trileptal 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.

My son takes Trileptal for his Epilepsy...(he is 16)...it's affecting his memory more and more; does anyone else here take this med and have similar problems? His dosage is 900mg/twice a day. Any lower dose and his seizures return. This has been the only med that has been able to control his seizures. He has frontal lobe epilepsy with seizures that only occured in his sleep (with a couple of rare exceptions). Thanks for your help.

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 started by calling the pharmaceutical company to inquire about assistance, but they have canceled their Provigil assistance program and also told me that depression is one of the few illnesses for which they do not provide assistance anyway. I then looked into other assistance programs, but they require enrollees to be without insurance, and giving up my health insurance is just not practical.

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.

Due to the severe burning sensation I have in my hands from my current MS flare up, my neuro has put me on Trileptal. I have read great things about this med in regards to TN but not much about peripheral nerves. Anyone have any experience with this med for burning sensation NOT on the face? Hope you all are well!!

The pain was an 11 on the 0-10 scale. Since the pain has only calmed down to a 7, my neuro added trileptal with the neurontin. The trileptal is being titrated and I'm at 750 mgs per day right now. Can anyone tell me at what dose of trileptal you got some relief from the constant crawling, burning, crushing type pains? Also does the side effect of nausea and just feeling crappy all over from trileptal eventually subside. I also have MS. Thank you.

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.

After 3 months, I am down to 900 mg of Trileptal, 2 mg Xanax, and 150 mg daily, down from 1800 mg daily of TRileptal originally, and a VERY slow introduction of Lamictal into my system. Of course this happens on the weekend, otherwise I would have called the pdoc by now-- anyway, let me know. Help is appreciated!

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?

I am on 900mg of trileptal and had a healthy baby boy in 2013. I am still on the same meds and currently 10 weeks preggo again. Good luck.

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.

in 2000 i was diagonosed with biopolor disorder i had my assorment of drug theropy i ended with a cocktale of trileptal, trazadone and lexapro when i found out i was pregnat in 2004. They took me off all my meds and have been med free until about 6 months ago when i went completely off the wall...They then put me on lexapro and ativan.. I went to a psychiotrist 3 weeks ago who took me off both of those meds and put me on Seroquel 150mg and trileptal 1200mg.

I am supposed to start trileptal this morning but worried about the side effects particularly dizzines. Has anyone had these symptoms? what are the likelyhood that I would become dizzy and nauseas while taking trileptal? I will be starting out w/ 150mg twice daily for 3 days then increasing?

Trileptal patient assistance

Common Questions and Answers about Trileptal patient assistance

trileptal