Hip pain symptoms and conditions

SIX HOURS POST REMOVAL- I had my mirena removed today after 3 years and nearly 3 months. My side effects included headaches, sore breasts, weight gain, nausea, severe hair loss, depression, severe pitting edema of my right foot, cramping, hip pain, exhaustion, severe mood swings, and acne. During the first six months I had constant bleeding, which I had been told to expect. I took regular pills everyday and the bleeding stopped. Then the hair loss started. My hair came out in clumps and was EVERYWHERE. I lost about 15 inches of my hair in spots. I went to the salon and got a fantastic hair cut, I attributed my hair loss to stress. Now I'm not too sure. I also didn't feel like I was myself with the odor that I developed. No matter how many times I showered I felt not regular. Slowly but surely over the past three years I have gained 30 lbs. I worked out to try to get the weight off, I lost nothing and in fact gained weight! The pitting edema of my left foot started in July of 08. I have been tested for everything including diabetes, heart problems, clotting disorders, pregnancy, high blood pressure, kidney problems, and the list goes on to the tune of $6,000. I went to my OB back in the spring and was told if they could find nothing else then they would remove the IUD. In the interim I lost my job and subsequently my insurance. I luckily was able to get coverage again and immediately set an appointment for the removal. Insertion hurt like nothing I have ever experience, removal was quick and almost painless. I also ended up with BV (bacterial vaginosis). I feel and look as though I am about 6 or 7 months pregnant. My belly is actually the same size as it was when my son was born. I weight about 15 lbs more. My breasts were extremely swollen and sore.

I instantly felt better after removal. My hip immediately stopped tingling. I have no back pain. It felt almost like a lifting if that makes sense. I am curious to see what the next few weeks will bring and I will definitely keep you all posted.

This is another update. I had the Mirena removed about 3 weeks ago and my hip joint pain has calmed down A LOT since then! My headaches are gone, my breasts don't feel like they're going to explode, and I am gaining some of my energy back. My hip pain is still there somewhat, but I am hoping in time it will disappear - in the meantime, Motrin helps immensely whereas it didn't touch it when I had the Mirena in. I will be having my regular doctor check out the hip just to be sure nothing else is going on, but I am CONVINCED that this device caused all of the above. I was really surprised that my gyno didn't fight me at all when I told her I wanted it removed. I told her that I felt the benefits no longer outweighed the side effects, and she told me if I felt that way it was best to get it removed. The removal was nothing compared to the insertion - she was done before I even realized she had started to remove it! I haven't had any cramping or bleeding since it was removed beyond the first day or two. I guess that makes sense since the Mirena was supposedly keeping the lining from building up in the first place - guess there's nothing to shed yet. All in all, I am glad I got it taken out, and I am here to tell anyone with similar symptoms to follow your gut and push for what you want - it's your body, not your doctor's!

Update. I received a response from my Gynecologist regarding my email listing the symptoms I have been experiencing since having the Mirena placed. She said some people are sensitive to the hormone that is in the Mirena even though it is a low level. She acknowledged the headaches could be related, but didn't think the weight gain was (I was told the same thing about the pill, yet the weight literally FELL OFF once I stopped taking it). She said she doesn't know about the joint pain - that it's not usually a side effect, and that there shouldn't be an odor to the discharge. She wants to evaluate the discharge & said I can have the Mirena removed at that time if I am more comfortable with that. I just don't understand how there can be SO MANY WOMEN who have these symptoms yet the doctors aren't aware of them being side effects! I truly believe the only research they do is read the literature the manufacturers supply them with and that's that. I am going to print out as much info as I can to present to her and tell her she needs to look into it further. And yes, I am having it removed on that visit because I CAN'T STAND the hip pain any longer.

