Class action suit symptoms and conditions

I have had COPD for years and treated with daily prednisone and Foradil but I wanted to come off prednisone so used Symbicort and Spiriva and was doing good until a new doctor put me on Advair 250/50 and my body went to h... I had terrible bronchitis with hacking cough for 5weeks, noise when on exhaling, severe leg pain, blurred vision, flu like symptoms and harder to breathe. Came off off Advair and felt better the next day. Saw another doc who yelled at me for stopping it but by the weekend I couldn't walk 5feet and this was using my oxygen machine. Stopped Advair and saw my regular doc so I'm back to my original meds and recovering. Yes, I think doctors get a kick-back and yes, there should be a class action suit.
Everyone......take charge of your own body!!!!!!

Wow, reading this is very scary. I also had a steroid injection about 4 months ago. It is in my lower back/upper buttocks. Now I have an indentation the size of a quarter and pain when I sit down for any period of time. I was searching for what it could be and found this site. My heart just sank. I called my doctor to see what he injected and sure enough, Kenalog. I am so upset about this and feel too uncomfortable to even wear a swimsuit or go to the beach anymore. I am very thin so this huge hole in my butt is very noticeable and people notice it all the time. It looks terrible, and from what I am reading it can get worse! I would love to be part of a class action suit against them, if anyone has any information please contact me with it.

HEADACHES,NAUSEA,MAJOR HAIR LOSS,EXTREMELY DRY SKIN,GALLBLADDER REMOVAL,FULL HYSTERECTOMY,PANIC ATTACKS,MOOD SWINGS,STOMACH/DIGESTIVE PROBLEMS,PARANOIA,NEAR LOSS OF JOB,PROBABLE LOSS OF MARRIAGE,MONETARILY DEPLETED,SHORTNESS OF BREATH,HEART PALPITATIONS,VISION TROUBLE,CHILDREN TRAUMATIZED,LOSS OF ENERGY,NEED FOR THERAPY,CURRENTLY USING THE CLYMARA HORMONE PATCH. I WAS ON THIS YASMIN DRUG FOR ALMOST FIVE YEARS, AND SYMPTOMS STARTED ABOUT 2 MONTHS AFTER I STARTED ON YASMIN. I WAS PUT ON YASMIN TO KEEP OVARIAN CYCSTS FROM BURSTING. I FINALLY TOOK MYSELF OFF OF IT DUE TO WHAT FELT LIKE A MINY STROKE AMONG SOME OF THE OTHER SIDE AFFECTS. I HAVE NOT BEEN ABLE TO FIND MYSELF FOR 5 YEARS, I DON'T EVEN KNOW THIS PERSON INSIDE ME. DOES ANY ONE KNOW IF CLYMARA IS OKAY TO BE USING W/WHAT YASMIN HAS DONE TO ME? IS THERE A CASE # NUMBER FOR ANY CLASS ACTION SUIT OUT THERE?

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.

I obviously have a COPD situation...last 5 years of shortness of breath etc..there is no question of the relief I got from Adaviar but I have had the constant pain under my rib cage...feels like an elephant is sitting on my chest...but worst of all since I started three months ago I have had 3 teeth break off. I assume there is a bone loss issue involved with the ingredients.
I am on Medicare so I don't have any dental coverage so my dentist is having a great time with my extractions. If there are others with teeth issues please let me know. Adaviar has been around for about ten years but that does not mean a Class Action suit would be out of the question here. I have talked recently with my Primary MD about trying something else but I would not mind so help with my upcoming Dentures.

