Joint pain symptoms and conditions

I'm currently taking Doxycyline for my Varicocele and so far I have been feeling very nauseated haven't been as hungry and I have anxiety in my stomach and I also feel shaky and nervous sometimes.. it is discomforting.Also I have been experiencing joint pain and an overall body ache.

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 am 50, pretty healthy, but have had a new condition of inflamed and severely painful joints and muscles limiting activity. Doc put me on 60 mg prednisone for 3 days, then 40 mg 3 days and 20 mg 3 days. First day was ok. Since then I have been a raving lunatic! I read the post about the person chasing their cat around and had to laugh and relate. I flipped off the neighbors workers because they were backing up a truck and it was noisy! It is all I can do to keep myself in check. I have canceled/rescheduled all unnecessary appointments until next week when I am finished. I "sleep" about 3 hours a night. Last night I peed the bed. I eat constantly. I have to work and concentrate (teach college) and that is so hard. I imagine my students must think I am on meth. I can't take it any more. I have 1 day left and I am not going to take the last one. I hope that this regimen will have calmed down the inflammation and if it recurs I will seek alternatives. AM NEVER going back to prednisone unless it is life or death situation.
Good luck to all those out there who have to take it long-term. Bless your hearts.

I am a 27 year old female and I have stage 4 endo and have had lots of rupturing ovarian cysts. The laporoscopy was pretty ineffective for me and I tried birth control and had severe vaginal bleeding during intercourse. So my doctor wanted to do 3 months of Lupron Depot and add back therapy with Premarin.
I have only had one shot of Lupron and that was on 10/16/09. I noticed side effects with in 24 hours. I had severe joint pain especially noticed in the right hip ( I was injected in my right side) severe migraines, awful mood swings, short term memory loss and that was all in my first week on the shot. I started feeling better like 10 days after the shot, but that was only short lived. Now even after three weeks into the shot, I am in so much pain in my joints, it is difficult to take care of my two toddler boys and my home. I now have a crazy rash on my butt, and still have so much pain in my body as well as feeling numb in my toes, left arm, and fingers. This drug appears to be more ineffective than effective and I feel like women need to explore other options before going down this unknown path. I found out through research on the internet that the Premarin that I was taking as an add-back is made from PREGNANT HORSE URINE and that the horses are treated like crap so everyone can get rich off them. There has to be other options for people that have already gone through the nightmare of endometriosis. I would take endo over these side effects any day.

Please help me I already post my side effects that after taking that med for 7 months I start having a joint pain ,my all body hurts I have no energy left ,I have stopped taking doxy from last one week but I m not recover .does anyone know how I will get normal I m continuously taking Motrin 800 mg for my pain but I'm worried how long I can be on Motrin but if I don't take Motrin I cannot even walk ,does anyone think arthritis but my blood work was negative ...plz help me

I am happy that I have come across this website. My son was born in July 2nd, 2009 and I had the Mirena IUD inserted on August 24th, 2009. The insertion wasn't all that painful, but the cramps that followed were. It lasted for approximately 2 weeks following and I had some spotting here and there. I have had serious cramping on my right side and after sexual intercourse, I always bleed and cramp on my right side. I have complained about my right wrist hurting bad and my thumb seemingly being dislocated. After reading these post I see that I could possibly have joint pain as a side effect. I can honestly say that the joint pain didn't start until after the Mirena insertion but I never associated it with that.

I thought that I'd love the Mirena because I wouldn't have to worry with pills or having to remember to take birth control, but the side effects are not worth it. I have also had some weight gain. Serious mood swings. Depressed moods and very emotional. Ive been short tempered about just minor things and I haven't been motivated to do much of anything around the house.

I'm debating on whether or not I should have the Mirena removed. I'd hate for any of my symptoms to get worse.

I took Zocor for 25 days when I suddenly had such pain at night in my upper arms that I couldn't raise my arms up at all. It's been 2 full weeks since I stopped taking Zocor, and every single night around 7 I develop severe pain somewhere in my body, usually in my hands, knees or feet. It's in a different place almost every night. Tonight it's in my left hand across the whole top of my hand, below the wrist. Can Zocor cause this kind of pain so long after stopping taking it? And I only took it for 25 days! Please help - this really hurts and I hope it will improve.

Joint pain in fingers, joint pain in knuckles, wrist weakness after a week on 10 mg daily dose of Zetia. Amazing reduction in bad cholesterol and triglycerides when used with daily maximum 80 mg dose. Zetia was discontinued because of these painful side effects. 68 year old male.

