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Can anyone tell me if it’s normal to feel VERY TIRED from the drugs?
My observations are:
1) The closer people are to the edge the longer it takes to drag them back
2) The usual 1 week “a bit under the weather” on treatment initiation is more like 2-4 weeks in cirrhotics
3) Cirrhotic viral loads, enzymes and bilirubin take longer to come good, and platelets take even longerThe reality for some people is that treatment arrives too late to drag things back, and transplantation will still be required.
I have one patient like that. He was in ICU when we started treating him 6 months ago, and has no viral load, but his liver was/is so shot he’s now on the transplant list. Without generics he would have been on the casualty list.
YMMV
And if you added Sofosbuvir to this you do probably have the mythical PERFECTOVIR!
YMMV
So enough results are in, and out of embargo so now I can say what I was dying to say at the time, well actually…..
Generic Sofosbuvir + Ledipasvir delivers damn good SVR rates and we repeated a trial Professor Gane did (26/26) with Sof+Led+Riba in GT3 and got 13/13 = 100% SVR – please don’t get excited this was in treatment naive low fibrosis GT3 only and the +Riba was essential.
Here is the data: http://fixhepc.com/forum/media-news/914-easl-slides-94-4-svr4-overall.html
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Looking very flash indeed Am I able to share this photo on my FB to show all my friends these wonderful people or should I not?
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Although we are surrounded by the cone of silence maybe if we all shout really loud somebody will hear it!
Something like….
In the time it took to give this presentation another 15 of our fellow citizens perished from a disease we have the power to cure.
We have the power to FixHepC.
My question to you, the audience, is do we have the will power? The will power to think global, but act local, and see cure deployed on a mass scale?
…Or would we rather blindly protect patent rights at the expense of patient lives?
Generics work. We’ve already seen them work for HIV and now we can see that they work just as well for HCV, so let’s deploy them and wipe Hepatitis C off the face of the planet…. just like we’ve done with smallpox and polio
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That is an awesome post from Mister99. Any relation to Agent 99?
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Hi Joy Your link is “currently under maintenance” so I will have to read it later..
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Why not spread your remaining doses out and take them every 48 hrs. The meds have a 1/2 life of 27 hrs which means they stay in our system for many weeks at a reduced dosage.
Rationing is definitely the way to go, but rather than every other day (and provided you’re up for it) if you have a shortfall the best way would be to open the capsules/split the tablets in 1/2 and take 1/2 a dose each day. Not as good as a full dose every day, but much better than a complete break. Failing that every 48 hours is a good option.
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4 hours after you take your last dose you can take all the PPIs you like.
At this point you will have absorbed all the medication so….
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The Medicines Patent Pool Signs First Sub-licences for Hepatitis C Medicine Daclatasvir
Four companies to help speed access to curative direct-acting antiviral in 112 low- and middle-income countries
Geneva, 20 January 2016 – The Medicines Patent Pool (MPP) announced its first round of sub-licences for the generic production of Bristol-Myers Squibb’s daclatasvir, a novel direct-acting antiviral that is proven to help cure multiple genotypes of the hepatitis C virus. Generic companies Cipla, Emcure, Hetero and Natco have signed non-exclusive, royalty free agreements with Bristol-Myers Squibb and the MPP to produce and sell daclatasvir in 112 low- and middle-income countries.
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Since only 1 out of 4 was potentially fatal, I figured the odds were acceptable.
You have to admit in retrospect, it was a pretty big leap of faith….
Plus I had someone telling me they would give them to their mother…..
The “mum” test remains my moral true north.
I confess I took some of the API myself before I sent it to my patient zero. The tests looked good and it didn’t kill me so I figured it should be ok.
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I was warned off early on then it quieted down.
Recently there has been a substantial increase in the daily hacking spam and a lot more probing of websites with automated tools.
The issue for Gilead is that the genie is out of the bottle and the writing is on the wall. Nothing they can do now will negate the fact there are now thousands of generics patients on treatment or past EOT and into SVR and that a good chunk of those results have been collated.
Even if Greg and I conveniently fell under a bus there will still be 2 other authors at EASL who could present the results.
Historically HIV generic use only takes off with the publication in the Lancet in 2004 of a paper sponsored by MSF and conducted in Cameroon that demonstrated – surprise surprise – generic HIV medications work.
If you can make functional HIV generics it stands to reason you can do the same with HCV generics, but for that you’ll just have to wait.
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12 April 2016 at 5:12 am in reply to: US Patient with balls as big as Sean, Tina and Hazel required #15263Hi GF,
If you could send an email to Andrew that would be great.
Although I’m sure we will need someone stateside to put a face to it, even putting an anonymous voice to it – with a familiar accent – should help draw the US media in, so it would be great if you could speak anonymously about it.
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Daclatasvir will deal with the L31M RAV. Ledipasvir won’t. For my money Sof + Dac is the way to go.
If you want to add in I would consider Simeprevir or Asunaprevir to attack the NS3/4A side of things.
YMMV
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