Class action law symptoms and conditions

I posted back in August or September 2008. I FINALLY had my Mirena removed and when I say FINALLY, I mean FINALLY. I went in late October to have it removed only to be told that it could not be located. I then had to have an internal ultrasound to locate the IUD. Thankfully she found it, but I was very scared of the pain of removal that I talked some more with my OB about it and decided to wait until the New Year to see if my symptoms had subsided. My symptoms were namely the horrible acne I started having after insertion. My periods at this point were non-existent, which was nice, but as a 37 year old woman, the acne was more than I could handle. Come 2009, the acne was still there - and when I say acne, I mean acne. I mean hard cystic acne that turns red and does not go away with time and medication. I have been a Proactiv advocate for a long time and sadly not even Proactiv was managing my acne on the IUD. So . . . January I went in to have the Mirena removed. The doctor knew it's general location and tried to remove it. She could not locate it and the procedure was extremely painful. Long story short, I had to undergo out-patient surgery and be knocked out to have it removed. I'm back on the Yaz and am already noticing a difference in my skin!

If you ever struggled with acne during your teens and early twenties, I would think twice about the Mirena. I struggled with acne and was finally at a point where my skin was "maturing" and the Mirena made me feel like that 14 year old with horrible skin all over again.

IMPORTANT INFO FOR ALL OF YOU MIRENA USERS: It is true. There is a class action law suit against Mirena for your side effects please call 850-916-7450. They will ask for your name and number at first. Then someone will call you back asking you for your name and address and your side effects so make sure you make up a list of every side effect you ever had or are having. They told me that they will be calling me back in 5-10 days. Good luck to all of you!!!!!

Hi ladies! I have had Mirena for about 6 months, and at first I did have constant bleeding, but then it stopped and I would have normal periods. I never experienced the depression I have now. I do suffer from an anxiety disorder, but have never ever felt this type of depression before. I don't want to parent my little girl, go out to do things, be at my job, etc. The worst part is the feelings I have about parenting, and I think I started having postpartum depression again. I did not have these feelings right after having Mirena inserted; but have for about 2-3 months now. I am on other medication for anxiety, but I don't think this depression is being caused by my other meds. Have any of you felt this way? Thanks for reading.

For me having the Mirena removed just last Thursday was the right decision. I was not using it for birth control but as hormone therapy for heavy, crampy periods. I had it inserted in July 2008 and bled every single day for the entire time, I had it removed last week and now I am bleeding very heavily but hopefully that will stop once all those hormones are out of my body.
While on Mirena I lost all sex drive, I became severely anemic and with that fatigued terribly, and moody, crying at nothing and screaming at my kids or husband for stupid reasons, I felt bloated and gassy and didn't have those problems before.
I am 42 years old and I hate my heavy bleeding in fact I want a hysterectomy, but not sure now what I will do.

For those of you who had the Mirena removed, how long did it take to stop bleeding afterwards? This is draining every last ounce of energy for me and I am taking iron supplements.

What sucks is the cost of this, Even with insurance I ended up paying a lot out of pocket to get this thing and then all the Dr. visits due to bleeding and side affects in the 4 months it was in and now the removal of it. I am wondering if there is any way that we can get a Class action lawsuit against Bayer for this horrible thing they are trying to sell to women.
I know there are some out there who have not suffered all these horrible side effects at least not yet or that they are aware of, but I truly believe that there is nothing good about this IUD and those of us and there are a lot of us who have suffered with this should be reimbursed or compensated for the pain and loss of parts of our lives and expenses with this. Does anyone else have any thoughts on this?

I have been making inquires as to how and if the fda will conduct investigations in to permanent damage left from this drug.Although on taking my son off this drug i saw a 90% improvement,i am still missing the final piece,is it that he lost 3 years to this drug or did it do damage that cannot be fixed,we as parents need to know.The FDA responded to my letter,they said if they see a trend in reports from medwatch,it may prompt an investigation .I am asking all who still have missing pieces to file a report.What has happened is a tragedy,we need to explore ever option for continued success for our childrens future.Good Luck to all,Keep Fighting

I was wondering if anyone knows if there is a class action lawsuit against Yasmin.

