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Drug Lookup

Before you fill a prescription or pop a single pill, be sure to use this drug lookup to do some research first. You'll find essential information about arthritis medications, including generic and brand names, common dosages, special instructions, possible side effects, interactions and important cautions.

Click on the type of drug here for a detailed chart filled with information:

Analgesics

Biologic Response Modifiers

Corticosteroids

DMARDs

Fibromyalgia Medications

Gout Medications

NSAIDs

Osteoporosis Medications

Sjögren's Syndrome Medications

 

Nancy Rodrigo
15 Oct 2011, 14:48
I've been living with psoriatic arthritis since 1995, I was 35; which very much like RA. Over the years my dx was changed to RA. I've been on all the meds. I became permanently disabled in 2001. I have degenerative disc disease-and have scoliosis from the RA. All my large joints are effected, just had reconstructive surgery to my right foot.

This is horrible disease to live with-and worse without proper pain management. I've read so many folks here who have poorly managed pain. I recommend seeing a pain specialist at your local medical center. There are different types of pain; nerve pain, muscle, bone, joint, skin-with drugs that help them-but you need a doctor who understands this. I go to Beth Israel medical center, NYC, pain and palliative care center.
I do have bad days, but when I have good days, I can walk miles, and be very active. Our quality of life is so precious.
: )
Nancy
sabrina
26 Sep 2011, 21:57
I am 40 yrs old and was diagnosed w RA and Fibro in Jan of this year. My dr started me on Methotrexate, Folic Acid, and Etodolac. I now take 7). 2.5 mg tablets/week of the Metho, and I hardly need to take the additional Eto for pain. I am blessed to say that I only occasionally experience a mouth sore. It's usually gone in a few days. I hardly feel sick at all, and before diagnosis I could hardly get out of bed. I have experienced the low immune system function however. I could not get over a simple head cold that turned into a sinus infection. I had to stop taking Metho for a few weeks while I took antibiotics. My advice to anyone taking meds. Drink alot of liquids with them. This is the best way to help your body pass them and keep your organs healthy. The second is eat a healthy diet. The third is educate yourself. No one is responsible for taking care of you but YOU. Don't expect your doctors to do it. None of my doctor(s) talk to each other.

God Bless
Erin
21 Sep 2011, 12:10
After about a year and a half of sometimes severe pain in my shoulders and other joints I finally went to my PCP and was diagnosed with RA in March. I'm 27 years old. Since I was diagnosed, she started me on Naporoxen but that didn't help the pain. She then put me on Sulfasalazine at the lowest dose, once a day. I am now up to two (1000 mg) in the morning and one at night. It works great and I haven't had any bad side effects (knock on wood!). My rheumatologist is optimistic about how I've responded to the meds but he has mentioned prednisone. I definitely don't want to start on prednisone because of the side effects but he also mentioned pairing the sulfasalazine with methotrexate or plaquenil. I'm in the process of doing some research but if anyone out there has been on any of these two meds, I'd like to know if and how they helped with pain or didn't help and side effects. Thanks!
Sandra Inberg
21 Sep 2011, 10:50
Sorry, I meant: Methotrexate.
Sandra Inberg
21 Sep 2011, 10:48
for those asking about Methothrexate, check this link, it lists all kind of information regarding this medication.

http://www.nlm.nih.gov/medlineplus/druginfo/meds/a682019.html
Allyson Hoff
15 Sep 2011, 04:43
Anne: I feel your pain. I hope you read this and reply!
Allyson Hoff
15 Sep 2011, 04:39
I meant 10 mg of Ambien.Also,Prednisone 40mg
OTC Vit D RX Vit D & is helpful seeing a psychiatrist for depression & anxiety meds. Try my suggestion on contacting Abbott Labs Foundation for help with your meds.Don't give up. What do all think of Methotrexate? I'm thinking about asking my MD about it. Anyone having adverse reactions?
Allyson Hoff
15 Sep 2011, 04:30
To All of you Dear People:
I feel your pain.I was diagnosed with RA 6 months ago. Have your DR.Call Abbott Lab Foundation for those who can not afford your meds. You can also call yourself. They even help those who HAVE insurance. The # is 1-800-222-6885.Good Luck! Does anyone get jittery from Prednisone? I can't sleep even with 19mg of Ambien! Any difficulty with methotrexate?
Please reply!!!
Denise
03 Sep 2011, 14:56
I've been on Plaquenil for 16 yrs, except for 2009 when I started an anti-inflammatory diet.
My hair lightened about 3-4 yrs after starting it. No joke. And I have terrible ringing in my ears, which eased off while I was off it. It takes 4 months to get out of your system when you stop it. I went back on it when I crashed - 200 mgs twice a day. Since I've flared back in July my rheumatologist started me on Mobic. I supplement all that with my "reserve" of Darvocet. I have a terrible problem reacting to medications. My liver doesn't tolerate NSAIDS, so he told my to try Mobic for a month. I'll see how it goes.
Megan
23 Aug 2011, 17:43
I am 33 and was just diagnosed with UCTD, but my Rhematologist is sure it is the early stages of RA. My great uncle has RA, my aunt whom passed away a year ago also had RA. She started me on Plaquenil. Has anyone noticed any strange side effects from this medication?
robert
23 Aug 2011, 10:32
i have extreme pain from arthritus IN my shoulder, knees ,feet, lower back,etc. nothing helps my lower back pain but strong narcotic med's, my shoulder i have taken darvocet for years the only med. to take away the extreme pain, i have a screw through my arm and shoulder.!!NOW DARVOCET IS TAKEN OFF THE MARKET..!!,And guess what the darvocet destroyed my heart..!!I'M HYPOGLYCEMIC and a DIABETIC, I Refuse to stick needles in me,i have been in so many fights and car accidents in my past that i have way too many prior injury's to list,would take all day,'LOL' i suggest what-ever works for you ;;get it;; pot-pills-etc..there are side effects,,i need heart surgery ,12 months ago, i didn;t do it..sick of being cut open,,MY ONLY SUGGESTION IS;; FRESH FOOD,, FRESH MEAT, FRESH VEGETABLES,FRESH FRUIT, FRESH SEA FOOD,NO CANNED OR PROCESSED FOOD, NO PIZZA, NO TAKE OUT FOOD,NO SALT, NO SUGAR, ''NO TV DINNERS ''DO NOT DRINK THE TAP WATER''unless its filtered,NO PASTA NO MACARONI ETC,[[drink spring water]], TAKE CARE ,;.GOD BLESS
Chuck
10 Aug 2011, 11:53
To Judy and all taking things like Vicadin and Tylenol. At my first stages of pain relief, I was taking as many as 20 Vicadins a day, 10,000 mgs. of Tylenol and for a couple of years, it is a miracle that my liver still works and found out that Vicodins are the number One cause of Liver Transplants in California. You can have a pharmacist compound vicodin medication with only tiny amounts of tylenol, but I would advise not using anything with tylenol. I understand fully the need for pain relief, and need for narcotics. But if your own doctor will not help, go to pain management if you can or even ask your pharmacist for the name of a local doctor who helps others with pain, etc. But also understand the costs of these doctors and medications, as so many of us are totally disabled from chronic pain and cannot work. At least I got SSD in 11 months from applying for it, it is something, but lost my beautiful home and so much more in the process. Good luck to all, just be careful
Chuck
Chuck
10 Aug 2011, 11:18
To all,
I have had so much chronic pain in my life, arthritis, in the neck and spine and joints, and so much other that it is too much to list, got sleep apnea and narcolepsy from not being able to sleep, massive pain meds and all the negative things with them, went into anaphalectic shock twice from aspirin, so cannot take any anti-inflamatories as they are all chemically similar to aspirin, had massive amounts of steroid injections in neck and back, and doctors now believe they were the cause of me getting The flesh eating bacteria and lost most of the back of my thigh to that from waste to knee, 41/2 months in the hospital, MRSA 3 times, Staph infections twice and one surgery to remove it. Lost most of my teeth from one med, only have 5 left, am an insulin dependent diabetic, so the infections had something to do with this, and the steroid usage, so cannot ever get them again. Had facet and ganglion nerves burned out of my neck 7 times, a most horrible procedure. Cannot have any kind of surgery as because of risk to additional MRSA infections again, possibly lose more toes, or foot or limbs, etc.