cannot believe how many stories I have read about mirena and hair loss etc..etc.. etc.. I have experienced many of the side effects that everyone is mentioning.. I actually feel I could live with most of them if it weren't for the hair loss. I have had ( copying from other post.. ridiculous right?)Tired all the time ~ Depression ~ Hungry all the time ~ leg cramps ~ HAIR LOSS TO THE POINT OF BALDING IN SEVERAL AREAS ~ oily skin and bad breakouts ~ Mood swings (huge...yelling fits at my husband and the kids) ~ fluttering in uterus~Sore breasts.. I have medium thick hair that is about 10 inches. I noticed a bald spot in June and now have discovered 4-5 others starting. I just had the iud removed today and my OB pretty much tried to convince me that there is no way that the IUD is causing my issues. I have never had any of these issues before. I got the Mirena on 4/30 of 08 and noticed slowly but surely all of the side effects mentioned. My OB told me that the progesterone could not be causing my issues because it is such a small dosage that it would be comparable to spitting in the ocean as far as the amount that is in my blood stream. She said because I am black and 35 that I may have an autoimmune disorder and that I should stop reading blogs. I told her that all of my research wasn't from a blog and that ALOPECIA is a side effect just not mentioned in my pamphlet that I can find. I understand what she is saying and that she is the one that is the dr. but nobody knows my body better than I do.. I am in it!! I have !never had any problems and have been healthy my entire life. There is no history of autoimmune disease in my family. I am going to my primary care doctor.. to have some blood tests done. I think that the mirena has caused an autoimmune response in my body.. it may not necessarily be the progesterone..although I don't rule it out no matter what she says . the progesterone is synthetic and has an androgynous like activity that is similar to testosterone the main thing that causes male pattern baldness. also Mirena is made out of Silicone.. perhaps those of us that are having hair loss are having it due to our body trying to fight off the foreign invader of the IUD itself. I was going to go and have the Paragard inserted.. because i was thinking it may just be the progesterone.. nope... I read that many women are complaining of ACNE and HAIRLOSS even with that because its made out of copper. So with that being said.. not sure what to do.. may have to go back on Yasmin.. didn't seem to have any problems with that.. I really just don't want to risk putting another hormone in my body.. We all need to get together and look into a class action suit because I am tired of being made to feel crazy by doctors.. sometimes what seems to not be possible is .. especially when there are so many women having the same problem. Feel free to e-mail me re: a class action suit.. if they took depo off Mirena needs to come of too. It seems like it has really screwed a lot of peoples system up.. Hopefully I won't find out I know have a thyroid problem etc.. etc..

OK..... looks like this site deleted my links on my previous post on where you can go to view the video on IUD self removal. Actually, you really don't need to watch it... it's so easy. If you can feel your strings, grip them tightly and firmly with your fingers, and just pull gently for a few seconds. I didn't feel any pain at all, just slight pressure. Mine came out in about 10 seconds.
It's been 24 hours since I've removed mine. I cannot tell you how much better I feel. Normally, every morning when I first wake up I start feeling really irritable, I start bawling in the shower and can't stop... I even run late to work because I can't stop crying long enough to put my makeup on. Throughout the day my moods will fluctuate depending on what's going on and how other people around me influence them. Today has been totally different. This was the first morning in months where I woke up and showered without crying. I feel like I've been "cleansed," I don't feel my blood pressure boiling over from the slightest family disturbance... in fact my kids were screaming and chasing each other this morning and this was the first time I didn't jump up and scream at them and send them off to their rooms for an hour! I'm going to call my GP tomorrow and see what he says about coming off of my antidepressant, because I clearly don't need it now that the cause of my depression is gone.
Good luck to everyone out there.... maybe we can all get together and turn this bad into good and file a class action suit against this company. I'm really scared about what it could do to some of these women who have depression before they even get this product.... this is a pretty serious situation here.

this is probably the worst thing Avelox caused, besides death, which would have happened without help..

7th day on Avelox for sinusitus - massive pain back of my head, sweating so much my clothes were soaked, threw up 2 times, legs were uncoordinated when trying to walk

Called 911 - paramedics took blood pressure - guess what.. 210/180.. something was definitely wrong. Rushed to hospital - passed out in ER - woke up with wife and family present - CT scan found my brain bleeding and brain surgery was performed to remove the clot..

