Google symptoms and conditions

I started NuvaRing in Sept 2009. I started noticing my right boob was VERY sore like it felt bruised. I also noticed that I didn't want to have sex with my boyfriend. We have only been together since May so you know we were hot n heavy until I was put this thing in! I got to where I didn't want to be around him or have him touch me and I noticed that I was horrible to my kids! I didn't want to play with them, I just wanted them to go to their rooms and leave me alone. I thought it was just me and my boyfriend having trouble and I was just waiting for him to kick me out! I was having headaches and moodiness and I just wanted to stay in bed. I also noticed I gained some weight. Now I didn't step on the scale but my pants went from a 10/12 to a 14! My boyfriend actually heard about some side effects on TV one day when he got home from work and he asked me to take the NR out because he was concerned. So, I did and lo and behold, I started my period 2 1/2 weeks early! So, now I'm "google-ing" the NuvaRing and I find all this on all these different sites...so it's NOT just ME...it's alot of women. I should have researched BEFORE i filled the script. No more NR for me...I can't stand the depressive and bitchy side of me and neither can my boyfriend!

Hi there... I came off of Yasmin just 2 weeks ago and thought I should share with you my story since yours is a skin issue. I took Yasmin for 3 years. This past year I would wake up some bumps on my lip.. then on my hands.. then (this is over a period of months) I would wake up and have a slightly swollen lip... this was over the last year or so. I would also get a feeling in my throat, like something was in it and swallowing felt funny.
WELL, 2 weeks ago, I took my bc like I always do, right before I go to bed and my lip starts to tingle and itch.. and in the morning my face was swollen 3x the normal size on on side, mostly at the lips... I couldn't really talk.. it was like those awful photos on google. It was angioedema and can kill you by swelling of the throat. I had also for about a year- an ear issue.. it would sound like I was talking under water and felt like swimmer's ear- related to the swelling I found out later. Turns out I'm allergic. I developed this allergy over the period of time I was exposed.

I just want to say to anyone out there that has FACIAL/LIP SWELLING, or swelling of the hands... GO TO THE ER. It can kill you. I got lucky.. my swelling started slow and after about a year if was full blown. It is not something to mess around with!I was prescribed an epi pen. I developed an allergy to a preservative in it and I'm not an allergen sensitive person. That was just the parms/doctor guess I might add.

The first year I took Yasmin I had numb and tingling toes. and the whole tie I've had on and off leg pain.. no sex drive, that's the truth..definite bloating issues about 6 lbs weight gain, sometimes more without change in diet. I haven't noticed any hair loss thankfully. Migraines. Lots of nausea in the morning, every morning like morning sickness. Car sick even when driving.. not normal! I used to work on an airplane and I never got motion sickness.

I'm now on day 4 of Mirena IUD and I'm having having severe diarrhea and trouble sleeping.. I really, really don't want to get pregnant. Our next step is a vasectomy for the hubby. I'm 25 and I weigh 140 5'10 if that helps. I wasn't an 'at risk' like the pamphlet said.

Well, I have one side effect I haven't seen anyone mention. My breasts feel weird, like they did at the beginning of my pregnancy. I've been trying to figure out a way to explain the way it feels, and its a combination of when I had a yeast infection in my breast while breast feeding (not nearly as painful though) and the way they felt when I was in my first few weeks of pregnancy. I also have constant cramping, its not terrible, but constant. Then I've also had joint pain in my hips, I've woke up in the middle of the night with my hands asleep. And you can't even imagine the weight problems I've had. I weighed 180 two days before I had my twins, 160 when I came home from the hospital, 135 in January, and now I'm 175. If I gain 5 more lbs I'll weigh as much as I did 8 months pregnant with twins. I've tried dieting and I still keep gaining. Then my DH also says that I am not the same person. He was the reason I started looking into side effects because he told me one night that I've changed since I got the IUD and it is making me crazy. I thought he was crazy, that it was just because I had babies and more on my plate now, but then I thought that maybe he was right, that my moodiness and weird feelings combined could all be from the BC. Then I started researching. There are too many woman posting problems with the Mirena. I think it should be taken off the market (and they should pay for everyone to have it removed). If you go to Google and just search for Mirena IUD, don't include side effects or problems, just type in "Mirena IUD", you will get an official site, a couple of drug websites, and the others are sites for side effects. That should tell you something. There's even an support forum.

