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Treatments > Drug Guide > Types of Drugs > Drug Guide: Corticosteroids
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Drug Guide: Corticosteroids

Steroids, or corticosteroids, are used to treat joint inflammation and inflammation of the organs.

What are corticosteroids?

They are a class of drugs designed to be similar to the hormone cortisol, which is produced naturally by the body’s adrenal glands to regulate the immune system. They are sometimes referred to casually as steroids and some doctors call them by their more specific name: glucocorticoids. In contrast, anabolic steroids, most widely associated with athletes, are related to the hormone testosterone and have no role in arthritis treatment.

What diseases are they used for?

Corticosteroids are used to suppress inflammation of autoimmune diseases, including rheumatoid arthritis, lupus, vasculitis (for example, arteritis and Wegener’s granulomatosis), ankylosing spondylitis, polymyalgia rheumatica, psoriatic arthritis, reactive arthritis, scleroderma and Sjögren’s syndrome. 

How are they used?

Corticosteroids are among the most effective drugs for relieving inflammation quickly and dramatically. They are used in high doses to reduce dangerous flares of inflammation – sometimes as a temporary measure, until other drugs take effect.

 In low doses, they are used to prevent flares and protect joints, eyes and internal organs from damage caused by inflammation.

Corticosteroids sometimes are used with disease-modifying anti-rheumatic drugs (DMARDs), such as leflunomide (Arava), methotrexate or sulfasalazine (Azulfidine). Combination therapy can increase the effectiveness of very low doses of corticosteroids. They usually are not used in combination with biologic response modifiers, a new type of DMARD, such as abatacept (Orencia), adalimumab (Humira), anakinra (Kineret), etanercept (Enbrel), infliximab (Remicade) and rituximab (Rituxan). 

What forms of corticosteroids are available?

Corticosteroid medications typically are taken orally. The oral versions are the only ones listed in this Drug Guide. 

Other corticosteroids are given intravenously when high doses are needed quickly for short periods of time.

Some forms of corticosteroids can be injected directly into joints for relief of pain and swelling. Cortisone shots commonly are used in osteoarthritis treatment. Those injections act locally, and so are not associated with systemic side effects. Topical corticosteroids are applied directly to the skin to relieve the inflamed skin lesions of cutaneous lupus erythematosus and psoriasis. If the topical corticosteroid is used over a wide area, systemic side effects may occur.

 

PATRICIA GOEING
19 Dec 2011, 09:42
RHONDA GARZA SOUNDS MORE LIKE OSTEOARTHRITIS I HAVE IT AT MY FINGERS ARE LIKE YOURS. I ALSO HAVE IT IN MY SPINE AND HIP. I JUST RECEIVED A CORTISONE SHOT IN MY BACK AND IT NOT ONLY TOOK THE STIFFNESS AND PAIN AWAY IN MY BACK BUT IT ALSO HELPED MY HANDS WHICH SURPRISED ME BECAUSE I THOUGHT IT STAYED LOCAL BUT LOW AND BEHOLD MY SWELLING WENT DOWN IN MY FINGERS AN I CAN MAKE A TIGHT FIST NOW AND BEND OVER WITHOUT PAIN AND STIFFNESS IT'S LIKE A NEW LEASE ON LIFE PLEASE GO BE DIAGNOSED WITH THE TYPE OF ARTHRITIS YOU HAVE AND START ENJOYING THE REST OF YOUR LIFE. GOOD LUCK TO YOU
pat
01 Nov 2011, 15:28
ive been having joint pain in my upper arms and my knees.i need something to help my joints,have told doctor,but noyhing,i get my pain pills tomorrow and hopefully they will help,have been told i have arthritis all through my body...thank you pat
Rhonda Garza
09 Sep 2011, 23:05
Ive read these comments by others and it scares me to go see a doctor, I believe I have R/A because of the nodules that have been growing on the joints of my fingers closest to my nails. They are painful when I lift or try to tie shoe laces, 2 of the fingers are turning at the joint by the nail. I have been eatting raw yucca root and I feel pain relief within 20 minutes and the funny thing is, just like pain med's it lasts about 4 hours. I hope this helps others
jackie
08 Aug 2011, 10:06
I have CAD, with 3 stents in my main artery.
I use nitrospray PRN for angina, Coreg BID.
Crestor. and 81 mg.coated aspirin.

