Hips symptoms and conditions

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.

I just want to say how happy I found this site. I'm not alone! I thought I was going crazy or that my body was shutting down completely. I had my mirena put in Sept. 2006 and my body has become something I don't even recognize. I am extremely bloated all the time and it hurts every time I eat and use the bathroom. I keep on thinking maybe I have Irritable Bowel Syndrome, but it doesn't make any sense because the symptoms showed up after I had the Mirena put in. I thought it might be food sensitivities so I got tested and have been trying to cut those foods out but it doesn't seem to be helping. I have tried all sorts of natural remedies but it never seems to go away.

I have gained 40 pounds since I the Mirena put in even though I have never have had weight gain problems before, I eat healthy and I am active. I also have a difficult time concentrating and focusing on anything. I also get dizziness, depression, irritability and mood swings. I also have been experiencing a sharp pulling or stinging in my uterus at times as well as joint pain (especially in my hips, knees) and painful intercourse with bleeding afterwards. My hair is also falling out and I have lost my desire for sex.

I've also noticed a drastic decline in my immune system. I have never been as sick as I have been in the last three years of my life. I seem to always be getting sick. For the first three months after the Mirena was inserted I had frequent bouts of yeast infections, bladder infections and still three years later I have these types of infections frequently. Not only this but I seem to catch everything that is going around when before the Mirena I hardly ever got sick.

Finally after reading the posts on this site I can trace all the changes in my body to when I had my Mirena put in. I am so upset that I have been suffering for 3 yrs with these side effects and it has taken until now for me to figure out that the Mirena doesn't just effect your uterus it effects your WHOLE body. I cant believe I trusted the doctor I went to when I had it put in that said that the hormones would only affect my uterus. NEVER, NEVER USE THIS PRODUCT!! It is coming out as soon as I can have it done! Please ladies if you know what it is like to have it removed let me know.

My total cholesterol was 220 and LDL was 157; I started taking 40mg last week and within 2 days I just felt horrible. I felt weird and yuck in my stomach. There was a fog in my head and 2 days ago I was so dizzy I was almost falling over; I had to catch myself with the walls and doors. The next day, yesterday, I started having higher blood pressure and racing pulse with heart palpitations every 45 seconds or so, which makes me breathe deep often. I have felt pain in the back, arms, neck, and hips. I have also had weight gain and stomach irritability. Last night was the first night I did not take my medicine and even though I don't feel all that better I will see how it goes. I fought taking this medicine for over a year now and since my cholesterol went up I figured I'd try it in hopes my level would drop, but I can't handle this, I'm only 38!

I have been on Yasmin for over 5 years, and just thought that I was a hypochondriac. After starting Yasmin I experienced severe nausea and unrelieved hunger pains. I saw a gastroenterologist who performed an EGD and Colonoscopy at the age of 20. It was normal and I was placed on Protonix to help with the GI issues. Also I have severe joint pains in my knees, hips, elbows and shoulders. I have been tested for everything from Lupus to Rheumatoid Arthritis, and it was all negative. I get headaches, have little sex drive if any, my skin is not clearer than usual and nor has it been since starting Yasmin. Thanks to all those people who have voiced their concerns and shared their stories, it makes us feel less crazy. I threw out all my birth control pills last night and I am going to try another form of contraceptive. I mean my headaches and chest pains have gotten so bad that they have forced me to go to the ER on several occasions. I DO NOT THINK THE BENEFITS OF YASMIN OUTWEIGH THE RISKS ASSOCIATED.

feel so so sad and just want to die, can't get out of bed for more than 2 hours at a time, so much pain in hips and legs that I just want to take handfuls of pills to stop the pain, no motivation to do anything, nausea and stomach ache all the time, and of course constant runny nose, can't make it up a flight of stars, swollen hands