I am taking prednisone and probably will for the rest of my life due to a rare lung disorder. I am down to 5 mg every day. When I first was put on it, I was taking 20 mg which wasn't too bad. The Dr. increased it to 80 mg. That was a living nightmare. My eyes hurt so bad from the pressure. My pressure in my eyes were very high. The Doctors did cut it down to 5 mg which isn't a good idea as you should taper off of it slowly. I still have some hip pain but it's not to bad. I do try to keep busy and that does help. It does make one's period irregular if you are a woman. I feel for those high school students taking this stuff. Also, it can make your sugar high so get tested for diabetes. This drug does suck but it also can be a lifesaver.

I've been on NuvaRing for a little over 2 weeks now, before that I had been using the OrthoEvra patch. The patch was working just fine but it's less convenient in the summer (esp in TX) because sweating does cause the sticky stuff to ooze around the edges and I often found the patch stuck to my clothing. So, back to the ring...the first few days I swear I could feel it inside me but I gave it some time and figured I would get used to it which I have. I haven't experienced any of the other symptoms you all are sharing about but I have had horrible pain in my hips. It's not a joint pain, I think it is actually swollen lymph nodes. My OB/GYN said they had not heard of this type of side effect and suggested Tylenol and fluids and of course to call back if worse or if no better in 3 days. Is anyone else having hip pain or issues with their lymph nodes (hip area)?

Was on Prednisone for 11 days for an injury to my neck. I knew nothing about the drug except what my doctor told me that it would reduce inflammation in my neck and help with pain.

Well, it did nothing for the injury and pain in my neck. BUT.... I had HORRIBLE menstrual cramps and got my period 8 days early. I've had my period for 9 days now AND terrible pain in my upper left leg. I thought the pain was related to my leg and as the days went by I realized it was in my left hip! It's so bad I can't lift my leg without extreme pain. I KNOW IT'S FROM this awful drug.

I've been off of it for 4 days and the pain is still with me. I called my family dr. and was told Prednisone doesn't do that. BULL!! The paperwork I got with it from the pharmacy show "Changes in menstrual periods" "muscle/joint pain" "bone pain".

I wish I knew this BEFORE I ever took it.

Does anyone know if these symptoms and problems will go away after stopping it? I called the pharmacy and was told it will take 2-3 weeks for it to get out of my system!!

Has anyone had problems that eventually went away after stopping the drug?

Thanks and I hope everyone else is okay soon! This drug should be off the market. I received no help for my neck pain at all!!

If you read my prior posts I have suffered with almost every and more.
I finally called my Dr that put the IUD in about my lower back and all my other symptoms of course she said that it was not related.
Anyhow, she suggested to get a steroid/cortisone shot in buttocks . so that is was I got from my family doctor. I was in more pain for 1 1/2 weeks and then I asked for a mild muscle relaxer which she prescribed that was Flexal. I took one for 3 nights in a row and honestly I have felt extremely better!!! Although, from prior visits I'm still also taking a low dose of a fluid pill every morning for my swelling/fluid in my muscles and hip pain and I also take a good Vitamin B complex every morning for my nervous system.
I 'm in a position waiting for my husband to have a bysectomy?(sp) therefore I have no other birth control. So maybe those of you that are i the same boat as me I thought maybe what i had done may help you all too.
Let me!! Although, I'm fine right now as soon as I can i will have mine removed. I don't know if my effects will come back but I never want them again. I am spotting a little bit which I'm glad because I feel that you have to have some kind of release at sometime. I just think that is not healthy and puts your hormones in turmoil and that is why we have so many side effects.

Im sorry for all of you ladies who have had issues with the Mirena but I love mine. I had it put in 1/09 7 weeks PP with my 3rd Daughter. I never had any cramping or bleeding with the exceptional spotting for the first 3 days and my sex drive is better than ever knowing I have less of a chance of getting pregnant than when I was taking the pill. No headaches or dizziness either. After reading all of your comments, I asked my doctor about all of those side effects when I had to go back a month later to check and make sure mine was in place. She said that they are possible side effect because every woman's body is different and some peoples bodies react differently as with any method of BC. There is still many women out there like me who have no side effects and Mirena is god-sent. I do apologize to all of you and hope you do end up finding something that is right for you.

<3 K.

