Muscle and joint pain symptoms and conditions

THANK YOU SO MUCH FOR THIS SITE! I was beginning to feel that I was getting old too quick. I have been on Lisinopril for about a week and for the past two days I have had such severe muscle and joint pain that it even hurts to type this, it is in my hands, elbows, knees, and feet, and I look like a little old lady going to the store all hunched over and barely able to walk and I'm only 29!!! I don't care what my doctor says I'm quitting this medication today and going back on my old meds. Hopefully this excruciating pain will go away.

Extreme Fatigue, Anxiety, Muscle and Joint Pain, Extreme Hair Loss, Chest Pain, Heart Palpitations, Vision Problems, Vibrating sensation on my insides, Tingling and burning in all extremities.

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 began taking Levaquin for a kidney infection. After the first pill (500mg) I had insomnia, joint pain and a little under the weather. I thought maybe it was a combination of the pill and still having the kidney infection. I figured the infection wasn't gone because the first med, Sulfameth/trimethoprim 800/160 I had a reaction too also. That was prescribed for 10day when I only was 4days into it with that pill. So I went from Friday to Monday without any medications. I felt that the kidney infection was still there because I was still hurting, not as bad as when I went to ER but knew it wasn't gone. So Monday night I started taking the Levaquin. Felt bad after the first pill but after taking the 2nd pill I became very weak, had ringing in my ears, eyes started to swell,had sweats nausea, stomach hurt and became very bloated, neck pain so bad I could hardly turn my neck. Pain running down into my shoulder blades, jaw pain, sore throat, nausea, felt like someone was squeezing muscle in left arm and squeezing muscle on left side of neck Started to have some muscle pain in right calf. Call Dr. on call and he said STOP taking the medicine, take some Benadryl and if gets worse go to the ER. Well, I took some Benadryl which made it seem a little better, but this is the day after and my muscles by my shoulder blades are so sore and have a burning sensation. I still feel somewhat weak but not as bad as last night. Seems I tired out real quick. This medicine made me feel like I was on the way out. I was prescribed it for 7 days and only took it for 2. Now I am very hesitant about taking anything as I have had reactions now to 2 different meds. Still don't know if kidney infection is gone or not. Does anyone know of any natural ways to rid yourself of kidney infection? I would appreciate any advice anyone has. All I know this has been 2weeks of @@@@ since I was diagnosed with this kidney infection.

I was diagnosed with ILC August 2007. I had bilateral mastectomy w/ reconstruction, chemo and started Tamoxifen. Then I had a hysterectomy and I started Aromasin about six months ago. Prior to starting Aromasin I had some muscle and joint pain from Tamoxifen but I could tolerate most days. Three months into Aromasin, I couldn't get out of my car. It literally took me 15 minutes one day and I had to trade cars with my daughter. Naproxen gave me upset stomach, ibuprofen wasn't enough, Tylenol wasn't enough, Hydrocodone kinda helped but makes you feel weird. My doctor decided to take me off of it and i haven't taken anything since. My side effects were: extreme stiffness, better with motion but joint pain was so bad i didn't want to move. I have been documented as having overall generalized weakness as a result. My doctor said Aromasin shouldn't make me feel this way but why is it doing this to everyone else (mostly) too? I am now being evaluated by a rheumatologist for arthritis. My joints still hurt so bad. I gained weight, cant concentrate, can't sleep, can't wear my shoes. my ankles hurt the worst after being on my feet. My ankles, knee joints, hip joints, neck, elbows, wrists, fingers, toes and jaw are all very painful now.
If i would have known all of this, i never would have had my hysterectomy and stayed on Tamoxifen. I can only hope at some point this will get better. I just pray the cancer doesn't come back in the meantime.

I am 72 years old and in 1995 I had an artery blockage and had angioplasty.Upon my release from the hospital I was put on several prescriptions, beta blockers, cholesterol, Aspirin, Vitamins, etc. which I had been taking regularly for 13 years without any problems. In 2008 after having chest pain and going to the hospital my heart doctor advised me I had Atrial Defibrillation and put me on Warfarin and also told me to stop taking all the vitamins I was using along with my daily aspirin dose and one of my prescriptions. Since then I have had constant shoulder and muscle pain in my arm and leg. I have had several treatments by a chiropractor and several physical therapy treatments and the pain has not subsided. My memory has gotten worse also however I thought that was due to my age until I read some of the above side effects of Warfarin. I definitely have a lack of energy and also changed my diet due to the Warfarin. I have informed my heart doctor about the problems and he advised it is not due to the Warfarin. I don't agree with him after reading all the posts, but I am not a doctor. I will continue my prescribed dosage and Pt/Inr tests as schedule for a while, but if my pain etc doesn't get better I will probably do like the lady's posting and stop the warfarin on my own.