I just got my Mirena removed today. I am SO excited. I have had it in for 1 year and it has been the worst year of my life. My symptoms were :MIGRAINES!- for which I was admitted to the hospital, they did all kinds of tests, and found nothing-( they even gave me an IV of morphine, and the migraine was so intense, i still felt it with the morphine.), arthritis- (or EXTREME ACHING in all of my joints, especially my hips, knees and lower back area., pain in my chest- like unable to breath, pain in my neck, I was sleeping 9 hrs a day and still exhausted and lately its been severe insomnia, cramping in my lower stomach and bloating really bad. I am 5"3, 21 yrs old, originally 107 pounds, and have two kids. After my daughter I was on Seasonique and although it made me have mood swings it was NOTHING in comparison to this. After my daughter I lost all the baby weight and then some. Even after I had my son in the 6 weeks before I got the Mirena, I lost all of the baby weight and was back down to 107 pounds. Now I weigh 130 pounds- and thats doing the same exercises and eating the same that I have always done. I have also never had ANY UTI's and I have had consistent UTI's since I have had it in, that have NOT gone away with various medications. I have had NO sex drive. Absolutely NONE, and I am 21years old! I felt very fatigued every day and it took all my strength and energy and mostly motivation that I HAVE TO provide for my family, to get up and go to work everyday. I read the brochure for Mirena when I got it inserted, and there were NONE of these side effects. I found some of these side effects on the Canadian website, and found people's horror stories of having Mirena in. I am SO happy to have finally gotten it out and am looking forward to being a normal healthy person again.

I've been prescribed Prednisone since April and just recently experiencing hair loss (I'm Female)

I recently back in April of this year received Cyberknife radiation for Adenocarcinoma with metastasis to my brain. After surgery to remove my brain tumor in March of 2009. I went though whole brain radiation and the Cyberknife to my lung. The doctor was very adamant that as the lung heals from radiation you will develop what they call wet lung or neumonesis sp? This will have to be treated separately, or severe coughing would continue. My primary care doctor in the mean time put me on Lisinopril 20 mg for hypertension. I have not gotten a good nights sleep in 2.5 months since, then came the pneumonosis. This cough persist to this day waking me from what little sleep I do get, and amazingly am now suffering from joint pain especial in my hips. It's to the point I can't even cross my legs anymore it hurts. When discussing this with my primary she says its in my head as of today and reading this site and side effects I am taking myself off of Lisinopril and will seek a second opinion, even a third if need be thank you all so much for posting your side effects from this drug.

Hi Everyone!
I too am thankful for having found this site. I had Mirena inserted back in April of this year. Can I tell you the pain was worse than child birth! I have 3 children and had NO drugs during child birth, so my pain threshold is high.It was so painful that after the long insertion time I almost passed out. Two weeks after having it inserted, I was riding in the car with my husband and had such bad cramping that I had to use my breathing from childbirth class! I had bleeding all the time. Not heavy, but annoying. I also felt like someone is up in my uterus pinching me hard it hurts so bad. my breasts are huge, my stomach is bloated (just in time for summer and the bikini...not) I have cramps, I feel depressed, nothing interests me anymore, I cant laugh with my kids,I am moody all the time and generally felt like crap. I made an appt. with gyno to have ultasound done to make sure it was in place correctly. It was. the OB told me I could have all these symptoms for up to a year! No way am I dealing with this for a year. I tried to hold out for a while longer and some of the symptoms have subsided a bit. The bleeding is less often, but I still get very bad pains. I have now also developed very bad back pain. It is located lower back/hips,and will sometimes travel into the front of my thigh. I thought it was due to a car accident, but having gone to a chiropractor and been fixed from the accident, it is still there. I thought it was in my head, but having read all the posts I feel pretty sure it is because of this Mirena IUD.
I made an appt. with my OB and I am having the darn thing removed!! I am glad I read these posts girls, as I was still not sure if I should leave it in for a while longer to see if things improve more. But I had to ask myself a question. Is it worth it? feeling bad physically ALL the time and sad?. the answer was simple. NO. It is coming out and I hope it wont be long before I feel like my old self again!
Best of luck to you all.

