disclosing some of the horrible side effects.

After you read a representative sampling of this website's testimonials, you certainly ask yourself inter alia: Can this be true? Did thousands of people inject an antibiotic from the fluoroquinolone family, which crippled them for longer or for shorter? Most of us, I suspect, never really get beyond the initial litmus test: Did this medicine poison me or save me? (The answer depends, of course, upon the age, gender, medical condition, and most importantly, the DNA make-up of the individual patient. For hundreds of thousands of patients this antibiotic is a boon. For thousands of other misfortunes this antibiotic is a disaster.) But there is another important question here.

Who gains from self-revelation? To be sure individual sufferers gain certain emotional catharsis from posting their adverse drug reactions (ADRs) to levaquin. E-postings are one-way anonymous tracks that form ruts on a well-traveled trail of tears. Unless these postings are hoaxes written by mischievious gnomes, then they consitute prima facie evidence for a causal link between levaquin injection and sundry crippling ADRs.

Curiously, this e-forum cannot be used as a tool for organizing thousands of potential litigants who might coalesce under a class action lawsuit. Yes, we can analyze each other's anonymous revelations to see if they muster our respective sense of the "ring-of-truth" re: levaquin toxicity, and we may contact each other one-on-one, but no-one can harness this intoxicating communication's technology to reach simultaneously all respondents en masse as a bloc.

So, who wins? The emotionally unburdened e-poster who learns belatedly that s/he is not alone and that prescription medicine likely caused more pain than the underlying malady for which s/he is being treated? Or big pharma that continues to manufacture and market a medication that poses downside risk to many consumers who unwittingly incur more damage than therapeutic value?

Indeed, who wins in a forum where consumers anonymously reveal their symptoms and unconfirmed suspicions? The answer is big pharma wins. Pharmaceutical companies data-mine our postings to estimate the frequency and bredth of ADRs about which consumers complain. House statisticians estimate the ratio of active complainants : silent complainants, i.e., the ratio of complaints who show up on this website to the far heftier percentage of complainants who never post on this website because either they are technology-challenged or they are incurious. House actuarians proceed to estimate how much operating profits their employers must set aside to cover losses in out-of-court settlements or in awards made to plaintiffs in class action lawsuits.

I think this is how the game is played in a behavioral sink where billions are made in a deregulated marketplace that allows predators and prey to interact anonymously. Sorry to be such a downer, but I fathom only the desperate plight of tens of thousands of levaquin consumers for whom no monetary award ever will compensate them adequately for their suffering, and the hundreds of millions of dollars at stake in court awards if consumers ever brought to bear their aggregate numbers and draw a bead on their big pharma tormenters.

I think it a true horror and shame that pharmaceutical companies have not devised a test which determines in advance which patient safely may consume levaquin and which patient's DNA places him or her at risk. I suspect the genome technology is available, but would dig too deeply into big pharm's bottom line. The economics of "parachutes-for-everyone" is infeasible. We are all guinea pigs in a B-grade movie featuring Russian roulette, billion-dollar pay-offs, and an FDA that pretends not to know.

I'm so glad I found this website - thanks to all of you who have shared. I had a Kenalog injection in May 09 and about a couple of months ago noticed an indentation in the side of my leg. I had it given in my leg instead of buttocks due to other health issues currently going on. It is sore sometimes and hurts sometimes when I bend down or exercise. I also had abnormal periods for several months and didn't realize that it was related to the injection. I had a sinus infection/ear infection and had to get on a plane to go out of the country the next day, otherwise I would have never done this. No one mentioned (or I think knew) anything about the possible muscle/skin side effects. Does anyone know about a class action suit regarding this? I've already made a report with the FDA. I am working with a dr that is doing soft tissue work on it weekly, this does seem to be helping, the indentation decreases quite a bit, but it the indentation increases if I don't have the soft tissue work. I'm hoping I won't have to have plastic surgery to fix this, but looks like I will looking at all the other postings. Does anyone know of a class action law suit regarding this? I tried the person listed in Delaware's e-mail listed on the posting, but it wouldn't go thru.

****KENALOG CLASS ACTION LAWSUIT****
Need a list of people that want to join Kenalog class action lawsuit A.S.A.P Please email me with name,state and all side effects. Include if you were treated for the side effects from a Doctor and/or hospitalized.
******

