Knots symptoms and conditions

When I took SMZ-TMP DS; The day after i could not move my legs without being in agony pain. I didn't think anything about it. The next day i had painful, red knots on my ankles and as the day went on they started to grow in size and more started to appear. I immediately stopped taking the drug and called my doctor. I could not sleep cause I was in so much pain. I would lay still on my back but when it was time to get up in the morning i had to literally lift my legs with my hands and get someone to carry me to the doctors office. He said that I had a very interesting case and that to never take this medication again. Right now I am still in a lot of pain and taking anit inflammatory medication to help with the knots and pain. I am still in bed not getting up and now I have 40 knots on my legs. He called the knots Erythema Nodosum. My tissue got infected with this medication.

I am 45 years old. I get the impression many of the ladies here are younger, as they speak of having younger children, so I will tell my side from a bit more "mature" (ie older!) perspective:

Had Mirena for a little over 9 months. My two MAIN side effects were a development of terrible cystic acne on my face, back, shoulders, hairline, behind my ears and straight down my spine, ending in a nice lovely rash just above my tailbone. These things were deep, solid knots under the skin, not average little pimples. Worse acne I've ever had, and at my age too!

Second, profuse sweating under my breasts and lower back, again just at my tailbone, right above my butt. After drying off from a shower, I'd run my hand back there and still feel soaked. This did not seem related to hot flashes. Just sweating, and I think that contributed to the acne, which was beginning to leave scars it was so deep.

I do feel like I gained weight, my pants were much tighter and I just felt bloated all the time.

Fortunately, no hair loss or emotional side effects. I've had anxiety for years and take Ativan (lorazepam) which keeps it pretty much under control. No loss of sex drive either. It seems there are a distinct set of side effects, and some get them in different combination than others, but we're ALL getting them one way or the other!

OBGYN said as the Mirena is only progesterone, I was missing the estrogen which were the 2 components of the pill I took for years with no trouble. He gave me a Rx for a low dose of estrogen. Now I am getting what I had in the pill in 2 separate forms, and having these awful side effects on top of it. It didn't help.

So I had Mirena removed 6 days ago. Luckily he found the strings, told me to cough, and pulled it out, no pain! I immediately went back on Alesse BC pill that same day, so no break in hormones, but I handled the BC pill fine all those years, so I"m just going back on it. Have been bleeding ever since removal, but I figure that is just my body "getting back at me" for not having periods for months. My first real one, due in about 3 weeks following the pill schedule will probably be the period from hell. Ok, I accept that. My uterus wants to get this poison toxic mess out of me, and I'm ok with that.

I'm crossing my fingers that I will miss the "crash" I've read so much about. As it seems to be mostly psychological, and I didn't have those side effects to begin with, maybe it won't be so bad, or at all. Of course that could just be wishful thinking on my part! So far, 6 days of having it out of me and I already feel 100% better! My face cleared up in a matter of days. The sweating stopped immediately. My pants are looser, although I still weigh the same. The bloated feeling is gone. I just feel thinner. Before, my profile in the mirror looked like I was 4 months pregnant! That too is going down quick. Good luck to all who have it removed. Things can only get better!

And don't let any doctor tell you you can't have it out! It's your body! You can demand whatever you want, especially if you feel like it is making you sick! Do not take no for an answer. You don't even owe them an explanation. Just a "Sorry, it's not for me..." at the most.

Good luck to all....