Wow, what an eye opening experience it is to read all these posts! I was just about at the end of my rope thinking something was horribly wrong with me. Now I firmly believe it's the Levoxyl that is wrong.

I went on thyroid meds about a year and half ago for just slightly under active thyroid. I was actually lulled into it because the Doctor assured me it was a completely safe medicine and taking it would help me lose weight. Always a welcome thing. So I started on 50 mcg. I noticed some degree of improvement. I was sleeping better and having more energy during the day. Next checkup, the levels are in the normal range but just barely. So he doubled the dose. Two weeks later I broke out in a horrible itchy rash. I actually thought about the meds but then I didn't change meds, I was just taking more. I called the doctor and he said, "No this medication won't do that." So I change detergent, soap, everything I could think of and nothing worked. Finally I said, enough and I skipped a dose. During the day the rash got a lot better. Next morning I took another one and within and hour I was itching like crazy again. I stopped taking them, waited a week and called the doctor again and told them. His reaction was "You have to take this." I said, No, I don't and I won't. He actually argued with me that the rash could not be caused by the meds. Now I realize at that point I should have called another doctor but he's in my town, convenient, yada, yada, yada. Anyway he called me in another med which he said was the same active ingredient but different brand. Enter Levoxyl. I've been on 100 mcg for 3 months during which time I have felt progressively worse. Most of these things I didn't attribute to Levoxyl until later. Initially I noticed I was having the hot/cold flash thing. I have no comfort zone. I'm either flushed and sweating or chilled so my nights are spent constantly either searching for cover or kicking it off. Next thing I noticed is that my breasts would swell. Naturally that was a concern but about the time I would decide I needed to see about it, they would be normal for a few days. Sleep? What's that? Tired all the time. Started having confusion and forgetfulness. I even told my co-worker I thought I was losing my edge. I was all of a sudden forgetting things I had done automatically for over 15 years. Then the really scary stuff started. I would wake up in the middle of the night with my heart racing and feeling like I was in a fight for my life. I was afraid to go back to sleep. Joint aches and pains across my upper back, my knee. Tingling in my feet. It just keep getting worse and worse. Still didn't think of Levoxyl. Then Monday of this week I didn't have a pill to take. I forgot to get it refilled. Monday at lunch I told my husband I felt better than I'd felt in months. Tuesday took the regular dose. By noon the mental fog was back, back was hurting and I just felt like crap. Tuesday night went to bed early because I was so tired. 11:40 woke up with the worse anxiety attack I've ever had. Heart was pounding and I was breathless. Wednesday morning I got up and the light came on. I did not take the pill. Entered Levoxyl in google and found this site. I am so angry at my doctor I can hardly stand it. I even went to the official Levoxyl website and all these side effects are listed except for the swelling breasts and confusion but I've noticed several posts here that list those. During those two days I didn't take the freakin' pill both problems improved greatly. This morning, I reluctantly took half a pill. I plan to to that every other day for a few days then skip two days, then three, until I'm off of it. I don't know at this point what I'll do about my thyroid but I won't take this stuff and I won't ignore feeling like crap again. This is crazy. Where is the FDA? Oh yeah, being entertained by the drug companies. What a shame.

Thanks to everyone who has taken the time to post here. It is a sad commentary when we can't rely on our doctors to take care of us but we sure can't. If he had just told me about the bone loss, I would never have started this drug in the first place. My Mother suffered with that and that is something I would not trade for a few lost pounds and a little more energy. No thanks.

