solodyn 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.

I'm wondering if there's any research supporting a link between solodyn and eye floaters. I was on Solodyn for about 2 months and my vision deteriorated over the same period of time. I have pretty severe floaters that distract me in reading and computer use. Previously a little farsighted but not requiring glasses. Optometrist says the back of my eye looks like "a spiderweb." No retinal detachment, glaucoma, cataracts, etc.

no results Abt two months ago, I was prescribed Solodyn, I use neutrogena creamy wash, Retin-A and some hydroquinone for the dark spots. The solodyn make me break out in a HEAP of HIVES !! so I stopped taking it about 3 weeks ago and now I have been prescribe Bactrim? It seems that antibiotics are the ONLY thing that cure my acne since I have really oily skin. The topicals dry it out in the beginning, and I only apply a little, but then my sebaceous glands quickly make up for the lack of oil.

I just found out that I am 6-7 weeks pregnant and I took Solodyn 115mg for the first month of my pregnancy! I am really scared that this might have harmed my baby. All the websites say to avoid becoming pregnant while taking Solodyn because it has been shown to cause harm to the human fetus. Has anyone been in this situation?

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.

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 have also been on Doxy 100 Mg for about a month now because of bacterial follicilitus on my thighs which does not seem to be working. My derm has put me on Solodyn now, I'm just wondering what test I should take to test for Lyme and if I should stop taking my antibiotics to test for it. Please help.

I saw a dermatologist and he said that it was folliculitis and prescribed me solodyn (minocyciline). The sores on my lips usually last a week, but I usually pop them and they are sore, but no blood or pus comes out. They heal and have dissapeared, but for a little redness that you can't really see unless you look closely in the mirror. Is there still a chance that this is herpes?

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?

If someone had hiv would it take two years or could it have been a reaction to the medication solodyn which does have a side effect of joint pain. I have been tested several times since that encounter and my hiv test even up to febuary when I got sick was negative and the three previous tests before that were negative.

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.

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.

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.

If you go on tysabri, or any other drugs, be sure and get on their patient assistance program. It is great help with the co-pays.

I am searching out any possibilities for financial assistance for a patient with multiple nonunion compression fractures of mutliple thoracic vertebra the worst being T6. His care includes Fentanyl 100mcg/hr patches being changed every other day. His insurance has lapsed and the pain in unbearable. What financial assistance is out there for this patient? I need any and all leads as it is imperative that he get contunuance of his relief as his family has sacrificed everything.

Solodyn patient assistance

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