I started taking Yasmin last October and the first three months I was on it, I was bleeding every day. It was the first time I ever got on a birth control pill. I stayed on the pill for a total of 6 months until one night I suddenly had severe abdominal pain along with nausea. It went bad from worse and I was rushed into emergency room later that day.

My diagnosis was acute pancreatitis due to high level of triglycerides. The doctors ran a series of tests, blood, ultrasound, CAT scan, and X-ray, etc. Their conclusion was Yasmin caused the dramatic increase of my triglycerides, and ultimately caused my acute pancreatitis.

My triglycerides level was below 200 before I started taking Yasmin and by May this year when I was diagnosed with acute pancreatitis, my triglycerides was over 4,300!

After spending 3 weeks in hospital for pain control and being off food and water for a total of 2 weeks, I was able to go home and get on with my life. My doctor told me I should never take any form of birth control pills nor any kind of hormone. I stopped taking Yasmin since the day I was admitted.

If anyone knows of a lawsuit or a lawyer that is working on a case against Yasmin, please let me know.

I have contacted an attorney in Delaware who is willing to pursue a possible class action suit. I explained my side effects from this drug and told him of the countless others that are suffering as well. He said if I was willing to do the "legwork" and gather up names of others who would like to join this suit, perhaps we could get a class action started. If anyone is interested please reply by contacting me at ***** Please be sure to type "Kenalog" as the subject and include your name, email address, and a description of your experience with Kenalog. I will than gather your responses and forward them to the attorney. He will than contact you individually, so please include a contact number. This will take some time. So please be patient, as you know these cases take time. I have spent 15 months trying to get some kind of help from various doctors, to no avail. Someone needs to step up and take responsibility.
Hope to hear from many of you. Thank You

i took cipro for a UTI over 10 years ago and have had floaters, neuropathy, tingling, and numbness in my hands and feet ever since then. it was not until THIS YEAR that i stumbled upon information on the internet about CIPRO and its side effects. but immediately following my use of the drug i went to a doctor who insisted i had carpal tunnel and i asked then why is it in my feet? then a neurologist who found nothing and patted me on my little college girl head, told me it was "just stress," and prescribed me narcotics to calm me down. i threw the prescription in the garbage on the way out of his office... then was tested for diabetes and briefly thought i might have MS. eventually, after many docs finding nothing and my family thinking i was a total hypochondriac, i just decided to ignore the symptoms. pain in my joints, floaters in my eyes, numbness and tingling in my hands and feet. after years i figured if i wasn't dying from whatever it was and it wasn't getting any worse, then i would just live with it. one day when it was particularly uncomfortable i did an internet search and came up with CIPRO info. there was a class action law suit at one time because right around the time i took CIPRO, it was a new drug and had not been sufficiently clinically tested. there's no recourse for me now, but i feel better having solved the mystery.

i am appalled to see so many people still suffering in 2008 and this drug still being prescribed. i'm sorry you're all going through this. i tell everyone i know not to ever take this drug. i feel lucky to be still functioning. i am very healthy, just have the annoyance of these symptoms that never go away.

I had nuvaring in for two years, developed a blood clot in my lung, almost died, and the only trigger the doctors can come up with is the nuvaring.

I took Levaquin for a sinus infection and my left arm completely froze up and I had to have two cortizone shots in the arm to get it to move. That was in February 2008. I told the Doctor about it and she didn't think it was Levaquin and I stopped it and got better than started it again and same thing again, my arm was paralyzed. My arm is better, but I am always in pain. My right arm had problems as well, but not as severe. Once I quit the Levaquin my right arm became normal. My left arm will never be normal again.
I think there should be a class action law suit!

Nancy B.