I have been on Lisinopril 2.5mg for HBP for a few months now. Not thinking it had anything to do with anything, I started to develop severe muscle and joint pain in my hips all the way down to my feet. I was starting to think I had arthritis or RLS. The pain is really bad and I have taken ibuprofen and used muscle rubs without success. I went on vacation for a week and accidentally forgot to pack the med. Well I had no problems until when I came back and started back on it. The pain has gotten so severe that I called my MD. She recommended I stop taking it and see her in a week. I even ordered a tens unit and started taking potassium supplements. I see on some posts not to take the potassium so I will set that aside for now. As for the coughing, I am a smoker and cough and hack my brains out anyway. So I can't really say its making me cough. This pain though has kept me up at night and I toss and turn because of the pain. I hope now that I stopped taking the med these pains will subside soon.

I started taking Zoloft in December of 2007. I have had anxiety my whole life and after being in an intense car accident I decided it was necessary for me to try medication. It worked miracles. I no longer have anxiety attacks and I'm able to focus and not let little things worry me as much. Over the last few months, however, I have noticed that I have been gaining a lot of weight. My diet has stayed the same and I've been exercising more than usual. NONE of my jeans fit me anymore AND I'm getting a few stretch marks on my hips. I am scared to stop taking Zoloft since it has been almost 2 years. I am currently taking 200 mg. Does anyone have any advice on weening?

After major surgery in mid-June I got an infection. I took a week-long dose of Levaquin. Approximately a week later, my shoulders, back, wrists, hips, knees and ankles became extremely sore and stiff all at once. It took two and a half weeks for those symptoms to disappear, however, my right hip is still affected so much that it hurts to walk. I am an otherwise healthy, young person. The pain does not dissipate when I sit, lay down, or stand in any position. It's really awful and completely has put a hold on my life. Just about everything I enjoy doing involves the use of my leg, and the pain stops me from living normally. I hate this! I wonder whether it's related to the antibiotic. My doctor has not been able to figure out what it is. I'm going to ask her to look in to this! Thanks for letting me vent..D.M. Washington

PLEASE READ BEFORE GETTING MIRENA.....I recently had my second child (which was unplanned) so i was all for it when my doctor told me about Mirena. She talked this big game telling me how great it was and it was perfect for a person like me, so i had it put in at my 6 week check up. To start, it kinda fells like mild to moderate labor pains when they put it in. Not even 2 days later i started experiencing swelling all over my body most of it was in my feet and legs, kinda like when your pregnant except i never had that with either of my children. I have constant pain in my back, hips, and feet. Weird fleshy discharge. I feel like you should when your on your monthly cycle with the bleeding, tired, crampy and hungry except its not just once a month, its been this whole time. I've gained 10-12 lbs in 2 months. I HATE it!.. To top it off it took me THREE requests to finally get them to agree to take it out and it comes out next week...They like to tell you they hardly ever have anybody get it removed but thats because you have to fight with them tooth and nail. It might actually be wonderful for some people but NOT for me!.....So warning to all other women out there BE WARE because i know i'm not the only one...

I'm so frustrated with the Depo injections in general. I received my first injection Nov '03...I was 19 years old it was highly recommended to me at the Health Dept because I'm a lazy pill taker and at the time I questioned the side effects, but the general pamphlet I received mentioned NOTHING of bone depletion being a side effect... and after the first few months of constant irregular bleeding, things were great, no periods, no pill, I was okay with gaining the 20lbs for it...about one year in one of my molars just randomly chipped, my dentist told me it wasn't anything to worry about, it didn't need a filing...less than two months later the tooth cracked down the center... I needed a root canal...one year later during my routine visit my dentist found 5 more molars that needed root canals.... 6 months later all my filings began coming out one by one... My dentist said I wasn't taking care of my teeth, but I brush 3 times a day and floss!! It's been 6 years since I started Depo injections, last year in Sept '08 during my yearly, the OBGYN looks at my file and says "oh I hadn't realized you've been on the Depo 5yrs, you need to take a year off, let your body rest" then she handed my some pill packs and a jar of calcium supplements and sent me on my way. I never even knew about the Depo Black Box Warning, now I realize why my teeth are falling out... I need a filing or root canal on every single tooth in my mouth, they are rotting from the inside out....I've put 7grand in my mouth so far... I can't even afford to keep up with it anymore... I wish I had known what not having a period was going to cost me. I'm 25 years old and I look like I've been doing Meth since I was 19.

