started clinical trials out of st. Pauls hospital in Vancouver BC
I take the teleprovere 3 tabs 3xday and ribavirin 200mg 2 tabs 2x day
and Peg interferon 180 1x week ..its free my enzyme has dropped from
50 in one month and they pay me to do it ...Canada Rocks ....
Booze is out but got a per for pot and went to the legal dispensary and scored some Killer BC purple Kush 10 bucks a gram and legal ....gotta love it here ..
I'm in the US and just started treatment. I have the Pegasys 180 shots once a week, plus the ribavirin 200mg (3) twice a day plus teleprevir, (2) 375mg tablets three times a day. I'm a Veteran so my medical has been free and thank G-d for that. The teleprevir is $400.00 a day. My doc told me every time he writes me a month's script for the teleprevir, it's like giving me a brand new Toyota Corolla...$ 12,000.00 a month.
http://en.wikipedia.org/wiki/Clinical_trials
http://clinicaltrials.gov/ct2/search
The first link will explain what a clinical trial is, the second is where to search for a clinical trial that fits your needs. (condition, location, ect)
what is clinical trail studys for Hep-c?
drugs in the states are the most expensive in the world , you guys get ripped of because of the insrance scams
one month of interferon is $600 in the uk
Yes, we have a few kinks in our medical system left to work out :o). In the U.S., drug manufacturers provide patient assistance programs for those that can’t afford the cost of meds; this includes uninsured as well as underinsured. Our problems are with the providers; without insurance, we can’t access doctors to prescribe or manage our care.
Hopefully, we (the U.S.) will eventually learn from other developed nations and provide universal health care for our citizenry as well some day. Things are changing here, but ever so slowly…
Thanks for your thoughts,
Bill
Mine was $1200/month...You want to see something REALLY expensive? Neupogen and erthropoietin (rescue drugs) are about $6000/month...Yikes, huh? ~MM
Picked up my first months supply of Inteferon and Ribavirin for $5.40. I was surprised as scripts have increased by a couple of dollars since the last time I needed some meds(a couple of years ago). I really feel sorry for those in the US that need this treatment.
What happens if you are broke do you just do without? If so, that is just wrong.
my insurance covers with a small copay , but I asked the pharmacy because I was
interested in some extra back up
I was quoted $2600 for Peg and $1500 for Riba per month.
Needles to say I am not getting extra meds from the pharmacy.
I was diagnosed with HCV 1A December 2008. I am very blessed I was able to get into a "CLINICAL TRIAL" study. I take Pegasys 180mg once a week, and Ribavirin 1200 mg (3 in morning, 2 at night)....all my medications, doctors visits, EKG's, eye exams, and all lab work are paid for. Also because I have to drive about 5 hr's to the "CALIFORNIA PACIFIC MEDICAL CENTER" in San Francisco they also pay my gas for travel. Although I am sick from the normal side effects of basic treatment all the medication is working fantastic. Also because I am in a "Clinical Trial" I am monitored very close, much more so then if I were just on regular treatment.
C.A.M ... in California
Thank you bill for the information its a great help to me since im new at all this. God bless you
Hi Leslie,
The manufacturers of the drugs for HCV provide patient assistance for those that are uninsured, or underinsured; call whichever number is pertinent to your treatment:
Pegassist (Roche Pegasys system): 1-877-734-2797
Commitment to Care (Schering- Plough PEG-Intron system): 1-800-521-7157
Good luck—
Bill
Iwas just dx with chronic hep c im supposed to see the Dr on 08/18/09 to start treatment i do not have any insurance and i see the cost of the meds are very expensive, Any advice for me please im desperate and i want to get well. My email address is ***@****. Thank u and may god bless everyone.
I was diagnosed with Hep C last year (Aug. 2007). I finally found a doctor to take my case, have been getting vaccines against Hep A and B through this past year [they have to be spread out]. My doctor no longer follows patients through 'treatment'. My recent focus has been to locate a nearby source to 'oversee' my treatments...today I learned I have found one. My online 'searching' gave me an education as to what seems to be the current [good results] 'cocktail' of Pegyasus and Ribivirin. Because I'm on Social Security Disability, and have Medicare and Blue Cross Blue Shield (supplement) insurance, and am in the 'low income' group, my Pegysus co-pay will be (max) $5.60 a month (for four shots - 1 per week) the no insurance cash cost for it would be $2,064/mo., the Ribivirin co-pay will br $2.25 (I don't remember what the 'cash cost' would be) Hope this helps. God Bless
I am so lucky. MY co pays were $20.00 each. The Ribavarin I could get a 3 month supply for $40.00 . Pegasys I could only get a month supply at a time. I found it interesting that no one mentioned the programs supposedly available by Roche Pharmaceutical. I have read and heard several times that if a person is unable to afford the medication for tx to call. I FOUND IT!!!!! If you knew how crazy my life has been you could really appreciate my last statement. Anyway it states if you cannot afford tx to your case managerabout medication costs. If you qualify we may be able to assist you financially. I know not everyone has a case manager and I iknow at 2 or 3 people are saying hey. The qualifications are probably so rigid I could meet the qualifications. If you do not have a case manager how is aware of this program I would suggest asking your pharmacist for the number. (It was a pharmacists that referred to another pharmecitical company. I had ins but they refused to pay for the specific med I was ordered. The company wrote my doctor and my insurance company. It approved for me at my regular copay. You never lnow if you do not check it out. I see this was more of an experiment to see response so I hope my info will help someone out there.
The real cost for me (without insurance) would have been $2,500 a month. With my insurance, I pay only $15 a month. Thank goodness for my insurance! I'd say your insurance is great too if you can get by with paying $40 a month.
guys, Can anyone tell me if these costs you are paying are with or without insurances? Because i just called my insruance, and they said, i only have to pay $30 for Pegasys for 34 days and $10 for generic ribavirin.
Thanks,
In canada there is a govt program that even pays for the co-pay...ITS called TRILLIUM
Mine was only $25/Mo (including both my pegasys and my ribavirin). Of course, that doesn't include the myriad of co-pays I shelled out to deal with my sides.
does anyone pay as high a co pay as I do? I have Blue Cross full coverage & I am considering asking my doctor to change the ribavarin prescription to generic. While $110.00 is not astronomical, I am feeling the economic pinch like everyone.
I wasn't certain ;)
But it was kind of instructive to see what different folks are paying in terms of their co-pay anyway.
That's hilarious! I did not know that. I missed that part.
Folks - we know that this is in response to a thread started in 2004, right?
the BOC trial even supplies the rescue drugs.