Law suit symptoms and conditions

I was given a Rx for Levaquin on Dec 17th (5 day dose). I started it on the 17th. By Saturday the 20th, I wasn't feeling good at all, my ankles, knees, hips, elbows, wrists and finger joints hurt. I only had one dose left so stupid me, I took it.

I have had pain ever since. I had read the sheet you get from the drugstore when I had the Rx filled. I remembered something about possible joint pain but didn't think much about it until the pain didn't go away after I stopped taking the drug.

Wednesday the 24th, I looked Levaquin up on an internet drug site and looked at the side effect list again. That is when I realized that the pain I was having was under the "notify your doctor" category. Their office was closed until the 29th. I tried to call the 29th but the phone was always busy. I finally got through today and told them my symptoms and told them to put in my chart to not give me that drug again. The nurse called back to say that they put it in my chart and to take otc stuff for the pain.
I have been taking Advil and a combination pill of glucosamine and condroitin (those are probably not spelled correctly - sorry). I am better but still not 100%.

Today is the 31st and my last dose of Levaquin was Dec 21. I am down to knee pain and a puffy feeling (not really swollen externally but feels swollen internally), left shoulder pain (worse in the morning when I wake up), my hips hurt off and on and my ankles hurt off and on. I am concerned about one of my ankles because I already have a haglund deformaty there so there is already damage to the area.

When I try to get out of a chair, I feel like I am 90 (I am only 49). I really hope this gets better soon. I haven't heard anything about a law suit or anyone who has a way to speed the recovery. Please, let me know if anyone knows how to help this get better faster.

OH MY GOD!!!! I thought I might be imagining things. I was prescribed Levaquin and clyndamycin on December 15 2008 for a urinary tract infection that appeared to have gone systemic. After 2 days my right knee swelled up. I went back to the Dr the next day and he looked up both antibiotics in his little book and said the clyndamycin could cause joint swelling and pain. He told me to stop taking the clyndamycin and take 600 mg of ibuprofen for the joint paig. His little book said nothing about levaquin. Well I kept taking the levaquin and the pain spread literally to every joint in my body. I could not walk and had trouble even holding a coffee cup. The pain was unreal. I completed the 10 day course of the levequin as instructed. The joint pain was getting worse. I called the Dr. again and they did blood work to rule out arthritis and stuff like that. He put me on prednisone which has significantly helped with the pain. He said it may be a coincidence that I have developed arthritis and that it had nothing to do with the UTI. Well as I was watching TV last night I saw a lawyers commercial for a law suit against levaquin and cipro. Then today got on the internet and found this site. I am going to call the Dr. and tell him to update his little book he looked up the levaquin in. My fear is how long after you stop taking this poison does the joint pain end? I wish I would have known all of this sooner. I will never take this drug again.

I have the dent at the injection site too. I have been so worried it was skin cancer. I recently saw the same doctor and asked about it and she told me it was probably a scar from when I was little! I told her it showed up in August. She said not to worry and she would do a biopsy if it got bigger. She even had in her records I was there for the kenalog shot in summer. I had the shot in early July. Please inform me of any class action law suit. I am now wondering if this also was the cause to my lack of sleep and loss of 20 pounds over the summer. I was not informed of any negative side effects.
Thanks
******

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'm 18 years old and live in Florida, while at the gynecologist for a routine visit my doctor strongly suggested that I start the Gardasil 3 shot cycle. After checking with my mom (who was unfortunately given biased information from my doctor without first doing research on the product) agreed since we both figured that my doctor would be knowledgeable enough on the subject (or you would think since she was the one administering the drug.) The first two shots went fine and I had no reaction at all. After the third shot (in October of 2007) I woke up the next morning with swollen hands and extreme swelling at the injection spot. I immediately returned to my gynecologist where I was told “there is no possible way you can be allergic to this medication” by my doctor, and that those reactions would go away in a few days. A few days following this I developed sores in the back of my throat and under my tongue, however my gynecologist still insisted there was no possible way it was an effect of the Gardasil (EVEN THOUGH IT WAS THE VERY NEXT DAY) & I had no previous illnesses. Within the week following I developed body-wide hives so severe that I cannot sleep and they affect my breathing. I’ve seen several doctors (allergist, dermatologist, primary physicians, and immunologists) none of which can determine why exactly I have these hives, besides that it is a “drug reaction” (it took 11 vials of blood to determine that). However when one of my dermatologists questioned Merck about it they simply said that there is no evidence and I cannot sew!!! That’s all they cared about! A law suit! WHAT EVER YOU DO, DO NOT GET THIS SHOT, TELL EVERYONE YOU KNOW! It has ruined my life. As an 18 year old girl living in Florida I love to go to the beach however because of these hives they get so severe when I’m exposed to sunlight I can no longer go. It’s also extremely embarrassing when people stare at them since they cover most of my body on a daily basis.

