Golimumab: Has anyone had experience of Golimumab? As I... - NRAS

NRAS

37,263 members46,132 posts

Golimumab

-Mii profile image
-Mii
15 Replies

Has anyone had experience of Golimumab? As I am starting this soon and would love to find out more about it!!

Written by
-Mii profile image
-Mii
To view profiles and participate in discussions please or .
Read more about...
15 Replies
Victoria-NRAS profile image
Victoria-NRASPartnerModeratorNRAS

Hi

Hopefully you'll get some responses from people who have been on this drug. It was approved in 2009, so is one of the newer RA drugs, but is a type of drug called an anti-TNF drug, and these as a class of drug have been around for a while now.

I thought you might also find our article useful if you haven't read it:

nras.org.uk/golimumab-simponi-

Kind regards

Victoria

(NRAS)

-Mii profile image
-Mii in reply toVictoria-NRAS

Thank you Victoria!

simponiaria.com/sites/defau...

-Mii profile image
-Mii in reply tobassiefromholland

Many thanks! Maria.

skinnycappuccino profile image
skinnycappuccino

Hello 2210 :) I've been taking Simponi (= golimumab) since 2012 and have been in remission for 3 years now :) It's worked wonders - I got my old life back. I hope it works as well for you! Good luck & let us know how it goes! Best, Christine xx

-Mii profile image
-Mii in reply toskinnycappuccino

Nice to hear that! I've been on methetrexate for 4 years tablet and injection and now going to try an TNF!! I am taking it monthly Christine, are you? Did you have any side effects? .... Many thanks Maria. ( do u take anything else with it?)

skinnycappuccino profile image
skinnycappuccino in reply to-Mii

Hello Maria :) Yes, Simponi is a monthly injection - I do it at home with the pen. I haven't had a single side effect in all the years I've been taking it :) I am taking 10mg Leflunomide (Arava) every evening as well. I'd prefer MTX as you only take that once a week but unfortunately I suffered from side effects from it. I think it's standard to take anti-TNFs in combination with a DMARD. Best, Christine xx

Sueymo profile image
Sueymo

I started it on 23rd Dec 2015, alongsiew 15mgs injection of methotrexate and full dose of sulphazalazine and feeling fantastic and no side effects. Good luck

-Mii profile image
-Mii in reply toSueymo

So nice to hear thanks x

LesBev profile image
LesBev

Hi. So pleased to have someone else on Simponi. I had my first injection in October so not reached the 3-4 month stage when the best effects are reached. I am not taking anything else due to horrid side effects. I have not had any side effects on this and this last month have felt a bit better, although the effects do seem to reduce after the 3rd week until the next dose. the pen makes it so easy and pain free to self inject.

I really hope you / we have found the one to help us towards remission! Please keep in touch with news of your journey and good luck.

Lesley

-Mii profile image
-Mii in reply toLesBev

Thanks Lesley would love to keep in touch! Maria x

kalel profile image
kalel

I was put on Simponi by my Dr but was later told by him that if you have a lot of active inflammation in your body then this injection does not always work as well for some people as something like Humira or Enbrel does and in the hospital that I went to they normally give this injection to people that have trouble injecting themselves. Of course everyone is different but for me this injection never worked very well. I hope you get some good results using Simponi. We are all different so the biologics that work for you may not work me.

On a personal note Humira worked very well for me and I was on this drug for a long time and then I had to stopped taking it and since then I have had to look into other methods to treat my ra because biologics don't seem to help with the inflammation that went on in my body. Take care.

-Mii profile image
-Mii in reply tokalel

Thanks for replying to me!

Aless2002 profile image
Aless2002

I've been on Simponi for about 4 years (would have to check with my rheumie!) and it's been by far the best one I've been on yet. Even when I had to inject myself-yuck! (no pre-loaded pen at that time) I was more than happy to keep using it as it worked!! Happily, the pre-loaded is available now.....I am SO interested to read Lesley's comment about the effects wearing off after 3 weeks. I knew I wasn't imagining that!!!! Despite that happening, getting 3 weeks out of 4 feeling pretty much normal is worth it.

Sueymo profile image
Sueymo

I've been on Simponi for 18 months and take it alongside 15mls of methotrexate.

It has really improved my life and am fortunate not to have any side effects. Good luck

Not what you're looking for?

You may also like...

Golimumab

Been two weeks and still not received my injections what’s going on ??? All my bloods were done
deejojo08 profile image

Golimumab (Simponi)

Has anyone got any recent experience with above biologic, I'm so desperate for it to work as my...
premierscfc profile image

Do biologics cause hair loss?( golimumab(simponi)

Does any one experience hair loss on a biologic? Does anyone take biologic on own without...
-Mii profile image

Moderation team

See all
KateL-NRAS profile image
KateL-NRASAdministrator
Donagh-NRAS profile image
Donagh-NRASAdministrator
Nicola-NRAS profile image
Nicola-NRASAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.