I have been on Simvastatin for about 4 months now. For the past 2 months, I have been having unexplained muscle/joint pain and tightness in my hips and thighs. I couldn't figure out what I'd done but thought it was just one of those things (slept wrong, stepped wrong, etc.). I've been working with a foam roller to get the knots out, even getting up in the middle of the night to work on the roller because it hurt so much. That helped some. Took Motrin but that didn't work at all! Added Omega 3 fish oil and glucosamine and that did help a little. Have been limping for 2 months now and it finally occurred to me, "I wonder if it's the Simvastatin?" I already knew I was sensitive to chemicals like sodium lauryl sulfate, so everything I see written here makes sense to me. I emailed my MD today and she said to stay off it for 3 weeks and see if I see any improvement, plus get blood work. I sure hope I don't have any muscle damage. Thank all of you for posting your experiences

wow. i am so happy i found this website. after reading everyone's posts, i now know that i am not alone. my doctor prescribed me Yasmin about maybe 3-4 months ago. i take BC to regulate my period & ease the pain of it (my cramps are unbearable and cause me to get very sick & sometimes pass out). and almost as soon as i started taking it, i was also having UTI-like symptoms, but with no infection whatsoever. my urethra was SO sensitive it even hurt to wash myself sometimes, peeing was painful, i was constantly irritated, dry, and red down there, and sex was nearly impossible. the lack of sex caused me to become somewhat depressed, because i knew my bf was unhappy, just as i was. & besides vaginal problems, i experienced headaches every 2-3 days, and my breasts were sore 24/7 and felt VERY dense, as if they had knots in them. i already have the beginning stages of fibrocystic breast disease (like my mother), so i figured there was NO WAY this pill could be healthy for me to take. so just a few days ago actually, i switched to ortho tri cylen. i've only been on it for about 4 days, so i'm crossing my fingers that those horrible symptoms stay away. for anyone you know who is thinking of going on BC, please tell them to stay away from Yasmin. this site and everyone's posts honestly made me feel so much better. i wish the best for all of you.

Hello,

I am so happy to find these posts. I started the generic Wellbutrin SR 100 MG in the morning about four months ago. She wanted me to increase my dose but there is no way I can handle it. I am also on Zoloft 50 mg for panic attacks. She added the wellbutrin to give me more energy and help with my low sex drive. It gives me lots of energy but I can not have caffeine or much sugar when I am taking it or I have a panic attacks. Also I am very short of breath, I thought this was just my anxiety but after reading all the other posts I am beginning to wonder if it is the wellbutrin. My sex life is a little better but not much, of course I am taking a very low dose. About a week after I started taking it, my back and neck was killing me. I went for a massage and she said I had knots all over my back and neck, this four months ago, I kept getting massages and they just keep getting bigger and will not go away! I am almost certain the wellbutrin is making me tense and causing these. I decided to call my doctor today and ask to go off of it.

What is funny is I was on it a few years back but it was Wellbutrin XL not generic. It was wonderful! I had the best sex life, I had so much energy and no side effects.

I just wanted to share my story.

I am so thankful I found this site. I wish I would have found this before I got my Mirena inserted. I had been on the pills(orthotricyclen) for years. I have two children my husband and I decided we did not want anymore, but just in case we did later on, we decided to do a more permanent birth control. Something I did not have to worry about wach day. I got the Mirena in late October 2008. I really trusted my Dr. when she told me all about how great this was and that everyone loved it! Well, I have wanted to get it removed twice since Oct. My Dr. told me to give it more time. I started out experiencing bad cramps!! I still have sharp cramps and pain off and on at any time. Then I begin having BAD acne in my chin area. I mean like very sore knots. It was like it started on one side and then just spread all over my chin area. oNE WOULD LEAVE AND ANOTHER WAS RIGHT behind it I have never had problems with acne before. When I mentioned this to my Dr. at my January 09 appt. she told me acne was not a side effect of the mirena, but I don't know where it could be coming from. I decided to have it removed. My appt is this Fri. 27 at 10:20. I can't wait. I am really hoping that I can get my body back on track and tame this acne. I think I am just going to go back to what I am used to.....the pill and stick with it. I tried something new, and it has not been a good experience for me. Now, after reading a few of the posts I am concerned about the effects I will have once it is removed. I will come back and let you know. Thanks to all the ladies who have posted here. It really confirms my decision to have the Mirena removed. THANK YOU!!