I'm 39 and have been on Coumadin for about a month. Was diagnosed with DVT in right calf after taking Yaz birth control for only about 4-5 months (no other pre-conditions - I'm a non-smoker, fairly active, not overweight, no recent airplane trips or long car rides.) I was on Yaz to treat severe problems with my period which has been the case since I was a teenager, but I was tired of having to call in sick to work every month, and had hoped Yaz would eliminate that problem. I had been on other BCPs when I was in my 20's, and never had any symptoms of clotting, so didn't think that it would be all that risky to try again, despite me being slightly older than the typical woman on BCP. Obviously, I am not taking Yaz anymore, and will not be able to take any other hormonal therapies for the rest of my life. But I guess that's minor compared to the risk of developing PE from an undiagnosed blood clot.

Anyway, I've been noticing I've been getting sudden, severe headaches since starting the Coumadin. I have a history of migraines but I usually only get one or two per year at most. Now I've had what feels a lot like a migraine twice in a matter of a couple weeks. My husband has also commented that I've been irritable and acting "spacy".

My INR has also been all over the place. They've been alternating me between 5 mg and 7.5 mg per day. For the first few weeks I was right where they wanted me - between 2 and 3, but then last Friday my results were 4.6!! Way too high. I go back this afternoon to see if anything's changed over the weekend, after skipping a dose and then doing 5 mg Sat. and Sun. I do hope they can find the right balance and don't have to keep tinkering with the dosage. I'm wondering if that's what's contributing to the headaches. Maybe if they can stabilize how much I'm taking from day to day, my body will adjust.

I wonder if anyone "official" is tracking the number of DVT/PE patients that can trace their onset of symptoms to Yaz. My sense is that this is a much more serious and prevalent side effect than their marketing dept. would like to admit.....

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.

MY STORY

My Mirena was removed on 29th May 2008.

I had the Mirena put in four years ago,I had terrible pain the day after, it was that bad I was going to go to the hospital Emergency to get the thing out but I put up(the worst thing I done in my life, Im paying for it now) with it and it and the pain got a bit better,had a lot of bleeding (spotting) for the first six months and then it finally went away. For the first year I thought Mirena was Great but then the problems started.I started to gain a lot of weight,facial hair,Very sore breasts, I also had a lump removed from my left breast a couple of years ago, but I didn't know until recently that it was most likely caused by Mirena. Some of the other problems I had, My stomach bloated, I look like I'm six months pregnant ,I have a cyst on my left ovary,dry skin,acne,strange depression,headaches,and the Worst of all I had to have my Thyroids REMOVED on 1st Nov 2006 and I'm pretty sure that was caused by Mirena as well, so now I have to take thyroid Medication for the rest of my life,I had the Mirena removed as soon as I done some searching on the internet for my unexplained medical problems, mainly my weight as I had weighed about the same my whole adult life and now I had put on a few stone and now I have to try and lose it,as for my thyroid I have trouble getting the Meds right its a real pain,blood tests all the time.I just don't feel I have much left in my life,depressed,sick all the time. I eat well as I have high cholesterol so its not that I over ate,I noticed you do feel a lot more like eating sweet things. I found a site called ****** and found out there are thousands of woman,girls with the same problems as myself and that there is a class action law suit going on to Sue. Its worth having a look at this site it helped me a lot.I feel so bad I don't go out anymore I don't see friends or family I'm to depressed about my weight now. I am in the process of trying to find out if there is a Class Action Law Suit in Australia.If anyone knows of a Class Action in Australia could they Please let me know. After having the Mirena removed about 6 weeks ago I thought I was doing ok only a bit of spotting,but about 3 weeks after having it removed I got my period and the pain was unbearable,I was in agony stomach cramps and I bleed so much I thought I was going to die from blood loss,also the scariest was the huge blood clots,very scary,must of been four years of period in 1 week I couldn't believe how bad it was, I felt really sick and weak,but thank goodness its eased off now after a week. I just hope now I might slowly start and feel like my old self. Im also on medication for heart palpitations,I get Heart palpitations (SVT) a few times a week,I had my heart palpitations just after my thyroid removal op and was put on ecg and my heart rate was 176 Beats per Minute I was rushed to Intensive Care and I had to have an injection called Impending Doom (It makes you feel you are going to die) to slow my heart rate,it worked and I was kept in intensive car for 3 days,very scary thing to go through I hope I never have to go through that again,my heart palpitations got worse while I was on Mirena and now I also take Magnesium to help control them as well as Metoprolol which I have been on for some years and I recently read that if you are on Mirena it increases the side effects of Metoprolol.

