humira skin rash

upper respiratory tract infection, headache, injection site reaction, skin rash, antibody development, sinusitis, and pain at injection site. Other side effects include: urinary tract infection, abdominal pain, and flu-like symptoms. https://www.drugs.com/sfx/humira-side-effects.html I'd tell your doctor you are experiencing this.

I have AS and was on Revellex for 1 year but then developed a skin rash reaction. I changed to Humira recently and was wondering if anybody has had success with humira who has ankylosing spondylitis. Any feedback would be appreciated.

m having a followup with a oncologist/dermatologist because one of the side effects of Humira is non-melanoma skin lesions (some cancerous). Besides, once a cancer patient, always concerned. Want the remaining Humira shot in my fridge?

he thinks that i will get some help from humira and i am to start that this week. i have done searches but only find info on humira induced lupus, nothing about treating lupus with humira. is anyone on here taking humira for lupus? any advise would be greatly appreciated. thanks!!

I have injected humira 2 weeks ago and after 3 days developed a itch and cant sleep. will it subside?

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.

However my Rhumy cannot give me an explanation whats causing my weakness or numb feeling. I have also had a skin biopsy done for a rash I have developed. Result was vasculitis. Now that I am having another episode of weakness on the left side my Rhumy has requested for another Brain and neck scan. I have had a neck scan done in 2013 to which they found that i had c4,5,6 damaged had a cervical op done.

At night time, I could not sleep because it felt as tho the bedclothes were also wet. The Humira made me very sick so I stopped that. I asked my doctor about the rash but he continued to state that it was a skin disorder and I should visit a dermatologist which I did on 3 different occasions. Of course the dermatologist said he could not find the reason for the rash after trying a couple of ointments. So on April 19, 2009 I stopped taking all my drugs. Nothing.

Do not use any cosmetic products at the sites. You can apply some calamine lotion at the rash as it will help in soothing the skin. You can take some OTC oral antihistamine medications like Benadryl or Claritin and see if it helps. For mild-moderate symptoms a weak steroid may be used (e.g. hydrocortisone as dermacort), whilst more severe cases require a higher-potency steroid (e.g. clobetasol propionate, fluocinonide).

Options--Go to a dermatologist. When using steroid cream put it only on the psoriaris marks, not on the skin that doesn't have red at all.It thins skin a little. I am in my 20's and I have some veins seem surfaced--I put it everywhere on accident. Do a light therapy box from Washu medicine or ask where one is. Just like at the Dead Sea spa in Israel I called and asked what there treatment was and then just did it myself at home. Sun, mud, sea salt bath and message.

Hello everyone, hope this posts finds you all well. I was hoping someone might have a trick to make taking the humira injector pen any less painful. I'm actually hoping I can talk my doctor into letting me get it in vial form so I can fill my own syringe and take it the same as I do the methotrexate. But that pen, its a killer. I always let it warm up from the fridge first is this a mistake maybe? Does it just burn naturally or does the injector pen make it worse?

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.

I am 32 a women 30 weeks pregnant first child. I was diagnosed with Chrons at 23 years old was on humira till I went off due to pregnancy complete remission when I went off. I had my gallbladder out two years ago and felt awesome since even went down in humira dosage. My husband and I had issues getting pregnant so we did IVF and sure enough it worked! Got positive confirmation in July 2013 and stopped humira that month. Symptoms started August 23 2013.

My gastro is going to start me on Humira and my question is, does Humira aid with digestion and stop the diarrhea. Thanks!

I felt so much better on the remicade and my rash cleared up over my entire body, I have a psoriatic rash over more then 1/2 my body, unfortunately I ended up with muscular dystonia (sp) where all my muscles froze up and I couldnt move my arms, hands, left knee and neck. Believe me when I say if I could have found a way to deal with the not moving I would have stayed on the Remicade, I felt it helped me THAT much.

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.

My son photographed and took close-up video of the rash/ shingles/hives ? The rash has eased along with the pain but my skin is very painful to touch. I spoke with a PH.D Opthamology researcher at the University Medical School who told me the varicella virus mutates rapidly. She felt my symptoms could be Post herpetic neuralgia PHN, Nystagmus/ fibromyalgia along with fibromyalgia of the eye.

Even when I was a teenager I never really had acne problems and have had almost completely clear skin since I was about 14. I wash my face with a gentle cleanser every day and make sure I moisturise daily. My doctor has told me that the Prednisolone is causing the acne, but he's a bit vague. He also told me the Salazopyrin was causing my chronic migraines 2 months ago when I wasn't even on Salazopyrin so I'm inclined to ask for another opinion.

I have RA and use Humira/methotrexate. How long do I have to be off Humira to get a yellow fever (and/or tyhphoid) vaccine? How long to I have to stay off Humira after the vaccine?

Well, narcotics work wonderfully for the pain, however you can't live life being on narcotics all the time. How would you work/drive/care for your children if your head is clouded by narcotics? I was like you - I had awful pain, started Humira and within a few months felt completely better. I am still on Humira and haven't had any flare ups (fingers crossed so that I don't jinx it) for two years.

now need to decide on a medication and have been giving the chose between the infusion and giving myself shots. My doctors seems to be leaning toward Humira shots. The idea of giving myself shots for the rest of my life is very overwhelming. My mother gives herself shots, and wants the infusion, but cannot because she would have to change medicines and her Embrel is working so the Dr. wont switch her. Does anybody have any insight to which is better.

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?

Humira skin rash

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