But wait, it gets better... 2 days in the ICU my brain swelled from the surgery and the fluid stopped circulating.. I was semi conscious in the ICU for probably 4-5 hours and nothing was done. My wife came in early in the morning and thought I was sleeping, but could not wake me.. The nurse said that a doctor was called and will be there later. I'm DYING right before their eyes in the ICU!!! My wife demanded I get a CT scan immediately. If she didn't I would have stopped breathing. Later CT showed my ventricles enlarged with fluid backed up so much that my brain and brainstem was ridiculously squeezed so much, my head was all ventricles and barely any brain showing in the CT. I attribute my current brain damage to this episode.

A shunt was placed in my head for about 3 days.. basically a needle is inserted into my brain and left there to drain the excess fluid.. After my condition stabilized, the shunt was removed.

Spent 1 week in the hospital, then transferred to another hospital to stay in for inpatient PT and treatment. I didn't know left from right, had double vision, was throwing up constantly, was hot, then very cold, my legs hurt, had hallucinations (was believing certain things were happening, that really weren't) was incontinent, had a new catheter inserted every single day, was taught to walk again, had to use a wheelchair.

I had always been healthy, was vegetarian and did not smoke cigarettes.. I exercised regularly, did not use drugs (i.e. - cocaine or methamphetamine which can cause high blood pressure leading to a stroke)

Didn't know what happened to me, but realized I had to be there.. After 1 month, decided to go home (the hospital was becoming too stressful, somebody was always screaming and yelling at night and the daily catheters were uncomfortable), to be back in the lifestyle I knew.. my wife, my granddaughter, my house, my dog, cats, and other pets were sorely missed.

Once home I found that I couldn't do what I used to anymore - could not mow the lawn, drive, speak well, walk properly, had double vision, a tingling on my face, a metallic taste in my mouth so bad that good food tasted bad.

My wife set me up for physical therapy three times a week daily outpatient at the hospital I was at. Vomited regularly from the daily dizziness.

This was most disturbing, I developed a pain in my left hand and left shoulder, to the point where I could not raise my arm above my head and had to sleep with my arm straight down for at least a year. After playing guitar for 30 years, I found myself unable to play my guitar anymore. My left hand had lost all its dexterity and was not usable. I did not realize what happened to me until my wife explained the entire thing to me.

In the next few weeks I spent each day trying to put "2 and 2 together" and figure out why this happened to me. When doing research on strokes, I realized that certain things happened to me that were not consistent with having a stroke. In my brain damaged condition, I remembered taking the antibiotic Avelox, based on a physicians prescription. I researched the adverse effects and to my amazement, the listed side effects were consistent with what happened to me.

I began a quest to file a lawsuit - was unable to find a lawyer willing to tackle such a huge case.. although one lawyer did file before the 2 year time limit expired.. I had MRI's performed on my hand and shoulder which revealed scarring and previous ligament tearing.

During the time of having more outpatient and in home therapy, I regularly visited a psychologist and my physician confirmed that the Avelox most likely caused the brain bleed, tendon tears, and other mysterious symptoms when I presented him with my research. I was unable to work and my only income was from monthly Social Security Disability benefits that didn't begin until 6 months after the incident.. leaving me with no income and unpaid bills for 6 months. The mortgage payments fell behind and soon foreclosure notices arrived. We decided that an alternative would be to sell the house.. it could not be sold after 1 years attempt, so my wife and I moved to an affordable apartment. I put household items in a storage facility. I either sold to pay bills or threw away much of my personal things,since I was devastated by what happened to me, I didn't think I was going to survive long after reading statistics on strokes.

