Humira hives
Common Questions and Answers about Humira hives
humira
Thank you for your response. The only new thing I have started on myself, is Humira. I'm due for my 3rd injection tomorrow. I have rheumatoid arthritis myself. Could there be any connection?
Both are supposed to do the same thing in the body. The only difference is Remicade is a made-protien where as the Humira is a human protien. With Humira you give yourself a shot every other week.
So far, after using both, I prefer the Remicade. I didn't mind the treatments as much as I do the Humira even though the Humira is more convienient (I hate having to give myself a shot.
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.
I am taking a slew of medications for my evergrowing list of problems (januvet for type 2 diabetes - diagnosed three monnths ago, humira shots for crohn's, isoniazid for a TB+ test, prevacid for GERD). I am mildly overweight, non obese, but do have fatty liver and history of chronically mild ALT elevations.
Is this dangerous?
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?
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.
That doesn't sound good at all. Combining the methadone and the norco could be too much. Maybe you should call your doctor tomorrow and let him know what's happening. I know nothing about the Humira. Your pharmacy could tell you about any drug interactions.
If I were you, I wouldn't take anything else until I spoke with my doctor and/or pharmacist.
COMPLAINT -- I am 32 year old male with no prior problems with alcohol (and I am not an alcoholic; I am a social non-binge drinker), and quite suddenly I now have severe response to alcohol. I don't think this is true for all liquors (so far it is happened to me after red wine, and mixed drink with vodka khalua).
My husband missed his dose of Humira by 24 hours a week ago. He is now vomiting regularly like he did prior to his diagnosis. Is this normal with a missed dose? He has been on Humira since September.
I just started Humira (2 shots so far) and have had a worsening of symptoms since the first shot. 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.
Any body else taking humira? I have Ulcerative colitis and thats the meds they put me on. My condition is pretty bad because all three of my doctors told me not to come off the meds. That it could cause problems and early delivery. Any one?
Hola, lobo.... No tengo ninguna experiencia ni conocimiento sobre humira... he leído ahora que son unas inyecciones para tratar la artrosis, es para eso para lo que te lo han recetado ? Llama a tu médico y consulta con él/ella o la enfermera si es normal que te siga doliendo.. cuanto antes lo consultes mejor y es normal que les llame para algo así. Si hay una reacción, lo sabrán y si es normal te tranquilizará que te lo digan.
night last 4 mths also Endep 10mg 2 before bed to help restlessness ....still in pain ....so now about to start Humira but I cannot afford to gain weight,, and the
forum makes me afraid to take.......as met have a few years ago ...any one still on Humira injection every fnight?.
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.
I have started Humira injections which is a tnf drug and since I started taking it three weeks ago I have had a constant headache. Is this normal as not even strong painkillers are helping.
I have injected humira 2 weeks ago and after 3 days developed a itch and cant sleep. will it subside?
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.
I'm 33 and have psoriatic arthritis and was recently started on Humira. Within a day of starting I had pain in my fingers, toes, shines and forearms (none of which I had before). Has anyone else experienced new joint pain after starting Humira?
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