ADVERTISEMENT
Advertisement
ADVERTISEMENT
 
Conditions > Rheumatoid Arthritis > Rheumatoid Arthritis Treatment > Medications for Rheumatoid Arthritis
Text Size   Plus   Minus   |   Print   |   Email  

Medications for Rheumatoid Arthritis

There are many different drugs used in the treatment of rheumatoid arthritis. Some are used primarily to ease the symptoms of RA; others are used to slow or stop the course of the disease and to inhibit structural damage. Most of these drugs fall into one of the following categories:

NSAIDsNonsteroidal anti-inflammatory drugs include more than a dozen different medications – some available over-the-counter, some available by prescription only – used to help ease arthritis pain and inflammation. NSAIDs include such drugs as ibuprofen (Advil, Motrin), ketoprofen (Actron, Orudis KT) and naproxen sodium (Aleve), among others. If you have had or are at risk of stomach ulcers, your doctor may prescribe celecoxib (Celebrex), a type of NSAID called a COX-2 inhibitor, which is designed to be safer for the stomach.

CorticosteroidsCorticosteroid medications, including prednisone, prednisolone and methyprednisolone, are potent and quick-acting anti-inflammatory medications. They may be used in RA to get potentially damaging inflammation under control, while waiting for NSAIDs and DMARDs (below) take effect. Because of the risk of side effects with these drugs, doctors prefer to use them for as short a time as possible and in doses as low as possible.

DMARDs – An acronym for disease-modifying antirheumatic drugs, DMARDs are drugs that work slowly to actually modify the course of the disease. In recent years, the most commonly used DMARD for rheumatoid arthritis is methotrexate. But there are about a dozen others that fall into this category. They include hydroxycholorquine (Plaquenil), sulfasalazine (Azulfidine, Azulfidine EN-Tabs), leflunomide (Arava) and azathioprine (Imuran). 

A person diagnosed with rheumatoid arthritis today is likely to be prescribed a DMARD fairly early in the course of their disease, as doctors have found that starting these drugs early on can help prevent irreparable joint damage that might occur if their use was delayed.

Biologic agents – The newest category of medications used for rheumatoid arthritis is that of the biologic agents. There are currently six such agents approved for rheumatoid arthritis: abatacept (Orencia), adalimumab (Humira), anakinra (Kineret), etanercept (Enbrel), infliximab (Remicade) and rituximab (Rituxan). 

Each of the biologics blocks a specific step in the inflammation process.  Humira, Enbrel and Remicade block a cytokine called tumor necrosis factor-alpha (TNF-?), and therefore often are called TNF-? inhibitors. Kineret blocks a cytokine called interleukin-1 (IL-1). Orencia blocks the activation of T cells. Rituxan blocks B cells. Because these agents target specific steps in the process, they don’t wipe out the entire immune response as some other RA treatments do, and in many people a biologic agent can slow, modify or stop the disease – even when other treatments haven’t helped much.

