Humira and prednisone
Common Questions and Answers about Humira and prednisone
humira
I was diagnosed with Crohn's 9 years ago. I have been taking Asacol (5-ASA) and Imuran (Azathioprine). Last february I was hospitalized for the first time and was put on prednisone. I am still on prednisone and my body won't let me get off of it. My doctor wants me to start Humira, but I am scared. I don't like reading about the side effects and things that can happen when on that drug. Does anyone have any experience with this drug (Humira)? I would really appreciate it.
Its the worst its ever been and I am miserable. I was on Azathioprine, Canasa, and a taper of Prednisone with no relief. Just started Humira yesterday. Four shots to the stomach....ouch! Today along with my flare symptoms (lots of bleeding, constipation, bloating, abdominal pain, fatigue, dry mouth, occasional nausea) I have the chills with a very low grade fever and my fatigue is worse than normal. Is this normal after starting Humira? What do others do to manage all of these symptoms?
I am 31 and was diagnosed with crohn's disease about two and a half years ago, but had symptoms for years before. I used to have problems with making it to the bathroom in time which was a horrible feeling, but I havn't had much pain.
Since being diagnosed with crohn's I have tried a few different medicine's. The first was Prednisone, then ASA, then another, and finnally Methotrexate and prednisone together which seemed to help tremedously.
There are enough other sites and posts of the same complaint and also in the first 6 months on Humira. It was about my 3rd injection I think when I started having tooth pain in my upper front teeth. Within a couple of days, my bottom front teeth stated hurting. I skipped a week of Humira under Dr advice incase I was fighting a sinus infection. Symptoms got better. Then I started back on my Humira last night and my teeth are killing me again.
m sure is a large part of my problem. I have been on various types of nsaids, plaquinel, prednisone, and celebrex - and a calcium channel blocker for the raynauds. I have never heard of so many drugs being used in combination before. But it makes sense for sure that they would compliment eachother. Do you find yourself with many side effects? Early on I was discouraged by a stomach ulcer and other stomach issues.
I have been treated for rheumatoid arthritis with Humira for 7 months including a combination of Humira and methotrexate for the past 2 months. I also take 5mg of prednisone, and 6 Azulfadine tablets each day. I was taking Humira once every fourteen days and I am on 15mg of methotrexate a week. About a month ago, I started experiencing numbness in my toes and feet. I mentioned it to my rheumatologist but she wasn't concerned and simply told me it wasn't rheumatoid arthritis.
My hands/feet have become swollen and my joints hurt more than before I started taking the Humira. I also have systemic vasculitis (Churg-Strauss Syndrome) and am on Cytoxan and Prednisone, but I have been taking both for more than a year and know the side-effects from each.
I am looking to see if anybody else has had the same happen to them or if they know what could cause this reaction with Humira.
Several ground glass opacities in my right lung showed up on a CT scan in July 2011. Enbrel was discontinued and coincidentally I took a regime of prednisone for an allergy problem - 60 mg for one week, then with a weekly taper. A repeat CT scan was performed in December 2011 and one ground glass opacity remained (15 mm), with a small focus of sold component within the ground glass density. A percutaneous biopsy was performed to rule out bronchogenic carcinoma.
During this time I have had uveitis (lasted for about 4 months) followed by gastritis (8 months), followed by strep throat leading to chronic tonsilitis and re-occuring bronchitis flares for 6 months that triggered asthma and now back to uveitis... Additional meds have been added to treat this, Pred Forte and Prednisone taper (uveitis), Prilosec and various other pump blockers (gastritis), 20days amoxicillin (strep) 10 weeks on amoxicillin (bronchitis), singulair and dulera for asthma.
Your antibody tests at 4 and 5 weeks would have detected between 90 and 95% of recent HIV infections and the 4th generation test that you had at 51 days provides definitive results (the 4th generation tests are conclusive 4 weeks following exposure). That you took prednisone the month before your exposure would have no impact on your subsequent test results.
I suspect the symptoms you have described are, at least in part manifestations of the anxiety you are experiencing.
meth got me sicker and sicker, cold after cold. now i am on just prednisone and pain meds etc. I cannot now take a tnf blocker, my immune system is so challenged. your sensations could be from the meds or your nerves. have some blood work done, like sed rate and wbc and see a neurologist. just my opinion and I am not a doc, just a very sick lady, 56 next month!
Naproxen, Vioxx, Celebrex, Diclofenac, Mobic, Sulfasalazine, Plaquenil, Clinoril, Lodine, Methotrexate, Neurontin, Methilprednisolone, Prednisone, HUMIRA injections. (These are the ones I remember). My current regimen is Humira 1wk., Leflunomide 1day and tapering off of Prednisone. But guess what?? I'm still in a lot of pain in my L/elbow and some pain in R/hand and wrist. I have come to doubt I actually have RA. Perhaps I have some weird unknow disease not known to the medical community.
I asked if it was ok to take with my HUMIRA and prednisone and was told it was fine. I was injected with the vaccine and became ill within 24 hours and my eyes became seriously inflamed. I sought medical care and saw a Opthamologist who diagnosed Iritis and Uveitis. Six months later my vision has deteriorated and I have considerable floaters. I have been referred to a major medical school, and Eye Institute.
Naproxen, Vioxx, Celebrex, Diclofenac, Mobic, Sulfasalazine, Plaquenil, Clinoril, Lodine, Methotrexate, Neurontin, Methilprednisolone, Prednisone, HUMIRA injections. (These are the ones I remember). My current regimen is Humira 1wk., Leflunomide 1day and tapering off of Prednisone. But guess what?? I'm still in a lot of pain in my L/elbow and some pain in R/hand and wrist. I have come to doubt I actually have RA. Perhaps I have some weird unknow disease not known to the medical community.
Prednisone can cause acne. I had UC for ten years until I perforated and had my colon removed and a J-pouch built 16 years ago. My son has UC and moved onto the Imuran last year. He did have some acne with the prednisone too. He has been in a wonderful remission this past year and is so enjoying feeling healthy. The only change he continues to make is to leave dairy alone as he realizes he is lacto intolerant. I hope you will get the same success.
He concluded that the relief (although moderate) provided by the NSAIDs was further evidence for Reactive Arthritis and that I should try Humira. I have been on Humira for about 6 weeks with no effect. If anything, pain has gotten worse (though worsening should probably be attributed to discontinuation of NSAIDs).
statistically 1 out of every 2-3 of us has hsv1 and 1 out of every 4-5 has hsv2 - a lot of folks who take humira, are already going to have herpes whether they know it or not! Of course you also can contract herpes simplex, either orally or genitally, while taking humira too.
It also can cause shingles to occur - you'd have to have had chicken pox in the past before starting humira in order to have a shingles reactivation.
5120 homogenous. Aditional blood being sent to Oklahoma for scleroderma 12 panel and he told me it would take up to 3 months to get results. Since I have symptoms of both lupus and scleroderma he's waiting to make a dx. Has anyone else had this kind of testing? He started me on prednisone and plaquanel. Anyone else started on this combo off meds?
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