Joint pain symptoms and conditions

What a Godsend this website is. I am a 48 year old female, and I have been taking Advair (the lowest dose) for about 2 months now, with steadily worstening side effects. Although I have to admit, my first dose of Advair was like a much need "breath of fresh air", the side effects are not worth it. In fact, I just got off the phone with my doctor, telling her I will no longer be taking the Advair. These were the side effects I have experienced: rapid heartbeat, rib pain, joint pain in my legs and fingers, loose bowels, and a noticeable change in weight / body shape. I have always been complimented on my tiny waist and flat stomach, but as of late I have noticed my waist size increasing, despite my usual exercise. In addition, the most serious and most disturbing side effects are insomnia and the onset of severe depression / anxiety / paranoia. I had issues with depression as a young woman in my 20's with anorexia, with no relapse until I began this medication. Yesterday, I had to pull over to a store parking lot to cry for no reason! If it were not for this website, I would have blamed myself for some sort of mental weakness or unhealthy thinking. Also, I have never experienced anxiety in my life, and while on this medication I have had several episodes of intense panic, where I was convinced I should immediately draft a last will and testament. My vision has been blurring in and out considerably, my voice sounds as if I have larynxitis daily, and I have also experienced profoundly increased thirst and urination. I have not had my blood pressure checked, but I feel like what must be an increase in this, as well. Lastly, the past few days I have noticed severe hair loss, which, until I read this website, I attributed to my recent dieting. (I have been desperately dieting and increasing exercise to try to regain my figure that this medication is apparently ruining. Until this time, I have weighed the same and had the same or stronger body than high school school (5'4'', 115 - 120 lbs.) God bless everyone who has contributed to this website to educate others about the horrors of this medication. My doctor wants to see me to "give me something else", but I am going look into alternative therapies (yoga, breathing exercises, teas, etc.) The comment that made the most sense on this website was the person who wrote "break up with your asthma...begin by taking a deep breath and telling yourself you no longer have asthma." Also, I have seen that God / Jesus can heal anything, so I am going to turn to Him in prayer instead of the doctors. After all, Who created our bodies to begin with? I will add you all to my prayers, and that God will help us all heal from this... both the asthma and the suffering created by Advair.

I can't believe what I am reading! I have been a competitive runner for over 25 years, and in the past two years I started running mainly trail ultras - races up to 70 miles. This March my husband noticed a huge dent in my left glute muscle that over the course of four races got worse and led to a secondary dent in my hip area. I just assumed I had injured my muscle somehow, but no amount of rest, PT, or stretching has helped.(it's been 6 months now) I developed hip bursitis, medium to severe pain in all my joints, including both knees, my left ankle, and extreme spinal stiffness.

None of the experienced PTs I've been to have seen anything like my dent, and they are baffled by my worsening condition. I'm so scared I'll have to give up running altogether, as my joints are failing me. My PT has advised me to go to my regular doctor to get bloodwork, X-rays, an MRI & all tests done to see if something is wrong with me that is beyond muscle-skeletal. Before all of this, I had low back issues but no joint issues at all.

I found this web site by chance, and suddenly I remembered that several months before noticing the dent, I received 2 steroid injections in my butt, as well as pills & cream for a super severe case of poison oak that covered my whole body and face. Do you think my doctor will tell me if it was Kenalog if I ask?

I, too, am very very interested in any other stories of severe joint pain and inability to run especially after receiving these shots. I hope we can help each other figure this out & get answers.

53 year old female who has taken "F" for almost 2 years - the past two months was the generic version. Have noticed a gradual onset of joint pain and heart palpitations, but am not one to see a doc unless I feel like I'm dying... So I wrote it off to aging. (-:
A friend recently mentioned that she had heard that Fosamax causes bones to be brittle, which caused me to wake up, look around and see what people are saying and what new articles or research are out there. Yeah, sure - there are lawsuits. Not a surprise in our litigious society. More importantly, however, are the comments from real people. Thanks to you who've posted your experiences!
I stopped the drug several weeks ago and seem to have an increase in joint paint. But I'm not going back to Fosamax! Also interesting to me is that around the same time I stopped the drug, I experienced an uncharacteristic downward shift in my mood/mental state. Not sure if there's a correlation to the drug or not...
It is reassuring to see some comments from people who indicate they feel better after weeks/months of being Fosamax free. I am a "gym rat" and very fit/weight appropriate. Weight training and nutrition will be my treatment of choose for osteopenia for now. With time, I am confident that the symptoms I'm experiencing will subside. And any future ailments for which I am prescribed a drug will be very carefully researched by me beforehand.
Be careful out there and stay informed!