And my reason for writing is, for 16 years I was told to do this by friends and family and didn't until this past year, finally smoked Marijuana and got more and better pain relief than I ever got from any and all the strongest narcotics, up to 360mg of Oxycontin a day, and actually was never a pot smoker in my life(age 54) And since the legalization of it in places like Holland, scientists have developed the most incredible pain relief strains, and not sure about writing about what is legal and not in here, but seeds can be found on the Net from Amsterdam and many other places, and grow guides, etc., unless you are lucky enough to live in a 'legal medical marijuana state', but it isn't hard to find, and you must find what works for you the foremost, and I would suggest trying it to all, it does help me, over the addiction probs with narcotics, and all the negative things with that. Just my 2 cents, peace to all
Chuck
Kim B.
20 Jul 2011, 13:09
I totally understand what everyone is going through....
I was diagnosed with SEVERE RA at the age of 22, 1-month after I had my son. The onset was within 3 days. I had my doctors so shocked, they ended up putting me in medical journals. I have been on EVERY medication there is within the last 8 years and nothing has worked for me. Next step... trials...
judy ullius
05 Jul 2011, 10:04
i take vicadin for back pain but only makes me tired not much help.
Aimee
12 May 2011, 09:44
I have had RA for 13 years (diagnosed when I was 25). Have been on methotrexate with folic acid for the entire time. It has worked wonderfully for me. I have even weened myself down from 8 pills to 5 pills a week). When I was pregnant (both times) and not on any meds at all, I had no problems or pain! The only side effect is it makes me extremely tired. I can't even keep my eyes open but I guess a small price to pay for no pain.
Anne
03 May 2011, 15:28
I was diagnosed with RA in Feb. of this year after neck pain and both knees swelling up to the point I could not walk. I tried 15 mg/day of meloxicam which helped a little bit but I still had "bad" days and have never been pain or stiffness free. My Rheumatologist wanted to start me on methrotrexate immediately but I held off because of the fear of side effects of a chemo drug. One day, my knees were hurting so badly, I called her up and asked her to go ahead with the methotrexate. I have been on methotrexate for 5 weeks now and have noticed a big improvement in my knees with minimal side effects. I take 10mg on Friday nights with dinner and Saturday I am pretty fatigued with a little nausea all day long. By Sunday, I am good to go. I feel that I will continue to improve since it has only been 5 weeks so I am optimistic. For those of you that are afraid of methotrexate, I suggest that you give it a try as I now have days that I forget that I have RA since the pain has become minimal.
Susan
06 Apr 2011, 12:25
Hi Karen,