While in the apartment, I needed an income and was forced to take what was in the scpoe of my limited ability. I accepted an early morning paper route and then made deliveries for a courier company using my own vehicle.. That was a 12 hour work day. Being completely upset over what happened, losing everything including my house.. I decided to attempt to escape the overwhelming things that happened and were still happening. I found a house for rent that was less than the apartments rent, except it was in North Carolina. At the time that seemed perfect, a 3 bedroom house located in a far away place where I could forget everything that happened and make a fresh start. Only problem is my wife not want to go, but I was adamant upon doing it. She helped me move everything, including all storage items.. I had moved to North Carolina, but soon found being alone and unable to find suitable employment unbearable. I was being contacted for back rent owed, but could not do everything alone - I became more depressed to the point of feeling suicidal, so I called my aunt in NY and she said just leave everything and get myself to her house. I did, leaving everything behind, and stayed with her for a month until my cousin invited me to stay with him.. which I did. I stayed with him for 3 months, all the while searching for employment.

With help from my family I moved back to my familiar area in NJ in the summer of 2008. I had lost everything..unable to be physical with my wife and being seperated for 18 months, she has requested a divorce. Currently I live by myself and am still slowly recovering, yet my left arm and hand are uncoordinated, my talking is difficult, slurred and gravely (diagnosed with dysarthria), my balance is bad and am dizzy every single day for the past 4 years.. Although brain damaged, I am attempting to rejoin the computer support business again.

My entire past, everything I knew and did, everyone I knew, who I was, etc.. is all a strange hazy memory. If I don't take a sleep aid, I wake up around 4am with racing thoughts, unable to sleep.. My depression and anxiety are so bad, it is difficult to function and interact with others. My psychiatrist has diagnosed me with post-traumatic stress disorder and prescribed Zoloft and Xanax.

Upon proper research, I have to blame the prescription and subsequent use of Avelox for causing the brain bleed which led to my life being completely and utterly destroyed. My intentions are to file suit against the manufacturer Bayer and/or the hospital for allowing me to die in the ICU

Shortly after beginning Yaz, I began getting dizzy at random, messy vision, fainting spells and an arrhythmia. I spent 2 days in the hospital and none fo the doctors attributed any of the side effects to Yaz, but that was the only new thing in my lifestyle. I also had been having incredible abdominal pain in the upper right area where my liver is. I have always been incredibly healthy and I started taking this to help the PMDD. Instead I am afraid that I have a frigging pending stroke coming my way or blood clot hiding in my brain making me pass out. Im scared and incredibly angry that all I did was try to get some help and instead had my life and my family's well being threatened. I am fighting to get an MRI on my head just to be sure nothings in there. I know I sound paranoid but suddenly getting an arrhythmia and passing out at random is scary. I am afraid to hold my daughter because If I faint, she'd get hurt. Another thing is at the beginning, I would dry heave a lot, but my doctor kept telling me to stick with it. She is STILL telling me this. Im stopping it tonight and joining a class action suit.

Ladies,

My Mirena was removed Monday morning and my blood pressure was 165/101. Yesterday I was feeling considerably better but still had numbness in my arm last night. This morning, 2 days after removal, my blood pressure was 138/92 - still high, especially for someone not overweight, but an improvement over Monday's pre-Mirena.

Thank you to my friend Jackie who has located the FDA website (below) to file complaints. We must ALL file!!!! Although this website has absolutely been a Godsend to me and others, it isn't enough that we air our complaints to one another then let the matter rest. We must take this off the market! Strength in numbers, Ladies!

http://www.fda.gov/downloads/Safety/MedWatch/HowToReport/DownloadForms/UCM082725.pdf

Seriously, does anyone know anything about how to get a class action suit initiated?

L.