I don't have a side effect to post THANK GOD. I want to thank all of you for posting your comments. These comments help people like me make more informed decisions. Our Doctor strongly encouraged my husband to have our 3 daughters receive this vaccine. I am so glad he waited to ask me - I have long been angry at the Government insistent on vaccines that don't seem necessary. In any case my research landed here along with a web site from a law firm looking for more more victims in the class action law suite they are waging. Many of you should call them. Also, a news article that was shocking on the subject. In this day and age any medication or vaccine should be researched on line with a buyer beware attitude - NOT through your doctor!!! I have seen many cases of drugs that cause side effects that doctor's and laboratory's say couldn't possibly happen.

I had the same steroid injection for tonsillitis this past January in both cheeks. I now too have noticed a large indentation in my right butt cheek. I was never informed of this possible side effect either. I would definitely be interested in pursuing a class action regarding the disfigurement of my previously favorite body-part. Had I been informed of such, I would have just had my tonsils removed!!

My BP had been slightly elevated for over a year and my doctor felt it was time for medication. He started me on 25mgs and continued to increase it till I reached 100mgs. I started having anxiety attacks, lightheadedness, dizziness and finally ended up so sick that I was in bed for three days. It was the toprol. I was only on toprol for 3months but found out that trying to come off the drug was the hardest thing I have done. I never had BP spikes before but at the end of the first 24 hrs. without Toprol my BP was hitting 200/104. I went to ER. Matter of fact, the spikes continued and I was in and out of ER until I was finally admitted for tests. The spikes were also accompanied by flushing, rapid pulse(122 beats per minute), lightheadedness and diarrhea.Many times I thought I was having a heart attack. I have seen two cardiologists, an internist and now an endocrinologist for these "BP spikes". All tests come back normal. No matter what the new medication is, nor how low my BP might stay for up to three days....the episodes still happen. My BP can go from a normal range too 200 systolic in a matter of less than 1/2 hr..........Has anyone else had spikes in their BP when coming off toprol. It has been 11 months since stopping this awful drug and I still I no answers....but I have a pile of medical bills.

Thank you very much for posting your experiences. My wife has the same adverse effects with nuvaring. We're gonna remove this thing asap. She has been so depressed and cry all the time for nothing since she started nuvaring. Her antidepressant are not working at all. Her sex drive has decreased substantially. She is getting panic attacks for trivial things. I am so pissed of with this worthless contraceptive. Somebody should file class action law suit against nuvaring.

Thanks friends for sharing yr experiences.

I am also a victim of having the Kenalog injection administered over 8 months 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. It is 8 months later and the indent appears to continue to deepen and lengthen. 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.

HI, i too have to say i am kind of relieved after reading this website that i am not alone with my experiences of the kenalog injection. I was given kenalog injections to treat hayfever, although i wasn't told the name of the injection. They did help and i probably would of continued this year if it wasn't for the side effects.
I was told that to have one a yr was safe, then just before xmas i noticed a dent on my hip, this started getting larger and looked almost like scare tissue, I too was worried i had some sort of flesh eating disorder. The dent is still there and i will never have that injection again. I also have been experience problems with my hips and pain around my coxis,i am not sure if this too is related to the injection. I was told by my doctor who is very good that the kenalog had eaten my fat tissue causing a dent and that it will get better in time.

I am on Femcon right now and today is my fist day of my brown pills. I have been nauseous for the past three weeks consistently. The hot flashes during the night started a few days ago and culminated in sleepless night filled with waves of emotional surges such as fear, sadness, and of course anxiety. My mouth has been dry for the past couple weeks. I have not gained or lost any weight, but I am also quite careful of what I eat. I have been spotting for the entire month. I would say my energy levels have also decreased and I have been more irritable in general. I will no longer taking Femcon and feel that I have been given a medication that caused my moderate to great difficultly. I am almost tempted to head up a class action law suit, as I have lost sleep, missed work, and struggled with too many issues to just forget about this. If anyone else is interested, please keep posting. I read the Femcon website and I do NOT see any of these side effect listed anywhere. Did I miss something?