I am a 61 year old mail. Two years ago I suffered chest pain resulting in the fitting of two stents was placed on Lipitor and had the usual liver function test which proved normal. Initially I was put on a low dose but as my cholesterol level did not improve eventually I was placed on 80mg which is the highest dose and this did lower my cholesterol level to a satisfactory level. A few months ago I had severe unexplained back pain which I thought might be due to the statin and when I stopped taking it, very quickly the pain went. I have restarted the medication for about 6 weeks now and in the last few days have had intense pain in my lower legs, hips and lumbar region. I have decided now to stop taking the drug and will be seeing my doctor shortly. Although I am taking other medication (amlodipine, perindopril and bisoprolol) for blood pressure I feel quite sure that my intolerable pain is due to the statin.

I had my Mirena inserted on 7/22 and I'm getting it taken out tomorrow (8/4)! This product needs to be taken off the market. I have already reported it to the FDA. I am a total picture of health (25 years old at 150 pounds at 5'11")--eat the right foods, exercise almost daily, no other medications,etc. Since having this thing inserted two weeks ago, I have felt TERRIBLE! Symptoms include: stabbing pains in the legs and hips, joint pains especially in the wrists, headaches, backaches, uterus pain especially in the right side (but left side as well), tingling in many parts of the body (toes, face, abdomen, legs, and arms), nausea, no libido, and blurry vision. I was fine with spotting (this is the only side effect that the doc mentioned), but the other side effects are ridiculous! This needs to be taken off the market immediately, so that other women do not suffer. I will gladly take a pill everyday to get this thing out of me!!

I took 500 mg of Levaquin more than two years ago and am still have severe tendon problems. I was a runner and triathlete. Now my hips and elbows ache so bad that just daily routines are difficult. I have heard that Levaquin has a dispropriate effect on athletes. So if you are a runner or triathlete do not take this drug. YOU WILL NEVER BE THE SAME. The information provided by the manufacturers regarding the side effects is false. The incident of injury for certain groups is much much higher than they report.

I was on levaquin august 2008 for a sinus infection. After about day 5 is was in pain. My joints ached terribly. My knees, my hips, my wrists, elbows and fingers. I have undifferentiated connective tissue disease with lupus like symptoms. I thought that maybe the levaquin made me flare. I stopped taking it on day 5 and after a week felt somewhat better. I am on meds for joint pain for my autoimmune condition but still had the joint pain with the levaquin. The physicians assistant that I saw said joint pain wasn't common. From what I'm reading here it's very common.

I switched from the small round white generic Wellbutrin to the large round yellow Wellbutrin 2 weeks ago. Not to my agreement, I just picked it up at the pharmacy and there it was. Anyway, today I went to the doctors for a rash and she told me that different manufacturers have different fillers in the pills, so I could be allergic to one of the components. I took my new Wellbutrin back to the pharmacy and the pharmacist gave me my old generic brand. The rash was on my stomach, the hips, my back...and it appeared Sunday night. Just a story in case anyone is experiencing something similar. If this doesn't make my rash go away, I will report back to let you know it in fact wasn't the change.
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pic of the different pills.

