enbrel versus humira

https://www.hopkinsarthritis.org/arthritis-info/rheumatoid-arthritis/ra-treatment/ It's definitely worth a visit to your doctor to discuss more budget-friendly alternatives.

I am having the exact issue you describe, except I'm on Enbrel. Just started seeing an ENT specialist to try to get to the bottom of it. The Enbrel works for my RA when I can stay on it, but then I get sinus infection and have to go back off... it's a constant cycle. Constant headache behind my eyes and sinus congestion. I take Allegra D for sinus and Bultalbital (prescribed) for the headaches, but it barely takes the edge off. Been dealing with this for years...

Lulu--I used to take humira, which is a TNF inhibitor like Enbrel. One of the rare side effects of both humira and enbrel is the development of MS or MS-like symptoms. I didn't pay enough attention to the warning because it seemed so remote and happened so rarely. However, it happened to me. If what I have is MS, the doctor isn't sure whether the humira caused it, or if I would've gotten MS anyway, but the humira hurried the process along.

I changed to Humira recently and was wondering if anybody has had success with humira who has ankylosing spondylitis. Any feedback would be appreciated.

does anyone know about any new medicine for psoriasis?beside dovonex,enbrel,humira.?

Ok, heres one for anybody out there. Has anyone tried the Enbrel, had no luck with it and gone on to either the Remicade or Humira and gotten results? It's a beautiful day here in the NE and the pup is telling me it's time to get out there! Make it a good day everyone and I will check in later today. Sue & Casey, ha ha!

Recently, the RA flared up and my doctor added Enbrel. I have severe headches and feel like my heart is beating so fast that i get dizzy. The doctor thinks that this is because I am on yet another medication and my body has to adjust. Is anyone familiar with this drug? Has anyone gone as far as to have a second opinion for their RA? I just find it scary to give you one drug to have to counteract side effects with another. Then they add more.

does anyone know if it is ok to take the redipen injection and humira injections at the same time.

now need to decide on a medication and have been giving the chose between the infusion and giving myself shots. My doctors seems to be leaning toward Humira shots. The idea of giving myself shots for the rest of my life is very overwhelming. My mother gives herself shots, and wants the infusion, but cannot because she would have to change medicines and her Embrel is working so the Dr. wont switch her. Does anybody have any insight to which is better.

I am seeing a new dr.next month and may be changing to Humira or Remicade. The Enbrel has helped my lower back and hip pain, but my hands are still swollen and painful. The one other thing that has a HUGE impact on how I feel is Stress and Lack of Rest/Sleep. This past week was very very stressful and today when I woke up I felt like the Tin Man and my hands are still swollen and painful and it's 11 pm.

The doctor has suggested Humira. He is reluctant. Then I have seen and gotten information on Enbrel. I would like to put him on something that is going to reduce the inflamation in his knees. He is 27 and can barely walk at times. In the past he was on methotrexate, naproxyn, something called "gold". None of these seemed to really keep it under control. He has been feeling pretty crappy these past couple of days and I am hoping that he doesnt have a flare up.

Tried everything out there, coal tar creams, Steroid creams, uv lights, psoralens, vitamin b6 injection...what have you. Then I tried Enbrel which gave me hope, because almost half of my body was cleared and after 2 years, I couldn't go beyond any further than a few stubborn patches. Finally I moved to Humira and Oh my my I have a new lease on social interaction. I can now wear my short sleeves in summer.

Remicade is a biologic injection, in the same class of drugs as Humira, Enbrel and Orencia. I have been taking Humira for rhematoid arthritis and it seems to be doing it's job as my rheumy says. It keeps me out of the emergency room with serious flares which had become a habit for me. These drugs are usually reserved for "rheumatoid" type arthritis and getting insurance companies to approve them is not normally easy.

Some people do much better on Enbrel than Humira. If you are having problems and experiencing side effects, it sounds like Humira might not be the right one for you. Please let us know what your rhuemy has to say about what you are experiencing. I hope something helps soon as I know what a misery it is to be in flare.

I am on one shot of Enbrel a week and the doctor I just fired was talking about putting me on Humira or Remicade. Remicade is an infusion medication and Humira is an injectable like the Enbrel. You may want to speak to your rheumy about perhaps trying one of those two. I was in between jobs and had no insurance and had to stop the Enbrel for 3 weeks, within 2 weeks the pain and stiffness was back worse than ever. The price of Enbrel is $1500.

I do get muscle twitches, not as often now as before MTX, but they are there. Had my dr appt last week and have put off Humira/Enbrel for another 8 weeks. It's looming out there, but so far I am avoiding them. MTX is enough!

