Would you have Tendonitis when you have Multiple sclerosis?
Summary: Tendonitis is found among people with Multiple sclerosis, especially people who are female, 50-59 old, also have Osteoporosis, and take medication Tysabri.
We study 169 people who have Tendonitis and Multiple sclerosis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
You are not alone: join a mobile support group for people who have Multiple sclerosis and Tendonitis >>>
Multiple sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath) can be treated by Copaxone, Tysabri, Avonex, Rebif, Baclofen, Betaseron. (latest reports from 224,251 Multiple Sclerosis patients)
Tendonitis (a condition that causes pain and swelling of tendons) has been reported by people with osteoporosis, sinusitis, high blood cholesterol, osteopenia, urinary tract infection. (latest reports from 9,549 Tendonitis patients)
On Jan, 25, 2015: 169 people who have multiple sclerosis and Tendonitis are studied.
Gender of people who have multiple sclerosis and experienced Tendonitis * :
Age of people who have multiple sclerosis and experienced Tendonitis * :
Severity of the symptom * :
|least||moderate||severe||most severe |
Top co-existing conditions for these people * :
- Osteoporosis (6 people, 3.55%)
- Muscle spasms (4 people, 2.37%)
- Bipolar disorder (3 people, 1.78%)
- Pituitary tumour (3 people, 1.78%)
- Intervertebral disc protrusion (2 people, 1.18%)
- Depression (2 people, 1.18%)
- Anxiety (1 people, 0.59%)
- Dyspnoea (1 people, 0.59%)
- Relapsing-remitting multiple sclerosis (1 people, 0.59%)
- Fibromyalgia (1 people, 0.59%)
Most common drugs used by these people * :
- Tysabri (94 people, 55.62%)
- Avonex (84 people, 49.70%)
- Rebif (14 people, 8.28%)
- Xanax (8 people, 4.73%)
- Betaseron (7 people, 4.14%)
- Baclofen (6 people, 3.55%)
- Provigil (6 people, 3.55%)
- Celebrex (5 people, 2.96%)
- Demadex (4 people, 2.37%)
- Acyclovir sodium (4 people, 2.37%)
* Approximation only. Some reports may have incomplete information.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
Do you have Multiple Sclerosis and Tendonitis?
You are not alone! Join a mobile support group:
- support group for people who have Tendonitis and Multiple sclerosis
- support group for people who have Multiple sclerosis
- support group for people who have Tendonitis
Recent conversations of related support groups:
Could your drug cause:
Other conditions that could cause:
Can you answer these questions (Ask a question):
More questions for: Multiple sclerosis, Tendonitis
You may be interested at these reviews (Write a review):
- Dont use copaxone. it caused huge necrosis of my flesh!!
I took injections for 1.5 yrs. No problem. Then received a batch that caused huge indentions in my skin. I am a body builder, very obsessed with how my body and skin looks. Now I have massive (1/2 dollar sized) craters in my thighs and upper arms. I can no longer compete. Copaxone ruined my life. So sad, I was diagnosed with MS, but it's the medication that destroyed me. it's the f**ing treatment
. Be careful. The drug companies don't care. They are just making $$$ off of you.
- Ceftriaxone reynolds syndrome & tenditis
Ceftriaxone intravenous, after a week hypokalemia hospital visit waited a week went back to the CDC physician he said that drug had nothing to do with it. I am allergic to 99% of antibiotics I can only take a z-pack for two weeks and then run into allergic reactions. We started back on the Cefriaxone as soon as it entered my system heart pain burning sensation every nerve had to be iced. Also the Reynolds was so bad my hands turned white the blue numb. Now pain in wrist and upper arm. The cdc physician knew I was allergic why!
- Ms relapse - changed to copaxone in april
I've never joined one of these sites but saw this site. I have had MS for 14yrs but changed to Copaxone in April, had a relapse last week and wondered how others were getting on with it. I have a puffy left calf/ankle which can be a side effect of Copaxone - have others had this - can you reduce the swelling?
If I haven't started using this site - my apologies!
- Developed systemic scleroderma while on copaxone for 10 yrs.
I just tested positive for both crest and systemic scleroderma. I already have ms and have been on copaxone over 10 yrs. I believe copaxone may have caused this. I dont blame the makers. I am sure it has helped more then hurt, but I wonder if this has happened to others. If so it should be something ppl are aware of. That there is a risk.
- Topamax for weight loss, causing diarrhea
I was taking Topamax for weight loss and it worked very well. After 2 months I started having diarrhea. I stopped Topamax and the diarrhea stopped. Is there any drug or supplement I can take Topamax that will stop the diarrhea?
More reviews for: Multiple sclerosis, Tendonitis
Comments from related studies:
From this study (3 days ago):
I have been told to put up the level of the drug Amitriptyline but I work and if I up the level then I will not be able to carry on working.
From this study (1 week ago):
I was on Tysabri for 6 months and ended up with breast cancer 2 months after I stopped taking it. Is there a correlation. I heard if you are Brac 1 or Brac 2 positive Tysbri could be the culprit. If anyone has family members that have had cancer, check if you are BRAC positive. It could save your life or at least a horrible ordeal.
From this study (1 week ago):
Have experienced tendonitus in both elbows, left knee, and lower abdominal groin area. Started about a year ago and has gradually gotten worse.
Post a new comment OR Read more comments
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.