I was diagnosised with RA last year, I'm 38 years old. We had been down the road with many drugs. My doctor suggested Cimzia, I had been on methotrexate but my body didn't absorb it. Cimzia has really helped me. Gave me back some energy, less pain. I'm glad i'm on it but it is expensive. I have no medical coverage now and I'm not sure I will be able to afford $1716.32 plus all the other medications. If you have a drug plan you should try it.
Michele
21 Mar 2011, 08:47
RE: Cas
OMG! When I read your post it was like I was reading about myself! I have almost everything you listed and the things that I don't have that you do are just swapped out for other problems like asthma and sleep apnea and various others. I go in for my surgery on my neck in April for my "protrusions" and had my endometrial ablation quite a few years ago. I am on 11 various medications daily which I feel is way too much for someone my age (45). And yes all this arthritis and other various disc diseases, etc., are hereditary as I got mine from my parents and there is 90% chance my kids will have it too. I found your post while searching for something my dad can take for his gout since they have discontinued his colchicine. Thank you for letting me see that I am not the only one in this kind of pain every day of my life! Yes it can be depressing. I am on anti-depressants as well (three different kind actually) so I know that feeling as well. You take care!
Roger Sellars
07 Mar 2011, 12:45
I was diagnozed with RA 12-years ago. 10-years ago I was put on Enbrel and it has been my saving. It doesn't work for everyone with RA, but it certainly has for me.
James
26 Feb 2011, 12:00
Iam a viet nam vet I seem to be plauged with joint and spine osteroarthrites ive had a total knee replacmeant and total hip replacmeants both now my lumbar spine is roting away the pain is terrible I take morphine and norco for pain it scares me these meds are very addictive i wish their was some other way.
Karen
08 Feb 2011, 08:42
I have had RA for awhile now. I am allergic to Ibuprofen, Penicillin and aspirin so it limits my choice of RA meds. I tried methotrexate but I had bad side effects. I can't stay on pednisone for a long time because it's not good as a long term solution. Currently I take 20 mgs. of Leflunomide a day. My doctor wants me to consider Cimzia and gave me some literature about it. I was wondering if anyone had tried it and what they thought about it or any other treatments.
edith colon
31 Jan 2011, 08:21
I am taking methotrexate for six weeks. the inflamation of my knees is alittle better. pain is the problem.knees does this med take longer than 6 weeks to take effect
doris
18 Jan 2011, 20:40
Recently diagnosed with arthrittis is lower back and degenerative disc disease. my doctor prescribed weight loss, daily walking, and Tramadol. If I take my medicine as prescribed I am pain free. I am bothered that I may be on pain medicine for the remainder of my life. I suppose i should be thankful that I am no longer in pain and am not so stiff i could not get out of bed. My doctor has told me that Tramadol does not have any long term side effect and should not damage my liver or kidney. I don't necessarily believe him, however. has anyone had any experience with Tramadol?
Cas
18 Jan 2011, 17:39
I forgot to mention i have been warned about steroids, I have the spinal needles of cortisone and apparently any type of steroid will flare up the myalgia.or counteract medications taken for myalgia.Can make it worse...the choice of devils.What to do?
Yesterday i started on the anti depressant Cymbalta which is supposed to help with fibro and musclular pain as well.So looking forward to see if it helps.
Prednisalone on my dog years ago, make his teeth fall out and his quality of life deteriorated so much he had to be put down.
what is it doing to us? long term?
Cas
18 Jan 2011, 17:29
My heart breaks reading all these messages. I felt like the only person in the world experiencing pain so severe I wanted to die.
I just found out last night I have arthritis, so I know nothing yet, and it was an xray I had taken because I thought I had fractured my wrist 3 weeks ago, when I fell into a pile of rocks. Since then my index finger has swollen so much, I now realise its arthritis.I cant use my whole arm or hand very well.I have a spinal disc protrusion L5/S1, and awaiting a neurosurgeon to talk operation.It is hell to live with. It started 4 years ago with sciatic pain,I planned a suicide, and the pain and depression almost took my life, but I did get referred to an excellent psychiatrist.I had a useless doctor! I also have chronic colitis, and they prescribed sulfa salazine which I am allergic to (that was for that condition) so its interesting to see it also is prescribed for OA.So I take nothing for chronic colitis, except iron tablets for anemia from blood loss from bowels.
I thought the anti inflamms (meloxicam)i tried were the greatest drug on the earth, except for the reflux, so I take Lexium and it works straight away to get rid of acid.But I only take the meloxicam sometimes because it makes me bleed more- also have menorrhoea- excessive blood loss from periods. Had an ablation operation which didnt work..
Once your immunity gets low, look at all the new conditions that come.If only we could get healthy from natural remedies so the drugs we take dont lessen our ability to help the body fight.I am really concerned about anti biotics, and refuse to take them, as they lower the immunity so greatly, no wonder alot of other illnesses arrive. I always take inner health when i have had them in the past as they kill all the good bowel flora- acidophyllis replaces.Surely they would weaken any immune system giving way to illness.So build up your immunity.....God this is depressing that so many are suffering so much pain. I had chronic fatigue when i was 26(now 42), but now I believe it wasnt that at all, because my pain and aching now is the same so it could have been arthritis all along.Doctors are pretty stupid alot of times, why is there not a data base of symptoms that they all access from the public like this forum! They should read it, I'm printing and taking to the doc.
I wasted $1000 on chiropractic treatments which did nothing.

But we get sucked right into the conventional medicine path, the drug companies make trillions and so health alternatives are not promoted.Its always the bottom line isnt it?
Has anyone even tried naturapaths and natural healers? We need people to help us who are intuitive. Our bodies are amazing_though it doesnt feel like it. We can be diagnosed from the iris-eye, not 10 different blood tests and other tests.Arthritis shows up in the eye.Our body provides us with its own map of health.I had an iris test 10 years ago and she saw arthritis! Doctors- beat that!
I am now searching for what to do about the arthritis, I dont get to talk to a doc till next week about it, so its pretty scary!!! to be left with this information from the secretary but no advice.I am in so much pain every day, arthritis in my hand is pretty devastating as I work online- typing.So this will be the end of my job if i cant type.I am self employed run my own business.Hours became less because of my neck and back pain.Now more. My mum had everything i have now,she just kept taking more and more medications, she died with organ failure!!! so it seems its hereditary, and my 23 year old son has spondylitis.What a horrible gift to give our children, poor breeding.
A lady i have been talking to has fibro myalgia and she recommended that lyricia.
so thats what I thought I have, now i dont know.All these mis diagnoses I hear about.Maybe i will see a naturapath and get diagnosed properly- the body tells all.
I'm sorry I'm not here to help with drug suggestions. I'm just in the middle of a big pain pool feeling crippled and hopeless with no clue yet, bit scared and just needed to talk to someone.One thing that helps me to walk and feel ok is a muscle therapist. After I have treatment, I am mobile again, and can get out of bed in 5 minutes not 15.My hips seize up most days and I am stuck trying to get out of bed before wetting myself! She is really someone who does help and i think fortnightly or weekly treatments fix me more than anything I have ever tried.
Please dont give up people there would not be these illnesses without a solution, in the balance of life. we just have to find it.
There is a reason for everything, and hopefully we can help each other. There IS a VERY good reason we are here. Louise hay and others cured themselves of cancer, so with the right tools, we can beat this.
Star
05 Jan 2011, 20:31
Tammy:

Maybe you have ankylosing spondylitus. Its a rhuematic disease without the rh factor. The symptoms are the same as rhuematoid arthritis. It can take up to 10 years to be diagnosed and sometimes never. I know because I am a 56 year old female who has been diagnosed with it 1 1/2 years ago. I was lucky enough to go to a doctor who knew about it. Its worth checking out.
Becki
19 Dec 2010, 13:05
After reading about everyone's experiences, I feel so bad for everyone.

I was diagnosed with OA in spine, knees, ankles, feet, toes, wrists, well everywhere, but most severe in lower spine and knees. I am to the point that I can't do anything for myself and my husband has to do all the housecleaning and cooking and errands, plus help me with a shower and even walking.

I am in so much pain I can't take it, and all my Dr. will say is to take ibuprofen. It doesn't do anything to take away the pain.

I am ready to just give up. I don't have any insurance as I lost that when I could no longer work. just at my wit's end.
Elisa jarman
16 Dec 2010, 04:10
GET OFF ALL THE MEDICATIONS!!!!!

I was on over 36 pills a day for Lupus, Fibro, Diabetes, and all the symptoms they cause. I did my own research and found multiple herbs that cure and take care of the pain of all of them!!!!!! Look up Neem oil for your skin problems Neem leaves to cure Lupus, Fibro, Diabetes, Cancer, and even AIDS!!!!!
Arnica, mugwart, aloe, chamomile, and emu oil help relieve the pain naturally.

I make my own soap and lotions because they do not have all the chemicals that the ones you buy in the stores do! THEY use LYE to make soap. Cos-tic LYE. Most of our illnesses are caused by what we eat the fertilizers they put in our food and the hormones they give our meat. Even to feed chickens cyanide in small traces so they lay more than one egg a day!