Ive only had it since 2010 but it was severe at the beginning! Flipped my world upside down. I was tried on Humira and Enbrel. They discontinued the Humira because it was not helping. They discontinued the Enbrel because of side effects. Now I am on Plaquenil. I also get Rituxan infusions.I am on 15 mg of Prednisone but being tapered because I have been on it since 2009 and they want me off it because of the problems it is causing me.

Hi. I've had RA for 17 years, on Enbrel for the last 8.5. I never wanted to go on MTX because the side effects scare me, and I enjoy a few drinks with friends. A new doctor has put me on it in conjunction with Enbrel because I have couple joints which have been causing me problems. Otherwise, I've been great on Enbrel. I am now in my 3rd week on MTX, and seveal joints are really flaring. I find this very depressing.

I took my first Humira shot in my leg on Monday and last night my leg began to hurt really bad. It is a pain that is hard to describe. I told my husband it was a "bone pain" it hurts down deep in the bone from my knee to my hip joint. Today it is hurting mostly in my hip joint.I take darvocet daily for pain and it really isn't helping and neither is naproxen. Is this normal after the first few days of the injection?

Still trying to get the dosages and combination of drugs right and may be going to Enbrel or Humira soon.

Hi, I also have AS, diagnosed in 2007 and have taken both Enbrel and Humira. Neither did the trick for me. Enbrel did nothing Humira gave minimal relief, it did help with my eye symptoms. I have also been on celebrex and several other medications. I was unable to get much relief with any of them, my lower back and hip would just kill me. About 9 months ago I completely stopped taking everything because they just werent helping and I just felt terrible.

I have now been through prednisone, methotrexate, Enbrel, Humara(Humira? sp) then back to Enbrel.......then nothing. The Enbrel worked very well, but I have massive anxiety about the biologics. I just don't trust them and and it's very frustrating. I feel like I'm between a rock and a hard spot. On one hand they really do make me feel better, pain and ROM vastly improved.

I thought I had the flu about 5 years ago.. turned out to be PMR and my joints were very painful.. could hardly walk.. it was in my feet and ankles, knees, and wrists.. anyway I took celery seed and Ibuprophen.. and it went into remission.. yeah! celery seed.. worked as well as the sterioids that others have been on.. and though I have had a flair up .. so has another person I know with it, who is still on the steriods.. so you might want to at least look into the symptoms..

My BD has been maintained by Humira 40Mg weekly and Imuran 200Mg daily for over a year. Prior to that Humira was bi-weekly for about 8 months and Enbrel was used for about 8 months prior to it. All in combination with Imuran 150Mg or 200Mg. During this time I have had uveitis (lasted for about 4 months) followed by gastritis (8 months), followed by strep throat leading to chronic tonsilitis and re-occuring bronchitis flares for 6 months that triggered asthma and now back to uveitis...

I think your best bet is to get a dx and a new treatment plan. If the Enbrel worked, have you tried Humira? There are lots of options out there. I am on methotrexate and plaquenil. I may have enbrel or humira added in the near future but am hoping to avoid it. Before we got to a plan that provided some relief, the pain meds covered up the symptoms. I now take Darvocet and flexeril or zanaflex if I need it instead of every 8 hours religiously.

I had an episode where I gave myself a shot of Humira in my stomach and ten mins later did not feel well. I felt very sick which traveled up my left arm into the side of my head and pain into the left temple into my eye which started twitching. The numbness has really never left except to say that it feels asleep and waking up. The eye twitching has gotten better but it's a twitching that circles the entire left eye.

Also, I forgot to ask this at her last rheumy appt, but how is Remicade any better than Enbrel or Humira? (SHe hasn't been on them, but I just wondered why he chose Remicade.) Any info you can provide would be most appreciated! My daughter is at the end of her rope.

I have rheumatoid arthritis have been on methothrexate since December and am supposed to start enbrel next week. I got very sick the first of March with pneumonia and pleurisy. I took levaquin for 10 days and I still have the pain so the doctor ordered a ct scan. I have a strong family history of lung cancer in non smokers, I have been a smoker for over thirty years. This is my second bought of pneumonia in a year and a half. Please help me with the ct scan results.

Hello, I have severe psoriasis 98% of body its not fun,my dermatologist said he has done everything he could to try to control it but failed.dovonex,enbrel,humira,etc. i have endstage liver cirriosis, he says thats why he can't control it. that i have toxins, my autoimmune system is shut down,i take immune supplements,i detox my body too. use salts(dead sea), sugar ,honey based bodywashes,lotions nothing works.anybody have any ideas? something new?

Enbrel versus humira

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