I wish I read this page before getting Budeprion. When I heard about my sister's weight loss and her rise in energy with Welbutrin XL I had to try it out for myself. I have been on Zoloft for the past four years for OCD and depression, but my depression was getting worse. I asked for XR but I ended up with Budeprion SR. The first few days were really great and I was less depressed and I could get out of bed. That't the time when you don't want to hear about the side effects. It's there. I had the nausea, stomach cramps, constipation. I just thought if I could get over the side effects it would work, but it only gets worse. My stomach is in knots and now I've developed sinus problems. This is quits! Every time I find a new drug for depression, and every time I get knocked out by the side effects.

I have hypothyroid. Have been taking Synthroid for about a year, 0.075MG a day. Had my levels checked 3 times since on the meds and still have never gotten to normal, but a lot closer. I have gained 20 pounds that I can't get rid of, which for me, is crazy. I have never had a problem dropping weight, and for the past month or so, I have started losing my hair. Not just losing it, but the texture and everything has changed. No matter what I do it looks dry and flat, and even when I condition it and also use a leave in conditioner, it still knots up and tangles. I have NEVER had a problem with tangles. It's coming out in handfuls. Im not taking any other meds, so I imagine it has to be the Synthroid. My problem is..What else can I take? I mean, I have Hypothyroid, so I can,t just leave it untreated, But I have no wish to be fat and bald either. Please...anyone know of others meds without these side effects?

I have had the SAME EXACT THING!!! The 1st time I had the shots I was at a knee specialist. He stated that it wasn't cortisone but a different med that does the same thing just better for you. Never could pronounce it!!! I started going to my family doctor to get them cause I trust her fully. However I got cortisone shots from her and was okay that evening. Woke up the next day and face was on FIRE, HOT, RED, FLUSHED all the above. BP was 170/102 was ILLLLL to my stomach like in knots and the WORST HEADACHE I have EVER had in my LIFE!!!! I will NEVER EVER do this again its HORRIBLE!!!! I took Benadryl and just knocked my miserable self out. Today is day 3 and I am still red and still major headache!!!!! Your not crazy and your not alone this is from the shots!!!

I was given Dexpak for a severe sinus infection. I took it for 5 days and could no longer take the side effects, so I quit it cold turkey. I have been off from work almost the whole month because of this drug.

The side effects I had from it were:

• anxiety
• hyperactive
• uncontrolled talking
• severe tremors and shakes
• overheating
• loss of appetite
• sitting still and the room spinning
• loss of vision
• severe headache
• loss of concentration
• unable to think
• no sleep
• all upper body muscles tied into knots
• esophagus swollen and raw
• dizzy
• personality change

After I quit I became ravenous the next day. I ate a lot of protein and fruit. It has almost been a week since quitting. I still have problems sleeping, headaches, a swollen esophagus, sore muscles and my personality is not quite normal. Hopefully I will get back to normal.

I had an injection into a Bursae about a week and a half ago. My face was hot and bright red for about three days, if i went out in the sun it made it worst almost like i was allergic to the sun. I have had headaches daily, since. Vicodin will not help these headaches, my heartburn was so bad i stopped taking all medicines, birth control, antibiotic, pain meds. My stomach hurt so bad the second night that i could not make a sudden movement. and i couldn't stand straight up. i have been so nauseated, ive thrown up twice, once i was taking a sip of milk to get rid of the side effects and as soon as i swallowed i puked, the second time i just smelled something. i have been bouncing around in the bed all night. and so depressed i need to be committed. my head has hurt so bad many days i don't want to hear my one and a half yr old speak. but i am stay at home mom and i have to do what i have to do. i had told my doctor that i had these effects, but another physician treated me. i told him and he assured me it would be a very small amount. also a my ankles hurt especially, feel like they are gonna snap, as well as all my other joints when i come off of these. someone email me plz *******

Anyone have room for my wife. I have had enough. She is sometimes pleasant but most of the time a real bitch. She has not connected the dots between the Femcon and her horrible mood swings. Sex was scarce enough but now I have almost forgotten why I liked it so much. PLEASE HELP! If she stopped today how long until I get her back?
(fyi: I am signed in under my wife's account. She will be so proud of me. I hope I survive! Pray for me please.)

