Dry eyes is found among people with Multiple sclerosis, especially for people who are female, 50-59 old, take medication Tysabri and have Multiple sclerosis. We study 257 people who have Dry eyes and Multiple sclerosis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
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Multiple sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath) can be treated by Copaxone, Avonex, Tysabri, Rebif, Baclofen (latest reports from 316,154 Multiple sclerosis patients)
Dry eyes (lack of adequate tears) has been reported by people with eye pain, rashes, drug ineffective, ocular hyperaemia, eye irritation (latest reports from 14,090 Dry eyes patients).
On Aug, 25, 2016
257 people who have Multiple Sclerosis and Dry Eyes are studied.
* 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.
Hi, I'm from Buenos Aires, Argentina and I'm 29 years old. This is my problem: After five hours of being asleep, I usually wake up with dry eyes. I must sleep again just to be mentally stable for the rest of the day. I have already try the problem with eye tears of all kinds. Question: Do you know what may be the cause of my problem? I really need to sleep better. A phychological condition can be the cause? Thanks!
I have been diagnosed for the past 5 years with MS. lately I HAVE BECOME EXTREMELY PARANOID, ESPECIALLY WHEN IT COMES TO MY PARTNER WHICH IS NOW AFFECTED OUR RELATIONSHIP. I also doubt my family and friends which is becoming quite upsetting as I don't want to lose my partner as he has been so patient through all this or my friends.
I am in pain everyday! My life sucks! I just want to know how to get some relief! Most days I don't want to get out of bed! My feet and legs hurt the most on me but lately my hands are starting to hurt! On my right foot I have a lump on the bottom of my foot, I have bunions(big) on both feet, ...
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 have been diagnosed for the past 5 years with MS. lately I HAVE BECOME EXTREMELY PARANOID, ESPECIALLY WHEN IT COMES TO MY PARTNER WHICH IS NOW AFFECTED OUR RELATIONSHIP. I also doubt my family and friends which is becoming quite upsetting as I don't want to lose my partner as he has been so ...
Hi, I'm from Buenos Aires, Argentina and I'm 29 years old. This is my problem: After five hours of being asleep, I usually wake up with dry eyes. I must sleep again just to be mentally stable for the rest of the day. I have already try the problem with eye tears of all ...
I took depakote for around twenty years. I had an MRI showing a T2-flair last year. I have almost all MS symptoms currently. I am no longer taking depakpte. I crave to eat the kind of thngs myelin is made of: like protein, meat connective tissue. High potasium foods, fat, cheese, green leaves, ...
Hi! I have had the hug for a couple years. It varys in degree day to day. Does anyone benefit from methocarbamol? I would love info as Neurontin and baclofen don't help a very great deal when the hug is at its worst. Thanks, Jeanne
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