I'm a 46 years old male normally good shape,I was put on Lipitor due to high cholesterol and family history of heart problems.I've been on lipitor for four years , 2years on 10mg, 1 years on 40mg and 1 year on 80 mg.
The last 6 months I have been experiencing severe archiles tendonitis to the point where I can hardly walk. I am extremely disatisfied with this drug and have read a lot of complaints regarding this drug.

Has anyone else experienced this side effect?

Please reply to this post.

Thank You

HI. I googled "class action law suit singulair"
This web site came up
http://class-action.legalview.com/
They have lawyers that will contact you. I contacted one via e-mail to see if there was one started, or how to start one. There was also another link on Google that referred to this legalview.com page. I let them know via my e-mail there were hundreds others just like my son. We shall see.....

My 11 year old daughter has been on the 5 mg chewable singulair for almost 2 years. She has changed from the shy, sweet, I love you and will not hurt your feelings child to a moody and negative person. She has recently said "nobody loves me" and "I wonder what the world would be like without me in it". We should all show them what it is like to live with depression and file a class action law suit.

I have taken Levaquin 500 mg daily for the last 7 days. I am quitting it today! I am so tired. Cannot sleep! Have severe pain in both of my hips! I do not have a history of sleep disorder or hip pain!!! I even have severe pain in both of my shoulders now as well. My doctors insist this isn't from the med. My pharmacist differs in that opinion!! This stuff is POISON!!!
I am a registered nurse and will preach this to any and everyone who will listen!!!
I only pray I will not suffer a tendon rupture even after I have stopped this med! If that happens I will contact an attorney! Can we get a class-action lawsuit for all of us and to prevent others from this terrible experience???

I am new to birth control. Last week was my third week on Yaz. The first 2 weeks on it, I was fine. No real symptoms, but the third week, I began having anxiety (which I have never had before) and my heart would race every now and then. Also, I had a major loss of appetite. I would have to make myself eat even though I felt like gagging. I would try to go to sleep, but the anxiety would be too bad. (I took my pill at 8:00 every night) So, I stopped taking them. Yesterday was my second day off of the pill and all I wanted to do was sleep. (I guess from the lack of sleep due to the anxiety/panic attacks) Today my appetite is slowly coming back.
I contacted my GYN and they said they have never heard of those side effects from Yaz...but I looked it up online and there are tons of women complaining of the same thing.
They now want me to try Loestrin...which I am very hesitant of. I don't want to get my body back to normal and then start with the same problems again.

I am getting married in October and of course we don't want a baby right away....I must say...the old school condoms are looking like a better option every day!

I to have a huge dent in my right butt cheek. I would be interested in a class action suit. This is ridiculous! It has been about three months since I received the shot. Has anyone noticed their dents getting better with time?

I have recently discovered that I too have had a major side effect from this drug. I only received one injection 5 months ago in the buttocks for an allergic reaction I was having and now I have a huge indention like crater in the area that looks like the tissue has been eaten away. I did not even know it was from that since it has been a while and only one shot. After finding this website and talking to my doctor's office. They did confirm that the shot given was Kenalog and in that spot which I was certain of after reading so many others who have this side effect as well.
I am very interested in joining a class action lawsuit. People need to be warned of these major effects. I would have NEVER allowed the injection to be given had I been warned.

I went on levaquin-2 rounds of it, due to pneumonia. I felt very out of sorts and discombobulated. Dizzyness, word recall problems, insomnia, diahrrea. My tongue was coated with a thick white film. One night my tongue and my hand felt very disconnected to me, and I had a strange but familiar taste or sensation in my mouth but I couldn't name it. It lasted 3 or 4 minutes. I think I may have had a petit mal seizure. I have been having trouble with my vision, things I read are blurry now, and I have never worn glasses, or had vision problems before. I have been off of this medication for 6 days now, and I am still feeling some of these side effects. I rarely have any side effects from medications. I will never take this again.