If you are taking this medicine, STOP! I took this medicine for about three months. I started to feel like I had a congestion. I cough lightly at first then into a hard cough which progressed into a hacking. My wife thought I was critically ill. I was spitting up clear congestion at work into my garbage can. This stuff is bad, I found this site and stopped taking the medicine. It took 3 week for the cough to subside. It’s been about 4 months, and I would say I am only about 98 percent back to where I started . About every 3 weeks I out of the blue start to slightly hack. I know one thing this is not a good medicine. When I started my BP was 138/109. My doctor told me to try this. Because of this medicine I could not do my job and my doctor never told me it was the medicine. When I told him he told me he didn’t think it was the medicine and prescribe some cold medicine

My mother is on Bactrim for a UTI. She has Alzheimer's disease, but can normally function pretty well. Two days after starting the three day treatment she got more confused and couldn't even figure out how to take her medication. Now she has leg pain, muscle weakness, and joint pain although I think it has helped the UTI.

I'm not a person that necessarily thinks the drug should be removed from the market because of what I've read here. We aren't reading posts from the thousands of people that it has helped without ill effects. All drugs potentially have side effects. There is always the potential for adverse reactions or allergic reactions. As a matter of fact, many people on this forum continued to take the medication when they were clearly having allergic reactions making themselves sicker in the process. We must be diligent and educate ourselves about medications and not just rely on someone else to tell us that it is fine. That being said, I feel for those on this board who have endured such suffering and hope that they recovered without incident.

Was on Vytorin for 2 years & experienced no noticeable side effects during that time. It lowered my cholesterol to 179. Had a hysterectomy (complete) in Dec., 2007. In May, 2008, I began a sudden on-set of severe numbness in both hands (especially when lying down)--classic carpal tunnel symptoms and intense pain in all joints. When I move from a sitting position to stand up, I can hardly do it. This is what I thought I would feel like at maybe 80 years old--not 46 yrs. I thought maybe it was because I'm not taking hormone replacements, but my doctor said it could be the Vytorin & he took me off of it. I've been off for 2 months, but the symptoms are not improving. The carpal tunnel seems to have lightened up a bit, but the joint pain (especially hips) has not gotten any better. I wonder if it ever will????? Also experience fatigue, foot pain, & weak fingers.

My husband initially took Prednisone after getting strange lesions, severe joint pain, severe fatigue and severe stomach cramps/nausea. It worked great he was tapered off and no problems for about 18 months. Then he go sick again (2/08) and has been up and down on Prednisone for 7 months- currently taking 60 mg. daily. Some doctors think he has Wegener's, but testing is inconclusive (Wegener's starts with upper respiratory stuff, which he also had). His mood swings are severe and he's a different person, twitching, hand trembling, muscle spams, malaise, anxiety/depression, very fatigued, insomnia, severe stomach cramps/vomiting. How do you tell which symptoms are the Prednisone and which are the disease process? They want to taper him to make him sick enough to get some test results that show organ damage or something, but everyone chickens out and he ends up getting increased. How long should he be on Prednisone and not be put on something stronger?

Husband taking 10mg. He is having dizziness, confusion, memory lapse, depression, short-temper, severe leg cramps, chills, loss of appetite, constipation and severe stomach cramps. We are discontinuing this medication. He thinks it's literally killing him like being poisoned.

i got mirena 3 years ago. i have felt bad every day since. never thought it could be linked to this device. i have had every symptom but hair loss and flakey skin. its been awful. i found this website last night. and it all clicked. the moodiness, fatigue, heartburn and palpitations, joint pain, headaches, nasal problems. hands going numb, i thought there was something really bad wrong with me. but since reading these blog. i know that i should start feeling better soon. I had it removed today. My husband and I want another baby. i had no idea this device mirena , is what caused all my problems. i even got so weak that i didn't feel like moving. had to force myself to get out of bed. so thanks everyone for this website.

amber

I have had three kenalog shots: once when i was 15 to combat severe allergies, sinusitis, rhinitis, nasal polyps, and everything else that can go wrong in the nose. I also have moderate to severe persistent asthma. Yet after this shot i was cheerleading, running the mile and 800m in track, and running the 3mile in cross country. I had another shot almost 2 years ago after a severe asthma attack made me go to the hospital and yesterday i had another shot.
I have never had any adverse reactions to Kenalog (besides weight gain, same with prednisone) and i am sorry to hear that so many people have experienced terrible side effects. I have never had any mood swings, period problems, dissolving of my butt cheeks, joint pain, etc.
Kenalog keeps me alive and breathing.