I am a 25 year old female who at 24 had never had any experience with birth control other than a quick prescription to a generic hormone to take care of a long period at 16 (due to stress.) Only a few pills were taken and I was fine. Now, at 25 I have been on YAZ for a year. I began taking it because I became sexually active at 24. Why? Well, I was mature both mentally and physically. I have had friends who became sexually active at a young age and who started birth control young. The side effects were pretty dramatic. I had seen a slim friend gain a whole lot of water weight. She even said it was the patch and later monthly injection causing the problem but the side effect was well worth the pregnancy prevention. I was against the use of birth control due to my preconceived notion of horrible side effects. However, once the monogamous sexual activity began I knew that I needed to take something. I had heard about YAZ and knew that it was something new and different. A different hormone used for prevention. I researched the pill and looked into any side effects. The posts I found seemed a little too ridiculous. I decided to find actual accounts and spoke to a co-worker who had been using YAZ for awhile. In fact, the majority of females I know use the product with no problem. Thus, after my yearly checkup I requested YAZ. My gyno welcomed the suggestion and even gave me several packs for free. It’s been a year without a problem. However, this morning I was hounded by my mother because there is a warning and lawsuit against YAZ and YASMIN (seen by a commercial-lawsuit.) This is due to severe side effects and death associated with blood-clots (when presented with heart disease, diabetes, etc.) I am a healthy 25 year old that frequents the gym weekly. I do not smoke. I drink every now and then. NO SIDE EFFECTS. My period starts after the 3rd pill is taken. It is quick and simple. I enjoy being able to plan things around my period. Cramps are light compared to what I use to go through. I can take one Ibuprofen the day of the third non-active pill and not feel a thing. I use to have horrible leg cramps and now I have no problem. My pre-menstrual mood has improved and I think it is because my period is no longer a strong factor in my life. I use to dread it and now I welcome it. I do not have any skin issues, no bloating, and no weight gain. Heartburn occurrence which is slim to none is similar to what I would have had before YAZ. I was appalled to find this site and to discover that people are having problems. I do not understand why people are so quick to blame this pill on everything. It seems like a lot of users who are posting on this site are extremely young. The body is still growing and maturing at 18 and even into the early 20’s. In my late teens, I was extremely moody and stressed due to college, etc. Any hormonal regulation then would have probably put me overboard! I am going for my yearly check up next month and will discuss this lawsuit with my gyno. I am concerned about this lawsuit. More importantly, I am concerned that this pill will be taken off the market. Call me a statistic but I like YAZ and would recommend it.

There is a class action lawsuit for anyone that took Yaz/Yasmin birth control. I just saw the commercial the other day from an attorney in Denver and it's nationwide. Please call Nolan Law Group - Valerie Romo at 888-630-9340. They are handling it nationwide.

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.

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

I had been on Yasmin for about three years, and just over a month ago I had a blood clot in my brain that caused two seizures. If any one has information on a class action lawsuit, I would greatly appreciate it.

I had a little case of pneumonia and the doctor prescribed avelox to me. since the first day i took it i experienced numbness in my legs and i was feeling very weak, i thought those symptoms were from pneumonia so i continued to take avelox. after taking avelox for 6 days i saw my doctor and i told him about everything i was feeling, numbness in my legs and arms, tingling in my whole body(even my lips), and i felt very weak. my doctor gave me some tests and everything seemed to be fine. but i kept feeling really bad, i started to get chest pain. i went to the ER and they ran some tests, they told me i was fine. they told me to go to a neurologist. later that day i read on the back of the prescription and i saw that everything i was feeling i saw as side effects on the prescription. By the time i saw that i have already taken all of the medication. now i'm waiting to see when the side effects will go away. i wonder why any of the doctors i went to didn't know these were side effects from the medication, i will never take this medication again.

I had a 103 fever Thursday went to my doctor Friday she prescribed this to me and I started taking it same day - that day - hardly any side effects until later that night...took a shower and I looked like I had spider webs all over me - then the real fun started...I started to swell up, I have not slept since that first night and needless to say, I have stopped taking the Avelox now. My fingers are so swollen they are like coctail weenies and it is hard to type - my legs are so swollen it hurts to wear shoes and I have bright red dots all over from my knees down. Is this permanent???? I'd rather not have this look for summer. : ( I feel like I am all "craked out" for lack of a better term but I am exhausted form the no sleep, etc. Oh yeah and the best part of this whole thing, I am so itchy I want to peel my skin OFF. Who the h*** lets this remain on the market?? Better yet - why do doctors keep prescribing it knowing all this - oh yeah I forgot MONEY...
I really hope all of this goes away? I am terrified cause most of the posts I have read thus far say most people deal with this for weeks +!!!!

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.

I was so glad to find this website. I was feeling terrible after having the Mirena in for around a year. I started looking online when I woke up several days in a row feeling so bad and nauseous that I was worried I was pregnant!

I was very fatigued, achy, having trouble sleeping, having strange acne breakouts on weird parts of my body, terrible abdominal cramps - yet no period, bowel problems, VERY slow to heal my sports strains/sprains, nauseous, random headaches (and I have NEVER been prone to headaches), odor, crotch drop, hair loss, forgetfulness, BAD mood swings/depression, dehydration. I looked and felt like I had aged 10 years...All this time I was blaming it on having a two kids, getting older, stress, etc.

Well, thanks to this site, I had my Mirena removed last week. I had no ill side effects from the removal and had a normal period for the first time in about 6 months. I felt incredibly better in a few days! I have more energy, I have slept much more soundly - the dark circles around my eyes are diminishing and I look much better. My routine bumps and bruises from soccer and taekwondo are healing at a normal pace and I don't feel achy all the time. Basically I feel great, and I hadn't for a long time. I feel like myself again.

