norvir copay

What is your doctor thinking? Is this an HIV Specialist? Are you multi drug resistant? You say your combo is Combivir : which is AZT and 3TC Truvada : which is Viread and Emtriva (which is almost identical to 3TC and should not be taken together) Viread : which is already in the Truvada! Prezista : which is a PI that MUST be taken with Norvir which you aren't on!

Initial counts were 423 viral load (not thousands - just 423) but T cell was 398. Immediately went undetectable. Put on Fortavase, Combivir, Norvir. Soon switched to just Fortavase 8 bid, combivir 1 bid. over time decreased to just 1 fortavase bid and 1 combivir bid. Been up in 700 - 900 T cell the whole time. No one can explain to me why numbers were odd to begin with. Also now that fortavase is off market my doc wants to switch me to Invirase, Combivir and Norvir.

The only side effects ill have in the soft stool from time to time, the tingling feeling in my hands and feet from the norvir this too is from time to time, they say the norvir also has gastro effects, I know when it will kill someone....lol.... As of last month my t-cells were 945. I have been positive for 5 years on meds for 4years...

I have a bcbs ppo and was supposed to have a copay at my first visit, but since I'd already paid a bit out of pocket they said it was covered

I started taking PEP on august 4th. I take truvada norvir and reyataz. I went to get a rapid antibody hiv test today and was negative. Should I still be worried and stressed? I haven't slept much since this happened.

I recently started the Norvir, Reyataz, Truvada combo. This is my first time taking "the meds" after being hiv + for 20 years. I have been on them for only 11 days. I have weird side effects: headaches, queasy stomach, and fatigue/weakness. I told my doctor, and he said, to "tough it out for another week, and he'll see if he needs to change the combination, or switch meds.

I started PEP 2 hrs later (truvada, norvir, raltegravir, and preszita), my initial results are negative. I do not know the viral load of the patient yet, i can only pray that it is low. I know odds are 0.3% but that doesnt settle my fears, i am young and want to live a happy healthy life with KIDS! DR. please tell me if you have honstly heard of any cases like mine that have converted. I am in awe and feel like my life is totally over and ruined.

Handsfield, I have started with antiretroviral therapy in April this year after my cd4+ further declined to 480 and viral load remained very high at 800,000 even after 6 months after exposure. I am currently on combination of Truvada, Prezista and Norvir which I take regularly every 24 hours. I feel much better than before meds, from time to time I have soar throat, nothing serious though. I didnt notice any significant side effects except temporary diarrhoea.

I was diagnosed with HIV in 2006, I was 26 years......I was at 129CD4 count.......When I started feeling sick I started treatment. I got all the way up to almost 500CD4 count....I was undetectable for 5 years until now docs were like wow! I went into the hospital back in Feb of this year for some kidney infection that the doctors was confounded about how I got and my CD4 was 2something and viral load 500+ AFTER 5 YEARS UNDETECTABLE!. Kidneys got clear & I left....

I went to the doctor and they tested me. I was negative. They gave me some medicine called truvada norvir and reyataz.They told me to come back August 28. The woman also told me she was undetectable and said her viral load is extremely low. I went with her to her doctor and her doctor did confirm that. What are the chances I have it? I am very scared to death right now.

been positive since 1988, maybe even earlier, didnt start on meds till 2007. Norvir, truvada and reyataz are my friends. My cd4 is 700 and viral load is undetectable. very fortunate to have meds at my disposal. I would advise folks who are positice,please take your meds.

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?

4 I have a compromised immune system and am on truvada, norvir, and reyataz. I have been walking and watching my intakes... I do have a sweet tooth sometimes but otherwise I eat pretty healthy. any ideas?

someone said Shared Solutions would help but I have not yet approached them. You might try calling them.

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?

m finding that so many of these drugs have special offers on their websites to help cover the copay cost. Big Pharma definitely wants us using their pills.... If you have a name brand drug you are using, be sure to look at their websites to see what special offers might be going on. I just started Restasis last week and they have all sorts of incentives/rebates to use their eyedrops.

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

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?

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!

Just to add Giliead pharma has be providing copay assistance so your copay would be just 5 dollars if you have applied for this with Giliead they have other support also you may want to visit their site. https://www.harvoni.com/support-and-savings/co-pay-coupon-registration?gclid=Cj0KCQjwyvXPBRD-ARIsAIeQeoGwAmTRV7zDZKKTTcjYh2WVswO7ySJ6vpO4-IUr92XCIul6QBfQXQUaAj1aEALw_wcB Best of luck hopefully you won’t have any issues getting approved.

I have been on the Lidocain patch for a few years and at my last PM visit he suggested the Lidocain cream 1%. My copay on the patch was $50 month and my copay on the cream $5 so I am using the cream which actually works better as I can apply the cream to my low back myself where the patch not so easy.

Some insurance policies cover the riba under their Rx plan but put the IFN into major medical, sometimes requiring 30% copay. That happened to me, and while I paid the first time out of pocket, the second treatment I went through the mfgr’s patient assistance program; they paid for 100% of both meds, with no copay or deductible to meet. Also, these drugs often require prior authorization; sometimes that can take a week or more to arrange.

I will not receive 1st month until Jan after copay help goes through. Rbeth did you have a super high copay from Optum? Yes the spec pharmacy was supposed to request assistance but never did, after weeks of waiting my Docs office complained and got immediate results. Upset1234 as far as I know CVS still covers Harvoni.

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