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Would you have Underactive thyroid (Hypothyroidism) when you have Multiple sclerosis?





Summary: Underactive thyroid is found among people with Multiple sclerosis, especially people who are female, 30-39 old, also have Depression, and take medication Avonex.

We study 454 people who have Underactive thyroid (Hypothyroidism) 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 Underactive thyroid >>>

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)

Underactive thyroid

Underactive thyroid (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development) has been reported by people with osteoporosis, high blood pressure, osteopenia, depression, multiple sclerosis.(latest reports from Underactive thyroid 43,269 patients)

On Nov, 26, 2014: 454 people who have multiple sclerosis and Underactive Thyroid are studied.

Trend of Underactive thyroid in multiple sclerosis reports

Gender of people who have multiple sclerosis and experienced Underactive thyroid * :

FemaleMale
Underactive thyroid91.48%8.52%

Age of people who have multiple sclerosis and experienced Underactive thyroid * :

0-12-910-1920-2930-3940-4950-5960+
Underactive thyroid0.00%0.00%0.00%2.34%17.27%30.76%32.91%16.73%

Severity of the symptom * :

n/a

Top co-existing conditions for these people * :

  1. Depression (24 people, 5.29%)
  2. Hypothyroidism (21 people, 4.63%)
  3. Hypertension (19 people, 4.19%)
  4. Multiple sclerosis relapse (16 people, 3.52%)
  5. Anxiety (16 people, 3.52%)
  6. Vertigo (13 people, 2.86%)
  7. Dizziness (13 people, 2.86%)
  8. Aphonia (12 people, 2.64%)
  9. Restless legs syndrome (12 people, 2.64%)
  10. Hemiparesis (12 people, 2.64%)

Most common drugs used by these people * :

  1. Avonex (305 people, 67.18%)
  2. Rebif (127 people, 27.97%)
  3. Tysabri (123 people, 27.09%)
  4. Baclofen (59 people, 13.00%)
  5. Synthroid (50 people, 11.01%)
  6. Neurontin (47 people, 10.35%)
  7. Provigil (37 people, 8.15%)
  8. Zoloft (31 people, 6.83%)
  9. Betaseron (24 people, 5.29%)
  10. Ibuprofen (23 people, 5.07%)

* 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 Underactive Thyroid?

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

Could your drug cause:

Other conditions that could cause:

Can you answer these questions (Ask a question):

  • Is it okay to take co enzyme q 10 with levothyroxine
    Is it okay to take Co Enzyme Q10 with Lovothyroxine. Will it stop my Levothyroxine from working properly. I am also on Simvastaton. Would appreciate any advice on this.
    Reply
  • Can my sister take phentermine with multiple sclerosis to lose weight
    I worry she is taking a pill that will affect the nervous system and may not be good for her body.
    Reply
  • Omeprazole or pantoprazole?
    I take an oral contraceptive, Diane-35 ED, which is not in the list of drugs to choose from on this site.

    Recently, the medication I was taking for my stomach ulcer (Omeprazole) became unavailable in my country of residence and was replaced by Patoprazole. I started taking it yesterday morning and by midday today the side effects were unbearable. I am nauseous, have diarrhea, and a very severe headache. This didn't happen with Omeprazole. Do you think this is a drug interaction or is there some difference between the two that I am perhaps sensitive to?
    Reply
  • Has anyone been prescribed methotrexate for granuloma annulare?
    I have had GA for 2 years now, however it has gotten progressively worse the past 6 months. It has now spread over 80% of my body. I am seeing an Endocrinologist next week as I believe my thyroid may play a big role in this. My Regular Dr. suggested I speak to Endocrinologist about a drug called Methotrexate. Has anyone taken this for GA, and if so, can you please tell me if it is working, side effects etc?
    I am desperate for some relief!
    Thanks
    Reply
  • I have been on armour 8 days started at 1 grain after having been on 88 mcg synthroid.
    Was on 88mcg synthroid. Test was 4.75 tsh and low t3 3.3. Switched 8 days ago to 1 grain armour and now feel shaky. Pulse 90. Had diarrhea and vomiting last night at 1 in am. Is it working too fast? Felt good earlier in week and slept all night for first time in months.
    Reply

More questions for: Multiple sclerosis, Underactive thyroid

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
  • Shortness of breath after taking levothyroxine for 8-10 yrs.
    I have been experiencing shortness of breath lately when taking the levothyroxine. If I stop taking it for a couple of days my shortness of breath is pretty much gone.
    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
  • My memory loss due to omeprazole
    I took omeprazole for 20 years until I developed edema of the lower extremities. I started having memory problems right away and they still persist even though I have not taken omeprazole now for about 6 yrs. I am hoping it will dissipate or clear my system. I do not have a constant memory problem but rather problems remembering words from time to time. I ended up having to take magnesium for leg cramps that developed from taking omeprazole.
    Reply
  • Lipitor bad reaction
    I was on lipitor for 5 years started at 10mg and the headaches started. At 5 years on I was up to 80mg and had severe migraines every day. Was also diagnosed with hypothyroidism and given synthroid. Also had a prescription for migraine meds that did nothing. My daughter found out she and her kids have celiac disease and her Gastroenterologist said I should have a blood test to see if I have the gene as well. My internist Poo poohed me and did not want me to have the test. That was when I totally lost faith in her. I insisted on the test and lo and behold I have 2 of the genes. I also had a rash that she kept telling me was from sweat, but gave me no other info. As soon as I stopped eating gluten the rash went away.About that time I had a headache so severe that I went to the ER. The dr there thought I was having a stroke. The pain was so bad I vomited several times. That's when I stopped the lipitor and synthroid and quit going to her. I am totally headache free now. Took about 6 months for them to totally go away. I can also sleep all night again. I don't know if the problem was from the synthroid or lipitor.
    Reply

More reviews for: Multiple sclerosis, Underactive thyroid

Comments from related drug studies (Check your drugs):

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  • I was diagnosed with Hypothyroidism in Sept. 2012 after 6 yrs. of taking Tramadol 50mg. I had gotten it under control using Red Yeast Rice 200mg 3 times a day, Niacin, and Multi-vitamin with iodine. I was told to eat more fish and add iodized salt to my diet which I had done. Then after starting t ...
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  • Was recently told that my white blood count was low, I believe that it is a direct result from my medication as I have no other symptoms. My question is , if I go off the medication will my blood count go up if it was indeed the medication causing the drop.
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  • I lived in a condominium where each of my neighbors smoked and after I began taking Tecfidera I developed a strong sensitivity to this. Other than myself, no one else could sense the smoke. I became so sensitive that I could tell when a neighbor would start and stop smoking. I then developed constan ...
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  • I feel like I don't belong, little disagreements make me cry with outbursts of yelling, always want to keep busy or don't want to do anything. Always biting down on my teeth or always feel like I am sucking on my tongue, cannot stay still sometimes always depressed
    Reply

More related studies for: Multiple sclerosis, Underactive thyroid

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