Tendons symptoms and conditions

I have had rheumatoid arthritis for 20 years,controlled reasonably well with a combo of methotrexate, naproxen and enbrel. I do a 10 day course of prednisone several times a year for bad flares. I absolutely hate taking prednisone because it turns me into a crabby, edgy, insomniac who can't stop eating. It makes me bloat and that REALLY makes me nuts because I've done so well at weight watcher's, I don't need that nasty, upset stomach over full bloat feeling. And the "roid head" headache thing ? I'm on the phone all day at work so that's bad, too. The insomnia is the worst, really, because I just lie there awake. When I stop taking it I return to normal within 2 days. I only do it when I am absolutely desperate - I already lost some tendons in my left hand to arthritis related damage so I tend to use the prednisone when the fluid builds up in the right hand or if I'm really too sore. I'm also aware that long term prednisone usage is a one way ticket to osteoporosis / osteoarthritis, so I really have to feel like I cannot deal before I take it. It's a hate/hate relationship.

I was prescribed tramacet which did nothing for me.. Ralivia was useless.. but Tridural, which is a type of Tramadol, is working for me very well. I take 300mg slow-release tablets every 24 hours. It is, however, extremely dehydrating at first, and gives me difficulty urinating. I used to be up 7 times a night to pee, and then sat there and had to concentrate to pee! I just thought I would ask if anyone else had the following problem with Tridural: I had been taking it in the afternoon, and I was extremely lethargic and sluggish midday when it began to wear off. I also had insomnia at nighttime. After suffering like this for a few months, I finally clued in to what was causing this lack of energy, and I decided to experiment with the time I took my pill. When I took it before bed, I was wide awake at 5am ready to clean the house! When I waited till morning to take it, my pain was too severe to get out of bed, and I was sluggish again (from withdrawal). Finally I set my alarm and took it at 4:30am, and by 7:30 am I am feeling terrific and am full of energy all day long. I just thought it was important to share this since the time of day really made a huge difference to my quality of life.
By the way, I am using Tridural for pain from "Enthesopathy" or migratory polyarthropathy. In my own words, all of my tendons in my body are weak and very painful. I have trouble walking and carrying my little kids, and some days I feel like all of my limbs are broken and I can't even function or be around my kids, they find it too upsetting.

Tendons were tight in my legs, fingers aching, and joints were hurting after taking this antibiotic. Besides the fever accompanied by the headache.

I had back surgery in July and caught two infections from the hospital, Staph and pseudonymous. I had a picc-line put in and was put on Cipro oraly and Ancef. I got Steven Johnson syndrome from the Cipro and almost died. I looked like a burn victim and swelled from head to toe that was three weeks ago. They pulled me off the Ancef and Cipro. It took a week of me running 103 + temps and the dr. kept telling me its a virous until the rash showed up and my tongue swelled and private parts and throat started to swell shut before they decided to admit me. Then once all that was done and they figured it out they put me on impernem to kill both infections. They pulled my picc-last week and put me on Doxycycline. I have done my research and know that the two are related I asked my dr. what the chances were of a reaction again he told me less then 1%. Ha! I am seeing an infectious disease dr. by the way. Since I started the Doxycycline last Thursday I have developed hives I called the dr. and was told they are not worried about it because I am not running a 101 temp and I am not swelling, plus they don't even know if the Pseudonymous is cured. What do I do? If I go off the antibiotics I will die and if I stay on them I am probably going to die. My joints hurt all the time now and I am only 31. Do I look for a new dr.? Can someone please help me? This is the only website I have found so far where people have had the same reactions as me. These antibiotics are dangerous they need to be taken off the shelf. Thank you and good luck to everyone who is struggling with this.

I took levaquin for 10 days and then cipro for 10 days after being misdiagnosed with bacterial pneumonia when I really had cocci mycidioidosus (valley fever) a creepy lung infection from a fungus that lives in the dirt here in Ca . Within a few days of stoping the antibiotics I experienced severe joint pain,dizziness,swollen neck ,hives,pain and tingling in my legs and feet,taste perversion,neck pain,hallucinations,nightmares,suicidal thoughts,dead skin,head ache,conjunctivitis. All of which I thought were valley fever related . A few weeks later I started noticing loss of vision and an inability to focus or concentrate on anything. I have ruptured 5 tendons and sometimes can't lift my right arm off the table.
I'ts been a year and 3 months and I still suffer from these side effects and about 3 months ago I started to notice some hearing loss and then ringing in my ears so load that it wakes me up!