Just to start of, I just got out of the emergency room for heart attack symptoms which I later found out were caused by my cholesterol med that I was just put on 2 weeks ago, Litportal. Well after looking this up on google and found out many people had the same affects I figured well if that made me have so much pain maybe I should look up Lisinopril w/ body pain. OMG, was I speechless. After reading the blogs I was sure that the Lisinopril was causing all my pain which doctors had diagnosed as Fibromyalgia after 8 years of testing. I was put on Lisinopril 8 years ago after my reg brand was not covered by my health insurance. Didn't think much at the time because it was suppose to be the no name brand of what I was taking. Well, it started off with weird things happening. Pain in my ankle and wrist like I sprained them. Shooting pain in arms and legs. Vision problems, numbness on one side of face, stomach pain, just feeling like crap. Months past then other weird things happening, not feeling like I slept at all even though I did for 8-9 hours, body aches all over, anything I did made me hurt. Then years past and it was everyday, wake up with pain and go to bed with pain. Not able to do simple stuff like play with my kids or go grocery shopping knowing I was going to hurt even more and that percocet was all that would relieve it. After 8 years of this I am totaling drained. Just cleaning my house kills me. Everything got even worse after the years and still gets worse. Going to the doctors knowing they think I am crazy and it's all in my head. Family members questioning my pain. I would always say, if you could be in my body for one day, just one day, you would know the hell that I have been through. But today, a new life came into me, after reading tons of blogs on the side affects of Lisinopril. I am just hoping that this is what it is caused from. I am 39 years old now, my 30's completely wasted, and do I mean wasted. To think that this has all been due to a little pill taken daily for 8 years. I thank everyone who has posted on this blog, because if it wasn't for you, I would have no hope. Now I do. And I am schedule for an appointment in 3 weeks to change my meds. What I thought I would have forever may soon be gone. Or at least some of it. Thank you.

This is not a new side effect, but the same day I started taking Levaquin for sinusitis, I suspected something was wrong. Within hours, ears were roaring. First night, NO sleep, and that's WITH Ambien CR. Day 2.....depression! Immediate. This is in spite of having a severe depression under control for over a year. Sudden. I really started suspecting Levaquin then, but thought it was a coincidence. Took it this morning. Deep, dark depression. After reading these posts, I knew my suspicions were correct. The depression is getting better after 10-12 hours after the dose. This is really scary stuff. Really scary. Oh, yes, and I had the stomach pains, also. Told my husband it was just hurting like a bruise, not like indigestion or gas. I will report it to my doctor so they will no it's a "no-no" for me....in spite of all the websites that said how safe it was. Glad I found this website. Thank God.

Hello I am 40 yrs old and got a lung infection which cause swelling in my lungs so the put me on high doses of prednisone via IV for 21 days in the hospital. The drug saved my life and took it at the same time.

After I got out of hospital i was on 60 mg for 6 weeks the 30mg for 6 weeks then 20mg the 10mg. It has been a living HELL over the last 5 months or so.

I told my DR. i have very bad blurred vision and he said it because the med runs my sugar up but I check my sugar and limit my sugar and it around 100 all the time which is normal soits not sugar. Then he said well them you need to see an eye dr. cuz your eyes are going bad. I begged to differ with him and told him if there was something wrong w my eyes then why is is one day I see fine and the next day all blurred and then back to normal!? it this stupid steroid if you ask me plus on day my right eye is bad and next day my left uggh!

The WORST side effect it the brain fog as yall call it. OMG I feel like im loosing my mind and going crazy. The dr. says hes never heard of such with a wise remark and says you know where your at now right? I know where i am and what I say but I feel like its not really happening. Its like im dreaming it. I feel like Im trapped in my head and I lookout blurry eyes.

