humira side effects chest pain

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.

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!

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.

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...

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.

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

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.

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.

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

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.

what i hate is the cyclosporine 500mg,and humira 40mg,thats for my psoriasis of my skin there side effects are the worst it effects my wbc which is .01%.i can't get sick.funny! they pulled out all my teeth so i won't get an infection.i have a warthins tumoron left side.now i found i have another tumor in front of my throat ,they done a biopsy but i have to do it again cause they need to use a ultrasound which i think he should have done in first place. what is your situation Sir_Osis?

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.

Pain is listed among the side effects of Humira and this could be it. Also, since it iwas your first time to give yourself a shot, here are some pointers I found online. "...you should always position injections at least 1 inch from recently used injection sites and avoid injection into tender, bruised, red, or hard areas. When you administer the injection you may pinch the area up when giving the injection (I hope that makes sense) Also you may want to apply a cool compress afterwards.

Also tightness in my chest as well as my left side feeling different from the right. Leg, hip pain with heaviness. Extremely sensitive to sounds and some touch as well as swallowing and breathing. I was also recently diagnosed with gastroparesis. My moms cousin had MS and I have a strong family background for autoimmune disease. Does any of this sound like MS?

You should also try checking your medication side effects. I highly recommend checking your medications to pin point the problem. I have begun taking Humira for my Crohn's Disease and my left arm feels like there are pins and needles in it. This is a side effect of my medication. So before you do anything else, please check your side effects list.

, and then there are cases like mine (I treated twice for 1A) who will have life long side effects to name a few....

s allergies, an infection, or a side effect from the Humira. Has anyone else had this happen shortly after starting this drug? I am planning to call my doctor on Monday but just trying to figure out what's going on.

They put me on pain meds through IV nearly cut the pain. Took chest X-ray, another ultra sound of the left side more towards middle now and blood work all normal. Set me home with pain patch and follow up with surgeon. So I did he set me for an MRI no contrast of abdominal and pelvic area showed nothing. I swear this is pancreatitis since it can't be gallbladder cause it's removed. This is acting just like my gallbladder did. But everyday I am in more more pain on that side.

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?

I have been to a cardiologist and that is not the issue. My question is can Synthroid cause chest pain side effects? They come upon me when I have to move suddenly or at the start of a walk/run. They (the pains) fade soon enough but the pain is enough to cause me concern.

Hi Ladies I just have as question about metformin whats the side effects some of you may have had? I start to take metformin today so maybe this will bring on my period. I had a natural m.c in nov 2008 and no AF as of yet.

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!!!

I also sometimes have a twingey feeling that comes and goes on the right side of my chest sometimes. In general, I just feel a lot more aware of the organs in my chest and neck area. Does anyone else experience this kind of feeling? Is this common, or is it something I should worry about? In your opininons, will it subside? Like I said, it is not painful exactly, just a very weird feeling.

Humira side effects chest pain

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