humira medication cost

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.

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

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

t have insurance/$$ to cover the cost of medication, they allow you to get 270 days worth of free medication. it helped me out tremendously... i did it before and received asacol, not sure if asacol will even work for you, but i found it to be more effective than pentasa. also there's a generic available for steroid enemas (not proctor and gamble), i believe... still expensive but helps out.

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.

I've been on Enbrel for about 5 years and it has been an extremely good medication for both the psoriasis and the psoriatic arthritis. My concern is what am I going to do now that my husband is retired and my health insurance won't cover the cost. I live in Canada and the cost of this medication is approximately $22,000.00 a year which my husband's company insurance covered but now that he is retired, it will not cover the cost for my lifetime.

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 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...

Usually the side effects are well, evaluated against the benefits of a medication before prescribing it. 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!

A doctor at the VA diagnosed you with this and prescribes your medication. The maintenance dose of Humira is typically 40 mg after the starting regime that is often higher doses. Are you still having symptoms at your maintenance dose? https://www.drugs.com/dosage/humira.

I have had Crohn's for 40 yrs; 30 yrs on steroids, 10 on methotrexate. Originally oral, 25 mg a week, but last 4 yrs weekly injections of 25 mg. I had a hemi-colectomy in March 09, with 15 cm of my small and large intestines removed. Unfortunately, I then had a big flare in late September requiring 2 weeks again in hospital. I was put on remicade: gastro said I would have only 3 infusions: 0, 2 weeks, 6 weeks, but still had faecal incontinence and failure to put on weight.

Hi, I've had a related disease, rheumatoid arthritis, for over 40 years. I take Enbrel, a medication in the same class as Humira. These drugs are indeed designed to slow - and if you're lucky, halt - the progression of the disease. I take methotrexate in addition to the Enbrel, and I know many people who combine mtx with Humira, too.

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.

Thanks so much for your input!!! Could you share the dosage amount of both please.

Have read that some people have found the automatic self injection thingie painful, although the manufacturer pack said the medication should be administered within 15 minutes of removal from the fridge, the Humira nurse said to take it out 20 mins before use, and I was pleasantly surprised at how painless using it was.

I have very severe pain on a relatively frequent basis, about 2 episodes a month. I am on humira and it seems to be helping all the other symptoms but the pain. My gi doc only ever offers antispasmodic meds. The pain I am feel IS NOT cramping...believe me I know what cramping is. Not sure what to do. Any advice would be appreciated. Before you ask I know it's not an obsruction...

s anyone out there that can give me more information on cimzia. Every medication I have tried either makes me worse, or I have reactions to. I created a reaction to Remicade and Humira just doesn't seem to work anymore. I am bleeding more than I have in years and I am only 18. My brother met a girl who takes Cimzia and she is having amazing results. I have, well, little hope that the Humira will turn around and stop working.

im looking for any information on Humira,im having tests next week to see if im suitable,the doctor at the hospital said they have had good results,in patients with Crohns,but id really like to hear from real people who have tried it,any info good or bad will be appreciated, thanks

I just got my first shot of Humira for my suspected psoriatic arthritus yesterday (i realize this is in RA, but there's no other section), and I had a quesiton. For those of you that take it or have knowledge about it, I know that it lowers your white blood count. People in my house are sick quite a bit during the year, so other than screenings (which I obviously will be getting), how do I protect myself? Supplements? Immune-boosting foods?

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?

I've been diagnosed with RA since 2006. On Methotrexate 20mg, Humira, and folic acid. In last 24 months I've had 3 bouts of pancreatitis (twice after gall bladder removal) with no cause determined gastro doc, and chronic burning sensation in legs, buttocks and lower back. (Similar to feeling of frostbite) Sensation increases as day progresses and greater sensitivity on sitting or clothes binding in areas.

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.

Hi, patients receiving humira are prone for developing serious infections. Lymphoma and other malignancies have been reported from patients receiving this medication. So, you can try to avoid infective zones and also restrict your physical work load. Take care.

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.

during a flare gas and the stools might smell worse. In my experience with Crohn's medicines do just stop working over time. I had two big flares in since I've been diagnosed with the disease. The first time prednisone worked like a charm. I was taking off and back on it between flares for smaller flares, well the other big one it help a little through IV's but it didn't work. So yeah medicines do stop working.

Humira medication cost

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