humira side effects insomnia

Common side effects of Humira include: 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.

Have you talked to your doctor about the side effects you are experiencing? Are you taking the Humira for RA?

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!

I have also heard that you may feel better if you inject it right before bed so you can sleep through most of the side effects. Please let us know how you do and if you develop any other side effects.

I had other side effects too.

Humira is an anti-inflammatory monoclonal antibody directed against TNF. Well, every drug including prednisone would have side effects and so does humira. Without a detailed evaluation, I would not be the best judge if this would be the most suitable drug in the situation; though it could be given a short period of trial to see how well you do on it. You may also like to get a second opinion from another gastroenterologist before making a change in the treatment plan. Hope this is useful.

However, I have found that to varying degrees Remicade and Humira give me the following side effects. I am trying to find out if these are normal side effects and if anyone has found a way to manage them. Physical therapy is not giving me enough relief at this point.

Thanks! I've just started had shot a week ago. Just curious about successes and side effects.

Even though you were on this med before and did fine you can go back on a med and have side effects. Or, side effects can show up at any time with any med. The weight gain is from the steroid, not from being inactive. My sister has to take a steroid sometimes and when she does she can put on a great deal of weight in no time. Humira comes with a long list of possible side effects. I really think this is what your Dr should be looking in to.

Losartan is not known to have many side effects. I've been taking it for a few months with no problems. Have you had any other medication changes? Do you take any statins for cholesterol issues?

I have not developed any bad side effects from the humira thankfully, and my DS-DNA is still negative. I am being closely monitored for SLE related symptoms just in case, but have had none besides the arthritis. Would like to know whic systemic, chronic connective tissue diseases I have one of these days, but, in the meantime, I'm happy with the combo of drugs I'm on....not entirely pain & stiffness free, but pretty close on most days...hoping it lasts!!!

Has anyone been on Humira and what kind of result did you have? Any side effects? I am on lots of meds which are not decreasing the pain. My doctor wants to put me on Humira and I was wondering if anyone out there has had any success with this drug. I am desperate to NOT be in pain anymore. Help...

What has been the most noticed side effects of Olysio/Sovaldi combo? Today is my first dose.

t help you with Remicade, as my gastro refuses to prescribe it for me, because of side effects connected with my recent breast cancer. My Crohn's is kept under control with weekly injections of 25 mg methotrexate, and 3 mg tablets daily of entecort. I do the injections at home - real easy, only takes a couple of minutes, so no tedious 3 hr round trip to the hospital. The local GP's nurse is unwilling to do cytotoxic injections.

Just wondering if anyone else is dealing with the following side effects due to taking benzo's and if anyone has found a way to alleviate any of them.

I have been on Sovaldi, Olysio and Riboviron for 4 weeks. I am finding that I feel very poorly with a laundry list of noxious symptoms. I feel very alone since my docs said that the side effect profile would be very tolerable. Many years ago I was on interferon and riboviron but could not tolerate the tx. I don't know if it is the roboviron that is causing the side effects. At this point I am pretty much bed-ridden. Is there anyone out there with a similar experience?

I am concerned about the potential serious side effects of this medication and the risk/reward for me. I am doing exercise rehab and intend to use herbal remedies on a daily basis for the inflammation if I do not use the medication.

Lulu--I used to take humira, which is a TNF inhibitor like Enbrel. One of the rare side effects of both humira and enbrel is the development of MS or MS-like symptoms. I didn't pay enough attention to the warning because it seemed so remote and happened so rarely. However, it happened to me. If what I have is MS, the doctor isn't sure whether the humira caused it, or if I would've gotten MS anyway, but the humira hurried the process along.

Most of the side effects are dose related. Here is more information about the medication: http://www.drugs.com/topamax.html . Sometimes, dividing the dose into several doses throughout the day may help. Also taking the smallest dose you can take is best to avoid the side effects. Initially, many people have side effects, but after your body gets used to the med. it goes away (usually after a week or 2).

The competition does sell versions of it (Remicade and Humira) but those are just as costly. Humira actually would cost me more. I was hoping there was a different class of medications outside those 3 that can do the same job for much less.. Thank you for replying.

Humira side effects insomnia

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