Would you have Earache when you have Multiple sclerosis?
Summary: there is no Earache reported by people with Multiple sclerosis yet.
We study people who have Earache 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 Earache >>>
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, Betaseron, Baclofen. (latest reports from 224,251 Multiple Sclerosis patients)
Earache (ear pain) has been reported by people with depression, stress and anxiety, high blood pressure, insomnia, bipolar ii disorder. (latest reports from 934 Earache patients)
On Jan, 27, 2015: No report is found.
Do you have Multiple Sclerosis and Earache?
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- support group for people who have Multiple sclerosis
- support group for people who have Earache
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More questions for: Multiple sclerosis, Earache
You may be interested at these reviews (Write a review):
- Ampyra vs kidney stones
Started taking Ampyra Sept 1, 2014.
Had a severe kidney stone in mid-September.
Another two weeks ago.
No family history or them. I also have no history of them.
Drink fresh squeezed lemon daily and lots of water.
Take Ibuprofen when it starts up.
Ampyra is helping with leg strength a tiny bit.
My MS is 40 years old so it is acting like it is old!
- 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!
- Penicillin vk induced drowsiness
I have been taking Penicillin VK and Acetaminophen for a severe pain I had been feeling in my ear. It's been 48 hours since I started taking them. Within the first 24 hours the pain had calmed down and I was feeling normal. However, since day 2 started, I have been feeling really drowsy. I keep falling asleep with no reason or desire to sleep. I just wanted to put this side effect out there for anyone else who might be feeling the same.
I am a male, 28years old, athletic build, 6 foot.
- 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: Multiple sclerosis, Earache
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