Does a decrease in carbimazole affect... - Fibromyalgia Acti...

Fibromyalgia Action UK

59,795 members66,878 posts

Does a decrease in carbimazole affect joints

chocolate49 profile image
3 Replies

Hello everyone and a happy new year to you all!

Diagnosed in nov/dec 2011 with over active thyroid put on carbimazole (20g twice a day)

By the april/may 2012 went under active so doc put me on levo as well (block and replace?)

However since aug/sept 2013 doc has been reducing carbimazole gradually as everything seems to be settling down. Went down to 20g (10g twice a day) for the period aug-sept. Seemed to be ok pretty much of the time. Oct/nov went on 10g (5g twice a day). Not too bad.

Since mid dec been on 5g just once a day. For the past week I have been feeling crap again though not as bad as the early days. My joints have been really painful (especially finger/thumb joints). Though my other joints have also not been very happy also.

Still on 75g levo also

Due to have a blood test next week to see how things are going, not sure I can wait that long.

Can anyone let me know if all the joint pain is as a result of the reduction of carbimazole?

I hope this all makes sense and I would appreciate any advice

Many Thanks

Written by
chocolate49 profile image
chocolate49
To view profiles and participate in discussions please or .
Read more about...
3 Replies
Mdaisy profile image
Mdaisy

Hello Chocolate49,

Welcome, I see this is your first post in the FibroAction community and you have been usually posting in Thyroid UK.

As the question is about Thyroid medication, please can I ask 'Did you mean to ask this question here or in Thyroid UK ?' :)

Happy New Year :)

Emma

FibroAction Administrator.

chocolate49 profile image
chocolate49 in reply to Mdaisy

Hi

Think I got a bit muddled and it should have been in the thyroid uk! I must be honest since the site has changed it does confuse me somewhat but since my thyroid went wacko everything seems t confuse me! Happy new year to you all :)

Mdaisy profile image
Mdaisy in reply to chocolate49

Hey, no worries ! :) Well at least now you can repost and you'll get the appropriate replies !

Emma :)

Not what you're looking for?

You may also like...

Fibro, Buprenorphine Patches and CBD Oil

Is there anyone that can give me any good advice. Over a good many years I was on a cocktail of...

Meds??

Well as I said earlier, I am new to fibro. Doc put me on amitriptyline 35mg taken in evening. As...

How does gabapentin affect people?

I went back to my gp today as following an appointment at the FM clinic was told should change my...

How does anxiety affect you in this pandemic

Hi everyone, before the pandemic I had anxiety under control but now it seems to be taking over...

Should I take Duloxetine again?

Hi I'm not sure whether I have been a member of this forum before, but think I haven't so will say...