I am a 42 year old male. I have been on Lisinopril for two years. I developed sore muscles and joint pain. I was so tired I wanted to sleep all the time. My blood sugar was up. Some one mentioned to me that some blood pressure meds can cause blood sugar to rise. I quit taking the Lisinopril for a day to see what would happen to my sugar. It went down, and then I noticed that my joint pain was gone and, my muscle pain and soreness was gone and I had much more energy. I go see my doctor tomorrow for other options.
The drug made me so tired over the years I could not exercise and I have put on 25 more pounds
side effects
depression, muscle and joint pain, muscle stiffness, tired, weakness, dizzy

Has anyone had the experience of previously taking Levaquin without side effects, then when taking it again, developed severe headaches, joint aches, muscle pain and weakness, etc? I am currently going through this. I've taken Levaquin before probably 2 or 3 times due to upper respiratory problems and not noticed any side effect but this time, I've taken 5 days worth, 3 in hospital 2 as outpatient dose and can hardly move. I had the same experience in 2004 with zithromax. Had taken it without side effects, then suddenly when taking it again developed such bad chest pain, I thought as did my doctor, that I was having heart attack and spent a week in hospital before figuring that one out.

I'm 46 and have been taking Advair for 7 years and I'm amazed at all of the side effects I've noticed of Advair that I've never had before. Asthma aside, I've always been healthy, moderately active and eat healthy yet noticed over the last couple of years I constantly feel like a puff ball from water retention and bloating - it's awful. My eyesight is worse, blurry and dry eyes. Constant muscle and joint pain, occasional dizziness and lightheadness, mood swings, just about everything . I've also noticed a decrease in libido and an increase in blood pressure. Does anyone have experience with a better replacement for it that I can discuss with my physician that does not cause any additional side effects from switching from Advair to a different long-term inhaler?

I am 27, married, and have been on birth control continuously for four years (right before we got married). I have been on Loestrin 24 Fe for five months and just stopped three days ago. I thought there was something wrong with me. Our whole marriage I've had sex drive issues, depression, tiredness, feeling sick all the time, and headaches. All of it got even worse on Loestrin 24. In talking with a co-worker and then doing research a few days ago, it occurred to me that my these problems could be a result of the synthetic hormones I've been taking in the form of birth control. Prior to Loestrin 24, I was on Ortho-Tricyclen, Ortho-Tricyclen Lo, and Yaz. I suffer from endometriosis and have problems with severe cramps and bleeding. My Gyn thought Loestrin 24 would help, with fewer inactive pills. Since taking Loestrin, the side effects mentioned above have gotten worse. In addition, I have had cystic breakouts on my chin and neck, horrible vaginal dryness, fluctuations between nausea and ravenous hunger (I've gained 8 lbs. in five months!), chest pain, muscle and joint pain that gets to be almost unbearable, moodiness, anxiety and paranoia issues, and hot and cold flashes. I think Loestrin 24 should be taken off the market. I've only been off of it for three days and already feel a bit better. My husband and I are now researching natural family planning. No more synthetic hormones for me. Keeping your body's estrogen levels so artificially high all the time is bad news. Not to mention it is a leading cause of breast cancer.

I was on 40 mg of simvastatin for 4 months with seemingly no side effects when my doctor said my cholesterol wasn't coming down quickly enough to suit him, so he added lovaza - had me taking both at the same time. Within 2 months I was noticing sore muscles but didn't relate it to the meds. After about another 2 months I was so bad I could hardly walk - extreme muscle and joint pain over my entire body, severe weakness, shortness of breath. Then I found out that both of those drugs can cause these side effects. I wish I had tied it together sooner. I have been completely off of them both for about 3 months and still have some pain in my feet, shoulders and elbows, along with severe pain in my hands, and I am still weak and short of breath. I don't know how long this is going to hang on, but I certainly hope it isn't permanent. I can't stand to think that I might have to live with this pain for the rest of my life. My hands are so close to useless, and I am so weak, that it's about all I can do to take care of my job and make a living. I haven't been able to work around the house for months. I want to work on my cars (my hobby). I have 2 antique cars that I enjoy working on and driving, but I don't think I'm going to be able to do very much with them this summer. My hands just won't let me. And the beauty of it all? My cholesterol numbers did not come down any great amount. Since I stopped taking the meds I have brought the numbers down by changing my diet - eggbeaters instead of whole eggs, less beef (venison is very low in cholesterol) more chicken & fish, oatmeal, plus I'm taking vitamin C, D3, garlic and cinammon for cholesterol and B complex for muscles, msm and glucosamine for joints. I also bought a hot tub, which helps with the pain and stiffness. This has definitely not been a fun thing. I just hope it goes away some time soon.