TMills
26 Jul 2010, 19:51
I was diagnosed with SLE and RA in 2000 and osteoarthritis in 2008. I was put on methotrexate by my rhuematologist and had a horrible reaction. He then put me on Remicade and it was working wonderfully, but my liver enzymes rose to almost 1000. Needless to say, I can't do Remicade anymore. I started a new injectable med today and pray it works as well as the Remicade was and that my liver doesn't have a fit again.
Jodi S
30 Jun 2010, 11:37
To Michael Neumann:
I had a similar experience. I have had RA for awhile and was on Remicade for about 18 months along with methotrexate and other meds. Since I got no relief from Remicade I was switched to Rituxan. I had no problems with the first three doses and then with the fourth, about 4 hours after it was finished, I started having seizures, I couldn't control my arms and legs no matter what they did at the ER. I was in the hospital for 5 days and off work for 2.5 months. They put me on so much prednisone in the hospital that it took 2.5 months to get back down to my usual 5 mg per day. Now, nobody will give me any IV RA meds and my insurance won't pay for the injectable kinds. I am on pain meds and still work 40 hours a week as a nurse but I too hope my life isn't as long as most. I won't do anything to end it myself as I don't believe I have the right to make a decision like that, but I hope longevity isn't something I have to deal with either. I'm 47 now and feel at least 90 most days. I just wanted to let you know that I understand how you feel and feel the same way. Keep on going as best you can and our day will come sometime. I am afraid that this new legislation about pain meds that is being discussed is going to cause a lot of us problems as they are putting a lot of regulations on prescribing pain meds. The docs will have to be certified in that area, the patients will have to go to education classes and go to a pain clinic. It will be difficult to have pain meds prescribed and I can't imagine the pain without them. It really scares me but I can only hope that God is merciful and helps in this situation. I just wanted to let you know that you aren't alone in how you feel. God Bless.
Margie
19 Jun 2010, 17:39
I have had RA for one year and before I was told that, I was planning on a very much needed knee replacement. My RA dr said absolutely no, I couldn't have the surgey due to my taking prednisone, CellCote and all my other meds. She said my body might rejec the implant. Just when can I have the surgery? I am in such pain from my knee, and then I have flares once in a while and that hurts also.
Beth
23 May 2010, 10:45
To Stephanie:
So sorry to hear of your plight and at such a young age. I am no expert but from your comment, I don't know why you can't get diasability. Have you worked in your life? If so, you paid for it and you now need it. Try a disability lawyer. They are experts and make sure they don't charge you unless they win your case. Also, appeal you claim. Go to one of their doctors for a second opinion (SSI). Hang in there and remember RA can and does go into remission. Do all YOU can do for yourself...good nutrition, gentle walking and range of motion exercises and feed your soul (rest without worry). Hope this helps.
rob
21 May 2010, 00:22
For men..there is evidence of lowered testerone levels with ra..dont know the cause and effect..but a few wonderful studies show treating the hormone levels and getting them back to previous levels actually puts ra back into remission..please ask your doctors about hormone levels and correlation with pain reduction if levels are brought up?...if anabolics can do this why isnt this better known..and why are we all allowed to suffer when we dont have to?...lets all go back to no pain...and heres a thought no pills???how much will quality of life improve..wow..no pain..no stiffness..no daily medications...poor drug companies would suffer...but wow...life back to normal???keep informed folks..this is actually true
Nancy Beavers
18 May 2010, 11:06
In response to Rochelle, I am using enbrel only and am doing great. 3 years ago I couldn't walk for more than 5 minutes before sitting down because it hurt. I bowl twice a week and am a high school bowing coach and have had no pain. The only time I feel pain is when the weather changes. I do sometimes have a little swelling in the thumb join on the hand I hold the ball in but it soon goes away.
Charles Hodgin
13 May 2010, 14:15
I, like everyone else who reads this, am dealing with RA. I was lucky for a long time as I was diagnosed in 1996 with the desease, but with methotrexate and salsalate was able to work and play without too much discomfort. Last year saw a big change as I started to have swelling joints again and incredible pain and weakness. I worked for the railroad industry as an electrician and found I could no longer perform my job safely. Anyway I have been put on embrel along with prednisone and methotrexate, and am still suffering. Isn't there anything that will take te pain away? My wife, who has fibromyalgia, gets some pretty good drugs for her pain, why isn't something like that available?
Louise
04 May 2010, 23:57
I have tried most meds for my arthritis and I am allergic to them. Do you have any other suggestions. thank you.
Stephanie C.
22 Apr 2010, 22:25
I have had RA for 2yrs now as of 2010 and I just don't know what to do. In 2008 I was a 28yr old healthy woman, well in March 08 my left shoulder "just drop as I worked" curling hair (was a cosmetologist). Well I didn't think it was much until April with weeks of sleepless nights,well with no health insurance I saw a many ER Dr.'s that just said I was havng muscle spasms. Well in May while walking I fell on the groung because my ankle just gave out. Well with more ER visits, no insurance and so many misdiagnosis I finally saw a Dr. that told me that I may have a torn rotator cuff and plantar facitias! Well by this time I am unable to work and in so much PAIN it was horrifing. Well finally after not being able to obtain ANY HEALTH INSURANCE from ANYONE I saw a Rheumatologist and he explained that I had ADVANCE STAGES OF RA that had deteriated the cartilage in my left shoulder, ankle and both wrist! Needless to say this was devestating to me.Well since then I have had to be on methotrexate, prednisone,for the last 7months Enbrel and now the Dr. wants me to go on Orencia. Well again it was a struggle to get the listed Rx above and now he wants me to take something that you have too have insurance for well I don't have an and have been denied for SSI and am really tired of not being able to get help for mself and others that are uninsured.And as if I need anthing else to go out my hip has lost its cartilage and the Dr. said I need a hip replacement! So in closing if there is something that someone thinks will help PLEASE PLEASE PLEASE let me know. It's really hard not being able to care for yourself and not do simple things. But I must sa it reall helps to know I'm not alone and someone understands m pain, my family is and has been with me and throughout the whole process and it means alot.
Sammy Lee Spangler
06 Apr 2010, 18:17
None
Anna
05 Apr 2010, 18:05
Christine,
I also suffer from RA and become discouraged because certain drugs have not worked for me. I understand feeling helpless but there is hope. When I start to feel sorry for myself I think about the fact that there are so many other people out there who are far worse off than I am and that this disease is not the end of my life. lean on the people u love for support and when u are feeling discouraged think of all the things you can do still. If you still feel so down consider talking to someone about it because nothing is worth taking ur life over. Staying positive is so hard but it can also make all the difference. Keep faith.
Christine
14 Mar 2010, 18:30
I live in Australia. Had RA since '92. In and out of hospital since then, having Prednisone drips, etc..Tried every drug going. currently I inject myself weekly with Enbrel, plus MTX weekly by inj, Celebrex Digesics ,panadol etc. ad nauseum..nothing helps. Going on another new Infusion drug hopefully in May, but can't remember the name.can't remember what feeling normal was like, only other sufferers know what this is like... hope this drug will work, otherwise I think I'll take my life, can't take this pain every day anymore...
Tammy
16 Feb 2010, 16:04
I have had RA for the last 10yrs and I've just about tried everything for it. The problem with most of the usual medication for RA, is I suffer really bad side effects. My RA doctor in Australia recommended "Plaquenil" 200mg and "Mobic" 15mg everyday. "Plaquenil" is used for Malia patients, and they found that those patients who also had RA, that there pain was greatly decreased. With most of the other meds,you have to have your blood tested for varies problems that can come about, but with "Plaguenil" no tests are needed. I have been taking it for about 6-7mths and feel soo much better.I do have some days where my hands hurt, but nothing like they use to. I currently don't have insurance, but you can get them at Walmart for $24.00 per script...which is really good without insurance. Also your diet is a major factor as well. Go to webmd.com and they will have you a list of foods to avoid. Try it, and I'm sure that with the meds and diet you will notice a major different.
anny
11 Feb 2010, 01:44
hi, i have RA last 22yrs, right now i am on prednisone 5 mg every day, 400 mg aleve(over the counter)once a day,50 mg enbril subq once a week,,work good with me, i work five 12 hours shift in a hospital as a RN,i stop taking methotrexate about a year ago b/c hair was falling alot,,,,,,,i am taking some indain herbs,i just started i didnot see any change yet, but if i do, i will inform......thanks
Cheryl Betts
09 Jan 2010, 00:13
i was diagnosed of RA last January 2009 and its so hard to stand specialy in the morning because my hands and ankle and knees are all swelling and i cant nothing at home because of the pain,,i was using predisone and Methotrexate for 5 months but my doctor told me that i need to stop the Methotrexate because my liver is elevated so my doctor precribed me an embrel and its been 3 months now that i used embrel but nothing is changes with the pain....anyone knows what food do i need to avoid ?