I was put on synthroid a year ago, due to a tsh level of 87. I pretty much felt better right away after taking it. First I took 50mcg and then it was upped to 100mcg. Everything went well until I had my latest tsh test. The level was going up again (tsh 5.4) so the doctor decided to put me on 125mcg. After about a week I began feeling like crap. Slugglishness, tiredness, muscle pain, joint pain, and it became progressively worse. I have an appointment coming up thank god. In the mean time I read 3 books on thyroid and it was mentioned that most people don't benefit from just taking T4 (ie. synthroid), despite the fact that the pharmac. and some docs say that body breaks t4 down into t3.
Some people's body cannot successfully break it down enough, some are cellular resistant to thyroid hormones, and those people absolutely need t3 in order to not develop Hypometablolism. The cell need the T3 to function. But unfortunately one can be hypo and still have good TSH levels, because this particular test only tests if there is enough T4 in the body.
Unfortunately, it's so hard to explain that to mainstream doctors.
One doctor I read about said it right: Don't just treat the test results but also the bodily symptoms, for everybody is different anyways. Just like our finger prints are unique, so is our hormonal metabolism.
I'm going to try to talk to my doc about this, but if he doesn't listen I will look for another doc until I found one that will. Good luck to all in this hormone jungle.

I was prescribed Levaquin for a bout of diverticulitis six weeks ago. About a half hour after taking it each morning, I felt completely unwell--dizziness, fatigue, overall weakness, odd sensations of pressure in my head, chest, and bladder, weird bouts of sudden joint pain. The worst side effect was terrible insomnia. I'd go to sleep OK, but wake up after 3 hours and not be able to get back to sleep, sometimes for the rest of the night. Instead of getting the rest I needed to get better, I was getting more and more exhausted. Now, a month after stopping the medication, my sleep hasn't returned to normal. I'm still awake in the middle of the night for two or more hours. Is this a residual side effect from Levaquin? Has anyone else experienced it? When can I expect my sleep to improve? Is there a way to detoxify from this drug?

negative -aches all over, joint pain, lack of energy and motivation, positive -nil asthma, greatly improved sinuses, less head congestion, was told this was the best drug for asthma, polyps-sinus, aspirin allergy. Have been taking singulair for two months, concerned have also noticed feelings of anger/mild depression. Am female 50yrs, breast ca 3 years ago taking femera for 8 months. Am worried whether to continue singulair aches are killing me but could be side effects of femera to scared to go off it. Want to live and have quality of live, have 13 year old, I need to be fit for parental duties/work.

Exhaustion, joint pain, headache, ankle swelling, shortness of breath, persistent (cold) sores in my nose…

I am 52 years old and have taken Lisinopril for approximately 7-8 months. During the past two weeks, the majority of my joints have suddenly begun to ache. My fingers, especially index fingers, and one wrist are extremely uncomfortable. Other than the side effects listed in the comments on these pages, has anyone lost their eye brows? Sounds crazy doesn’t it but I first thought it was a side effect of hormone replacement therapy. I gradually stopped taking the HRT (ugh!) but continued to lose my eyebrows and now I notice my eyelashes are thinning. After trips to two dermatologists, neither had an explanation and both denied the HRT drug would cause the hair loss. I was and am extremely frustrated. I am not sure what made me research side effects for Lisinopril again but I finally saw something on an internet site saying that ONE percent of people could suffer hair loss. I’m sure my doc will be disappointed that I want off this medication. The only meds I take regularly are Lisinopril and Dyzaide (low dose). I have taken the Dyzaide for several years.

