Would you have Bone spur when you have Multiple sclerosis?
Summary: Bone spur is found among people with Multiple sclerosis, especially people who are male, 60+ old, and take medication Avonex.
We study 6 people who have Bone spur 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 Bone spur >>>
Multiple sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath) can be treated by Tysabri, Copaxone, Avonex, Rebif, Baclofen, Betaseron. (latest reports from 224,251 Multiple Sclerosis patients)
Bone spur (bony growth) has been reported by people with pain, multiple sclerosis, osteoporosis, neck pain, hyperlipidaemia. (latest reports from 148 Bone spur patients)
On Jan, 27, 2015: 6 people who have multiple sclerosis and Bone Spur are studied.
Gender of people who have multiple sclerosis and experienced Bone spur * :
|Bone spur||36.36%||63.64% |
Age of people who have multiple sclerosis and experienced Bone spur * :
|Bone spur||0.00%||0.00%||0.00%||0.00%||0.00%||88.89%||0.00%||11.11% |
Severity of the symptom * :
Top co-existing conditions for these people * :n/a
Most common drugs used by these people * :
- Avonex (6 people, 100.00%)
- Neurontin (1 people, 16.67%)
- Vicodin (1 people, 16.67%)
- Xanax (1 people, 16.67%)
- Hydrochlorothiazide (1 people, 16.67%)
* 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 Bone Spur?
You are not alone! Join a mobile support group:
- support group for people who have Bone Spur and Multiple sclerosis
- support group for people who have Multiple sclerosis
- support group for people who have Bone Spur
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Other conditions that could cause:
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More questions for: Multiple sclerosis, Bone spur
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.
- 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?
- A self-conducted trial with prozac in a case of "benign" ms
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.
More reviews for: Multiple sclerosis, Bone spur
Comments from related studies:
From this study (4 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 (2 weeks 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 (4 weeks ago):
Bone spurs appears on heels at time of Accutane use as an adolescent. Now bone spurs are appearing on one elbow, becoming painful. (As I read about it, I now know more bone spurs may be accumulating in other parts of the body).
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