Doctor visits symptoms and conditions

i had mirena inserted at my 6 week check up after my son was born in march 2008... i only kept it in for 2 months. i was constantly bleeding and had more clots in my blood than i had ever had before. my doctor tried to talk me into keeping it in but i told him i just couldn't tolerate the bleeding. i never had any problems with any of my female specific doctor visits before or during my pregnancy. i've always been on the heavy side so my weight hasn't been a factor in the issue. since having the iud removed it seems like my problems have increased, i skipped periods all the time with no cause, no pregnancy, when i did bleed it was heavy and for weeks at a time with horrific sized clots (golf ball). every time i would go to the doctor they would tell me nothing was wrong, until march of this year when to my surprise... the doctors told me i had poly-cystic ovaries. they gave me loestrine 24 fe to help my periods and keep away the cysts but it didn't work, i still have unpredictable periods and still get cysts. they told me a 4cm cyst was nothing to worry about... HA! all my tests are still "normal" so i'm at square one still, but i'm almost positive all my problems were caused by that stupid mistake of an iud Mirena.

I wish I would have read these blogs before I decided to get the Mirena! I usually research everything but for some reason thought I didn't have to since my male obgyn said it was so great. I had it put in two weeks ago and am having it out this Thursday. Since it went in I have been bleeding, cramping severely enough to go to the ER, extreme faintness and dizziness, can't sit in any position without pain in pelvic area and it is not getting any better. I can't focus, work, sleep, nothing. I just want to feel normal again! I wish I would have researched before agreeing to do this! Not to mention the $250 I paid before seeing what insurance will cover and about 4 doctor visits and 1 er visit so far related to this! I'm not willing to ride it out any longer after reading other comments. I just hope it comes out easily!

I am a 53 yr. old woman who had aortic Valve replacement surgery in April 2007. I had a St. Jude valve put in and have been on Warfarin ever since. I usually go for a couple months with a steady INR and then, for no apparent reason, it goes out of whack and I have to adjust the level (with repeated doctor visits) to smooth things out. I have gained 20 lbs since my surgery, and cannot lose it, no matter what I do! I ride an exercise bike an hour a day, or walk a 3 mile route. NOTHING helps. I have recently said that if I had it to do all over again, I would choose a Bovine valve (even with the knowledge that surgery would probably have to be repeated later in life) just to be able to avoid the side effects of Warfarin. I have also experienced light-headedness, left sided chest pain, fatigue, coarse thinning hair, but by far, the worst is the weight gain!!

I am a 41 year old woman who had an epidural injection using Kenalog in my lower back (for stenosis, disc herniation, degenerative disc disease, etc.). My first injection was on 4/1/09. About two weeks after the injection, my period started a week early. I had light to moderate spotting, not quite like my normal period. I also noticed that I broke out with major acne, had bad mood swings, constant urination and increased hunger. I had a second injection in my back on 429/09. I told my pain management Dr. what I had been experiencing, and he said that it was the side affect of the drug, Kenalog.

I just saw my GYN for my yearly pap smear and told him what I had been experiencing. He said he had never hear of anything like what I was going through as it related to an epidural injection, though he also admitted it wasn't his area of expertise. Due to my age, my GYN commented that the spotting I was having could be due to my body changing and getting ready for menopause. He said that spotting was very common in women my age. He gave me a prescription for Progesterone 100mg to start taking for 15 days to see if that stopped my spotting (and hopefully return my cycle back to normal). He also did a uterine biopsy to rule out any other causes. My uterine biopsy came back normal. I'm currently taking the progesterone and my period seems to be tapering off, but it still hasn't stopped. It went from spotting to more heavy bleeding to spotting again. I'm due to stop the progesterone on Tuesday 5/26/09 so we'll see what happens there. It's officially been six weeks of having a period.

I'm very frustrated that I've had a menstrual cycle this long. I canceled my other future epidural injections as right now, by back in doing much better (the injections did help, though the side affects are the pitts!). If my back flares up, I will seek other solutions as I will NEVER have any Kenalog again.

For those women who've had the same issue with their menstrual cycle, did your cycle ever return to normal? If so, when???