I am being treated for ulcertive colitis. I have been on prednisone since Sept of 08. I started out on 40 mg. In late Oct. my doctor started tapering me off 5mg per month. Each month following the tapering date, I would get sick. As I look back, all the signs of withdrawal were there. This Jan. I tapered once again, but the window was only 3 weeks. I hit rock bottom. If there was a symptom, I have it. Nausea, burning in my digestive tract, diarrhea every time I eat, muscle ache, numbness in my legs, swollen feet, sore bones and joints. ( The worst was in my feet. I ended up seeing a podiatrist. He thought plantar faciaitis until I told him about being on prednisone. The small bones in my foot were swelling, The muscles in my calf were buning they were so sore. That was last week. Today my other foot started. I can hardly walk. In addition to that, I am lightheaded, have elevated blood pressure, and fatigue. I also had some vision problems that sent me to the doctor. I went through a ton of testing which all were negative. It seems that pseudotumor is another symptom of withdrawal. I have a history of that. It would have been nice to know that. As I look back each month, I had different muscle and joint pain that lasted about a week. I was put on an acid reducer in Dec. to help my stomach, but in all of this time, I was not told that these all may be withdrawal symptoms. I have been off work for two weeks now in addition to the days I missed each month. My physician is now controlling the tapering procedure. They up the dose to 10 mg again. They plan on weaning me by 1mg doses. This has been a terrible experience for me. I have only been severely sick one other time in my life. This pain is awful. It is chronic. This drug may be beneficial, but it is like poison too. Anyone who takes this should really ask a lot of questions, and be careful..

I started taking synthroid in November and have experienced severe muscle and joint pain. I took myself off of it! I can't wait to see my new endocrinologist on March 3rd. By the way, I haven't taken it for two weeks and I still feel absolutely awful.

Hello I'm a 41 year old female, and I took Lipitor 20 mgs for 6 months about two years ago. When I called my doctor's office to complain about side effects they told me it couldn't be the Lipitor because I had been taking it for a month already, and would have had problems before that. I eventually took myself off of the drug 5 months later. Here are some of the side effects I experienced:
Itchy fingertips, increased blood pressure, 30lb weight gain, shaky hand writing, acne, poor driving skills, poor memory, hair loss, "frozen joints", IBS, incontinence, low grade fever, itchy feet, numb toes, numb hands, foggy brain, joint pain, muscle pain, foot pain, plantar pain, dizzy, jaw pain, back and neck pain, week ankles and wrists, nasal allergies, skin rashes, migraines, heartburn, Increase in Astham, heart palpitations, knee pain, difficulty standing up from sitting position, difficulty climbing stairs, water retention alternating in feet, hands, arms and legs, almost constant taste of bile in my mouth.
These are only the ones I can remember. Two years down the road everything but the muscle and joint pain and weakness is gone. even those have improved a lot. I stopped taking the Lipitor and lost all 30lbs I had gained on it, without dieting, in a months time. I still have two toes on each foot that are partially numb. I have trouble climbing stairs, and getting up from a sitting position. I can do both, but I move slowly while doing them. The pain in my muscles and joints drives me crazy, but I'm grateful that the rest of the symptoms have cleared up. My doctor never believed me about my symptoms, and neither does my new doctor really. Went to the emergency room for asthma that was not responding to my inhaler, and they were about to let me go home when I mentioned to the doctor that I had been on Lipitor. Suddenly a huge battery of tests were ordered including a CT scan and a stress test. When I asked the doctor why he said that they just wanted to be sure that it wasn't something other than asthma. Why did they do that after hearing about the Lipitor? Do they know something? Are there doctors who believe that statins are killing and seriously injuring people? I'm so angry. Even as I sit here typing I know when I stand up I will have massive amounts of pain that I will have to "walk off". My quadriceps have not recovered, and remain ridiculously weak.
If I can stop one other person from going through this I will be happy. Thanks everyone for taking the time to list your symptoms. It makes me feel better to know that someone believes me, and knows what I am going through.