Before I was a very confident independent person but now I feel scared all the time i feel hopeless and ive went through 3 girl friends over the summer because of the extreme forward attitude the med gives me. I am not the same person I was. I some time just want to die. I'm extremely tire if i do any exercise at all.

Plus I have all the other typical side effect like the moon face and weight gain. I don't even look the same cuz my eyes have huge bags under them and a double chin I never had.

I feel for all of you because i know what your going through.
I saw one comforting post in here where someone said within 2 weeks of completely getting off the pred. he was his normal self.
I CAN TELL YOU HOW GLAD I WAS TO READ THAT!

Please if you have finished the med and have got back to normal don't forget about this post. Please let us know because we need any hope we can get to keep our chins up and not loose hope and go completely crazy or worse kill ourselves.

I have about 4 more months of this LIVING HELL and I will surely let you all know if it get better. If you have come off of it and are reading this PLEASE let us know if we get back normal at least w the brain fog. I can take all the side effect ok except for the crazy dream zone zombie feeling.

I WOULDN'T WISH THIS KINDA HELL ON THE DEVIL HIM SELF!!
Let's pray for each other that the Lord keep out minds strong until we get off the nightmare drug call Prednisone.

side effects:
brain fog, blurred vision, puffy eyes, depression, confusion, dizzy, moon face, buffalo neck hump neck, hopelessness

I was prescribed Avelox for a sinus infection that would not go away. After 4 days of taking it I have had severe cramping in my joints around my ankles, knees, shins and calf muscles. I have pain in my fingers too. I feel totally out of it, and dizzy. I have little to no appetite. This is a terrible drug, and should be pulled off the market. I was desperate to get rid of my sinus infection, and now I find myself having bigger problems from the side effects of this drug.
I have had pain now for 4 days. Does anyone know when this pain goes away?

I'm so glad to find this forum. I've been on Yasmin for 7 months since March 2009. My gyne recommended me to take it because of my acne problem, heavy period and cramps. Ever since I started taking it, I was happy about it. My face is cleared of acne and my period only lasts for 3 days and very light without pain. I was a happy camper until the 4th month into taking Yasmin. I started to have patches of rash on my right temple, then a week later on the left temple and upper lip too. At first I thought it was due to my new face toner. So I stopped using it. I didn't think it would be the pill as any allergic reaction usually would should up 1-2 months after taking it. The rash got worst after 2 weeks, it started around my waist, more like hives this time. I can't stop itching my skin even in my sleep. It was unbearable. The hives comes and goes. And it spreads bigger and bigger to behind my neck and back. I drives my NUTS and my skin is very dry. I saw my family doc, and he thought it was eczema/fungus. He gave me some steroid cream to apply. It helped but didn't make the hives go away. I kept looking for the cause of the hives, but have no clues. After I read many people who posted in this forum also suffered the same problem, I can conclude that Yasmin is the reason. I'm stopping the pill today!!!! Hopefully, the hives will go away soon.

Hey Guys,
I'm new to all this but just wanted to share my story with everyone so I feel like i'm not so alone! I'm 23 and was diagnosed with SLE 3 years ago.
It started in my joints and then moved to my kidney's real fast. I now have stage 4 nephritis, finished 6months of cyclophosphamide in Feb and have been on no less than 40-20mg of pred for about 2years. Just when things were starting to look better it has stared in my blood so they are trying to up my dose again. It has thinned my bones so I am on special meds for that now too.
I know taking the pred is something I need to do to live but it comes at a really high price. I don't even look like the same person I used too because of the moon face. I know it's shallow but at 23 it is almost as bad as having to live with this disease. I now have really low self esteem and get anxious all the time, which is affecting my job. As much as I want to come off I also worry that I would have to stop work again as the pred is what keeps me going. All I want to do is get off it though! Anyone know any alternatives? Also, just wondering if you guys are still drinking alcohol while taking pred?
Thanks for listening guys!