I had a severe reaction in 2006 (posted with you in 2007. My question now: is there a class action suite or are lawyers just looking into the possibility of a class action suite

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 am a 48 year old female who had just recovered from pneumonia and was prescribed avelox for a lingering sinus infection. Within hours after taking just 1 400 mg pill, I began experiencing a severe reaction. First there was a rash all over my body, with swelling and flushing all over. Then I became nauseated to the point of dry heaves and my temp went to 104 digress. My body then had neurological shakes, I could not control them -- just like Parkinson. I had no energy to move. My husband rushed me to the ER where I was treated with steroids, liquid benadryl, nausea medicine and IV fluids. After a few hours, I was released. Two days later, after another trip to the ER because of tingling, rash and no blood flow to extremities the same treatment was given. It has now been two weeks and I am just now feeling like I am coming out of this and getting back to normal. I have just spent over 10 days in bed, untold amount of money at ER and lost two weeks of my life.. BTW, the ER Doc said he would never prescribe Avelox to anyone due to the numerous reactions he has seen. If there is a class action suit, count me in.. Never let anyone take this drug..

I WAS GIVEN AVELOX AFTER I HAD A SINUS INFECTION WITHIN A COUPLE MONTHS. I WAS ALSO PRESCRIBED PREDNISONE. THE FIRST DAY I TOOK THE AVELOX I RAN A FEVER. I STARTED THE PREDNISONE THE NEXT DAY. I FIGURED I WOULD FEEL BETTER ONCE THE AVELOX KICKED IN. HOW WRONG. IT TOOK ME THREE TRIES THE NEXT DAY TO GET THE DOCTOR ON THE PHONE BECAUSE I HURT SO BAD. EVERY MUSCLE, EVERY JOINT IN MY BODY HURT. I DID NOT MOVE OFF MY COUCH. THE DOCTOR TOLD ME HE DIDN'T KNOW WHAT I WAS TALKING ABOUT BUT I COULD MAKE AN APPOINTMENT THE NEXT DAY. MY MUSCLES HURT SO BAD AND THE JOINT PAIN WOULD GO FROM ONE TO ANOTHER WITH WEIRD CHILL LIKE FEELINGS AT TIMES. MY MUSCLES IN MY ARMS AND LEGS WERE VISIBLY SHAKING WHEN I RETURNED TO THE DOCTOR THE NEXT DAY. HE BLAMED THE PREDNISONE. BUT TOLD ME AFTER A DAY OFF OF IT IF I STILL DIDN'T FEEL RIGHT TO STOP THE AVELOX. YA THINK? THREE DAYS LATER AND I AM STILL IN PAIN. AFTER 4 DAYS OFF WORK I HAD TO RETURN AND I HURT ALL OVER. DURING THAT TIME I CRIED FROM THE PAIN. MY STOMACH HURT, AND I WAS NERVOUS. I THOUGHT MAYBE I WAS LOSING MY MIND I HAD SO MANY DIFFERENT SYMPTOMS AND HURT SO BAD. WAS SO GLAD I FOUND THIS SITE. SOMEBODY NEEDS TO SUE THE DRUG COMPANIES. I WOULD LIKE TO SUE THE DOCTOR TOO.

ok i'm 27 and I've had Mirena almost 5 months now and no periods since end of 2nd month...last few days I have a strange feeling around the area the IUD would be inside like tingles and just bothersome (as if body was trying to expel it or something...hoping i;m no preggo).....Anybody know what is going on?

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK 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. Here's my case: 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. It is over a year later and the indent remains and continues to cause discomfort. 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 and strongly urge others to report their adverse event to the FDA (see link above).

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.

y story is but an echo of many of the others so there is no use to repeat what is being said. I do believe there is due cause for a class action suit. I hold the FDA and those responsible for its poor performance as well as the drug manufacturers and the pharmacies responsible. I just found out about the recall of metroprolol today when I went back to my local Walgreens to pick up a refill of my prescription. I was told by the pharmacy that four days ago that they had to obtain a new authorization from my doctor to refill it. Today a different pharmacy technician told me they had to send their supplies back to the factory because met-succ was no longer made by tthat company. I thought that strange, and I asked why the recall. I was told it wasn't really a recall, but the company wanted the meds returned to it. In answer to my "what is wrong?" I was told their was nothing she knew of, that the medicine was fin, the company just wanted it back and that I should talk to my doctor for a replacement.

