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Would you have Chills when you have Multiple sclerosis?





Summary: Chills is found among people with Multiple sclerosis, especially people who are female, 20-29 old, also have Hypertension, and take medication Avonex.

We study 2,912 people who have Chills 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 Chills >>>

Multiple sclerosis

Multiple sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath) can be treated by Copaxone, Tysabri, Avonex, Rebif, Betaseron, Baclofen. (latest reports from Multiple Sclerosis 223,215 patients)

Chills

Chills (felling of cold) has been reported by people with multiple sclerosis, rheumatoid arthritis, high blood pressure, osteoporosis, pain.(latest reports from Chills 45,468 patients)

On Nov, 27, 2014: 2,912 people who have multiple sclerosis and Chills are studied.

Trend of Chills in multiple sclerosis reports

Gender of people who have multiple sclerosis and experienced Chills * :

FemaleMale
Chills77.92%22.08%

Age of people who have multiple sclerosis and experienced Chills * :

0-12-910-1920-2930-3940-4950-5960+
Chills0.00%0.00%1.02%5.65%18.78%31.04%29.96%13.54%

Severity of the symptom * :

leastmoderateseveremost severe
Chills0.00%50.00%25.00%25.00%

Top co-existing conditions for these people * :

  1. Hypertension (58 people, 1.99%)
  2. Depression (51 people, 1.75%)
  3. Insomnia (28 people, 0.96%)
  4. Pain (25 people, 0.86%)
  5. Anxiety (22 people, 0.76%)
  6. Hypothyroidism (20 people, 0.69%)
  7. Headache (19 people, 0.65%)
  8. Muscle spasms (17 people, 0.58%)
  9. Prophylaxis (17 people, 0.58%)
  10. Fatigue (17 people, 0.58%)

Most common drugs used by these people * :

  1. Avonex (1,601 people, 54.98%)
  2. Tysabri (838 people, 28.78%)
  3. Rebif (474 people, 16.28%)
  4. Extavia (174 people, 5.98%)
  5. Betaseron (149 people, 5.12%)
  6. Copaxone (125 people, 4.29%)
  7. Gilenya (123 people, 4.22%)
  8. Baclofen (120 people, 4.12%)
  9. Neurontin (110 people, 3.78%)
  10. Aspirin (80 people, 2.75%)

* 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.

Do you have Multiple Sclerosis and Chills?

You are not alone! Join a mobile support group:
- support group for people who have Chills and Multiple sclerosis
- support group for people who have Multiple sclerosis
- support group for people who have Chills

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More questions for: Multiple sclerosis, Chills

You may be interested at these reviews (Write a review):

  • 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!
    Reply
  • Seizure disorder med problems (1 response)
    Velafaxine 150 mg. 1 per day.

    In process of switching from Topiramate 50 mg. 1 pill in morning & one at night (going off of this because of kidney stones) Was on this medication approximately 10 years.

    Lamotrigine 2 25mg pills in morning and 2 - 25 mg. pills at night.

    On the 3rd day of the 2nd week of switching I started the nightmares. I took a one hour nap and had a nightmare that seemed like it went on the entire time. Even if I slept for 20 minutes I had a dream or nightmare. I've sometimes been known to have vivid dreams but never this constant in my entire life. Also, very seldom do I have such terrible dreams. So many in one evening. They are an occasional thing, not an all night long thing.

    Also, I have sinus trouble occasionally. The same day the nightmares began I got a terrible headache behind my one eye and under my eye. I have no drainage yet anyway. Not sure if this is during the start up of this medicine, but if I had known it could cause trouble with sinus I would never have started it.

    I was put on this as a quick back up plan when the medicine we agreed upon - Levetireacetam made me feel drunk feeling and I had to be careful just walking around my homes and steps.
    Reply
  • 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.
    Reply
  • Chills while on tizanidine
    Extremely sensitive to cold and have chills several times a day
    Reply
  • Trying to figure out my diagnosis . no doctor can figure it out (3 responses)
    I have been having these fainting spells since I was 12 .. It starts with lower abdominal pain followed by feeling light headed then I black out and my body shakes kind of like a seizure but last a few seconds then I come to ..then I feel nausea and also I have chills
    Reply

More reviews for: Multiple sclerosis, Chills

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  • Fever over 102, chills, horrible pain began on day 5 taking medication. Red blotchy rash began appearing late following day on chest and back and gradually spread. Blood blister-type rash on legs. Went to ER after 4 days. Told I have sulfa allergy. Given iV fluid and meds. Need follow up blood test ...
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More related studies for: Multiple sclerosis, Chills

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