humira injection cost

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've just had my 2nd injection of Humira today (on 20mg, 2x month). Both times I've had no energy and felt bad for about 12 hours after the injection. Anyone else have this type of reaction to the injection?

I hve hsv1&2 for over 6 yrs nw ,no flare up for two yrs.I just started humira then out the blue I flared up,nw I'm due for my 15th day injection but hve to wait for my Doc to call to let me know if I'm able to continue the humira injection wth this active virus.I think the humira reactivated the virus,wow! What u suspect she'll say?

are you checking with the manufactory on cost savings cards? I have been on Humira for over a year and the manufacture subsidies the cost to were i pay 25 a month for two 40m pens.

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. This may help decrease injection site discomfort." That said, if this does not work out for you, I hear that enbrel stings but is not painful.

anyone getting Humira, my hubby refuses to pay out of pocket $2000 for starter pack

s on how this inflammation formed so quickly after surgery.

ve been on Humira for about 6 months and I have been messing with my injection times a lot over the past couple months. Humira is the only thing that keeps me going, but I have to do it weekly. I noticed when I missed my dose, when I was doing it bimonthly, my symptoms would just keep getting worse. We did a few psychological tests to see if my symptoms were coming back due to an emotional connection. That was quickly proven otherwise as I started to vomit and have bloody stool.

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?

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

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...

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.

I have had 5 shots of humira and after the fisrt shot I felt like a scaitica but didn't think it was the now I can fell it go down my left leg, both calves tignly and i feel it in my neck also like spams, is this from teh humira? I called my dr and she idd not seem concerned? it has done wonders for my RA not at this cost. my finger tips fell tingly my clafs there is a pain in my butt that runs down my leg.

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?.

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?

does anyone know if it is ok to take the redipen injection and humira injections at the same time.

Tried everything out there, coal tar creams, Steroid creams, uv lights, psoralens, vitamin b6 injection...what have you. Then I tried Enbrel which gave me hope, because almost half of my body was cleared and after 2 years, I couldn't go beyond any further than a few stubborn patches. Finally I moved to Humira and Oh my my I have a new lease on social interaction. I can now wear my short sleeves in summer.

umm in the usa without insurance, n im chronic.

Also had just given myself Humira injection.

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...

I have had two shots of Humira, I constantly have sinus issues, pain pressure, teeth hurt and hedaches. I got them on enbrel and after 9 years it quit working, so tired remicade but after 4 infusions I had such a bad insus probelm I quit it also raised my blood pressrue a lot. I don't seem to be able to handle hard core antibidoics so I can take zpack, and it helps, but I always seem to be back on it alteast every two months.

Which Part D insurance plan has the best coverage and cost factor for the humira pen. I dose 40 mg every other week.

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 been on Humira for about 1 1/2 years. An injection every other week for about a year and my DR. up my dosage to once a week for the past 4 months or so. I'm still in pain though.

My 16 year old daughter has a rare auto-immune disease called "Takayasu Arteritis". Her medicines consist of Prednisone 10 mg daily (down from 40 mg), Azathirophrine 150 mg daily, Methotrexate 1cc 25mg injection weekly, Humira 40mg 1cc injection weekly, & Levothyroxine .5mcg daily. Despite these medications, her Sed-rate ranges 13 - 40 and its checked every 2 weeks along with CRP which ranges 3.2 - 12.

I think it was after some 6 months or so that I had the infliximab infusion on a Monday, delayed my mtx injection until the next day and had a violent reaction with pruple spots all over my body, very high temperature, nausea, vomiting, diarrahea and a pain up my spine. We agreed to stop the mtx as it seemed I had made antibodies against it.

Remicade is a biologic injection, in the same class of drugs as Humira, Enbrel and Orencia. I have been taking Humira for rhematoid arthritis and it seems to be doing it's job as my rheumy says. It keeps me out of the emergency room with serious flares which had become a habit for me. These drugs are usually reserved for "rheumatoid" type arthritis and getting insurance companies to approve them is not normally easy.

I am still waiting for an answer from the pharmaceutical company on the Humira, as I also have NO insurance. I am on Endocort (steroid with a LOT less side effects than prednisone), Pentassa, Depression meds, Trammadol (pain), percocet (pain), azathioprine 75mg. Still, I am in pain almost daily. Every once in a while I have a good day. I am really having a hard time, mentally and physically. I have always been very active, early to rise and then go go go go...

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!

Humira injection cost

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