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Community > Expert Q & A > Rheumatoid Arthritis > If In Remission, Can I Stop Medication?
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If In Remission, Can I Stop Medication?

Q: With taking injections of methotrexate and Humira, along with naproxen and folic acid, I have had very little joint pain, swelling or morning stiffness for at least three months. Does that mean my RA and psoriatic arthritis are in remission, and can I stop medication, or at least the injections temporarily?  

A: You may well be in remission, but you should not stop medication by injection. The combination of an immunosuppressant (methotrexate) and a biologic agent (Humira) can result in a near-complete cessation of symptoms in a high percentage of people. Your excellent response with very little pain in the joints and no morning stiffness or swelling for the past three months could be classified as a “clinical” remission.

But without the injections, the diseases most likely will come back within four to eight weeks as strongly as before you started taking those medications. Most important, if the disease becomes more active, you will have an increased risk of damage to the joints. I certainly understand your desire to stop medication or use less, but you must balance it with the need to keep the RA and psoriatic arthritis under control, in order to halt the progression of your diseases.

Once a clinical remission is achieved, we attempt to lower the amount of medications while maintaining the remission. I recommend you talk to your rheumatologist about first reducing your dose of naproxen, which is an NSAID. People in clinical remission usually can discontinue their NSAID; because it does not halt the progression of RA or psoriatic arthritis, stopping it does not increase the risk for disease-related damage. Once the NSAID is discontinued, sometimes the methotrexate dose can be lowered next, but this is an individual decision to be made with your rheumatologist. Rarely can a person stop a biologic agent and maintain a clinical remission. 

Paul Howard, MD, Rheumatologist 

xavier
22 Dec 2011, 13:52
?i have ra trying the natural thing that not working but i see on all the natural labels that i am taking it says good for your immune system that not what we want we want to bring it down so we have to do the opposite so that would be like eat wrong get little sleep and over workouts all that stuff will lower your immune system am i wrong or right
Bridget
14 Dec 2011, 20:47
I've been on Humira and Metho for about 2 yrs i hate the meth.It makes me so sick for a few days after taking it and I have no energy at all been off work for the last 2 yrs and cant seem to get any thing done because the way i feel does anyone else have this problem.
VIRGINIA
06 Dec 2011, 19:10
i HAVE STOPPD TAKING THE IM METHOTREXATE AND FEEL VERY WEAK..i AM STILL ON THE PREDNISONE FOR GIANT CELL ARTERITIS AND AM FEELING JUST OKEY.. HOW LONG DOES THE WITHDRAWEL LAST WHEN DISCONTINUING THE DRUS VIRGINIA
jacqui
29 Aug 2011, 14:11
i have been on methotrexate and humira and was doing great then got a chest infection and went on antibiotics so had to stop all other meds and now al my joints flared up and little white spots under skin on fingers and docs says may be gout now so i confused but feel real poorly now
xavier
20 Aug 2011, 12:12
i stop metho & humira after taking metho for 10 years and humira 6 years its now 6 mounth later and it comming back i was hopeing i could last longer i guess it will never go away i was just hopeing eather you die from meds or ra we just have to face the it its a long 10yrs i hope i can have 40 more
May
26 Jul 2011, 06:14
I was diagnosed with RA in 1994 and have tried various Rx. I started Enbrel in 2009 and switched to Humira in 4/2011. The shot makes you symptom free. But you do wonder how long it will last. My doc told me that eventually the med will become less effective, then you switch Rx. Because the infection on the base of my finger nail area, the doc thought that may be allergic reaction. I switched to Humira

I often tried to extended the time between the shots, like once a week and I will slowly increased to every 2 wks. The longest was up to almost 8 weeks (1-2 yrs ago)and the symptom came back. Recently the same redness swelling happened again. I stopped the Humira(Shots have to stop when there's infection.) My family doc prescribed me antibiotic Rx & cream. It took 3 tries of 10 days, 10 days & 15 days to calm the inflammation down. I haven't gone back to the shots since then. Today is the 10th weeks. I still get morning stiffness as usual on my hands when I got up and with some hand stretch, I am OK. Last blood test was OK, red blood cell a bit low. I have anemia all my life and tried to donate blood years ago and got rejected. Dr. prescribed Iron pills, didn't help.

