maxalt patient assistance

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.

t mean to interrupt but I am actually a pharmacist and thought I could clarify the maxalt questions.... Maxalt is not a beta blocker. It is a 5HT1B receptor agonist. Basically it's a triptan drug that is used for vascular migraines. Vascular migraines cause vasodilation of blood vessels and that dilation causes pain. Triptan drugs cause vasoconstriction of those blood vessels and thus reduced the pain caused by pressure.

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 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.

She proclaims that she diluted and injected her migraine medicine (Maxalt) because she keeps throwing it up. Her symptoms, however, where those of an opiate overdose....blue hands and face, low respiration, eyes rolling backwards, staggering, tremoring arms upon waking up, disorientation, etc. Does anyone know what the side effects would be of injecting maxalt? I find this impossible to believe that it would knock her out and turn her blue.

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.

does either imitrex or maxalt contain caffeine? I was taking Maxalt for migraines and it worked great! Now my insurance has decided I need to try Imitrex before they will approve coverage for the Maxalt. The Imitrex took about 2 hours to have any effect, but eventually my headache subsided. Since then I have had recurring headaches for 4 days.

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?

My question is, are these rebound headaches from the Maxalt? I use the Maxalt no more then once to twice a week. This could also be sinus headaches too, I'm not 100% sure as I feel pressure in my head also. Is it okay to take the Maxalt 1-2 times a week? I also have a spinal cord nerve injury and I do take the long acting oxycontin every 8 hours for the pain.

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.

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.

They have been increasing in quantity and severity until about a year and a half ago I had to stop working completely. I am on a combination of darvacet, tramadol, topomax and maxalt. The combination leaves me in bed about 18 hours a day. I have had two MRIs. One with contrast and one without. Neither shows any good reason for my pain. The headache never goes away and I have no idea what makes it hit so hard every few days (room blacked out and crawling to the bathroom). Am I the only one.

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.

My friend had called me and I told her that I was too sick to talk and that I had run out of my Maxalt. My friend is a life saver! When she got off of work, she picked up my Maxalt and brought it to me. She also brought me some hot dogs, chips and pop because I had nothing to eat in the house. Hubby left on Wednsday and took the kids up to the cabin, so I've been here alone. I thought that was extremely nice of my friend to go and do that for me.

When I was having frequent migraines and my insurance would only pay for one refill of Maxalt each month, I obtained prescriptions for both Maxalt and Relpax and filled both each month. They worked equally well for me.

d have trigeminal neuralgia, tinnitis, one eye would blur, and he often lost the hearing in one ear. And then the global head pain would come on. All abortive medications except Maxalt would fail to work, and even Maxalt didn't work all of the time. His attacks would last hours to days, sometimes bad enough that he was vomiting and suicidal from the pain level.

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.

Maxalt patient assistance

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