God bless all of US
Anneli
07 Jan 2010, 00:01
I was diagnosed with RA close to 9 years ago at age 21. Since then I have been on medication but had to stop taking these when we wanted to start a family. In the end we struggeld so much to fall pregnant due to frequent flare-ups that I wasoff methotrexate for close on 3 years. Our baby was born in Oct 2008 and since then I was back on methotrexate but I haven't improved as much as we would like. We want to have another baby but I am currently not healthy enough to be of the methotrexate and not sick enough for my medical aid to pay for biologicals like Enbrel to get me healthier. What are we to do?
toyosi
18 Nov 2009, 11:04
Gd day to you,
please am writing you because my mum has arthritis and both of her knees are swollen in which gives her difficulty in climbing the stairs or working too much.please any prescribtion of drugs to use would do her a great deal.thanks and God bless you real good.
jill
10 Nov 2009, 19:04
It looks like someone was reading my mail. I have most of the symptoms and pain, but no one has mentioned Reynauds. Even in the summer,esp. at the grocery store, my hands turn white then purple then red and hurt. I have read that it is related to RA. Anyone else?
Lately I am in horrible pain in my hands, neck and elbows and the joints on my index finger are getting very large and ugly.
Rochelle
07 Nov 2009, 16:47
i would love to know if anyone has been using enbral with out methetrexate or anything else with it as i have been perscribed it and am worried as i havebeen alergic to everything else
cris
04 Aug 2009, 09:21
i would like to know more about mehotrexate 2.5mg tables orange
Michael Neumann (Missouri)
26 Jun 2009, 18:17
I am 56 and I can remember the pain way back in middle school,(us indians say many moons ago) I tried remicade, worked great for the first three infusions, no pain, no other meds, 4th gave me a heart attack...neadless to say my RA doc took me off the treatment and will not put me on any other meds like remicade, so I am stuck taking prednisone and pain meds for the rest of my hopfully short life.I'm not suicidal but I sure don't want to live in severe pain.If anyone has a secret formula please advise. I would be eternally greatfull.....
toni
03 Jun 2009, 19:18
i have been on all the drugs enbrel, hummira, remicade i keped getting lung infections because i smoke no no i have to quite. i take predison 5mg 1 time day and metrotrexate 2.5mg 4pills 1 time week now dr wonts me to go on orencia i donot hear good things about it.new drug out called cimzia any one on it let me know.thanks
brigitte
18 May 2009, 22:15
Hi Gail

