difference between humira and remicade

Both are supposed to do the same thing in the body. The only difference is Remicade is a made-protien where as the Humira is a human protien. With Humira you give yourself a shot every other week. So far, after using both, I prefer the Remicade. I didn't mind the treatments as much as I do the Humira even though the Humira is more convienient (I hate having to give myself a shot.

29, 2009 - Rheumatoid arthritis patients who take the biologic drugs Remicade, Humira, and Enbrel do not appear to have an increased risk for developing cancer in the first few years of use, researchers in Sweden report. The study is one of the largest and longest population-based investigations ever into the cancer-causing potential of the drugs, known as tumor necrosis factor (TNF) inhibitors.

On doctor suspects that because I have not taken Humira injection for about a month that it might have played a role in this mystery, Has anyone had anything similar to this or have insight on success and failures from Humira and Remicade, I really appreciate any and all responses and insight

I last had my last Remicade four weeks ago and then tried my first loading dose of Cimzia. I am very ill from the Cimzia. Does anyone know if I could move back to Remicade if only 8-10 weeks have passed. My side effects on Cimzia are comparable to the.side effects on Humira that caused me to stop using the drug. Remicade is only marginally effective now for my Crohns but the side effects are minimal. Any thoughts would be appreciated.

Johnson and Schering have described the drug as the new standard of so-called tumor necrosis factor blockers, a group of drugs that includes Enbrel from Wyeth and Amgen, and Humira from Abbott Laboratories. Unlike Simponi, those drugs are generally injected once every week or two weeks. The drug class works by engaging and neutralizing a protein that, when overproduced, causes inflammation and damage to bones, cartilage and other tissue.

I'm 33 and have psoriatic arthritis and was recently started on Humira. Within a day of starting I had pain in my fingers, toes, shines and forearms (none of which I had before). Has anyone else experienced new joint pain after starting Humira?

Hi just making inquires about the treatment inflaximab treatment for ulcertative colitis if it has helped you and how long before you notice a difference I have only had one infusion and ready for the next one this friday.... I am also on azithroprine and prednosolone and lots of minerals and vitamins and other drugs for gerd etc.

I'm on Remicade infusions and I was told that I was not supposed to use biologics when sick. You might want to talk to your gasto.

My Doctor has not put me on anything yet, she want's me to choose between Humira and Remicade, but the thought of taking either scares me to death because my immune system is already weak.

My sister has psoriatic arthritis and takes Remicade by IV monthly. It has made a tremendous difference in her pain level. We talk often about our symptoms being alike in so many ways. I am just wondering if your doctors have treated you with Remicade?

Just wanted to let you know that I was on pegasys and riba for 24 weeks and remicade became svr with absolutely no side effects at all....everyone is different and react differently to all meds. I have been on remicade for almost 10 years with no side effects and met MANY MANY people who never experienced any side effects and better health. Just to let you know that this wasn't a study.

I have had Crohn's for 40 yrs; 30 yrs on steroids, 10 on methotrexate. Originally oral, 25 mg a week, but last 4 yrs weekly injections of 25 mg. I had a hemi-colectomy in March 09, with 15 cm of my small and large intestines removed. Unfortunately, I then had a big flare in late September requiring 2 weeks again in hospital. I was put on remicade: gastro said I would have only 3 infusions: 0, 2 weeks, 6 weeks, but still had faecal incontinence and failure to put on weight.

Humira is my choice if I can talk my GI into it, I can’t see backing up all the way to Remicade when Humira may do the trick. I had Iron infusions 2 years ago and ended up with clots in my arm so I'm not looking forward to Remicade infusions.

The competition does sell versions of it (Remicade and Humira) but those are just as costly. Humira actually would cost me more. I was hoping there was a different class of medications outside those 3 that can do the same job for much less.. Thank you for replying.

I am sorry that you have chrons. No fun right? Hopefully you will hear from those who have tried Humira. I was on Remicade and it did wonders. I am no longer on it because I have 2 fistula's and had to have bowel resection. But I went from barely could go to feeling really good on Remicade. Good luck, hope it works wonders.

Just as you had built antibodies against the mtx injection you can also build antibodies against the Remicade and when you stop taking it and try to take it again you might have a reaction as you did with the mtx injection. I am so sorry that your chrons is so bad. Also, there are many new products out there for chrons and hopefully one will work.

Hey guys! I was wondering if there's anyone out there that can give me more information on cimzia. Every medication I have tried either makes me worse, or I have reactions to. I created a reaction to Remicade and Humira just doesn't seem to work anymore. I am bleeding more than I have in years and I am only 18. My brother met a girl who takes Cimzia and she is having amazing results. I have, well, little hope that the Humira will turn around and stop working.

My son was diagnosed with T1D at age 22 mos. He is now 13 and in the past year has been diagnosed with Crohn's. He is currently on Remicade, which only seems to treat his Crohn's symptoms for about 4 of the 8 weeks between infusion treatments. The good thing is that Remicade does not adversely affect his diabetes management. We are still looking for a regimen that will keep his Crohn's at bay the entire time between treatments.

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.

ok so i have Ankylosing Spondylitis and my hubby is in med school, he just learned of a procedure (surgery) that puts like a fake cartialge between the spinal bones. and that prevents the bones from fusing together. now i have never heard of it and it sounds scary, like do they cut my whole back open or just little incisions? its supposed to take 2 months to recover and 6 months to be fully back to normal.

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 was diagnosed with Crohn's 9 years ago. I have been taking Asacol (5-ASA) and Imuran (Azathioprine). Last february I was hospitalized for the first time and was put on prednisone. I am still on prednisone and my body won't let me get off of it. My doctor wants me to start Humira, but I am scared. I don't like reading about the side effects and things that can happen when on that drug. Does anyone have any experience with this drug (Humira)? I would really appreciate it.

she had her first surgery last jan. She was on remicade acouple years ago and it was working well for awhile and then it stopped working. now in the last 2 years she is loosing her hearing. she has lost 50% of her hearing so far. They dont know if it is from the crohns or all the meds she was on. Has anyone experienced hearing loss she is now being fitted for hearing aids.

ve been diagnosed with the disease. The first time prednisone worked like a charm. I was taking off and back on it between flares for smaller flares, well the other big one it help a little through IV's but it didn't work. So yeah medicines do stop working. (If i was you I'd see if you can get on a state insurance thing since you do need meds, i'd apply.) But talk to your doctor about other medication such as remicade or humira.

My wife is now uninsurable, and we cannot afford the state insurance (HIPPA) . I'm self employed, and they say we overqualify for the Remicade offered for uninsurable familys. My wife (46 yrs.old) has had this for the past 6 years and has had both knees replaced and it's now working on her ankles and wrists. Without the Remicade infusions I'm afraid that this will get worse and do serious damage to her other joints. Any suggestions from anyone would be greatly appreciated.

I have had two shots of Humira, I constantly have sinus issues, pain pressure, teeth hurt and hedaches. I got them on enbrel and after 9 years it quit working, so tired remicade but after 4 infusions I had such a bad insus probelm I quit it also raised my blood pressrue a lot. I don't seem to be able to handle hard core antibidoics so I can take zpack, and it helps, but I always seem to be back on it alteast every two months.

Difference between humira and remicade

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