I was prescribed Paxil and started out at 10mg. then they gradually increased it up to 60 mg a day. Later on they added I think it was 200 mg of Wellbutrin. I was on Paxil for I think 2.5 to 3 yrs. What happened was I was so out of it I didn't know what day it was. The HMO would have to call me to remind me to come in that day for my doctor visits. I slept most of the time and was just worthless. I didn't care about anything much and didn't have the energy to do much of any thing. This was a drastic change in me and my family hung in there with all this. I actually drove which is not a good idea at all. But when they put you on this you don't realize how bad you are on this stuff and once you are on it for so long then you are either a captive at home not able to do anything or you try to take back some part of your life. You also can't just go off of it cold turkey at 60 mg. I tried and it got bad and went back on it. After I got really bad all I did really is drive to therapist appts or to nurse practitioner who managed the Paxil and Wellbutrin. After being on 60 mg of Paxil and Welbutrin for awhile/months and I was so out of it, that is when they said we need to back me off of it. I think it accumulates in your body and I think you can kind of have an overdose in a sense. They didn't really monitor it that well and took their sweet time recognizing it. But they didn't say anything about it. I think that is what happened to me but no one at the HMO said that. Instead they got me scared that I was going to run out of therapy sessions allowed while on Paxil and that is why they were going to back me off of Paxil. I guess another patient had that happen to her and they didn't want that to happen to me. I then say my therapist very rarely while I was backing off of the Paxil. She acted like I was ready to handle everything on my own. I had no idea that suicidal thoughts were in my future when backing off of this drug. But they sure knew it, a lawsuit in California had been filed the month after I started taking the drug and it was all about the lack of disclosure about the withdrawal issues. First I got off of Wellbutrin and then they slowly backed me off of Paxil. It was physically wrenching. Throwing up and diarrhea all at the same time. Painful is not the word. I have given birth to two kids and pneumonia and this was much worse! Chills, tremors, I felt sick all the time. This went on for months. When I talked to nurse practitioner they pretended that it was no big deal. I wasn't sure what was happening. I finally got pissed off about the whole thing and never called them back and they didn't follow up either. Not even therapist. They hoped I would go away quietly which I did. When you are in the throws of this and you know who did this to you, you really don't want any more of their harmful help. It took at least a year to feel better. There is this uneasy weird feeling and zinging noise that lingers for a long time. But my memory is a fraction of what it was. My short term memory is very difficult. I know that Paxil was responsible for this. How do I know? Well when you are on Paxil and if you have a recall on a bad incident and you start to emotionally react to it, Paxil will offset it by making you sleepy. It literally targets your emotional reactions and those thoughts connected to it. It tries to disconnect the feelings from the thoughts. These disconnects also disconnect your ability to remember other things. Even after I got off of Paxil I noticed that I would get sleepy when I thought of stressful things. It has taken me about three years and I am talking better and can remember many more words. I talked very simply for so long since I couldn't recall basic conversation. It targets emotional responses and I got to a point where I was really numb about a lot of stuff due to the constant tapping down by Paxil. I feel like it disconnected those connectors to your brain that talk to each other. My family made jokes about me and how simple I got and how I couldn't remember anything. They are worried that I have alzheimers disease or will get at this rate. I could not work on Paxil at those high doses I was on and while I was withdrawing. I found that afterwards my memory was so bad that I missed so many simple things that I would have never missed before. I am concerned that my memory lapse will cause a big mistake that may hurt someone. I was out of work for so long. I volunteered to keep myself busy until I got too bad. It would keep me busy. I also noticed that while on Paxil I was uninhibited and said things that hurt folks and I was unable to monitor myself like normal and couldn't determine what was not appropriate to say all the time. I had an emotional disconnect to myself but also to others. This hurt some folks and cost me a job. My memory is so bad that I have to write down important things if I really want to refer to it again. I also have given up on going back to school. I couldn't test well at all. I can not remember what I did 5 minutes ago let alone a chapter I have read. I am only 52 now and I feel so much older due to this. I suffer from Fibromyalgia and IBS. I was so upset with my doctors at HMO since they didn't warn me of the withdrawals. When they put me on Paxil I was adamant about not taking an addictive drug. My family has had a history of addiction and I was not going there. I know how bad it can get. Paxil's withdrawals is very much like the withdrawals that addicts go through. I was devastated by not only how doped up I was on Paxil but also all time I wasted on it and with the year just trying to withdraw from it. Then the time just trying to get some of my memory back to function. I am mad that there is no way I could go back to school to better myself. I am mad that no one warned me of any of this and if they would have I wouldn't have taken it. How many of you would take a drug knowing that you memory would be messed up? Not many. Certainly not me. My daughters know what a tyrant I am about drugs and alcohol. This is not something I would have opted for if the whole truth were known. They certainly don't warn you that your memory will be like swiss cheese afterwards. No one in my family has had such memory loss. No alzheimers disease. In fact quite the opposite is the case. My grandmothers were very clear at older age, so menopause can not be a big factor and beside this happened before menopause. Also grandfathers and father were very clear getting older. My family noticed a definite change while I was on and after Paxil. The irony was that when I started to go back to HMO for regular care which took me a long time to trust them enough for them to do even that, someone at HMO had put in my automated chart that I was allergic to Paxil. They won't say who put it in either. I was not allergic to it but they are now saying that I had a bad reaction. But what I say is after seeing so many "bad reactions" on websites like this I am convinced that this is more than isolated cases but rather the norm of what happens to patients who take it. HMO doesn't want to admit wrong doing. Paxil seems to have kept a lid on it. Besides how do you measure a bad memory and how do you prove it after the fact? You are getting older and who is to say it isn't genetic. But I was on it for maybe 2.5-3 years. I was so out of it I don't remember how long I was on it. I also was suicidal when coming off of it. I even called a crisis line since I couldn't trust the HMO. I was irrational. For those of you still on it I think you are doing more harm than good. I don't believe all the facts have come out about the side affects from these types drugs. Who would be doing the studies? Certainly not he drug companies, FDA is a joke and if you think the attorney generals are doing much think again. Yeah a couple states like CA an NY they did settle on suits about suicide for kids but they settled quietly. The doctors who prescribe these drugs also are in a catch 22 like my HMO. They don't want to be linked in this and will avoid it too. What attorneys can afford to go up against all those high powered attorneys for those loaded drug companies? Not many. No one is actually dying from this and that is another reason there won't be much done on this either. Fortunately today we can hook up online and share our stories and this is the first step in documenting what is really happening to patients.