I had a Kenalog injection in May. I was on vacation in Vegas and had bad allergies and ear pain due to my allergies. I went to an urgent care center and they injected the shot in my right butt cheek. I noticed an indention in that spot today and never would have linked it to the injection. I did online searches and put it together. I called the urgent care center and spoke with a nurse who told me that muscle atrophy at the injection site is a side affect and yes it can take several months to show up. In my case exactly 5 months to the day. The doctor called me back. I asked why he did not tell me about the side effects. His response was that only 1% of people get this kind of side effect. I highly doubt that this is accurate considering I can google it and find many people with the same reaction. I asked if it will go away and he said it may never go away. I am 27 and in shape. I am interested in pursuing this legally if it does not go away. It is pretty upsetting.

I've been on and off singulair for several years. I had a horrible bout of bronchitis that then triggered bronchial reactive disease and I now have allergic reactions to certain chemicals (some spray deodorants, etc.) Singulair worked so much better for me than advair, I was thrilled to be able to talk and breathe. As a teacher I would sometimes have to stop the lecture to get my breath again and drink some water if I inhaled the slightest amount of chalk dust or something.

After reading the comments on this website I am going to discontinue taking singulair. I used to be this skinny person and never, ever worried about my weight. At the age of 37 I had a rip-snortin' major depressive episode with insomnia that had me miss 3 days of sleep (this is on no medication of any kind) and panic attacks and suicidal thoughts and impulses that I'd never had before. Imipramine was my first prescribed med (in 1991) and worked like magic. It cheered me up, calmed me down and made me sleep. I went from 135 pounds to 155 pounds in just several months. I finally got switched to effexor and trazodone, but there's really not been much weight loss. I'd hover around 150-160, but then with singulair added in the last several years I am 170 lbs. I can't believe I am a fat person now and do not over eat. I can't go off my psychiatric medication because it runs in our family and if I taper off I am...uh...crazy. My insomnia is tenacious when I am without medication and then that makes depression and anxiety worse. I never want to have a panic attack again.

I just ran out of my singulair prescription about a week or two ago. I am breathing and speaking fairly normally and my husband and I now have to pay for our own health insurance which is exorbitant and I just didn't feel like renewing the prescription in order to save money. I was pondering my weight gain today and just decided to google singulair and weight gain and I just can't believe it.

I have also experienced hair loss, but my hair is so thick it still looks basically the same. My husband and I have noticed over the last several years that I lose lots of hair after I wash it and there is a mass of hair in the shower stall.

My memory may have been adversely affected by taking singulair. I thought it's just getting older. I am 55. It's been the last several years that I have started to have problems remembering things. I have always had to work with my husband in helping him remember things (it's been life long with him: he is an absent minded professor. He has a genius IQ, is an M.I.T. grad, is an excellent engineer and can't remember his mother's birthday, what plans we have for the week-end, no matter how major, etc. to save his life.) I feel like I am becoming more like my husband in being hopeless and helpless about remembering what's happening from one day to the next. It could very possibly be the singulair. There has been a marked difference in my memory over the last several years. It is embarrassing. I sub for the school district and once showed up on the wrong day at a school and another time didn't show up and they had to call me up and get me out of bed to go to work. I also teach piano and never used to forget who was coming when. Again, I don't know if I can blame this on singulair causing memory loss, but there would be times when someone would knock on the door and I'd be surprised to find a piano student standing there. I feel like I am getting Alzheimer's. My grandmother had it for 17 years. My mom has always been afraid of getting it but she is 80 and is just now starting to show signs of real forgetfulness. I explained to her what my lapses in memory are like and she is shocked to hear that they are similar to hers. My mind just will completely go blank. I will have this thought, get distracted, and just a moment later will struggle to remember the previous thought and there is just a void, peace, blankness, white screen in my mind. Maybe it is getting older, but maybe it's the singulair. Since I'm just recently off it I'm going to pay attention and see if my memory improves or if it is just old age.

Also, my joint problems have been nearly ruining my life the last several years. I don't know if this is exacerbated by my singulair use or not. Bursitis in the hips runs in my family like crazy. We re-sided and painted our house several years ago and my bursitis started to flare up and has been bad since then, but it's also about the time I started taking singulair. I had to quit a sales job this summer because my bursitis has become so bad. Sometimes I can hardly walk. It is nearly unbearable. I get cortisone injections every 6 months, but need it every 2 months. I wonder if my discontinuation of singulair will ease my joint pain? I'm going to track that as well.