This drug has ruined my life.I have lost 2 profitable businesses,a house a car .a commercial building, my credit score is 309 from 760 a year ago.All from a stupid antibiotic that should not be sold in the first place unless you are going to die if you don't take it.....personally I would rather be dead I think.

I think that we (the 1000's of people effected by this drug) should protest,march at ORTHO McNEIL's doorstep and perhaps the FDA....write a letter ,call or write to OPRA...do something ...It's not right that they get away with selling this crap.

Please email me ...I see 1000's of you on these sites...lets get busy!

******

Thanks for reading

Took Doxy for 2 years for Lyme and Babesia. Never had a problem with it. I stopped taking it for 8 months, then the Lyme disease symptoms returned. So I started back up on it. I noticed migrating pain in all of my joints...even every toe. I stopped taking it for a week and the joint pain pretty much resolved. I started it up again and sure enough, joint pain returned mainly in my knees and hands. Constant cracking of my thumbs, knees, toes,elbows. It also caused my tendons to become very tight and sore in my right hand. Making it hard to hold my dog's leash or open a door knob. Whether it was a bad herxheimer reaction or just my body deciding it was sick of this drug......I may never know.

Hi all, ive been on flomax about a month or so now, and have started having pain in muscles and tendons of arms and legs, anyone else having these side effects?, also i have experienced the other known side effect, reduced semen, and a kind of burning feeling in the groin area. Bryan in Indiana.

I took this poison 5 years ago and I'm still suffering the effects of it. PLEASE send it MEDWATCH reports so that they can get this off the market.
For all of you just starting your journey into hell, only time will help you. Take hot baths, don't over exercise ( you will tear tendons), change doctors tell everyone you know not to take any FLUOROQUINOLONE (LEVAQUIN, CIPRO, ETC.)

My local hospital prescribed Avelox for a sinus infection since Amoxicillin wasn't working. My fever jumped up to 102 the first 2 days so I called my family doctor. He told me to keep taking the meds for 2 more days and if my fever persisted to call him back. I experienced the high fever on day 3 and then was in a world of shock when I took the 4th pill. My body went numb, I was speaking but had no idea what I was saying, dizzy, the fever subsided during the day but spiked back up to 102 that night and I was very irritable. I made a doctors appointment the next day and the doctor told me to take the meds at night and I wouldn't have those reactions. After reading these comments and my day 4 episode, I had it in my head that I was not going to take any more pills. Then I called a nurse friend who assured me that it wasn't the antibiotic making me feel that way.....it was the extra strength Tylenol. She advised me to take the pill. I took the pill and not two hours later, my body went numb, I became dizzy, my tendons in my right knee and left foot swelled and I couldn't sleep. After my body went numb, I took the rest of the pills and flushed them down the toilet. I'm still feeling the affects of the pills and it's been 2 days. I've been swallowing gallons of water to flush it out of my system. I lost an entire week of work and pretty much my normal life. I'd much rather have sinus pressure in my head then deal with these side effects.

I am a 62 year old male who works out and is in good shape. I developed a case of diverticulitis and was prescribed a 10 day course of Avelox, 400 mg. per day. I began taking the pills and they worked on the diverticulitis. However, after 7 pills, I developed pain above and below the knees and down at the ankle. This pain is in the tendons. It feels like a permanent Charlie Horse. I went to the doctor today and his belief is that I do indeed have a side effect, since I am in otherwise good health, the pain is in both legs, and the onset coincides with taking Avelox. Unfortunately, he said they do not really know the mechanism of this reaction; they don't know how long it lasts; don't know if it goes away, etc. Now I must really watch myself for who knows how long because of the danger of popping a tendon. This is incredible to me. Seven pills and perhaps permanent damage? I am wondering if any of the people who have posted tendon issues have improved or gotten worse after time.

I had posted my condition earlier.
http://www.medications.com/effect/view/36140
I am still working on my muscles and tendons. It's been a long road.

