Multiple sclerosis is reported only by a few people who take Mestinon. We study 1,503 people who have side effects while taking Mestinon from FDA and social media. Among them, 4 have Multiple sclerosis. Find out below who they are, when they have Multiple sclerosis and more.
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Mestinon has active ingredients of pyridostigmine bromide. It is often used in myasthenia gravis. (latest outcomes from Mestinon 1,571 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 influenza like illness, urinary tract infection, weakness, gait disturbance, fatigue (latest reports from 278,805 Multiple sclerosis patients).
On Aug, 22, 2016
1,503 people reported to have side effects when taking Mestinon.
Among them, 4 people (0.27%) 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.
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, and I am testng to see if alkaline water made with ordnary baking soda, helps currently, as my skin is acid and disolves metal, so my acid body may be disolving my faytty meylin even wen I try to replenish it with these things. Self talk type hypnosis seems to help as does exercse. Does anyone have any advice for me?
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 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
Hello group I'm Marnie I ve had ms since 1988. I found out in 2012 I have IgG subclass 3 but I had been sick for years before going to Cleveland clinic in 2012. I thought it seemed odd that I had these two different immune diseases. I also took the Avonex therapy. So I started researching ...
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