For me: weight gain, hair loss, joint pain, some dizziness are possible side effects from singulair.

Thank you to everyone who has contributed to this site. I am never taking singulair again.

I don't know if I can blame Zocor on my weak thighs--my doctor says that muscle weakness as a result of the drug should include all of my muscles. I've also developed an extremely itchy neck-also not sure if this is related. Weight keeps going up in spite of increased exercise and limiting daily caloric intake to below 1500 calories.

I am a generally active and fairly healthy 77 yr old who had been taking 10 mg of Lipitor for over 12 years with no obvious adverse effects. Recently I started having pain in my right leg, severe enough to wake me at night. This was followed by a significant weakness in both legs, and for a while, accompanied by a lightheartedness. The doctor had me take a series of lumbar and leg x-rays which didn't show much of significance. He wrote a prescription for physical therapy, which I did not follow.
I did internet research on my own which made me aware that Lipitor could be the cause, in spite of the fact that I had tolerating the drug for so many years. I told the Doctor of my suspicions and we agree to stop the Lipitor for at least 6 weeks to see. A few days later, all my symptoms were gone. So be cautious, adverse effects from Lipitor can occur anytime.

I am 61 years old. I started taking Lisinopril 10mg, once a day about 6-7 months ago. Because of cough, I switched to Diovan 80mg, once a day (samples from my physician friend). After running out of Diovan samples, I started taking Lisinopril 5 mg, once a day again about three months ago. For better BP control, I ended up again taking Lisinopril 10 mg, once a day about 5-6 weeks ago. I started to simultaneously suffer from having persistent, extensive and progressively worsening joint and muscle pains in my both sides of neck, both shoulders, both upper arms, left elbow, left lower arm, both wrists, both hands, all fingers, both knees and left calf muscles. I had difficulties walking, moving my arms, shoulders, doing anything with my hands at the peak of the pains about 7-8 days ago. In the night, my fingers were very stiff and uncomfortable that I hardly could make a fist and I had difficulties getting up to go to bath room because of pains. I felt like I were a 90 years old man. Even Cataflam and Advil did not work well to relieve the pain. As a retired physician, I started to suspect it was Lisinopril-induced side effects. I searched on Google and found this web site. Now, I realize that I am not alone. I got my Lisinopril from CVS Pharmacy. I immediately stopped taking Lisinopril about one week ago. All my joint and muscle pains have been dramatically subsiding (although not completely disappeared) without taking any NSAID pain killer. Even "cough problem" became much worse during the same time. I am convinced that Lisinopril I got from CVS caused my serious, extensive, multiple joint and muscle pains. Perhaps, FDA should look into this side effect: whether it is common ACE inhibitor related side effect or it is possible manufacturer, country origin of the product related problem (made in a non-USA country and imported by CVS?). I would never take Lisinopril again. Posted by myh810.

i went 2 the specialist yesterday that put me on the prednisone due 2 me having crohns as the joint pain in my ankle has been so painful and his now told me that the prednisone has giving me arthritis im really upset about it im 25 and im in a lot of pain the specialist said 2 go home and rest my ankle for the weekend its been 2days and its still not better iv got 2 go back and see him on Monday and if it hasn't improved which i doubt it will his going 2 change my medication he wanted 2 up the dosage of prednisone to 30mg as im down to 10mgs now and i told him that i have received every side effect possible 2 the prednisone and its just starting to reverse and there is no way im going to le you put me on a higher dosage i want 2 come off this drug as quick as possible and he surgesseted another medication that will help with the arthritis in my ankle but it will make me nausea i told him id rather that then all the symptoms iv been having in the last month then be put back on the prednisone

iv been diagnosed with crohns 2months ago iv now been on prednisone for 4weeks i started on 40mg and now down 2 15 the last week my ankles have swelled up and now my right ankle is so painful to touch and walk on, and nothing is making it better, pain killers don't work, massaging it doesn't work, putting deep heat on it so to night i iced it for 15 mins and put a heat pack on it several times the pain went away for 10mins and came back its so painful im almost in tears, im down 2 15mg now so im not eating as muchas i was b4 i wasn't getting full i just keeped eating, my mood swings arnt as bad iv got moon face as they call it and i hate it as theirs no shape at all 2 my face, im getting pimples as will iv retained all this fluid and i feel like a marshmallow can someone please tell me that this pain will go away or is their something i can take 2 make it go away this is the worst medication in the whole world when i get off the prednisone and i have another flar up id rather have the runs and stomach cramps then all this drama iv been having in the last 3weeks iv also changes my whole diet and its made a huge difference 2 how i feel