I am writing because I saw an ad today about Levaquin-

If you've been harmed by Levaquin, call our lawyers for a screening at
1 - 8 0 0 - B A D - D R U G
They specifically mentioned torn and damaged tendons.

I was diagnosed with pneumonia on July 6 and prescribed Levaquin 500 mg for 10 days. I took my last pill tonight and could not understand the pain in my right hip, red eyes which I suspect comes from the insomnia I have been experiencing since July 10. I am still having difficulty sleeping and tonight I feel extremely tire with discomfort in the back and shoulders. I wish I had read these comments earlier, I would have discontinue using this drug. I have not experience any depression, but lack of appetite, stomach pain and upset stomach. I have had intermittent diarrhea. How long will it take for this drug to get out of my system.

I started feeling much better very quickly after being off Lipitor now 7 months. However, the symptoms I had using the RX has cause significant problems. I fell so many times with my weak joints and muscles, that I had severe problems. I now need to have knee replacement surgery after falling so many times injuring my knees and weakened muscles to support myself. I am getting cortisone shots in that knee, as well as physical therapy. My MRI shows a torn meniscus, stretch PCL very thin, cartlidge loss and debris, still swollen with csyt after all these months. With no meds, and lack of being able to exercise, I now have hig-chol back. On and on it goes.... a real catch 22. Take care of yourself, watch out for symptoms. I ignored sx's thinking it was stress but after reading adverse reactions, it fit me to the T.
My original posting re: Lipitor is Forestseaski on Jan. 2, 2009

C.

I have been on simvastatin for 2 yrs . The past six months have had foot pain my doctor described as neuroma.By the time I started physical therapy the pain was in my arch + tendons. I went to physical therapy for two months, the therapist became concerned when improvement peaked. Still have burning nerve pain. I think its time for natural supplements . I hear "red Rice Yeast" is effective.
S. M.

54 year old Male, Retired Marine, Very physically active, with Type II Diabetes; 5mg. Thanks for this Website. Started Lisinopril 3/25/09. Took it for 25 days, found this website and stopped taking it immediately. I had severe JOINT PAIN. It started in my hands, then feet, knees were next, then moved into my shoulders. The pain was the worst I've ever felt. Approximately 60 days after stopping the drug I went to see the Dr. after the Pharmacist told me Lisinopril should have been out of my system after 2 weeks. The Dr gave me Steroids (Prednisol) which completely eliminated ALL pain in 2 days . I was tested for Polymyalgia Rheumatica, however the my Sed Rate was normal. The blood tests did reveal that my RHEUMATIOD FACTOR is elevated (34.3 where the normal range is 0.0-20.1 IU/ML). Was told that if the pain returned, then I would be referred to a Rheumatologist. 3 Days after finishing the dosage pack of Prednisol, the pain/swelling in my hands and shoulder has returned. Going back to see the Dr today to discuss next steps.

Although the doctors don't agree, I believe Lisinopril caused this pain, and although out of my system now, triggered something that isn't going away.

The rest of this describes the roving pains I experienced.

Hand pain included swollen fingers, inability to make a fist or type on a keyboard. After light yard work on Sat., shooting burning pain up the inside of both arms. Trying to close your hands into a fist, you can feel the tendons up your arm burn with pain. Motrin did not alleviate the pain. Hot water did not help.

Pain in my knees each morning. The pain worsened over night and frequently causes you to wake up. The pain was like your knees were being squeezed in a vice. No position is comfortable. Motrin sometimes helped, but after awoken, getting back to sleep was impossible.

Feet swollen. Couldn't wear any shoes for extended periods. Loosening the laces helps, but still caused pressure which becomes unbearable and the shoes have to come off.

Shoulders; This is the strangest one. First pain was in the left shoulder, like I had impacted a brick wall at a full run (actually no trauma occurred). The pain felt like someone had stabbed it in my shoulder in the socket. At it's worst, no position is comfortable. Had to put my arm in a sling. 5 Days later, the same type pain moved to the right shoulder.