If you have ANY of these symptoms that everyone is talking about...don't write it off to anything else, and don't let your doctor tell you it's due to other things. You know your body and what is normal. If you are wondering at all why you feel bad - get the thing OUT and do it NOW! (My GYN was very understanding and compliant to my request, but still insisted that my symptoms were most likely due to stress than anything else). At least you will have peace-of-mind knowing that you eliminated the IUD as a cause of your symptoms. You can always have a new one put in if you find that not to be the case.

I hope this site is correct regarding the class action lawsuit, because I am seriously considering joining it. Mom's have it hard enough without this IUD complicating their lives further!

My daughter was on Yasmin for about a year approximately 3 years ago.She constantly felt ill and was always at her regular doctor with excruciating head aches, dizziness, respiratory problems, bladder infections, kidney infections etc etc.A battery of tests including CAT scans etc showed nothing.Then came the manic mood swings, depression, rage and severe panic anxiety attacks which grew worse over time.(We are talking about a former gymnast who lead her team to the State finals in H.S. and used to be cool, calm and collected tumbling on a 4inch wide balance beam 4 feet off the floor!) She finally stopped taking Yasmin after I spoke with a gynecologist I met during mutual sports activities our children shared. He told me to get my daughter off of Yasmin immediately. It took about 6 mos. before she was close to being back to normal. Taking Yasmin caused a number of issues for my daughter - some of which I believe she still deals with today in the aftermath of the effects of this drug. PLEASE if there is a class action lawsuit against these people for putting this out there, she DEFINITELY needs to be a part of it and retrieve some sort of compensation. Thank you!

Okey-dokey. I guess they deleted my post because I included my email address. So here it is again...

There is a class action lawsuit in the works against Bayer pharm. regarding Yaz & Yasmin. There are many women you have had heart, lung and/or thyroid problems, myself included. If you are interested in more information I can put you in touch with the firm conducting the lawsuit. Please send me a private message.

I got my Mirena removed two weeks ago after seven years of carrying it around in my uterus. I had horribly painful periods before (like vomiting and fainting from the pain horrible), so I was glad to be rid of that.

What I'm not glad about, however, is the thick black BEARD HAIR that I've developed (which returned after expensive laser treatments), losing about a quarter of my previously thick hair (now I have to wear extensions to appear somewhat normal), and walking around for seven years with acne, a pooch that had me constantly pregnancy testing, hoohoo odor that sometime persisted despite bathing AT LEAST daily, and oh, the wonderful gas, bloating, and bowel irregularities that caused me constant anxiety in the tiny, quiet house I live in with my boyfriend.

Then there is the chronic pain for the past two years that they can't find the cause of - could this little miracle have anything to do with it?

I've brought these things up to doctors, all who knew I was on Mirena, and was always blown off. But it's obviously related, along with the my eyesight now being that of an 80-year-old, my very own snowstorm of dandruff no matter what I wash with, and, quite possible, the depression that no medication makes a dent in. None of which I had before Mirena came waltzing into my life.

Here's hoping for a return to normal now that it's out, and perhaps a lucrative class action lawsuit in the future that nets us each at least enough to get electrolysis and a hair transplant.

I THINK WE WERE DUPED!

Is anyone thinking that the drug company knew all of this, and therefore has been marketing specifically to women who have just given birth... this way, the postpartum symptoms are the scapegoat:

bleeding
cramping
hair loss (very common 3 months after.. I believe I lost more than most)
insomnia (very common after delivery due to motherly hormones have
you on high-alert))
No sex drive (because we're either breastfeeding, hormonal, or just feel
fat)
Mood swings (because of our ever-changing post-partum hormones)
depression, crying (must be Post-Partum Depression!)
Joint pain, back pain (we're carrying our new baby around too much)
Bingeing and Food cravings (we're home alone and bored or
breastfeeding)
No sex drive (we are bitchy, unsociable, depressed, feel overweight and have no energy.. I'm surprised they still want to have sex with us?!!)

I was 19 years old when I was put on Yaz. About 1 year after using Yaz, I had my gallbladder removed. My gallbladder was diseased and the doctor told me if I was to wait any longer it could have possibly ruptured. Then 3 months later I had a softball cyst removed from my right ovary, and use told that I now have endometriosis. Then 6 months after that i had another cyst the size of a grapefruit removed. I am going to school for nursing and while on the Yaz pill I always thought I was a failure and that I would never make it through the nursing program. I was always having mood swings, depression, bad headaches, stomach problems, bad back pains, and ovarian cyst always popping up and growing. If someone could please let me know how to contact someone about the class action lawsuit it will be very helpful. Thank you

google the class action lawsuit for mirena. i joined in. so should you. it has ruined a part of the happiest time of my life. don't let them get away with it.

I had the shot administered in my butt On November 2008. I now have a huge indent, on my butt, t is also discolored. This is ridiculous, we need to file a Class Action Suit, and have this shot off the market.