Be so careful coming off of these drugs. Give yourself plenty of time to get normal. Make sure you are seeing a therapist you can trust and is trustworthy. It takes an alcoholic about a year to rid their bodies of the toxins that have built up in their tissues. I do believe that is also true of Paxil. Be kind to yourself and get good support while doing so. It can be a very lonely physcially and mentally anguishing time. Think of yourself like someone who has had a brain injury or stroke. You need to practice to get things to reconnected as best as possible considering. You will never be like before you took Paxil but with time and patience and hard work it can get better or you can develop ways to compensate or work around or cope with such memory loss. Financially this can be devastating and it was for us. The loss of income and finally a bankruptcy. We paid dearly for taking this drug. It can be very frustrating and you have to look long term. I think it is very easy and cheap for HMO's to pass out pills rather than schedule needed appointments for therapist and other alternatives. Before they started to take me off of Paxil I was warned by my HMO that I had exceeded my number of appts allotted for a 2 or 3 yr period. So I may end up without any therapy while on Paxil. That is the reason why they decided to back me off. I had apparently used something like 32 appts in two or three years and I was getting close to not being able to have any for a long while. This was interesting approach since by then they knew that suicide was linked with Paxil. They will put you on Paxil and they will leave you high and dry without at therapist if you actually use one regularly and use up a normal amount of visits. I have very little compassion for HMOs. What was amazing was listening to the nurse practitioner tell me if these drugs don't work there are lots of other ones we can use. These are the easy going drug pushers of today and they prescribe these drugs without much thought. They make it cheap and easy and they will swear to your face they aren't addictive but are basing it on very little research. They regurgitate what ever the drug companies tell them. The cost cutting with HMO's is almost frightening. I also have problems sleeping too. I wonder if the drug messes up your serotonin levels since it does make you sleepy so much of the time and when you are off of it the brain is fried from all that artificial serotonin that it no longer knows how to manufacturer it well. I think that is what maybe causing my Fibromyalgia since this is a condition where you muscles never repair themselves at night due to lack of sleep is one theory. I was always a deep sleeper before all of this. I think there maybe a connection.
Finally depression. When you can't remember what you did 5 minutes ago or simple things it gets more than frustrating, you get depressed at how limited you are now. The pain from the fibromyalgia is constant and that too is depressing. I wish someone could put together the data on this to prove the link to memory loss and how it has affected our serotonin levels.
The only way you can stop companies is to sue them. Government won't do it really. A class action suit might work.