The doctor was observing me for very low globulin G levels and had me on 500 mg Keflex for a month trying to make my body "respond"? I took a bad sinus infection, went to my ENT, and he took me off the Keflex and put me on Cipro (500 mg) twice a day. I had taken this almost two weeks when my ongoing appt. with the first doctor came due. I called her office and they said I must come on in to get my lab work done. I did and she saw how sick I really was. She took me off Cipro and put me on Levaquin which I had never taken. During the first three days, I got sicker and sicker.
I thought it was just the "sickness" getting worse. One day I sat staring into space for over an hour without realizing what I was doing. Also, that day I noticed large knots in various places (under the skin). I live alone and became increasingly concerned. May I say, during that space in time,
I lost 25 lbs almost immediately. Nassau, sinus worse, felt terrible, and
hurt like the dickens. I could not sleep (and still have problems with it) and thought it all me, having never read anything about side effects. That night at 2a.m. I found the sheets that came with it, read, and identified with
everything written on the paper. I had to take one hand and put it under the opposite arm at the shoulder to help move it from my side. The muscles in the upper arms were like - separated. I found large knots under
my arms as on my body in various places. I could not raise my arms away from my sides. At 8 am I phoned the doc's office. They said, oh! it couldn't be that bad. I faxed the underlined, highlighted sheet to them and fifteen minutes later they called. The doctor said not to take any more
and it should be out of my body in 48 hours, if not see my primary phys.
She knew my GP had retired to help with her son, and had talked to me about taking her place until I got someone. A lot of it was out of my body in approx. 48 hours but my right arm (upper) and upper right leg was a mess. It is some better after April - Oct. taking medicine, therapy, and exercise but I still limp, especially when I get tired. There had been no strength for a long time. It was like the muscles separated and tendons enlarged, strutted, are very painful. The challenges are great up and down steps, etc. Can't lay on that side at night, put pillows under and between legs and when the doctor examining did a "frog-leg" with the right one, it didn't want to hold me up for several days. When I walk it gets to hurting very badly. Can't cross my legs when I sit. Wiggle and turn when sitting.
The very bad thing is this: The doctor never tried to help me get over this. When I went to other doctors for help, most of them looked the other way completely. For example, I tried to tell my new primary about the problems and pain from the muscles and tendons - he suggested lab work and a colonostomy. A rheumatologist kept saying I had "hip" pain. He did sent me for therapy though with a diagnosis of tendinitis in the upper arm.
He never addressed the case and cause. I would like to know if this is something to last the rest of my life. What can be done? You can only have therapy so long. An assistant told me to look this up on the internet.
I did not know this existed but I'm glad to know it has not all been my
imagination or "in my mind". My symptoms: dropped 25# in about three weeks, nausea, depression, sleepless, severe pain, taunt stretched tendons, droopy separated muscles,dizzy, and more. If anyone has any answers of who to contact and what to expect, please tell me. I've had anyone I talked with or saw to make note to never give this to me again.
God bless all experiencing these bad side-effects and make us well
again. --By ******

I am a healthy female with little to no history of adverse reactions to medications. I was prescribed a 10 day dose of Levequin (500 mg) for a minor but stubborn skin abscess. After the third day, I woke up with significant joint soreness in my fingers. Progressively the soreness spread daily to my wrists, elbows, ankles, knees, hips, etc. I did not suspect the antibiotic at first, but I know my body, and I know something was WRONG.
After my 8th dose I decided to look online...it is at least good to know that what I'm experiencing is definitely from Levequin. Thank you all for sharing your stories.

I especially found MERCEDESLANE posting on April 15th interesting. I guess this person works in the health care system. Considering this uncompassionate individual, who apparently wants everythone to know he has a Mercedes, can't spell (whine), and does not have basic grammar skills. Wow...my faith in the our health care system is stronger than ever. But what do I know, I'm just an "IDIOT" with shingles that needs to have a couple of glasses of whine while I pop my remaining Levequin.

