Multiple sclerosis is found among people who take Orencia, especially for people who are female, 50-59 old , have been taking the drug for 2 - 5 years, also take medication Humira, and have Rheumatoid arthritis . We study 16,009 people who have side effects while taking Orencia from FDA and social media. Among them, 28 have Multiple sclerosis. Find out below who they are, when they have Multiple sclerosis and more.
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Orencia has active ingredients of abatacept. It is often used in rheumatoid arthritis. (latest outcomes from Orencia 16,862 users)
Multiple sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath) has been reported by people with multiple sclerosis, relapsing-remitting multiple sclerosis, depression, pain, gait disturbance (latest reports from 423,460 Multiple sclerosis patients).
On Oct, 19, 2016
16,009 people reported to have side effects when taking Orencia.
Among them, 28 people (0.17%) have Multiple Sclerosis
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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.
Hi, I was on Simponi Aria and had a terrible allergic reaction to it, so now we are trying Orencia. I had irregular heartbeat on Simponi Aria which went away a month after stopping infusions. I have now had 2 Orencia infusions and the irregular heartbeat is back! I fit the profile to a tee - over 60, taking mexo, and have under one month of treatment. My question is this: Does the irregular heartbeat stop and is it dangerous?!
I'm a 45 single mother of two girls 10 and 8.5 ...been on disability since 2009..ex husband trying to take my girls away because of my ms ...although I'm functioning quite well. I own a house ..car...volunteer and the kids school ...I use to help with he pain and to give me energy but it's starting to get a bit carried away now and I need help
Is anyone's Cushing's the result of Steroids used to treat their M.S., or does everyone have some type of tumor? I'm in the beginning stage of diagnosis. Abnormal midnight saliva & still waiting on ACTH results. The waiting is the worst part of all... Thxs
I'm a 45 single mother of two girls 10 and 8.5 ...been on disability since 2009..ex husband trying to take my girls away because of my ms ...although I'm functioning quite well. I own a house ..car...volunteer and the kids school ...I use to help with he pain and to give me energy but it's ...
Hi everyone, Thank you for letting me join your group. My name is Mary, (Mary1016), the major illnesses I suffer with is Complex Regional Pain Syndrome/RSD, small fiber peripheral neuropathy diagnosed with biopsy two weeks ago. I was told the neuropathy was already severe and the thing to do ...
I have ms and the doctor has prescribed atenolol. I am really worried about taking it. Filled the prescription but keep reading all these sight effects. I live by myself. Go to work everyday but I just don't feel comfortable. Any advise would be great or experience with this.....pls
I' am 50 and was diagnosed with RRMS 3 yrs ago.I went through menapaus last year. I'm taking avonex and just started Premarin for vaginsl driness. I'm just curious about the side effects of Premarin because I don't want any relapses. Also my blood pressure has steadily gotten higher since the ...
I have been diagnosed with MS sense 2009. I having more active lesion. Now I think I am developing Dupuytren Contrature because I hands have curved to my wrist very painful and unable to straighten twice with in the last year.
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
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