2 days ago I just happened to come across this website. I was in tears reading all of your stories. It sounded like it was me writing! You have given me the answer to all my misery over the past 3 years! My marriage nearly failed from all of this. I was married in July 2005, had a son in March 2006 and immediately had the Mirena IUD inserted. I thought it was the best thing on earth! No side effects... that I was aware of!! It all came on so gradually that I blamed my symptoms on post-partum hormones and a change in life-style. I remember I became a total bitch towards my husband very shortly after I got the Mirena. I gave up exercizing, ate like crazy (partially probably due to breastfeeding), and I had absolutely no sex drive, which was a 180 for me, because previously I wanted sex everyday! I blamed this on hormones too, or maybe my weight gain... just not feeling sexy anymore. When my son was 12 months old, I had the Mirena removed, only to try to get pregnant. We had a daughter in December of 2007, and I immediately had the Mirena re-inserted. As time went on, I was the bitch I was after my son was born.. again, I blamed it on my hormones. My back was killing me all of the time.. I blamed that on having to carry my daughter around. Then the insomnia hit me.. wow! I would lie awake in bed till 6:30 in the morning, and this was after my daughter finally started sleeping through the night. Maybe I had insomnia the months prior but never noticed because I was up all night long with my daughter anyways. I was miserable, depressed, moody, and incredibly mean towards my husband (thank God not towards my kids). He's a saint to still be here. Last summer I started getting pain in my joints. Some days I couldn't lift my kids because my wrist was so sore... or I was limping because of my hip or my knees. I was also incredibly depressed at this point. I was getting virtually no sleep, was pissed off at my husband all the time, and looking after 2 kids was draining me. My husband, being non-confrontational, was lying to me all the time try not to rock the boat. I found out he was lying to me, and I thought he was having an affair. I was crying all day everyday... finally after everyone told me I was depressed, my doctor put me on anti-depressants, and a bedtime pill called Elavil to help me sleep and to help with my joint pain. We went to marriage counselling (still are). After 2-3 sessions with an amazing counsellor, we realized I was not suffering from depression. Thank God, because the anti-depressants were making me even more miserable and I was binge eating like crazy! My husband and I, with the help on counselling, have since dealt with all of our problems. So why am I still so unhappy? Why is my join pain coming back? The Elavil is not working for my pain anymore. My body feels like I have the flu. Achy, but more intense and joint-specific. I have no energy or motivation to do daily tasks like laundry, clean the kitchen, or even take a shower and get dressed. When my kids wake from their nap, I feel like crying because I don't feel like a good mother is caring for them. 3 days ago I was with my husband and kids and had to leave because I began to cry. My husband came to ask me what was wrong, and I just said that I was in so much pain, I couldn't stand it. The truth, which I did not tell him was: I literally could not take another day like this. If I don't get better, I don't want to live anymore. I was not contemplating suicide, but I'll tell you this.. if I hadn't found this website when I did, who knows what I would have done!
Looks like I know how to make a long story even longer! LOL.
My husband and I went out for a romantic dinner on Friday to celebrate Valentines. I told him what I had discovered.. actually, I just handed him this website on my iPhone. AS he read your stories, we both were in tears! The last 3 years should've been the happiest of our lives, and we were robbed by this devil-IUD!!
Last night I couldn't take it anymore. I was crying and my husband said, "why don't you just go to a walk-in clinic and have it removed?" So I did! It was painless and I have no bleeding or cramping as of yet! I don't know if it's psychological, but I feel terrific today. My joints are achy still, but my mental state is on cloud nine! I have energy today and have been playing with my wonderful adorable kids all day. Let's hope it lasts. I will keep you all posted!
I hope my story helps someone as much as you have all helped me. You have saved my marriage, and probably my life. Thank you all!!

Hey all i'm a 25yr old Caribbean woman who has polycystic ovaries.....two years ago i had a jumbo cyst removed from my left ovary ..... a year before that was the first time that i started noticing that my period that was usually like clock work became more and more unpredictable..... (here for two days , then gone for five months) anyway my surgery passed well and everything seemed normal .....but then the cysts came back ( tiny ones) and the irregularity started again..... I was put on Yasmin...(reluctantly) i had never used bcp prior (I heard the horror stories though).... i already suffered from severe mood swings and bout of depressions but this pill made things a hundred times worse... I also had bouts of dizziness, nausea etc i'm very poor lol seriously speaking and doctor visits are anything but cheap in my country soo i'll still monitor it for a while longer.

I am relaying the story of the granddaughter of my boss. She was 15 when she got the first shot of Gardisil in May of 2007. Within hours of the shot, she collapsed and an ambulance was called because she had distressed breathing. She was taken to a hospital and was in intensive care for 2 weeks in and out of consciousness. In the meantime, her mother tried to get the shot records from the doctor's office that gave the shot. They did everything in their power to:
A.Dismiss the correlation between the shot and the girl's collapse, despite the girl being in good health before the shot.
and
B.Keep the parents from getting hold of the vaccination records.
It was like pulling teeth to even get the vaccination batch numbers, and finally the office told the parents that somehow, the girl's health records went "missing". Luckily, the parents still had copies of most of the doctor visits, plus the "aftercare" paper following the shot with vital information on it.