I have had my Mirena in for about a month now give or take a day or two. And I hate it! The day I had it put in my doctor said I could use a tampon. Worst pain ever and that includes child birth. Since then I have been to the ER over a pain by my left and right hip bones. They brushed it off. It continued, they finally looked into it with an ultrasound and it turns out I have a cyst on my left ovary. I knew that could happen. But the headaches are unreal and the pain in my hip area is so bad that my doctor actually prescribed me 800mg ibuprofen. I want it taken out but knowing that I am so young and that I specifically went to this doctor because he offered it I am afraid they will try to get me to keep it in. Someone please help!

I had mine removed less than a week ago after using it for almost 2.5 years. Like most, I did my research post insertion (I'm finishing up my PhD and have always been very 'body aware') and thought I knew what I was getting into. I've had 2 children (now 11 and 13) so I'm familiar with the pregnant feeling.
My life has been pretty turbulent for the last 3 years (grad school, divorce, cross-country move, intense new romance) and I blamed my symptoms on stress. The last 9 months, however, have been relatively calm. With that background, here's the low down:
Long term symptoms (since within a few months of insertion): Mood swings (very up to very down), Depression (with poor response to treatment), Bloating, Bleeding (sometimes almost all month...mellowed after 1 year), Cramping, Hair loss, Vision effects, Mental fog (pregnancy brain), Weight gain (20 lbs in 2.5 years), Hip pain
More recent symptoms that finally tipped me off: Acceleration of mood swings and brain fog, Lethargy, Acceleration of wt gain (despite consistent workouts and diet), Spike in blood pressure (feeling heart beat in finger tips...like when I was pregnant...verified by nurse at removal appointment. Mirena documentation says remove it if you get a spike in BP), Panic attacks (totally irrational with no external explanation, lasted for days), Suicidal thoughts (SO not like me).
In just in the few days since removal, my mental clarity has improved immensely. Nothing like being foggy when trying to write a dissertation! My energy level is way up. While I've been working out regularly for a few months with continued wt gain, I can feel it coming off now, already. My moods are much, much better. Little things have been throwing me way off track for a long time. I had a couple emotional knocks last night that just rolled right off (no gruesome details, just know that a week ago I'd have been in a puddle of tears). My blood pressure is down and food cravings are gone. Hips feel much better.
Doc at Planned Parenthood said that she has seen a few women in her clinic who have had problems and wanted the Mirena removed (cost me $94). She thinks it might be the beginning of the wave. I had no idea that the hormones in the device could be causing so much trouble. Over the last year, especially, I have adjusted my whole life and lifestyle to stabilize my moods (and maintain a relationship with my very patient partner), not linking them to all the other symptoms. Ugh. I am relieved and angry at the same time. The difference, pre and post, is night and day.
FYI, I had a few hot flashes the day after removal, along with a mild headache for a few days. I was on my (light) period when I had it taken out and it's still tapering off. Moods were pretty rough the first afternoon post-removal (another suicidal rant in my journal) but consistently good since then.
I'm going to circulate a cautionary message with my girlfriends and grad student peers. I sure would have liked to have known long ago what was causing me so much trouble.