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pic of my rash

Happy to have Mirena out of me! I had Mirena inserted in 7/07. I had it removed on 7/13/09—YEAH!. My sister, who is a Sonographer (she does ultrasounds), noticed my weight gain and that I haven’t been myself for a while (moody). She said that so many women complain to her about Mirena when she is doing ultrasounds for them. Most of them tell her about the weight they have gained and their moodiness. My sister said… “You workout all of time and watch what you eat. You shouldn’t be gaining weight.” I was 150 lbs when Mirena was inserted and two years later, I weigh 168 lbs. I workout intensely five or more days a week and earned the 2008 Olympian title at my gym (which took a year of hard work to acquire), but my weight keeps creeping up no matter how hard I try. My workouts keep getting harder because my body is heavier… it’s so frustrating! Following my sister’s advice, I decided to do some research on Mirena and found this site. THANK YOU! I was so relieved to know that I wasn’t crazy and that others have experienced the same symptoms as me. Here are some of the other symptoms that I experienced from Mirena: constant bloating, I ached from my hips down to my knees (which I attributed to my hard workouts, but was wrong), mood swings, hot flashes in the middle of the night, acne on my chin, dark hair growth on my chin, dull cramps in my lower stomach, back ache, fatigue, fluttering in my stomach (which felt like a baby), sensitive breasts, pain during intercourse, spotting after intercourse (almost every time). I’m not sure how long it will take me to get my body back, but am so glad that I’m on my way. I’d like to thank everyone who posted symptoms on this site, you’ve changed my life.

I am 26 yrs old and had the Mirena inserted when my son was 2mos old in Feb 08. I still have a very light period, however I have major discharge all the time, tons before my period. My cramps are similar to the beginning throes of labor as my back and hips hurt extremely bad. I have NO SEX DRIVE, I am moody and feel distant to my husband. I am typically a very high strung person, yet now I want to sleep all afternoon when I get home from work. I keep migraines to the point of having to visit a neurologist...have the appt scheduled but haven't been yet. I don't feel depressed, just distant. I have dizzy spells. I want this thing gone.

tri-sprintec was awesome for me. I took it for 2 months and my boobs went from a 36b to a 36c. I stopped taking Sprintec because I didn't have the money at the time to get a refill and my parents would kill me if they knew I was sexually active *17 years old* and I am currently scheduling an appointment to start taking it again! (: My face also cleared up.

I started taking Levaquin on Saturday for preventive measures for knee surgery. I had taken Keflex the week before and had an allergic reaction to it. Extreme itching on my hands, hips, shoulders and feet. I broke out in hives and my lips, eyes, hands and face swelled up. I quit taking Keflex and then a week later, they started me on Levaquin. So this morning, Tuesday, I had been on Levaquin for 3 days, I woke up feeling fine. I was up for about 10 minutes and the back of my head was itchy. I itched it and noticed that my fingers and hands were starting to swell. I took a sip of coffe and my lips were starting to swell. Within 10 min. I was swollen, itchy, in an extreme cold sweat, my throat was swelling and I could not breath very well. I grabbed my phone and called 911 and I could barely remember my address. I told the dispatcher that I was going to pass out and I did. When I came to I could hear the dispatcher trying to get my attention. When I got back on the phone after passing out, she said paramedics were on the way. They showed up about 2 min. later. My blood pressure was 101/53. I ended up going to the hospital and on the way there, they gave me a shot of epipedirine and benadryl. When I got to the hospital there were 8 people working on me. I got a shot of pepcid and a shot for the rash that was covering 90% of my body. I was still having a hard time understanding questions and was having a hard time staying focused to answer questions. I was in the ER for about 4 1/2 hours for anaphylaxis but they finally got it under control. Now I get to have epi pens to carry around with me since this was such a severe reaction. I was told to look into an allergy screening so I think I might see how much the insurance will pay on that and maybe get that done.

I am a 58 year old female Who has been taking Simvaststin for 16 months .
I have been increasingly bothered with mainly night leg pain ( bilateral) that radites to my hips and back. It's like a tooth ache. I too have had to resort to taking pain medication at night to sleep. During the day when I sit for long periods my legs ( especially the thigh area) aches and standing up , walking etc does not alleviate the ache. It is not constant at this point but very frustrating.
After reading the posted notes I am contemplating going off the Simvastatin for a while to see if my symptoms improve.
Any thought?

Thanks!