I've posted several times before, but it ahs been a while since I've updated on here. So a recap: Almost 33, have 3 kids(ages 13,11,and 7) Had insert on 12/27/07 after having used depo for many years with no major side effects...issues continually worsened over next few months. Had removal early May, 2008. Several issues cleared up within the first few weeks after removal, such as the joint pain, swelling, heartburn. Brain fog and moodiness became much better. Libido returned gradually as well. But I still have had no success in losing the weight gained over the last 6 months. Still 30 pounds heavier thatn was at insertion...increased workouts, decreased caloric intake, only lost 4 pounds in almost 3 months. Family doc even put me on meds to help with the weight loss, and they had opposite effect...I actually was hungry all the time and felt completely stoned! Acne still unrelieved to the point that I know have an appointment for a 2nd dermatologist as my first one ran out of options for me! Completely unable to clear up my face. Family doc wants to put me on antidepressants, but I don't' think that's the answer. Plus after all the problems I've had...don't trust a whole lot of meds anymore...especially ones that are known for reducing your libido! (Plus after all this and to STILL be overweight with acne...he'd be pretty depressed too!) Bloodwork all came back fine...actually a "Picture of perfect health!" The only thing he did say was that my testosterone level, although in normal range, was at the high end of normal. However, as I'm still young 30's, no one tested my hormone levels before...so I don't know what is normal for me. Will be talking to him about using an anti-androgen, like aldactone, to see if that will help. Not using any form of hormonal birth control any longer. As old-fashioned as it is...I now use a diaphragm and spermicide...and I'm actually pretty happy with it. I'm happy for all those ladies who had a flat belly again within a few weeks, and their faces cleared up almost instantly...but I must admit I'm jealous. I wish it was that easy for me. Good luck to all of you. Will post again in the future.

I STARTED LEVAQUIN, 1ST ROUND FOR STAPH INFECTION POST OP BURSECTOMY. AFTER THE 2ND DAY, I ASKED DR. FOR PAIN MEDS JUST TO CONTINUE ANTIBIOTICS. I HAD TERRIBLE JOINT PAIN, AND COULD BARELY WALK. I ALSO STARTED GETTING PITTED EDEMA. THE DR CONTRIBUTED THE EDEMA TO IV FROM SURGERY AND DISMISSED ALL THE SYMPTOMS I COMPLAINED ABOUT FOR THE LEVAQUIN ASSUMING I WAS A DRUG SEEKER I GUESS. AFTER THE FOLLOWING WEEK, MY SYMPTOMS SEEMED TO GET BETTER. I AM NOW ON ROUND 4 ( 500MG LEVAQUIN X 7 DAYS) I WENT TO DR BECAUSE MY PITTED EDEMA RETURNED. I ACTUALLY HAD A ROLL WHICH COVERED MY ANKLE. MY FEET WERE HUGE. THE PA SAID HE DIDN'T KNOW WHAT CAUSED IT, BUT SAID IT WAS NOT LEVAQUIN. BY THE NEXT DAY I COULD BARELY WALK. MY KNEES HIPS AND BUTT MUSCLES HURT SO BAD. I HAD A LUMBAR FUSION A FEW YEARS AGO, AND