I am a 48 year old female with a-fib. I am not overweight...just started falling apart since now I am menopausal. I've been on Warfarin for 6 weeks. My INR has hardly moved. I'm now on 8 mg and have my INR test on Monday. I started at a 0.9. Now I'm at 1.20 and have been there for three weeks in spite of upping the warfarin. I've not changed my diet except to exclude greens and green tea when I began the therapy. Everything else is consistent.
I just started exercising again a week ago. Something I haven't done in five years since I lost my sister. I bought a Total Gym and enjoy it. It has helped me get some energy back, has helped alleviate some of the mental fog, and has lowered the incidence of anxiety attacks. (I've been getting anxiety lately...since the mental fog and memory lapses...that bothers me since I love to read and write and the mental fog seems to be taking the joy out of it now.) The reason I decided to start strength training again is because of the joint pain I have been experiencing lately. I didn't have it before warfarin. I do now. Only one joint, though. The strength training does help, but every once in awhile, that sharp pain comes back to visit. It's just a little less now.
I plan to tell the doctor that I have begun strength training again. Not just because it's good for me and my heart, but it seems to help with the side effects of menopause and warfarin...without adding another drug like an antidepressant.
Warfarin...I believe is a life saving drug. BUT, I have to do my part too.

BTW, if I didn't have triple thick hair, I would complain about hair loss. Right now, it's a non issue for me. Just saves money at the hair dresser.

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.

I'm partial to Mirena. I had it for all 5 years, but still debate as to whether my weight gain, hair loss and joint pain were related. I got it shortly before my boyfriend of 2 years broke up with me, starting drinking a bit more and was in general stressed out. So stress & alcohol equals weight gain. Weight gain (30 lbs in a year) equals joint pain. The hair loss is another story. It might be stress, but I went long periods afterward without stress and I could pull out rat size clumps of hair once every few weeks from my shower drain. I had it removed on October 6th 2009. I immediately started NuvaRing. 3 weeks later, I'm DONE with that. That's another story. Overall, though, I don't think the majority of the side effects were caused by Mirena and the 5 years I had it in were good. I won't get another one, just because I'm still skeptical. I think I'm going to take some time off birth control with hormones. We'll see how it goes. I can't say I'd recommend Mirena due to all of the horror stories I've read. Maybe in a year, if all my symptoms go away, I won't be so wishy washy.

I'M SO GLAD THAT I FOUND THIS WEB SITE BECAUSE I JUST DIDN'T KNOW WHAT WAS WRONG WITH ME. I THOUGHT I WAS JUST FALLING A PART. I HAVE HAD THE MIRENA FOR 14 MONTHS AND I HAD HEAVY BLEEDING FOR THE FIRST 8 MONTHS AND THAT ENDED. I HAVE SEVERE HEADACHES, INSOMNIA, DEPRESSION AND NUMBNESS AND TINGLING IN MY FEET. SOME MORNINGS I WAKE UP AND IT'S LIKE I CAN'T GET OUT THE BED BECAUSE I HAVE JOINT PAIN. I'M ONLY 38 YR OLD. I HAVE NEVER HAD ANY OF THESE PROBLEMS BEFORE THE MIRENA. ONE LAST THING I HAVE ALSO LOST THE DESIRE FOR SEX! IT'S GONE. I'M IN THE PROCESSING OF TRYING TO GET THIS THING OUT OF ME. ASAP . LADIES THINK TWICE BEFORE YOU GET THE MIRENA.

well im so glad i found your site. i thought it was just me. the headache every single day. the strange cramps for no reason. the joint pain. the unexplained mood swings. im getting this thing out of me asap

I had that Kenalog and it's been a total nightmare...My doctor Dermatologist injected into my two index fingers on each hand. The itching has been insurmountable and absolutely horrible....I haven't been able to sleep, wash dishes, do anything with my hands....I am telling you I am about to go out of my mind. I went back to her..and now she put me on Prednisone and Singular...now I am reading the side effects of Singular. She never told me what type of shot she was giving me for the pains in my hands that i was getting. I have had cortisone shots for joint pain before...for I figured that what it was that she was giving me...later to find out it was this damn Kenalog. I would have never agreed to such a thing until I had looked up the side effects. This has been a night mare completely...

The itching is so bad, that I have broken the skin, I have a rash completely on both fingers. It so sad...and she's charged me a fortune for it too, and the second time I had to come back for help. What the hell is wrong with people..?

DON'T TAKE THIS DRUG...UNLESS YOU DO CAREFUL CONSIDERATION..!!!PLEASE

I am so glad I am not crazy and all alone. I've had my Mirena since January for perimenopause and was still getting my period every month until this month. No I have such cramping, joint pain I can barely walk and my lower back is killing me. I am scheduled for a hysterectomy this Wednesday, I CAN'T WAIT, I'll be done forever.

Has anyone had terrible joint pain from the Mirena? I didn't know where it was coming from, every time i would sit down for awhile then get up my joint ached so bad, i had never noticed this before, i told my doctor about it and he said i was just starting to feel the effects of getting older, i couldn't believe that, i am 38 years old and already being this stiff, i told him that i would not be able to move around by the time i was 50 if i felt like this already...and i was going to the gym at least 3 to 4 times a week so i was getting a lot of exercise, well i had my Mirena taking out about 3 weeks ago, mainly because my blood pressure kept going up and i had never had problems with this, so i thought maybe it was from the Mirena since i wasn't on anything else and i ate right and exercised, well i happen to notice the other day that i no longer have the joint pain i was having, i couldn't believe it, it had to of been from the Mirena, i feel so much better now, my sex life is back to normal and my blood pressure is staying down without medications, please don't listen to the doctors when they say its not the Mirena, we know our bodies more than anyone.