When the girl finally began to be able to sit up again and eat on her own, she experienced mental fuzziness, memory problems, and speech problems. She had perpetual tingling and jolts of pain on the arm that had gotten the shot, in her side and abdomen and down both legs. Three weeks after the shot, she tried to get up out of bed and found she could not walk. She was diagnosed tentatively with Guillain-Barre Syndrome, also with nerve damage. It took her three full months to walk again without help, and even now, a year and a half later when she comes into the office she still has a bit of a limp. She lost over 25 pounds, which is pretty sad as she was not overweight or anything. She now looks very skinny and sickly. She had to quit school and started being home schooled because of the physical and memory problems and depression. I feel so sorry for her and her parents, who thought they were doing the right thing.

six months ago my dentist prescribed 500 mg and 500 mg of penn every eight hours for five days,, along with vicodin for a horribly painful gum infection in my root canal. To this day I wonder if I will fully get rid of all side effects of the Met. After 3 days I was soo dizzy and with extreme blurred vision, the pharmacist and dentist office stated it could not be the ant but the vicodin. I stopped the vicodine and just stayed with Motrin. I had the worst vertigo and blurred vision you can imagine, I felt like an infection was now in my brain, (yet was not) I felt like I had a toxic infection in my body. I would fight to concentrate mentally, I was very fatigued and sick feeling. This went on long after the tooth pain. It took about three months of strining for mental concentration, dizziness, toxic feelong to begin to go away. By the fifth month I could finally feel my personality had returned. Yet my vision has not and has only gotten worse. My dizziness is every so often. During the first months I kept running back and fourth to my doctor with no avail. It was the eye doctor MD that said he was very suspicious that I had an toxic allergic reaction to the Met. Between doctor visits, eye doctor visits, cat scan I have run my medical bills high. I am extremely worried about going blind.
It has now been six months - my health, my vision, my family, my job, my personality have all suffered from this.... Don't take this drug............

I was on Minocycline (a cousin to Doxycycline Hyclate) for years. I’m not sure how long exactly as I didn’t write down the date that I started, but I believe I have been on it around 3-4+ years. Well I went to a dermatologist and he instantly looked at the outer area of my arms (just above the elbow) and recognized I am suffering from skin discoloration, and prescribed Doxycycline, and told me to stop taking Minocycline right away. I also have this blue-gray skin discoloration on my back near my shoulder blades. I took my Minocycline for the next two weeks till the Doxycycline came in then stopped the minocycline, and started Doxycycline on Sunday. I take a 100mg pill twice daily with a meal, and thus far have had no issues. Keep in mind that I have been on Minocycline for the past 4 years or so and maybe I’ve been suffering similar side effects on that drug, thus I would be unable to see the difference with Minocycline’s cousin Doxycycline. I am pretty sure the first year or two that I was on Minocycline I was depressed (other things in life may have contributed to this depression, but now that I see all of these people saying they have had mood swings, I must state that I have had many more mood swings in recent years then I ever remember before being on these meds). I have also been extremely sleepy the past few years. I used to NEVER be able to fall asleep in public, but (I believe about the same time I started Minocycline) I gained the ability to sleep anywhere. Now I mean, anywhere. I can sleep even after I get anywhere between 6 and 14 hours of sleep. I have had approx 7-9 hours of sleep on average for the past 6 months, yet am always tired. I can’t remember the last time I haven’t been sleepy, and have had many doctor visits to attempt to discover the reason for this, but hadn’t read the side effects of Minocycline. I’ve still been pretty sleepy since Sunday, but I’ll hope that this Doxycycline isn’t as bad. Anyone else have a similar issue, where you used to be awake, but now you are always sleepy (wake up in the mornings a bit dizzy and confused), and have a hard time concentrating on one thing at a time?

