Anyone else with side effects from pr... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,356 members10,544 posts

Anyone else with side effects from pregablin?

Kittybaker profile image
7 Replies

I was diagnosed with fibromyalgia on top of APS a few months ago. Started on Gabapentin but the side effects were so strong with dizziness and feeling spaced out (only 300g) my GP then put me on Pregablin. The first week was fine, I felt really well. Pins and needles dispersed and the aching joints. The following week I started getting suicidal thoughts, crying, anxiety and just severe unrational thoughts and a higher emotional state.

I am now as if to day back on Gabapentin but only 100mg to see if that will keep the pain and pins and needles away. I was wondering if anyone else has had these symptoms when on Riveroxoban?

Written by
Kittybaker profile image
Kittybaker
To view profiles and participate in discussions please or .
Read more about...
7 Replies
MaryF profile image
MaryFAdministrator

While your GP tries to address these problems, do please also get your vitamin D, iron and B12 tested ad be aware with us lot the Fibro often turns out to be under active thyroid combined with low vitamin D, iron, sometimes B12 and Sjogrens Disease, the trouble with Thyroid is they only do the TSH test which is very unreliable. I did a barrage of private tests, which I paid for but this was worth the money as it showed up very clearly that Fibro was not in existence, but actually a severely under active Thyroid, let me know if you want details of the tests. MaryF

Hughes-Comrade profile image
Hughes-Comrade

Yes. I felt like a zombie. I then tried Lyrica (a relative) and ended up in ER.

Kittybaker profile image
Kittybaker in reply to Hughes-Comrade

That sounds awful!

Lure2 profile image
Lure2

I tried Lyrica perhaps 15 years ago (the same as Pregablin).

A Neurologist before I had a certain diagnose of APS prescribed it. I was very bad on it and had to stop it.

Hope you have got an APS-Specialist who understands what APS stands for, too thick blood.

Best wishes from Kerstin in Stockholm

Kittybaker profile image
Kittybaker in reply to Lure2

Thank you Kerstin

Yes I have been under Dr Sarah Lewis who has been my specialist for the past three years.

My doctor liases between Sarah and my other specialist who diagnosed me with Fibromyalgia

I am trying the new dose of Gabapentin so hopefully this will work better

Fra22-57 profile image
Fra22-57

Yes I am on Pregabalin and have APS , Fibromyalgia and Rheumatoid Arthritis

At present I am slowly trying to reduce from 450mg day.Stuck at 350mg as crippled up.

Yes it has made me very spaced out in past at point where I had to just shut my eyes n have my husbands arm to hold onto. Think my body has got used to drug. I used to have very bad suicidal thoughts but talked myself through them.I still have an occasional one but wouldn't do anything.

If does help enormously with the pain but maybe you need smaller dose or something more suitable

Kittybaker profile image
Kittybaker in reply to Fra22-57

Thank you for the reply, it's reassuring to know others have felt the same.

I am trying a tiny dose of 100mg of Gabapentin to see if that helps. I suffer from terrible puns and needles and joint pain.

I sometimes wonder if the side effects are worth it with Gabapentin/pregablin. The pain is horrible but I hate the side effects

You may also like...

Hydroxycloroquine side effects

diagnosed with LA several months ago and also have Lupus diagnosed 1994. Last week my Rhuematologist

Does anyone else suffer from stuttering with APS?

say struggle to get my words out. I was only diaganoised 6 weeks ago with APS and Lupus. I should...

Clear liquid suddenly streaming from nose has anyone else ever had this?

liquid was streaming from my nose, it stopped then started again 5 mins later. It has stopped now...

Anyone else sick of feeling horrible?

for three weeks (doc gave me exercises to do without even an examination). On the 5th week of...

side effects on warfarin?