Joint pains symptoms and conditions

I am 56 years old and I was put on Lisonpril about three months ago.

We had just moved to a different town with a new doctor. The reason I went to the doctors was that I had a bicycle accident where I went over the handle bars (front brakes locked up on me). I was also due for a periodic check up. I was sore from my bike accident (jammed my LH wrist, RH elbow, both shoulders and knees). The doctor had no x-ray machines so he sent me to the urgent care, nothing was broken. My doctor said that I would be sore for awhile and gave me some Vicaden pain medicine.

Due my periodic exam the doctor suggested that I go on Lisopril because I am a diabetic, even though my blood pressure is OK. He said that he actually takes it because of the preventive nature of the drug.

Well, as the weeks went on I continued to have aches and pains in my joints (wrist, elbow, shoulders and shoulders), wch I thought was from my bike accident. I also play seniors softball which is not a very agressive sport. Well I've had a pulled hamstrin and archilles tendon pull during playing. Thought this was normal but these injuries continued to plague me.

At nights sleeping my shoulders & neck would ach. My knees would shoot pains. My ankles constaintly ache, day & night.

A friend of mine told me about taking black cherry juice for joint pains, maybe from gout. After taking this black cherry juice it seemed to help, but still not normal.

Today I stopped at our local taven to have a berr and talk softball with the guys. I broke out in a heavy cold sweat and almost pasted out, lightheaded. I thought I was having a heart attack or something. Being very concerned I told my wife who is an RN. She read the side effects of Lisonpril and it clicked. This web site helped me figure it out also.

I am taking myself off Lisonpril today and expect improvement and my life back. I thought all this was from my accident and getting older. I am excited to see the results, which I feel very positive about.

ive been on mirena since march 2008. at first i thought this was the best birth control product out there. however for over two years i have been riddled with allergies, sinus infections, upper respiratory tract infections, tiredness, headaches, joint pains, muscle aches, gastric and bowel problems, cyst like acne, mood swings tachycardia (rapid heart rate), anxiety. at first i thought all these were related to getting older (im 29) and work related stress so i wrote it off. but being a person who has never been sick in my life to all of a sudden being sick once a month is crazy. this has been the only thing i could think of that i could think the problem is. i hate to remove the iud because it is so convenient but i am sick of being sick. the doctors dont tell you of the not so obvious side effects like these. i just hope that no permanent damage has occurred.

I have had two shots of Lupron, as a result I've gained almost 30lbs, had very bad joint pains and little hot flashes. I also experienced hair loss and became moody at times. However, my doctor did warn me that I would gain weight as a result of the shot and that I may experience hot flashes. December 2009 will make one year since my first shot the second shot was in April and I"m just beginning to feel normal again. It is now November 2009

It has been interesting for me to read this posts. I have been wondering about the long term side affects to singulair- mostly because my 11 year old has been on Singulair for several years now. We spent many of nights in the ER for asthma when he was little and no Dr. did testing. When he was 5 his pediatrician tested him for allergies and put him on Singulair. We have had a great experience with it. I find it interesting that many of the health issues on here- joint pains, bouts of depression, weight gain...I personally experience all of them and i am not on any medication. My 11 year old does not experience any of the mentioned side affects. I wanted to find out long term side affects for my own personal knowledge. Prior to Singulair, he was on Zyrtec which was not a good fit.

ive had the marina in for 5 years now and ive suffered mood swings joint pains headaches spots i itch all over like something is crawling all over me sweating crying my hair don't grow any more but ive got this huge belly on me i look pregnant but my boobs have shrunk i wont it out ive heard its very painful to get out and my doctor has refused to take it out ive had 4 mini strokes since having the dam thing in panic attacks sacred to even go out my house plz tell me im not going nuts

This is not a first-hand experience, yet I would like to share the side-effects occured to my Mom. She was having high blood sugar levels for some time,
The Doc' insisted on Jenuvia though expensive and he said that since it is
produced naturally(from human body itself), there are no known side-effects.
Well I searched for Jenuvia side-effects because my Mom was complaining about increased heart rates, head aches and after going through the experiences on this page, well her joint-pains too can be attributed to Jenuvia.
India is not cautious of the usage of medicines, lack of monitoring authorities,Medics going for quick relief and perks on costly medicines from
Pharma Giants.. and to add a huge diabetic population in need of help..
It could adversely affect lives of millions.