I have been on Lipitor for over a year know after having a heart attack at 43 and having two stents put in. I was diagnosed with Fibromyalgia by in 2002. Recently, I have been having more arm, leg, back, pelvic, hip and hand pain then ever before. I am going to talk to my doctors now about the side effects. I have just know decided to start halving my Lipitor and may ween off of it completely. I'm on Niacin and Zieta in addition to the Lipitor. Have also been having a lot more digestive problems lately...am to be scheduled for a upper GI. I came here looking for info on the fact that although since being on Plavix (didn't realize Lipitor could be culprit) I have had bruising...today I found knots under two bruises on my upper arm. Not only are there knots but they (the bruises) are a different shade of blue (if that makes sense). Thanks to all who have shared their stories.

i was prescribed Levaquin in April for pneumonia. I took 1 pill in the morning and by mid-evening felt gross. My stomach was in knots, head was fuzzy. I decided to NOT take any more and let my body fight it. Last week I had awful pain in my ear/jaw and thought it was my tooth so didn't go to the DR. right away. Finally I couldn't handle the pain and went. He said I had an ear infection and immediately wrote a script for Levaquin despite me telling him how it made me feel in April. He said it was no big deal, the feelings would go away. I came home and against my better judgment took what I had left from April. (6 pills) I am done them now, but was looking up Levaquin on line because I feel like crap, my ear and jaw still hurt like hell, and tonight my leg started to hurt. I have a flaming esophagus as I sit and type this at 2 in the morning because I cant friggen sleep. Pain my chest feels like I inhaled glass. My husband said he noticed I haven't been acting right...news to me. I'm cranky because all this crap did was make me feel worse. DR. told me to take 2 aleve in the a.m. and Tylenol/Motrin every 4 hours after that for pain. I just got done reading that NSAIDs shouldn't be taken with Levaquin. Nice to know after the fact. My stomach has been turning for 5 days and food is absolutely disgusting. I have awful diarrhea from this med too, which the doctor said was normal.. good to know that spending hours on the toilet was"normal". I've been teary too. Crying over nothing, literally sitting at the pc playing a game of cards and I busted into hysterical sobbing OVER CARDS!! Hopefully I will feel better in a few days and nothing else happens. DO NOT TAKE LEVAQUIN!!! Save yourself the trouble.

(33yr) Was given Omnicef for an ear infection. After 3rd dose broke out with huge patches of red whelps. Stop taking, but then my joints started to ache and I had large knots on the bottom of my feet and hands. Diarrhea and vomiting, severe stomache cramps and low blood pressure... followed by antiphylatic shock. While I was in the ER the discovered I was also having a heart attack.

It has been 3 weeks and every time I come off the steroids, the rash and other symtoms return.

Has anyone else had similar problems.

I have been on this pill for about a week now and I have had a series of diarrhea. My stomach is always in knots. I also noticed some spotting, something I have never had from any other birth control.

Hi, thought I'd share my positive story about having Mirena removed. Having it removed was no doubt the best decision even though two doctors told me that it was not necessary and the loss of hair, graying and loss of libido could not be due to Mirena since it releases minute amounts of hormones locally. Not only have I seen a return to my libido but the hair loss has stopped. this cannot be placebo effect. Even my husband has noticed the difference (no more clogged drains). Thank God! I felt like I was aging at the rate of knots. I now feel so much happier, healthier and more attractive. For all out there who are wondering if it's the Mirena causing hair loss etc, I sincerely believe it is probably very much the case, despite what the medics will tell you. Best wishes.

Alright. After observing my daughter for two full weeks after discontinuing Singulair, I have decided to share our story.