First of all, a big thanks to all of you who have shared your experiences. I am a biochemist, with a background in pharmaceutical research...I chose the Mirena IUD after careful consideration of it's active ingredient, Levonorgestrel. The side effect profile seemed pretty acceptable...until I started to experience nearly ALL of them...I am 33 years old and had the Mirena IUD placed in October of 2008 after the birth of my second child in June of 2008. The initial reaction was to be expected...cramping, a little spotting etc...nothing to be alarmed about. I still have yet to have a period (which I really don't miss so no problem there) I never gave a second thought to this until now...for the past month or so (coinciding with the weening process, since I have been nursing the entire time, I believe the side effects were not as noticeable) I have been experiencing the following (that may or may not be related to Mirena as my OBGYN has so adamantly pointed out, but after reviewing your posts I'm willing to bet they're connected) and are in order of occurrence: Major, but temporary, hair loss after 2 months or so; Major respiratory infection lingering over a month with difficulty breathing, tightness and pain in the chest at around 6 mos; And in the past month, several instances of motion-like sickness/ nausea, dizziness, blurred vision, major impatience/ mood swings, loss of appetite (pregnancy-like symptoms...yep, I was thinking man I'd be pretty pissed if I was that 0.01% pregnant statistic), and as of this past weekend, my first aurora migraine with tunnel vision and serious nausea and vomiting, to the point where I went to Urgent Care...who referred me to the ER...who wants to perform a battery of tests including a head CT. I have an appointment with a trusted GP tomorrow to discuss possible root causes...but it is to coincidental that so many women are experiencing these same symptoms! I am certainly leaning towards having this removed. CAN THOSE OF YOU WHO HAVE HAD THIS REMOVED PLEASE RESPOND IF YOUR SYMPTOMS SIGNIFICANTLY IMPROVED OR WERE RESOLVED!!! THANK YOU!
These side effects seem to go well beyond a 5% rate of incidence according to all of you who have reported. I will investigate further and keep everyone posted. As someone who is highly experienced in the pharmaceutical industry, you bet your a$$ I'm going to get to the bottom of this! Good luck ladies!

Hi all! Well I got my mirena taken out on Wednesday. The Dr. was very sweet I told her my symptoms and she said lets take this out then! While she was down there she said " Hmm I'm going to look at a swab under the scope." She came back in and said that the mirena gave me a bad infection! I had to take some strong one time antibiotic that killed my stomach! I can't wait to start to feel better. I did notice I can see a lot better then I did, no more blurry eyes. The last 3 1/2 years have been utter hell for me. I've been in and out of different Dr. offices not finding anything. I was dizzy all the time, I started out small after I delivered my baby and gained 60 lbs since it was put in. I had a shooting pain on my right side, horrible anxiety attacks, blurred vision, fuzzy mind, head aches, ovarian cysts, lower back pain and bloated belly. I am so relieved I got this disgusting thing out of my body!!! I hope my life will go back to normal now.

I'm a 26 year old female that has had the lovely experience of taking Lupron twice in my life. I was diagnosed with endometriosis at the age of 19 after having a lap. I had been suffering from excruciating back pain for months. The lap only helped for 3 months and then the pain returned. My doctor recommended Lupron for 4 months and so I jumped at the chance to feel better. I actually did ok with the shots. I experienced the hot flashes, fatigue and crazy mood swings but I was willing to try anything to feel better. After the 4 months, my life returned to normal and I had 5 good years of pain free life with normal periods. My body on the other hand did not react well to birth control so I couldn't use it. For the last 2 yrs, my husband and I having been trying to conceive with no luck. 1 yr ago my periods took a wild turn. I began bleeding so heavily that I was bleeding thru my tampons every 5 min and began passing clots the size of a half dollar. These episodes would last for bout 3 hrs. This continued for 3 months and so my doctor recommended Lupron again. I was cautious about taking it again, but I was desperate. This time around I suffered from weight loss, nausea, severe bilat hip pain (due to low bone density), and receding gums along with all the usual Lupron side effects. My dentist said my gums and teeth looked like I was 60 or 70. FYI, I have never even had a cavity!!! I'm now 3 months post Lupron. I still haven't started my period again but my symptoms have subsided. Its just a waiting game now. I hope to get pregnant soon but I will probably go on fertility drugs very soon. All I can say about this drug is that it worked for me the first time and I hope it did the second time. It definitely was not easy and I don't recommend anyone going into it lightly. Good luck to anyone who is thinking about it and I feel blessed to have gotten out of it with a lot less problems than other men and women

I have had serious hip pain, especially when extending my left hip, and even worse with abduction of my left leg. I had absoluetly no pain before taking Fosamax. My doctor insists, the pain is only arthritis, and had nothing to do with the Fosamax.