I was Dx. with RA years and took prednisone
for a short while. Lab Another doctor dx. me with
Fibro and CFIDS. He changed the prednisone to
Cortef 10 mg tabs -2 in a.m. and 1 in early
afternoon. Combined with infrared therapy and hydro therapy. Lost 50 lbs. and went into remission. positive for RA elevated CRP
and SED rate x-rays showed no evidence of RA
No joint changes. JUST PAIN. Dr. did not believe me.

New doctor changed my rx from prednisone to
cortef.
Moved from Florida to N.C. and soon experienced an acute FLARE! RA, hands and ankles show visible deterioration, PAIN is
disabling Right ankle replacement recommended, second opinion agreed. CRP
again is VERY HIGH so ankle surgery is postponed. The doctor (Rheumatologist) wants
me on a DMARD and they all seem to be contraindicated if patient also has heart disease. I want to know what is best for
me? I found a place to go to receive infrared and hydrotherapy. Can you provide
feedback? If allopathic is your practice,
I doubt you would agree with Functional/Alternative treatment protocol.
Della Shuler
19 Jul 2011, 12:05
Prednisone is like a blessing and curse. I have multiple conditions like many that have posted here: Hashimoto's thyroiditis, osteo-arthrtis, RA, Fibro and degenerative disk disease to name a few. Methotrexate didn't help me at all. I was allergic to Arava. I took Remicade for 8 months, then had to stop when I fractured my ankle. Resuming almost 18 months later it turns out I am allergic to this medication.

I now have been on prednisone for five years. My rheumatologist cut my dose back as low as we he could, because I had become pre-diabetic. I get skin infections all the time, which means I can try any of the other biologicals.

Unfortunately, I need major abdominal reconstruction, and my surgeons don't want me to come of the prednisone completely, because my body won't be able to make its own cortisol So, I'll have to have a super does of "shock" steroid" when the surgery is done. In the meantime, the predisone weakens my bones and in the past seven years of use has caused four of my teeth to crack and be removed.