Don't believe me...... do your own research. Please do yourself a favor LOOK UP NEEM and see what it can do to relieve your pain! You can even grown your own tree, they grown quickly. So you don't have to pay anyone to heal you! good luck in life and I pray you are healed!
LESLIE C
19 Oct 2010, 12:23
I WAS TAKING ENBREL FOR 10 YEARS, WITH ALL SYMPTOMS OF MY FIBRO AND PSORIATIC ARTHRITIS GONE. IN 2008 I WAS DIAGNOSED WITH STAGE 3 MELANOMA AND HAVE BEEN OFF THE MEDICATION FOR 2 YEARS, ALL OF THE PAIN IS BACK AND THE DOCTORS WONT LET ME TAKE IT BECAUSE IT SUPPRESSES YOUR IMMUNE SYSTEM, DOES ANYONE HAVE NEW SUGGENSTIONS AS TO WHAT I CAN TAKE THAT WORKS?
Jitendra
15 Oct 2010, 03:21
I have RA since last 3 years but I am comfertable with drug " Methotrexate " 2.5 mg one tablet/ 3 days ( 2 tablet in a wek ).I got too much relief after using this drug.Now I can work all my activities.I do not fill any side effects.
Robt
22 Sep 2010, 15:33
I take Limbrel.. You need to google it. It works, 80% of my pain is gone.
brenda price
04 Sep 2010, 08:19
I was told by my doctor to take the methotrexate to mainly ward off the deformity that can occur in the future. Is that true or does it also have another purpose?

Also, have there been studies done on the RH factor? on how it affects different people versus how high or low it is? The reason I ask, is mine is always the high 600's or low 700's and I am always asked how severe is my pain. I feel myself fortunate for I am usually not in pain except when I have a flare up about three times a year.
Rajan.S.
24 Jul 2010, 09:47
I have suffering of R.A.from Nov 2007.
And also suffering of G.B.SYNDROME from Mar 2008.At present My Doctor prescribed the following medicines for R.A.
1.Calcium Tablet 500mg -1/day.
2.Folic Acid.....5mg. -1/day.
3.Misprosto 100mg with
Diclofenac
Sodium 50mg Tablet...-1/day.
4.Sulfasalazine.u.s.p.1gm-Tablet-1/day.
5.Methylprenisosolone.ip.4mg.Tablet-1/day.
6. Physiotherapy 1 Hour/day.
Now i am recovered 70% from R.A.
Please suggest how to recover completely from
R.A.
Regards,
S.RAJAN.
Bernadette Carter
21 Jul 2010, 11:28
I've just been dianosed with seronegative
r/a, as you can tell i dont know a thing
my doctor is putting me on mtx 2.5 mg
also folic acid.what do you think,here's a little background. i've been going through this for at least 20 years i'm always in pain
in one place or another. the pain used to last for maybe 2 weeks now the pain last for a month or more, nothing i take helps. all of a sudden my hands decided to go up on me
and wont let go, i think my legs are going
up next.can you help
Kimberly Simmons
08 Jul 2010, 09:01
I have had fibromyagla for 13 years now and it get worse with each passing year. I have been on oxycotin for over 2 years for the pain its the only thing that helps me get through the days. I have to set my alarm clock one hour ahead of time to get up and take my meds. just so I can get up out of bed. My pain is so bad most days that I wish I would just die!! I sit and cry all the time because I hurt so much all over my body. I have had injections tried all medications everything there is for my condition and all that helps is pain medication. I am now addicted to it but I have to take it in order to get through the day and work. I can't afford not to work and my meds cost me around $1,000.00 a month.I am now in looking for a pain clinic to take me because I have no insurance and can't afford that eighter.Will the pain ever stop and will I make it through another day?
Carley
22 Jun 2010, 14:40
I was just diagnosed with RA about a month ago. I started getting symptoms when I was a senior in high school, just 17. I had pain in my right big toe, feet, and my left index finger. 3 years later at 20, my rheumatoid factor was positive along inflammation in my blood, and everything hurts. I have slight erosions on a few joints, but nothing terrible. My neck started up a couple weeks ago, which really scared me. My rheumatologist put me on methotrexate and I just took my first dose yesterday. He never told me I had to wait to take the folic acid the morning after, nor do the directions on the pill bottle. I took it along with the methotrexate, but now I'm reading you're not supposed to take it the day of. I was wondering if this is true, or if it matters, or what. If someone could let me know how they were told to take it, that would be great!
Fernando
20 Jun 2010, 14:03
can ANYONE tell me their experience w/ Anakinra ( Kineret)?
MARTY
18 Jun 2010, 19:34
i want some info on ropinirole
ba
04 Jun 2010, 17:09
My daughter got RA at 23. I research the antibiotic therapy for her, and begged the doctor to give it to her for months. She was finally put on minocin, and she was free of pain within 2 years. She is still going strong. Check it out, especially for the newly diagnoised cases.
Karen
03 Jun 2010, 17:17
I'm on my first month of Actemra. Other RA drugs stopped working although Orencia worked well for two years. Take methotrexate, Ultram, azathioprine, Meloxicam, carisoprodol, Ambien AR, metropolol, Folbic, etc., etc. Continue to work full time as a high school teacher so the stress is overwhelming right now. Aleve Arthritis helps. Mornings are difficult, especially since I have to get up so early. Had neck surgery last year and that helped. Two days after the Actemra injection, I had the best sleep in years but I've been in lots of pain since then. I hope the second dose is better.
Michele
03 Jun 2010, 15:23
Hi Barb!
I too have OA in every joint in my body,my elbows and knees being the least painful of the lot. I've had OA for about 10 years now. I'm 50. It started in my hip and now after 10 years I have it everywhere! I've had surgery to replace worn vertebrae in my cervical spine but after 4 years the pain has returned.

I can definitley feel your pain! I was on 800 mg of Ibuprophen 3x daily and Vicodin for breakthrough pain.

My PCP now discontinued the Ibuprophen (alot of reflux) and started me on Ultram. It seems to have changed how I perceive pain but if I overdue it walking or sitting or standing it has no effect whatsoever. That's when I cry.

People, including doctors, have no idea what or how this pain feels unless they have it themselves. It's debilitating, it's depressing, it's disgusting.

I do feel your pain, honestly!
Brittney Urban
22 May 2010, 15:26
I am 17 years old and I have Juvenile Rheumatoid Polyarticular Arthrits. I was diagnosed when I was 2 years old. I've defintely had my fair share of flare ups and swelling. I have been on Methotrexate both orally and by injection. This has defintely been a big help but it was terrible side effects, mostly causes a nauseous feeling. Any suggestions on how to stop them??