THIS WAS MORE PAINFUL. I STOPPED THE DRUG BECAUSE MY BIG TOE STARTED GOING NUMB. SYMPTOMS STARTED TO DISAPPEAR BY NEXT DAY, BUT THEN MY ARM INFECTION RETURNED SO I RESTARTED LEVAQUIN. THIS TIME, BY 2ND DOSE AL SYMPTOMS RETURNED. NOW MY BIG TOE WENT COMPLETELY NUMB ON TOP HALF AND MEDIAL SIDE. I COULD NOT USE KNEES AT ALL. IF I COULD HAVE MADE IT TO THE STORE, I WOULD HAVE GONE AND BOUGHT A WALKER. I AM 45. I DECIDED TO STOP DRUG AND START SOME KEFLEX I HAD IN CUBBORD. SYMPTOMS WERE GONE IN ABOUT 2 DAYS. I STILL LIKE CRAP, BUT I CAN WALK NOW AND THE SEVERE FEET, LEGS, KNEES, HIPS , BUTT , WRIST PAIN ARE SO MUCH BETTER. I DID HAVE TO LAY FLAT WITH LEGS ABOVE HEART FOR 2 DAYS TO HELP GET RID OF EDEMA. I READ ONLINE WHERE OTHERS HAD THESE PROBLEMS ALSO. I HAVE TAKEN LEVAQUIN BEFORE AND HAVE NEVER HAD A PROBLEM WITH IT. I HAVE TO WANDER IF THERE IS SOME KIND OF FACTORY TAMPERING OR INGREDIENT CHANGE ETC, THAT COULD PASSABLY BE HAPPENING. MY MEDS WER PURCHASED AT SAVEMART AND KAISER. I HAVE TAKEN THIS DRUG MANY TIMES PRIOR TO 2005 AND ALWAYS HAD GREAT RESULTS. I AM GOING TO SEE IF ANY OF THESE COMPLAINTS WERE PRIOR TO 2005. I READ WERE SOMEONE SAID TO DRINK A LOT OF WATER . I AM NOT A BIG WATER DRINKER SO I MUST ADMIT IT HELPED. I READ WHERE ANOTHER LADY HAD MULTIPLE TESTS, AND FINALLY THE ONLY THING THAT CAME BACK ABNORMAL WAS A LAB TEST TO SHOW MUSCLE DETERIORATION. I ALSO DID A COLON CLEANSE. SOMETHING I ALREADY HAD THAT I USE ON OCCASION. SO, I DONT KNOW IF IT WAS A COINCIDENCE, BUT AFTER THE COLON CLEANSE, DISCONTINUE OF LEVAQUIN, LOTS OF WATER, AND CUT DOWN ON ANY SALTY FOOD, THE ONLY SYMPTOMS STILL LEFT ARE MY KNEES. I STILL CANNOT GET UP OFF THE FLOOR, OF BEND DOWN WITHOUT SOMETHING TO HOLD ONTO. BUT THEY ARE IMPROVING AND THIS IS DAY 3. EDEMA IS COMPLETELY GONE. MY SIDE AFFECTS PAPER STATED DANGER OF TENDON RUPTURE AND IT ALSO STATED NOT TO EXERCISE. SO, IT CANNOT HURT TO DO A COLON CLEANSE. IF NOTHING ELSE, IT HELPS GET RID OF LEFT OVER TOXINS IN BODY. I WOULD ASK FOR A GOOD ONE AT AN HERB STORE. BUT MAKE SURE YOU DRINK LOTS AND LOTS OF WATER. I THINK DEHYDRATION HAS PARTLY TO DO WITH MUSCLE PAIN ETC. ALL 3 DOCTORS I SPOKE WITH REFUSE TO BELIEVE THIS IS THE CULPRIT. I AM GOING TO DEMAND THEY PUT MY SYMPTOMS AND PUT THAT I STATE I BELIEVE LEVAQUIN IS CASING OR CONTINUING TO CAUSE THESE PROBLEMS IN MY MEDICAL RECORDS. ASK DR TO READ BACK TO YOU WHAT THEY DOCUMENTED IN YOUR CHART. INSIST THEY PUT IT IN YOUR CHART. IF THERE ARE ANY PROBLEMS WITH THIS DRUG DOWN THE ROAD, YOU WILL HAVE IT DOCUMENTED. NOT ANY OF MY DOCTORS DOCUMENTED THE THINGS I TOLD THEM ABOUT LEVAQUIN WHEN I ASKED. I AM NOW GOING TO INSIST THEY DOCUMENT IT IT ALL, AND PROVIDE ME A COPY OF THE MEDICAL RECORD AFTER IT HAS BEEN DICTATED. PS. IT IS NOW CAUSING CRAZY NIGHTMARES, DEPRESSION. I CAN LIVE WITH THAT, BUT THE PAIN ON A SCALE WAS A 9. GOOD LUCK, AND IF ANYONE FINDS A DOCTOR WHO HAS EXPERIENCE WITH THIS, PLEASE POST IT. THANK YOU DK