I got my first Lupron shot in Aug and I've had nothing but serious muscle and joint pain and also constant sweating, I'm always hot. I've gained weight, I've also had more anxiety. I'm about to get my 2nd and last shot next week..I'm debating on even getting it....

I'm a 54 year old female prescribed 10 mg zocor(simvastatin) for slightly elevated cholesterol. Took it for 7 months before I clued in to the cause of my many symptoms. Muscle and joint pain, head fog, blurry vision, weight gain, stomach upset, fatigue, etc... The muscle and joint pain were excruciating at times --especially in my left hip...which had gotten so bad I needed a walking stick for support. I felt so darn old wondering if I would even feel normal again.
After reading many postings I decided to stop my zocor(simvastatin) 6 weeks ago and am very happy to report an improvement in many of my complaints...although far from where I want to be.
I am curious as to the withdrawal effects others may have experienced. The first week coming off I had stomach aches and I had awful headaches which thankfully did stop. The stomach aches and touchy digestive system still plague me though. Am I the only one experiencing this?....

I'm a 54y/o female prescribed zocor for slightly elevated cholesterol. Too it for 7 months before I clued in to the cause of my many symptoms. The muscle and joint pain, head fog, blurry vision, weight gain, stomach upset, fatigue, etc... The muscle and joint pain were excruciating at times --especially in my left hip...which had gotten so bad I needed a walking stick for support. Felt like I was 95--and never going to feel normal again!
After reading many postings I decided to stop my zocor 6 weeks ago and am very happy to report an improvement in many of my complaints...although far from where I want to be.
I am curious as to the withdrawal effects others may have experienced. The first week coming off I had stomach aches and I had awful headaches which thankfully did stop. The stomach aches and touchy digestive system still plague me though. Am I the only one experiencing this?....

I have been on Wellbutrin XL for 2 years with no ill side effects and it has worked well. 2 1/2 months ago my script changed to the 'generic' BudeprionXL. Since this change, I have been experiencing severe muscle and joint pain, my hands go numb, my skin crawls to the point that I have scratched myself to the point of bleeding. Sleeplessness has just recently started to occur and my teeth have also become very sensitive. General irritability has also set in. I have not yet started to get the headaches most get with the Budeprion and it a good thing as I'm already taking 1600 mg a day of Advil to try and arrest the muscle and joint pain. After reading these other ill effects of this drug I'm now very scared and will be calling my doctor to get her to represcribe Wellbutrin -only- 'no generic'. It is clear to me the FDA did not do the proper research or makes me think TEVA has a friend in the FDA's office.

I started simvastin on Aug 11. Lately I got severe lower back ache every time I get up in the middle of the night and every morning but the lower back ache goes away as I starts my day after 1 hour. I am also experience short memory loss.
Pls advice if this is a serious side effect of the drug.
Thanks....hw

My wife has been ill and was recently diagnosed with a sinus infection, upper respiratory infection, and middle ear infection. She was prescribed Avelox, along with a combination of corticosteroids, a NSAID, and another medication.

Today was her third day, and LAST day of taking Avelox. The adverse reactions began yesterday when she began complaining of body aches and dry mouth. After waking this morning, she found that her entire neck was swollen, stiff, and sore to touch. We believed that this problem was probably glandular, caused by the sinus drainage, and we expected it to subside through the day.

As the day went on, she began to feel fatigued and the soreness continued to increase, escalating to tenderness and a physical pain response to touching her neck.

She took her third dose of Avelox at 9 p.m. and the reactions escalated from that point. Within an hour she felt her lips began to tingle with a numbing sensation, and believed that her tongue was swelling. She also began to feel the soreness and pain spread across her body, extending to her abdomen, arms, and legs.

Luckily, I have a significant amount of medical and emergency response training based on my career, and was previously a pharmacy technician. On top of that, I'm blessed with a father who is a DoctorPh. and has spent over 20 years in hospital pharmacy. I recognized the signs of these reactions and called my dad. We agreed that the Avelox was the problem and gave my wife 50mg of Benadryl.

It is now 1:40 a.m., and the effects are still ongoing, however they appear to be subsiding. In total, my wife experienced: muscle and joint pain, stiffness, numbness and tingling of the entire body, swelling of the tongue and neck, gastrointestinal pain, nausea, body chills including uncontrollable chattering of the teeth, an epidermal pain response to any physical stimulus (even the slightest touch), and also another reaction that I have not seen listed anywhere else -- her entire lyphatic system seems swollen and tender. You can actually feel the swollen nodes across her body (neck, arms, legs, etc.).

