Review: could Copaxone cause Immunosuppression (Immunodeficiency disorders)?
Summary: Immunosuppression is found among people who take Copaxone, especially for people who are female, 30-39 old, have been taking the drug for 1 - 2 years, also take medication Venlafaxine hcl, and have Multiple sclerosis.
We study 10,161 people who have side effects while taking Copaxone from FDA and social media. Among them, 7 have Immunosuppression. Find out below who they are, when they have Immunosuppression and more.
You are not alone: join a mobile support group for people who take Copaxone and have Immunosuppression >>>
Copaxone has active ingredients of glatiramer acetate. It is often used in multiple sclerosis. (latest outcomes from 10,380 Copaxone users)
Immunosuppression has been reported by people with rheumatoid arthritis, multiple sclerosis, crohn's disease, multiple myeloma, osteoporosis. (latest reports from 6,913 Immunosuppression patients)
On Jan, 29, 2015: 10,161 people reported to have side effects when taking Copaxone. Among them, 7 people (0.07%) have Immunosuppression.
Time on Copaxone when people have Immunosuppression * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Immunosuppression when taking Copaxone * :
Age of people who have Immunosuppression when taking Copaxone * :
Severity of Immunosuppression when taking Copaxone ** :
How people recovered from Immunosuppression ** :
Top conditions involved for these people * :
- Multiple sclerosis (6 people, 85.71%)
- Depression (4 people, 57.14%)
- Relapsing-remitting multiple sclerosis (1 people, 14.29%)
- Psoriasis (1 people, 14.29%)
Top co-used drugs for these people * :
- Venlafaxine hcl (2 people, 28.57%)
- Venlafaxine (2 people, 28.57%)
- Baclofen (1 people, 14.29%)
- Carbamazepine (1 people, 14.29%)
- Folic acid (1 people, 14.29%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
Comments for this study:
Marie (3 years ago):
using Capaxone and have ongoing insommnia ... wondering if okay to take melatonin? thx
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Do you have Immunosuppression while taking Copaxone?
You are not alone! Join a mobile support group:
- support group for people who take Copaxone and have Immunosuppression
- support group for people who take Copaxone
- support group for people who have Immunosuppression
Drugs in real world that are associated with:
Could your condition cause:
Can you answer these questions (Ask a question):
- Has anyone using copaxone found that the actually have stiff persons syndrome, not ms?
I was diagnosed with ms 23+ yrs ago. 15 yrs ago, I was put on Copaxone. For the 1st 6mo I had gradual improvement, which then plateaued. After 15 yrs, it was discovered that I didn't have ms, but Stiff persons syndrome (sps). After going off of the Copaxone, over the course of 2 wks, my symptoms became so bad that I could not walk without assistance. I have contacted the drug company, and they have shown some interest, but I think they would be more interested if I could present info on other people with similar experiences. I am very serious that this could be a possible treatment for sps. As a pharmacist for 30+ years, I do have some knowledge of drugs.
- I have ms with some outbreaks of andgiodema in my mouth. i can't figure out what causes this. i have been tested by an allergist for the basic foods and molds.he came up with nothing.
This issue has been going on since June 2012.I have been tested for all basic allergies. Kept a food diary of all the foods i had the day of and before a breakout.came up no causes for an angeiodema. Can my ms have something to do with this. What can I do.
More questions for: Copaxone, Immunosuppression
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.
More reviews for: Copaxone, Immunosuppression
Comments from related studies:
From this study (1 week ago):
All are multiple sclerosis-related symptoms.
From this study (3 months ago):
Started with spasticity, in my legs about 5 months ago, now I have had physical therapy, and have developed intense heel pain for last 4 months. Dr's and nurses just keep telling me to use the baclofen and if needed a cane.
From this study (4 months ago):
Was put on simvastatin for 5 days, when severe pain hit. Was taken off of it immediately. Put on steriods. SED rate elevated. Prednisone helped just a little, but when weaning down, pain got worse. It has been 6 weeks off medication.
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