neupogen copay assistance

Here are some patient assistance numbers from the mfgrs. I haven't used these in a while, so if one of them doesn't work for you let me know and I'll straighten it out: Pegassist (Roche Pegasys system): 1-866-422-2377 Commitment to Care (Schering- Plough PEG-Intron system): 1-800-521-7157 Amgen Pharmaceuticals (Neupogen) 1-888-762-6436 http://www.needymeds.org/drug_list.taf?

I've arranged to get the neupogen at the hematologist for the copay price of the visit. It worked out better that way for me, rather than pay the price through the specialty pharmacy. Explore what your insurance will cover and all your options. I believe there is also assistance for this if needed. Hopefully this won't be an issue for you.

Laura, aka Lulu54 mentioned that there may be copay assistance programs available. I went to the Genentech website and found a wealth of information about assisatance for payments associated with many conditions. None of these were MS. I have a call in to them. but sustpecty that since Rituxan for MS is off label there is no program at Genentech. Does anyone know of any fiancial assistance programs for Rituxan?

does anyone know of any copay assistance programs that would help with copayments .for my osteoarthritis?

Are there assistance programs out there to assist with cost of Neupogen if my Dx prescribes. I am on a basic health program and co-pay 50% for all meds.

They have copay assistance if you have insurance. They sent me a letter to reapply and the deadline for 2012 was December 5 2011. I am not sure if that deadline is for reapplying. You have to reapply every year. The Copay assistance is a separate arm of TEVA I believe not for profit. It is a limited amount per year of assistance. You send in your tax returns or pay stubs, etc. to show your income.

I think most of us will have insurance and pay a copay -- the highest, to be sure, but still a copay. I understand Vertex is not only offering assistance for those without insurance but they even have a program to help with copays for those who do. The Incivek website is here and you can contact there assistance here: http://www.incivek.

I have Blue Cross/ Anthem insurance but have a 30% copay for the injections and 40% copay for the pills, which will be about $900 a month out of pocket expence. since this is a non elective tretment i dont have a choice but to get the treatment, but i do need help paying for it. Is there any kind of program that will help me offset the copay cost for this program?

Vertex does have a copay help program which give a 20% copay help. After a 20% copay card from Verrtex, my out of pocket, roughly $14,000 for a 12 week treatment. I just cant afford this. Is anybody working on a drug coverage appeal for Incivek or have you found other means of assitance?

Does anyone know about any financial assistance programs? I'm in Arizona. My neurologist wants me to take Tecfidera and just found out that I'm not eligible to get the $10 copay because I'm on MEDICARE. Been on SS disability since 1992 and have take four of the injectables for MS. Had to stop all of them because of side effects.

if Rebif has been working you hate to make a change. There are very good patient assistance programs and like C wrote, they often bring the copay down to zero. I believe Rebif and Copaxone are about to fall off the list of drugs eligible for us in the UK on the NHS... they didn't feel the efficacy of the drug was worth the cost. One of the injectables fell off our formulary last year too, I think it might have been betaseron would no longer be covered.

Well I am again left hanging by Teva copay assistance. I went through being accepted to SS discount program never to have them come through. Then they suggested I apply for needs based through the Chronic Disease Fund in July they accepted me a day after I refilled even though I faxed in the paperwork asap. They would not honor it until my next three month refill in October. I sold my mother's gold necklace to pay the three hundred dollars.

I think my neupogen was about 40 a month.

Now if you need the helper drugs, neupogen and procrit, they have no copays either so you will pay your highest copay -- if your insurance company will cover them. Procrit may have a generic but I am not sure if it will be your lowest copays. You, my copay, for example would be 40+60+60 and another 60+60 if I need the helpers per month. That is just the meds. When I treated, my doctor appointments and labs all came under another copay with the doctor.

I looked on the blue cross blue shield web site and found I could have them sent to me through their preferred pharmacy for a $69 copay for pegasys and no copay for ribaviron. Hope my experience saves you a lot of money!! There's a number to call to get the fax number to give your doctor to send in the prescriptions. Welcome and good luck!

Neupogen copay assistance

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