Yes, Humira will indirectly help in controlling diarrhea and digestion. Let me explain this. Humira or adalimumab is a biological response modifier and tumor necrosis factor (TNF) blocker. Thus, in Crohn’s it will modify your body’s response to disease (bloating, tenderness, diarrhea, indigestion etc). This is because any immune mediated disease like Crohn’s produces excess of an inflammatory protein called TNF-alpha, which causes cellular damage along with pain and inflammation.
As most of us know Humira (adalimumab) reduces the effects of a substance in the body that can cause inflammation.
Common Humira side effects may include: headache; nausea;
cold symptoms such as stuffy nose, sinus pain, sneezing, sore throat;
rash; or redness, bruising, ITCHING, or swelling where the injection was given.
So what you are experiencing is not unusual - however I think you should give your MD a call as Sherry also suggested. He/she needs to know about your reaction.
Yesterday my rheumatologist has finally decided to give me something other than anti-inflammatories and anti-depressants for my list of symptoms which he has decided are due to either Ankylosing Spondylitis, Psoriatic Arthritis (Palindromic Rheumatism was mentioned too) or possibly all of the above, with a side order of Fibromyalgia. Just wondering if anyone here has taken Humira (Adalimumab) as I've read about it and am freaking out a bit!
From the Journal of the American Academy of Dermatology
“Our results indicate that adalimumab seems to be a safe option in treatment, even for patients with liver cirrhosis.”
Best to discuss all medications with your liver specialist even over the counter and herbal supplements.
I have RA and have been diagnosed 1 year ago. Apparently I'm a severe case. It just keeps progressing. I've been on Plaquenil, Methotrexate for 8 months now. Started Humira injections about 3 months ago. About 2 weeks ago...my left thigh was itching...so I scratched. You should see the bruise I have now. It's been more than a week and its dark purple and measures 6" wide by 6"lenght. Should I worry about it?
Is this just a side effect from the meds?
I must admit...
Usually the side effects are well, evaluated against the benefits of a medication before prescribing it. Humira is a good medication to induce remission and symptom resolution, tough there are a few side effects associated. However all side effects may not necessarily develop in everybody. I would suggest discussing the pros and cons in detail with your treating rheumatologist.
Let’s hope for a favourable recovery.
Take care!
A doctor at the VA diagnosed you with this and prescribes your medication. The maintenance dose of Humira is typically 40 mg after the starting regime that is often higher doses. Are you still having symptoms at your maintenance dose? https://www.drugs.com/dosage/humira.
Hi,
I've had a related disease, rheumatoid arthritis, for over 40 years. I take Enbrel, a medication in the same class as Humira. These drugs are indeed designed to slow - and if you're lucky, halt - the progression of the disease. I take methotrexate in addition to the Enbrel, and I know many people who combine mtx with Humira, too.
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.
Thanks so much for your input!!! Could you share the dosage amount of both please.
I have very severe pain on a relatively frequent basis, about 2 episodes a month. I am on humira and it seems to be helping all the other symptoms but the pain. My gi doc only ever offers antispasmodic meds. The pain I am feel IS NOT cramping...believe me I know what cramping is. Not sure what to do. Any advice would be appreciated. Before you ask I know it's not an obsruction...
im looking for any information on Humira,im having tests next week to see if im suitable,the doctor at the hospital said they have had good results,in patients with Crohns,but id really like to hear from real people who have tried it,any info good or bad will be appreciated,
thanks
I just got my first shot of Humira for my suspected psoriatic arthritus yesterday (i realize this is in RA, but there's no other section), and I had a quesiton. For those of you that take it or have knowledge about it, I know that it lowers your white blood count. People in my house are sick quite a bit during the year, so other than screenings (which I obviously will be getting), how do I protect myself? Supplements? Immune-boosting foods?
Anyone taking humira and feel like they are sick coming down with a cold for a week after injection? Not a full blown cold but the start of one. I feel like this always and this is my 3rd dosage ( counting the starter kit), so I'm new to humira. I've noticed if I'm stressed, I'll even get a sore throat. I know humira suppresses your immune system but are you supposed to feel like you're coming down with something every injection or will this go away with time?
I've been diagnosed with RA since 2006. On Methotrexate 20mg, Humira, and folic acid. In last 24 months I've had 3 bouts of pancreatitis (twice after gall bladder removal) with no cause determined gastro doc, and chronic burning sensation in legs, buttocks and lower back. (Similar to feeling of frostbite) Sensation increases as day progresses and greater sensitivity on sitting or clothes binding in areas.
Of course it seems a lot of folks have the same questions you do after reading humira info online - found a lot of questions asking if humira causes herpes.
If you already have herpes simplex, either orally or genitally, it could cause it to reactivate. Most people never get tested for herpes to know that they have it.
Hi monicaroni, I have been taking Humira almost 8 months. I take humira for Crohns Althougth reap the benefit for the AS. I am thinking that you probably had a concurrent infection brewing when you Started Humira. Good Luck managing your AS, I appreciate how difficult it can be with mobility issues, and treating pain.
As you well know Humira is an immuno-suppressive
drug , which mainly inhibits TNF (tumor necrosis factor).
There's a growing amount of evidence of the development of Autoimmune conditions, related to TNF inhibitors, such as Remicade, Humira and other biologics.
during a flare gas and the stools might smell worse. In my experience with Crohn's medicines do just stop working over time. I had two big flares in since I've been diagnosed with the disease. The first time prednisone worked like a charm. I was taking off and back on it between flares for smaller flares, well the other big one it help a little through IV's but it didn't work. So yeah medicines do stop working.
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