Brittney Urban
barb
10 May 2010, 22:25
i was diagnosed with oa about a year ago im allergic to nsaids and almost all antibiotics . my doctor has me taking vicodin 500 mgs twice daily and predisone 5mgs once a day. most days this works but somedays i cry from the pain.i am very active and cant function somedays cause i have oa in every part of my body. has anyone else had systoms like this
Jacquie
27 Apr 2010, 14:14
For over a year I have been a "mystery patient" horrible joint pain everywhere in my body, all tests came back negative. Finally went to Cleveland Clinic and was diagnosed within the hour! pseudogout or RS3PE. I'll know more at my followup in4 weeks, but wanted to mention that the Specialist put me on COLCHICINE and within days I am feeling better! its amazing and no side affects.

good luck all
Tish
20 Apr 2010, 10:51
Follow up on my comment of May 19 2009. Now nearly a year later. The generic doxycycline brand I was taking decided to reformulate and again my joints started aching and the Rheumatoid Arthritis started to attack every joint in my body. I quickly switched to the BRAND Vibramycin, doubling the dose to two 100 mg per day capsules, and within two months things were getting back under control. After two months I started alternating months between a generic minocycline - one 100 mg capsule per day, and the Vibramycin - one 100 mg capsule per day. Every week I could see improvements, and finally a week ago I noticed that the last hold-outs, my weak wrists, had regained their former strength. I have virtually no symptoms of RA at all. NONE. I can make two fists, (ok...the index finger in my left hand has the tiniest vestige of some stiffness when I curl it up), I have zero joint pains anywhere, I have plenty of energy, can sleep soundly with no pains. Life is good. I know that the demon is lurking inside me just waiting for me to take the wrong pill (should the manufacturer do a reformulation or my pharmacy switch generic brands), but at least I know to look for the symptoms and quickly switch to the BRAND while fining another generic. The reason I switch is this: Minocycline is the drug of choice. It is better able to get deep into the joints. But it can turn your teeth a little greyish after years of constant use. So I minimize those side effects by alternating with it's half-sister drug, Doxycycline (I use the brand, Vibramycin). No side effects, but since I have to buy the Brand product, the price is very high (my health insurance will not cover much of anything when it comes to prescriptions, so I am lucky these work). I feel wonderfully fortunate to have found out about this antibiotic treatment as soon as I was diagnosed, and also lucky to have a Rheumatologist who is willing to prescribe it, as long as it works. When I read about the hazardous possible side effects of other treatments, I just shudder.
Billie
20 Apr 2010, 09:43
This is my first visit to this site.

In October 2009 I was diagnosed with lower lumbar degenerative disease. Since then I have also been diagnosed with OA, restless leg syndrome and ocular roscea, and in the care of a primary physician and a rheumatologist. Currently my meds for OA include: Hydrocodone and Meloxicam 15mg - both as needed. I cannot take Celebrex as it is a sulfur-based drug and I'm allergic to that type of drug [tightness in the chest and severe indigestion]. Has anyone had experience with taking Meloxicam for OA? It would be most helpful to hear from you.
Jane
19 Apr 2010, 14:21
Anyone out there with good/bad experience with Celebrex?
Thanks.
Brenda
11 Apr 2010, 19:31
I was diagnosed with RA last Nov. I am nearly 68 so feel fortunate it waited this long to appear. I am currently taking methotrexate, 15mg a week. I have had a few very painful "flare-ups". I find that a little marijuana is the most effective drug with, the fewest side effects, that helps me feel like getting up and moving.
Teresa
09 Apr 2010, 09:17
I have platued out on everything,I will be starting a new drug in 30 days ACTEMRA.Don't know if I can go that long - terrible pain all day, every day, I have to work to keep health ins. I do everything I can to stay mobile.I am scared.
Teresa Fusco
Mari
09 Apr 2010, 07:45
Hello: I feel very sad while I'm reading all these stories. I have been diagnosed with RA since 2008 (30 years old)and the whole year was horrible because of the lot of pain I was feeling all the time. Now I'm a littler better because of med (methrotexate 15 mg/weekly inj)but every single day I'm in pain. I feel tired all the time and my mood changes a lot.
I was using relafen, prednisone, ibuprofen, folic acid.My Dr want to try another treatment with Rituximab but I don't becuase I want to have a baby soon, so I decide that I just going to stop any medication at all.
Jane
01 Apr 2010, 08:21
I have RA for 4 years unresponsive to other meds. I just started on ACTEMRA. So far no reaction except for a salty taste which I am not sure is connected or not.Does anyone have any experience with this med?
Maria
24 Mar 2010, 23:15
Just diagnosed with Osteoarthritis (erosive) and the rheumatologist has prescribed Methotrexate 5 mg once a week and Folic Acid; why not first try less powerful med? this drug scares the living daylights out of me with all its possible side effects like headaches, I suffer from migraines already! He ordered chest x ray and hepatic test also and said would not require me to take the med until after those results but he did not give me any choices of meds, I truly feel I may do alright with swimming, diet changes and milder drugs. I have such anxiety since the diagnosis I am thinking of a second opinion as to the treatment drug.
MARC
19 Mar 2010, 06:13
Hello Again

I started taking Salazopyrin (sulfasalazine) last night for the first time, only 1 tab though.

What can one expect taking this drug, felt a little dizzy sometime after.

I am also on Lyrica twice daily, venlor once daily, tripeline once daily, zopivane at night, some quinine based tab once daily, MTX 1ml(25 mg) inter muscular once weekly and tramal or tramcet as require for pain.

One hell of a mix, as what to expect with the new tab I do not know.

Had RA now (diagnosed properly) since 2005/2006, I missed the two year window though, my fault.
At 41 this really gets to you sometimes, been bed ridden on two occations and in hospital twice as well for the RA.

I had to change jobs to suit, no longer on the floor but in the engineering office (company helpd out a lot)of a aircraft maintenance organization, large aircraft.

By far the RA is worse now than in the begining.

Hope new cocktail works.

