humira patient assistance

Try contacting the manufacturer of your medication (will be listed on the box or container) and ask them if they have a patient assistance program - many of them do - and they usually are for either a great discount or even for free.

could anyone give me ideas as to where or who i would contact to get some patient assistance for acute hep c treatment? I am not working, cannot wait on s.s. disability. I try to do some construction work when available, but it is really rough.

Procter & Gamble has a patient assistance program: http://www.pgpharma.com/patient_assistance.shtml if you can prove that you don'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.

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?

I am outside the US and need to contact my humira, but cannot call an 800 phone number. Is there any other number that I can call to ask for nurse assistance?

I would try getting her meds straight from the company. There are a few websites that offer assistance. My husband is starting Humira (expensive) he get's it free from the company. As her dr about a perscription assistance plan, we like pparx.com...hope this helps, you can also try other companies by typing helping with perscription drug costs in your search engine.

You might be able to apply directly to the patient care assistance program for Humira.. Their phone # is: 800-222-6885. It's called Abbott Patient Assistance.. Best wishes to you!

I am 22 white circumcised male, also Crhons patient on Humira (at that point was 1 month of Humira) Does that increas my chances of hiv? 2. If she was totally dry, does that mean that there were less potential infected fluids? 3. What keeps me a litle better is that many people insist that cuba has one of the smallest percentages of aids in the world, and the majority of the hiv + are males. Could you confirm? 4.

I was reading the post about suboxone prices ,someone wanted to know if the was any assistance for the cost . I did some research this is what I found RECKITT BENCKISER suboxone patient assistance programs 1-866-512-2216 I don't know what are the guidelines but its worth a call . Any little bit I am sure would be very helpful. If I find anything else I will post it.

I am 22 white circumcised male, also Crhons patient on Humira (at that point was 1 month off Humira) Does that increas my chances of hiv? usually my imune works fine amd i barely catch anything 2. If she was totally dry, does that mean that there were less potential infected fluids? 3. What keeps me a litle better is that many people insist that cuba has one of the smallest percentages of aids in the world, and the majority of the hiv + are males. Could you confirm? 4.

This can be a tough decision. I inject both methotrexate and Enbrel once a week; both are virtually painless. Sometimes I don't even feel the needle, it's so small. The upside is, self injecting is much more convenient. You'll get so fast at it that you'll be done in under a minute and get on with your day (or night, if you inject at bedtime). Humira is taken once every two weeks, I believe, though it varies from patient to patient.

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?

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.

I wanted to share some encouraging news for people who have Chronic Hep B and have financial difficulty affording Baraclude. I contacted Brystol Myers Squibb and applied for the Patient Assistance Program. The website and application is here: http://www.bms.com/products/Pages/programs.aspx It took about a week and they have approved me to receive the medication and are shipping it to my home.

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.

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

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.

This is my understanding of the patient assistance programs for Incivek. The list price, which no patient will have to end up paying, is $49,200 for 12 weeks. HOWEVER, the patient assistance programs, are more than generous. Typical Co-pay for the three prescriptions that will be needed will be between $50 and $250 each.

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 changed to Humira recently and was wondering if anybody has had success with humira who has ankylosing spondylitis. Any feedback would be appreciated.

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?

Humira patient assistance

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