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.

I am a diabetic for 10 years and I am januvia for 2 years, now I have developed joint pains in my fingers of both the hands. Does any one has similar side effect from this medicine?

I took levaquin (750) for a bronchial infection about 9 months ago. My doctor gave me individual samples with no info. on any side effects. Like most people, I trusted my doctor and took the pills without question. The aftermath has been a complete nightmare as I have suffered severe joint pain, depression and an atypical anxiety that at times that feels like a drug induced brain fog. I've seen numerous specialist searching for an underlying process causing the symptoms but nothing is ever found. Since the beginning I've contended that the Levaquin was at the root of my problem, but no doctor has ever given that thought any consideration. Prior to the Levaquin I was perfectly fine with no history of any joint pains or mood disorders. Does anyone have any ideas on how to reverse or heal the process?

I took levaquin for an ear and sinus infection in 2007. On my last 500mg pill, I had such a cramp I could not walk. Since then I have had severe food allergies, severe muscle and joint pains,kidney problems and rheumatoid factor is real high. Before taking this drug I have never any joint pains, or kidney problems. I was recently diagnosed with aggressive Rheumatoid Arthritis. It has been 2 years since I took Levaquin, but the side effects weakened my body and did a number on me.

I have been on Prednisone 40mg x 5 days and am now reducing to 30mg x 5 days followed by a 10mg reduction q 5 days until I am off the med. I have read your blogs and my heart goes out to you all.

Has anyone lost their sense of taste? I can only taste salty things, but just the salt only. I have the nausea, stomach pains, depression, mood swings, inability to focus and a tremendous amount of 'floaters' in my eyes. In general, I am extremely drug sensitive, but the Prednisone has brought me to a place I don't want to be.

I welcome your input on the sense of taste issue. Thanks in advance for your comments.

Wow, I'm so glad I found this site!
I was diagnosed with pleurisy 2 and a half weeks ago following a virus, a few weeks before, so naturally, as my asthma nurse has always told me, I've doubled up my Advair (or Seretide as it's called here in the UK!) for that entire time.
Previously I was taking one puff once a day in an evening which I never had any problems or side effects with, it just controlled my asthma really well. Now I'm taking 2 puffs twice a day (morning and night) and for a few days now I've been having terrible joint pains in my hands, feet, elbows and knees. Have been searching the internet for what it could be and think I might have found the answer! Hopefully if I decrease my meds back down the pain will improve!
Like a lot of people on here, though, I was NEVER told about any potential side effects to Seretide, just that it was a wonder drug.

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

I was prescribed Bactrim DS to treat an ORSA Staph infection following some vein surgery in my right leg. The original prescription was 1 pill 2xday with a refill after 7 days if needed. Since the infection did not seem to be responding very well and I had not developed any side effects (at day 7) I told my Dr. I was going to refill it. I continued to take it another 4-5 days when I then developed bumps and a slight rash on both of my lower legs. I went to the Dr. (my primary physician - not the vascular surgeon - who had originally prescribed the Bactrim) and was told it didn't "appear" to be an allergic reaction to the medication since it wasn't on my torso. Within two days the rash had intensified and spread all over my legs. Then within another 3 days it spread to my arms. The itching is relentless and varies between raw, searing, burning pain and plain old itch. Last night I cried myself to sleep for lack of any way to relieve it. The newest side effects are nagging pain in my right knee ( I've never had any joint pains before) and a feeling of tightness in my chest. I'll be calling my Dr. back tomorrow, if only to find out just how long I can expect this joy to last.

I will never, ever, take Bactrim or any related medications again.

Someday, some genius research scientist will invent a test to determine an individual's tolerance to this drug - BEFORE they take it and develop side effects.