Right after I was diagnosed, I found a wonderful TaiChi master and have been practice since '95. I do about 2 hrs.in the morning and night time 2 hrs in school most of the week. It has helped me tremendously. I try to eat healthy and light, sleep well at night (afternoon nap is wonderful) and stay stress free. Nothing could be worse than the pain I have suffered before. So there is nothing can stress me now a day. I will keep my fingers crossed and counting the days!
Linda Knittle
16 Jun 2011, 22:35
I have been on methotrexate, plaqinil, and arava for 11 years, and have been doing great! now I have to have a bowel resection, due to diverticulitis that will not heal, I was told by my Rhumatologist to stop all of these meds, due to the upcoming surgery, so far I feel great, been off the mtx for 4 weeks now, and the other meds off a week, hopefully I can stay in remission until I get this problem resolved. what are my chances?
Dolores Ramirez
17 May 2011, 14:06
I just started Bee Venom therapy about 2 weeks ago. If you can stand the pain and go to a Doctor that knows what they are doing, it helps with RA pain and energy. Look it up on the internet. That along with eating no sugar, being on a glutton free diet, exercise and meditation has helped me with this awful disease I have had for almost 20 years. I have been on every medicine and they all stop working after a while. I am now referred to Stanford University. I am getting a bike called E3 SX Ergonomic Recumbent to get more aerobic exercise. I think keeping myself leaner is advantageous to my joints.
Carole
25 Mar 2011, 10:30
My SED RATE has hit the roof! 94......

It was 73 and it has jumped up in the last few months. I had been on Metho but was told to stop it as I broke out in a rash on my legs.

I am now with a new Rheumy and he wants to start me on Orencia infusion (Biologic).

I am allergic to soooo many medications, and this Rheumy told me this is the way to go as it is a 1/2 hr infusion.

I am worried about this, as the side effects might be devestating to me. Sore throat, flu like symptons, swelling where the injection (IV) goes...etc. I am a singer and cannot afford to lose my voice.

Has anyone had exprience with this???
Neroli
03 Feb 2011, 19:53
Diagnosed psoriatic arthritis 2004. Tried methotrexate, SSZ with NSAIDS, Plaquenil, became resistant or intolerant to them all.
Stopped eating gluten Nov. 2007 and eliminated nightshades completely in July 2009. Began Humira injections January 2009 when PsA flared up again after stopping other meds. Have taken Humira shots only ever since with remission of both arthritis and psoriasis. Stopped shots for two months Oct/Nov 2010 and symptoms returned so I am back on Humira again since December.
So far no side effects.
Jim Livingstone
02 Feb 2011, 18:38
I was diagnost with rheumatoid arthritis in 1983 and took arthritis Meds continuously thereafter.
My VA Rheumatologist told me to stop taking Methotrexate in 8/2008, after taking it for 5 years, as a result of being diagnosted with Kidney Cancer, and I now don't take any medication for my arthritis. As a result I have put myself on the "No Nightshades Diet" written by Norman Childers, this being "no tomatoes, no potatoes, no peppers, & no eggplant" in my diet. If I CHEET on the diet I will have a bad flare-up within 4-days. I have been on this diet for 2.5 years, and I feel I am in remission.
Jim
EJ
14 Dec 2010, 10:04
I was diagnosed with RA in 2007 and have been on variety of medication trying to get my RA under control. I finally ended up on Enbrel and took it for little over a year.
After I found out I was pregnant in February 2009 I stopped taking Enbrel and have been in remission ever since. It has been almost 2 years and I have not taken any kind of medication.
Does anyone know if I should continue not taking medication as long as I feel fine or is my RA worsening without me knowing it? I really do not want to get back on the medication but I also don’t want my RA to come back worse than ever. Has anyone experienced long period of remission without medication?
Heather
03 Dec 2010, 19:15
I am wondering if maybe I have been misdiagnosed. About five months ago in July, I woke up one morning feeling terrible. The joints in my hands were very sore and my lymph nodes were swollen and my neck was stiff. The next day, I woke up with the same thing and my neck got more stiff throughout the day. I went to the Dr. and they prescribed an antibiotic assuming Strep throat (though strep test was negative). There were a couple of days after that where my elbow was stiff or my shoulder, but that was the only real joint pain I had and my joints never got red or had nodules. My neck, however, continued to be stiff and I would get fatigued every couple of days or so. After several trips to the Dr., I finally got a blood test and my RA factor was 85. My sed rate was normal. I was referred to a Rheumatologist, but by the time I went in September, my symptoms had subsided. He tested me for Parvo, but that was negative and he said he had to assume that I had RA. He said that I was probably in remission and he expected to see me back in the office in about 3 months with a flare up.
Fast forward to December, I have not had any problems in months. No joint stiffness, no fatigue. I have not been taking the Plaquinel he prescribed but I have been taking Lysine (an amino acid). I had one incidence of neck pain again after I got a stomach virus and did not take my Lysine for 2 days. Once I started taking the Lysine, my neck pain subsided.