Our daughter started taking Singulair last August (2007) to relieve her allergy symptoms. I'd like to add she is an identical twin, whose sister did not need to take the medication, for she had mild allergy symptoms that were easily relieved by taking Allegra. So we clearly have a side-by-side case study where one twin took the Singulair and the other did not. About two weeks later we noticed changes in her behavior and thought it was due to the new school routine and changes, etc. Then she started not eating, and when she did eat, she ate very little. Both girls are in a select soccer league are physically active 4-5 times a week.

Long story short - she stopped eating, lost weight, stopped growing and is now 2.5 inches shorter and 15 lbs. lighter than her identical twin. They are fifth graders, I might add, so 15 lbs is ALOT of weight at their age. She was withdrawn, known to have deep depressive episodes, reacted adversely to everything and, in general, wasn't acting herself since last August. She was not enjoying life at all.

She is usually a quick-witted child, one with a sunny disposition and who interacts with others very well. She is joy packaged in a colorful bottle, ready to share her thoughts with you.

We took her to her pediatrician, a nutritionist, a psychologist and all said she was clearly depressed and that is what led to her changes in eating. No kidding, I thought. But why? What has happened that could have changed her so drastically?

I had never felt so far away from my child as I had with her during this time period. We are a close family and we pride ourselves on being able to freely express how we feel.

My dear mother-in-law saw that the FDA was probing the side-effects of Singulair with children and she mentioned it to me, because she knew that is what my daughter was taking was taking. I never thought about the connection, because I take Singulair. I will add I also take an antidepressant and have made an appointment with my doctor to discuss all of this.

After talking with our pharmacist and getting an exact date as to when she started taking it, I called her pediatrician and discussed it with him. We had not been to him since October, because we took her to everyone else (psychologist, etc), so he had not known exactly what was going on with her mental health. He did, however write in his notes (and told me when I called), "Discontinue Singulair if symptoms persist." Hmmmm. Exactly why I wasn't told this from the beginning, I don't know and am very bothered knowing he wrote that on her chart.

Well, after taking her off it two weeks ago she is now back to her happy, connecting and eating self. People (her father, twin, and I included) noticed a change in three days from stopping use of Singulair.

She has changed IMMENSELY since getting off the Singulair that it has been easy to pinpoint her taking that medication as the reason she has been absolutely miserable for the past SEVEN MONTHS. I thank God it wasn't longer and that she didn't suffer any longer than she already did, but it was a true hell to watch her go through what she did and to watch her decline and to not know (professionals included) what to do. Words diminish how we felt and how we feel now after having her back.

So there you have a side-by-side comparison. One identical twin thrived while NOT taking Singulair and the twin who did take it suffered terribly, physically and mentally, while she was taking it.

The allergy relief she experienced was clearly not worth the internal suffering she endured while taking Singulair. I wish we could turn back time and give her those seven months back.

3 weeks after putting in the NR, I went to work explaining to my co-workers that I "had a hangover" and needed to eat some bread , as my 3 glasses of birthday wine from the night before really had done me in. After a baegal, and an energy drink, I noticed my eyes had this weird kinda haze, and my head over my ears was really starting to ache. The worse it got, I finally voiced to the girls how "weird" I felt, and with their own experience, we figured out it was a migraine. A migraine? I had never felt a headache like this before. this alone made me anxious, and made my heart palpitate (which I was already familiar with) I left work early because I was having difficulty concentrating, and i felt bad for having everyone work in the dark with me. I got home and did nothing but sleep ALL night into the next morning. When I woke, it felt like just breathing was making me more nauseated by the minute. I vommitted all morning, had no lunch and am still queezy 6 hours later. I was glad to find this site to answer the question of this being due to the ring or not. I took it out, with no plans to re-insert, and my stomach is still in knots. as a nurse my advise to other women is: reconignize the common/small symptoms, before the big/scary ones occur.