So if you have had any bad experiences with Mirena please let us know,it will help others with their problems, hopefully. I just wish I never got Mirena and my advice is DON'T its not Worth the risk,if the Doctors had of told me about the BAD side effects I would NEVER of had it put in. Sorry about going on so long, Good Luck to you all,

Thanks Net.

google mirena-side-effects.****** (a mirena help,info site)

UPDATE

I have had it out nearly 3 months now my painful breasts feel normal again,I haven't lost any weight yet, but will soon hopefully,I do feel a lot better but still get some of the symptoms back just before my period.

I get sooo mad when i think of what Mirena done to me and all the other women and how bad some of their side effects have been. I get mad when i read some of the other ladies stories and the terrible things they have gone through ,

Perforations,Miscarriages,IUD's lost in their body,

Hystorectomy,and the rest. I want to wish them all the best, and we WILL get Better and Bayer ,Mirena will PAY some day for what they have done to US..

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 posted for my 14 year old daughter a couple of weeks ago. I am happy to say that we stayed off of the YAZ after going to the hospital 2 times, sonograms, cat scans.... worried about spleen rupture ~ pains in the side, back, shoulder, throwing up THE WHOLE SHABANG! pretty much every side effect there is listed for this horrible drug she had. Well...turns out she had mono/epstein barr a couple of months ago so it kicked it up again after it was getting better. DOCTORS PA's....push push push meds. We need to be more informed about what we take into our bodies. MEN WOMEN CHILDREN just because they prescribe it doesn't mean we should take it. we are the guinnea pigs here. Yes there will probably be a law suit and it will like the patch be taken off of the market. But where will we be??
So my thought on this drug is that doctors need to be taking blood tests of a variety of things before saying ~ yes it is ok for you to take this. Because there are some (I say SOME) people who aren't as sick as others... some people drink booze so their liver will be elevated some people have dormet problems that will cause this pill to reek havoc on your system... everyone needs to get a grip on taking meds.... it is whats causing havoc on our bodies. we take all these pills. its crazy.

I can't believe that this drug is legal and that it has not been taken off the market. I have been on it for a year and couldn't understand why I was gaining weight, nothing helped to get those pounds off. I started at 160 and now at 195 and growing. Three years ago I had triple bypass, weight 150, some of the meds caused some weight gain, but nothing like this. My joints was so sore in the morning I couldn't hardly walk, I just knew I was going to be using a walker if this kept up. BTW I'm 65 female, always been active and busy, now I just do what I have to or can and that doesn't make me happy. I have recently been having crying spells and sore throat, voice lost, and enlarged tongue. The enlarged tongue caused me to do some searching on side effects.....I am so glad I found this page. I haven't taken any puffs of Advair since., that was 3 days ago. My tongue is starting to shrink, my joints aren't as sore, my crying is stopping. The weight is still with me and might never lose it, time will tell. I don't seem as hungry and eating less so maybe there is hope. This is a drug that should have Big warning all over it. Advair has taken a year of my life at this point. If there is ever a law suit I would be the 1st to sign. I didn't have that many breathing issues and really didn't understand why the Dr. put me on it.
I usually check up on drugs before I take them, this one slipped through the cracks, guess cause it wasn't a pill. At this point I just hope that others find this in time and stop using Advair before it ruins their lives.
God Bless
Barbie Kay