I have had the worst year and a half of my life-it should have been the happiest! I was on Yasmin for about 7 years. This last year I had gotten engaged and was excited to marry the man of my dreams! The first few years on Yasmin everything was fine-I did not notice any changes. Over the last few I seemed to recognize some anxiety and started having panic attacks out of the blue. Well, in July 2008, I went to the Dr. and was misdiagnosed as having an ulcer-I really had mono and walking pneumonia?? I was having all kinds of anxiety and they could not figure out why I was sick. I went to all kinds of specialists-neurologists, cardiologists, gastroenterologists, etc. They said nothing was wrong. I received a call from a friend of mine who is a nurse. She knew of my symptoms that had compiled over the last year and asked if I was on Yasmin. She told me to stop the pill but I did not think that this was causing me all of these problems. I ended up having severe insomnia, massive anxiety and panic attacks, irritability, moodiness, muscle aches, night sweats, chest pains, racing heart, depression, the list goes on...I wanted to cancel my wedding! I thought that I was going insane! I ended up at a therapist looking for some help. She was able to help me get through my wedding (December 2008)-thank God!
One of my friends wanted to get off the pill to try and get pregnant and decided to do so after my wedding. After 3 months, she was able to stop her anxiety and depression medicine...correlation?? She was on Yaz!
I immediately stopped the pill (March 2009) -that was the icing on the cake! I have NOT had a period since March, I still have anxiety and am in fear every day that something is going to happen to me.I still have insomnia and feel scared that all of this is taking a huge toll on my body-especially my heart. I just want my hormones to go back to normal so that all of this will end!
Does anyone have a similar story? Any advice as to when I will get back to normal?
Please do not recommend Yasmin or Yaz to anyone ever! It has ruined my life in every aspect. It has affected my relationships, work, school, my well being.
I would love any feed back and/or comments-help!

Hi, I am a mother of 2, and not quite 23 years old and got the Mirena inserted at my 6 week check up after having my second. I read all the literature that the Dr. gave me and I was sure that Mirena was the right thing for me (no where in the brochures did I read anything about the symptoms Ive read about here or anywhere else on the internet). I started having incredibly horrible mood swings, bloating, fatigue, nausea (sooo bad, every day) back pain, neck pain, no sex drive (!!!), depressed, lazy, headaches (to the point where I thought my head was going to explode), constantly hungry, acne, smelled maple syrup constantly, complaining all the time about everything, weight gain (only 7 lbs but I just had a baby, I need to lose weight, and I'm nursing),chest pain, and some other symptoms but the most important one is the stomach pain i was having. The pain in my stomach felt like a knife, and I kept having pain in my right side. So after a few days of this pain I went to the dr. he ordered an ultrasound of my abdomen and I am scheduled to get that done Wednesday. My doctor thinks that I may have gallbladder disease or something else seriously wrong with me that we suspect is induced by the Mirena. Keep in mind that I've had this thing in me for about 4 months!!! So after my doctors appointment I typed into google "side effects from Mirena" and Omg, I wish that I had done that before I got the thing inserted, those brochures about the Mirena make it seem like a Godsend and I am all for a lawsuit due to the problems I am having and the depression Ive felt. My 3 year old has suffered from my mood swings, every time id feel it coming I had to make her go to her room :( that poor girl deserves to have a mother that is not so depressed and ill that she can actually play, and both of them deserve that really, and im doing the best I can.... anyways I removed it myself yesterday, i had a hard time finding it but I took it out and I feel as if a huge burden has been lifted, EXCEPT I have been cramping very bad, spotting and incredibly sick, i also read about this thing called "the mirena crash" no matter how long you've had it in, if the hormones were in your system then you are effected and can feel very ill from it (and it can happen to women who had no problems while on it at all, even after 5 yrs). Im hoping that I have nothing wrong at my doctors appt on Wednesday when I get the ultrasound, and it may just be a cyst, turns out that is a side effect of mirena as well, that and bleeding the first several months (oh yeah, I did for about 2 months maybe 10 weeks altogether) Im also hoping that my daughter whom I am nursing is not sick as well :/