I am praying that by Christmas, I will finally be able to try a different biological and get off of steroids for good!
Tammie Lucas
21 Jun 2011, 21:30
Hi, I'm 47 years old. I've been diagnosis with Fibro and RA since February this year. I've know I had this problems two years ago. Everytime I would go to my primary doctor complaining about my joints aching, he would give me pain med and say I just have a pull muscle. Well, in January I went to him and ask him to refer my to a rheumatogy, because I want him to check me for Fibro. Well, I was diagnosis with something extra(RA), but at least I know I wasn't going crazy and now I can at least be treated with some pain meds. Now I'm taking Prednisone and Plaquenil. Pray for me.
Debbie Moore
09 Jun 2011, 08:31
I have Lupus (SLE), fibromyalgia, spinal stenosis, spondylosis, ruptured discs and all kinds if "Itis's" and have developed severe diabetes and brittle bones (have broken 6 in 16 months!) and I have been on predinisone 27 years and altho it has always helped the pain, it has caused many, many more problems nobody can begin to imagine. If you don't already have diabetes and you stay on steroids a long time, most likely you WILL end up diabetic. If I had known 27 years ago what I know now, I would only have taken it when I had vasculitis in my brain (which caused 3 strokes) I am only 50 yet my body is way more aged than that. I would advis everyone to think long and hard before you put that bitter little pill in your mouth cos you are playing with fire, honetly. Now my adrenal glands don't want to work on their own and the doc says I'll never be able to be off prednisone most likely. They are DANGEROUS for long term use and they will increase your blood sugar. Even with me taking several shots of insulin a day and being on the ADA diet, my A1C is 10.5 !!! It was much lower before I had the swine flu but since a near fatal illness from the swine flu, my health has just gone downhill. The steroids shut down your immune system and you can fight illnesses off like everyone else. This is just my personal experiences with predisone and just want to warn others because it was an easy out to help with crippling pain but go on opiods before you go on steroids because you'll end up on them too, anyway!! I am 50 and probably take 50 pills a day, too, and 3-5 shots! And I am just as sick as always, but nowadays I won't let myself stay immobile by laying in bed too much. I am on my way back into a wheelchair unfortunately cos my spine is crumbling now but I am fighting it every step of the way while making the necessary adjustments to my home to get around easier when I am completely confined to my wheelchair. Thank God there are ways to lead a prodcutive life despite terrible pain and disabilities with the Act for Disabled Americans and The Lupus Foundation and The Arthritis Foundation and The Cancer Foundation and Kindey Foundations (I've also had kidney cancer) and ones associated with Strokes and Stroke Prevention. Use the programs that are designed to help you in whatever health you are in because it could save you much pain and money in the long run. ALways try to take the meds with the least long term side effects also. Just food for thought. Hope it helps someone else before they end up like me - really OLD before my time and a much shorter life expectancy! God be with you! Sincerely, Deb
Felisha Lean
08 Jun 2011, 10:49
I have had RA for a year now and after having infusion with Remicade for the past 12 months - which did not work! - my doctor switched to Orencia. I am so happy with my first infusion of Orencia...I know this will be what works for me! My Rheumatologist also sent me to a Pain Management Clinic and this doctor prescribed Tramadol for pain, Mobic for anti - inflamation and Prilosec for possible stomach upset. I am also on methotrexate, once a week. Go Go Go to a pain management doctor! I was on Prednisone for a year - bone wrecking pills! - because I was in screaming pain and that was the only thing that would take the pain away...but, this Anesthesiologist knew exactly what I needed and now I am in very little pain! Don't give up!! Count your blessings to be living in the US and God bless.
brenda wilhelm
03 Jun 2011, 11:55
Is the med Methotraxate is a pill or what . Do this med work let me know . ty brenda
Readytokickbutt
21 Apr 2011, 12:52
Janet, maybe your mom needs to switch something other than metrotrexate. She's been on it for the past 20 years, her body is probably immune to it.
helen Forte
19 Apr 2011, 12:07
hOPE SOMEONE HAS SOME INFORMATION ON DIET FOR pOLYMYALGIA RHEUMATICA. THERE SEEMS TO BE A LOT OF INFO ON RA BUT NOT PMR. I WENT ON PREDNISONE THE END OF FEB. 2011 IT HELPED THE PAIN IMMEDIATELY, AND I WANT TO DO AS MUCH AS I CAN TO HELP OR RID MYSELF OF THIS DISEASE.ANY INFORMATION WILL BE MOST HELPFUL.
THANK YOU IN ADVANCE.
Janet
01 Jan 2011, 20:36