Hello Friends, it's been a week after i finished my 21 day Doxy treatment for lyme, Im still feel lot of fatigue and joint pain, i went to see my doctor yesterday, he explained the fatigue is a normal side effect after finishing the treatment. I feel so weak headache and migraines. The doctor told me to take pro-biotics and vitamins to recover faster i just started taking the pro-biotics today so i have to wait how it goes. the dizziness, migraines and fatigue doctor said it's a normal symptom of Doxy,, I hope these side effects will go away soon. if anyone has the same side effects after the treatment please write me.
Drink a lot of water.

thanks for sharing your stories,, we are not alone here.

Hello, this is E. again. My son took a nap, so I was able to read a lot of the posts. Many things that occurred to me over time were things that I thought came with the change of life of being married and having a child. Just life, in general also. But, now that I think of who I was before motherhood and being a wife, it just doesn't add up. I believe now the additional things that were happening to me were indeed extra side effects of the pill. They include, no sex drive, weight gain, migraines/headaches, fatigue/tired, joint pain, anxiety, depression, panic attacks, insomnia, nausea, and stress. I have been hospitalized and have had certain procedures done for some of these symptoms. Today I am stopping the pill due to the reasons of my previous post. Within time I will let you all know if there have been any improvements. Take care, E.

sorry forget to mention. any recovery from Lyme disease?

I have stopped taking lisinopril now for about 2 months. My sinus problems are 99% gone, but my joint pain has worsen. Can anyone tell me how long the joint pain will last?

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

Within 5 hours of first dose, I had "severe body aches" like those with the flu. My joints and muscles hurt so much that night that I had to call my parents to help me take care of my kids the next morning. I told the doctor who prescribed it, and he said to try to stick it out for the week...what horrible advice! Thinking it was crazy advice, I reluctantly took doses 2, 3, and 4 and experienced the joint/muscle pain each time, but I guess I just somehow tolerated it as if I had the flu. My hands became rather puffy as well. After the 5th pill, I woke up in the middle of the night with HORRIBLE joint and muscle pain, which was so awful that I could barely move; I was able to move a little bit, with extreme pain all over my body--particularly my knees, wrists/hands/thumbs, feet, and shoulders. I felt and heard unnusual snapping, cracking, and popping all over my body when I would move around at all. I stopped the med immediately, and noticed some improvement over the next several days. It has since been 9 days since the last dose, and I still have considerable pain in my knee, my thumbs/wrists, and arms. Unable to do my regular exercise, I tried gentle swimming and light water aerobics several days ago, but found even that to be too painful to do. I'm still unable to pick up my young children, drive without pain (mostly in right knee and muscles connecting to it, when pushing the brake) and am still somewhat limited in typical daily activities. Also, for the last 5 days or so, I've had a strange nodule present on a tendon in my thumb which has been hurting since taking the antibiotic. This has been a very frightening experience, to say the least.

Hello friends, thanks for posting all this information about Doxy and Lyme disease that makes me feel I’m not alone here, I finished my 21 day treatment for Lyme disease yesterday, but after completed the treatment I feel so weak, tired and little dizzy I have not energy left, I m wonder it’s part of the side effects, and still in my system. I hope these symptoms go away soon and be normal again. The joint pain seems to get little better or maybe it’s too soon to tell.
Has anyone gone through all these? Thank you friends and we are not alone out there…

All i can say is WOW! i am so happy i found this website..
I too have suffered side effects and till this day am suffering from Levaquin.
In Feb of 08 i was diagnosed with Prostatitis and was given a 14 day dose of Levaquin. Hours after the first dose i started experiencing pain in my lower extremities,me thinking it was caused by the prostatitis i continued the doses.By the second dose i was in absolute pain in basically all my insides and started having this metal taste in my mouth.Not ever being allergic to any type of medicine i continued the doses only getting sicker and worse.By like the 6th pill i was having anxiety,insomnia,hallucinations,nightmares whenever i was able to close my eyes,partial psychosis,rashes on my face that would get bright red then go away and the skin would peel off.I would be so thirsty water couldn't quench it,suicidal thoughts.I developed a pain in my left calf and behind my left arm in the tricep that till this day bother me.Joint pain,ringing in my ears,excruciating headaches like someone was jabbing a knife in my head,lost 30lbs cause of the colitis it caused,neuropathy,and so much more,it was a total nightmare.
I went in for discomfort of my prostate and doctors couldn't understand why all the other symptoms only a week later,they were completely clueless and told me i was making this stuff up cause i was having an anxiety attack.. I was a perfectly healthy 33yr old before levaquin. The doctors sent me for test after test from HIV to LUPUS only to tell me its all in my head,that i was a healthy man to move on with my life.I would try to sleep and have all these terrible thoughts and would swear i slept for 3 hrs only to see that 20 minutes have gone by,i was gentle to the touch.My family had no clue,they thought i was going nuts.I was pretty bad for months after,the effects started going away little by little,i was back 50% to myself by like June of 08.Since,i still have the pain in my left calf from time to time,tremors,joint pain..I have since joined the gym and have been taking supplements that have helped a lot with my joint pains.
This stuff is poison and should be taken off the market..

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.