When a class action lawsuit is filed, let me know....this drug should be taken of off the market immediately. We started all of this with an OB/GYN that prescribed this “miracle pill” and now have had to go not only to our primary doctor, but also a psychiatrist, gastrenologist, college campus counselors, psychologists, psychiatrist, and the campus medical doctors; All the while, accumulating enormous doctor bills. All the doctors say, "No, Yasmin won't cause those problems" (except the college campus doctors..wonder why? Hmm.. could it be that they are not in private practice?)....well, I beg to differ. Everyone needs to give this website to their doctor so the doctors can hear from the patients that have taken this drug, and not listen to the pharmaceutical companies that are pushing this drug to be the "miracle pill". Maybe if enough people complain and go to the media, we can get rid of this drug!
My daughter who is 18 was put on Yasmin because of irregular periods, hormonal imbalance, etc. We were told it was the new “miracle pill”. It will make you loose weight, regulate your periods, clear up acne, you name it, it will fix it. Yeah, right.
She started taking this pill in March 2007. She was off at college but called to tell me she was experiencing horrible headaches, behind the eyes. She complained about her stomach hurting, but we just figured it was the stress of freshman year at college. Then she said she got where she couldn’t eat when she went to a restaurant. When she came home in May for the summer, I noticed a total personality change. For example, she was always a neat freak, and now she wouldn’t clean her room. The first day when she drove home, she started crying she was so mad about the traffic. Yes, she has always had a little road rage, but this was ridiculous.
By June, not only could she not be in crowds, like at a restaurant, but now she is having full blown panic attacks and IBS. We called the OBGYN and they said, “Yasmin won’t cause this, go see your primary doctor”. I knew that the only thing that had changed with her was taking the YASMINE. I knew it had something to do with all of this so I “Googled Yasmin” and this website (http://www.medications.com/se/yasmin) was the first one I looked at. All of her symptoms matched everyone else’s! I am so glad we found this website, it explained everything and I had her to stop Yasmin immediately.
So we went to the primary doctor, explained about the Yasmin and how we thought it was the culprit of everything. Of course this doctor also says, “Yasmin won’t cause that”. We told him to look it up on the internet and see how there are over 3000 complaints on this drug, more than any of the other drugs on the market.
Besides the emotional problems she starting having, her pulse and blood pressure was sky high, so he puts her on medicine for that, and puts her on an anxiety medicine and sends her to a psychiatrist. She is very thirsty all the time, and develops IBS. She can’t eat without having pains in her stomach. So, now we’ve have gone from having just irregular periods, to all of the above, plus a psychiatrist.
The psychiatrist doubles her medicine (and puts her Pamine for the IBS) because the panic attacks are gone, but she still is having a lot of nervousness, anxiety, can’t sleep at night, crazy thoughts, worrying all the time, etc. A month later he changes her medicine again, to Effexor. The first 2 weeks, she does okay, but the packet doubles the strength after 2 weeks. It takes 4 weeks for it to take full effect. Right after she doubles this medicine, it is like her senses are on hyper-mode. She can taste everything that is in her food (chili powder, seasonings, etc…), taste the metal in water, and she can hear someone’s phone vibrating, in another room.
Then she goes back to college at the end of August 2007, and it’s horrible. The Effexor is having bad, bad side effects. We called the psychiatrist that she was using at home and he doubled the dose. That was the worse thing they could’ve done. The side effects were worse than ever. I had her to immediately go to a psychiatrist on campus. She told him the whole story and he believed her! Needless to say we switched doctors. He then lowered her dose back down to ½ a dose and hopefully can slowly get her off of all this medicine.
The newest thing she has developed is being hypoglycemic. The campus psychiatrist sent her to a campus medical doctor and he told her that they would get to the bottom of this. He tested her for everything under the sun. Low blood sugar is the only thing they found. But, she hasn’t taken the Yasmin since May. No telling what the results would have came back like if it was done at the time she was taking Yasmin.
Thank goodness she has counselors and doctors there at the campus that believes that Yasmin can cause all of these problems, and are working with her. From what I have read from the people that have used this medicine, although most doctors do not agree, Yasmin takes like 6 months to get out of your system. I think I am going to believe the testimonials of the people who take this medicine, over a doctor who prescribes it.
If everyone goes to the media, their doctors, the FDA, congressmen, and make them aware of these horrible effects, surely we can get this drug off of the market! Does anyone know a class action lawyer that would pursue this? For my child to have to go through all of this is ridiculous, not to mention costly. What do we know of the long term effects this drug will have if it is doing all of this when you first start taking it?
If you have the same concerns as me about this drug, and would be interested in looking into a class action lawsuit, please email: ****** I would be interested to see how many would want to pursue this.

Hello,

I read about how YAZ birth control pill affects the body and psych and I am now scared. This is my 2nd day of YAZ (I've never been on birth control pills ever and I am 27 years old), it's all new to me but after reading all these negative posts about Yaz I don't know what to do. Before the birth control pills, I was depressed, annoying, serious weight problems - 210 lbs :~~((, low energy, low libido, always tired, terrible migraines every 2nd day, ridiculously increased appetite and excessive hunger, hair where it shouldn't be, menstrual blood clots, excessive cramping etc
I have all these problems for 3 years now and now that the family doc. put me on YAZ birth control pill I am even more scared - mainly of more weight gain, it would be a tragedy for me, I am fat enough already and what's worse I can't lose the weight, exercise doesn't help, diet doesn't help, NOTHING. Will YAZ birth control pill worsen my already tragic condition? I just don't know what to do and what to believe ... I appreciate any advice or help you can give me ... Thank You to all!