After reading the comments hear I believe we all have been given the runaround. It sure seems like our pharmaceutical companies are trying to copy the Chinese. It looks like collusion between manufacturers of generic drugs and insureance companies. I do not think the doctors were privy to this.

Yes, I'm mad as hell. I hope I live long enough to see a good resolution to this matter.

H. R.

I'm taking no more of that poison

I am so glad I found this!!! I too took this pill before bed without a lot of water and I woke up in the middle of the night thinking I was having a heart attack!!! I cannot eat anything without it burning like there is a ulcer in the esophagus!! I have been off this medicine for 4 days and I still am on the slim fast diet because I cannot eat anything!!! How long does this pain last? Is it permanent? I don't know whats going on I am starting to get really nervous!! If this many people are having the same problem we should file a class action suit this is ridiculous!! I cannot not live like this the rest of my life! I am normally a very healthy person and I'm only 29 so hopefully this did not do any serious damage! So does anybody been off of this and not feel like a flame thrower is in your chest anymore????

I was put on Yaz when i was between 19-20 also and after only 6 days on it i had to stop it. I had horrible mood swings, depression to the point i plotted my own death (scary!), paranoia, serious abdominal and calf cramping, as well as headaches, nausea, fatigue, and serious fits of crying for unknown reasons. My boyfriend walked in one day to find me collapsed and hysterically crying on my kitchen floor with no known reasoning behind why i was crying except for the fact that i dialed the wrong number to order pizza...Yaz's side effects, still effect me today and have ultimately ruined my relationship because of serious mood swings, paranoia, and excessive fatigue. Despite that i only took Yaz for 6 days it still greatly effects my life. if you ever find a class action suit against them let me know and ill be right there next to you!

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

has anyone had the mirena removed and did the symptoms/side effects subside? if so, how long does it take to get back to normal?... from the sounds of this site..seems like a class action suit is in order??

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.

This note is very hard to write. I had a kidney stone removed using laser surgery and the urologists prescribed the 500mg of levaquin to prevent infection. I took the first pill while under the influence of dilaudid, so I didn't realize my dizziness, loud ringing in my ears, nausea, headaches, lack of appetite, insomnia, and joint pain were the result of the levaquin. I thought I was just reacting to going cold turkey off the dilaudid. I took two more pills. I haven't slept in two days and I am the most exhausted I have ever felt in my life.

This stuff is poison. I can't believe the cavalier attitude of the physicians who proscribe these powerful chemicals and the FDA is doing a very weak job keeping bad medicine out of the hands of these shills for the drug companies; i.e., the doctors.

I stopped today and I pray that I will recover from this very nasty experience. It has been as bad or worse as the kidney stone attack. I hope the other victims of this hoax cure win their class action suit and shut down this dangerous drug.

I had my mirena inserted in Mar/Apr of 2007 and I experienced nothing but hell like the rest of you. Following insertion I was dizzy, had horrible mood swings, was extremely bloated and fatigued all the time. I also experienced horrible acne which included those horrible cysts that form under the skin, they never came to a head and lasted what seems like forever. I bled all the time from light to heavy, never knew if I was actually having my cycle or what, the blood was dark in color and had a horrible odor. I need not forget the joint pain or what felt like a charlie horse, and nausea. I also believed it played a part in my hypertension. Needless to say I had it removed in June of 2008 and I still don't feel I've fully recovered. Now I am experiencing pains on the right side and center of my abdomen and am still experiencing mood swings and joint pain. I also suffered from lower back pain and I'm happy to say that pain seems to have subsided. I wouldn't recommend the Mirena to my worst enemy!! Ladies pay attention to your bodies you know them better than anyone else, if any of these symptoms sound even remotely similar to yours I would advise you have that horrible little device removed asap. If anyone knows of a class action suit I would be happy to join (my cousin as well since her symptoms are the same if not worse than mine). Please post any info you have available so that we may all follow suit.