This is a total nightmare and i need advice! I was on Lamictal for a year and about six months into my health began to slowly deteriorate. It started with shortness of breath and heart palpitations and eventually attacked every system of my body. My symptoms are muscle pain, spasms and knots to the point that i can't turn my neck sometimes, joint pain (mostly knees), stabbing floating pain everywhere, headaches, frightening tingling in my extremities and a few times my entire body, sore throat, flu-like feelings, stomach cramps, bloating and heartburn. The list goes on. I have been off of it now for two weeks. My psychiatrist has never seen this type of reaction before and is not convinced it is the Lamictal. I have been to every single type of doctor and the ER twice, had extensive lab work, CT scan and two MRIs. I have been off Lamictal now for two weeks and am not feeling much relief. I am so scared and frustrated and please need advice. Has anyone else experienced this? Does it ever go away? I feel like I am literally living a nightmare with no-one to turn to for advice because no-one seems to know ANYTHING!!!!

It all finally makes sense!!! I'm 26 yrs old, have been on 3 bc's in my life for Polycystic Ovarian Syndrome and this past bc was Yasmin. Weird things have been happening and I never thought to link them with the bc but after reading all of these stories it makes perfect sense. Here I'm thinking that I have severe IBS and zero sex drive b/c I'm just a medical disaster but these other woman have opened my eyes. The worst side effect of all is the story that I am about to tell you and I hope that nobody else has this problem. My gyno put me on Yasmin the 8th of Aug. ('07) and at the end of Aug. beginning of Sept. I noticed a big sore knot on the back of my ankle. I thought nothing of it until another one appeared under the skin of my other ankle. I went to my doctor (who is my regular and gyno) and she told me that she didn't know what these lumps were but were NOT caused by my bc. She gave me antibiotics and sent me on my way...one knot went away and another larger one appeared. I went back to her and she gave me a 2nd dose of antibiotics, one goes away and 2 more appear. So this time she sends me to an Orthopedic Specialist who takes x-rays and has no idea what is wrong. He tells me to go see a dermatologist. I went to a dermatologist 2 weeks ago who tells me that I have a blood flow problem. My blood is thick (never had this problem in my life) and has problems flowing back up from my feet in my veins. He diagnosis me with Lipodermasclerosis...ok, so I ask him if this could be caused by my taking Yasmin...YEP! So, I stopped my bc that night. Now I am going to wait the three months for the Yasmin to completely leave my system before I know for sure that this was the cause of the knots on my ankles. Please let me know your thoughts and if anyone has had this same issue. Thank you!

I've been taking Omeprazole for the last 4-5 days for the "possible treatment of H. Pylori" while we are waiting on a nuclear gallbladder test. After I started taking this I noticed my stomach going into cramps. Just like when you have a tummy bug and you get spasms or knots in your tummy. Very uncool, painful, and the only thing that seems to make it stop is eating and making my tummy full. (At least 90% of the discomfort and pain leaves when I do that) so I have been off of it for a little over 24 hours, and this morning I woke with some tummy cramps again. I'm thinking it may take a couple of days for everything to return to normal. I'm not going to take it anymore. (drugs - geesh - if you hear a commercial say it treats arthritis but may cause lymphoma - good god, why do that? Sorry I just think it's horrible about some drugs not that I have arthritis but I'd rather take a pain pill for it than turn around and get cancer)

My 16 yr old son was prescribed this drug 9 days ago for a severe sinus infection. He came home from school yesterday with several small raised welts on the creases of his arms. I took him immediately back to his Dr who said he was having an allergic reaction, prescribed steroids and said it would get worse before it got better. Within a few hours his elbows had visible knots in different places, then his knees did the same thing, then his feet started getting knots on the bottom and he had different whelps breaking out on his torso and lower stomach. We immediately took him to the ER last night when he said his tongue "felt funny". The attending immediately diagnosed an acute severe allergic reaction and gave him a huge steroid and Benadryl dose. He released him because the itching had stopped and his tongue no longer felt funny. Last night he kept drenching himself with sweat during sleep. Today so far some of the whelps are gone but he has some pretty severe joint involvement with visible knots around the elbow and knees and feet.