Regards,

Marc.O
Anne
11 Mar 2010, 00:10
I have been takeing 25mg of Methotrexate once a week and 5mg of folic acid every day for the past 2yrs,for RA
When I started I couldnt walk unaided my husband had to lay me down in bed as I was unable. I could not even pull up my doona if I got cold at night.I was seriosly thinking my future was not worth it,but now I am 99% pain free.I do have a slight curve in my left fingers but slowly they are getting straighter.I'm not having any side affects but I always have my monthly bloods done so my doctor can keep a good eye on any changes
Gary Clausing
28 Jan 2010, 17:21
My doctor just gave me Limbrel to try. A food supplement that's not OTC? Anyone tried this yet?
Georjean McKeeman
22 Jan 2010, 15:12
I liked it better when you printed the drug guide in the magazine - it was easier to compare the analgesics and the NSAIDs. Because of reduced kidney function, I have been taken off any NSAIDs and put on Tylenol, which does not fully take away my pain many days.
Betsy Beck
17 Jan 2010, 18:27
Is anyone taking Limbrel? Can you tell me if it is working and if it has any side effects?
bonnie
15 Jan 2010, 23:22
was diagnosed w/ ra when i was 16 or 17.now 32 married and mother of 3 energetic and brave little men..9yr and 5yr old twins.it has been getting very hard for me to do simple things that iwas able to do before.ihad my first hip replacement in 2002 very thing was fine fora couple of years till 2008 when i was having trouble walking.i saw a dr where i live and needed to get a hip revision because my hip socket was dislocating.in feb 2009 i had my surgery it was the worst 7wks of my life.i was away from mykids because of complicaions.now still suffering but hopeful with all your stories ineed to try to be openmindedand rely on the dr to give me what i need to be here and watch my children grow.i will be starting on remicaide therapy next week and i am scared to death.i am on 7 mg prednisone and that is pretty all that iam taking for my ra.i thank everyone for your comments i hope i helped.this website has been a good vent for me its a blessing from god that there is so many of us and that we are not alone.please everyone keep up with your hopes and pray to any faith that you belive which gotten me through so much
DonnaMarie
15 Jan 2010, 22:53
Hello everyone!
Last year I was experiencing some very bad pain in my back and body.. I have fibromyalgia, chronic fatigue. I was put on Tramadol, and Lyica from one dr.. Then i was refered to a different dr and was told i have sever arthritis in back back and hips so then was also put on lodine and plaqunil. so four different pain pills some days they help but some days they don't. Does anyone have any advise on what steps to take next? oh yes I am also only working pt and started working out. So sick of being in pain and stiff all the time. One dr said next step may be medical marijauna, not sure if I want to take that step or not. Iam also have applied for SSI and have been denied. Any help would be greatly appereicated. Thank You, DonnaMarie aka always in pain
Peter Mason
14 Dec 2009, 06:26
I have RA in my kneck, shoulder and wrists, I have had a knee replacement which is great, I have joined a Gym for gentle exercise and to reduce my weight. I am on Tramadol and paracetamol four times a day which give me bearable relief, I also have PMR which I take prendicalone, and it was amazing the results in six hours were fantastic, except you have to live with the side-effects. Does anyone know if vegetable and fruit juices help, I have tried cider vinegar and the Hayes Diet, not much good, although to be fair the Hayes diet is not easy when you live on your own.
Curt
04 Dec 2009, 08:38
OOOPS!!! Sorry, I mis spelled the meds, "OXAPROZIN".
Curt
04 Dec 2009, 08:35
OOps! Sorry I forgot to mention that I've been taken the meds for over 6 months/ sence May 2009. I have a good dr. and he knows that I lost my job for this and he has helped me get through this.
Curt
04 Dec 2009, 08:01
I currently take "OXYAPROZIN" the generic of "DAYPRO" and I am conserned about the side affects, so far the only ones that's noticeable to me at this point is that I am gasy!!! I have noticed no other side affect. This really does help with my arthitis, when I get up in the morning, I feel fine, I can walk again. I was told that I have "ORTHOARTHRITIS" and it is in my right-left ankles, left knee, right hip, right shoulder. I am only 45 yrs old and I'm still trying to get a hold onthe fact that my body is giving out on me, this "SUX". I don't know what is going on inside my body, but I am waiting to see if anything else is going to happen, me and my body have a pretty good relationship.
Sunnie Joy
20 Nov 2009, 12:00
I have been on Plaquenil 400mg daily since RA diagnoses 1yr ago.The results have been pretty good,until recent "flare" alot of pain in feet bones,ankles,hands,etc.the recurrent episodes of pain are hard to deal with .I dont care for the pain meds & cant take NSAIDS with Zollinger_Ellisons Syndrome.What else would help get thru these episodes.
Warm water swimming at a local high school $2 a day three times a week has been a Godsend.But not during this... Anyone have any suggestions ?
linda j
27 Oct 2009, 18:34
I have been diagnosed with accute RA, Fibro and osteoAR. I have been on prednisone 4 mg bid since 04/09. It was like a miracle drug for me. I was actually able to hold a spoon a mug of coffee with only one hand. I have recently gone thru a divorce and I think the stress has caused a really bad flareup. My Rheumatologist has just prescribed methotrexate. After reading the internet blogs, the patient blogs and the medical info brochure... I am scared to death! I am only 57 yrs old, active and am afraid to take a drug used to also treat cancer patients? Please send any advise. I am looking into antibiotic alternatives and will let you know about that.
Natural
16 Oct 2009, 09:11
I have been on every drug in the book for RA. I have never been given antibiotics. I will certainely ask my doctor. I haven't had the pleasure of being pain free since being diagnoised with RA in 1997. I have had 2 knee replacements. 2 being twice on both knees. Big mistake because the pain and swelling are more intense. I currently take prednisone 10 mg BID, Sulfasalizine BID, plaqenil, Methotrexate, Remicade Infusion. I am taking myself off the Methotrexate because I am losing my hair. Also I am on the cancer drug Imuran. I'm sorry I only have a temporary fix with the Remicade I get every 8 weeks. I was in the middle of a career in entertainment and it hit me. My mother suffered with it for 20 years and because of several combination of medications, they destroyed her liver. Going by statistics that RA usually affect the youngest and oldest, which neither I am, but when I was told I had it, I went into depression and some times now feel I still am. I recently had surgery to repair my right wrist. Now my left ankle and foot is bothering me. It stayed swollen for months. I got a cortison injection and it went down but my weight went up. I've been dealing with my weight for years because of the Prednisone and the steroid injections. I am happy that I came to this site because I have learned a lot from the comments here and will continue to read and give my testimony. Anyone wishing to share can send me an email personally at bettyeb@clayton.k12.ga.us I am getting married next year and need to lose 35 pounds. I will make sure to stay heart healthy. These insurance companies are terrible with paying bills, yet I continue to move forward with faith that one day I will be pain free before I leave this earth. Dreaming...Right? Take care!
Leslie
22 Sep 2009, 12:31
