Ligaments symptoms and conditions

Im still on the fence about Ativan...I am taking a 1mg tab once a day along with my 100mg og zoloft. The ativan is for my dystonia, which is a result of certain surgeries i had to rid myself of cancer. The dystonia would flare up and become horrible (meaning my neck,left shoulder and left side of my back would twitch like crazy)and this eventually lead to the ligaments in my shoulder becoming so loose from the twitching that I have had to have two more surgeries to correct that problem. Since taking the ativan on a daily basis, I have has almost NO ticks or twitches. however, while i don't have as much anxiety, i do feel more depressed and my doctor upped my zoloft...

UPDATE from Yesterday)))>>> well thanks to everyone i quit taking it yesterday BUT!!!---> today when i woke up i had a horrible head ache and it seemed to be coming from my left eye. i looked in the mirror and i have a really weird yellowish glazed tint in both my eyes and in my left eye a blood vessel has burst. i also noticed ive developed a skin rash on my right side of my stomach and on my left calf. My joints kept me up all night in constant pain which felt like someone was ripping apart my ligaments. I had a minor anxiety attack last night (Ive NEVER had anxiety before) and my body just feels weak, drained, and i keep getting really weird muscel spasms in my upper thigh. I tried to go out to the store earlier and as soon as i stepped into the sunlight a migraine hit me, and ive never been sensitive to light....Ive had a feeling of helplessness and worthlessness more in the past 24 hours than i have in a year. Im also experiencing horrible lower back pain and stomach pain around where my kidneys are.... I did have a small amount breast tenderness when i woke up and im not sure if that's another side effect...(no im not pregnant, had multiple urine tests in the last week)...I think ive only went potty maybe once today...and that was at like 9am...its now almost 9pm. Im pretty sure if this isn't over with or doesn't improve by 10pm im going to the hospital.....i cant drink water and im pretty sure im getting dehydrated....my skins turning pale, i have dark rings around my eyes.....etc.......has anyone else suffered with these things? Levaquin is by far the MOST painful, riskful, antibiotic ive been on...They should definitely take this sh*t off the market!!! =[[

I was given Cipro 500mg twice daily for a UTI. After 4 days on the medication I developed severe joint and tendon pain. Every joint in my body was in pain! I have called the doctor and they had me stop taking the medication. I continue to have pain in my joints. By the end of the day, my knees are killing me! Will this ever go away. I am seeing the doctor tomorrow, I am so upset over this, I am in my mid-30's and am feeling like I am 80! I am a grade 1 teacher and have 3 young kids at home, I hope things will get better!

I went back to my PCP today. Yes the one that gave me the Levaquin. He was very nice and even agreed it was the Levaquin I took back in December. He said that these types of side effects we all are describing are RARE (I would have kicked him for all of us, but my legs hurt to bad).

But he did acknowledge pain and my symptoms (listed in my December post) and prescribed me Prednisone for my ligaments and Lyrica for my nerve pain. He also said it was going to be a long haul. I know that some of you are dying to telling why these meds are bad too, but I am going to try it because I haven't really been out of my bed for two weeks.

I just wanted to let you all know, that maybe some doctors are starting to listen... and that we should keep speaking out and warning others about the HIGH risk of our side effects.

PLEASE READ THIS! UPDATE FROM ROCCO21ELM

I suffered terrible joint/muscle pain after taking Levaquin for 9 days. After reading all the posts here I was terrified that it was going to be an ongoing problem but it's been about a month now and the pain is nearly gone completely. Worry and fear seem only make the pain so much worse!
Pleae go to the doctor for a blood test. If everything comes back negative then you can relax. I suggest a proper diet, (AVOID foods known to cause inflammation and eat more foods that are anti inflammatory! Stretching in the morning, and swimming in warm water, hot baths help, and above all else, have a positive attitude. It goes a long way!! Good luck to all of you.