I thought that RA was a progressive disease and that it gets worse with time. My condition (whatever it was, or may be), seemed to improve with time. I don't know what to think. I go back for a follow-up in a couple of weeks. I'm interested to see what he says.
Judi
06 Nov 2010, 02:36
A few years ago we got a new R.A. doc at the clinic. He said he didn't think I had RA. So he slowly took me off of my Metho.and Hydroxicloriquin. After a couple of months I had a hugh flair up. I had to go back on predisone until I could get the Metho. and Hydro. to start working again. Doc said that had been the last test to see if I really had R A . However, he didn't tell me that little bit of information until I had the flair up. My bones feel like they are hurting now.
vivian
05 Nov 2010, 17:02
hi i have a 6yr old daughter wit JIA,she has been in remission for 20mths and was taken off meth but after 7 weeks she is limping really badly n can barely walk for more than 3 minutes at a time. I have an appt for the doc but its not for a few weeks,she has had bloods tests and her arthritis markers were quite high. Apart from neurofen and physio is der anything else i can be doing to make her more comfortable?
Sarah
23 Sep 2010, 15:01
I am here to comment on the "stoppong Humira and or Methotrexate". I am on meth Humira and Plaqunil. When I was diagnosed in Nov 2009. I started Meht the plaqunil then Humira. I felt better so I went back to work and exercising in July after not moving for 3 years. I felt good on the outside but had a rude awakening when my doctor was upset that I was being so active. She was also expressing her dissaproval of my decline in my blood work.This made me realize I didn't know what the blood work was for and how she could see things wrong on the inside i could'nt see on the outside. So I sought a book entitled Inflamation Nation recommended by another person who has their RA in great control for years now. The author is Floyd Chilton and the book just makes sense . I am going to try the inflamation free diet-lifestyle and ditch the meds for a month. I will follow up with what I find out.

Sarah
Mary Ellen
21 Sep 2010, 13:24
I took Humira for over two years after the Methotrexate, which I took for several years, stopped working. My new doctor noticed that I had no signs of RA on my bloodwork, so we decided this past January to stop the drug and see what happened. I haven't had an injection since January and feel just fine. I have no idea what this means, but it's been a long time since my last remission and this one is much longer. I have more energy without the drug, but it did work for the RA quite well. As far as side effects, constant bloodwork and doctor visits are necessary.
Melissa
15 Sep 2010, 16:22
I was on Humira for 9 months for psoriatic arthritis and had to stop due to Humira-induced psoriasis. A year later, my blood tests show no arthritic signs (remission?), but my hip (original problem area) has deteriorated such that I am having a total replacement next month. Don't know if the Humira actually stopped the arthritis, but I'm still glad I got on and then off it.
Betty Somerville
07 Jul 2010, 20:41
I would like to ask what kind of drug that Humira is???? How does it work, and what are the side effects. I have been taking it for about 6 weeks now. I am worried about the side effects, as the doctor says I need to be monitored (by liver and kidneys.)
thanks Betty
karan
18 Apr 2010, 14:04
I was on Humira for 6 months (after trying MTX and steroids) i was symptom free almost immediately after starting the injection, i ahve not had an injection for 6 weeks as my liver function result has doubled. i am still symptom free and hope i am in remission, will wait and see what the blood test tells us in 2 weeks.
Lisa
02 Mar 2010, 21:38
I have been on methotrexate since June last year and had one shot of Humira--got super sick after that first injection. I have made diet changes and FEEL GREAT, but just got results back and my C-Reactive Protein is up from 10 to 72. Does anyone have any thoughts on this? Why would my scores be high, but my comfort AWESOME? Please advise.
Jim Paradisi
04 Jan 2010, 10:57
I've stopped taking the methatrexate with the ok from my doctor.It's been 4 months.
I feel great.Can you get to the place when you can stop taking humira,injection?Are there any cases when people have stopped everything and stayed in remission?
Wes
26 Oct 2009, 23:30
Well, I stopped Humira cold turkey...I'm 31 years old and I'm sure its probably not the best way to stop treatment. I've been lucky enough to not inject Humira into my body for 11 weeks in a row. I still feel great and have been swimming laps at my gym three days a week...usually 50 - 66 laps at a time. I started swimming for the first time "freestyle" about 3 months ago. Wish me luck that I will continue to have no major RA symtoms. I'm taking probiotics, vitamins, and fish oil. Nothing else for imflammation for 11 weeks in a row....I was on Humira for almost a year prior.
jason w
13 Oct 2009, 18:05
all i can say is this the doctors have us on tnf for them not us all rheumys the same also all drugs they use are the same tnf will kill me soon if i dont find another way this field od medicine is frankensteinish i dont fear arthririts i fear the drugs
Jim
30 Mar 2009, 17:36
I would be interested in a response relative to SSZ. I was taking 2500 mg / day and recently lowered to daily doseage to 2000 mg (2x500mg morning then evening). I get twinges in my joints but no real pain. May it be advisable (upon consultation with my rheumatologist) to reduce further with possible elimination?

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