I am very thankful to have found this sight. I am sorry that so many people have experienced similar effects, however their stories have assisted me and my wife extremely. Our physicians office will definitely be receiving a complete and detailed account of the experience with this drug. Thank you again!

In December of 2006 i was taken from school to the emergency room for sever menstrual contractions. It was the first time i had ever experienced that kind of pain during my period. Literally it felt like i was going to have a baby.
My doctor put me on Loestrin and it worked beautifully. My periods stopped completely after 2 months. I had no symptoms at all, no side effects either. Now that i have been on it for almost 2 years my periods are coming back (only lasting about 3 days), my cramps are returning, ive developed muscle and joint pain, my lower back stiffens up making it difficult to stand or walk for more than 15 minutes, i get dizzy easily, and now ive developed brown spots on my back near my shoulders. if any one else has these spots please let me know so don't think im crazy. My doctor says i have a fungal infection but iv had it for 6months now. IDK!!

I was prescribed Levaquin by my Dr. for a sinus infection. There were 10 pills and I was to take one a day. No one mentioned any of the side effects or drug interactions except to not take antacids within 2 hours of taking the meds. During the coarse of me taking the medication I began having substernal chest pains which I thought was just horrible heart burn, but it got so bad that I woke up screaming multiple nights from the pain. I also started having pain in my ankles, legs and especially my knees. The pain in my knees gets so bad that I think my knee caps are going to shatter when I walk especially when going down the stairs. I didn't know any of the drug interactions and my father in law who is a physical therapist has always advised me to take ibuprofen for muscle and joint pain so that's what I did, but little did I know that was only increasing the effects on my central nervous system. I am also experiencing bouts of nausea, confusion, light headedness, difficulty sleeping, anxiety and I actually thought I was having a mental breakdown.. I was freaking out on my husband and very depressed even having suicidal thoughts. It wasn't until my mother randomly mentioned that she had heard about the FDA issuing the Black Box warning that I connected the dots and had already finished the meds. I called my doctor's office right away and was told that the symptoms I am having are not side effects of the medicine. Maybe the Dr. doesn't listen to the news either.

In response to Wewe's post, I've been wondering the same thing. Since taking my daughter off Singular almost 2 months ago, I'm seeing a different almost typical kid. Four years ago about 2 months after starting Singular my daughter was diagnosed with anxiety. As her condition got worse she was diagnosed with depression. We started to see OCD and tics so they were added as a diagnosis It was determined that it was related to strep infections so she was diagnosed with PANDAS. She was started on Zoloft and klonidine. The Zoloft made her worse. Her fears of hurting herself got so intrusive she was hospitalized. Her cholesterol was high too. The Zoloft was discontinued and Prozac was started. She's had therapy all 4 years. She also neede physical therapy due to muscle and joint pain. Now she's doing better, off Singular. Does she really have PANDAS, OCD? I don't know. She's still on Prozac, we just did a slight decrease this week. Is this medication the trigger for underlying conditions. Learned behaviors can be unlearned, but are there lasting physical effects? If a gene has been turned on, can it be turned off? I wish we knew the answers to help all of our kids.

taking lisinopril -2 yrs. tues. 6/2/08 - started feeling like the flu. by wed. was so sore in places i had never had muscle and joint pain, all i could do is lay...by wed evening was feeling a little better so, ok it's the flu. took med to go to bed and had one of the most miserable nights ever...what i call severe neck and left arm pain. could not raise or put weight on my rt. hip,leg, knee or foot (those were just the worse spots). by the by been i have been having very poor sleep about 4 months. managed thru thurs, by fri i was convinced it was lyme. saw physician...of course all blood was normal. on sat. 6/7 i kept thinking it was the lisinopril because i would start feeling better (not over the pain, just better) in the evenings and then be right back in severe pain by 2 am.

Just an update about the class action suit discussed previously, and Aamaya had provided us with the Florida attorney, Justin Wikin: I got a letter in the mail yesterday stating that they would not be pursuing suit against them. They said that they deal mainly with wrongful death cases and it does not mean that the case does not have merit, just that it is not their specialty. I will be doing some research here locally in Ohio to see if I can locate a practice to pursue this. If anyone comes up with something, please let us all know.