I started using Yasmin right before I was married May 2006. We wanted to have children but, wanted to wait a little bit. I bled the whole month and experienced major weight gain. I had cramps and felt awful on it. I didn't feel like myself. My husband and I started to try for children in Sept of 2006. We stopped taking it. I continued to bleed when I stopped taking it.

A few weeks later we got a positive sign on a pregnancy test. We were so excited!! A few days later I started to bleed. I went to the doctor and after blood tests and ultrasounds they found something on my right ovary. At first they thought it might be cancerous. After more tests we found out it wasn't cancerous but there was a cyst.

I had had previous doctor visits with nothing showing. A clean bill of health. Now all of a sudden I take these pills and I have a cyst on my ovary. We continued to watch it and they came to the conclusion that I would need to have it removed. In November I had my right ovary removed.

Our chances have lessened since the removal, I stopped taking the pill at the end of January. We have yet to get pregnant, and have been trying most of the year. I continue to have my period monthly but, we are not pregnant yet. I find it difficult to lose weight too, although I'm still trying. I don't know if we are ever going to get this stuff cleared out of my system. No one ever warned me of possible cysts, of the dangers of using vitamin C, and we were told that we should have no problem, as soon as we stopped taking it we should have no problem getting pregnant!!
LIES, LIES, LIES.

I'd be interested in participating in a class action lawsuit. We may never have kids because of this.

My 4year old grandson has been on 20mg adderall Xr for aprox 2 months .. It has helped with his hyperness but soon after taking the drug he becomes emotionl and completely beligerant. He acts out and screams at you. This goes on for hours. Ive discussed this with doctor and he wants to up the dose.. Almost afraid to. Dont want to think that grandson could get anymore beligerant. He was hyper before the meds not beligerant. Where can I go to find more on this.?

Hello,

I haven't been on lately posting my symptoms because for the first time after 8 months of Post Yasmin Hell, I have started to see real progress.

After taking Yasmin for 7 months, I stopped and have been so so sick, it was unbelievable. Over 50 various Doctor visits and nothing at all could be found. I lost my appetite and 13 pounds, had anxiety and heart palpitations, nauseous all the time and just so so ill. I have never been sick all my life... never...aside from colds of course.

Nothing really helped... vitamins, food... nothing. If you really think about it.. . we ingested a POWERFUL horomone suppressent. How can we think that taking vitamins or herbs will solve the problem? Believe me, it might help a little... a very little but far far from the solution.

I notice that my worst symptoms were cyclic and each month I could be assured that I would get worse and going through this month after month with little improvement was taking a toll and I just wanted to literally give up already. The rate of improvement was ridiculous!! 1 % perhaps... less?

So then I told everybody my absolute last resort was taking an antidepressent because my general Dr. told me that it has been used off label to help PMDD which is a menstrual disorder. My other Dr. also told me it has been PROVEN to help gastrointestinal problems also.

I know most of you are scared and skeptical about taking another drug, just how I was. I kept saying.. I am not depressed, etc etc. I was worried about side effects etc. But after a while it came down to a point of.. I NEED TO TRY SOMETHING ELSE!!!!

So if Prozac has been shown to help with female horomone problems I should give it a shot and see if it will help mine, because believe me, it couldn't really get any worse. How can someone live through or six months of hell??? You long term sufferers know what I am talking about.

So I did a TON of studying on Prozac / Fluoxetine and found that this proven drug is the easiest of all the SSRI's as far as side effects and withdrawal. I also read that taking a low dose is just about as effective as taking a normal dose. For example, would you give the same 20 mg. dose to granny as well as Shaquille O' neal?

To give you the best news already: I have finally turned a corner and am starting to feel so so much better, month by month. Prozac has finally reversed this cyclic monthly hell. I had ABSOLUTELY no side effects because I researched and researched and realized I only needed a small small dose. I started at 10 mg. EVERY OTHER DAY. This dose is very low and yet very effective. The usual dose is 20 mg. daily.. which is too much.

My appetite started to slowly come back, my anxiousness went down. My general sense of well being became better and better. Yes of course, the monthly cycles would sometimes pop up once in a while but this time 75% better than before.

So for all of you who like me made the mistake of taking a powerful horomone altering drug Yasmin and still not getting better, you may need to try Prozac because I am proof that it does work. Don't be afraid of withdrawal or side effects because the low dose you need will cause none of these... ask your Doctor. It is not only used for depression because believe me, I never had any depression issues at all, but Yasmin caused my body CHAOS, and no vitamins can really help that kind of mess. Prozac is helping by pushing my horomone system back to it's normal activity as well as helping my digestive system AND my overall well being.

