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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 168 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

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 Multiple Sclerosis 223,215 patients)

Tendonitis

Tendonitis (a condition that causes pain and swelling of tendons) has been reported by people with osteoporosis, sinusitis, high blood pressure, high blood cholesterol, osteopenia.(latest reports from Tendonitis 9,383 patients)

On Nov, 25, 2014: 168 people who have multiple sclerosis and Tendonitis are studied.

Trend of Tendonitis in multiple sclerosis reports

Gender of people who have multiple sclerosis and experienced Tendonitis * :

FemaleMale
Tendonitis89.58%10.42%

Age of people who have multiple sclerosis and experienced Tendonitis * :

0-12-910-1920-2930-3940-4950-5960+
Tendonitis0.00%0.00%0.00%2.35%8.82%27.65%41.76%19.41%

Severity of the symptom * :

leastmoderateseveremost severe
Tendonitis0.00%0.00%100.00%0.00%

Top co-existing conditions for these people * :

  1. Osteoporosis (6 people, 3.57%)
  2. Muscle spasms (4 people, 2.38%)
  3. Bipolar disorder (3 people, 1.79%)
  4. Pituitary tumour (3 people, 1.79%)
  5. Intervertebral disc protrusion (2 people, 1.19%)
  6. Anxiety (1 people, 0.60%)
  7. Dyspnoea (1 people, 0.60%)
  8. Relapsing-remitting multiple sclerosis (1 people, 0.60%)
  9. Tremor (1 people, 0.60%)
  10. Pain (1 people, 0.60%)

Most common drugs used by these people * :

  1. Tysabri (94 people, 55.95%)
  2. Avonex (84 people, 50.00%)
  3. Rebif (14 people, 8.33%)
  4. Xanax (8 people, 4.76%)
  5. Betaseron (7 people, 4.17%)
  6. Provigil (6 people, 3.57%)
  7. Baclofen (6 people, 3.57%)
  8. Celebrex (5 people, 2.98%)
  9. Parcopa (4 people, 2.38%)
  10. Paxil (4 people, 2.38%)

* 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

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More questions for: Multiple sclerosis, Tendonitis

You may be interested at these reviews (Write a review):

  • Ceftriaxone reynolds syndrome & tenditis
    (Posted by a 53 year old woman who has Reynolds Sydrome , Tendonitis, Hypokalemia, and takes Ceftriaxone )
    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
    (Posted by a 47 year old woman who has MS, and takes Copaxone)
    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.
    (Posted by a 41 year old woman who has Multiple Sclerosis, Scleroderma, and takes Copaxone)
    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
    (Posted by a 59 year old woman who has Overweight, Multiple Sclerosis, Tibia Fracture, and takes Topamax, Aubagio, Cymbalta, Celebrex, Fosamax)
    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?
  • A self-conducted trial with prozac in a case of "benign" ms
    (Posted by a 59 year old woman who has MS, and takes Prozac)
    I want to show that, with the approval of my doctor, I started taking Prozac (10 mg daily) to see if the number of the lesions on my brain remains the same. After 14 months no new lesion showed on the MRI. I should mention that I have a mild form of MS, if one may put it like this, but the previous three years my lesions had doubled as compared to the past 15 years. Not wanting to start an Interferon or other immune-suppressing treatment I chose Prozac. At first, I had a lot of problems (insomnia and bouts of crying and indifference) but after a few months they eased off. The only really bad symptom is sexual, i.e. difficulty or rather impossibility to orgasm. In 2-4 months I will take another MRI and check the results, and come back with details, hoping they could be of help for other persons with MS.

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