I had my mirena inserted one year ago, july 7th, 2008. I had it removed July 6th 2009 and I thank god that I did. This past year has been a blur. Headaches, weight gain of nearly 20lbs, acne, especially on my chin, greasy hair, puffy bloatedness, constipation, sudden fits of anger, back aches, lower back aches, lethargic, no energy, full body and joint pains and aches insomnia, bad dream, moodiness, depression, extremely sore breasts. ALL since I had this introduced into my body. I am hoping that things will improve. So far this past week I feel a tad better but still have no energy and, of course, the weight hasn't fallen off, but I am hoping that PUFFY look goes away as I continue to eat properly and exercise daily. I will keep you posted as to how I am feeling, week to week.

I am 50 years old. Two years ago was diagnosed with very high LDL and low HDL. I told my doctor then that I did not want to go on statin drugs, but 3 months of Niaspan didn't help the cholesterol, and I hated the hot flashes and flushing that could come at any time after taking a dose. So my doc put my on Zocor.

Two years later I my bad cholesterol is within normal limits but my good cholesterol is still too low, even with fish oil and borage oil taken regularly. Almost immediately after starting the Zocor I started experiencing light-headedness and dizziness that would last for up to a minute--even lying down in bed! My doctor prescribed Meclizine for the dizzy spells--more stinking drugs! I get migraines at least twice a month. For the last six months now I have been experiencing increasing muscle pain, joint pains in the knees, elbows and fingers, and now have been having stabbing pains in lower back around the kidneys. I would wake up in the middle of the night with shooting pains and stiffness in my left knee and cramps in my calf muscles. The first joint of my middle finger had become extremely soar so that I could not make a fist or grip tightly. I have had a recurring stabbing pain in my chest under the left pectorals muscle. My feet and toes are soar--especially my left foot. When I exercise even the slightest or do some long walking or outside work, my muscles in the arms and legs get very soar and tender, then stiffen up. I had to see a massage therapist to loosen up my legs last week! Six months ago I would be up at the crack of dawn, ready to start my day, but recently I have become very lethargic and tired with little zeal for any physical activity. I have had intermittent pain in my left testicle. We recently moved and I started seeing a different doctor. After a physical exam, he brushes off these symptoms.

Well, I stopped taking the Zocor a week ago, and already my fingers are much better, although my knees and elbows are still soar. The dizziness has gotten worse but I'm hoping that after my body re-adjusts and flushes the simvistatin that that will subside, too. I have drastically changed my diet to drop 15 to 20 pounds and lower the cholesterol with better eating habits and swimming exercise; hopefully that will help alleviate the pain, too.

I am a 48 year old woman, 5'1" (now 145 pounds). I had Mirena inserted almost exactly 5 years ago, and am scheduled to have it removed in 2 weeks. I gained 25 pounds over the course of the last three years; prior to that, my maximum weight for my whole (non pregnant) life was 123 (I was at 120 when Mirena was inserted, four years after the birth of my second child). I have always been very healthy, never abnormal blood tests except during my two pregnancies was tested as pre-gestational diabetic and had to watch my carbs.

I never put it together with Mirena until just recently, when I started doing research on hypothyroidism after a friend told me that my symptoms could be due to that problem. Depression, hair loss, acne on my back, and the terrible weight gain. I went to see my G.P. who referred me for blood work. I hoped to see evidence of low thyroid function (actual TSH value, 3.12 -- I was told this is normal on a range of .4 to 4.5). I also discovered that I now have high cholesterol (269 triglycerides, 251 total cholesterol, 46 HDL, and 151 LDL). My fasting (14 hours) glucose # is 99 (I was told this is normal on a range of 65-99 mg/dL), and my vitamin D, 25-OH is 21 (also was told this is still normal but low on a range of 20-100 ng/mL). I tried to give blood six months ago, and was turned down because of anemia, so I've been eating a lot of spinach, greens, and more red meat than I normally would, so I was interested to see if I am still anemic -- the red blood cell count is 3.8 (told it was normal on a range of 3.8-5.1 mill/uL). I mention these specific results because although I was told they were normal (except for cholesterol), when I physically went to the doctor's office and requested a copy of the results and did some research online I see that my thyroid IS actually low-functioning -- according to guidelines revised six years ago, anything over 3.0 is considered hypothyroid and should be treated. Plus, isn't a fasting glucose of 99 pretty high? Yet my doctor's only suggestion: diet and exercise. Good grief, I've been on a diet since I had my first child, 13 years ago. True, I don't exercise regularly (I'm a teacher and mom of 2; I never seem to have the me time.) I guess I have an excuse to get a gym membership now.