I was just like all of you, coming back month after month because just when I thought I was getting a little better, the bad cycle hit me again like a truck and I thought I would never get better. I avoided Prozac because I thought it was bad and that how can an antidepressent help me? I was wrong, Prozac has been the ONLY thing that has helped my cycle get back on track. Ladies who are still long term sufferers of Post Yasmin hell, read up on Prozac and it's off label uses of treating Pre menstrual dysphoric symtom, as well as digestive treatment.

Also, although SSRI's are all in the same class, they can have very different effects on individuals. For example just because Zoloft didn't agree with you, that doesn't mean Prozac will do the same thing. The ignorant DR. probably gave you too high of a dose as most Doctors do.

The best way of finding out is starting on a low dose. You should see no side effects at all. Well the one side effect that was welcomed was a sense of calm and sleepiness. So much better than the panic attacks...

FYI. I have realized that Yasmin has hit me XTRA hard because Yasmin has a high dose of ESTROGEN, and my body before Yasmin was the opposite... testosterone high! I am ultra fit, love working out and don't possess the typical estrogenic female body, meaning I don't have big breasts or typical softer female features. So being on Yasmin really changed the dynamics of my body.

Again, if any of you have similar symptoms of me and is a classified long term sufferer (6 mos. or more), my sincere advice is to talk to your Doctor about Prozac and give it a shot at a low dose. There should not, I repeat should not be any side effects and you should start to get better month by month.. and this time at a much faster pace.

Victory! My optometrist...yes, I did say, my optometrist reported my Yasmin problem to the FDA. After 5 months off of Yasmin...and MANY doctor visits later, my general practicioner also has reported the horrible problems I have been having. I went to the gyn Tuesday (still having problems in that area too) and she finally started to listen. Maybe word is getting out now. It will be so nice to be able to see again without the spots or blurriness!

Virginia, USA

I am a 23 yr old female and it all started for me after my 3rd month on yasmin. I was just finishing my period when I awoke one night with shooting stomach pains on my right side. I went to the bathroom, came back to bed and must have passed out b/c the next thing I knew, my husband was shouting at me to wake up and on the phone to 911. I went to the hospital right away and after a ct scan on my brain and stomach and lots of blood tests nothing was found....however, we knew there had to be a reason that I passed out and experienced such severe stomach pains. I went off the pill immediately after that night. Then 4 nights later, the panic attacks started in-I went to the emergency room again that night to find out I just had my first panic attack --which I never had before in my life-
It has been a month since I have been taking it-and after numerous doctor visits they now think I am suffering from gallbladder attacks. I read on here once that a girl had to have her gallbladder removed after being on yasmin. I am a healthy person and have never had any serious health problems or anxiety/panic attacks before taking these pills. These last 4 months have been the worst of my life. I am off to the hospital tomorrow for more testing on my gallbladder and liver and I am still having occcasional anxiety/panic attacks. I wish all of us could have one big meeting so we could knock this pill out for good. E-mail me with any concerns you might have-I would love to talk about it!

side effects, how about feeling as if i am falling apart. i am a dance major and 28 years old.
i feel as though my life is over. my body feels like i am a hundred. i am thinking of
not taking my meds. it can't be any worse than the way i feel now. i am either really tired or
can't sleep. i have to take something to make myself go to sleep then i can't wake up for school. i have blurred vision/vision changes, constipation, my body hurts all over, my back is
badly injured, i have persistent headaches, chest tightness and pain, sore throat often. . .theres
more too, the biggest thing is i thought that i was going crazy with all these doctor visits and
questions until i read this web page. thank god, maybe someone has an opinion to relate!

Having been diagnosed with COPD, I am prone to respiratory infections. I take Levaquin every few months for 10 days at a time and also anytime I am in the hospital by IV drip.

The medication sure does the trick and I probably owe my life to it many times over. However, I do get a rash, mostly on my arms, every time I use it. The rash is crusty and blistery and itches like crazy. I have some ointment a doctor gave me but it really doesn't seem to help.

I was never told anything about side effects of this medication and figured out myself, even after doctor visits for the rash, that it was caused by the Levaquin. Doctors aren't too smart sometimes.

It's a great medicine but, as with all medications, people should be careful and pay close attention to any changes in their body anytime they take any medication.

My husband took Reglan for 6 month for acid reflux disease. (Prescribed by the VA, Fort Wayne, IN). After SEVERAL doctor visits for shaking, sleepiness, TD etc... a psychiatrist suggested his symptoms were due to this drug. It has been over 2 years now; he is still disabled, has spent over 4 weeks in a mental hospital, and will most likely be mentally challenged for the rest of his life. This drug should be banned. Please be careful on what drugs you take and weigh the side effects to the benefits of the drug.