oh and for anybody out there thinking that the only women gaining weight are fat to begin with, well I am usually 105 lbs, after my baby I weighed 145, lost some weight, went down to 130ish gained it all back then some, losing weight is easy for me because I diet and exercise like I should, now I am doing all that and nursing a child.... and hello weight, when it really should be goodbye... well goodbye mirena I WONT miss you!!!!

I feel compelled to share my daughter's horrendous experience, which we (and some of our docs) believe was a reaction to Bactrim. Her chills, high, high fever, night sweats, itching and majorly swollen lymph nodes mimicked lymphoma. She had a biopsy of one of the swollen lymph nodes and it revealed Kikuchi' s Disease or Kikuchi-Fujimoto's Disease. Google it. Thankfully, it was benign and self-limited, but it made her very very sick and it was scary and most probably triggered by her allergic reaction to Bactrim - taken for acne. We will never take this drug again.

Warning to Avelox users

As I am reading all these posts I am very alarmed. I just got out of the hospital because of an allergic reaction to Avelox. I developed a potentially fatal reaction called Stephan Johnson Syndrome. Please google this, as it might save your life. From what my doctors said, Avelox is a major offender of this syndrome. After reading the posts I see that a great many of you have the same symptoms I did. Even if the side effects don't seem that serious, stop taking the medication right away and consult your doctor. People who are most in danger are people with low immune systems and people who are allergic to other medications. PLEASE, I beg all of you to check this out, it can cause death in a matter of days. Fortunately for me we got to it early. Best of luck to all :)

I have been taking prednisone for three years and I love it! It has helped me out with breathing problems and arthritis pain. I take a small does every day. And when I am without it I have trouble breathing and have painful arthritis pain. This drug has done wonders for me.

I was on Yasmin for 1.5 years. Ended up with chest pains, severe Vitamin D deficiency, B12/Folic Acid deficiency, elevated potassium and unbelievable fatigue/exhaustion along with muscle loss. I have now been off for almost 3 years and do not feel completely recovered. I'd encourage folks to google Yasmin/Yaz lawsuits as they are just beginning and I expect will eventually come off of the market due to finally, recognized increased risk of these pills with pulmonary embolisms, stroke, heart attack and blood clots. Also, if you google Yasmin Survivors, there is an international forum of women who have been sharing and contributing now for last 3 years as well.

I've stopped taking Yasmin a little over 1year ago. I went to the Dr. the day before my wedding because I had a large lump in my right forearm that was really painful. They sent me to get an ultrasound done because hey weren't sure what it was. Come to find out I had a blood clot. I was only 23 and it was the day before wedding. I had to self inject my self twice a day for 5 days with blood thinners and then take coumain for 6months. I wasn't able to go on a honeymoon. I felt like a human pin cushion, getting my blood tested twice a week. Taking Yasmin was the worst thing I have ever one for myself. No one should take this B.C. and if you are you should stop. IT'S DANGEROUS! Women have died from taking. I was lucky!

All I can say is shortness of breath, pulmonary embolisms and DVT's almost did me in 3 years ago. A week in CCU and a year or more on Coumadin. After a year I needed a blood transfusion because of an iron deficiency. Finally had endometrial ablation procedure and all is well. No periods or side effects. Completely off of meds and after 3 1/2 years I will be finished paying off all of my hospital bills in two more months!

I would also just like to add that I have developed a ganglion cyst in my right wrist, and do experience frequent joint pain. I don't know if this can be attributed to the use of Yasmin.