I have been on Diovan HCT 160 for several years. The other day I woke up with joint pain in my hands. The next day it was in both ankles and arches of my feet, also both elbows and my right knee felt swollen and painful. I am a physical therapist and am
In tune with my body. I know this is atypical joint pain and not from physical activity. I was afraid of rheumatoid arthritis so I am shocked and a bit relieved to read others with same effects. I am going to my MD for full blood work and a new BP med for sure. I will post any new info if it might help others.......

Have been taking topamax for 4 months and now have hand and feet tingling. major spelling and memory loss issues. My question is Does any one else have HIP PAIN??? I can't think of any reason why I have it now... except for the addition of the topamax.Thanks, TL

At about the time i started to take Lipitor (10 mg) two years ago, I started to experience severe neck pain which I attributed to spending 8 hours bending over y laptop. I went through physiotherapy, and the therapist recommended a cylindrical pillow which proved o be quite effective. However, my biceps tended to be sore when I woke up. Last week I suffered excruciating pain in the right hip joint. My doctor appeared to finally link my problems to Lipitor advised that i stop taking Lipitor immediately. The hip pain subsided within a couple of days, but a vague feeling of fatigue and dizziness persist.

I hate this pill! I have been on it for a month. I been getting bad back and hip pain and I am always tired, I can sleep for 12 hours just like last night and be up for 3 hours and want to go right back to sleep, I noticed my hair has been coming out when I get out of the shower and also when i brush it (more then usual), I'm gaining weight and that's bad for me cause I have weight issues and I can't stop eating! All I want to do is eat. As for my sex drive and moodiness its better then when I was taking ortho tri cyclen, with ortho tri cyclen when I was in the mood it would go away instantly, my moodiness was crazy I would break up with my boyfriend over the tinest things. I think I'm done with taking birth control, I didn't like either way I felt with either one.

Also I spotted for 6 days not even heavy, idk if I should take a pregnancy test or not. I called pph and they said it could be because I don't take my pills at the same time but they don't know. sometimes I miss one pill and ill take it the next day wit that day pill but I never take it at the same time sometimes I take it an hour or two later. Should I take a pregnancy test?!

I have been on Diovan HCT for about 9 years!!!! I have felt like crap for about 5 of those years! I recently was searching the internet to find out a possible diagnosis for my feet swelling! I showed this to an ENT dr. at a recent appt. and she thought it could be Cellulitis, however the antibiotics did not help the redness and swelling in my feet. Now, after extensive research, I do believe I have GOUT. After trying to figure out why I would have GOUT at age 39, I have read that the "thiazide" can caused elevated levels of uric acid, which forms crystals in the joints. I also have "anemia" which doesnt get better with medication and the reason I felt I was constantly tired over the last few years. I have also had severe joint pain...foot pain, back pain and hip pain. And an overall feeling of listlessness. After reading an article listed on the FDA's site on this drug, I fully believe this drug is the cause of 90% of my problems. I am going off this tomorrow, and calling my Endocrinologist. Did I mention I have diabetes too? Which has severely exacerbated in the last few years. Try this site for viewing adverse reactions (hopefully this will work)

www.fda.gov/medwatch/safety/2006/Nov_PIs/DiovanHCT_PI.pdf

I am scared to death after reading what everyone is going through. I was put on Levaquin for 10 days and got to day 9. My joints ached so bad I thought I had arthritis, and even had my Dr. do blood tests for it (I had no idea it was the Levaquin). I am only 35 years old and never worried about arthritis before this. Also, within 5 days I started developing hives all over. Again, I was stupid and didn't realize until day 9 that the hives were because of this med. I told my Dr. and he told me to stop taking it which of course I did. I assumed the hives would go away after the med was out of my system. But a week later the hives were unbearable. I was put on prednisone (another issue altogether) and that helped the itching, but now every time I try to go off or back off the prednisone the hives come back- and they are terrible! Now my Dr. thinks the hives were from something else because there is no way that the Levaquin is still in my body. But after reading what other people are going through on this med, I am convinced this stuff is as everyone says- POISON!! I am so worried about the joint and hip pain that was so bad I couldn't stand for long without excruciating pain in my right hip. It felt like I had a one hundred pound weight just sitting on it. And my hands were the worst. I have a newborn and could barely pick him up without worry that I'd drop him. I don't know what to do.. Is there anything to do?? I'm still on the prednisone, and have been for a month. I need to get off of it but every time I do I itch so bad with the hives that I cannot function. Also because of the prednisone I noticed last night that I am getting "moon face" my face is swelling up and there are a million side effects from that drug too. How long does this last? Has anyone else fought the hives that come with this? Please help me, I am so scared!

