Experiences with

Enbrel

How has enbrel been for anyone who has taken it? Did you tolerate it well? Not sure why I am having any fear now.... thanks in advance

Hi I’m 44 and I have psoriatic arthritis since I was 23 and psoriasis since I was about 16 I started Enbrel when I was 30 and helped tremendously for 11 years then stopped working so was changed to IMRALDI about 1.5 years on that and i started to have injections site reaction was changed to Benapali

Dear All, I would be very grateful for others experiences whilst on a weekly Biologic prefilled and weekly Methotrexate tablets with Folic Acid 5mg 6 days a week. My daughter is 32 years old and having a Laparoscopy Operation to remove bilateral ovarian dermoid cysts on 16 May. When should she come

c) Price differential between Enbrel and Benepali. Anyone know what the savings are? The list price of originator etanercept (Enbrel, Pfizer) is £89.38 per 25 mg pre-filled pen or pre-filled syringe (excluding VAT; BNF online, accessed March 2021).

I didn't have any major skin reactions, unlike previous biologics Enbrel, Humira which I couldn't continue because of skin reactions. So I am now wondering if this change to Tyenne is causing an allergic reaction/side effect.

I had several biologic treatments , some of which did not really control the RA well… The best biologic was Enbrel (Etanercept) weekly injections. It gave me my life back for 14 years until I had my second knee replacement operation in 2018.

I have already tried Baricitnib, Enbrel, rituximab (allergic reaction). The consultant mentioned adulilumab or Filgotinib. Has anyone got any experience of these drugs? my consultant seemed to think side effects for methotrexate were rare?? Anyway hope everyone is ok xx

Been on Enbrel injection and methotrexate and have all been fine until last year . 2 years.

Hi all, I need to make a trip in 2 weeks to thailand and the travelling time will be around 16 -17 hours. It will also be my first time travelling with the pens, and I'm a bit freaked out. I have the DR letter, the supply and all in order but I dont know which the most efficient way to carry it

The next medication to try was Enbrel. The Enbrel injections were easy and effective for awhile, but Enbrel stopped working after one year. Now my Dr has ordered Rinvoq tablets. I have only been taking Rinvoq for a few days now. Is anyone taking Rinvoq for their RA? Results?

Treatment so far is Enbrel and prednisone. I'm working on tapering off the prednisone, and now down to 10 mg from 40mg daily. I have surgery in a week for torn rotator cuff.

They are: Eliquis, Jardiance, Xarelto, Januvia, Farxiga, Entresto, Enbrel, Imbruvica, Stelara, and Fiasp and certain other insulins made by Novo Nordisk, including NovoLog.

where do I start. For one apologies to you lovely helpful kind ppl on here. Sorry for my lack of time I've been in an alful Place again since Dec this times with on going open sores that won't heal then make don't laugh I've 10 inch of blond hair I'm brunette by the way so big huge scabs for good had

Hey all,I am 39. Last few years have had a period 22 days, 34, 23, 35, 22, 33 etc. July I had 2, one starting 6 days after the other finished. Since then every 2 weeks. I have hashimotos thyroid diagnosed 6 years ago and the past 2 years have thought my levels were out due to severe fatigue, brain

I am 46. I have had a rough couple of years. In lockdown I discovered I had gallstones and a large kidney stone. It was only the gallstones causing attacks. That was removed successfully. I then had a ureteroscopy to remove the kidney stone. This lead to ureteral spasms months afterwards. I then had

Just in case anyone is affected: [i]Class 3 Medicines Recall: Theramex HQ UK Ltd, Evorel Sequi, EL (24)A/41[/i] [i]Theramex has informed the MHRA that some cartons of Evorel Sequi contain the incorrect combination of patches. An error at the packaging site means that a limited number of packs

I started these patches 3 days ago and pretty soon after starting my anxiety was horrendous and has just continued getting worse. I don't know if some of it's in my head but I'm having constant adrenaline dumps and just feel like I have so much negative energy that I can't sit still. Should I push through

**** I have posted screen-shots of recent results from Aug 2024 in the comments. Bit of a cock-up with timings - so it was a non-fasting, blood test taken about 7 hours after I’d had my levo (87.5mcg, been on that dose since April 2024. I’m also on HRT Evorel Sequi patches 50) - doesn’t seem to have

I would be so appreciative if you could help me. I am 37 and recently diagnosed with poi. My doctor has been fantastic and supportive but has openly said that he knows very little about my condition and specifics for helping me with the symptoms of it. Q.1 Could i be on the wrong estrogen? I

Afternoon everyone. So after months of getting nowhere fast, my GP results confirmed that my estrogen levels are very low after my repeat test after 6 weeks. Delighted to finally get somewhere! They have prescribed evorel 50 patches to start. As i expected, they won't do anything about thyroid as the