Hi all, my mum has RA and Ostio and has been on methotexate for 20 years, usually gets a kenalog injection for bad flare ups but was refused recently, due to risk of thinning bones, did not get second opinion on the matter. and is in bad pain all the time with no relief. there must be something we can do. cannot take strong painkillers as they upset stomach. always takes 1 cocodemol which i say is not enough for the type of pain, any good painkillers out there that you would recommend ? anything new? thank you for any replies.
Lorraine Szymkowski
29 Oct 2010, 16:16
For Stanley Adams....I was on prednisone for about 2 years and I had passed out and my elbow had split open. My doctor put me in the
hospital. I had celulitus. The prednisone thinned my skin and I ended up with sores. I was in the hospital 3 times (each time another sore opened up) They had me on a heavy amount of antibiotics. After my 3rd stay in the hospital (10 days each time) I
called the doctor and wanted to get off prednisone. I was told the celulitis was caused by that drug. I have not had another
bout of it now. I have to say, the prenisone
did take away a lot of pain but I was very
upset with ending up in the hospital so often. I have fibro and arthritis. Be careful
Stanley Adams
18 Oct 2010, 20:00
Many cortisteroids will cause a spike and quickly in blood sugar's. This can cause a response in some people as you mention. I take prednisone daily and cortisteroids by injection when necessary. Sometimes all of the other meds that I take or the illness itself causes hypo-insultin effect or a drop in blood sugar and yes I shake and have jerks for a while.
eileen segal
26 Jul 2010, 15:40
i had 2 series of syn visc one and then the 3 shots seems i walked betttet with cortisone
Karen R
16 Jun 2010, 02:33
Can I get some form of cordticosteroids otc? I am at this moment in extrudiating pain makeing it almost unbearable to type. The pain starts at the neck through shoulder blade
Charles Teply
02 Jun 2010, 00:11
This is for MaryAnn VonderVor. If she is taking a statin for cholesterol, they can cause excruciating pains in your legs and back, If you are on one of these tell your doctor your symptoms and Have your doctor determine the cause. I switched from Lipitor to another statin, and I had so much pain in my knees and thighs, that I could barely walk. I also had back pain. It took a month for these to subside after being off all statins. I went back ti lipitor with no ill effects, but My brother had these pains on lipitor and now uses crestor with fine results.
Donald Rager
10 May 2010, 20:27
I have had RA for 34 years and have been on predisone for 31 years at 5 mg I was on methotrex for 8 years but 10 years ago I got NHL and the Dr though it was caused from the
methotrex I AM NOW TAKING Rituxan). an have been getting along fine
j forney
05 May 2010, 11:55
My cousin(84)and I are both on methotrexate. She has developed swollen feet and lumps in her left arm. The lumps are under the skin, red, sore, & itchy. It started with only one and now there are many large lumps. This started after she was given a TB test. Has anyone else experienced anything like this?
MaryAnn VonderVor
11 Dec 2009, 09:44
I have been taking so many different perscriptions, not together, but tried it all and I still have severe pain daily in my whole right side especially in my lower righ calf and up to my waist, at times it even makes my back terrible. I am at a loss as what to do as many of the specialist also do including pain management. Any help would be appreciated. Thank you.
Len L Peterson
05 Nov 2009, 13:01
Can Prednisone cause chills? I had a colon resection and was given stress steroids for the operation (high doses). Then the steroids were gradually reduced to 5 Mg which I have been on for several years prior to the operation. I had severe chills after the operation and previously experienced chills even on the low doses of Prednisone. Can this drug cause chills such as I have experienced?
mary ellen calcaterra
04 Nov 2009, 09:41
I just had shot in knee first time im 6 week i woke up and i could walk with no pain or limp. But my face is swollen and very read.
Susan
20 Oct 2009, 10:48
This information is so lame. Everyone who has arthritis knows more than this. This is why I steer away from patient info. and go for the professional discussions. Writers think patients are idiots.
Adriana Cashman
25 May 2009, 21:40
Where are the answers to the above?
Mwafak
22 May 2009, 21:37
Dear sir
How do I best manage severe sjogren disease during pregnancy third trimaster,detailed information please-----thanks in anticipation

Mwafak
Dexter R. Barbee
05 May 2009, 14:03
I am 69 yrs old and had polio in left leg at 17 mo. old. As years progress and many operations later my leg mainly is just there. I have no use of my foot and very llittle strenth in knee and hip. Terrific pain in foot has the Dr. thinking artificial ankle for pain only. No muscle to attach to. Also fusion but with a weak knee will cause me to fall. Havew been taking cortizonew shots that work for a couple months. What is maximum I should take per year and side effects.

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