Hello Every one i am a 28 yr old female / i have had asthma all my life and took many meds that really mess me up one was alupen / i went into cardio arrest at the age of 4/ in 2004 i was alone with my kids when i got an asthma attack / i had them before but never like this i called my husband to take me to the ER / i got into the car i told my kids to put their seat belts on and thats the last i remember. I blacked out waking up in icu on life support. doc ask what i was taking i told him i had a albuteral therapy advair and my singular pill / i told him the advair was making me sick / over weight and he said no its not the advair / but like i said ive taking about every asthma med out there and nothing made me so sick to the point of death like advair. i did call the 1-800 to find out about the law suit.

Hello: I am so sorry that all of us are suffering since taking this pill. My experience with Yasmin was brutal and 3 years later I know am told that I have developed b12 deficiency or a very serious, but treatable condition called pernicious anemia. I never had it before then pill. I took Yasmin for only 5 months and felt sick the whole time. Headaches, strange moods, even a popping sound in my head some times, bizarre symptoms. I called my OBGYN and told he I was stopping. She said the pill did not cause this, but if I felt it was related to stop. AND IT WAS! She now admits to feeling bad for this. She did not mean it. Doctors only know what they read from the literature of a drug. I stopped taking it and was in the hospital within three days. I was in shock. Night sweats, tingling skin, no energy, stomach problems of every kind. Severe pain in my left ovary, suicidal depression and on and on. The worst part is that I began to get sicker and sicker. 3 years later of still being sick. The only thing that has helped my system is acupuncture and a serious diet change to aid my system, I find out that I have a serious b12 deficiency, which I never had. They call it an autoimmune disease which impedes you from processing b12 and all this starts in the tummy! I lost a baby during this time while pregnant, now we know it was this! The Yasmin pill has been pulled off the social medicine of some European countries due to such severe side effects. Their is a girl on this blog getting names together to start a class action suit. I am in. No one can get me my three years of suffering back, or my lost baby or my lost work. I am a professional flamenco dancer and let me tell you it is not easy to perform with a serious b12 deficiency which affects nerve endings, heart tissue and neurology! And the cure for this is b12 injections for life! If you want me to forward your name to the girl with the attorney you can write me at:****** Well I am going to keep trying to be well. I am young and have a whole life ahead of me.

I was just discharged from the hospital on Saturday. I had been taking Yasmin for almost two years now and until recently, had no problems. Last Wednesday I went to the ER for severe pain and inability to breath with my left lung. They admitted me after finding a blood clot in the right, as a result of Yasmin! Turns out, I had pneumonia in the left and since I had no symptoms that the clot was there, the pneumonia saved my life! I too had to take those fun Lovenox shots in the stomach and now I'm on Coumadin for 6 months. I am 29 years old, never smoked a day in my life. I do not drink, I am a healthy weight and I work out regularly. I do not have a history of blood clots in the family. How could this happen especially with a drug my doctors told me was safe?

With the amount of occurrences, I'm interested in a class action lawsuit as well. I will never take a birth control pill again EVER.