Also, for the last year I've had increasing pain in my shoulder (I couldn't lay on my side, for example, and lately I can't reach behind me or over my head). An x-ray turned up mild bone degeneration, but not enough to cause the pain I've been having. I was referred to an orthopedist, who today diagnosed a shoulder rotator cuff injury (I've had no injury; he says it is a common degenerative complaint in the over-40 crowd). He gave me a cortisone injection and I'll be on PT for a while to see if the pain goes away. If not, I'll have to have an MRI and surgery to correct the tear.

I'm posting all of this in case it might be useful to someone out there who might be going through the same thing. I had a thyroid test done about six years ago at my OB/GYN, and it was normal then (though I don't have the number; I'll get it in 2 weeks at the OB/GYN). It will be interesting to learn whether my thyroid level has gone up since Mirena. Also, although my research suggests that the effects of these synthetic hormones do not wear off for some time, possibly even years, I will finally feel like there may be hope if my symptoms improve over the next few months when Mirena is gone. If so, I will share it with you.

If you are reading this, perhaps you have a similar story. I wish I had been more aggressive about checking out the possible causes of my many symptoms, but I let them go for years because, I guess, I just figured I'm a healthy woman who is no longer young. (Oh, one more thing: for the first year or even two years that I had Mirena, I had incredibly heavy periods. The blood flow was similar to that during the day or two after the vaginal births of my daughters. Don't know if that's significant, but it took a couple of years for my periods to get fairly normal on Mirena.)

Has anyone had side effects pop up after 3 years? Yes, you heard me. Three years. Hair falling out. Joint pain. "Foggy headedness." Chest discomfort. Gotta be that. Please share.

Sorry to post again, but NO ONE REPLIED TO MY POST!

I am 5 days post removal and need reassurance. Unlike everyone else, I have NOT felt better right away. I am just as tired (if not more), more irritable, and JUST GOT ACNE on my face and arms 2 days AFTER removal! I'm still dizzy and the brain fog is just as bad. Have not bled a drop at all.

I know everyone is different, but my removal experience has been completely different... don't feel better, no bleeding/clots, no immediate improvement. IS SOMETHING WRONG WITH ME??? Was it not the Mirena after all???

My Mom was prescribed Levofloxacin ( AKA Levaquin) by her retarded doc for a mild cold and a sore throat.
After taking 2 tablets of 500mg each my mom is down is severe pain all over her body! she has joint pains, neck pain, arms, palms shes got severe pain all over her body!
She also has severe itching on the palms and her arms as well..
Headaches,
Things aren't looking good.

She in real pain! She tells me she just wants the pain to stop and that she was better off with the cold and sore throat.

She has stopped taking Levaquin.

Anyone got anyway to help her? something?? She is asleep now but tmr Im going to ask her to drink some kefir..

Thanks

hi everyone

i just thought i'd post about mirena post removal. i had mine removed 8 weeks ago after 6 months of unbearable side effects. i am now finding they are all fading away. the joint pains i was having in my hips knees and wrists was horrendous, so much so i was being tested for lupus and arthritis, my muscles were also tender and easily fatigued. these symptoms have slowly diminished and are now almost gone completely.