I have been on prednisone for 5 1/2 months now, I was hospitalized starting in February until like the 25th of March for a bad exacerbation(sp) of my ulcerative colitis. I have taken prednisone for 9 1/2 months out of the last 17 months. I have experienced everything from growing facial hair I don't want to loosing what hair I do in a short period of time. Most of my hair loss started after I weaned off the prednisone about one week ago, or lets say it got much worse. I also while on prednisone got have got to experience the lovely side effect of pysicosis(sp) and am on meds to couter react what it has did to me. This is a evil and horrible drug, I hate it with a passion for all the harm it has did to me. I now have joint pain, restless sleepless nights, night sweats, tremors, not to mention the rapid weight gain. And to top all this off I am still not in remission, so this drug was used all in vain. Please be careful using this awful drug and if you have to use it, only use it for a few weeks at the time and not long term...the side effects can be horrendous and sometimes like in my case permanent to some extent. I do wonder about the hair loss, it has been worse this time than ever...I hope it stops soon.

I have had my mirena since April of 2006. For the first two years it was the most wonderful thing in the world ( no cramping, spotting or periods). But lately I have been feeling very horrible. I have no desire to do anything. I am very tired, moody, gained weight (just around stomach area), depressed, joint pain and sik to my stomach. After reading a lot of the posting on this website. I realized that a lot of the women feel just like me. Now I know that I am not crazy. I also scheduled to have mine's removed on August 1, 2008 (yay!!!).

tramadol has been great for me . I have mod to severe joint pain and it is the only thing that helps. Curbs my appetite so I have been able to lose weight. Gives me great energy so I am by far in a better mood . Only negatives about it are Dry mouth and mild constipation .

I have been taking 20mg of Lisinopril and 5mg of Felodipine for about a year now, and I am experiencing excruciating joint pain. The back of my knees ache even while sitting and the bottom of my right foot keeps me from walking freely because it hurts so much. My wrists and fingers hurt too. I am overweight, so I just figured it was due to excess weight, but reading these posts made me realize that this is not normal. I am in pain all day long. I feel like I'm going crazy because I can't just get up and go- I struggle to do anything. I did not want to see my doctor because I've switched medicines before- used to take 50mg of atenolol but fatigue was horrible, so doc gave me hydrochlorothiazide and it gave me a terrible rash on my face. I thought I was done switching meds- does anyone know what is a good bp medicine? I'm tired of being tired and in pain.

I have experienced most of the side effects that others have listed here. Mental fog, dizziness, blurred vision, horrible fatigue, cold intolerance, weight gain, joint pain, etc. These started approximately one month after insertion. I have been to my PCP multiple times and have been evaluated for things ranging from hypothyroidism to lupus. All tests have come back negative. No one has once suggested that it may be due to the Mirena. I am going to have it removed at my next visit and I would be willing to bet that many of my symptoms will be resolved.

7-18-2008
I HAD THE DEPO LUPRON SHOT IN 2004 FOLLOWING A LAP. AFTER THE FIRST SHOT (A 1 MONTH) FAILED MY DR. GAVE ME A 3 MONTH SHOT, IMMEDIATELY FOLLOWING I HAD SEVERE JOINT PAIN, INDIGESTION, COUGH, DEPRESSION, DIZZINESS, HOT FLASHES PLUS A LOT MORE. AFTER 2 MONTHS I DEVELOPED A LUMP IN MY BREAST, MY DR GAVE ME ESTROGEN (THEY ARE NOT SUPPOSE TO BE USED TOGETHER. I WENT ALMOST INSANE!!! NOW 4 YEARS LATER MY TEETH ARE GETTING CAVITIES IM 37 AND HAD MY FIRST ON AT 35.
MY JOINTS ARE VERY PAINFUL I LIVE ON ALEIVE AND IBUPROPHAN.
MY DOCTORS SAY THERE IS NOTHING WRONG WITH MY JOINTS (GO FIGURE). TO AN ONE WHO IS THINKING OF THIS SHOT FOR ANY RX DON'T.

I am a woman in her early 60's. I have slightly elevated BP abd it does tend to spike first thing in the morning, after waking and is much lower (normal) at night. I have tried several different BP meds and had side effects of all of them. The Doctor recently put me on Toprol XL 25mg. After about three weeks, I really did not feel well - extreme fatigue, severe leg and joint pain, depression. I just could not function. I know I am extremely sensitive to medication. I decided to come off the Toprol, after only three weeks and go back to Lisinopril 2.5MG. Now, after only two days of not taking Toprol, I truly feel very weird. Far less tired, but extreme dizziness and a kind of spaced out feeling. Is this just the withdrawal from Toprol...and after only three weeks of taking it? Plus, my BP seems to be very low - the lowest I have ever recorded it. 112/55 last night. Does coming off Toprol actually have a reverse effect and plummit your BP until it is out of your system. If so, why has my doctor told me to triple upon the Lisinopril now I am back on that. Dealing with even slightly elevated BP has become such a major issue for me.

rash - mostly on arms. few spots on neck and abdomen,high fever, severe sore throat (thought I had strep), severe joint pain (mostly knees- could barely walk, jaw, elbows, wrist), tingling skin, itchy face and eyes, chills, nausea, depression (crying).

I have had my mirena for almost 6 weeks now - I am still having some bloating, indigestion, and joint pain - all of which my doctor says should not be related to Mirena. Also, moodiness and anxiety -which she said could be due to my post partum state or the fact that I am nursing - so we left it in for now. She said to give it another month or two - UGH - I don't want to give up on it - but it seems that those that have had it removed are feeling much better - please continue to post comments after removal for those of us on the fence about what to do.