I have waited long enough to tell my story. I am a 29 yr old single mother of 3. I started YAZ in Feb of 2008. I took it for 11 days. ELEVEN DAYS. It was about 4 days in that the headaches started. I couldn't stand light, I wore hoodies and sunglasses. I was nauseated. Saw double, black spots. Motion sickness.I could barely make it to work. I was out of control. I did not have control over my mind. I was crazy. My friend almost took me to the hospital to have me committed. There is no history of this in me or my family. The headaches would last from the time I woke up til the time I would go to sleep. Painkillers was the only thing that would keep me asleep through the pain. My dr immediately stop the the pills. I saw an eye doctor and they found nothing. They ordered an MRI. They found T2 Foci scattered throughout my brain. VERY unusual in someone my age. What that is, is my protective covering of my brain cells had been damaged there were gaps in its covering. I soon developed a stutter and a slur in my speech. The pain then moved throughout my whole body. They said fibromyalga and daily migraines. I'm now on topamax daily which gives me breaks in my headaches. I still get them daily. I still have pain in my body daily and I'm on painkillers daily. I have found a new dr who is wonderful. Who has recently taken blood. Who thinks that maybe it could be lupus. So I started researching Lupus...my symptoms and rashes match up. There is also a DRUG INDUCED LUPUS. and ORAL CONTRACEPTIVES is a KNOWN drug that can cause this!!! BUT IS THAT ON THE LABEL???? NOOOOOOOO!!! I was perfectly healthy before yaz, in kick boxing and now I walk and have the memory of a 60 yr old and my brain is permanently damaged. I have another MRI coming up to find out if there is more damage and I will find out the results of the blood work to find out what is wrong with me...but I blame all of this on YAZ and I hold them responsible. I SAY CLASS ACTION LAW SUIT....just have to find a firm with big enough BALLS to do it!!!

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?

My son has been battling sinusitis for a few months . I didn't know sinusitis could be so bad. His doctor prescribed Levaquin three days ago and I read the side effects and realize it was a risk because my son has seizures.After 2 dosages and sleepless nights with headaches and him not being able to function I've stopped giving it to him.
Thanks for such a great website!
The benefits don't out-weight the risk.

I too, have been having weird symptoms over the last several months and just connected it all with having a Kenalog shot 7 months ago. In October 2007, two months after my injection, I developed severe anxiety and panic attacks. I thought it was related to perimenopause. Then, in January, I started having lots of muscle and joint pain all over my legs and hips. I've been a healthy and active person, so this was very unusual. I saw an orthopeadic surgeon who diagnosed me with a strained rotator cuff and bursitis on my hips. Now, just two weeks ago, I woke up with a large indentation on my left glut. Right where the Kenalog injection was given. My doctor had no clue what it was and said she might refer me to a Plastic Surgeon. I am SO relieve to find this board. It all clicked when I read everyone's postings. Now I just want to know if it will get worse or eventually go away. I did find some interesting information about the drug. BTW, the nurse or doctor NEVER said anything about side effects before giving my the injection. I am seriously going to pursue a law suit, so we can get this terrible drug OFF the market and no one else has to endure this disfiguring problem. If ENOUGH of us join together in a law suit, it might be worth suing the drug manufacturer. But we have to somehow get organized. Anyone intersted in pursuing this?

Here are some facts about the drug I found online.

Kenalog is not appropriate for everyone. A thorough medical history should be assessed prior to prescribing this medication. Patients with a medical history which includes skin infection, tuberculosis of the skin, chicken pox, herpes, cold sores, sunburned or wind burned skin, chapped skin, open sores, diabetes, or a stomach ulcer may not be able to take Kenalog or may require careful monitoring while undergoing drug therapy with this medication, depending on the condition and the severity of the condition.

The American Food and Drug Administration rated Kenalog as a pregnancy risk category C. This medication has been known to cause harm or birth defects in unborn babies. It has yet to be determined whether or not Kenalog passes through the mother’s breast milk and affects a nursing baby. The prescribing physician should avoid prescribing this medication to women who are pregnant, nursing, or have a high likelihood of becoming pregnant.

There is a risk of side effects associated with Kenalog, some of which are severe. A patient who is experience a serious side effect or an allergic reaction should seek immediate emergency treatment. An allergic reaction will present with symptoms which may include facial swelling, such as swelling of the lips, mouth, tongue, or throat, hives, and difficulty breathing. Other serious side effects which require immediate emergency medical treatment include symptoms such as insomnia, blurry vision, mood changes, halo vision, fatigue, weight gain, facial puffiness, or irregular heart rate.