Hi I'm 29 and diagnosed with Reactive Arthritis. My sed rate and CPR were very high and I was sent to a Rheumatologist who prescribed Indomethacin and Plaquenil.I've been on those meds for over a month now and I don't see a difference. I still feel a lot of pain in my feet (heels) and I got the sausage toes. I had an MRI done because my neck was getting stiff and had lower back pain. Those results came back saying I have bulging disks in my neck and back. Does any one have any advice?
Pam
09 Sep 2009, 13:37
Janet--I had gastric bypass surgery so medication for me is tricky. I either have to take Tylenol (which is not that strong of course) or a narcodic (not productive at work nor do I wish to become addicted). I am having success with Tramadol HCL. 50 mg will take enough of the edge off to allow me to function at work, drive, etc and 100 mg will take my pain away but will make me tired. Might ask your doctor his/her opinion of Tramadol.
Pam
Julie
07 Sep 2009, 12:28
I am 37 yrs old and recently had a child in December 2008 by February of 2009 I started swelling in my hands and feet. Tests have been run many times to try to figure out what was the problem. All tests come back with signs of RA then I was sent to a rheumatolagist for more tests. I was given Prednisone 5mg taking 1 tablet a day, Methotrexate 2.5mg once a week 8 tablets 4 in the morning 4 in the evenings. The doctor is trying to take me completely off of the prednisone. But then she seems to think that I need to go to the next level by taken other medications with injections like embrel,etc... I really do not want to do more injections since I have been a diabetic since I was 12. I am on an insulin pump for that these sticks are bad enough I dont need more...Can anyone help or give me any suggestions on this please ??????????
jesse swann
20 Aug 2009, 22:07
this message is for tish if your reading any of these postings im very interested in what you have to say my husband just got diagnosed with RA a couple months ago and they wanted to put him on methotrexate he is 29 years old and in pain everyday i want to help him in any way i can i dont want him to take this medication do you think the minocin will help him.
greg klinker
20 Jul 2009, 20:24
I have had type 2 diabetes for the last 6 years. I am taking metformin [1000mg daily]actos [45 mg daily] simvastatin [20 mg daily]. Recently diagnosed with arthrirtis. What prescription/over the dounter meds can and should I take. aleve works well but according to the label 10 days max. What is best?
janet
17 Jul 2009, 15:32
I have just been diagnosed with moderate osteo arthritis in the knee and i am difficulty coping with the pain, i take co-codamol and ibrufen, any suggestions please fo alternative pain relief.
Yazmin
15 Jul 2009, 20:00
I'm 29 years old and was recently diagnosed with RA. RA factor came back at 1000....extremely high. Doc prescribed Methotrexate and Prednisone....he told me about harmful side effects to liver, lungs and kidneys. Is there any other medications which I can take...that are not as harmful on organs??? Maybe something natural?
Please help
Yazmin
15 Jul 2009, 19:56
I'm 29 years old and was recently diagnosed with RA. RA factor came at 1000...extremely high. Doc placed me on Methotrexate and Prednisone....side effects seem very harmful. Is there any other medication that I can take, that is not is not as harmful??? Maybe something natural instead? Help
Marie
13 Jul 2009, 13:29
I have Fibro & OA. I tried everything on both subjects, and nothing seem to work. My doc put me on Armix and so far so good. I was Savella for a week and started to get bad stomach pains. I am taking Lyricia, Cymbalta, flexeril, Skeletain. Nothing seem to help me except Marijuana. It helps my muscles to relax, and I feel comfort with it. It lift me up, where I can do my chores, like vacuming not so painful. Alot, people do not understand this is a natural drug, and helps alot of people with all kind of chronic pain..They use it for cancer patients. Why not Fibro Patient?
vickie
07 Jul 2009, 09:38
ok i had a stint put in for my heart in january sence then my right leg has bothered me bad at times and some times my left now i have to go to another doctor this doctor is saying i may need a stent in my leg meanwhile my doctor has given metramadolfor my other aches and pains i know i have arthritis but is this a good drug and does any one know why all of a suddenly mylegs are aching he said poor circulation butwhy they didnt before thanks vickie
Kamary
25 Jun 2009, 09:58
I am a 25 y/o and very active. I have apparently had RA for years and was finally diagnosed in early 2009. Multiple procedures done for years; trigger finger surgeries, cortisone shots in fingers. I started mtx, plaquenil, clinoril, remicade infusions, and predisone. The dr. tells me i am atypical due to the severe affects on my lungs, pleurisy. Still no pain relief. Just trying to figure out a baseline at this point.
Joyce Lancaster
23 Jun 2009, 21:09
I Have Cerebral Palsy and take Naproxen it's good you print the side effects Some Dr's over prescribe meds.
Debbie
21 Jun 2009, 18:29
I too am interested in the supplement that Carla is talking about, but seems to be omited from her 5/9 post. Could you please let me know what it is. Anything is worth a look at when it comes to RA.
tammy
17 Jun 2009, 15:18
I have been dianosed with arthritis about 4 years ago and DRS. said I had rhemotoid but since then been ruled out, when I first started having symtoms I was having pain everywhere , DRS. put me on prednizone and plaqunil the medicine has helped me get back to my life but still dont know what kind of arthritis I have test after test.Does anyone else have this problem?
Catheirne
13 Jun 2009, 13:49
Has anyone had an experiences with Simponi or know where I could find some patient reviews?
Lois Ciaburri
11 Jun 2009, 19:54
Can anyone tell me if they have taken rituxin and what there experience was with it and also arava i have read about people who have taken it losing hair and teeth and internal bleeding can anyone tell me about this
Lynn Olive
06 Jun 2009, 14:48
I was diagnosed with RA in 86. I am now almost 62. I was on a pill form of gold for 10 years before I went out of remission. Since then I have been taking plaqunel. I am now experiencing pain and swelling in the balls of my feet and my first finger joints. I also have a new Rheumagologist. He suggests methotrexate. I also have congestive heart valve, my second mitral replacement was 9 years ago, and a pacemaker/defibrillator. Too top that off I was diagnosed with Celiac disease two years ago. The side affects of the methotrexate scare the heck out of me. I am trying to see what other options I may have.
Linnell Naughton
01 Jun 2009, 18:38
why doesn't carla say which..natural supplement helped her so much.It may help others, can she share please?
Robert
26 May 2009, 15:43
Hey.........I'm 79 and have been the Naid route, then Hydrocodone and now Oxycodone but, 4 - 5 times a day and the side effects!!!! I'm gonna look into the antibiotic route. Thanx ever so much for that testimony.
Tish
19 May 2009, 09:52