I am on dr. Weil Antiinflammatory Diet. see his website. drweil.com

they really help and i don,t miss the food as much as I thought I would.
apryl
09 May 2009, 09:44
I have been showing signs of RA for years. It runs in my family on my mother's side. I am unable to work now due to the pain and other medical issues. Now I have started seeing a PA that listens to me and understands that it is not just writing me off like many doctor's in the past have done. I don't have insurance now due to the problems but she wants me to get tested. I can't pay for these test. Anyone know how to do this?
Gail Wallace
20 Apr 2009, 10:58
Since RA is a consequence of inflamation in the body has anyone thought about or had any sucess in taking foods out of their diet that cause inflammation? I have been on methotrexate, arava and plaqunial..had slight reaction to humera have a possitive PPD of .8 (TB bug) which has been treated....I am now being considered for infusion therapy. Lynn's entry of March 12th has me alittle spooked about the copay....when you are disabled and on a fixed income you can only do so much...
Janet Washburn
19 Apr 2009, 09:55
I have had RA 20 years and lots of treatments. I had the most success with Remicade,but also take prednisone & methotrexate. I had to give up the remicade as no ins. any longer as unable to work, so I enrolled in a clinical trial for tocilizumab for two years. Otherwise I would be bedridden again. It helped the first year but now I am having severe pain in my left leg. The thing that scares me is this article on TB as I lost an aunt to TB I am one of 9 kids and the only one to get RA. Thank God for that.
Lynn
12 Mar 2009, 09:45
I have been on Arava, Enbrial, Humera, Methotrexate and for the past 3 months I have been on infusion of Orencia. My question is, Is there any funding available for patients with RA, I have a full time job and own my own home, its small and old and in need of so much but it is mine, and my problem is the copay is 165.00 per month and I cannot afford it anymore, I don't know if I have been on Orencia long enough but I have notice absolutely no change, I have the same problems I had before treatment began I am on the lowest dose offered I would be willing to keep taking it if they increase the dose which they are supposed to do if I can get some sort of assistance.
I have spent over 600.00 and I just can't keep doing it.
Thank you for your time
Lynn
David Matthews
09 Mar 2009, 08:31
I have had Rheumatoid Arthritis for approx 15 years and have been on Napratec OP for most of that time, however for the past 4 weeks I have experienced extreme pain in a knee joint both ankles and an elbow, this is effecting my sleep and work as well as making it difficult to do everyday things such as getting dressed.
Would a drug such as methotrexate be of benefit to me
Col
06 Mar 2009, 13:31
Will biologics work for pain if there is not alot of inflammation?
Meena Benny
05 Mar 2009, 13:40
For two years I was a trial patient testing abatacept (orenia), the last drip received December 2009. For the past two weeks I've been in pain. From the specialists I gather this product is not available in South Africa. Please advise who I can contact as to when this will be released in South Africa

Regards

Leave a Comment

The comment function provides the opportunity to comment on the content above.

General comments or questions to Arthritis Today editors and medical experts can be submitted here. Past medical questions and answers are available here.

Promotion of products and services and other inappropriate comments are prohibited and will be removed. If you spot one of these before we do, please send an alert.

All fields are required but only your name and comment will be displayed. Your e-mail address will not be used for any other purpose.

Name:
Email:
Text:

ADVERTISEMENT
Advertisement