Started taking lisinopril April 6th of this year. Have had many of the symptoms listed in these posts. I just thought I was still having symptoms from being sick. I have had a lot of anxiety and depression, as well as chest pain and heart palpitations. My hands were ice cold and had severe stomach pain. My head felt very cloudy and numb. I have had every blood test possible, 2 EKG's, a brain MRI, cervical MRI and brain MRA, and a chest x-ray. So far, everything is normal. I saw this site a few weeks ago and on June 8th, I stopped taking lisinopril. I have started feeling better, not completely, but definitely better. I am supposed to go back to my doctor on the 29th. He did not agree with me that these symptoms could all be caused from this drug. He reluctantly agreed that I get off it for these 3 weeks. I am still taking Hydrochlorot with no symptoms. Not sure what to tell him when I go back. Are any of the other blood pressure drugs safe???

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

I was prescribed levaquin back in May for a sinus infection. Have suffered from severe side effects, worst of which being joint and muscle pain, stomach pains, weakness and hives (last dose was taken 10 days ago). This has been the most physical discomfort and pain that I've ever been in. In addition, my ability to concentrate and recall easy things has lessened.
The "Bafoon" of a doctor that prescribed this claimed he didn't know what was wrong with me after a normal blood test. My new knowledgeable doctor told me that some people can't even walk after taking Levaquin. She says it takes on average 7 days to 6 weeks to feel improvement. Being a 36 yr old woman, having to move turtle speed, and feeling like I'm in a 90 year old body is very depressing.
If anyone has any information on any class action or mass tort litigation lawsuits please send me the information. This drug is poison and should not be prescribed for minor infections!!!

I've been searching for answers on LONG TERM side effects of Lupron hoping that it could give me answers as to what's going on in my body now!
23 yrs ago my fertility dr. gave me Lupron to inject MYSELF EVERY DAY (experimental back then). I had SEVERE endo since the age of 16 and was fighting that as well as trying to get pregnant thru invetro. I was 26. At 29 I had an emergency hysto. Now at 48plus I have chronic tendonitis where the tendons will shred off of the joints. I have been diagnosed with C spine and T spine disease, osteoarthritis and a mystery that I'm going to have to go to the Mayo to figure out (hopefully). I have tumors that are growing in my lower back...growing around nerves, tendons and bone, They aren't sure why they are there, why they are growing, or even what they are. Surgery removed 2 of them...but pathology shows foreign matter other than tissue/bone. All they DO know is that it is not cancer. One year ago I started losing weight (25 pds) for no reason. I'm now holding my own at 112 and hoping to figure all of this out. I can't help but wonder if Lupron or any other experimental drugs I was on has something to do with this. Is there anyone out there that used this drug so long ago??

I have a history of sinus infections. After two rounds of Augmentin did not clear up my latest one, my doctor finally gave me the steroid pack and Avelox. He had tried to avoid the steroids. I have had them so many times. I finished my steroids 5 days ago and my Avelox yesterday. I read the side effects and did as it suggested. Since it mentions low potassium would not be good I ate a banana every day and had some orange juice to keep my potassium levels up. The drug warms against taking any pain killers such as Aleve, Advil, etc. One earlier reviewer admitted taking Aleve and had a bad reaction... well.... bad move.... I have had no real side effects that I can say for sure are Avelox related. I did feel a little less focused at times, but was not obviously groggy or woosey. I did have a little abdominal discomfort that I usually do not have with drugs, but it was short-lived and only occurred 3 of the 10 days. Many people have bad effects because they do not follow the warnings against anti-acids, pain killers, low potassium, etc. Some people are more likely to react to any medicine, while others like me rarely have a side effect. My tendons did not hurt... nothing.... People who are out of shape, have a poor physical life style, etc. sometimes help contribute to the drugs reactions by being in basically poor physical health to begin with. America is one of the fattest, out of shape nations out there due to our abundance of everything. The majority of persons can take Avelox with no real issues. I will take it again. I truly feel concern for those who had problems, but sometimes we are partly guilty by how we don't take care of ourselves when we are well...... As with any drug, some persons will react no matter what... It's often just a matter of inherited genetics...... Be safe everyone, and take time to evaluate how you take care of your body and really decide to do better. For the record I am almost 58, 5-9 158 pounds and work out semi-regularly.... Take care of that temple God gave you. Its the only one we get on this Earth,,,,,,