I have been taking Singulair for about two years now and I have been getting increasing fatigue so profound I have had to go from a 40 hour week to a 15-20 hour week. I have noticed increasing pain in my feet and legs which which affects my ability to stand and walk more each day. I also have stiffness in the ligaments of my hips, knees and feet. Medical tests show no arthritis in any of these areas. My memory is not as sharp and I have very restless sleep averaging 4-6 hours a night. My mind seems to be constantly running with thoughts and my concentration is gone out the window. After reading the the comments on this site, I am surely going to have my doctor change my medication to something else!

In January I was diagnosed with polymyalgia rheumatica and temporal arteritis (giant cell arteritis). I was put on 60 mg prednisone and an array of other meds to help with pain, inflammation, water retention, and stomach problems from everything. I've lost some vision from the TA. I've experienced the weight gain, the moon face, stomach problems, depression, fatigue, muscle weakness, lack of memory and concentration, and generally feel miserable. The brain fog is awful! I don't trust myself doing much of anything these days!

When I was first put on the prednisone it completely took away all my TA and PMR symptoms. I could walk and get up and down again, didn't have the headaches, and didn't hurt all over.
My doctor tried to taper my dosage about 6 weeks ago and all my symptoms returned and increased as I went down on the prednisone. He upped me back to 60. That time the symptoms didn't go away. They lessened but were still there.

He's trying to taper again, and I'm down to 30 mg now and feel worse and worse. My sed rate has been normal, so the doctor thinks it's from the prednisone. Does it mimic all the TA and PMR symptoms? I also am having a lot of hand and feet cramping.

Does anyone else have these two illnesses? I would be interested in your experience. I want off these meds! Anyone found an alternative approach that's helped?

God bless!

I have just started taking ultracet today. I was prescribed 2 tabs 4x's a day. I have taken 4 tabs so far. The pain is better but the pharmicist told me and my partner to watch out for psychotic episodes since I am taking 20 mg of Paxil a day. SCARY!!! So far just stomach upset. But not intolerable. NO PAIN!! I have suffered from chronic pain for 3 years after I tore my scapula away from the muscle and ligaments. I do feel a little wired. I was also told it was non habit forming. I have taken morphine and loritab but cannot handle the withdrawl. I think 8 tabs a day is a lot. Let you know as the days progress. Especially about the psychosis. My Dr. was informed about the Paxil and said it should not become a problem. We will see.

after taking the first 6 pills my heart started fluttering and I had to go to the bathroom most of the night. Called my Dr. and he said to cut the dose in half. I have infection in my ligaments in my thighs, so far no change in the pain.

I have taken this drug over the last three years for prostrate infections - if you get a bad case of prostitus you might end up taking it for 30 days as the prostrate is a dense organ and this is the only drug I've found that actually eliminates the bacteria causing the condition.

Recently I have started to develop more side effects to the drug than the usual joint pain - as like the others all my doctors said it wasn't the levofloxin but in reality it was - my recent symptoms are chest pain WHEN DOING SIMPLE EXERCISE LIKE LONG WALKS (external I have no cardiac problems) - over the heart area, in the front center where the ligaments attach and in the left and right shoulders plus center of my back, the pain is so bad it causes shortness of breath.

You can do real joint damage if you exercise while taking this drug and injuries come easy and with no warning. Joint pain is the normal and it takes about a month of flushing your with system with water for the effects to begin to diminish.

The instructions indicate that it should be taken with lots of water - DON'T OVERLOOK THIS WARNING AND TAKE LOTS OF WATER WHEN ON THIS DRUG AND YOU WON'T HAVE AS MUCH TROUBLE WITH THE SIDE EFFECTS - THIS IS VERY IMPORTANT AND I DON'T THINK THEY STRESS THIS ENOUGH.

My boyfriend tore some ligaments in his ankle and is taking lortab for pain. He has experienced sudden blackouts twice. He took one 7.5 mg dose.