i had terrible gallbladder type pain but on both sides under my ribs, also now gone

i had headaches, now gone

i was impossible to live with because of my mood swings and irritability, now gone, just a bit more pms'y than i would have been prior to the mirena

constant bleeding and gross sludgy discharge, now gone

bacterial vaginosis, gone

unbearable tiredness. getting better

low libido, getting better

brain fog, getting better

hair loss, getting better

32 year old male here. I was prescribed Levaquin 500mg 2 days ago for 10 days after being diagnosed with cellulite which is a bacterial infection in the blood. I had a swollen and sore groin on the right side. I already take prilosec once a day for acid reflux. Since starting Levaquin the infection seems to be clearing up, but the heartburn is pretty vicious. Yesterday I thought to myself hmm, maybe I didn't take my prilosec but I thought I did. So, I took a second prilosec but with no results. Today again as listed on the bottle I waited two hours after taking the Levaquin and then took my prilosec, but no luck. I've since taken a second prilosec and a couple of tums. As I drove home from work the heartburn started reoccurring. Thats when I googled it and came to find this site and that I'm not crazy. I also had sharp pains in my wrist and hands today and feel really run down and almost mildly depressed. I can live with joint pains and feeling a little run down, but the heartburn really does effect your eating and sleeping. I guess I'll have to see how the next 7 days go.

I am 34 years old. Back in 1985 I had most of my thyroid removed, due to a tumor attached to it. Since I was 10 until my late 20s, I was on Synthroid. By age 19 I had 3 knee surgeries to remove arthritis. I have suffered most of my life with joint pains, dry skin, weight that is like a roller coaster, and being tired most of the time. In my 20s I was put on Levoxyl. I has been on Levoxyl for several years now. Since being on Levoxyl I have been fighting anxiety, racing heart, joint pain in fingers and ankles, sudden dizziness to the point where i have to sit or pass-out. I feel like I'm 80 and not 34. After reading this site I am printing all this out and taking it to my doctor. No telling how much damage has been done after all these years.

Ironically, when I was in high school, I was sick for 2 years; I had migraines so bad I couldn't read, write or even watch TV. I was nauseated every day.. felt a bit better in the evenings. But my eyes were so sensitive to movement, if i was to move my eyeballs just to look at something move on the TV screen, I would be in agony. At the time, my mother was so worried about me, she took me to see every specialist there was in the city (Winnipeg), I missed 2 years of high school. After seeing about 50 doctors, finally one asked me if I was on the birth control ill and told me to get off it. 3 months later I was completely cured! Since then, i have been so afraid about birth control. i have used nothing but condoms.. until my son was born, my maternity doctor recommended the Mirena. I was skeptical because it had hormones in it, but she assured me they were different hormones then what were in the BC pill, and she said the risks were so low. I thought I would try it, and be on the look-out for the same symptoms I had with the pill. But I didn't have any. No visual problems, no nausea, no headaches... so I thought it was the greatest thing on the planet. Meanwhile, I was miserable, angry at my husband all the time, had no interest in sex whatsoever, was not sleeping.. I thought it was post-partum hormones. We decided our son needed a sibling so i had Mirena removed to get pregnant, and after our daughter was born in Dec '07, i had it put back in... again, thinking I had post-partum depression or something. Even 6 months later after I quit breast-feeding, I still couldn't lose the weight. I was eating chocolate and peanut butter by the cup every single day, crying all the time, had no energy to look after my kids and wanted to nap all the time, and cried when I couldn't! Then a few months later all of a sudden my joints started hurting. My wrists, elbows (like tendinitis), then a couple of days later I was limping because my hip or my knees hurt or my ankles felt swollen and weak. I felt like a hypochondriac because I was always complaining of something. Did I mention the hair loss?
So, sorry for the long story. But most of my symptoms have disappeared since removal if the Mirena this past Valentine's day 2009. However, as I was forewarned, I have recurrent symptoms every month while PMSing. I have never suffered from PMS in my life, until I had Mirena removed. I get depressed, eat more, and my joints hurt so bad, and sex repulses me. My poor husband; A couple of weeks ago I got so grossed out during sex that I made him feel like a creep.
These last 2 weeks, I wasn't supposed to have joint pain, because i wasn't PMSing anymore. But it has gotten worse. That's when I put up my post asking if anyone else has this pain. I was beginning to think I had Fibromyalgia. I also have very dry burning eyes, which is also a symptom on Fibromyalgia. I saw my doctor twice last week, and she thinks I may have it too. Is anyone out there in a similar boat?