I am a 29 y/o male.this month i got a terrible sinus infection, probably due to a month's struggle with allergies. I was initially prescribed Augmenting but after just 1 pill i was up all night with stomach cramps & diarrhea. I was scared to take another dose so my dr. prescribed me Levaquin as an alternative. After reading the warnings I became very worried due to the fact that I already have lower back/hip and joint pain issues. I also work evening freight at Home Depot. After 1 Levaquin yesterday morning, I went to work ready to take it easy and not hurt my body more than it already does... after about 30 minute of simply opening small boxes and putting light-weight merchandise on the shelves, i began to feel extreme tension/aching in my hands and fingers.I was being very careful with my back & neck, but never even thought this might effect my hands??? I woke up this morning hoping it would be gone... no such luck, even after a full night's rest they still feel like i have arthritis, and no my hips (S.I. joints)are popping out like crazy. i am about to take the 2nd dose, only b/c my ears nose and throat do feel much better. I am just glad I picked up paperwork/and can afford to take a few days of LOA if this gets any worse. It is hard for me just to type this now : (. I'm scared.

i WAS ON A Z-PAK FOR 5 DAYS FOR A SINUS INFECTION. i GOT WORSE, SO ON THE WEEKEND, i WENT TO URGENT CARE BECAUSE i COULDN'T BREATHE. aNYWAY, THEY GAVE ME A SHOT AND LEVAQUIN. oH MY GOD, WITHIN 3 DAYS, I COULD HARDLY MOVE MY KNEES. jOINT PAIN SUPER BAD!!!!!!!!!!!!!!!!! i CALLED MY PRIMARY DOCTOR AND THEY SAID TO STOP TAKING IT. wELL I HAVE BEEN OFF
OF IT FOR 10 DAYS AND MY KNEES ARE GETTING A LITTLE BIT BETTER.
THEY THROBBED AT NIGHT, SARP PAINS IN MY CALF. A STETCHING, PULLING BEHIND MY KNEE FOR MANY DAYS. iT WAS AWFUL THE WORSE THING i HAVE EVERY FELT. oF COURSE MY PRIMARY DOCTOR SAID IT WASN'T A REACTION TO THE ANTIBIOTIC. i KNOW IT WAS, THE MEDICINE IS FINALLY GETTING OUT OF MY SYSTEM.

I took Levaquin shortly after a complete hysterectomy. I was intrigued to hear that this drug causes tendon damage. I took at least a year to heal, I felt like the tendons in my stomach were torn, lifting caused great pain. I couldn't sleep or lay down crooked, I always had to keep my body flat. If I sat up it had to be straight up, no slouching as it cause great pain in my stomach. Apparently the uterus is cut off of tendons. Everyone said I should have healed so much faster. I couldn't wear slack for at least a year. I took the Levaquin for a sinus infection. The doctors decided that I was having interstitial cyctitus causing all the pain, I still have that but it causes pain lower. I had diarrhea for 6 weeks after taking it. Someone told me you're aren't supposed to take it and lay down, you're supposed to sit up for at least an hour, which I couldn't, and it wasn't a caution on my medicine bottle-this was in April of 2007. My stomach area still isn't great, I get a tearing feeling when I throw the ball too much to my dog or do too much housework, or cleaning/scrubbing. What a nightmare. Did anyone else experience tendon damage of this same type?

My son (14 years old) was given levaquin for a sinus and ear infection
2 weeks ago. Around the same time he began practices for his high school baseball team. He complained about his legs being stiff and aching. We assumed it was the intense practices causing his muscles to ache. After a week on the drug, he could barely walk and his knees were swollen. We were very concerned and looked up the side effects of levaquin on the internet. We were shocked and angry when we found out that levaquin should not be given to children under the age of 18 because on the possibility of joint and tendon problems. Today we went to the orthopedist and he drained a lot of fluid off of both knees (it looked like about a 1/2 cup from each).The doctor thinks it has to be a side effect of the drug, because the symptoms began at the same time. He doesn't
think after examining the knee and having him perform certain tasks that he has damaged any tendons. He has all the symptoms of rheumatiod arthritis. He is very athletic and plays competitive sports and we are praying that his knees are not permanently damaged by this drug. Parents please research all drugs and there side effects before giving them to your children! Doctor's DO make mistakes!! The pharmacist failed us too.

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