Well ladies let me tell you what... I must be super sensitive to this crap!! I started the ring because I had used it years ago and LOVED it!! I mean LOVED it! It WAS the only bc that didn't give me any issues... they really must have changed it... I'm gonna list my new symptoms and reasons for taking this crazy thing out...

Nausea,
Headaches,
Visual Migraines... spots in eyes
Dry Mouth
Breast Pain
ALL of my hair is FALLING OUT
in 3 days gained 10lbs!!
Mood swings
Think i'm pregnant every day!
Still get cysts (which was my need for the ring)
Horrible constipation/diarrhea... IBS like
Lack of energy
Itchy scalp
Leg pain
Hip pain
All the symptoms of thyroid issues!!
Circulation issues
Took Sudaphed and almost had a stroke!! BP was 180/110 WOW!!
normally is 117/67

My advise... GET OFF THE NEW RING... The old one was great...this new one is DANGEROUS!! I have worked with doctors for years... they prescribe things that the cute sales reps bring...

Contact me if you have felt the same... It's good to know there is someone out there that has been thought it too!!

Wow! I must be the latest in a long line of Lipitor users and apparently pain sufferers. I have been on Lipitor for over a year. I am 56 years old, active and healthy (thank God). Around November 2008, I noticed a "twinge" in my left hip while sleeping. This has gotten progressively worse over the months and I thought it was due to arthritis (which runs in my family). But after reading these blogs, I am not so sure. If anyone has anything definitive regarding this, ie: tests, studies, etc., I would really appreciate a point in the right direction for more information. I was thinking (until today) that I was headed for hip surgery or something equally drastic. Now that I have a clue that it may be the Lipitor, I want to investigate further and then, if necessary, change to another medication that won't break me down like this. My heart goes out to anyone that has suffered through hip pain. It is a miserable, painful condition that saps your energy and your desire to even move sometimes. I appreciate any help you can offer. God bless all of you. - L. B. ******

I began having right hip pain a month after the mirena was inserted. I assumed it was from running. All the doctors I have seen for the past year stated I strained a muscle. They ordered MRI's and physical therapy. I have completed all, but still have the same hip pain-over a year now. Has anyone had hip pain due to the mirena? And did your hip pain stop completely after your mirena was removed? I am considering getting it removed. Although the doctors tell me they are not connected, I can't help but think there is a coincidence.

I have been on lipitor 10mg for about 6 mths (after reacting to lipex with severe hip pain and going off that). Am now experiencing abdominal pain, severe headaches, excruciating neck pain and to top it off a droopy eyelid and loss of extreme peripheral vision after a bout of flashing auras and fluid like waves in the outer edge of my eye. After tests my retina is not detaching so what is the cause then. My cholesterol is high when not on lipitor and am wanting to lower it without drugs. I could do with losing 10kg weight but will that bring down the cholesterol. I walk every morning for 30-40 mins. Diet is healthy, a few junk things each week but not overly so.

I've been on 10 mg of Lipitor for approx 2yrs. A few months back I began experiencing severe constant right hip pain. A could walk through it, but had many sleepless nights due to the unrelenting deep pain. I had difficulty lifting my right leg without support from my arms. I'm 54 and otherwise in pretty good health. I stopped taking the Lipitor about 2 weeks ago and while I still have some pain it has decreased about 75%. I can sleep at night and am even pain free some of the time. If anyone has had a similar experience would appreciate knowing and if the pain eventually subsides and any suggestions to support the healing process.