I am very disappointed that this magazine totally ignores the antibiotic approach to treatment of Rheumatoid Arthritis. Numerous clinical trials have been conducted over the past four decades with results published in well recognized medical journals showing on the average a 75% very good response to Minocin and to Doxycycline. When I was diagnosed in the fall of 2006, the first three months were spent trying to treat with NSAIDS, which were of absolutely no value. Then, after having done intense online research, after reading dozens of journal articles and a few books on the topic, I asked my Rheumatologist to put me on Minocin. He did...100mg once a day. Within 3 weeks the effects were noticeable. Within 2 months my flares had totally stopped. Within 6 months any evidence of the disease had disappeared. I stayed on Minocin for 6 months, then switched to Doxycycline, using a generic tablet, 100mg once a day. For the next 12 months I was totally symptom free, I had reduced the dosage to three times per week. Then I changed pharmacies and received a different generic brand. After three months, flares started up. Things went spiraling downwards. I finally realized that possibly it was the generic brand change that caused the problem. I was almost ready for a wheelchair...my hands became paws, getting up out of a chair was a tremendous feat of accomplishment. Went back to the original brand, (that was December 2008) and now (May 2009) am again virtually symptom free. (Dosage was upped to 100 mg 2xday). I can turn the key in the ignition with no problem, I only have one finger that is stiff (probably permanently so). The antibiotic treatment will work for many people (I personally know someone who went from a wheelchair to a relatively normal life using minocin, was on it 12 years, has been drug free for the past three years, and is still in complete remission of the disease). This magazine is paid for by the drug companies who do not want you to know that a $15 a month prescription could well do better than your expensive biologic treatments. For that reason, I am cancelling my subscription to this magazine. They do not cover ALL treatments equally!! I encourage them to contact me and my doctor if they have any questions.
Deb
10 May 2009, 12:14
to Carla regarding her 5/9 post. That is the natural supplement you are on? My dad is 81 and suffering! Thanks!
carla
09 May 2009, 20:06
I have had RA for over 25 yrs. I have been on every drug available. Some worked well, others never worked. I was on Prednisone for 18 yrs and methotrexate for 14 yrs and still didn't feel great. I was finally able to get off of these 2 drugs as well as acid reflux med and HRT med with a natural supplement. That was 4 years ago. I got something from this supplement that NO drug every gave me, HOPE. I feel so blessed to have found a product that builds up my immune system and reduced the inflammation in my body. That is just the beginning.
Don't discount the great alternative supplements available today. They can really change your life.
Tyna
22 Apr 2009, 05:50
In the past been told I have arthritis in my spinal column and numerous other places. I also don't know of to many places that don't have bone spurs. Vioxx "for me" was the most wonderful drug that was made. I could take one and sunshine. But as you all know this is no more. I've been given several of the drugs mentioned in the comments above and just went to a rheumatologist. He started me on 5mg of prednisone 2x a day that was 2 weeks ago. Seems to be working, swelling going down. Oh I should mention going to ortho for treatment previous. I went in one time my hand was swelled around the knuckles about 5x the size it should be and pain. X-ray, MRI and no answer. Anyway I see my med report areas that are diagnosed with osteoarthritis but he's going to treat me for rheumatoid. Now he wants me to take the "malaria drug" can't remember the name either. Said it will take 3 months to actually work. For only 2 more weeks will he give me prednisone and cut it to 5mg 1x a day for a week then 2 1/2mg for a week. I've never heard of the antibiotic mentioned above but will definately give him a call in regards to it. All the side effects including nausea, vomiting, eye problems, the side-effects sound worse than the problem. I also have COPD, factory work all your life can do that, so some of the medications I can't take either. Any more info out there on anyone that has taken the "malaria drug"? I realize not all will be the but did it actually work at all for anyone. Also I'm told I can't be on the prednisone for to long to many side-effects.
Take Care.
Mary Ann Snow
21 Apr 2009, 14:23
When I was first diagnosed in 1996 I was put on Naprosan. My body didn't respond well, then I got in to a Rheumatologist and he put me on Plaquenil. This did wonders for the inflamation - nothing for the pain. When I told my Dr that when I took antibiotics for sinus infections I felt great, he doubted me. I then found Dr Browns book as well as an article from Tufts Univ advocating the use of minocycline. I was on it for over 2 yrs and did wonderfully. Until my Dr decided I didn't need to take the antibiotics anymore. He put me on Prednisone for 2 yrs, I gained 60 lbs, and went back to the pain. Needless to say - I've since found a new Dr.
edie elliott
21 Apr 2009, 11:50
My 17yr old son was recently dx with enthesitis related arthrits. was on prednisone,but weaned off. now using methotrexate and enbrel shots-doing very well. his symptoms started with toe and heal pain-was diagnosed by a rheumatologist, after foot x-rays and a bone scan. Any other sufferers of enthesitis??
sue
21 Apr 2009, 07:41
I've been diagnosed with RA - majority of discomfort in heels... is this RA or somethning else? medication isn't working for heel pain... not sure what to expect with RA...
Paula J. Kintzel
31 Mar 2009, 01:22
I was on mxt, it was reduced due to my lab. Then i became short of breath, ankles swelled up and heart rate stayed above 130 for about 3 months. I was taken off mxt. i was diagnosed with asthma, and saw a cardiologist. The symtoms went away on their own after the 3 months. I am still not on anything but meloxicam for my RA and having small flairs. Not sure where to go from here re: meds.
Susan Butler
30 Mar 2009, 10:20
OOPS!! Forgot some inportant details in my first post. I was diagnosed with RA over 20 years ago. Started out on Voltaren, then was prescribed the "malaria drug" - can't remember name, sorry. Took them for years. Then went to Arava - hair fell out, liver enzymes when up, severe diarreha for over a year (10-12 tiimes a day). At that point was taken off Arava and began drugs in first post. Hair has never come back like it was - very disappointed about that - I know that's silly. Anyway - more info I should have put in first post. Sorry.
Susan Butler
30 Mar 2009, 10:14
I have been taking Enbrel Injections, Methotrexate, and Prednisone for quite some time. My bruising mainly on my arms and hands has been horrific. I am 60 years old and realize age has much to do with a lot of things, including my aging skin. Was taken off Prednisone gradually late 2008. Scratches remained and were not healing. I play with my dogs and do some yard work. I was prescribed antibiotics and taken off all the rest of my medication for 6 weeks now. Sed rate has gone sky high and sores are healing but not quickly. What are the chances of the bruising coming back once I am back on Enbrel and Methotrexate? Dr. L. seems to think it was all from the Pred. but since I am off everything now and have no significant easy bruising, I'm not sure.
Nell
30 Mar 2009, 09:57
I am surprised that you have no information on antibiotics, particularily Minocin, which has been very successful in treating RA, with very few side effects. For anyone interested, read "The New Arthritis Breakthrough" by Henry Scammel which highlights the work of Dr. Thomas McPherson Brown who was a pioneer in antiobiotic therapy for RA.
khyati
24 Mar 2009, 04:16
My grand mother is having a sever knee pain and its not reducing after taking so many drugs.before 3months she had a knee trasplantation operation..but still pain is as it was..can you give drug guide?thank you
Erma
19 Mar 2009, 08:26
My 73 year old father has rheumatoid arthritis, severe. He's tried methotrexate/humira/prednisone but to no avail. He is being treated at his local VA hospital. Right now, he can hardly walk. The doctor gave him gengraf, 100 mg, twice a day and then one 25mg once a day. Is this more dangerous because of the side effects? Thank you.
lee Reid
15 Mar 2009, 12:04
My wife has shoulder pain, it has affected her sleep significately. She was using 80mg Geodon but it has become so expensive to use.
We are looking for an alternative form of this drug that we can afford.
Lee Reid

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