Arava patient assistance

Common Questions and Answers about Arava patient assistance

arava

Avatar m tn 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.
Avatar f tn She says that I am a sero-negative ra patient. My concern is that I am not totally convinced that I have ra. I know I have all the symptoms and do get worse when I am off of my Arava but I also wonder if I could have Lupus because I have a lot of the symptoms of it and my sister has it. My mother has fibro so I wonder if maybe that is what I have instead as well. Things are continuing to get get worse and my dr is wanting to start injection therapy for my symptoms.
256161 tn?1196879046 0) I was wondering if anyone here has taken Arava (Leflunomide) and their side effects? I started it almost 3 weeks ago for the RA and Sjogrens and have started to have nausea, hair loss, skin sensitivity, burning or tingling of skin, and restless legs (already had, but much worse now), vivid dreams, and torso pain like a cramping sensation in back and sides. I have read too much bad stuff about this medicine and I am hoping someone has had a good experience with it.
Avatar m tn I have an Auto Immune Disorder of the connective tissue as labeled by my Rheumatologist. I take Plaquenil 200mg, and Arava 20mg daily. I have been on the Plaquenil for over a year and the Arava for 5-6 months. I am still having flares and experiencing pain on a daily basis. I'm a 28 year old male. My tested positive for ANA but the doctor hasn't labeled me with Lupus. I see my Rheumatologist on the 18th of December and I'm looking for the next step in my treatment.
Avatar n tn i take the leflunomide (arava) but also take pills for the reflux, which does help. I take renitidine i believe it is called. I found it worked pretty good for the swelling myself. I am also on the Embrel, but still do not have R.A under control. I just wanted to say that the arava was the best drug i have taken up until i was put on the embrel. I live in B.
199177 tn?1490498534 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.
Avatar n tn Have you tried xenazine ( chemical name is tetrabenazine)? We've also found clonex gives some relief.
158939 tn?1274915197 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?
Avatar m tn Peace be with you. While I am not a doctor, this is a patient forum, I may be able to provide some help. (The ask a doctor arthritis forum is located here http://www.medhelp.org/forums/Arthritis/show/101) Lefora is a brand name for leflunomide. This medication is classified as a DMARD, a disease modifying drug. There are other DMARDs that may be tried in place of Lefora. Examples would include Methotrexate, Imuran, Arava and Plaquenil.
Avatar n tn Prior to that she was on Arava for five months and it almost killed her. She lost 60 lbs, had heart issues, urinary tract infections, had no appetite and was incredibly weak. Her RA doctor said it was not the Arava. It was. I took her to the Lahey Cllinic and they confirmed it. I had taken her off the medication before going to the Lahey Clinic but it was a binding med. so it stayed in her system for months afterwards.
1622229 tn?1299050798 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.
Avatar f tn 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.
Avatar f tn Hi, I was recently diagnosed with psoriactic arthritis and the doctor put me on Arava. I've been on it for 4 weeks with no relief. In fact, the pain has increased in all of my joints and my toes have decided to join in on the fun as well. My question is has anyone had any experience with this drug in the amount of time it takes to start working? Is it usually immediate or does it take time to "build up" in your system before it begins to work?
Avatar n tn i am 22 years old..i have RA(still desease) from about 10 years, i have tried almost everything..metothrexate(didn't well work),arava(had a baaad effect on me!!),remicade(no improvement),humira(had it about 4 times but had lots of problems with purshasing it and without good effects also),and i had also a both replacement surgeries for my hips ..
1713494 tn?1327519682 Would your local mental health service have access to that information? Maybe whereever you go for governement assistance (financially) they may have some info. Have you tried a google search?
Avatar f tn Without the patient assistance program I probably wouldn't be SVR - when my insurance refused to let me extend, they coudln't have made it easier and didn't even make me feel bad about needing them to help.
Avatar n tn I am also on Copaxone - can I suggest that you talk with them again at Shared Solutions and ask what criteria they use for patient assistance? They fund for people without insurance or underinsured through NORD - national organization of rare disease. Unfortunately it sometimes takes more than one phone call to connect with the right people at SS to get help. If you can't work it out with SS you might talk to your neurologist about other options.
Avatar m tn If in need, call the Schering-Plough Patient Assistance Program at 1-800-521-7157 and/or the Roche Patient Assistance Program at 1-877-757-6243. November 10, 2008 http://www.hepatitis-central.com/mt/archives/2008/11/choosing_and_af.
Avatar n tn My pain hasnt been relieved totally with this med and the rheumatologist wants me to start on Arava in combination. Im scared of the hep c coming back with both of these meds. Opinions needed.
572651 tn?1530999357 There are so many drug assistance programs out there for us in the US who are not on medicare/medicaid or live in Massachussetts. I'm thinking it might be helpful to start a thread of some of these so everyone is taking full advantage of the drug companies' generosity. Ok, you know I'm being facetious with that comment - they want us to take their drug and are bribing us to do so by helping with the copay.